Abstract
Despite recent progress, ischemic heart disease poses a persistent global challenge, driving significant morbidity and mortality. The pursuit of therapeutic solutions has led to the emergence of strategies such as ischemic preconditioning, postconditioning, and remote conditioning to shield the heart from myocardial ischemia/reperfusion injury (MIRI). These ischemic conditioning approaches, applied before, after, or at a distance from the affected organ, inspire future therapeutic strategies, including pharmacological conditioning. Gasotransmitters, comprising nitric oxide, hydrogen sulfide, sulfur dioxide, and carbon monoxide, play pivotal roles in physiological and pathological processes, exhibiting shared features such as smooth muscle relaxation, antiapoptotic effects, and anti-inflammatory properties. Despite potential risks at high concentrations, physiological levels of gasotransmitters induce vasorelaxation and promote cardioprotective effects. Noble gases, notably argon, helium, and xenon, exhibit organ-protective properties by reducing cell death, minimizing infarct size, and enhancing functional recovery in post-ischemic organs. The protective role of noble gases appears to hinge on their modulation of molecular pathways governing cell survival, leading to both pro- and antiapoptotic effects. Among noble gases, helium and xenon emerge as particularly promising in the field of cardioprotection. This overview synthesizes our current understanding of the roles played by gasotransmitters and noble gases in the context of MIRI and cardioprotection. In addition, we underscore potential future developments involving the utilization of noble gases and gasotransmitter donor molecules in advancing cardioprotective strategies.
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Introduction
Coronary artery disease persists as a major contributor to worldwide mortality and morbidity, driving extensive research aimed at safeguarding the myocardium from ischemic damage. Ischemic preconditioning (PC), postconditioning (PostC) and remote conditioning (RC) are extensively studied adaptive mechanisms. These procedures involve brief exposure to ischemia/reperfusion, occurring prior (PC) to prolonged ischemia, at the immediate onset of reperfusion (PostC), or in a remote organ (RC), respectively, thereby initiating cardioprotection. Yet, pharmacological conditioning, achieved through specific drug administration, can mimic the effects of ischemic PC and PostC, providing an alternative approach to heart protection. Conditioning protection is evidenced by notable reductions in arrhythmias, decreased infarct size, and alleviated cardiac and endothelial dysfunction [e.g., see Refs. 24, 60, 61, 64, 67, 68]. While the cardioprotective benefits of ischemic or pharmacological conditioning strategies have been demonstrated across various species, including humans, the presence of cardiovascular risk factors, comorbidities, and associated medications (comedications) may disrupt cardioprotective signaling pathways [5, 44, 92, 154]. In addition, the potential cardioprotective effect of female sex, with differences possibly existing between pre- and post-menopausal women, should be considered. However, there is currently no evidence indicating sex-related disparities in infarct size and cardioprotection in pigs [93, 106].
Nevertheless, the precise cellular mechanisms underlying the cardioprotective pathways remain elusive in male and female, although several signal transduction cascades have been proposed. The initiation of cardioprotective modalities involves mainly the occupancy of specific surface receptors by various ligands, leading to intracellular signaling transduction, including redox signaling by reactive oxygen species (ROS) [7, 69, 144, 152], S-nitrosylation by nitric oxide (NO) and its derivatives, and S-sulfhydration by hydrogen sulfide (H2S) [5, 7, 144]. These modalities interact and regulate an integrated pathway, impacting one another’s function. Notably, enzymes may undergo phosphorylation and/or nitrosylation at specific or distinct sites, resulting in alterations in their activity. The cardioprotective pathways, namely the survivor activating factor enhancement (SAFE) pathway, the reperfusion injury salvage kinase (RISK) and the NO/cyclic 3′,5′-guanosine monophosphate (cGMP)/protein kinase G (PKG) pathway, were initially associated with ischemic conditioning [see Refs. 91, 93, 95, 226]. Enhanced understanding of these pathways holds promise for advancing cardioprotective strategies, including pharmacological interventions, in clinical practice. In particular, we outline the elements of RISK pathway involving intracellular mediators such as phosphatidyl-inositol-4,5-bisphosphate 3-kinase (PI3K), protein kinase C (PKC), mitogen-activated protein kinase (MAPK), glycogen synthase kinase-3β (GSK-3β), and extracellular signal-regulated kinase 1/2 (ERK1/2), as well as the SAFE pathway influenced by janus kinase-signal transducer and activator of transcription (STAT) pathways [24, 226]. Convergence between these pathways occurs at various steps but mainly on the mitochondria and, specifically, on the mitochondrial permeability transition pore (mPTP) [24, 60, 61, 226]. Indeed, these factors and organelles represent a direct or indirect target for various gases, which exhibit biological effects, and among them, oxygen (O2) and NO, along with their derivatives, ROS and reactive nitrogen species (RNS), are well known for their biological activities.
For approximately four decades, it has been recognized that our organism possesses an enzymatic apparatus capable of generating gases with distinct biological effects. Termed collectively as gasotransmitters, including NO, H2S, sulfur dioxide (SO2) and carbon monoxide (CO), these gases constitute a group of endogenous, highly reactive, and regulatory molecules. As we will see in the specific paragraphs gases play a crucial role not only as endogenous factors, but also in cardioprotection induced by pharmacological conditioning using exogenous gasotransmitters as well as noble gases. Indeed, noble gases, traditionally labeled as ‘inert gases’, have gained recognition more recently due to their manifestation of distinctive biological effects.
Here, we focus on the cardioprotective effects of gasotransmitters and noble gases, allocating only some discussion to the role of ROS/RNS. The cardioprotective effects of ROS/RNS have been comprehensively reviewed by our group and others, emphasizing the intricate signaling mechanisms involved in cardioprotection; for reviews on the role of ROS/RNS in cardioprotection, see Refs. [7, 69, 144, 152]. In addition, some volatile anesthetics are gaseous molecules known for their protective effects [12, 203, 229]. Specifically, this review aims to provide insights into the roles of gasotransmitters and noble gases in myocardial ischemia/reperfusion injury (MIRI) and cardioprotection, while also discussing potential future directions for developing agents that modulate these molecules for cardioprotective purposes. The literature search was performed using the PubMed databases, employing as keywords the distinct gases in combination with conditioning and cardioprotection. By curating recent (last 20 years) English-language publications, we present an overview of current research and anticipate innovative approaches to enhance the effectiveness and broaden the clinical applications of cardioprotection.
The vital gas, oxygen, in ischemia/reperfusion and cardioprotection: focus on supersaturated-oxygen (SSO2)
Given the vital role of O2 as a fundamental gas for life and as a component of certain gasotransmitters, it is necessary to acknowledge its significance not only for life but also for potential therapeutic applications. Therefore, before exploring the cardioprotective effects of gasotransmitters and noble gases in the context of MIRI and cardioprotection, we briefly discuss O2, considering both its essentiality and its detrimental or therapeutic paradox, such as the concept of SSO2 therapy.
The regulatory influence of O2 extends from embryonic ontogeny to pathological processes, making it a key participant in various cellular activities [112]. Oxygen is a crucial element for the survival of all mammals, playing a fundamental role in generating biological energy required by cells [112]. Fluctuating O2 levels influence cellular physiology, with evidence suggesting that variable O2 levels, rather than persistently low levels, pose the greatest harm [112].
The “oxygen paradox” arises from the dual role of O2 in both MIRI and cardioprotection [7, 144, 152, 203]. This paradox involves the harm caused by reoxygenation following ischemia, known as reperfusion injury, juxtaposed with the therapeutic potential of slow release of O2 [43, 133, 150] and gentle reperfusion [122] or super-reoxygenation [113, 190, 230]. In the context of ischemia/reperfusion, “compartment syndrome” refers to increased pressure within tissue compartments, impeding blood flow and causing potential damage [34, 110]. Although the term “compartment syndrome” is typically applied to peripheral muscle reperfusion injury rather than the heart, we employ it here to underscore the significant impact of edema on O2 delivery during reperfusion in the setting of MIRI [34, 48]. SSO2 has emerged as a potential therapeutic approach to mitigate MIRI-associated damage, particularly in addressing “compartment syndrome” [96, 230]. SSO2 is obtained through aqueous oxygen, creating a metastable saline solution with a higher concentration of dissolved O2 than the liquid carrier [191,192,193]. Catheter-delivered SSO2 serves as a pragmatic alternative to traditional hyperbaric oxygen therapy (HBOT) in critical care settings.
Research indicates that SSO2, similar to HBOT, assists in arterial vasoconstriction, addressing compartment syndrome without the risks associated with high gas-phase [O2]/tissue interfaces [191,192,193]. Preclinical studies demonstrate that intracoronary SSO2 infusion significantly reduces infarct size and the edematous area at risk in post-ST-segment elevation MI (STEMI) reperfusion scenarios [191,192,193].
The primary mechanism contributing to SSO2-induced cardioprotection is the acute improvement of microvascular flow, leading to the normalization of left ventricle ejection fraction [193]. SSO2 facilitates gradual reperfusion at relatively low pressures, reducing microvascular damage compared to abrupt reperfusion [177, 178]. The hyperosmotic effect of hyperbaric dissolved O2, coupled with reduced capillary hydrostatic pressure, aids in removing edema fluid through Starling’s principle, interrupting the cycle of MIRI and microvascular responses [177, 191,192,193].
SSO2 also addresses the inflammatory responses associated with MIRI, as evidenced by reduced myeloperoxidase levels in animal models [86, 191]. The resolution of the “oxygen paradox” is attributed to SSO2’s positive effects on microvascular flow, improvement of left ventricular function, and reduction of infarct size [10, 190]. The time course of SSO2-induced improvements, including the reduction of precapillary resistance, remains to be elucidated. In summary, SSO2 shows promise as a therapeutic intervention in MIRI scenarios by effectively addressing oxygen-related complications and inflammatory responses. Hence, here we see “the paradox of paradox”: the detriment posed by reoxygenation following ischemia (i.e., reperfusion injury), are counteracted by the therapeutic potential of SSO2. Alternative experimental strategies to mitigate the adverse effects associated with the oxygen paradox include stuttering and slow reperfusion [177, 183], or controlled O2 release by oxygen-loaded nanodevices. These nanodevices can act as biocompatible drug carriers, enabling the gradual release of O2, potentially along with therapeutic agents [43, 132, 150] (see also “Nanodevices to deliver gases”).
While preclinical and some clinical evidence suggest the potential improvement of MIRI with SSO2, it is essential to consider the implications of hyperbaric oxygen therapy, which may exacerbate heart failure [174], and it is advised to avoid hyperoxia in cases of chronic cyanosis [121]. Moreover, a meta-analysis has revealed weak and inconsistent evidence, along with modest statistical power, regarding the safety and efficacy of oxygen therapy [88]. Therefore, caution is warranted in the use of O2 in these contexts. Adequately powered studies are imperative to gain a better understanding of the role of SSO2 in patients undergoing coronary revascularization.
Biological gasotransmitters
The intricate signaling pathways in which gasotransmitters—CO, H2S, SO2 and NO—are involved represent a multifaceted network of interactions characterized by the high reactivity and diffusive capacity inherent to these gaseous molecules. The intricacy of these pathways stems from both their chemical properties and the diverse cellular responses they modulate in the dynamic cardiovascular environment.
Gasotransmitters are versatile signaling mediators. They play a pivotal role in orchestrating cellular reactions critical to the complexity of cell physiology and pathophysiology, including MIRI [9, 112, 200, 220]. Their presence is integral to the delicate equilibrium between the potentially detrimental effects of ischemia and reperfusion. For instance, as signaling molecules, CO, H2S, SO2 and NO engage in a sophisticated crosstalk with cellular components, influencing vasodilation, inflammation, apoptosis, and oxidative stress [87].
The high reactivity of gasotransmitters and the capacity to rapidly traverse cellular membranes facilitate their widespread influence on various cellular components. Their diffusive capacity enables them to permeate tissues and reach subcellular compartments. Indeed, gasotransmitters, as well as derivative, ROS and RNS, are considered among the major factors involved in signaling pathways regulating mitochondrial function involved in cardioprotection [113, 200, 220].
As researchers explore gasotransmitter-mediated cellular responses, we expect this summary to be a valuable resource for understanding the complex dynamics involved in cardioprotection. A summary of the experimental studies on gasotransmitter-induced protection can be found in Tables 1, 2, 3 and 4.
Nitric oxide and cardioprotection
The importance of NO in both normal physiological processes and pathological conditions is well established. However, for a more in-depth understanding of its various roles, readers are encouraged to refer to recent reviews that offer comprehensive insights [3, 6, 7, 85, 153].
Sources: The synthesis and primary metabolic pathways of NO are extensively discussed elsewhere [9, 26]. In brief, endogenous NO is produced enzymatically through the conversion of l-arginine by a specific group of enzymes known as NO synthases (NOSs). These NOS enzymes, which exist as homodimeric oxidoreductases, are expressed constitutively in various cell types. Neuronal NOS (nNOS), inducible NOS (iNOS), and endothelial NOS (eNOS) are expressed by various tissues; therefore, they are also called NOS1, NOS2, and NOS3, respectively [3]. In particular, iNOS and nNOS highlight the involvement of novel cellular actors in cardioprotection. Various cell populations, such as immune cells [4] and pericytes [39], appear to play a role in the cardioprotective capacity of NO and other gasotransmitters (Fig. 1). In addition to these cells, emerging evidence highlights the significant role played by erythrocytes in mediating NO protective effects. Erythrocytes contribute to NO bioavailability and signaling pathways, thereby exerting a notable influence on cardioprotection against MIRI. Nitric oxide can also be generated in tissues through either direct disproportionation or the reduction of nitrate and nitrite to NO under acidic and highly reduced conditions that are present in disease states like ischemia [70, 94, 117, 119, 223]. Actually, during myocardial ischemia, NO synthesis increases independently of NOS pathways, impacting outcomes via concentration-dependent mechanisms [70]. Endogenous NO favors myocardial hibernation during ischemia by reducing O2 consumption and preserving function, thus preventing necrosis [117].
Cardiac protection: Recent progress in unraveling NO’s involvement in cardiac biology has highlighted its crucial role in defending against MIRI [6, 7, 9]. The cardioprotective effects of NO are not solely induced by “conditioning” mechanisms. For instance, upon β-adrenergic stimulation, the nNOS, which is bound to ryanodine receptors in the sarcoplasmic reticulum, modulates NO levels, facilitating calcium release and controlling inotropy [49] (Figs. 2 and 3). Therefore, NO plays a pivotal role in safeguarding the β-adrenergic-mediated heart function regulation. Moreover, NO influences the calcium release through S-nitrosylation, modulating key proteins, such as calcium channels. Inhibition of nNOS by superoxide (O2(−)) as well as by peroxynitrite (ONOO(−), formed by the reaction of NO with O2(−)), hinders β-adrenergic stimulation, impacting calcium release and consequently cardiac inotropy [28, 55]. Altered NO levels and increased O2(−) result in nNOS uncoupling, and blocked phospholamban phosphorylation. The formed ONOO(−) affects cardiomyocyte action potentials, induces lipid peroxidation, and damages mitochondria. Moreover, ONOO(−) influences cardiomyocyte function through the effects on sarco-endoplasmic reticulum calcium ATPase (SERCA). Indeed, elevated ONOO(−) levels promote calcium sequestration via SERCA, affecting cardiomyocyte relaxation [15, 35]. Nitric oxide actively contributes to protection induced by various factors, such as physical exercise [42, 147] and the stimulation of β3-adrenergic receptors [126, 159]. In particular, nNOS exhibits cardioprotective effects during exercise by modulating O2 consumption. Endothelial NOS contributes to cardioprotection by inhibiting the β-adrenergic response through the regulation of the L-type calcium channel. During exercise, the increased ratio of eNOS dimer to monomer, coupled with reduced peroxynitrite levels, promotes eNOS dimerization and activation, further enhancing cardiac protection [40, 41, 124, 208]. During exercise, iNOS levels are low, while elevated levels are induced in reactive hypertrophy through various signaling mechanisms. Increased levels of NO during exercise enhance mitochondrial O2 consumption, regulated by angiotensin II in cardiomyocytes. Notably, cardiomyocytes control NO diffusion and compartmentalization, with heme-centered proteins such as cytoglobin and myoglobin scavenging locally released NO, thus regulating this gas diffusion within the heart [57, 58].
Conditioning: In simple terms, the previously mentioned cardioprotection protocols (namely PC, PostC and RC have revealed cooperative and protective signaling pathways, including the RISK, SAFE, and NO/cGMP/PKG pathways [46, 166,167,168, 183] (Fig. 3). These pathways involve phosphorylation and dephosphorylation mechanisms with various kinases, including NOS. Furthermore, redox-dependent protective pathways are implicated, where ROS, S-nitrosylation by NO, and NO derivatives such as nitroxyl (HNO) play integral roles [113]. Therefore, NO participates in signaling cascades by activating enzymes such as guanylyl cyclase (GC) and it functions as a key element in redox signaling, engaging in reactions with O2(−) and sulfur groups.
The NO molecule plays a central role in initiating and mediating the late phase or second window of protection in ischemic PC. The cardioprotective effects of NO are particularly intriguing for the iNOS, which also displays a role in protecting the mitochondria. Actually, iNOS is primarily involved in inflammatory responses and reactive hypertrophy in the heart, but it is also involved in the second window of ischemic PC [142]. This has been demonstrated in both ischemic PC and pharmacological cardioprotection [85, 142, 195]. The widely accepted idea that increased iNOS activity in the later phase of PC enhances NO availability reinforces iNOS as a protective protein against MIRI. Yet, excessive NO production and iNOS expression and uncoupling were observed in cardiac allograft rejection, suggesting involvement of NO and O2(−) in tissue injury through ONOO(−) formation [2]. Despite limitations in current approaches, studies indicate that NO scavengers may extend acute cardiac graft survival by limiting NO’s actions and treatment with NOS inhibitors improved cardiac injury significantly [156]. However, the precise role of NO and NO/O2(−) ratio in organ rejection is still debated, necessitating further research on their effects on different cell types.
It has been suggested that NO interacts with elements of the electron transport chain (ETC) and/or the mPTP to alleviate post-ischemic myocardial damage (Fig. 2). However, the precise molecular events of this action remain elusive. Nevertheless, this interaction with mitochondria offers a fundamental molecular explanation for the mechanism behind NO-mediated cardioprotection, emphasizing NO as a common mediator of protection across various interventions against myocardial ischemia and reperfusion [6, 7, 153]. A comparable protective function is attributed to PostC, with both protection (PC and PostC) being hindered by the NOS inhibitors [81, 108, 151].
As seen above and summarized in Fig. 3 and Table 1, within the heart, NO plays a pivotal role in various signaling pathways involved in cardioprotection against MIRI. However, there is contradictory evidence that endogenous NO is involved in ischemic PC. For instance, endogenous NO did not alter infarct size development and was not implicated in the protection against infarction through classical ischemic PC in rabbits ex vivo [123] and pigs in vivo [158]. These findings underscore the complex and context-dependent nature of NO's cardioprotective mechanisms. It is also useful to differentiate between the NO that exerts cardioprotective effects within the heart and the NO that circulates in the form of cardioprotective, bioactive plasmatic nitrite. Circulating nitrite deriving from remote site contributes to cardioprotection by ischemic RC [166,167,168, 202]. These studies evidenced that circulating nitrite serves as a significant source of NO with cardioprotective properties. Furthermore, as highlighted erythrocytes contribute to the bioavailability of NO through the reduction of nitrite [51, 52, 201]. These distinct sources and mechanisms underscore the multifaceted nature of NO-mediated cardioprotection.
Pharmacological conditioning: Notably, drugs such as angiotensin-converting enzyme (ACE) inhibitors, statins, and angiotensin-receptor blockers, which boost NO levels, show benefits in mouse models of myocardial infarction (MI), supporting the potential importance of NO in conditioning cardioprotection [46, 100, 149, 150, 179]. Undoubtedly, the endothelium serves as the primary source of NO, yet its role in MIRI has often been overlooked, although the coronary circulation and endothelial dysfunction are implicated in MIRI as both causes and targets [65, 66]. In light of this, the replacement of endogenous NO with NO donors holds great promise in these conditions. Preclinical studies have unveiled various mechanisms of coronary microvascular injury that can be addressed through ischemic and pharmacological conditioning, suggesting potential clinical translation to enhance patient outcomes in MI [for reviews see 65–69]. When NO or HNO are administered before ischemia trigger protective responses similar to ischemic PC [113, 143, 198, 207]. For instance, the administration of exogenous NO, such as S-nitroso-N-acetylpenicillamine, demonstrated a beneficial effect in reducing infarct size [123]. In addition, the diethylamine-NO donor has been widely used as preconditioning mimetic [113, 143]. Moreover, the donors of HNO, a sibling of NO, are gaining recognition for their pharmacological attributes, which encompass offering functional assistance to failing hearts. In addition, HNO demonstrates the ability to precondition myocardial tissue, safeguarding it from MIRI, and exhibits actions that counteract vascular proliferation [113, 143, 200, 220].
To sum up, NO and derivatives have a plethora of targets, but the protective impact of NO and HNO operate mainly through mitochondria, interacting with different components of the ETC, mitochondrial ATP-sensitive K+ (mitoKATP) channels, and elements of the mPTP [78, 104, 150]. These interactions significantly reduce MIRI (Table 1).
Hydrogen sulfide and cardioprotection
In addition to NO, H2S is regarded as a cardioprotective gaseous mediator.
Sources: At least, three enzymes in mammalian tissues produce H2S endogenously from cysteine. Actually, endogenous H2S is generated through enzymatic or nonenzymatic routes within mammalian tissues [14, 18, 145, 221]. Key enzymes involved in this process include cystathionine γ-lyase (CSE) and cystathionine β-synthase (CBS), both utilizing homocysteine as a substrate. In addition, 3-mercaptopyruvate sulfurtransferase (3-MST) can catalyze H2S synthesis in conjunction with cysteine aminotransferase (CAT). CSE exhibits localization in the kidney, liver, vessels, and heart, CBS is found in the central nervous system, and 3-MST is expressed in the liver, heart, brain and kidney. The catabolic pathways of H2S involve: (a) oxidation to thiosulfate catalyzed by mitochondrial thioquinone oxidoreductase, S-dioxygenase, and S-transferase; (b) generation of methyl mercaptan and dimethyl sulfide through a reaction catalyzed by cytoplasmic thiol S-methyltransferase; (c) interaction with methemoglobin leading to the production of thiol hemoglobin [7, 10, 106, 168].
Cardioprotection: Apart from ischemia/reperfusion injury, heart failure, hypertrophy, fibrosis, myocardial infarction, arrhythmia, and several physiological and pathological processes have all been shown to be prevented by H2S. Its cardioprotective effect may be attributed to mechanisms such as NO interaction, ion channel regulation, antioxidative action, mitochondrial function preservation, apoptosis reduction, anti-inflammatory responses, and angiogenic actions [6, 7, 9, 20, 114, 170]. Despite identifying multiple mechanisms, additional research is necessary to determine the precise molecular mechanism of cardioprotection in various cardiac diseases to open the door to novel therapeutic targets based on H2S production and/or modulation.
Conditioning: During MIRI, the plasma level of H2S and CSE in the myocardium are reduced, while the mRNA expression level of CSE is increased following reperfusion, which contributes to a sort of positive feedback. Indeed, in KO model for CSE oxidative stress and MIRI are exacerbated [89]. In rodents, conditioning protection is mainly mediated by the RISK and SAFE pathways (Fig. 3), activated at the onset of reperfusion [87, 89, 118]. Findings indicate that naturally elevated levels of H2S act to safeguard the heart against MIRI, suggesting their potential as significant therapeutic targets.
Pharmacological conditioning: The majority of studies on this gas considered exogenous donors (Table 2). The administration of different H2S donors before reperfusion reduces infarct size and the plasma level of troponin-I significantly in MIRI mice [89]. Pretreatment with H2S, acting as a modulator of an ERK1/2-dependent pathway, also reduces endothelial cell death in vitro [235]. The protective effect of H2S is reported when the administration is either before (PC-like) or after (PostC-like) prolonged ischemia [5,6,7, 9].
In a porcine model, H2S treatment significantly improved hemodynamics, reduced infarct size, and displayed anti-inflammatory effects, suggesting potential therapeutic utility in clinical settings encountering MIRI [189].
Besides the influence on RISK and SAFE pathways, the cardioprotective effects induced by exogenous sodium hydrosulfide (NaHS) depend on mitochondrial ETC enzymes and also lead to mitoKATP channel opening (Figs. 2 and 3) [6, 7, 9]. Accumulating evidence has reported a crosstalk between H2S and NO. In fact, CSE knockout mice displayed a reduction in NO levels due to reduced eNOS expression. In this model, the treatment with H2S induces an increase in NO bioavailability and restores eNOS protein expression, which subsequently attenuated oxidative stress and MIRI. Recently, it was observed that S-sulfhydration, a post-translational modification involving the interaction of H2S with cysteine residues in proteins, alters the structure and biological activities of protein targets. In mice, application of pharmacological postconditioning using NaHS at the onset of reperfusion significantly enhanced S-nitrosylation of cardioprotective proteins, concurrently mitigating post-ischemic contractile dysfunction and reducing infarct size [198].
In the apolipoprotein E knockout model, the administration of NaHS induces increased plaque stability and blood lipid levels and reduced plaque formation [222]. Intriguingly, the Andreadou group displayed an interplay between eNOS, H2S, and CO-synthesizing enzymes in human atheroma in plaque stability and simvastatin effects [182]. Limited research has explored the interplay between CO and H2S in signal transduction, and the synergistic mechanism remains incompletely elucidated (see also “Carbon monoxide and cardioprotection”).
Sulfur dioxide and cardioprotection
Sulfur dioxide stands out as an additional gasotransmitters, showcasing diverse biological impacts, including antioxidative, anti-inflammatory, antihypertensive, and antiatherogenic effects.
Sources: Pioneering discoveries reveal that endogenous SO2 formation occurs within the cardiovascular system, exerting a prominent vasorelaxant influence [37, 74]. Subsequent findings identified SO2 products in various organs, such as the brain, stomach, lungs, liver, spleen, and heart [75, 109]. Aspartate aminotransferase is indicated as the key enzyme for SO2 synthesis. Conversely, SO2 catabolism involves the hydrogenation of bisulfite and sulfite ions, which are then oxidized to sulfate [74, 75].
Cardioprotection: Current knowledge establishes SO2’s engagement in apoptosis and oxidative stress, elevating antioxidant enzyme expression (e.g., SOD2 and GSH-Px1) and decreasing ROS production [105]. Simultaneously, in rats with isopropylarterenol-induced myocardial injury the antiapoptotic effects of SO2 are attributed to increased B-cell leukemia/lymphoma-2 (Bcl-2) expression, Bcl-2 associated protein x inhibition, mitochondrial membrane stabilization, decreased cytochrome c release, and diminished caspase activation [84]. Furthermore, SO2 plays a role in intracellular calcium homeostasis, with disruptions linked to cell death in numerous pathological conditions [74, 75]. Sulfur dioxide emerges as a pivotal regulator in various biological processes under both normal and pathological conditions associated with cardiovascular diseases. Recent investigations into the impact of SO2 on cell apoptosis have gained significant attention, revealing its regulatory influence on vascular smooth muscle cells, endothelial cells, cardiomyocytes, and other cells implicated in the pathogenesis of arterial hypertension and myocardial damage [234]. This multifaceted role positions SO2 as a crucial player in cardiovascular health, influencing cellular processes and offering potential therapeutic avenues in cardiac disorders.
Ischemic and pharmacological conditioning: Preconditioning with SO2 diminished myocardial infarct size, plasma lactate dehydrogenase, and creatine kinase activities in rats, alongside reducing myocardial caspase-3 and -9 activities. In addition, this pretreatment substantially elevated the expression levels of myocardial phosphorylated‑protein kinase B (p-PKB/p‑AKT) and phosphorylated‑PI3K-p85. Notably, the administration of the PI3K inhibitor LY294002 effectively nullified all the beneficial effects initiated by SO2 preconditioning. Furthermore, exogenous SO2 preconditioning improved cardiac function and reduced phosphorylated-ERK1/2 protein expression in isolated rat hearts with MIRI, suggesting the involvement of the ERK-MAPK pathway. Inhibition of ERK1/2 activation by the inhibitor PD98059 abolished the cardioprotective effects of SO2 [73]. Additional data on SO2 preconditioning strongly support the theory that the PI3K/Akt and ERK pathways play pivotal roles in mediating the protective effects against MIRI in rats [234] (Table 3; Fig. 3).
Carbon monoxide and cardioprotection
Sources: Carbon monoxide, being an easily diffusible gaseous molecule, originates from diverse sources within biological systems. The primary origin in mammals is attributed to heme oxygenase (HO) and HO-like activity. Carbon monoxide is generated through the degradation of the heme group via HO, which includes the constitutive forms HO-2 and HO-3, and the inducible form HO-1 [6, 19, 22, 53].
Cardioprotection: In the cardiovascular system, including the heart, CO-induced vasodilation occurs through the classical NO pathway, involving soluble GC (sGC)/cGMP, and PKG pathways. In addition, CO impedes endothelin-1 synthesis, prevents platelet aggregation, and inhibits L-type Ca2+ channels, collectively contributing to the cytoprotection of cardiomyocytes [22, 171]. Upregulation of HO-1 and its metabolites is known to activate various cell protection pathways, particularly during MI and hypoxia. Notably, during hypoxia and MI, there is a substantial increase in HO-1 expression, leading to heightened CO production [53]. Indeed, HO-1, in part, contributes to damage recovery and tissue repair by generating bioactive products such as CO. Carbon monoxide initiates a cardioprotective and antiapoptotic environment in the myocardium, akin to the effects observed during the late phase of preconditioning. This suggests that the presence of CO induces a state in the myocardium that mimics the delayed preconditioning, contributing to protection against cardiac damage and apoptosis [195].
Pathophysiological interactions between CO and H2S have been validated in a model of myocardial ischemic PC. In a rat model of pulmonary hypertension, H2S was observed to elevate HO-1 expression in the pulmonary artery and increase CO concentration in plasma [20, 164]. Carbon monoxide demonstrates cardioprotective properties, primarily through the opening of mitoKATP channels. This process inhibits the long-lasting opening of the mPTP and regulates mitochondrial ROS production. Although information on the cardioprotective effects of CO is limited, it is suggested that at low concentrations, CO facilitates the preservation of mitochondrial function. Under these conditions, CO has been observed to maintain the stable potential of the mitochondrial membrane, particularly during the ischemia/reperfusion period [9, 131, 171]. The mitochondrial level is a key site of CO action, where it induces the opening of mitoKATP channels and inhibits mPTP opening [22, 171]. Moreover, CO modulates several signal pathways implicated in cardioprotection, including NO/GC, MAPK, and ROS action (Fig. 3). In addition, CO has the capacity to impede platelet activation through both cGMP-dependent and cGMP-independent pathways [171]. In addition to the NO and cGMP pathways, CO exerts its anti-inflammatory properties by inhibiting cytokines such as tumor necrosis factor-alpha (TNF-α) and interleukin-1β (IL-1β) [135]. Apart from its anti-inflammatory effects, CO has proven its value in the field of organ transplantation, leading to improved outcomes [132]. Furthermore, in a porcine model of cardiopulmonary bypass, CO demonstrated its beneficial effects by enhancing cardiac energetics [98].
HO-1 expression and activity increase in hypoxic states, decrease during reperfusion, and correlate with heightened myocardial damage [171]. Protective action of CO is attributed to increased heme availability, a substrate for HO-1, and elevated HO-1 activity during reperfusion [22]. Indeed, the absence of HO-1 significantly increases vulnerability to ischemic injury [79].
Pharmacological conditioning: The majority of studies deal with exogenous CO, whose administration simulates HO-1 induction, resulting in heightened inotropy, reduced apoptosis, and diminished infarct size in rat hearts. Moreover, CO operates through a PKB/Akt-GSK-3β-nuclear factor erythroid 2-related factor (Nrf2) pathway, fostering mitochondrial biogenesis. Indeed, the influence of HO-1/CO on mitochondria is pivotal for the differentiation of stem cells into cardiac myocytes within the heart [155, 197]. Mitochondrial function likely plays a crucial role in CO-induced cardioprotection, impacting gene regulation, downstream signaling, and cell survival. Protective role of CO in the heart relies on HO-1 levels, triggered by tissue injury leading to the release of cellular contents, including elevated heme levels. This, subsequently, initiates HO-1 and endogenous CO generation, both highly cardioprotective and replicable by exogenous CO. Subtle concentrations of CO form transient bonds with cytochrome c oxidase, generating minimal levels of ROS. These ROS, in turn, activate signaling complexes involving Nrf2, hypoxia-inducible factor 1alpha (HIF-1α), and nuclear factor-kappa B (NF-κB)/inhibitor of NF-κB. Carbon monoxide also boosts the expression of peroxisome proliferator-activated receptor-gamma coactivator-1α, Nrf1, and Nrf2, thereby promoting CO-induced mitochondrial biogenesis for tissue preservation and regeneration [16, 21, 155].
Preconditioning triggered by CO demonstrates its ability to offer neuronal protection against apoptosis. This phenomenon highlights the capacity of CO to create a preconditioned state that safeguards cells from the process of programmed cell death [165, 206]. Two recent studies highlight the therapeutic potential of CO-releasing molecules (CORMs) in myocardial protection. Portal et al. show that CORM-3, a water-soluble CO-releasing molecule, exhibits substantial cardioprotective effects against hypoxia-reoxygenation in adult cardiomyocytes, emphasizing its potential as a therapeutic agent for MI [157]. In another study, Iqbal et al. demonstrate that CORM-A1 significantly reduce infarct size in a porcine model of acute MI [82] (Table 4).
Noble gases
Noble gases belong to a family of six naturally occurring gases: helium (He), neon (Ne), argon (Ar), krypton (Kr), xenon (Xe) and radioactive radon (Rn) [72, 209, 231].
Noble gases possess a defining trait: a fully occupied outer shell of valence electrons. This characteristic imparts inertness or, at the very least, diminished reactivity with other compounds under typical atmospheric pressure and temperature conditions. It is this distinctive feature that leads to their common designation as inert gases.
Nonetheless, a few of these noble gases exhibit potent biological effects. For instance, Xe is the only noble gas that shows anesthetic properties under normobaric conditions, while none of the other five gases has these properties [27, 72].
There is increasing evidence during the last 20 years that these so-called inert gases have strong cardioprotective and neuroprotective qualities [32, 50, 72, 116, 183, 209, 213, 214].
However, how these gases exert their cardioprotection is still a matter of debate. For Xe, it was shown that it may cause conformational changes in two proteins: annexin V, which has a hydrophilic pore inside and is meant to bind to cell membranes via a calcium-dependent mechanism, and urate oxidase, an intracellular globular protein with large hydrophobic cavities [25]. The Xe binding sites of the corresponding proteins consist of flexible gas cavities devoid of water. It has been demonstrated that Xe affects a number of cell membrane receptors. These include the nicotinic acetylcholine receptor [223], the 5-hydroxytryptamine 3 receptor [199], the plasmalemmal adenosine triphosphate-sensitive potassium channels (KATP) channel [11], the two-pore domain potassium channel TREK-1 [54], and the N-methyl-D-aspartate (NMDA) receptors [47]. In particular, it has been shown that at the glycine site of the NMDA receptor, Xe competes with the co-agonist glycine [33, 59]. However, this knowledge is primarily derived from neural cells. Thus, it is unclear if these Xe effects on neural cells also contribute to its myocardial protection. Nonetheless, it has been shown that regarding cardioprotection KATP channels—at least the mitoKATP channels—play a crucial role in the PC of the heart [134] and, therefore, might be a key mediator in noble gas-induced cardioprotection.
Here, we will briefly report and discuss the recent studies displaying cardioprotective effects of some noble gases (Ar, Xe, and He) with the main focus on the underlying molecular mechanism involved. A summary of the experimental studies on noble gas-induced cardioprotection can be found in Tables 5, 6 and 7 and Figs. 2 and 3.
Argon and cardioprotection
The name argon in Greek: αργός means inert. Argon has anesthetic properties under hyperbaric conditions and is relatively abundant in atmospheric air where it is found at a concentration of 0.93%. It is non-corrosive, non-flammable and non-toxic, with a density 38% higher than that of air and its solubility in water and plasma is 24 times less than that of carbon dioxide [125]. Despite being considered ‘biologically’ inert, recent evidence suggests that argon may have significant pharmacological effects [125, 204]. It has mainly been investigated for its neuroprotective effects but there is some evidence from both in vitro and in vivo studies that Ar exhibited cardioprotective effects and that these effects are mediated by activating ERK1/2 and Akt while regulating c-Jun N-terminal kinases (JNKs) in a biphasic manner [90, 99, 115, 141, 163] (Fig. 3 and Table 5).
Xenon and cardioprotection
Xenon is regarded as a gaseous anesthetic; despite being costly and scarce, it offers several special benefits such as cytoprotectivity and quick diffusion, along with minimal hemodynamic side effects [38, 169].
The noble gas Xe induces cardioprotection whether applied before (PC-like effect) or after (PostC-like effect) an infarcting ischemia [50, 62, 160, 175, 219]. In particular, in pathological conditions, applying 20% Xe along with 34 ºC hypothermia during early reperfusion can also reduce the area of the MI in rats [175]. Regarding the cardioprotective mechanisms of Xe, it has been suggested that the mitoKATP channel and phosphatidylinositol-dependent kinase-1 are first activated by Xe. These two in turn activate PKC-ε, which in turn activates p38 MAPK. Two downstream targets of p38 MAPK, mitogen-activated protein kinase-activated protein kinase-2 and heat-shock protein 27 (HSP27), are then phosphorylated, which causes HSP27 to translocate to the particulate fraction and increases F-actin polymerization [217,218,219]. In addition to p38 MAPK, ERK1/2 and cyclooxygenase-2 (COX-2) are critical mediators of either Xe early preconditioning [216] or Xe induced late preconditioning [211]. Xenon can also cause GSK-3β- and Akt-phosphorylation, prevent Ca2+ from causing mPTP to open, and maintain mitochondrial function [120].
The minimal side effects of Xe are in line with the minimal effects on cardiac function. Differences were observed between global or regional administration of 50% or 70% Xe in dogs. Regional administration of Xe in the left anterior descending artery only reduced local myocardial contractility when Xe was given at 70% but did not affect global hemodynamics, coronary blood flow and regional myocardial function in the circumflex coronary artery-dependent myocardium [160]. In isolated guinea pig hearts, 40% or 80% of the Xe did not significantly change the NO-dependent flow response, the electrical, mechanical, or metabolic effects. This may be because Xe did not change the major cation currents in the guinea pig cardiomyocytes [196]. Xenon (20, 50, and 65%), in addition to basic intravenous anesthesia, has been demonstrated to cause a reduction in total hepatic O2 delivery and venous hepatic O2 saturation, as well as a downregulation of heart rate and cardiac output without altering mean arterial pressure or hepatic arterial blood flow [80, 205]. However, it has not been observed to impair intestinal oxygenation in pigs. Actually, pigs with hepatic venous blood that was supplemented with pentobarbital and buprenorphine received 73–78% Xe, which increased the amount of O2 in the blood [170]. These data suggest that the effects of Xe on heart rate and hepatic O2 levels may be influenced by concomitant intravenous anesthesia.
Since Xe is scarce, expensive, and difficult to administer (only by gaseous route), it is challenging to use Xe outside of controlled respiration and hospital conditions. In addition, it is unlikely to be applied to the management of acute and chronic heart conditions. Researchers have recently solidified Xe, enabling its oral or intravenous administration, by incorporating it into cyclodextrins, starch derivative excipients commonly used as drug carriers [162, 228]. For instance, the saturation point of Xe in water is 0.22 mM only. The solubility of Xe was increased from 0.22 to 0.67 mM when 2-hydroxypropyl-β-cyclodextrin was added as a cage molecule. Supplementing these xenon-enriched solutions by gavage decreased hypertension, left ventricular hypertrophy, and cardiac dysfunction in aged ApoE-knockout mice fed a high-fat diet for six weeks [228]. The acquired information provides opportunities for the creation of medications based on the lyophilized-cyclodextrin-xenon complex that are suitable for transportation, storage, and use in medicine, including outside of hospitals (Table 6).
Helium and cardioprotection
Helium does not have any anesthetic effects, thus it may be used in awake patients in situations involving ischemia–reperfusion, such as percutaneous coronary interventions for STEMI patients. As He has a low density, it helps patients with airway diseases breath by lowering their energy requirements. Since there are ventilators that enable the application of He via both invasive and non-invasive ventilation strategies, He may also be used in patients undergoing organ transplantation or during heart or vascular surgery. Helium therefore could be a great substitute for Xe or Ar in clinical ischemia/reperfusion scenario because it is a noble gas that is significantly less expensive and there are no known adverse effects of He on regional or global hemodynamics.
Over the last 25 years, several investigations have demonstrated that He has vital cytoprotective properties on endothelial cells [185,186,187], the brain [1, 23, 31, 56, 104, 107], the gut [36], the liver [232] and the heart [1, 45, 63, 76,77,78, 127,128,129,130, 141, 214].
Helium administration prior to ischemia, known as He preconditioning, exhibits a significant reduction in the infarct size in the model of MIRI, specifically observed in young rats but not in aged rats, and in Zucker lean rats but not in Zucker obese rats [63, 76, 77] (Table 7). The elicitation of helium-induced cardioprotection is associated with the activation of PI3K, MAPK/ERK1/2, p70S6 kinase, cyclic AMP-dependent protein kinase (PKA), COX-2, opioid receptors, mPTP opening, and NO production by eNOS [48, 76,77,78, 136,137,138,139,140,141, 215]. In addition, the threshold of helium-induced preconditioning was lowered in vivo by inhibiting GSK-3β or p53 through a mPTP-dependent mechanism [140].
Furthermore, He was cardioprotective when given after ischemia (He-PostC) in the Zucker lean rat or Male Wistar rat models of MIRI. These protective effects on rats are associated with upregulating autophagy-related genes, downregulating apoptosis-related genes [128], raising calcium channel, voltage-dependent, L type (alpha-1D subunit), caveolin-1 and caveolin-3 (Cav-1 and Cav-3) protein levels, and activating ERK1/2 and Akt [45, 77, 128, 215]. According to Smit et al. [186], He preserves post-ischemic endothelial function; eNOS blocking did not reverse this effect.
However, in male adult Wistar rats, a prolonged 30- or 60-min of 70% He dose during reperfusion does not cause cardioprotection [127]. Although the burst of inflammatory cytokines did not decrease, the prolonged inhalation of He may have contributed to the proinflammatory response by raising IL-1β and cytokine-induced neutrophil chemoattractant 3 in the myocardium of the at-risk area, but not in the not-at-risk area [127]. However, when considering the clinical application of noble gases, different approaches have been undertaken for Xe and He. In a study with healthy volunteers, utilizing a forearm blood flow model to explore endothelial function, He was found to alleviate post-ischemic endothelial dysfunction. This improvement occurred without any observed impact on plasma levels of cytokines, adhesion molecules, or microparticles [186]. Furthermore, a clinical study found that neither He-PC (3 × 5 min of 70% He and 30% O2 applied before aortic cross-clamping) nor the combination (15 min of He applied before aortic cross-clamp release and continued for 5 min after start of reperfusion;) had any effect on the activation of p38 MAPK, ERK1/2, or the levels of PKC-ε and HSP27 in the hearts of patients undergoing coronary artery bypass grafting (CABG) procedures. Moreover, in these patients, postoperative troponin release was unaffected by helium-pre- or helium-postconditioning [184].
For Xe, it was shown, that unlike hypothermia alone, the addition of Xe to hypothermia reduced myocardial damage in patients following out-of-hospital cardiac arrest and return of spontaneous circulation [8]. The combination of Xe with hypothermia was linked to a more substantial recovery of left ventricular systolic function compared to hypothermia alone. This suggests that Xe possesses cardioprotective properties in this clinical context [173].
However, a multinational, randomized clinical trial examined the cardioprotective effects of Xe anesthesia in patients undergoing CABG surgery, comparing it to anesthesia based on sevoflurane or propofol. Among the 492 patients who received either propofol, sevoflurane, or Xe, a decrease in troponin I release was observed in the Xe group compared to the propofol group, as well as in the sevoflurane group compared to the propofol group. However, the difference in troponin release was minimal, and it remains uncertain whether this observed effect holds clinical significance [71]. In line with these results, a study in patients with American Society of Anesthesiologists physical status III undergoing aortic surgery under either Xe or total intravenous anesthesia did not find significant differences in global myocardial performance, myocardial contractility or laboratory values between the groups [13]. Furthermore, in a randomized trial in 30 patients who underwent elective on-pump CABG receiving balanced anesthesia of either Xe or sevoflurane, Xe rather triggers proinflammatory effects and suppresses the anti-inflammatory response [17]. The clinical relevance of these findings, however, has not been determined in this study.
Taking these results into account, even though the noble gases can be easily applied in the clinical situation, their cardioprotective effects so far have not yet been strongly supported by larger randomized trials. Therefore, additional studies are necessary to clarify these discrepancies between experimental and clinical studies. For instance, the presence of a threshold in the hypertensive heart is suggested by the fact that, in spontaneous hypertensive rats, only a triple intervention of He-PostC can reduce MIRI, in contrast to the healthy Wistar Kyoto rats [129]. According to an in vitro study He-conditioning enhanced fibroblast migration, but not the release of extracellular vesicles of protective medium or soluble factors from the cardiac fibroblasts, contributed to cardioprotection [83]. According to a recent study, a dose-dependent improvement in lipopolysaccharide-induced left ventricular dysfunction and cavity enlargement can be obtained with intraperitoneal injection of 99.999% He; the optimal dose, in this study, was found to be 1.0 ml/100 g [234]. In terms of mechanisms, in this study, He decreased the phosphorylation of NF-κB, inhibited the expression of toll-like receptor 4 and then attenuated the expression of TNF-α and IL-18 (Table 7).
Interactions between gasotransmitters and noble gases
From the preceding discussion, it can be inferred that noble gases frequently act on the same targets as gasotransmitters, either directly or indirectly, leading to the induction of endogenous gas formation and signaling pathways activation. The synergistic interactions between gasotransmitters and noble gases in cardioprotection scenario have become a focal point of scientific exploration [6, 7, 9, 139], and recent studies have delved into the experimental intricacies surrounding their collective impact. Notably, investigations suggest that these gases protect endothelial cells [209, 211, 212] and collaboratively induce vasorelaxation within the cardiovascular system, bolstering their individual and synergistic cardioprotective effects. As seen above, this phenomenon has been examined in controlled experimental settings, employing various in vitro and in vivo models of MIRI. Experiments involving perfused hearts, isolated vessels, and animal models have provided valuable insights into the specific mechanisms through which the interplay of NO, H2S, CO, and noble gases—Ar, He, and Xe in particular—manifests as a shield against MIRI (Tables 1, 2, 3, 4, 5, 6, and 7) [209, 231].
As seen above, the metabolic alterations observed in cardiovascular system cells during chronic illnesses (comorbidities) and their response to hypoxia are intricately linked with the involvement of endogenous gasotransmitters as well as with exogenous gases, including noble gases. As concern gasotransmitters, we have mentioned that they are generated as part of metabolic processes. For instance, NO is produced during the breakdown of arginine to citrulline, H2S is formed during cysteine metabolism, and CO is a byproduct of heme metabolism. The reader is redirect to recent reviews for the discussion on how these metabolic processes contribute to cardioprotection, specifically regarding gasotransmitters in the context of comorbidities [5,6,7, 9, 148, 180, 239]. These gaseous molecules play pivotal roles in modulating vascular tone, promoting angiogenesis, and ensuring cellular survival against hypoxic conditions and oxidative stress induced by IR. As seen, their effects are mediated via the modulation of signaling pathways that influence mitochondrial function and metabolism, and the activity of key regulators of intracellular processes, including but not limited to PKG, PI3K, MAPK, JNK1/2, sGC, cGMP, NF-κB, HIF-1α, as well as ion channels such as mitoKATP channels and large conductance calcium-activated potassium (BKCa) channels (Figs. 2 and 3). Indeed, BKCa channels are paradigmatic in elucidating the interaction and cardiovascular protective effects of gasotransmitters. Gases activating BKCa channels may confer protective effects and reduce vascular resistance during episodes of hypoxia and MIRI [180]. BKCa channels are target of H2S on cardiomyocytes under hypoxic conditions as well as upon endogenous CO stimulation of cardiomyocytes. Carbon monoxide modulates the function of these channels by interacting with reduced heme. Nitric oxide triggers the activation of BKCa channels indirectly through pathways associated with PKG and PKA signaling. Cellular functions related to Ca2+ storage and energy synthesis heavily rely on the capacity of these channels across cell and organelle membranes. Indeed, effective strategies to mitigate MIRI include activating energetic metabolic pathways such as glycolysis, glucose and ketone oxidation, as well as hexosamine biosynthesis, and deacetylation. Yet, protection can be achieved by reducing the activity of the malate-aspartate shuttle, mitochondrial O2 consumption, fatty acid oxidation, and mitochondrial succinate metabolism, requiring novel reversible and specific inhibitors. Currently, the most promising metabolic therapy for MIRI seems to involve targeting glycolysis, O-GlcNAcylation, and the metabolism of ketones, fatty acids, and succinate, either individually or in combination [239]. We have reported above the impact of gases on mitochondrial function and O2 consumption. Moreover, evidence suggests that their involvement in cellular metabolism extends to regulating energetic substrate utilization [131, 146, 169]. For instance, tyrosine residue nitration in mitochondrial key proteins contributes to regulate mitochondrial and cellular function after MIRI [239]. Consequently, the combination of gasotransmitters holds the potential to modulate metabolism, mitigate mitochondrial damage, and ultimately reduce MIRI. The crosstalk between gasotransmitters and noble gases has been probed at the molecular level shedding light on potential molecular targets for advanced cardioprotective strategies [181, 188, 213]. Controlled studies utilizing gasotransmitter-releasing compounds and precise administration protocols have demonstrated the therapeutic promise of these molecules in mitigating MIRI [82, 133]. Similarly, experiments employing various delivery methods for noble gases, including inhalation and controlled release, have showcased their organ-protective properties with a focus on detailed dose–response relationships and pharmacokinetics [227].
In conclusion, the ongoing research in the intricate interplay between gasotransmitters (NO, H2S, SO2, CO) and noble gases (Ar, He, Xe) paves the way for novel therapeutic strategies, underlining the potential of these molecular shields against the global health challenge of ischemic heart disease.
Nanodevices to deliver gases
Nanoparticle-based drug delivery has gained significant popularity as a strategy to optimize the therapeutic potential of drugs. Despite notable improvements, formulating gases presents unique challenges not encountered with liquid and solid active ingredients. The challenges and failures of gases-oriented therapies in the field of cardioprotection have been recently and extensively reviewed [6, 7, 9, 146]. In brief, drug formulation and tolerance as well as comedications and comorbidities may affect the outcomes [44, 92]. Specifically, in comorbidities, elevated production of ROS/RNS can influence cardiac gases-dependent signaling and induce adaptive changes in the expression and activity of enzymes producing gases as well as antioxidant enzymes. Initially, these changes may serve as protective mechanisms in metabolic syndrome and diabetes [148]. However, prolonged exposure to oxidative, nitrosative, and nitrative stress can deplete these protective mechanisms, leading to increased ROS/RNS production and reduced gases bioavailability (especially for NO and H2S) in the myocardium. Furthermore, heightened oxidative and nitrosative stress can impair the NO-sGC signaling pathway, limiting the ability of NO to perform its essential signaling functions in the heart. The upregulation of ROS/RNS production in the presence of risk factors also promotes the activation of redox-dependent transcription factors like NF-κB, which stimulates the expression of various proinflammatory mediators, contributing to the development of cardiac dysfunction and remodeling. The dysregulation of gases-dependent signaling may affect the therapeutic effectiveness of conventional drugs used in managing metabolic syndrome, hypertension and diabetes. Conversely, modulation of gases-dependent signaling could underlie the therapeutic benefits of established and newly developed treatment approaches, such as ACE inhibitors, specific β-blockers, and sGC activators as well as NO or H2S donors conjugated with other pharmacological agents such as non-steroidal anti-inflammatory drugs [6, 7, 9, 114, 146] A deeper understanding of these pathological processes and pharmacology of gas-enhancers holds promise for developing more effective therapeutic strategies to combat comorbidities and its cardiac consequences related to gases-dependent signaling. Gas molecules or noble gases, released from formulations for therapeutic purposes, have been studied, although insufficiently. Gasses can be modified into prodrugs called gas-releasing molecules (GRMs) and subsequently released from these GRMs. For instance, the development of CORMs stemmed from the need for compounds capable of transporting and releasing controlled amounts of toxic CO within cellular systems. This approach offered a promising avenue for studying the pharmacological effects of the gas and elucidating its mechanisms of action [82, 133, 157]. Extensive coverage is given to various nanosystems and their roles in efficient shuttling, targeting, and release of therapeutic gases. Diverse ways have been proposed in which GRM prodrugs, in delivery nanosystems, respond to intrinsic and extrinsic stimuli for sustained release, offering a comprehensive overview of their design and application in nanomedicine [133]. Considerable investigation has been conducted into the utilization of inorganic materials for the loading and delivery of drugs. These include, photothermal agents [100, 102, 233], photon‐to‐photon conversion agents such as lanthanide [237], catalytic metal ionic species [111], photocatalytic nanomaterials [210, 236] and polymer‐based nanomaterials [162, 176, 224, 228], to name only a few used for gas-loading in different pathological conditions (Table 8). In a related context, recent developments introduce two types of O2-loaded nanodevices (ND) based on alpha-cyclodextrin and cyclic nigerosyl-nigerose. These NDs demonstrate protection against hypoxia/reperfusion-induced cell death in vitro, serving as biocompatible and biodegradable drug carriers for simultaneous O2 and therapeutic delivery [43, 150]. Advances in solidifying Xe within cyclodextrins make oral or intravenous administration feasible [162, 228]. Hence, O2- NO- and/or Xe-loaded NDs, conjugated with an ischemic myocardium-targeting peptide (that is protein/peptide‐modified materials), could efficiently deliver to the infarcted heart. This methodology involves synthesizing ND formulations that integrate O2, gasotransmitters, and/or specific noble gases, achieved through thoughtful modifications around the glucose ring to enhance efficiency. In addition, lipid nanoparticles have proven effective in drug delivery and play a significant role in controlling the release and diffusion of gases within biological tissues in gasotransmitter applications [133]. Several stimuli-responsive GRMs have been tested for therapeutic gas release, emphasizing the importance of efficient and targeted delivery at diseased sites. Intrinsic stimuli, such as pH, offer high biocompatibility but demonstrate weaker driving forces for gas release compared to external stimuli such as magnetic, ultrasound, and near-infrared light (NIR)-triggers. Controllable external stimuli generally exhibit high release efficiency and specificity. Combining intrinsic and external stimuli can enhance responsiveness. Critical challenges for intrinsic stimuli include the need for improved sensitivity. External stimuli, such magnetic, ultrasound, and NIR triggers due to their superior characteristics might be preferred (Table 8). However, external stimuli may cause tissue irritation at high powers [133].
While there have been a few clinical trials conducted on the gasotransmitter H2S (refer to Table 1 in [9]), a multitude of studies have explored NO donors, nitrates, and nitrites, which are beyond the scope of this review. In particular, evidence from clinical practice indicates that H2S may produce inconclusive outcomes in patients with cardiovascular diseases. A clinical trial investigating the impact of Na2S on patients with acute STEMI was withdrawn by the researchers (NCT01007461), while another study, known as the Groningen Intervention study for the Preservation of cardiac function with sodium thiosulfate after STEMI (GIPS-IV; NCT02899364), demonstrated neutral findings [30]. To our knowledge, CO is often studied as toxic agent and only one trial has been conducted thus far involving CO in patients with stable chronic obstructive pulmonary disease (NCT00122694). Overall, further experimentation is crucial to advance the GRMs and/or stimuli for potential clinical applications in gasotransmitter and noble gases research. Nevertheless, the synthesis and testing of these formulations are deemed essential, particularly in the cardiovascular field and relevant myocardial infarct models, providing a promising avenue for future clinical applications, recognizing the imperative of adopting a multitarget approach in addressing MIRI [29]. This strategy underscores the potential efficacy of exploiting gaseous diffusibility as a readily attainable means of achieving multifaceted therapeutic goals.
Conclusions
In summary, we highlight the diverse yet interconnected roles of gasotransmitters and noble gases in modulating molecular pathways to promote cell survival and overall tissue health. While gasotransmitters such as NO and H2S, produced by various cell types, contribute significantly to various physiological processes, noble gases such as He and Xe emerge as promising candidates for organ protection. Their ability to modulate molecular pathways and promote cell survival underscores their cardioprotective potential. However, collaborative efforts between experimental and clinical researchers are essential to bridge the gap between laboratory findings and real-world applications. Prospective studies may focus on establishing optimal dosages, timings, and combination therapies involving both noble gases and gasotransmitter donor molecules. Integrating advanced imaging techniques, molecular profiling, and systems biology approaches will contribute to a comprehensive understanding of the intricate molecular pathways involved. Of course, it is crucial to acknowledge the influence of cardiovascular disease, confounders and risk factors on endogenous cardioprotective mechanisms. Here, we highlight the need to address the impact of cardiovascular comorbidities on the regulation of gasotransmitters and noble gases, as well as the challenges associated with the clinical application of their cardioprotective potential [5, 44, 154, 184, 187]. Moving forward, incorporating information on the effects of cardiovascular risk factors on individual gasotransmitters and exploring new avenues for therapeutic strategies will be essential for advancing the field and optimizing patient outcomes. Research in various areas has emphasized the significance of interactions among gasses, suggesting the need for integrated investigation into their role in MIRI and cardioprotection. Gasses influenced pathways intersect in common downstream effectors during processes such as cardioprotection, vasodilation and angiogenesis. Therefore, effective therapeutic approaches may require the utilization of multiple gases or their pharmacological modulators, considering also their potential in affecting cell metabolism [9, 131, 146, 169, 239]. This multidimensional approach is crucial for developing more effective and targeted cardioprotective strategies.
Data availability
This is a review article, and therefore, there are no original data to be made available.
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C.P. and P.P. are supported by the Progetto di Ricerca di Rilevante Interesse Nazionale (PRIN) with identification numbers 2022S74XWB and 2022AA37N3, respectively.
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P.P. and C.P. wrote the first draft of the manuscript. G.A. and N.W. revised the manuscript critically for important intellectual content. S.F. contributed significantly to the manuscript revisions, including ensuring accuracy in figures, tables, and references. All the authors revised the manuscript. All the authors have read and agreed to the published version of the manuscript.
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Pagliaro, P., Weber, N.C., Femminò, S. et al. Gasotransmitters and noble gases in cardioprotection: unraveling molecular pathways for future therapeutic strategies. Basic Res Cardiol 119, 509–544 (2024). https://doi.org/10.1007/s00395-024-01061-1
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DOI: https://doi.org/10.1007/s00395-024-01061-1