Abstract
Psychedelics have experienced renewed interest following positive clinical effects, however the neurobiological mechanisms underlying effects remain unclear. The paraventricular nucleus of the hypothalamus (PVN) plays an integral role in stress response, autonomic function, social behavior, and other affective processes. We investigated the effect of psilocin, the psychoactive metabolite of psilocybin, on PVN reactivity in Sprague Dawley rats. Psilocin increased stimulus-independent PVN activity as measured by c-Fos expression in male and female rats. Psilocin increased PVN reactivity to an aversive air-puff stimulus in males but not females. Reactivity was restored at 2- and 7-days post-injection with no group differences. Additionally, prior psilocin injection did not affect PVN reactivity following acute restraint stress. Experimental groups sub-classified by baseline threat responding indicate that increased male PVN reactivity is driven by active threat responders. These findings identify the PVN as a significant site of psychedelic drug action with implications for threat responding behavior.
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Introduction
Clinical studies suggest that psychedelics may provide rapid-acting and long-lasting improvements in psychiatric conditions including treatment-resistant depression (TRD), alcohol use disorder (AUD), and smoking cessation1,2,3,4,5,6,7,8,9,10. Psilocybin is currently in phase III clinical trials for TRD11,12,13, and symptom improvements have been observed after a single dose12,13. Psilocybin is dephosphorylated into its active metabolite psilocin, which crosses the blood-brain barrier14 to evoke alterations in synaptic structure and function15,16,17. The 5-hydroxytryptamine 2 A receptor (5-HT2AR) has been shown to be a primary receptor mediating the hallucinogenic effects of psychedelics17,18,19,20. However, recent evidence suggests that the antidepressant21,22 and synaptogenic effects15 may be independent of 5-HT2AR activation, with recent work implicating the BDNF TrkB receptor22. Despite advancements in knowledge, the neurobiological mechanisms underlying the fast-acting and long-lasting effects of these drugs remain unclear.
Psychiatric disorders including post-traumatic stress disorder (PTSD), anxiety, and major depressive disorder (MDD) are associated with dysregulation of the hypothalamic-pituitary-adrenal axis (HPA axis)23,24,25,26, which orchestrates the central and peripheral stress response27,28. The paraventricular nucleus of the hypothalamus (PVN)29 is an integral hub within the HPA axis but has also been implicated in a wide array of affective, social, and stress-related behavioral responses. To investigate the effects of psilocin on PVN function, we utilized histology, fiber photometry (FP), and simultaneous behavioral recording to measure changes in PVN activity and the corresponding behavioral response to an aversive stimulus. Additionally, we performed restraint stress to examine how prior psilocin exposure altered PVN reactivity following an acute stressor. Here, we provide findings pairing PVN reactivity with behavioral responding to an aversive air-puff stimulus and demonstrate sex differences in baseline responding. Additionally, we test how the serotonergic psychedelic, psilocin, alters PVN activity, highlighting sex-specific effects of psilocin administration on stimulus-evoked PVN reactivity and behavior.
Results
Increased activity within the paraventricular nucleus of the hypothalamus (PVN) following psilocin administration
Male and female Sprague Dawley rats (~8 weeks old) were injected with vehicle or psilocin (2 mg/kg, s.c.) 2 hr prior to perfusion. Immunohistochemical analysis and quantification of PVN c-Fos expression as a marker of basal neuronal activation was performed. As injections are inherently stressors, vehicle control groups are included to account for any injection-related confounds, and c-Fos+ expression in both groups may be elevated compared to basal conditions. Following analysis of coronal sections including the PVN, we found that psilocin administration significantly increased c-Fos expression in the PVN of males (t(8) = 2.603, p = 0.03; Fig. 1A) and females(t(8) = 2.324,p = 0.04; Fig. 1B) compared to vehicle control, suggesting that psilocin administration resulted in increased stimulus-independent activity in the PVN for both males and females.
Acute stimulus-evoked effects of psilocin on PVN reactivity and behavior
Male and female Sprague Dawley rats (~8 weeks old, 250-300 g, Fig. 1C) received microinjections of the genetically encoded calcium sensor pGP-AAV-syn-jGCaMP7f-WPRE followed by fiber optic implantation into the PVN (Fig. 1C). Group sizes were determined based on previous work30. After 3 weeks to allow for viral transfection and recovery, fiber photometry recordings were performed in conjunction with exposure to an air-puff stimulus (Figs. 1C, D). Baseline recordings were conducted to determine PVN reactivity prior to drug administration. Animals were assigned to groups following baseline recording sessions to ensure that reactivity between groups was consistent at baseline, thus accounting for any potential differences in viral transfection and GCaMP expression between groups. Following baseline recordings, animals received administration of vehicle or psilocin (2 mg/kg, s.c.). Follow-up recordings were performed 2- and 6/7-days post-injection. On day 8, recordings were performed after a 20-minute restraint stress to test for the effects of an acute stressor on PVN reactivity and the potential effects of prior psilocin administration. To assess changes in individual threat responding, maximum speed values (velocity) and distance traveled were collected within the 10 sec period following air-puff to align immediate behavioral responding with PVN reactivity. Following the completion of all air-puff fiber photometry experiments, brain tissue was collected, and site verification was conducted to ensure proper virus infection and fiber placement (Fig. 1E). At baseline, both males and females exhibited increases in PVN reactivity in response to the air-puff stimulus. However, PVN reactivity in the males was significantly greater than in the females (2-way ANOVA: Finteraction(19,608) = 5.646, p < 0.0001, Fig. 1F), with a significantly greater increase in Peak Point (PP, t(32) = 2.406, p = 0.02). Therefore, males and females were split into separate groups for all analyses moving forward.
In males, no differences were observed between groups in locomotor behavior or time spent in the center of the open field box during habituation or the inter-stimulus interval (ISI) period (Fig. S1A). Following baseline air-puff, there was a significant increase in PVN reactivity, with no differences seen in Area under the Curve (AUC) or PP between vehicle and psilocin groups (Fig. 2A). There was a significant interaction in baseline max speed following air-puff, with a greater increase in velocity seen in vehicle control animals at 2 seconds compared to the psilocin group (2-way ANOVA: Finteraction(9189) = 2.444, p = 0.01, Fig. 2B). All animals showed an increase in distance traveled following air-puff, but no differences were seen between groups (Fig. 2B). On the day of injection, male subjects received either vehicle or psilocin (2 mg/kg, s.c.) injection and were placed in their home cage for 30 minutes prior to being connected to the fiber photometry system and placed into the open field box for video-monitored habituation. Following injection, psilocin treated animals showed significant reductions in distance traveled during the habituation period (2-way ANOVA: Ftime(14,224) = 15.65, p < 0.0001; Finteraction(14,224) = 1.795, p = 0.04; Ftreatment(1,16) = 13.41, p = 0.002; Fig. S1B). Additionally, psilocin treatment significantly reduced time spent in the center as compared to vehicle control, with significant differences seen at 4 and 5 minutes (2-way ANOVA: Finteraction(14,224) = 3.160, p = 0.0002; Fig. S1B). Following air-puff, there was a significant increase in reactivity for both groups, with psilocin treated animals showing significantly greater PVN reactivity (2-way ANOVA: Finteraction(20, 320) = 1.951, p = 0.0092; Ftreatment(1,16) = 5.478, p = 0.0325; Fig. 2C), with increases seen in both AUC (t(16) = 2.798, p = 0.01) and PP (t(16) = 2.334, p = 0.03) of the PVN reactivity trace compared to vehicle control (Fig. 2C). Additionally, psilocin treated males exhibited significantly lower velocity following air-puff as compared to vehicle control (2-way ANOVA: Ftime(9,189) = 10.12, p < 0.0001; Ftreatment(1,21) = 6.246, p = 0.02; Fig. 2D left) and less distance traveled compared to vehicle control (2-way ANOVA: Ftime(1,21) = 7.647, p = 0.01; Ftreatment(1,21) = 4.896, p = 0.03; Fig. 2D right).
Next, female PVN reactivity and threat-responding behavior were tested following the same timeline as above. At baseline, there were no differences seen between groups in locomotion or time spent in the center (Fig. S2A). Following the air puff, PVN reactivity was significantly increased, with no differences seen between groups (Fig. 3A). In the 10-seconds following the baseline air puff, animals showed increased velocity and distance traveled, but no differences were seen between groups (Fig. 3B). On the day of injection, psilocin treated females showed significantly less locomotion compared to vehicle group overall (2-way ANOVA: Ftime(14,266) = 39.80, p < 0.0001; Ftreatment(1,19) = 8.943, p = 0.008; Fig. S2B). For time spent in the center, changes across time were dependent on the treatment group (2-way ANOVA: Finteraction(14,266) = 1.922, p = 0.024; Fig. S2B). Following injection, PVN reactivity in the females was increased, however there were no differences between psilocin and vehicle groups (Fig. 3C). Similarly, all animals showed increased velocity and distance traveled in response to the air-puff, but no differences were seen between groups (Fig. 3D).
Prolonged effects of psilocin on PVN reactivity and behavior
Given clinical findings suggesting prolonged effects of psychedelics following a single dose, male and female subjects were tested at 2- and 6/7-days post-injection to assess prolonged changes in behavior and PVN reactivity. In the males, at the 2-day follow up, there were no differences seen in locomotion or time spent in center (Fig. S1C). There was a significant increase in reactivity following the air-puff in both groups, with no differences seen between groups (Fig. 4A). Animals showed an increase in velocity within the 10-seconds following air-puff, however no differences were seen between groups in velocity or distance traveled (Fig. 4B). At the 6/7-day follow up, there were no differences in locomotion or time spent in center (Fig. S1D). There was a significant increase in PVN reactivity in response to the air-puff, with no differences observed between groups (Fig. 4C). Additionally, all animals showed an increase in velocity and distance traveled following air-puff, but no differences were seen between groups (Fig. 4D).
In the females, on the 2-day follow up, there were no differences seen between groups in locomotion (Fig. S2C). However, for time spent in center, there was an interaction of treatment and time with significant difference between vehicle and psilocin treated rats at minute 7 during habituation (2-way ANOVA: Finteraction(14,266) = 2.208, p = 0.008; Fig. S2C). At 2-days post-injection, there was a significant increase in PVN reactivity in response to air-puff, but no difference seen between groups (Fig. 5A). Velocity and distance traveled increased immediately following air-puff, but no differences were seen between groups (Fig. 5B). At the 6/7-day follow up, there were no differences between groups in locomotion or time spent in center (Fig. S2D). Following air-puff, there was a significant increase in PVN reactivity that did not differ between groups (Fig. 5C). Interestingly, there was a significant interaction in velocity wherein psilocin-treated females showed greater velocity at 2 seconds compared to vehicle control (2-way ANOVA: Finteraction(9,198) = 1.938, p = 0.04; Fig. 5D), however, no differences were seen in distance traveled during that 10-second period (Fig. 5D).
Effects of psilocin on PVN reactivity and threat responding following acute stress in male and females
One potential appeal of psychedelic compounds is that they appear to provide prolonged therapeutic adaptations related to reductions in symptoms of anxiety and depression. Given that stress exposure can instigate differential activation of stress-responsive circuitry, we wanted to test whether prior psilocin administration altered PVN reactivity following exposure to an acute stressor, so animals underwent a 20-minute restraint prior to the air-puff photometry recording session. To confirm restraint-induced stress, animals were tail bled immediately following restraint to measure peripheral corticosterone (CORT) levels. Once blood was collected, animals were placed into the open field box for habituation prior to fiber photometry recordings to test the reactivity of PVN following an acute stress exposure. Following the 20-minute restraint stress CORT levels were elevated consistent with previous findings31 in both males and females, however no significant effects of prior psilocin administration were found (Fig. 6A). In alignment with previous findings32,33, females showed greater concentrations of CORT compared to males regardless of treatment (2-way ANOVA: Fsex(1,34) = 51.52, p < 0.0001; Fig. 6A).
In males, there were no differences seen in locomotion or time spent in the center across the entire recording session (Fig. S3A). Following acute restraint stress, the air-puff was able to elicit a significant increase in PVN reactivity, but no differences were seen between groups (Fig. 6B). Similarly, there was an acute increase in velocity and distance traveled following air-puff, but there were no differences between groups (Fig. 6C). In females, there were no differences seen between groups in locomotion or time spent in the center across the session (Fig. S3B). Following restraint stress, there was a significant increase in PVN reactivity, however, no differences were seen between groups (Fig. 6D). Similarly, there was an acute increase in velocity and distance traveled following air-puff, but there were no differences between groups (Fig. 6E).
Active vs. passive threat responding in males and females
Upon exposure to the air-puff stimulus, animals either employed an active or passive threat response (Fig. 7A). An active response was defined as darting behavior involving an escape from the quadrant within which the air-puff was administered. A passive response was defined as immobility that did not involve an active escape from the quadrant where the air puff occurred. In the males, 58.3% of the vehicle group and 44.4% of the psilocin group employed an active response to the air puff at baseline (Fig. 7B) with a significantly higher proportion of vehicle active responders at baseline (p = 0.01) and injection (p < 0.0001, Fig. 7B). In the females, 66.7% of the vehicle group and 83.3% of the psilocin group employed an active response at baseline (Fig. 7C), with a significantly higher proportion of psilocin active responders at baseline (p = 0.01) and 6/7-days post injection (p < 0.0001), and greater proportion of vehicle active responders on the day of injection (p < 0.0001) and 2-days post-injection (p = 0.03, Fig. 7C). In the females, most of the animals in the psilocin group employed an active threat responding strategy, and therefore, groups could not be further split into active and passive responding subgroups without compromising power. However, the proportion of active vs. passive responders was more evenly split between the males, allowing for secondary analysis to determine the effects of psilocin within these threat-responding subgroups.
Psilocin produces increases in PVN reactivity in active responding but not passive responding males
To further assess the active and passive responses to threat phenotype, additional analyses were conducted within each group across the entire behavior period, including the 10 min habituation period and 5 min post puff ISI. Here, we examined the effects on immobility and time spent in the center as these behaviors are thought to be involved in the effect. In the active responding males, there were no differences between groups in time spent in the center or time spent immobile at baseline (Fig. S4A). Following air-puff, there were significant increases in PVN reactivity, but no differences seen between treatment groups (Fig. 8A). All animals displayed an increase in velocity and distance traveled following the air-puff, however there were no differences between groups (Fig. 8B). On the day of injection, there were no differences between groups in time spent in center. However, the active responding psilocin-treated males showed greater immobility compared to vehicle control (2-way ANOVA: Finteraction(14, 84) = 2.382, p = 0.007; Ftime(14, 84) = 6.672, p < 0.0001; Ftreatment(1, 6) = 10.19, p = 0.01, Fig. S4B). Following air-puff administration, the active responding psilocin treated animals showed a significantly larger response in PVN reactivity (2-way ANOVA: Finteraction(29, 203) = 8.247, p < 0.0001; Ftreatment(1, 7) = 12.80, p = 0.009, Fig. 6C), with a significant increase in AUC (t(7) = 2.992, p = 0.02, Fig. 8C) compared to vehicle control. Interestingly, psilocin active responders showed a significantly greater reduction in active threat responding behavior (increased passive responding) compared to vehicle control (Fisher’s: p = 0.0004, Fig. 8C inset), suggesting that increased PVN reactivity was associated with decreases in active threat responding behavior. All animals displayed an increase in velocity and distance traveled following the airpuff, and there were no differences between groups (Fig. 8D). No differences were seen between vehicle and psilocin active responding males at the 2- and 6/7-day follow-up.
In the passive-responding males, there were no differences seen in immobility time or time spent in the center at baseline (Fig. S4C). At baseline, there were significant increases in PVN reactivity to the air puff seen in both groups, with a greater AUC but not PP observed in the psilocin treated animals as compared to vehicle control (t(7) = 2.410, p = 0.046; Fig. 9A). All psilocin treated passive responders showed a subtle increase in velocity and distance traveled following air-puff, but there were no differences between groups seen (Fig. 9B). On the day of injection, there was a significant interaction of time and treatment for time spent in center seen in the psilocin treated males (2-way ANOVA: Finteraction(14, 112) = 2.540, p = 0.003, Fig. S4D). Additionally, psilocin treated passive males spent significantly more time immobile than vehicle control (2-way ANOVA: Ftime(14, 112) = 12.37, p < 0.0001; Ftreatment(1, 8) = 11.14, p = 0.01, Fig. S4D). Following air-puff administration, there was a significant increase in reactivity following air-puff in both groups, with no differences between vehicle and psilocin treated animals (Fig. 9C). Interestingly, in the vehicle treated passive males there was a greater reduction in passive threat responding (i.e., increased darting) in response to the air-puff compared to baseline, with no changes in threat responding seen in psilocin passive responders (Fisher’s: p < 0.0001, Fig. 9C inset). Additionally, in the vehicle treated passive responder males there was an acute increase in velocity and distance traveled following air-puff, but there were no differences between groups (Fig. 9D). These findings suggest that drug sensitivity is potentially driven by male subjects that employed an active baseline threat response, however, as behavioral subgroups were identified after data collection, sample sizes were out of our control and are smaller than other experimental groups.
Discussion
In the current study, we utilized immunohistochemistry and fiber photometry in combination with in-vivo behavioral recording to determine the effects of the psychedelic compound, psilocin, on stimulus-independent activity and stimulus-evoked reactivity within the paraventricular nucleus of the hypothalamus (PVN). This study provides insight involving the real-time analysis of changes in threat-responding behavior paired with simultaneous fluctuations in calcium dynamics within the PVN after administration of the serotonergic psychedelic psilocin. This work provides a deeper understanding of generalized changes in PVN reactivity following psychedelic administration and a valuable foundation upon which future studies will develop causal inferences regarding the role of changes in PVN reactivity in the behavioral effects of psychedelics. However, one limitation of this study is that there were no cell-type specific approaches employed, and therefore specific mechanisms underlying changes in PVN reactivity remain to be determined. In both males and females, we found that psilocin administration (2 mg/kg, s.c.) produced increases in stimulus-independent activity as measured by c-Fos expression within the PVN. Next, utilizing fiber photometry we found that the air-puff stimulus evoked an increase in PVN reactivity at baseline for both males and females, with a greater level of activation seen in males as compared to females. Following injection, psilocin-treated males showed increased PVN reactivity compared to vehicle control. Interestingly, the increases in PVN reactivity seen in males corresponded to decreases in velocity and distance traveled within the same 10-second timeframe. In females, there were no differences between the vehicle and psilocin groups in PVN reactivity, and, additionally, no differences in velocity or distance traveled immediately following air-puff. While this observed sex-specificity is in contrast with the c-Fos data, it is important to note the differences between stimulus-independent activation and stimulus-induced activation. Stimulus-induced changes can be impacted by a variety of different mechanisms and could point towards differential cell-type expression or innervating circuitry between sexes that could govern differential stimulus-induced activation. Future work will investigate upstream mediators of the PVN as well as employ a more cell-type specific approach to address these questions.
Given the observed persistent effects of psychedelics in clinical trials and previously published work30, we assessed PVN reactivity at multiple time points following injection. In males, acutely elevated PVN reactivity to the air puff following injection was restored at the 2- and 7-day follow-up time points. In both males and females, PVN reactivity remained consistent between groups at 2- and 7 days following injection. To assess the effects of prior psilocin exposure on PVN reactivity following an acute stressor, we utilized a 20-minute restraint stress immediately followed by fiber photometry recording in the PVN. We found that prior psilocin exposure did not alter PVN reactivity following acute restraint stress. To ensure that 20-minute restraint was sufficient to elicit a stress response, serum analyses were performed demonstrating levels of CORT indicative of a stressful experience31 in both males and females following restraint, with higher levels seen in females. Prior exposure to psilocin did not alter serum stress-associated CORT levels in males or females. These data suggest that psilocin does not interfere with the hormonal response to acute stress or the ability of the PVN to increase reactivity following acute stress exposure.
The PVN appears to be a highly relevant region as it pertains to the subcortical effects of psychedelic drug compounds. Previous work has shown that 5-HT2AR agonizts such as DOI, produce increases in c-Fos expression within the PVN34 and increased plasma levels of corticosterone35. Similarly, studies have shown that administration of the 5-HT2AR agonist psychedelic lysergic acid diethylamide (LSD) produced substantial increases in c-Fos expression in the PVN, with increases seen up to 4 hr following administration, the latest time point examined in the study36. Clinical work suggests that dysregulation of the PVN is a characteristic of several psychiatric disorders. For instance, post-mortem studies have shown increased CRF mRNA levels in the PVN of patients with MDD37. Patients with major depressive disorder (MDD) have been shown to have increased CRF+ neurons in the PVN38. Similarly, it has been shown that patients with MDD and bipolar disorder exhibit increases in oxytocin, and vasopressin neurons39. Additionally, patients with MDD and BD show selective neuronal loss in the PVN40. Preclinical studies have shown that exposure to a stressor promotes increases in oxytocin (OXT) release both within the PVN and systemically41. Additionally, chronic variable stress has been shown to double synapses onto CRF neurons within the PVN in rats42. Given the prominent role of the PVN in HPA axis activation, known activation of PVN following administration of 5-HT2AR agonist psychedelics, along with the well-documented dysregulation of the HPA axis associated with psychiatric illness, the PVN is a central site that likely contributes to the clinically observed therapeutic effects of psychedelic compounds.
The current study provides insight into in-vivo PVN reactivity to an aversive stimulus and identifies a sex-specific mechanism of action for psilocin administration to alter PVN calcium dynamics and changes in threat responding immediately following exposure to the stimulus. Here, we showed that psilocin administration produced increases in reactivity within the PVN in males, but no significant effects were seen in females, and no differences in either sex were seen at more prolonged time points. Interestingly, these effects are in contrast to previous findings from our group, wherein we found acute sex-specific effects of psilocin administration causing increased CeA reactivity in females only30. One potential mechanism for this could involve known inhibitory PVN→CeA circuitry, wherein oxytocinergic projections from the PVN to the CeA activate GABAergic cells in the lateral CeA (CeL) that then inhibit output neurons of the CeA located in the medial CeA (CeM)43. It is possible that psilocin produces sex-specific activation of this circuit in males such that an increase in acute reactivity in PVN→CeA circuitry that is having an inhibitory effect on CeM neurons would reduce/prevent an increased activation in the CeA in males.
Another potential circuit mediating these effects is a disynaptic hippocampus→bed nucleus of the stria terminalis (BNST)→PVN projection that has been shown to have an inhibitory effect on the PVN44. One study showed that following exposure to a stressor, there is an increase in CA1 spine density in males and a decrease in females45. Given that CA1 pyramidal neurons have been shown to display high levels of 5-HT2AR expression, and activation of these 5-HT2A receptors increases the firing of these neurons46, differences in density could contribute to differential activation of the known inhibitory hippocampus→BNST→PVN circuit. However, the lack of cell-type specificity is a limitation of the current study, and further work is needed to fully characterize the cell-type specific mechanisms behind the increases in PVN reactivity seen in response to the air puff. Additionally, circuit mapping to identify potential upstream mediators of the observed effects will be an important future direction for this work.
Previous work in the lab showed that a single administration of psilocin produced prolonged decreases in central amygdala reactivity in male, but not female Sprague Dawley rats30. In the present study, no such effects were found, suggesting that acute stress-induced activation remained unperturbed. Although we did not find any effect of psilocin on prolonged PVN reactivity, these data have been included as we find the lack of prolonged effects within the PVN to be of interest. These findings demonstrate stability in PVN reactivity to an aversive stimulus that is maintained following psilocin administration. The PVN is an essential region mediating autonomic functioning and orchestrating sympathetic nervous system activation. Previous work has suggested that PVN functioning is influenced by complex local excitatory and inhibitory circuitry47,48. For instance, it has been shown that local nitric oxide and y-aminobutyric acid (GABA) containing neurons within the PVN function to promote tonic inhibition over sympathetic outflow. This regulation of neuronal activity within the PVN is crucial to avoid hypertension and other, potentially lethal cardiovascular outcomes49,50,51,52. Thus, given the tightly regulated activity within the PVN due it’s heavy involvement in autonomic and cardiovascular functioning, it is possible that a single administration of a drug would not produce any enduring changes in function. This may also explain why exposure to the 20-minute restraint stress didn’t alter PVN reactivity to the air-puff stimulus. Stress exposure promotes excitation of corticotropin-releasing factor (CRF) expressing neurons within the PVN, leading to HPA-axis activation. Recent work suggests that within the PVN there are also CRF sensitive neurons expressing the corticotropin releasing factor receptor 1 (CRFR1) that serve as an inhibitory feedback mechanism within the PVN to prevent hyperreactivity of the PVN and as a result the HPA axis48. Given the observed increases in peripheral corticosterone following restraint stress, it is likely that PVN CRF release would also have activated these CRFR1 receptors in an attempt to dampen hyperreactivity. This could also account for the reactivity of the PVN not being altered following the acute restraint stress. However, it is possible that the observed stability in PVN reactivity may not be seen in subjects modeling psychiatric disease states, for instance, following acute stress exposure. Future studies will examine the effects of psilocin on PVN reactivity within subjects demonstrating anxiogenic pathology to better understand how these drug effects are modulated by psychiatric disease states.
Here, we replicated previous findings that females primarily employ an active threat response30,53,54, whereas males are more evenly split between active and passive responding. Interestingly, it appears that active responding males showed slightly greater basal PVN reactivity than the passive responders, with a similar trend seen in the max speed following air-puff. This discrepancy between active and passive responder PVN reactivity may provide clues for future work investigating the neurobiological mechanisms underlying these divergent behavioral phenotypes. Here, we showed that active responding psilocin-treated males exhibited a significant increase in PVN reactivity compared to active vehicle, while passive responders showed no difference between groups, suggesting that increases in PVN reactivity seen in males were driven by the males that exhibited active responding at baseline. These findings replicate previous findings showing an effect of psilocin on brain region reactivity in active, but not passive responding males30. Together, these findings demonstrate that an animal’s implicit stress-responding strategy and the underlying neurobiology driving this behavioral adaptation may be predictive of drug sensitivity, which could have implications for the clinical use of psilocybin and other psychedelic compounds. While these findings suggest that threat responding strategy may be predictive of psychedelic drug sensitivity, a limitation of the study is that subgroups were determined post hoc and were therefore outside of our control. As a result, sample sizes were relatively small. Given these findings, understanding the neurobiological underpinnings governing this active threat response may offer clues to the mechanisms behind psilocybin’s effects. Recent work suggests there is divergent circuitry from the paraventricular nucleus of the thalamus (PVT) to the CeA and nucleus accumbens (NAc) controlling active vs. passive responding to a stressor, specifically PVT→CeA circuitry promoting passive responding and PVT→NAc circuitry promoting active responding55. It has also been shown that females have a greater spine density and proportion of large spines within the NAc56,57. Together these findings point to a potential explanation for the increased prevalence of active responding in females. Activation of the PVT→NAc pathway along with a NAc that includes increased structural and functional susceptibility to engagement could promote active vs. passive responding in females.
Interestingly, we showed in this study that males exposed to psilocin exhibited a significant reduction in active responding velocity behavior. Activation of CRF+ neurons within the PVN has been implicated in peripheral stress response. CRF+ neurons activate CRF receptors leading to peripheral sympathetic nervous system activation58,59. As activation of the PVN increased during the 10-second window in which rats displayed decreased max speed and active/darting behavior, it is possible that the psilocin induced increases in activation we found are not targeting CRF neurons within the PVN. One potential mechanism behind an increased activation of PVN neurons resulting in decreased flight behavior following psychedelic drug administration could involve oxytocin (OT) neurons within the PVN. Previous studies have suggested that OT administration increases serotonin release in the dorsal raphe (DR) promoting a reduction in anxiety-like behavior, an effect that was blocked with a 5-HT2A/2C antagonist60. This work suggests that these 5-HT2AR expressing neurons within the DR may also express oxytocin receptors, so presumably, the same mechanisms may occur in 5-HT2AR expressing neurons in the PVN. Additionally, it has been shown that the endogenous release of OT within the PVN promotes inhibition of CRF+ cells61. Given that psilocin is a potent 5-HT2AR agonist, activation of these neurons could also activate local OT inhibitory circuitry which could explain decreases in darting behavior. While the current work provides a deeper understanding of generalized changes in PVN reactivity following psychedelic administration, a limitation of this study is that there were no cell-type specific approaches employed, and therefore specific mechanisms underlying changes in PVN reactivity remain unknown. Future work is needed to examine cell-type specificity in order to better characterize the alterations in reactivity seen in the PVN following psilocin administration.
All together, these data provide insight into the involvement of the PVN in psychedelic drug action. Given the relevance of HPA activation on psychiatric disease states, understanding how these drugs alter functioning within this stress-responding circuitry will provide key insights into better understanding how these drugs may elicit their therapeutic effects and provide potential predictive relevance in treatment responsiveness in human clinical populations.
Methods
Stereotaxic surgery
Male and female Sprague Dawley rats (200–400 g, ~8-weeks old at arrival, Envigo, Indianapolis, IN) were group-housed in a humidity- and temperature-controlled (22 °C) vivarium on a 12 hr light/dark cycle with ad libitum access to food and water. At ~9-weeks, animals were anesthetized using isoflurane with an initial bolus of 5%, followed by maintenance at 2–3%. Animals then underwent intracranial surgery using a (KOPF) stereotaxic frame. Bilateral infusions of pGP-AAV-syn-jGCaMP7f-WPRE (Addgene plasmid# 104488-AAV9) were performed at a rate of 100 nl/minute into the PVN using coordinates from bregma (AP: −1.8 mm, ML: +/− 0.5 mm, DV: −7.5 to −8.0 mm). Following injection, the needle was left in place for 5 minutes before retracting. Immediately following microinjections, three skull cap screws were put into place followed by implantation of a dual-tip fiber optic cannula (DFC_200/245-0.37_9mm_GS1.0_FLT), with fiber tips spaced 1 mm apart, placed at 0.3 mm above injection site (coordinates from bregma AP: −1.8 mm, ML: +/−0.0 mm, DV: −7.2 mm). Once fiber was in place, Metabond dental cement (Parkell, Brentwood, NY) was used to fix cannula in place and allowed to dry for 10 minutes before removing cannula holder and retracting stereotaxic arm. Animals were treated with 2.5 mg/kg of Flunixin on the day of surgery and for two days following. Following intracranial surgery at ~8 weeks of age, animals were single-housed in flat-lid cages with waterspout access, and food bowls to avoid damage to implants. All procedures adhered to the University of North Carolina Chapel Hill’s Institutional Animal Care and Use Committee (IACUC).
Drug Administration
On the day of injection, psilocin (Cayman Chemical) was dissolved in 2% glacial acetic acid and brought up to a 1 mg/ml dilution in 0.9% saline. Animals then received subcutaneous (s.c.) injections of either vehicle (2% glacial acetic acid in 0.9% saline) or psilocin and placed back into their home cage for 30 minutes prior to the beginning of habituation in open-field box. For the c-Fos cohort, animals received s.c. injections 2 h prior to perfusion and collection of brain tissue for immunohistochemical analysis.
Fiber photometry recording
Animals underwent fiber photometry/behavioral recordings at ~12 weeks of age. All fiber photometry recordings were taken using the previously mentioned TDT RZ5 (Tucker-Davis Technologies, Alachua, FL) real-time processor and Doric external components and were also conducted in the same plexi-glass chamber30. To test how the PVN would respond to the air-puff stimulus, baseline recordings were taken capturing changes in fluorescence (ΔF/F) following air-puff administration. Animals were split into their respective groups (vehicle vs. psilocin) following baseline recordings, to ensure that baseline PVN reactivity was equivalent between the two groups at baseline. Cohorts were split into two subgroups and ran consecutively to ensure that all animals were running within the first half of the day. On each day of recording, animals were placed in the chamber for 10 minutes for habituation. On the day of injection, animals were given an injection of either vehicle or psilocin (2 mg/kg) and then placed back in their home cage for 30 minutes prior to being connected to the fiber optic patch cord and the beginning of the habituation period. On the restraint stress days, animals first underwent a 20-minute restraint followed by a blood collection through tail bleed. Following these procedures, PVN reactivity was tested following the same air-puff parameters as mentioned above. For all fiber photometry experiments, the same male experimenter handled animals and recording. To avoid potential confounding effects of an added stressor, females were not checked for the estrous cycle.
Air-puff stimulus
The air-puff stimulus30 consisted of a custom made circuit controlling a solenoid that was connected to the air source within the room. Air pressure was regulated with a psi gauge and the solenoid was connected to the TDT system through a BNC cable. Activation of the solenoid through a button command on the TDT system opened the solenoid allowing for an 500 ms burst of air (85 psi) directed at the face of the animal. Tubing was connected to a metal pole and was inserted through a hole in the sound attenuated chamber containing the open field box environment that the animals were held in during recording sessions. This was manually lowered into the arena and aimed toward the animal’s face before activating the circuit box and delivering an air-puff and simultaneous tagged event in the TDT system for peri-event signal analysis. Within each air-puff session, animals were exposed to a 500 ms 85 psi air-puff directed towards the face of the animal followed by a 5-minute inter-stimulus interval (ISI) and then a final repeated air-puff. For each animal, an average of the two air-puffs was collected and used as the reactivity readout.
Locomotor behavior
Locomotor activity was assessed in a clear, plexiglass open field apparatus (50 cm×50 cm) which was located within a sound dampened activity cabinet. Behavioral sessions were recorded and analyzed with ANY-maze video tracking system (Stoelting Co, IL, USA). Behavioral measurements were collected within two time periods: a 10-minute habituation prior to the onset of the air puff and then a 5-minute ISI immediately following exposure to the air puff. Analyzes across time were calculated a 1 min resolution for the overall locomotor behaviors, and additionally at 1 s for the immediate post puff behavioral analysis to correspond with fiber photometry time points. Measures of locomotor activity included distance traveled (m), max speed (m/s), % time spent in the center zone, and time immobile (at 65% sensitivity, animal must remain immobile for at least 2 s). The center zone was defined within the tracking software ( ~ 7.6 cm×7.6 cm; 45% of total area), and the time spent variable was calculated as (time spent in center zone/(total time spent in center + time spent in periphery)) × 100). A total of 8 subjects (3 females and 5 males) were excluded from behavioral analyses that included habituation time period (locomotion, time spent in center, immobility) due to technical difficulties with behavioral video recording.
Restraint stress
Restraint stress procedures were performed using a Broome Rodent Restrainer (Braintree Scientific, Braintree MA). Animals were placed in a restraint stress tube with a foam insert to help protect against excessive bumping of the cannula on the plexiglass walls. Animals were restrained for 20 minutes. Following the 20-minute restraint, animals were kept in the tube for a 1–5 min for the collection of an ample volume of blood through the tail vein for cortisol analysis. Immediately following restraint stress and blood collection, animals were placed in the open field box for air-puff administration and PVN reactivity recording.
Perfusion
Animals were first anesthetized using isoflurane prior to perfusion. Upon entry to the heart, the circulatory system was first flushed with phosphate-buffered saline (PBS) followed by at least 120 mL of 4% paraformaldehyde (w/v). Brains were then stored in 4% paraformaldehyde (w/v) for 24 h before being transferred to a 30% sucrose solution. Tissue was sectioned into 40 µm thick slices using a freezing microtome and then stored in a cryoprotectant solution (comprising 30% v/v ethylene glycol and 30% w/v sucrose in phosphate-buffered saline) at 4 °C until further use.
Corticosterone assay
Tail blood was collected in 1.5 mL microcentrifuge tubes (Fisherbrand, Waltham, MA, CAT#05-408-129) and kept on ice. Blood samples were centrifuged, and serum was collected in 0.2 mL PCR tubes (Eppendorf, Enfield, CT, CAT#951010006) and stored at −20 °C. The serum was analyzed for corticosterone using a commercially available CORT ELISA kit (Arbor Assays, Ann Arbor, MI, CAT#K014-H5) that was performed per the manufacturer’s protocol. Results from the corticosterone assay are expressed as nanograms/milliliter (ng/mL).
Histology/Immunofluorescence staining
To assess changes in basal activity while under the acute effects of the drugs, animals in both groups were given subcutaneous injections of either vehicle or psilocin (2 mg/kg). Given that injections are inherently stressful, it is possible that both groups would have elevated levels of c-Fos expression within the PVN. While this could confound baseline levels of c-Fos, this perturbation is controlled between groups. Prior to injection, animals were perfused, and brain tissue was collected for analysis. 40 μm sections (AP coordinates −1.6 mm to −2.16 mm) were collected and prepared for immunohistochemistry (IHC) to stain for the protein c-Fos. The IHC protocol is as follows: wash in PBS, 30 min incubation in 50% methanol/PBS, 5 min in 3% hydrogen peroxide, blocking solution (0.3% Triton X-100; Thermo Fisher), 1 hr at room temperature (RT) in 1% bovine serum albumin, 24 hr incubation at 4 °C in rabbit anti-cFos (1:3000, Millipore Sigma; ABE457). Day 2: wash in 0.1% Tween-20 in tris-buffered saline (TNT), 30 min in TNB blocking buffer (Perkin-Elmer FP1012), 2 hr in goat anti-rabbit horseradish peroxidase (HRP; 1:200, Abcam ab6721), TNT washes, and finally a 10 min at RT incubation in tyramide conjugated fluorescein (1:50) in TSA amplification diluent (Akoya Biosciences, NEL741001KT). Following IHC, slices were mounted on slides using Vectashield ® HardSet™ Antifade Mounting Medium with DAPI (H1500, Vector Laboratories, Burlingame, CA). Images were acquired using a Keyence BZ-X800 fluorescence microscope. Images were taken at 20x magnification and the BZ-X800 Analyzer program was used to create stitched images for quantification. Quantification utilizing ImageJ62 was conducted to manually count labeled, c-Fos+ cells. PVN region was outlined and counted by two separate experiments. The experimenter was blinded for counting. Counts were taken per hemisphere and averaged to obtain a value for each subject.
Statistics and reproducibility
Collection of raw fiber photometry signal and subsequent data analysis to include binning of data into 500 ms time bins and bootstrapping confidence intervals were performed using Matlab (Version 2023a, The Mathworks, Inc.) and a custom written Matlab script (https://doi.org/10.5061/dryad.3ffbg79qr). For all binned trace data visualizations, we applied a bootstrapping confidence interval (CI) method (99% CI, 1000 iterations)63. This approach involved calculating a hypothetical ‘mean’ ΔF/F by repeatedly resampling the subject mean ΔF/F with replacement, aligning with the number of samples. The sample size (n) for all analyses matched the number of subjects per group. This bootstrapping procedure was performed 1000 times to generate a nonparametric distribution of population mean simulations for each time point within the window. A statistically significant increase (>0%) in Ca2+ transients following air-puff administration was identified by data points where the lower bound of the 99% CI exceeded 063,64,65 These significant increases were indicated on graphs by color-coded lines above the trace bin plots. All comparisons of proportions were done using Fisher’s exact tests. Comparisons of c-Fos, PP, AUC, and CORT concentrations were done using unpaired t-test to compare between groups at each time. 2-way RM ANOVAS were used to compare binned trace plots and behavioral data metrics between groups. All data were graphed and statistically analyzed with Prism 10.0.3 (GraphPad Software, MA, USA). For fiber photometry recordings, subjects were excluded from group data analysis if site verification revealed incorrect GCaMP injection location and/or fiber placement was outside of the PVN but was still included for behavioral analysis. Sample sizes for all experimental groups are listed within figure legends. Experimenters were blinded during manual cell counting and manual behavioral scoring. The experimenter was not blinded to condition during experimentation or during data analysis as these were all automated processes measuring changes in physiology and, therefore, did not involve any subjective interpretation during data collection. Sample sizes were determined based on previous work in the lab30, however no a priori power calculations were conducted.
Reporting summary
Further information on research design is available in the Nature Portfolio Reporting Summary linked to this article.
Data availability
All data generated in this study, including a source data file containing raw data values for each figure, have been deposited in the Dryad database [https://doi.org/10.5061/dryad.3ffbg79qr]. Source data are provided in this paper.
Code availability
Custom written MATLAB code and resulting MATLAB structures have been made available on the Dryad database [https://doi.org/10.5061/dryad.3ffbg79qr].
References
Bogenschutz, M. P. & Johnson, M. W. Classic hallucinogens in the treatment of addictions. Prog. Neuro-Psychopharmacol. Biol. Psychiatry 64, 250–258 (2016).
Davis, A. K. et al. Effects of psilocybin-assisted therapy on major depressive disorder: a randomized clinical trial. JAMA psychiatry 78, 481–489 (2021).
Johnson, M. W., Garcia-Romeu, A. & Griffiths, R. R. Long-term follow-up of psilocybin-facilitated smoking cessation. Am. J. drug alcohol Abus. 43, 55–60 (2017).
Johnson, M. W. & Griffiths, R. R. Potential therapeutic effects of psilocybin. Neurotherapeutics 14, 734–740 (2017).
Griffiths, R. R. et al. Psilocybin produces substantial and sustained decreases in depression and anxiety in patients with life-threatening cancer: A randomized double-blind trial. J. Psychopharmacol. 30, 1181–1197 (2016).
Roseman, L., Demetriou, L., Wall, M. B., Nutt, D. J. & Carhart-Harris, R. L. Increased amygdala responses to emotional faces after psilocybin for treatment-resistant depression. Neuropharmacology 142, 263–269 (2018).
Carhart-Harris, R. L. et al. Psilocybin for treatment-resistant depression: fMRI-measured brain mechanisms. Sci. Rep. 7, 1–11 (2017).
Nutt, D., Erritzoe, D. & Carhart-Harris, R. Psychedelic psychiatry’s brave new world. Cell 181, 24–28 (2020).
Barrett, F. S., Doss, M. K., Sepeda, N. D., Pekar, J. J. & Griffiths, R. R. Emotions and brain function are altered up to one month after a single high dose of psilocybin. Sci. Rep. 10, 1–14 (2020).
Ross, S. et al. Rapid and sustained symptom reduction following psilocybin treatment for anxiety and depression in patients with life-threatening cancer: a randomized controlled trial. J. Psychopharmacol. 30, 1165–1180 (2016).
Agrawal, M. et al. Assessment of psilocybin therapy for patients with cancer and major depression disorder. JAMA oncol. 9, 864–866 (2023).
Goodwin, G. M. et al. Single-dose psilocybin for a treatment-resistant episode of major depression. N. Engl. J. Med. 387, 1637–1648 (2022).
Raison, C. L. et al. Single-dose psilocybin treatment for major depressive disorder: a randomized clinical trial. JAMA 330, 843–853 (2023).
Eivindvik, K., Rasmussen, K. & Sund, R. Handling of psilocybin and psilocin by everted sacs of rat jejunum and colon. Acta pharmaceutica nordica 1, 295–302 (1989).
Shao, L.-X. et al. Psilocybin induces rapid and persistent growth of dendritic spines in frontal cortex in vivo. Neuron 109, 2535–2544. e2534 (2021).
Raval, N. R. et al. A single dose of psilocybin increases synaptic density and decreases 5-HT2A receptor density in the pig brain. Int. J. Mol. Sci. 22, 835 (2021).
Ly, C. et al. Psychedelics promote structural and functional neural plasticity. Cell Rep. 23, 3170–3182 (2018).
de la Fuente Revenga, M. et al. Prolonged epigenomic and synaptic plasticity alterations following single exposure to a psychedelic in mice. Cell Rep. 37, 109836 (2021).
Vargas, M. V. et al. Psychedelics promote neuroplasticity through the activation of intracellular 5-HT2A receptors. Science 379, 700–706 (2023).
Halberstadt, A. L., Chatha, M., Klein, A. K., Wallach, J. & Brandt, S. D. Correlation between the potency of hallucinogens in the mouse head-twitch response assay and their behavioral and subjective effects in other species. Neuropharmacology 167, 107933 (2020).
Hesselgrave, N., Troppoli, T. A., Wulff, A. B., Cole, A. B. & Thompson, S. M. Harnessing psilocybin: antidepressant-like behavioral and synaptic actions of psilocybin are independent of 5-HT2R activation in mice. Proc. Natl Acad. Sci. 118, e2022489118 (2021).
Moliner, R. et al. Psychedelics promote plasticity by directly binding to BDNF receptor TrkB. Nat. Neurosci. 26, 1032–1041 (2023).
Gillespie, C. F. & Nemeroff, C. B. Hypercortisolemia and depression. Psychosom. Med. 67, S26–S28 (2005).
Holsboer, F. Blunted corticotropin and normal cortisol response to human corticotropin-releasing factor in depression. N. Engl. J. Med 311, 1127–1137 (1984).
Abelson, J. L., Khan, S., Liberzon, I. & Young, E. A. HPA axis activity in patients with panic disorder: review and synthesis of four studies. Depression anxiety 24, 66–76 (2007).
Condren, R., O’Neill, A., Ryan, M., Barrett, P. & Thakore, J. HPA axis response to a psychological stressor in generalised social phobia. Psychoneuroendocrinology 27, 693–703 (2002).
Jankord, R. & Herman, J. P. Limbic regulation of hypothalamo‐pituitary‐adrenocortical function during acute and chronic stress. Ann. N. Y. Acad. Sci. 1148, 64–73 (2008).
Feldman, S., Conforti, N. & Weidenfeld, J. Limbic pathways and hypothalamic neurotransmitters mediating adrenocortical responses to neural stimuli. Neurosci. Biobehav. Rev. 19, 235–240 (1995).
Gray, T. S., Carney, M. E. & Magnuson, D. J. Direct projections from the central amygdaloid nucleus to the hypothalamic paraventricular nucleus: possible role in stress-induced adrenocorticotropin release. Neuroendocrinology 50, 433–446 (1989).
Effinger, D. P., Quadir, S. G., Ramage, M. C., Cone, M. G. & Herman, M. A. Sex-specific effects of psychedelic drug exposure on central amygdala reactivity and behavioral responding. Transl. Psychiatry 13, 119 (2023).
Kalil, B., Leite, C., Carvalho-Lima, M. & Anselmo-Franci, J. Role of sex steroids in progesterone and corticosterone response to acute restraint stress in rats: sex differences. Stress 16, 452–460 (2013).
Haleem, D. J., Kennett, G. & Curzon, G. Adaptation of female rats to stress: shift to male pattern by inhibition of corticosterone synthesis. Brain Res. 458, 339–347 (1988).
Kant, G. J. et al. Comparison of stress response in male and female rats: pituitary cyclic AMP and plasma prolactin, growth hormone and corticosterone. Psychoneuroendocrinology 8, 421–428 (1983).
Zhang, Y. et al. Evidence that 5-HT2A receptors in the hypothalamic paraventricular nucleus mediate neuroendocrine responses to (−) DOI. J. Neurosci. 22, 9635–9642 (2002).
Mikkelsen, J. D., Hay‐Schmidt, A. & Kiss, A. Serotonergic Stimulation of the Rat Hypothalamo‐Pituitary‐Adrenal Axis: Interaction between 5‐HT1A and 5‐HT2A Receptors. Ann. N. Y. Acad. Sci. 1018, 65–70 (2004).
Frankel, P. S. & Cunningham, K. A. The hallucinogen d-lysergic acid diethylamide (d-LSD) induces the immediate-early gene c-Fos in rat forebrain. Brain Res. 958, 251–260 (2002).
Raadsheer, F. C. et al. Corticotropin-releasing hormone mRNA levels in the paraventricular nucleus of patients with Alzheimer’s disease and depression. Am. J. Psychiatry 152, 1372–1376 (1995).
Raadsheer, F. C., Hoogendijk, W. J., Stam, F. C., Tilders, F. J. & Swaab, D. F. Increased numbers of corticotropin-releasing hormone expressing neurons in the hypothalamic paraventricular nucleus of depressed patients. Neuroendocrinology 60, 436–444 (1994).
Purba, J. S., Hoogendijk, W. J., Hofman, M. A. & Swaab, D. F. Increased number of vasopressin-and oxytocin-expressing neurons in the paraventricular nucleus of the hypothalamus in depression. Arch. Gen. psychiatry 53, 137–143 (1996).
Manaye, K. F. et al. Selective neuron loss in the paraventricular nucleus of hypothalamus in patients suffering from major depression and bipolar disorder. J. Neuropathol. Exp. Neurol. 64, 224–229 (2005).
Nishioka, T., Anselmo-Franci, J. A., Li, P., Callahan, M. F. & Morris, M. Stress increases oxytocin release within the hypothalamic paraventricular nucleus. Brain Res. 781, 57–61 (1998).
Miklós, I. H. & Kovács, K. J. Reorganization of synaptic inputs to the hypothalamic paraventricular nucleus during chronic psychogenic stress in rats. Biol. psychiatry 71, 301–308 (2012).
Knobloch, H. S. et al. Evoked axonal oxytocin release in the central amygdala attenuates fear response. Neuron 73, 553–566 (2012).
Cole, A. B., Montgomery, K., Bale, T. L. & Thompson, S. M. What the hippocampus tells the HPA axis: Hippocampal output attenuates acute stress responses via disynaptic inhibition of CRF+ PVN neurons. Neurobiol. Stress 20, 100473 (2022).
Shors, T. J., Chua, C. & Falduto, J. Sex differences and opposite effects of stress on dendritic spine density in the male versus female hippocampus. J. Neurosci. 21, 6292–6297 (2001).
Zhang, G. et al. Examination of the hippocampal contribution to serotonin 5-HT2A receptor-mediated facilitation of object memory in C57BL/6J mice. Neuropharmacology 109, 332–340 (2016).
Herman, J. P., Tasker, J. G., Ziegler, D. R. & Cullinan, W. E. Local circuit regulation of paraventricular nucleus stress integration: glutamate–GABA connections. Pharmacol. Biochem. Behav. 71, 457–468 (2002).
Jiang, Z., Rajamanickam, S. & Justice, N. J. CRF signaling between neurons in the paraventricular nucleus of the hypothalamus (PVN) coordinates stress responses. Neurobiol. stress 11, 100192 (2019).
Stern, J. E. Nitric oxide and homeostatic control: an intercellular signalling molecule contributing to autonomic and neuroendocrine integration? Prog. biophysics Mol. Biol. 84, 197–215 (2004).
Watkins, N., Cork, S. & Pyner, S. An immunohistochemical investigation of the relationship between neuronal nitric oxide synthase, GABA and presympathetic paraventricular neurons in the hypothalamus. Neuroscience 159, 1079–1088 (2009).
Zhang, K. & Patel, K. P. Effect of nitric oxide within the paraventricular nucleus on renal sympathetic nerve discharge: role of GABA. Am. J. Physiol. -Regulatory, Integr. Comp. Physiol. 275, R728–R734 (1998).
Pyner, S. Neurochemistry of the paraventricular nucleus of the hypothalamus: implications for cardiovascular regulation. J. Chem. Neuroanat. 38, 197–208 (2009).
Gruene, T. M., Flick, K., Stefano, A., Shea, S. D. & Shansky, R. M. Sexually divergent expression of active and passive conditioned fear responses in rats. Elife 4, e11352 (2015).
Mitchell, J. R. et al. Darting across space and time: parametric modulators of sex-biased conditioned fear responses. Learn. Mem. 29, 171–180 (2022).
Ma, J. et al. Divergent projections of the paraventricular nucleus of the thalamus mediate the selection of passive and active defensive behaviors. Nat. Neurosci. 24, 1429–1440 (2021).
Wissman, A. M., May, R. M. & Woolley, C. S. Ultrastructural analysis of sex differences in nucleus accumbens synaptic connectivity. Brain Struct. Funct. 217, 181–190 (2012).
Forlano, P. M. & Woolley, C. S. Quantitative analysis of pre‐and postsynaptic sex differences in the nucleus accumbens. J. Comp. Neurol. 518, 1330–1348 (2010).
Rajamanickam, S. & Justice, N. J. Hypothalamic corticotropin-releasing factor neurons modulate behavior, endocrine, and autonomic stress responses via direct synaptic projections. Current Opinion in Endocrine and Metabolic Research, 26, 100400 (2022).
Carrasco, G. A. & Van de Kar, L. D. Neuroendocrine pharmacology of stress. Eur. J. Pharmacol. 463, 235–272 (2003).
Yoshida, M. et al. Evidence that oxytocin exerts anxiolytic effects via oxytocin receptor expressed in serotonergic neurons in mice. J. Neurosci. 29, 2259–2271 (2009).
Pati, D. et al. Endogenous oxytocin inhibits hypothalamic corticotrophin-releasing hormone neurones following acute hypernatraemia. J. Neuroendocrinol. 32, e12839 (2020).
Schneider, C. A., Rasband, W. S. & Eliceiri, K. W. NIH Image to ImageJ: 25 years of image analysis. Nat. Methods 9, 671–675 (2012).
Bland, J. M. & Altman, D. G. Statistics notes: bootstrap resampling methods. BMJ. 350, h2622 (2015).
Bird, K. D. Analysis of Variance Via Confidence Intervals. (Sage, 2004).
Choi, E. A., Jean-Richard-dit-Bressel, P., Clifford, C. W. & McNally, G. P. Paraventricular thalamus controls behavior during motivational conflict. J. Neurosci. 39, 4945–4958 (2019).
Acknowledgements
This work was supported by National Institute of Health grants AA026858 (M.A.H.), GM135095 (D.P.E.), and by the Brain and Behavior Research Foundation NARSAD Young Investigator Award (M.A.H.)
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D.P.E. contributed to the initial conception, experimental design, apparatus design, surgical procedures, behavioral recording, histology, data analysis, custom code, data visualization, the initial draft of the manuscript, and manuscript editing. J.L.H. contributed to the behavioral recording, behavioral analysis, a section in methods, and manuscript editing. S.E.M. contributed to CORT assay, CORT analysis, and section in methods. S.N.M. contributed to CORT assay. S.G.Q. contributed to histological analyses, schematic illustrations, and manuscript editing. C.S.R. contributed to histology and draft editing. D.T. contributed to histology and manuscript editing. M.E.S. contributed to histology and manuscript editing. M.W.H. contributed to histology and manuscript editing. C.W.H. contributed to the behavioral recording and manuscript editing. M.A.H. contributed to the initial conception, experimental design, behavioral assay, and acquisition of funds.
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Effinger, D.P., Hoffman, J.L., Mott, S.E. et al. Increased reactivity of the paraventricular nucleus of the hypothalamus and decreased threat responding in male rats following psilocin administration. Nat Commun 15, 5321 (2024). https://doi.org/10.1038/s41467-024-49741-9
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DOI: https://doi.org/10.1038/s41467-024-49741-9
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