Abstract
Sodium–glucose cotransporter 2 (SGLT2) inhibitors have exerted cardioprotective effects in clinical trials, but underlying mechanisms are not fully understood. As mitigating sympathetic overactivity is of major clinical concern in the mechanisms of heart failure treatments, we examined the effects of modulation of glucose handling on baroreflex-mediated sympathetic nerve activity and arterial pressure regulations in rats with chronic myocardial infarction (n = 9). Repeated 11-min step input sequences were used for an open-loop analysis of the carotid sinus baroreflex. An SGLT2 inhibitor, empagliflozin, was intravenously administered (10 mg/kg) after the second sequence. Neither the baroreflex neural nor peripheral arc significantly changed during the last observation period (seventh and eighth sequences) compared with the baseline period although urinary glucose excretion increased from near 0 (0.0089 ± 0.0011 mg min−1 kg−1) to 1.91 ± 0.25 mg min−1 kg−1. Hence, empagliflozin does not acutely modulate the baroreflex regulations of sympathetic nerve activity and arterial pressure in this rat model of chronic myocardial infarction.
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Background
Sodium–glucose cotransporter 2 (SGLT2) inhibitors were developed to treat diabetes mellitus (DM), but they are now recognized as a new class of drugs to treat heart failure [1, 2]. The cardioprotective effect of SGLT2 inhibitors has been demonstrated in several clinical trials (DAPA-HF [3], EMPEROR-Reduced [4], EMPEROR-Preserved [5]), but its exact underlying mechanisms of action are not fully understood. The mechanisms may be multifactorial, including glucotoxicity attenuation, improved cardiac loading conditions via the body fluid volume reduction, and improvements in cardiac metabolism [6,7,8]. Although the sympathoinhibitory effect of SGLT2 inhibitors may also help facilitate cardioprotection [9,10,11,12,13], whether SGLT2 inhibitors acutely modify systemic sympathetic nerve activity (SNA) remains to be clarified. SGLT2 is primarily expressed in renal proximal tubules [14], thus the potential sympathoinhibitory effect may be related to the suppression of sympathoexcitatory reflexes from the kidneys. Renal sensory nerve activation can yield sympathoexcitatory reflexes in diseased kidneys while eliciting inhibitory renorenal reflexes in normal kidneys [15, 16].
Glucose reabsorption via SGLT2 depends on the sodium gradient across the plasma membrane, which is maintained by Na+/K+ ATPase activity. Hence, glucose reabsorption is energy consuming. The ATP level in the renal proximal tubules decreases shortly after renal ischemia [17], indicating a high metabolic rate and limited ATP storage in proximal tubular cells. Increased organ work or oxygen deficiency may cause renal stress, thereby activating sympathoexcitatory reflexes. The glucose reabsorption by the proximal tubules increases as the filtered load is increased by either an elevation in plasma glucose concentration or an increase in glomerular filtration rate until it reaches a threshold [18]. Increases in the filtered load above this maximal reabsorptive capacity results in glucosuria. Hence, DM represents a pathological situation of increased organ work with the proximal tubular cells working at their maximum reabsorptive capacity. We have examined the acute effect of an SGLT2 inhibitor, empagliflozin, on the baroreflex open-loop static characteristics in Goto–Kakizaki diabetic rats [19]. The study revealed that intravenous empagliflozin administration did not acutely attenuate SNA despite a significantly increased urinary glucose excretion. Therefore, the possible sympathoinhibitory effect of empagliflozin may be an indirect effect associated with chronic improvements in renal energy status and general disease conditions.
The present study used a rat model of chronic myocardial infarction (MI) to test the hypothesis that empagliflozin acutely mitigates systemic sympathoexcitation. We employed an open-loop analysis of the carotid sinus baroreflex [20] because this method allows us to test the drug effect on SNA over a wide range of carotid sinus pressure (CSP). For instance, the sympathoinhibitory effect of a central antihypertensive, clonidine, is more evident in the low CSP (high SNA) range than in the high CSP (low SNA) range [21]. Generally speaking, heart failure causes renal hypoperfusion and induces potential tubular damages [22, 23]. If renal dysfunction in post-MI rats causes centrally-mediated systemic sympathoexcitation via renal afferent nerves, the inhibition of SGLT2 might reduce energy consumption at the kidneys and attenuate the sympathoexcitatory reflexes, resulting in systemic sympathetic suppression.
Methods
Ethical approval
Male Wistar–Kyoto (WKY) rats were purchased from Japan SLC. The rats were cared for strictly following the Guiding Principles for the Care and Use of Animals in the Field of Physiological Sciences, which have been approved by the Physiological Society of Japan. The Animal Subjects Committee at the National Cerebral and Cardiovascular Center reviewed and approved the experimental protocols (No. 22033). As a reference, the data of body weight and heart weight obtained from age-matched WKY rats used in another study (No. 23013) were reported. We also included the previously reported data of plasma creatinine concentration obtained from WKY rats with unilateral renal denervation [24] and Goto-Kakizaki diabetic rats [19].
Preparation
The proximal left coronary artery (before branching into the anterior descending and circumflex arteries) was permanently ligated with a 5–0 Prolene suture (Ethicon, Johnson & Johnson, NJ, USA) at 8 weeks of age following a previously described procedure [25]. Of 30 rats that underwent coronary ligation, 12 survived for > 8 weeks and were subjected to an acute experiment described below, and the data from 9 rats were eventually analyzed because of the incomplete dataset.
The rats were anesthetized with an intraperitoneal injection (2 mL/kg) of a urethane (250 mg/mL) and α-chloralose (40 mg/mL) mixture. The anesthetic mixture was diluted 18-fold with physiological saline and continuously infused via the right femoral vein (2 mL·kg−1 h−1). Ringer’s lactate solution was continuously infused (4 mL kg−1 h−1) to maintain fluid balance. A respirator was used to ventilate the animals with oxygen-enriched air. Arterial pressure (AP) was measured from the right femoral artery. A cardiotachometer (AT-601G, Nihon Kohden, Japan) was used to determine the heart rate (HR) from the AP waveform. Central venous pressure (CVP) was measured via a catheter inserted into the left femoral vein and advanced to the inferior vena cava. Body temperature was maintained between 37 °C and 38 °C using a heating pad and a lamp.
A left flank incision exposed the postganglionic branch of the splanchnic sympathetic nerve. A pair of stainless-steel wire electrodes (AS633, Cooner Wire, CA, USA) was attached to the nerve and fixed with silicone glue (Kwik-Sil, World Precision Instruments, FL, USA). The electrical signal was band-pass filtered between 150 and 1000 Hz, full-wave rectified, and low-pass filtered at a cut-off frequency of 30 Hz. A ganglionic blocker, hexamethonium bromide (60 mg/kg), was administered at the end of the experiment to assess the noise level of SNA recording. The splanchnic SNA was chosen as a proxy of systemic SNA because the splanchnic vascular bed plays a substantial role in the systemic circulatory control [26].
The bilateral carotid sinus baroreceptor regions were isolated from the systemic circulation [27, 28], and a servo-controlled piston pump system (ET-126, Labworks, CA, USA) externally regulated CSP. Reflexes other than the carotid sinus baroreflex were minimized by sectioning the aortic depressor and vagal nerves in the neck region.
Urine was collected via polyethylene tubes (KN-392-SP 8, Natsume, Japan) that were inserted into bilateral ureters through a horizontal abdominal incision. The urine was accumulated on a balance dish, and urine volume (UV) was gravitationally assessed. The readout (resolution: 0.1 mg ≈ 0.1 μL) of an electronic balance (HR-150AZ, A&D Company, Japan) was recorded in synchrony with the hemodynamic data [29].
The left renal artery was isolated by gently dissecting the surrounding tissues. An ultrasonic flow probe (MA1PRB, Transonic Systems Inc., NY, USA) was attached to the renal artery to measure renal blood flow (RBF).
Protocol
CSP was decreased to 60 mmHg for five min and then increased stepwise up to 180 mmHg in increments of 20 mmHg every minute. The stepwise CSP input sequence was repeated and denoted as S1 through S8. Empagliflozin (MedChemExpress, NJ, USA) was dissolved in dimethyl sulfoxide (DMSO) at 10 mg/100 μL and diluted with polyethylene glycol and physiological saline to a final concentration of 10 mg/mL (10% v/v DMSO, 45% v/v polyethylene glycol 200, and 45% v/v physiological saline). The empagliflozin solution was intravenously administered at 10 mg/kg (1 mL/kg, bolus) at 1 min after S2 completion [19].
Data analysis
The CSP, SNA, AP, HR, RBF, CVP, and UV data were stored on a laboratory computer system at 1000 Hz via a 16-bit analog-to-digital converter. Data were averaged during the last 10 s of each step for each of the S1–S8 sequences to assess the open-loop static characteristics of the carotid sinus baroreflex. Renal vascular resistance (RVR) was derived from RVR = (AP − CVP)/RBF. Urine flow (UF) (in μL/min) was derived from a 1-min increment of UV. Then, normalized UF (nUF) (in μL min−1 kg−1) was calculated from UF divided by the body weight of the rat. Urine samples were combined for two consecutive sequences for urinary glucose, sodium, and creatinine concentration measurements. The S1 and S2 sequences are referred to as the baseline (BL) period. The S3 and S4, S5 and S6, and S7 and S8 are referred to as T1, T2, and T3 periods, respectively. Further, the hemodynamic data are reported as averaged values for BL, T1, T2, and T3 periods.
The SNA was normalized in each animal because the absolute amplitude of SNA significantly varied across animals depending on recording conditions. The value obtained after the ganglionic blockade was defined as 0%, and the value corresponding to the CSP of 60 mmHg during BL was defined as 100%. Regardless of the normalization, the acute effect of empagliflozin on SNA, if any, can be detected as the relative change from the BL value.
A four-parameter logistic function (Eq. 1) quantified the static characteristics of the baroreflex total arc (AP as a function of CSP), HR control (HR as a function of CSP), and the neural arc (SNA as a function of CSP) [20, 30]:
where P1 is the response range; P2 is the slope coefficient; P3 is the midpoint pressure on the CSP axis; P4 is the lower asymptote of the sigmoid curve.
Linear regression quantified the static characteristics of the baroreflex peripheral arc (AP as a function of SNA) (Eq. 2) [20]:
where b0 and b1 denote the intercept and slope, respectively. The SNA–RVR relationship was likewise analyzed using linear regression.
The baroreflex equilibrium diagram was obtained by plotting the neural and peripheral arcs on a pressure versus SNA plane [31, 32]. The operating-point SNA and AP values were determined at the intersection point of the fitted neural and peripheral arcs on the equilibrium diagram.
The AP–nUF relationship during a stepwise CSP input approximated a straight line in our previous studies [24, 29, 33]. The intercept (nUF-intercept) and slope (nUF-slope) were estimated using linear regression. In addition, the following logarithmic function was adopted to quantify the AP–nUF relationship because the relationship was slightly curvilinear in the lower AP range in the present dataset:
where log10(·) is the common logarithm; G and x0 denote the gain and x-intercept, respectively.
Blood and urine samples
An arterial blood sample was obtained once at the end of the experiment. The plasma sample was frozen at −80 °C after centrifugation. Urine samples obtained during BL, T1, T2, and T3 periods were also frozen at −80 °C. Later, the glucose, sodium, and creatinine concentrations were measured by outsourcing (SRL Inc., Japan).
The urinary glucose and sodium excretions were calculated from the product of the average nUF and the urinary glucose and sodium concentrations, respectively. Creatinine clearance (Ccr) was calculated as the value per kidney by halving the average nUF for compatibility with our previous reports [19, 24, 33, 34]. The plasma creatinine concentration was assumed to be unchanged significantly throughout the experiment.
Statistical analysis
The final analysis excluded data from three rats due to trouble in the UV measurement and failure to obtain stable SNA and CVP recordings, respectively. Eventually, data from nine post-MI rats were analyzed. All data are expressed as mean ± standard error (SE) values. Time-dependent changes in the baroreflex static characteristic parameters, urinary excretion-related data, and AP–nUF relationship parameters were analyzed using one-way repeated-measures analysis of variance (ANOVA) with the Greenhouse–Geisser correction, followed by Dunnett’s test (Prism 8, GraphPad Software, CA, USA). A nonparametric Mann–Whiney test [35] compared the plasma creatinine concentration with the values available from our previous reports, as a reference. P-values of < 0.05 in all the statistical analyses were considered significant differences.
Results
Table 1 summarizes the body weight, heart weight (biventricular weight), and normalized heart weight. The post-MI rats demonstrated a range of cardiac remodeling. The absolute heart weight and normalized heart weight were significantly heavier in post-MI rats than those in age-matched normal WKY rats subjected to experiments different from the present study (n = 5, age: 17.5 ± 0.7 weeks, P = 0.606; heart weight: 0.903 ± 0.018 g, P = 0.004; normalized heart weight: 2.251 ± 0.043 g/kg, P < 0.001 by Mann–Whitney test). Further, Table 1 summarizes the concentrations of plasma glucose, sodium, and creatinine measured from the arterial blood sampled at the end of the experiment. The plasma creatinine concentration was significantly higher in post-MI rats than that in WKY rats with unilateral renal denervation [24] (n = 9, 0.39 ± 0.02 pg/mL, P < 0.001 by Mann–Whitney test) or that in Goto–Kakizaki rats [19] (n = 7, 0.33 ± 0.05 pg/mL, P = 0.002 by Mann–Whitney test).
Figure 1 illustrates an example of time series obtained from one post-MI rat. The stepwise increase in CSP suppressed SNA, followed by AP and HR reductions. RBF decreased as the AP decreased in this animal. CVP did not decrease with decreasing AP but demonstrated fluctuations during low AP levels. The low AP might have caused respiratory center hypoperfusion and induced spontaneous respiratory activity, which affected CVP through intrathoracic pressure changes. Empagliflozin administration caused slight SNA, AP, and HR decreases, but the effects were transient. The SNA responses during T1, T2, and T3 were not significantly different from that during BL. The maximum AP increased during T1, but the increase subsided during T3. HR decreased, whereas RBF and CVP slightly increased after empagliflozin administration in this animal. Acute vertical changes in the UF plot were artifacts due to manual urine removals. The UF demonstrated near parallel change with AP, and the mean levels and amplitude significantly increased after empagliflozin.
Figure 2 summarizes the group-averaged static characteristics of the carotid sinus baroreflex. Empagliflozin increased the lower asymptote of the total arc without affecting other parameters during T1 (Fig. 2a). Empagliflozin did not significantly affect any of the fitted parameters in the HR control (Fig. 2b) and the neural arc (Fig. 2c). Empagliflozin significantly increased the intercept of the peripheral arc during T1 (Fig. 2d). The slope of the peripheral arc tended to be different among the four periods, with the mean value increasing with time.
In the baroreflex equilibrium diagram (Fig. 3a), the operating-point SNA (the downward arrowhead) decreased after empagliflozin, and the difference from BL was statistically significant during T1 and T2. The operating-point AP (the leftward arrowhead) increased during T1 relative to BL. The SNA–RVR relationship approximated a straight line (Fig. 3b). Empagliflozin increased the intercept during T1, but the effect waned during T2 and T3. The slope of the SNA–RVR relationship tended to be higher after empagliflozin compared with that in BL. The CVP response was not consistent across the animals although the mean data points of the CSP–CVP relationship distributed in an inverse sigmoidal fashion (Fig. 3c). Empagliflozin significantly increased the maximum CVP during T1 relative to BL. The mean data points of the CSP–RBF relationship also distributed in an inverse sigmoid fashion (Fig. 3d), but the RBF response was not consistent across the animals. Empagliflozin did not significantly affect the minimum, maximum, or mean RBF.
Figure 4 presents urinary excretion-related data. The average nUF (Fig. 4a) increased after empagliflozin. The nUF peaked during T1 and remained increased until the end of the observation period. The urinary glucose concentration was 17.4 ± 2.0 mg/dL during BL and markedly increased after empagliflozin (Fig. 4b). The urinary sodium concentration was not significantly different between BL and T1 but decreased during T2 and T3 compared with BL (Fig. 4c). The urinary creatinine concentration significantly decreased after empagliflozin (Fig. 4d). The glucose excretion was near 0 (0.0089 ± 0.0011 mg·min−1 kg−1) during BL and markedly increased after empagliflozin (Fig. 4e). The sodium excretion significantly increased during T1 but returned toward the BL value during T2 and T3 (Fig. 4f). The Ccr per kidney transiently increased during T1. The mean value of Ccr decreased during T2 and T3 relative to BL although the difference was not statistically significant in the post hoc analysis (Fig. 4g).
Figure 5 illustrates the relationship between AP and nUF per kidney during the stepwise changes in CSP. For the linear regression analysis (Fig. 5a), empagliflozin significantly increased the nUF-intercept during T1, but the increasing effect was not seen during T2 and T3. Instead, empagliflozin significantly increased the nUF-slope during T2 and T3 relative to BL. The R2 values between linearly estimated and measured nUF values were 0.883 ± 0.028, 0.887 ± 0.030, 0.910 ± 0.020, and 0.918 ± 0.020 for BL, T1, T2, and T3 periods, respectively. For the logarithmic function analysis (Fig. 5b), the gain significantly increased after empagliflozin throughout the observation period. The intercept on the AP axis was approximately 55 mmHg for all of the BL, T1, T2, and T3 periods. The R2 values between logarithmically estimated and measured nUF values were 0.912 ± 0.024 (P = 0.074), 0.931 ± 0.025 (P = 0.004), 0.940 ± 0.022 (P = 0.027), and 0.949 ± 0.020 (P = 0.027), respectively, where the P values were calculated between the linear and logarithmic estimations using Wilcoxon signed-rank test.
Discussion
The acute effects of an intravenous administration of empagliflozin on baroreflex function and urinary excretion were examined in post-MI rats. The baroreflex neural arc, which describes the baroreflex-mediated SNA response over a wide CSP range, remained unchanged while the effect of empagliflozin on urinary glucose excretion was confirmed during the entire observation period. There was a transient increase in the intercept of the peripheral arc after the empagliflozin administration. During the last observation period, AP did not change relative to BL despite the increased UF.
Effects of empagliflozin on open-loop baroreflex function
Renal energy status can affect systemic SNA via renal afferent signaling [9]. For instance, adenosine-sensitive nerve endings in the renal pelvis increase systemic SNA to produce hypertension in one-kidney, one-clip rats [36]. Heart failure may predispose the kidneys to oxygen deficiency because of decreased cardiac output as well as RBF [22, 23]. The post-MI rats in the present study demonstrated a moderately increased plasma creatinine concentration, indicating renal injury development. The expected SNA inhibition was not detected in the baroreflex neural arc (Fig. 2c) although the SGLT2 inhibition reduces ATP consumption associated with glucose reabsorption at renal proximal tubules. The result is consistent with our previous study on Goto–Kakizaki diabetic rats demonstrating a lack of acute neural arc modulation after empagliflozin administration [19]. The sympathoinhibitory effect of empagliflozin may not be acute but chronic and indirect through renal protection and general disease condition improvement. A study by Gueguen et al. [12] revealed that 1-week empagliflozin treatment, but not a single acute dose, attenuated the exaggerated sympathetic response to lowering AP in diabetic rabbits.
The lower asymptote of the total arc increased during T1 (Fig. 2a), with an increased AP-intercept of the peripheral arc (Fig. 2d). This increase might have partly resulted from a volume loading effect of the empagliflozin administration because of the increased maximum CVP during T1 (Fig. 3c). Changes in RVR might have also contributed to the increase in the AP-intercept of the peripheral arc. The mean SNA–RVR relationship displaced upward during T2 and T3 relative to BL (Fig. 3b) although the difference in the fitted parameters was not statistically significant. The increased RVR after empagliflozin may be mediated by tubuloglomerular feedback (TGF) [8]. SGLT2 inhibition at proximal tubules increases the amount of sodium reaching the macula densa of the distal tubules. This information causes constriction of afferent arterioles to protect the glomeruli by reducing the intraglomerular pressure. The present study revealed an increased amount of urinary sodium excretion during T1 (Fig. 3f), possibly induced afferent arteriole constriction through TGF. Whether vascular resistance in other body areas increases after empagliflozin administration remains unanswered in the present study. Empagliflozin can relax resistance mesenteric arteries in vitro [37]. However, the peripheral arc should have displaced downward if the vasodilative effect of empagliflozin was dominant, as in the case with an angiotensin II type 1 receptor blocker, telmisartan [34] or a soluble guanylate cyclase stimulator, vericiguat, administration [38]. Another factor contributing to AP maintenance after empagliflozin administration is the differential volume regulation between interstitial and intravascular fluid volume by SGLT2 inhibitors [39]. SGLT2 inhibitors reduce the insulin:glucagon ratio that increases hepatic glucose production [40, 41]. The increased hepatic glucose production moves the water from the interstitial space or cells into the vessels because water moves with glucose [42].
The upward peripheral arc displacement may have increased the cardiac afterload and is disadvantageous for the failing heart. However, hemodynamics were not acutely deteriorated after empagliflozin administration in the present study. Recently, a direct cardiac effect of empagliflozin to improve cardiac energy status is suggested despite the lack of SGLT2 expression in cardiac tissues [43]. Such an off-target effect of empagliflozin might have helped the failing heart better tolerate the increased afterload. A slight peripheral arc improvement, i.e., an increase in the slope and/or the intercept of the SNA–AP relationship, caused a marked operating-point SNA reduction as the sigmoid curve of the neural arc intersects with the peripheral arc near the upper plateau in post-MI rats compared with normal rats [44]. The baroreflex equilibrium diagram predicted a significantly reduced operating-point SNA with a slight increase (T1) and no change (T2) in the operating-point AP, though these changes became statistically insignificant during the last observation period (T3) (Fig. 3a). The present finding indicates that keeping AP slightly above the baroreflex threshold pressure could reduce systemic SNA and might help terminate the vicious circle of heart failure associated with sympathetic overactivity. Mechanical circulatory support might achieve somewhat exclusive goals of elevating AP while unloading the failing heart [45]. Instead of elevating AP, stimulating baroreceptors is explored as an alternative approach to treat heart failure [46].
Effects of empagliflozin on urinary excretion
AP increases with SNA in the present experimental settings (Fig. 2d), and AP positively correlated with nUF (Fig. 5) although sympathetic activation exerts an antidiuretic effect through renal vasoconstriction, renin release, and promotion of sodium and water reabsorption [47]. Hence, pressure diuresis outweighs the neurally mediated antidiuretic effect [29]. Empagliflozin increased the mean nUF, thereby facilitating extracellular fluid volume normalization and relieving heart failure-related congestion. Additionally, empagliflozin increased the slope or gain of the AP–nUF relationship (Fig. 5), thereby allowing finer control of extracellular fluid volume in response to AP changes. The slope of the AP–nUF relationship became steeper toward the lower AP range, yielding a convex curvilinearity in the post-MI rats, although the AP–nUF relationship was more linear in our previous studies on normal WKY rats [24, 29]. The x-intercept of the logarithmic function may point to the minimum AP necessary to keep urine production (Fig. 5b). This nonlinearity probably helps avoid excess fluid loss after empagliflozin administration.
Limitations
We only examined the acute effects of empagliflozin under anesthetized conditions while MI was induced chronically. Hence, the results cannot directly be extrapolated to an interpretation of the long-term effect of empagliflozin in a conscious state. As we did not test empagliflozin on sham-operated rats, it remains uncertain whether the observed results were specific to chronic MI rats. Second, the surrounding structures, including the renal nerves, could be damaged to some extent during the flow probe attachment to the left renal artery. Hence, the results of RBF and RVR need to be carefully interpreted. Third, cardiac function was not assessed in the present study. A continuous, stable recording of left ventricular pressure is challenging in the present experimental setting because the large change in the cardiac loading condition can induce ectopic beats possibly through contact of a catheter tip with the ventricular wall. The measurements of cardiac output and left atrial pressure in addition to CVP (≈ right atrial pressure) may allow us to estimate changes in stressed blood volume [48]. Further studies are required to quantify the relationship between changes in UF and stressed blood volume after empagliflozin. Fourth, the vagal nerves were sectioned to establish the open-loop condition of the carotid sinus baroreflex. Although we did not measure cardiac SNA, the HR data may roughly reflect changes in cardiac SNA because of vagotomy. The HR did not decrease significantly after empagliflozin, indicating that empagliflozin did not significantly affect cardiac SNA. Direct measurements of renal afferent and efferent nerve activities are also desirable to strengthen the discussion, though the present results did not support acute modulation of sympathetic regulation by empagliflozin.
Conclusions
The effect of empagliflozin on open-loop baroreflex function was examined in post-MI rats. The sympathoinhibitory effect of empagliflozin was not detected within the observation period. AP, at a given SNA, was well maintained despite a significant increase in urine excretion. Empagliflozin would take more time to manifest a significant hemodynamic effect in this rat model of chronic MI.
Availability of data and materials
The datasets used and/or analyzed during the current study are available from the corresponding author on reasonable request.
Abbreviations
- AP:
-
Arterial pressure
- BL:
-
Baseline
- Ccr :
-
Creatinine clearance
- CSP:
-
Carotid sinus pressure
- CVP:
-
Central venous pressure
- DM:
-
Diabetes mellitus
- DSMO:
-
Dimethyl sulfoxide
- HR:
-
Heart rate
- MI:
-
Myocardial infarction
- nUF:
-
Normalized urine flow
- RBF:
-
Renal blood flow
- RVR:
-
Renal vascular resistance
- SGLT2:
-
Sodium–glucose cotransporter 2
- SNA:
-
Sympathetic nerve activity
- TGF:
-
Tubuloglomerular feedback
- UF:
-
Urine flow
- UV:
-
Urine volume
- WKY:
-
Wistar–Kyoto
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This study was partly supported by grants from Grants-in-Aid for Scientific Research (JSPS KAKENHI 22K08222), Takeda Medical Research Foundation, the research program of Japan Agency for Medical Research and Development (22ama121050j0001), the research program of the Ministry of Internal Affairs and Communications (SCOPE: JP225006004), the Intramural Research Fund for Cardiovascular Diseases of National Cerebral and Cardiovascular Center (21-2-7, 21-2-9), the research grant from JST (JPMJPF2018), and the research grant from NTT Research, Inc. The authors confirm that these parties had no influence in the study design, contents of the article, or selection of this journal.
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TK and KS conceived and designed the study. TK and ML performed the experiments. TK analyzed data. TK, ML, AN, YY, SY, HM, MF, KU, JA Jr, and KS interpreted the results of the experiments. TK prepared the figures and drafted the manuscript. TK, JA Jr, and KS edited and revised the manuscript. All authors read and approved the final manuscript for publication.
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Male Wistar–Kyoto (WKY) rats were purchased from Japan SLC. The rats were cared for strictly following the Guiding Principles for the Care and Use of Animals in the Field of Physiological Sciences, which have been approved by the Physiological Society of Japan. The Animal Subjects Committee at the National Cerebral and Cardiovascular Center reviewed and approved the experimental protocols (No. 22033). As a reference, the data of body weight and heart weight obtained from age-matched WKY rats used in another study (No. 23013) were reported.
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KS received honoraria from ONO PHARMACEUTICAL CO., LTD. and Boehringer Ingelheim GmbH. Other authors declare no conflict of interest regarding this study.
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Kawada, T., Li, M., Nishiura, A. et al. Acute effects of empagliflozin on open-loop baroreflex function and urinary glucose excretion in rats with chronic myocardial infarction. J Physiol Sci 73, 20 (2023). https://doi.org/10.1186/s12576-023-00877-1
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DOI: https://doi.org/10.1186/s12576-023-00877-1