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Article

The Hypothermic Effect of Hydrogen Sulfide Is Mediated by the Transient Receptor Potential Ankyrin-1 Channel in Mice

by
Emoke Olah
1,†,
Zoltan Rumbus
1,†,
Viktoria Kormos
2,
Valeria Tekus
2,3,
Eszter Pakai
1,
Hannah V. Wilson
4,
Kata Fekete
1,
Margit Solymar
1,
Leonardo Kelava
1,
Patrik Keringer
1,
Balazs Gaszner
3,5,
Matthew Whiteman
6,
Julie Keeble
4,
Erika Pinter
2,3 and
Andras Garami
1,*
1
Department of Thermophysiology, Institute for Translational Medicine, Medical School, University of Pecs, H-7622 Pecs, Hungary
2
Department of Pharmacology and Pharmacotherapy, Medical School, University of Pecs, H-7622 Pecs, Hungary
3
Janos Szentagothai Research Centre, University of Pecs, H-7622 Pecs, Hungary
4
Centre for Human & Applied Physiological Sciences, King’s College London, London WC2R 2LS, UK
5
Research Group for Mood Disorders, Department of Anatomy, Medical School and Center for Neuroscience, University of Pecs, H-7622 Pecs, Hungary
6
Institute of Biomedical and Clinical Sciences, University of Exeter Medical School, University of Exeter, Exeter EX1 2LU, UK
*
Author to whom correspondence should be addressed.
†
These authors contributed equally to this work.
Pharmaceuticals 2021, 14(10), 992; https://doi.org/10.3390/ph14100992
Submission received: 25 August 2021 / Revised: 24 September 2021 / Accepted: 25 September 2021 / Published: 29 September 2021
(This article belongs to the Section Pharmacology)
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Abstract

:
Hydrogen sulfide (H2S) has been shown in previous studies to cause hypothermia and hypometabolism in mice, and its thermoregulatory effects were subsequently investigated. However, the molecular target through which H2S triggers its effects on deep body temperature has remained unknown. We investigated the thermoregulatory response to fast-(Na2S) and slow-releasing (GYY4137) H2S donors in C57BL/6 mice, and then tested whether their effects depend on the transient receptor potential ankyrin-1 (TRPA1) channel in Trpa1 knockout (Trpa1−/−) and wild-type (Trpa1+/+) mice. Intracerebroventricular administration of Na2S (0.5–1 mg/kg) caused hypothermia in C57BL/6 mice, which was mediated by cutaneous vasodilation and decreased thermogenesis. In contrast, intraperitoneal administration of Na2S (5 mg/kg) did not cause any thermoregulatory effect. Central administration of GYY4137 (3 mg/kg) also caused hypothermia and hypometabolism. The hypothermic response to both H2S donors was significantly (p < 0.001) attenuated in Trpa1−/− mice compared to their Trpa1+/+ littermates. Trpa1 mRNA transcripts could be detected with RNAscope in hypothalamic and other brain neurons within the autonomic thermoeffector pathways. In conclusion, slow- and fast-releasing H2S donors induce hypothermia through hypometabolism and cutaneous vasodilation in mice that is mediated by TRPA1 channels located in the brain, presumably in hypothalamic neurons within the autonomic thermoeffector pathways.

1. Introduction

Hydrogen sulfide (H2S) was considered to be an environmental toxin before it was identified as an endogenously produced mediator in the 1940s (for a review, see [1]). At present, H2S is recognized as an important gasotransmitter, which plays roles in a wide spectrum of physiological processes in the brain as well as in peripheral tissues in health and disease [2,3]. H2S is synthesized both centrally and peripherally by specific enzymes including cystathionine β-synthase, cystathionine γ-lyase, and 3-mercaptopyruvate sulfurtransferase, but alternative H2S-producing pathways are also known [3,4]. Endogenously, H2S is present within the nM to low µM concentration range and it is catabolized by enzymatic and non-enzymatic processes [5]. In the past decades, the role of H2S has been implicated in a number of physiological and pathological conditions [2,3,4], including the regulation of core body temperature (Tb) [6].
In 2005, Blackstone et al. [7] reported that the inhalation of H2S induces concentration-dependent hypometabolism and hypothermia in mice without causing behavioral or functional damages to the animals. The authors hypothesized that the thermal effect was evoked through the H2S-induced inhibition of the terminal enzyme complex in the electron transport chain and called the condition as suspended animation-like state [7]. The hypometabolic and hypothermic response to H2S inhalation was also shown by other authors [8], and similar results were obtained by the administration of the H2S donor sodium hydrosulfide (NaHS) in anesthetized rats [9] and by infusion of dimethyl trisulfide in conscious mice [10]. However, the thermoregulatory role of H2S was debated later, when Hemelrijk et al. [11] could not reproduce the H2S-induced thermal effects and concluded that H2S exacerbates hypoxia-induced hypometabolism, but H2S in itself does not decrease metabolic rate and deep Tb. The mediation of hypoxia-induced hypothermia by H2S was supported by the results of Kwiatkoski et al. [12], showing that production of H2S increases in the hypothalamus of rats exposed to hypoxia. Further complicating the issue, in larger animals the effects of H2S on metabolism and Tb remained contradictory, because H2S-induced hypothermia was shown in pigs by some authors [13,14], whereas other groups did not find an effect on Tb in pigs [15,16] and in sheep [17].
Several mechanisms underlying the thermoregulatory effects of H2S have been proposed (for review, see [6]), but the molecular site of action and the thermoeffector mechanism underlying H2S-induced hypothermia has remained unclarified. Peripheral and central inhibition of H2S-synthetizing enzymes were recently both shown to influence the fever response in rats, but neither of them altered deep Tb in afebrile animals [18,19]. Within the central nervous system, endogeneous H2S production in the hypothalamus was shown to be involved in the hypothermia associated with endotoxic shock [20] and hypoxia [12]. However, injection of low doses of sodium sulfide (Na2S), i.e., an H2S-releasing salt, into the lateral ventricle or the medullary raphe did not cause any significant effect on Tb of euthermic rats [19,21]. With regards to the thermoeffector mechanism, although it is well known that H2S plays a role in the regulation of the vascular tone [3,6], it is unknown whether skin vasodilation, a principal autonomic heat-dissipating thermoeffector [22], is recruited in the H2S-induced hypothermia. A plausible molecular target for a thermoregulatory effect could be a sensor that is expressed on neurons located within the thermoeffector pathways, therefore its stimulation can directly lead to a change in deep Tb via modulation of the activity of one or more thermoeffector organs. Interestingly, H2S has been shown to interact with transient receptor potential (TRP) channels also including temperature-sensitive receptors, e.g., TRP ankyrin-1 (A1) and vanilloid-1 (V1) (for a review, see [23]), which channels are expressed within the neural thermoeffector pathways [22]. The TRPA1 channel can be of crucial importance for the thermal action of H2S, since TRPA1 channel-mediated effects of sulfide donors and polysulfide were identified in a plethora of experimental models used for the study of pain, inflammation, vasomotor responses, as well as neuronal, urinary, and cardiorespiratory functions.
An extensive list of studies that describeTRPA1-mediated effects of H2S was recently collected by Pozsgai et al. [24]. However, thermoregulatory effects were not mentioned by the authors. The diverse existence of H2S-induced TRPA1 activation in different homeostatic processes may suggest that it could also be involved in thermoregulation. In support of this possibility, TRPA1 was shown to be essential in the autonomic thermoregulatory response, particularly in cutaneous vasoconstriction, following cold exposure in mice [25]. Seemingly contradicting this finding is a previous study [26] that found that TRPA1 channels do not play a cold sensor role for autonomic thermoregulation in rodents. However, it is important to note that even if a TRP channel does not play a thermosensor role in the thermoregulation system, its modulation with ligands can still lead to changes of deep Tb, as was shown in the case of another temperature-sensitive receptor, TRPV1 [27]. In summary, the question of whether and how the TRPA1 channel is involved in H2S-induced hypothermia has remained unanswered.
In the present study, we have investigated the thermoeffector mechanisms of the hypothermic response to fast- and slow-releasing H2S donors, then we used Trpa1 knockout mice to show the contribution of TRPA1 channels to the response. We also studied TRPA1 expression in thermoregulation-related brain nuclei to explore the possible site of action for the hypothermic effect of H2S.

2. Results

2.1. Central Administration of Na2S Decreases Deep Tb in Mice via Inhibition of Thermogenesis and Induction of Vasodilation in the Skin

First, we studied the thermoregulatory effect of Na2S, a fast-releasing H2S donor [28], administered intracerebroventricularly (i.c.v.) in C57BL/6 mice by using respirometry thermometry (for details, see Experimental Setups in Materials and Methods). In response to Na2S, the mice developed a decrease in deep Tb, which was more pronounced at the higher dose, whereas saline did not cause any effects (Figure 1).
The hypothermic response to Na2S developed rapidly at both of the applied doses, and at 20 min it reached the biggest mean decrease of −0.5 ± 0.3 °C at 0.5 mg/kg and −0.8 ± 0.3 °C at 1 mg/kg (p = 0.045 and 0.005, respectively). The effect of the treatment on Tb was significant [ANOVA, F(2506) = 41.158, p < 0.001] and so was the effect of time [ANOVA, F(21,506) = 1.809, p = 0.015]. The effect was significant for both the lower and the higher doses of Na2S as compared to saline (p < 0.001 for both). At the 0.5 mg/kg dose of Na2S, deep Tb was significantly lower than in saline-treated mice at 20, 170, and 180 min, while at the 1 mg/kg dose the drop in deep Tb was significant between 20–180 min compared to saline.
In the same experiments, we also measured the rate of oxygen consumption (VO2), which was regarded as an indicator of non-shivering thermogenesis (i.e., one of the principal autonomic thermoeffectors), as in previous studies in mice [29,30]. The Na2S-induced hypothermia was brought about by a fall in VO2, which changed with similar dynamics as deep Tb (Figure 1). Similar to Tb, the effect of the treatment on VO2 was significant [ANOVA, F(2506) = 28.860, p < 0.001] and so was the effect of time [ANOVA, F(21,506) = 1.654, p = 0.034]. The effect was significant for both the lower and the higher doses of Na2S as compared to saline (p = 0.024 and p < 0.001, respectively). At the 1 mg/kg dose, VO2 was significantly lower than in saline-treated mice between 20 and 110 min. Since the expected effect was hypothermia, these experiments were performed at a subthermoneutral ambient temperature of 22 °C. Mice and rats exhibit cutaneous vasoconstriction in a subneutral environment as also indicated by their low tail-skin temperature [30,31], which did not allow us to study the potential contribution of skin vasodilation to the Na2S-induced hypothermia in this setup.
In order to determine whether cutaneous blood perfusion is affected by central Na2S administration, as our next step, we measured changes of skin blood flow intensity on the lumbar back of anesthetized mice with laser speckle contrast imaging. The i.c.v. administration of Na2S (1 mg/kg) caused a prompt elevation in the cutaneous blood flow intensity, which reached the highest average of 14 ± 6% already at 2 min, then it decreased somewhat but remained higher than in the saline-treated mice throughout the experiment [ANOVA, F(1250) = 74.081, p < 0.001] (Figure 2). The effect of time was not significant [ANOVA, F(24,250) = 0.881, p = 0.629]. The blood flow intensity was significantly higher in response to Na2S compared to saline at 1–4, 6, and 20–24 min.
The rapid, dose-dependent development of the hypothermic and hypometabolic response to centrally administered Na2S suggests that the site of action for the released H2S is located in the central nervous system. To test whether the hypothermic effect of Na2S can be triggered from a peripheral site, next we studied the thermoregulatory response to the intraperitoneal (i.p.) administration of a high dose (5 mg/kg) of Na2S. As expected, i.p. infusion of saline did not have any effect on deep Tb (Figure 3). In contrast with the i.c.v. administration, when the mice were infused with Na2S i.p. their deep Tb did not differ significantly from that of saline-treated mice at any time points during the experiment (p > 0.05) even though a 10 times higher dose was delivered i.p. than the i.c.v. administered lower dose which caused hypothermia (see Figure 1). The effect of time was also not significant [ANOVA, F(21,286) = 1.285, p = 0.183]

2.2. Central Administration of GYY4137 Decreases Deep Tb in Mice

We also wanted to know whether the observed thermoregulatory effects of Na2S can be triggered by GYY4137, which is a slow-releasing H2S donor [28]. When administered i.c.v. in the respirometry thermometry setup, GYY4137 (3 mg/kg) caused a marked hypothermia and hypometabolism as compared to saline treatment (Figure 4). In accordance, the effect of treatment was statistically significant on both colonic temperature [ANOVA, F(1242) = 108.220, p < 0.001] and VO2 [ANOVA, F(1220) = 41.420, p < 0.001]. The effect of time was also significant on colonic temperature [ANOVA, F(21,242) = 6.815, p < 0.001], but not on VO2 [ANOVA, F(21,220) = 1.019, p = 0.441]. Between the GYY4137-treated and saline-treated mice, deep Tb differed significantly at 80–100 min (p < 0.05) and 130–180 min (p ≤ 0.001), and the difference in VO2 was significant at 20–30 min and 160–180 min (p < 0.05).

2.3. The Hypothermic Response to Na2S and GYY4137 Is Attenuated in the Absence of the TRPA1 Channel

Previously it has been shown that the TRPA1 channel mediates different effects of H2S, including nociceptive, inflammatory, vasomotor, and neurophysiological effects (for a review, see [24]), but it has remained unknown whether it contributes to the development of the H2S-induced hypothermia. Therefore, next, we investigated whether the TRPA1 channel is involved in the thermoregulatory responses to different H2S donors. For that reason, we used mice with (Trpa1−/−) or without (Trpa1+/+) a homozygous mutation in the Trpa1 gene and compared their hypothermic responses. As expected from our experiments in C57BL/6 mice (Figure 1), the i.c.v. administration of Na2S (1 mg/kg) caused a sudden, pronounced drop in the colonic temperature (>1.5 °C) and VO2 (>40 mL/kg/min) of the Trpa1+/+ mice (Figure 5A). However, in the Trpa1−/− mice the hypothermic and hypometabolic effects of the same dose of Na2S were markedly attenuated [ANOVA, F(1308) = 73.278, p < 0.001 and F(1308) = 62.496, p < 0.001, respectively, for intergenotype difference]. The effect of time was also significant on colonic temperature [ANOVA, F(21,308) = 2.535, p < 0.001], but not on VO2 [ANOVA, F(21,308) = 0.173, p = 1.000]. The Trpa1+/+ mice had significantly lower deep Tb between 30 and 180 min, as well as reduced VO2 between 60 and 180 min post-Na2S administration as compared to the Trpa1−/− mice.
We also studied the thermoregulatory effect of GYY4137 in Trpa1−/− and Trpa1+/+ mice in the thermocouple thermometry setup (Figure 5B). The i.c.v. administration of GYY4137 (3 mg/kg) caused a marked fall in the deep Tb of Trpa1+/+ mice; however, the hypothermic response to the same dose of GYY4137 was significantly attenuated in Trpa1−/− mice [ANOVA, F(1264) = 31.819, p < 0.001]. The effect of time was also significant [ANOVA, F(21,264) = 8.579, p < 0.001]. The colonic temperature of Trpa1−/− mice remained significantly higher than that of Trpa1+/+ mice between 20 and 80 min post-GYY4137 administration.

2.4. Trpa1 mRNA Is Modestly Expressed in Brain Neurons within Autonomic Thermoeffector Pathways

Our thermophysiological results suggested that the thermoregulatory responses to H2S donors are triggered from the central nervous system. We, therefore, studied the expression of the TRPA1 channel in thermoregulation-related brain structures. Since the specificity of commercially available antibodies for the TRPA1 protein is debated [32,33], we measured its expression at the mRNA level with two different techniques: real-time-quantitative (RT-q)PCR and RNAscope in situ hybridization (for details, see Measurement of Trpa1 mRNA Expression in Materials and Methods). Importantly, in both cases, the mice were carefully perfused before the brain sample collection. This step was required in order to avoid the contamination of the samples with blood, which was repeatedly shown to contain a detectable amount of TRPA1 channels [34,35,36]. First, we used RT-qPCR to assess Trpa1 mRNA in the hypothalamus of the mice, but we did not find any detectable amount, although the expression of Trpa1 mRNA was clearly present in the trigeminal ganglion, which was used as a positive control (Figure S1, Supplementary Materials).
Because the turnover of the TRPA1 protein in neurons may not necessitate a high rate of mRNA transcription, then we used RNAscope in situ hybridization, a highly sensitive method that can detect transcripts as single molecules [37]. We found detectable Trpa1 mRNA transcripts in all of the studied thermoregulation-related nuclei, viz., in the medial preoptic area (Figure 6A), dorsomedial hypothalamic area (Figure 6B), lateral parabrachial nucleus (Figure 6C), and rostral raphe pallidus (Figure 6D), although it should be noted that the number of the Trpa1 transcripts was low.

3. Discussion

In the present study, we show that fast- and slow-releasing H2S donors cause hypothermia which is mediated by reduced thermogenesis and increased cutaneous vasodilation. The hypothermic and hypometabolic effects are triggered from the central nervous system and both of them are strongly attenuated in the absence of the TRPA1 channel. TRPA1 channels located on hypothalamic neurons within autonomic thermoeffector pathways can be suggested as the molecular targets for the H2S-induced hypothermia.
First, we showed that injection of H2S donors into the lateral ventricle of the brain caused hypothermia and hypometabolism. These effects were more pronounced at higher doses in the case of Na2S. Our findings are in line with previous reports about the hypothermic response to H2S inhalation [7,8] and NaHS administration [9], whereas they contradict the results of other authors showing no significant thermoregulatory effect of centrally administered Na2S [19,21]. An explanation for the contradiction between the results obtained with Na2S can be that in the previous experiments Na2S was microinjected at low doses i.c.v. (870–1000 nmol/kg) [19] or into the medullary raphe (0.7–0.8 nmol/kg) [21], whereas in our study the doses were 6.4 and 12.8 µmol/kg and the lower dose of Na2S had modest thermoregulatory effects. Therefore, it is likely that Na2S was delivered at subthreshold concentrations to evoke a thermoregulatory effect in earlier studies. In accordance, NaHS also caused hypothermia when infused (to unspecified site) at a rate of 18–72 µmol/kg/h for 4 h [9]. It should be mentioned, however, that after the administration of the donors, H2S concentrations were not measured in the studies, thus a direct comparison of the H2S-induced effects at the different doses is not feasible. An alternative reason for the different findings can be that our experiments were performed in mice, whereas in the previous studies rats were used [19,21], which raises the possibility that the thermoregulatory effect of central H2S differs between mice and rats. Indeed, the lack of the hypothermic effect was reported in larger (non-rodent) animal species by different groups [15,16,17].
Next, we demonstrated that Na2S administered in the same way (1 mg/kg i.c.v.) as in the hypothermia experiments also increased the blood perfusion in the skin of the trunk (viz., lumbar back). Cutaneous vasodilation is an autonomic thermoregulatory response, which is recruited to decrease deep Tb (or to prevent its elevation) through increased heat dissipation to the environment [22]. In small rodents, heat-exchange organs with non-hairy skin, e.g., tail and paws, are the predominant body parts for heat transfer between the body and the environment [38]. Our experiments were performed in anesthetized mice placed on a heating pad that was in contact with the ventral surface of the animal including its tail and limbs, therefore, the heating could have interfered with H2S-induced changes in blood flow in these body parts. On the contrary, the heating had minimal local effects on the vasculature in the skin of the lower back, thus we assessed the effects of H2S on the blood perfusion in that region. The use of the trunk blood perfusion for the assessment of heat dissipation is also justified by the recent finding that in mice the trunk contributes more to the whole-body heat loss than in rats and it is likely that the largest fraction of total heat loss comes from the body trunk in mice [39]. The involvement of skin vasodilation—in addition to reduced thermogenesis—in H2S-induced hypothermia indicates that H2S acts on two distinct efferent thermoeffector pathways or perhaps on neurons that are situated in the common afferent or efferent part of the warmth-sensitive pathways before it divides into separate branches to the different autonomic thermoeffectors. Theoretically, a direct effect of H2S on the vessels and the brown adipose tissue can be also mentioned, but that scenario is unlikely, since in our experiments the systemic (i.p.) administration of a high dose (10 times higher than what was effective i.c.v.) of Na2S did not have an effect on deep Tb (Figure 3), thereby indicating a central (intrabrain) site for the thermoregulatory effects.
While Na2S is considered as a purer donor of H2S than NaHS, both substances yield H2S in a bolus instantaneously, which may question the physiological relevance of their effects (reviewed in [40]). In order to circumvent this issue, we also tested the thermoregulatory effects of GYY4137, a very slow-releasing H2S donor [41], which was used repeatedly to study the true physiological functions of H2S in a variety of experimental models, as reviewed by Whiteman et al. [42]. The i.c.v. administration of GYY4137 caused hypothermia and hypometabolism in the mice similar to Na2S. However, the dynamic of the response was different since the decrease in both VO2 and deep Tb developed slower and its extent was more pronounced than in the case of Na2S. The difference in the dynamics of the hypothermia between GYY4137 and Na2S is well in harmony with their different capabilities of H2S generation, because H2S is released from GYY4137 in a slow and sustained manner, which was shown to evoke slow-onset vasodilatory effects [41].
Last, we wanted to discover the molecular target responsible for the hypothermic response to H2S. Temperature-sensitive members of the TRP channel superfamily can function as thermoreceptor elements in the thermoregulation system [22], but nonthermal activation of some of these TRP channels can also occur and contribute to the regulation of deep Tb independently from whether the given channel is a thermosensor or not, as it was discovered in case of TRPV1 [43,44]. With regards to an interaction between H2S and thermosensitive TRP channels, strong evidence accumulated until present days for an action of H2S on the TRPA1 channel in a vast number of different experimental models [24], but whether TRPA1 also mediates the hypothermic effect of H2S was unknown until now. In the present work, we studied the thermoregulatory response to H2S donors (Na2S and GYY4137) in the genetic absence of the TRPA1 channel by using Trpa1−/− mice. We showed that the hypothermic and the hypometabolic responses are both attenuated in Trpa1−/− mice as compared to their Trpa1+/+ littermates. The contribution of TRPA1 to the thermal effect of the H2S donors used in the present study is in harmony with our previous report about the hypothermic effects of a polysulfide, dimethyl trisulfide, which was also attenuated in Trpa1−/− mice [10]. However, polysulfides activate TRPA1 320 times more potently than H2S [45], thus it was crucial to understand whether H2S delivered by different non-polysulfide donors can evoke TRPA1-mediated hypothermia. The present findings clearly indicate, for the first time to our knowledge, that hypothermia induced by either fast- or slow-releasing H2S donors is mediated by the TRPA1 channel in unanesthetized mice.
Since in our experiments we also showed that the hypothermic response is triggered from the central nervous system, then we focused our attention on the expression of the TRPA1 channel in the brain. Because nonspecific binding was shown for different commercially available antibodies against the TRPA1 protein [33,46], we investigated the expression of the channel at the mRNA level in the hypothalamus of the mice, which brain region harbors high number of neurons within the autonomic thermoeffector pathways [47]. We did not detect the presence of Trpa1 mRNA in the hypothalamus of mice with RT-qPCR. This finding is in accordance with a previous study, in which TRPA1 (formerly also called as ANKTM1) was not detected in the brain of mice [48]; however, it contradicts previous reports showing some TRPA1 expression in the hypothalamus of rats [49,50] and in the brain of mice [51,52]. It must be noted that in our experiments and in the study by Story et al. [48] the mice were perfused before the brain sample collection, whereas the animals were not perfused in any of the other studies [49,50,51,52], thus those results were also influenced by Trpa1 mRNA originating from the components of the blood. In particular, TRPA1 was repeatedly detected in whole blood [34,35,36] and it is expressed in various peripheral blood leukocytes [53], monocytes [54], and lymphocytes [55,56]. In another study, extremely long exposure times for Northern blots were needed to detect Trpa1 transcripts in the brain of humans suggesting low-abundance expression [57], but also questioning the sensitivity of the method for the detection of Trpa1 mRNA. Considerable between-study differences in TRPA1 expression (3.6% vs. 56.5%) were also present in the dorsal root ganglia [48,58], which were presumed to be due to the detection sensitivity of in situ hybridization [59].
RNA integrity can be a critical issue in gene expression studies with qPCR, because fragmented RNA impairs qPCR amplification. The brain is characterized by a higher RNA degradation rate than other tissues [60], which also warrants for the need of more sensitive techniques to study gene expression in brain tissue. In contrast with qPCR, which requires the intact cDNA sequence (from the 5′ of the forward primer to the 3′ end of the reverse primer) for amplification, RNAscope requires the annealing of only 3 pairs of the 20 possible double Z probes to produce a detectable signal. Therefore, shorter mRNA molecules could still be detected by RNAscope probes in brain samples. In accordance with the higher sensitivity, with RNAscope we detected some Trpa1 mRNA transcripts in all of the studied brain nuclei within the autonomic thermoregulatory pathways. The low-abundance expression of Trpa1 mRNA in the studied thermoregulatory brain structures may indicate that these neurons play a minor role in the effect of H2S, but it has to be noted that mRNA expression does not necessarily correlate with the rate of protein translation, since a low mRNA expression can be associated with high protein levels, as shown in different studies [57,61]. Importantly, despite its low mRNA expression, TRPA1 is thought to play critical physiological functions in various tissues [57,61,62,63]. Similar to TRPA1, another temperature-sensitive TRP channel, TRPV3 was also shown to contribute to neurophysiological functions despite the low abundance of its mRNA in vagal afferent neurons [64]. It should be also mentioned that TRPA1 protein levels can be controlled via regulation of the protein’s lifetime by modulation of its ubiquitination status [57]. This may result in the presence of functional TRPA1 proteins on the neurons despite the low abundance of Trpa1 mRNA. It was shown that de-ubiquitination of TRPA1 by the ubiquitin hydrolase protein CYLD increases the cellular pool of TRPA1 proteins [57] and CYLD expression was detected in different brain regions of mice, also including the hypothalamus [65]. Consequently, it is possible that the TRPA1 channel is expressed to a sufficient extent at the protein level to mediate the effects of H2S directly from the studied thermoregulation-related neurons. However, it cannot be excluded that TRPA1 channels in other brain structures are the primary sites for the action of H2S and modulate the activity of thermoeffectors through their projections to neurons within the thermoregulation pathways. In support of that scenario, physiological function for TRPA1 was found in the somatosensory cortex [66], in the hippocampus [63,66], as well as in the supraoptic and solitary nuclei [67,68], which brain regions are also involved in the regulation of deep Tb [47,69,70].
The involvement of TRPA1 was shown in the development of hypothermia in response to diverse stimuli, such as acetaminophen [71], relative hypoxia [72], and thiazoline-related innate fear-eliciting compounds [73]. Although these agents should not be considered as selective activators of TRPA1, the hypothermic response to them was markedly attenuated or completely absent after the pharmacological or genetic blockade of TRPA1 channels yielding to the conclusion that activation of the TRPA1 channel by the applied stimuli mediates the hypothermia [71,72,73]. In one of these studies, the TRPA1 agonist cinnamaldehyde induced a marked hypothermia in Trpa1+/+ mice, which was significantly reduced in Trpa1−/− mice [71]. These findings support our conclusions about the involvement of an H2S-induced activation of TRPA1 in the hypothermic response, but future research is warranted to reveal the exact nature of the interaction between H2S and TRPA1 and its contribution to the hypothermia.
Until the H2S-TRPA1 interaction in association with the hypothermic response is fully understood, alternative mechanisms of the hypothermic effect must be also stated. H2S can influence a variety of cellular structures and TRPA1 can be a channel that is important as a downstream mediator in different signal transduction pathways. In particular, the activation or expression of TRPA1 can be modulated by kinases, transcription factors, hormones, and reactive oxygen species, which can be activated by sulfides (for review, see [24]). Interestingly, through their activation in the central nervous system at least some of these signaling pathways can also contribute to a decrease in deep Tb in response to different stimuli, as proposed, for example, for AMP-activated protein kinase [74], p38α mitogen-activated protein kinase [75], and estrogens [76]. Despite the involvement of TRPA1 in the signaling pathways, their activity does not necessarily depend solely on TRPA1, hence the blockade of the channel (e.g., in Trpa1−/− mice) may not lead to the inhibition of the whole pathway, which could explain why some (attenuated) hypothermic response to the used sulfide donors was still present in Trpa1−/− mice in our experiments. Whether H2S triggers hypothermia through the direct or indirect activation of TRPA1 channels remains the subject for future research.

4. Materials and Methods

4.1. Animals

Experiments were performed in 109 adult mice of both sexes. As in our earlier studies [10,26], male Trpa1−/− and Trpa1+/+ mice (n = 18 and 14, respectively) were obtained from the Laboratory Animal Centre of the University of Pecs, where they were bred from breeding pairs generously donated by Dr. Pierangelo Geppetti. Seventy-seven C57BL/6 mice were also obtained from the Laboratory Animal Centre at the University of Pecs where they were bred and kept under standard pathogen-free conditions. The mice were housed in standard polycarbonate cages kept in a room with ambient temperature maintained at 24–25 °C and humidity at 30–40%. The room was on a 12 h light–dark cycle (lights on at 5:00 a.m.). Standard rodent chow and tap water were available ad libitum. At the time of the experiments, the Trpa1−/−, Trpa1+/+, and C57BL/6 mice weighed 26 ± 2, 26 ± 3, and 27 ± 4 g, respectively. For thermophysiological experiments, mice were extensively habituated to staying inside wire-mesh cylindrical confiners, as described previously [30]. All procedures were conducted under protocols approved by the Institutional Animal Use and Care Committee of the University of Pecs (registration no.: BA02/2000–6/2018, approved on 27 February 2018) and were in accordance with the directives of the National Ethical Council for Animal Research and those of the European Communities Council (86/609/EEC).

4.2. Surgeries

4.2.1. Anesthesia and Perioperative Care

Mice were anesthetized with i.p. administration of a ketamine-xylazine cocktail (81.7 and 9.3 mg/kg, respectively) and received antibiotic protection intramuscularly (gentamycin, 6 mg/kg). During surgery, mice were heated with a temperature-controlled heating pad (model TMP-5a; Supertech Instruments UK Ltd., London, UK) placed under a surgery board. Each mouse was subjected to one of the surgical procedures described below. The experiments were performed 4–8 days after the surgery.

4.2.2. I.c.v. Cannula Implantation

For the i.c.v. substance administration, A 22-G steel guide cannula (Plastics One, Roanoke, VA, USA) was implanted into the right lateral cerebral ventricle using a stereotaxic manipulator (Narishige Scientific Instruments Laboratory, Tokyo, Japan), as described previously [77]. In brief, after incision of the scalp and removal of the periosteum, two supporting microscrews (Fine Science Tools, Heidelberg, Germany) were driven into the skull and the guide cannula was inserted through a small hole drilled in the skull 0.5 mm posterior from Bregma and 1.0 mm lateral from midline. The tip of the cannula was placed within the right lateral ventricle (2.0 mm from dura). The cannula was fixed to the supporting microscrews with dental cement and closed by a dummy cannula.

4.2.3. I.p. Catheter Implantation

For the i.p. administration of substances, a polyethylene (PE)-50 catheter filled with pyrogen-free saline was implanted into the peritoneal cavity, as described elsewhere [30,77]. Through a small midline incision on the abdominal wall, the internal end of the catheter was fixed to the abdominal wall with a suture, while the external end of the catheter was exteriorized at the nape and heat-sealed. The surgical wound was sutured in layers. The catheter was flushed with 0.1 mL of saline on the day after the surgery and every other day thereafter.

4.3. Experimental Setups

Thermoregulatory experiments in unanesthetized mice were performed in either the thermocouple thermometry setup or the respirometry thermometry setup. The experiments were conducted at an ambient temperature of 30 °C in the thermocouple thermometry setup and an ambient temperature of 22 °C in the respirometry thermometry setup, which is subneutral for mice in these setups [77]. Cutaneous blood flow measurement was performed by laser speckle contrast imaging in anesthetized animals.

4.3.1. Thermocouple Thermometry

The mice were placed in cylindrical confiners and equipped with copper-constantan thermocouples (Omega Engineering, Stamford, CT, USA) to measure colonic temperature (a form of deep Tb). The colonic thermocouple was inserted 3 cm deep beyond the anal sphincter, fixed to the base of the tail with adhesive tape, and plugged into a data logger device (Cole-Palmer, Vernon Hills, IL, USA) connected to a computer. Mice in their confiners were then placed into a temperature-controlled incubator (model MIDI F230S; PL Maschine Ltd., Tarnok, Hungary) set to an ambient temperature of 30 °C, which is slightly below the thermoneutral zone for mice in this setup. When the mouse was pre-implanted with an i.c.v. cannula, a needle injector (Plastics One, Roanoke, VA, USA) was fitted into the guide cannula and connected to a PE-50 extension, which was prefilled with a solution of Na2S or GYY4137 or with saline. The injector needle protruded 1.0 mm beyond the tip of the guide cannula. The extension was passed through a port of the incubator and connected to a 10-µL syringe (model 701N, Hamilton, Reno, NV, USA). When the mouse had an i.p. catheter, it was connected to a PE-50 extension, which was prefilled with the substance of interest and connected to a syringe placed in an infusion pump (model 975; Harvard Apparatus Inc., Holliston, MA, USA). The PE-50 extensions preloaded with the substances were wrapped in aluminum foil in order to prevent the photolytic oxidation of sulfide ions by UV light, which reaction can occur in aqueous sulfide solutions [78].

4.3.2. Respirometry Thermometry

The mice were equipped with thermocouples and PE-50 extensions the same way as in the experiments in the thermocouple thermometry setup. Then, the mice in their confiners were transferred to a Plexiglas chamber of the four-chamber open-circuit calorimeter integrated system (Oxymax Equal Flow, Columbus Instruments, Columbus, OH, USA). The chambers were sealed, submerged into a temperature-controlled water bath, and continuously ventilated with room air (200 mL/min). The fractional concentration of oxygen was measured in the air entering and exiting the chamber, and the rate of oxygen consumption was calculated according to the manufacturer’s instructions using the Oxymax Windows software (version 3.1).

4.3.3. Laser Speckle Contrast Imaging

The mice were anesthetized, then the fur on the lumbar back-skin was clipped and the animals were placed in a ventral position on a heating pad (model TMP-5a; Supertech Instruments UK Ltd., London, UK) to maintain their deep body temperature at 36 °C for the duration of the experiment. A needle injector was fitted into the preimplanted i.c.v. guide cannula and connected to a PE-50 extension, which was prefilled with a solution of Na2S or with saline. The blood flow intensity on the lumbar back-skin of the mice was measured by a PeriCam PSI system (Perimed AB, Järfälla, Sweden), which applies laser speckle contrast analysis technology. The system measures blood perfusion by recording changes in the speckle pattern as motion blurring in the regions of interests. If there is more movement in the region, e.g., due to higher red blood cell flow, blurring will increase and the speckle contrast will be lower, which correlates with blood flow. The change in blood perfusion (recorded in arbitrary perfusion units) during the experiments was expressed as percentage compared to the baseline value determined at the time of substance administration.

4.3.4. Drugs and Drug Administration

Na2S nonahydrate (Na2S·9H2O) was purchased from Sigma-Aldrich (St. Louis, MO, USA). On the day of the experiment, Na2S·9H2O was freshly dissolved in pyrogen-free saline to achieve final concentrations of Na2S of 1.5, 5, or 10 mg/mL. For the i.p administration, the working solution (1.5 mg/mL) of Na2S (or saline) was infused over 4 min (3.3 mL/kg) to deliver Na2S at 5 mg/kg. For the i.c.v. administration of Na2S (at doses of 0.5 and 1 mg/kg), the working solutions (5 and 10 mg/mL, respectively) of Na2S (or saline) were infused (1 µL/min) over a 3 min period.
The slow-releasing hydrogen sulfide donor GYY4137 was synthesized at the University of Exeter Medical School, as described elsewhere [41]. On the day of the experiment, GYY4137 was freshly dissolved in saline to make a working solution of 30 mg/mL. By infusing this solution into the lateral ventricle (1 µL/min for 3 min), a total dose of 3 mg/kg of GYY4137 was delivered i.c.v. Control mice were infused with saline.

4.4. Measurement of Trpa1 mRNA Expression

4.4.1. RT-qPCR

Three month-old male C57BL/6 mice (n = 7) and Trpa1−/− mice (n = 2, for negative control) were deeply anesthetized with an overdose of urethane (2.4 mg/kg) and perfused transcardially with 30 mL of phosphate-buffered saline (PBS). Brains and trigeminal ganglia were quickly dissected after decapitation, frozen on dry ice, and stored at −80 °C. Then, brains were sliced using razor blades on a coronal brain matrix (Ted Pella, Redding, CA, USA) to obtain 1 mm thick coronal sections, according to the technique described by Palkovits et al. [79]. A microdissecting tool (Ted Pella, USA) of 1 mm diameter was used to punch the hypothalamus between coronal planes of −0.5 mm to −2.5 mm caudal to Bregma, based on the atlas by Paxinos and Franklin [80]. Eight tissue punches were cut and pooled in order to collect samples representative of the entire hypothalamus of each animal. The microdissection procedure was performed on a dry ice-chilled mat and the punches were immediately snap-frozen in precooled Eppendorf vials on dry ice. Then, the samples were stored at −80 °C until the RNA isolation procedure.
Total RNA from the microdissected mouse brain samples and trigeminal ganglia were extracted with Direct-zol RNA Microprep kit (Zymo Research, Irvine, CA, USA). The concentration and purity of total RNA quality were assessed by a spectrophotometer (NanoDrop 2000, Thermo Fisher Scientific, Waltham, MA, USA). For further analysis, only those RNA samples were used that showed an A260/280 ratio between 1.9 and 2.1 and an A260/A230 ratio higher than 2.0. The RNA samples were treated with DNase I (Zymo Research, USA) to remove genomic DNA. Using Maxima First Strand cDNA Synthesis Kit (Thermo Fisher Scientific, USA), 1 μg RNA was reverse transcribed into cDNA. Applied Biosystems QuantStudio 3 RT PCR System (Thermo Fisher Scientific, USA) was used to perform qPCR experiments, using SensiFast SYBR Lo-ROX Kit (Bioline, Taunton, MA, USA) according to the manufacturer’s manual. All qPCR experiments were performed in technical replicates and included a melt curve analysis to ensure the specificity of the signal. Reverse transcriptase minus control showed the lack of genomic DNA contamination. The geometric mean of the reference gene Ct values was determined and Trpa1 mRNA expression relative to the reference genes beta-actin (Actb) and glyceraldehyde-3-phosphate dehydrogenase (Gapdh) was calculated. Primers used to amplify target loci for RT-qPCR are listed in Table 1.

4.4.2. RNAscope In Situ Hybridization

For RNAscope studies 3 month-old male C57BL/6 mice (n = 4) were perfused as described above using 30 mL PBS followed by 100 mL of 4% paraformaldehyde in Millonig’s phosphate buffer. Brains were postfixed for 24 h at room temperature, rinsed in PBS, dehydrated, and embedded in paraffin using standard procedures. 5 µm sections were cut using a sliding microtome (model HM 430; Thermo Fisher Scientific, USA). The RNAscope Multiplex Fluorescent Reagent Kit v2 (ACD, Hayward, CA, USA) was used according to the manufacturer’s protocol. In short, sections were heat-treated, deparaffinized, H2O2-blocked, boiled, and pretreated with Protease Plus. Subsequently, the sections were hybridized with probes specific to mouse Trpa1 mRNA and with 3-plex positive and negative control probes. Sequential signal amplification and channel development were performed. Nuclear counterstaining with 4′, 6-diamidino-2-phenylindole (DAPI) was applied and sections were mounted with ProLong Diamond Antifade Mountant for confocal imaging. Probes and applied dilutions of fluorophores are listed in Table 2.
In accordance with earlier studies [81,82], cortical samples were stained for the ppib mRNA (red) as positive technical control (Figure 5E) and the bacterial dabP mRNA staining (red) was used as negative technical control (Figure 5F). According to the atlas by Paxinos and Franklin [80], fluorescent images of the medial preoptic area (+0.14 mm to +0.02 mm from Bregma), dorsomedial hypothalamic area (−1.58 mm to −1.70 mm from Bregma), as well as the lateral parabrachial nucleus and rostral raphe pallidus (−5.34 mm to −5.40 mm from Bregma for both) were acquired using an Olympus Fluoview FV-1000 laser scanning confocal microscope and Fluoview FV-1000S-IX81 image acquisition software system (Olympus, Tokyo, Japan). The confocal aperture was set to 80 µm. The analog sequential scanning was performed using a 40× objective lens (NA:0.75). The optical thickness was set to 1 μm and the resolution was 1024 × 1024 pixels. The excitation time was set to 4 µs per pixel. Blue and red virtual colors were selected to depict fluorescent signals of DAPI (nuclear counterstain) and of Cyanine 3 (Trpa1 mRNA), respectively.

4.5. Data Processing and Analysis

Data on deep Tb, VO2, and blood flow intensity were compared by two-way ANOVA. As in our previous studies [27,29], ANOVA was followed by the Fisher’s LSD post hoc test. Sigmaplot 11.0 (Systat Software, San Jose, CA, USA) software was used for statistical analyses. Differences were considered significant when p < 0.05. All data are reported as mean ±SE.

5. Conclusions

In conclusion, we show that slow- and fast-releasing H2S donors induce hypothermia through hypometabolism and cutaneous vasodilation in mice and that the hypothermic effect of H2S is mediated by TRPA1 channels located in the brain, presumably on hypothalamic neurons within the autonomic thermoeffector pathways. Our findings highlight the importance of central TRPA1-mediated H2S signaling in the thermoregulation system. In severe forms of systemic inflammation (e.g., septic shock), which is often associated with hypothermia [83] and by enhanced production of H2S [40,84], the interaction between TRPA1 and H2S can play a crucial role in the development of the response and, as perspective, may serve as a therapeutic target. Furthermore, the H2S-induced activation of central TRPA1 channels may pave the road to the development of controlled induction of hypothermia, but future research is needed to reveal the true thermopharmacological potential of the central TRPA1-H2S interaction in health and disease.

Supplementary Materials

The following are available online at https://www.mdpi.com/article/10.3390/ph14100992/s1, Figure S1: Representative electrophoretogram of the RT-qPCR products.

Author Contributions

Conceptualization, J.K., E.P. (Erika Pinter), and A.G.; methodology, V.K., V.T., E.P. (Eszter Pakai), M.S., B.G., M.W., J.K., E.P. (Erika Pinter), and A.G.; software, V.K., V.T., A.G.; validation, E.O., Z.R., V.K., V.T., E.P. (Eszter Pakai), M.S., L.K., P.K., B.G., and A.G.; formal analysis, E.O., V.K., V.T. H.V.W., K.F., M.S., and A.G.; investigation, E.O., Z.R., V.K., V.T., E.P. (Eszter Pakai), H.V.W., M.S., B.G., and A.G.; resources, B.G., M.W., J.K., E.P. (Erika Pinter), and A.G.; data curation, E.O., V.K., V.T. H.V.W., K.F., M.S., and A.G.; writing—original draft preparation, E.O., Z.R., V.K., and H.V.W.; writing—review and editing, E.P. (Eszter Pakai), L.K., P.K., B.G., M.W., J.K., E.P. (Erika Pinter), and A.G.; visualization, E.O., V.K., B.G., and A.G.; supervision, B.G., J.K., E.P. (Erika Pinter), and A.G.; project administration, B.G., J.K., E.P. (Erika Pinter), and A.G.; funding acquisition, B.G., J.K., E.P. (Erika Pinter), and A.G. All authors have read and agreed to the published version of the manuscript.

Funding

This work was supported by the National Research, Development and Innovation Office (FK 124483 to A.G.), the Medical School, University of Pecs (KA-2019-27 to A.G.), the New National Excellence Program of the Hungarian Ministry for Innovation and Technology (UNKP-20-3-II-PTE-877 and UNKP-21-3-II-PTE-1317 to Z.R.), the Higher Education Institutional Excellence Program of the Ministry of Human Capacities in Hungary (20765-3/2018/FEKUTSTRAT to A.G.), and the European Union, co-financed by the European Social Fund (EFOP-3.6.1-16-2016-00004 to B.G. and A.G.). A.G. acknowledges the Janos Bolyai Scholarship of the Hungarian Academy of Sciences. B.G. was funded by the National Research, Development and Innovation Fund of Hungary, financed under the 2020-4.1.1-TKP2020 funding scheme (Project No: TKP2020-IKA-08); NAP 2017-1.2.1-NKP-2017-00002; GINOP-2.3.2-15-2016-00050; MTA-TKI14016; EFOP-3.6.3-VEKOP-16-2017-00009; and EFOP-3.6.2-16-2017-00008. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.

Institutional Review Board Statement

All procedures were conducted under protocols approved by Institutional Animal Use and Care Committee of the University of Pecs protocols (registration no.: BA02/2000-6/2018, approved on 27 February 2018) and were in accordance with the directives of the National Ethical Council for Animal Research and those of the European Communities Council (86/609/EEC).

Informed Consent Statement

Not applicable.

Data Availability Statement

Data is contained within the article and Supplementary Materials.

Acknowledgments

The authors are grateful to Roghiyah Riahi for her help with the thermoregulatory experiments and to Aniko Varnagyne Rozsafi for her excellent technical assistance.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Szabo, C. A timeline of hydrogen sulfide (H2S) research: From environmental toxin to biological mediator. Biochem. Pharmacol. 2018, 149, 5–19. [Google Scholar] [CrossRef]
  2. Murphy, B.; Bhattacharya, R.; Mukherjee, P. Hydrogen sulfide signaling in mitochondria and disease. FASEB J. 2019, 33, 13098–13125. [Google Scholar] [CrossRef] [Green Version]
  3. Kimura, H. Hydrogen sulfide (H2S) and polysulfide (H2Sn) signaling: The first 25 years. Biomolecules 2021, 11, 896. [Google Scholar] [CrossRef]
  4. Szabo, C.; Papapetropoulos, A. International Union of Basic and Clinical Pharmacology. CII: Pharmacological modulation of H2S levels: H2S donors and H2S biosynthesis inhibitors. Pharmacol. Rev. 2017, 69, 497–564. [Google Scholar] [CrossRef] [Green Version]
  5. Stein, A.; Bailey, S.M. Redox biology of hydrogen sulfide: Implications for physiology, pathophysiology, and pharmacology. Redox Biol. 2013, 1, 32–39. [Google Scholar] [CrossRef] [Green Version]
  6. Branco, L.G.; Soriano, R.N.; Steiner, A.A. Gaseous mediators in temperature regulation. Compr. Physiol. 2014, 4, 1301–1338. [Google Scholar] [CrossRef]
  7. Blackstone, E.; Morrison, M.; Roth, M.B. H2S induces a suspended animation-like state in mice. Science 2005, 308, 518. [Google Scholar] [CrossRef] [Green Version]
  8. Volpato, G.P.; Searles, R.; Yu, B.; Scherrer-Crosbie, M.; Bloch, K.D.; Ichinose, F.; Zapol, W.M. Inhaled hydrogen sulfide: A rapidly reversible inhibitor of cardiac and metabolic function in the mouse. Anesthesiology 2008, 108, 659–668. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  9. Aslami, H.; Heinen, A.; Roelofs, J.J.; Zuurbier, C.J.; Schultz, M.J.; Juffermans, N.P. Suspended animation inducer hydrogen sulfide is protective in an in vivo model of ventilator-induced lung injury. Intensive Care Med. 2010, 36, 1946–1952. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  10. Pozsgai, G.; Payrits, M.; Saghy, E.; Sebestyen-Batai, R.; Steen, E.; Szoke, E.; Sandor, Z.; Solymar, M.; Garami, A.; Orvos, P.; et al. Analgesic effect of dimethyl trisulfide in mice is mediated by TRPA1 and sst4 receptors. Nitric Oxide 2017, 65, 10–21. [Google Scholar] [CrossRef] [PubMed]
  11. Hemelrijk, S.D.; Dirkes, M.C.; van Velzen, M.H.N.; Bezemer, R.; van Gulik, T.M.; Heger, M. Exogenous hydrogen sulfide gas does not induce hypothermia in normoxic mice. Sci. Rep. 2018, 8, 3855. [Google Scholar] [CrossRef]
  12. Kwiatkoski, M.; Soriano, R.N.; Francescato, H.D.; Batalhao, M.E.; Coimbra, T.M.; Carnio, E.C.; Branco, L.G. Hydrogen sulfide as a cryogenic mediator of hypoxia-induced anapyrexia. Neuroscience 2012, 201, 146–156. [Google Scholar] [CrossRef]
  13. Simon, F.; Giudici, R.; Duy, C.N.; Schelzig, H.; Oter, S.; Groger, M.; Wachter, U.; Vogt, J.; Speit, G.; Szabo, C.; et al. Hemodynamic and metabolic effects of hydrogen sulfide during porcine ischemia/reperfusion injury. Shock 2008, 30, 359–364. [Google Scholar] [CrossRef]
  14. Bracht, H.; Scheuerle, A.; Groger, M.; Hauser, B.; Matallo, J.; McCook, O.; Seifritz, A.; Wachter, U.; Vogt, J.A.; Asfar, P.; et al. Effects of intravenous sulfide during resuscitated porcine hemorrhagic shock*. Crit. Care Med. 2012, 40, 2157–2167. [Google Scholar] [CrossRef]
  15. Dirkes, M.C.; Milstein, D.M.; Heger, M.; van Gulik, T.M. Absence of hydrogen sulfide-induced hypometabolism in pigs: A mechanistic explanation in relation to small nonhibernating mammals. Eur. Surg. Res. 2015, 54, 178–191. [Google Scholar] [CrossRef]
  16. Drabek, T.; Kochanek, P.M.; Stezoski, J.; Wu, X.; Bayir, H.; Morhard, R.C.; Stezoski, S.W.; Tisherman, S.A. Intravenous hydrogen sulfide does not induce hypothermia or improve survival from hemorrhagic shock in pigs. Shock 2011, 35, 67–73. [Google Scholar] [CrossRef]
  17. Haouzi, P.; Notet, V.; Chenuel, B.; Chalon, B.; Sponne, I.; Ogier, V.; Bihain, B. H2S induced hypometabolism in mice is missing in sedated sheep. Respir. Physiol. Neurobiol. 2008, 160, 109–115. [Google Scholar] [CrossRef] [PubMed]
  18. Soriano, R.N.; Braga, S.P.; Breder, J.S.C.; Batalhao, M.E.; Oliveira-Pelegrin, G.R.; Ferreira, L.F.R.; Rocha, M.J.A.; Carnio, E.C.; Branco, L.G.S. Endogenous peripheral hydrogen sulfide is propyretic: Its permissive role in brown adipose tissue thermogenesis in rats. Exp. Physiol. 2018, 103, 397–407. [Google Scholar] [CrossRef] [PubMed]
  19. Kwiatkoski, M.; Soriano, R.N.; Araujo, R.M.; Azevedo, L.U.; Batalhao, M.E.; Francescato, H.D.; Coimbra, T.M.; Carnio, E.C.; Branco, L.G. Hydrogen sulfide inhibits preoptic prostaglandin E2 production during endotoxemia. Exp. Neurol. 2013, 240, 88–95. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  20. Fernandez, R.A.; Soriano, R.N.; Francescato, H.D.; Sabino, J.P.; Coimbra, T.M.; Branco, L.G. Cryogenic role of central endogenous hydrogen sulfide in the rat model of endotoxic shock. Brain Res. 2016, 1650, 218–223. [Google Scholar] [CrossRef] [PubMed]
  21. Sabino, J.P.J.; Oliveira, L.V.C.; Soriano, R.N.; Kwiatkoski, M.; Branco, L.G.S.; da Silva, G.S.F. Role of hydrogen sulfide in ventilatory responses to hypercapnia in the medullary raphe of adult rats. Exp. Physiol. 2021. [Google Scholar] [CrossRef]
  22. Romanovsky, A.A. The thermoregulation system and how it works. Handb. Clin. Neurol. 2018, 156, 3–43. [Google Scholar] [CrossRef] [PubMed]
  23. Guo, J.; Li, G.; Yang, L. Role of H2S in pain: Growing evidences of mystification. Eur. J. Pharmacol. 2020, 883, 173322. [Google Scholar] [CrossRef] [PubMed]
  24. Pozsgai, G.; Batai, I.Z.; Pinter, E. Effects of sulfide and polysulfides transmitted by direct or signal transduction-mediated activation of TRPA1 channels. Br. J. Pharmacol. 2019, 176, 628–645. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  25. Aubdool, A.A.; Graepel, R.; Kodji, X.; Alawi, K.M.; Bodkin, J.V.; Srivastava, S.; Gentry, C.; Heads, R.; Grant, A.D.; Fernandes, E.S.; et al. TRPA1 is essential for the vascular response to environmental cold exposure. Nat. Commun. 2014, 5, 5732. [Google Scholar] [CrossRef] [Green Version]
  26. De Oliveira, C.; Garami, A.; Lehto, S.G.; Pakai, E.; Tekus, V.; Pohoczky, K.; Youngblood, B.D.; Wang, W.; Kort, M.E.; Kym, P.R.; et al. Transient receptor potential channel ankyrin-1 is not a cold sensor for autonomic thermoregulation in rodents. J. Neurosci. 2014, 34, 4445–4452. [Google Scholar] [CrossRef] [PubMed]
  27. Garami, A.; Pakai, E.; McDonald, H.A.; Reilly, R.M.; Gomtsyan, A.; Corrigan, J.J.; Pinter, E.; Zhu, D.X.D.; Lehto, S.G.; Gavva, N.R.; et al. TRPV1 antagonists that cause hypothermia, instead of hyperthermia, in rodents: Compounds’ pharmacological profiles, in vivo targets, thermoeffectors recruited and implications for drug development. Acta Physiol. 2018, 223, e13038. [Google Scholar] [CrossRef] [Green Version]
  28. Papapetropoulos, A.; Whiteman, M.; Cirino, G. Pharmacological tools for hydrogen sulphide research: A brief, introductory guide for beginners. Br. J. Pharmacol. 2015, 172, 1633–1637. [Google Scholar] [CrossRef] [Green Version]
  29. Banki, E.; Pakai, E.; Gaszner, B.; Zsiboras, C.; Czett, A.; Bhuddi, P.R.; Hashimoto, H.; Toth, G.; Tamas, A.; Reglodi, D.; et al. Characterization of the thermoregulatory response to pituitary adenylate cyclase-activating polypeptide in rodents. J. Mol. Neurosci. 2014, 54, 543–554. [Google Scholar] [CrossRef] [Green Version]
  30. Garami, A.; Pakai, E.; Oliveira, D.L.; Steiner, A.A.; Wanner, S.P.; Almeida, M.C.; Lesnikov, V.A.; Gavva, N.R.; Romanovsky, A.A. Thermoregulatory phenotype of the Trpv1 knockout mouse: Thermoeffector dysbalance with hyperkinesis. J. Neurosci. 2011, 31, 1721–1733. [Google Scholar] [CrossRef] [Green Version]
  31. Romanovsky, A.A.; Ivanov, A.I.; Shimansky, Y.P. Selected contribution: Ambient temperature for experiments in rats: A new method for determining the zone of thermal neutrality. J. Appl. Physiol. 2002, 92, 2667–2679. [Google Scholar] [CrossRef] [Green Version]
  32. Guinamard, R.; Hof, T. TRPA1 and TRPV1, do we hold you in our heart? Acta Physiol. 2021, 232, e13695. [Google Scholar] [CrossRef] [PubMed]
  33. Virk, H.S.; Rekas, M.Z.; Biddle, M.S.; Wright, A.K.A.; Sousa, J.; Weston, C.A.; Chachi, L.; Roach, K.M.; Bradding, P. Validation of antibodies for the specific detection of human TRPA1. Sci. Rep. 2019, 9, 18500. [Google Scholar] [CrossRef] [Green Version]
  34. Bell, J.T.; Loomis, A.K.; Butcher, L.M.; Gao, F.; Zhang, B.; Hyde, C.L.; Sun, J.; Wu, H.; Ward, K.; Harris, J.; et al. Differential methylation of the TRPA1 promoter in pain sensitivity. Nat. Commun. 2014, 5, 2978. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  35. Gombert, S.; Rhein, M.; Winterpacht, A.; Munster, T.; Hillemacher, T.; Leffler, A.; Frieling, H. Transient receptor potential ankyrin 1 promoter methylation and peripheral pain sensitivity in Crohn’s disease. Clin. Epigenetics 2019, 12, 1. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  36. Sukenaga, N.; Ikeda-Miyagawa, Y.; Tanada, D.; Tunetoh, T.; Nakano, S.; Inui, T.; Satoh, K.; Okutani, H.; Noguchi, K.; Hirose, M. Correlation between DNA methylation of TRPA1 and chronic pain states in human whole blood cells. Pain Med. 2016, 17, 1906–1910. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  37. Femino, A.M.; Fay, F.S.; Fogarty, K.; Singer, R.H. Visualization of single RNA transcripts in situ. Science 1998, 280, 585–590. [Google Scholar] [CrossRef] [Green Version]
  38. Romanovsky, A.A. Skin temperature: Its role in thermoregulation. Acta Physiol. 2014, 210, 498–507. [Google Scholar] [CrossRef]
  39. Skop, V.; Liu, N.; Guo, J.; Gavrilova, O.; Reitman, M.L. The contribution of the mouse tail to thermoregulation is modest. Am. J. Physiol. Endocrinol. Metab. 2020, 319, E438–E446. [Google Scholar] [CrossRef]
  40. Whiteman, M.; Winyard, P.G. Hydrogen sulfide and inflammation: The good, the bad, the ugly and the promising. Expert Rev. Clin. Pharmacol. 2011, 4, 13–32. [Google Scholar] [CrossRef]
  41. Li, L.; Whiteman, M.; Guan, Y.Y.; Neo, K.L.; Cheng, Y.; Lee, S.W.; Zhao, Y.; Baskar, R.; Tan, C.H.; Moore, P.K. Characterization of a novel, water-soluble hydrogen sulfide-releasing molecule (GYY4137): New insights into the biology of hydrogen sulfide. Circulation 2008, 117, 2351–2360. [Google Scholar] [CrossRef] [Green Version]
  42. Whiteman, M.; Perry, A.; Zhou, Z.; Bucci, M.; Papapetropoulos, A.; Cirino, G.; Wood, M.E. Phosphinodithioate and phosphoramidodithioate hydrogen sulfide donors. Handb. Exp. Pharmacol. 2015, 230, 337–363. [Google Scholar] [CrossRef]
  43. Garami, A.; Shimansky, Y.P.; Rumbus, Z.; Vizin, R.C.L.; Farkas, N.; Hegyi, J.; Szakacs, Z.; Solymar, M.; Csenkey, A.; Chiche, D.A.; et al. Hyperthermia induced by transient receptor potential vanilloid-1 (TRPV1) antagonists in human clinical trials: Insights from mathematical modeling and meta-analysis. Pharmacol. Ther. 2020, 208, 107474. [Google Scholar] [CrossRef]
  44. Romanovsky, A.A.; Almeida, M.C.; Garami, A.; Steiner, A.A.; Norman, M.H.; Morrison, S.F.; Nakamura, K.; Burmeister, J.J.; Nucci, T.B. The transient receptor potential vanilloid-1 channel in thermoregulation: A thermosensor it is not. Pharmacol. Rev. 2009, 61, 228–261. [Google Scholar] [CrossRef] [PubMed]
  45. Kimura, Y.; Mikami, Y.; Osumi, K.; Tsugane, M.; Oka, J.; Kimura, H. Polysulfides are possible H2S-derived signaling molecules in rat brain. FASEB J. 2013, 27, 2451–2457. [Google Scholar] [CrossRef] [PubMed]
  46. Poole, D.P.; Pelayo, J.C.; Cattaruzza, F.; Kuo, Y.M.; Gai, G.; Chiu, J.V.; Bron, R.; Furness, J.B.; Grady, E.F.; Bunnett, N.W. Transient receptor potential ankyrin 1 is expressed by inhibitory motoneurons of the mouse intestine. Gastroenterology 2011, 141, 565–575.e4. [Google Scholar] [CrossRef] [PubMed]
  47. Morrison, S.F.; Nakamura, K. Central neural pathways for thermoregulation. Front. Biosci. 2011, 16, 74–104. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  48. Story, G.M.; Peier, A.M.; Reeve, A.J.; Eid, S.R.; Mosbacher, J.; Hricik, T.R.; Earley, T.J.; Hergarden, A.C.; Andersson, D.A.; Hwang, S.W.; et al. ANKTM1, a TRP-like channel expressed in nociceptive neurons, is activated by cold temperatures. Cell 2003, 112, 819–829. [Google Scholar] [CrossRef] [Green Version]
  49. Kozyreva, T.V.; Evtushenko, A.A.; Voronova, I.P.; Khramova, G.M.; Kozaruk, V.P. Effect of activation of peripheral ion channel TRPM8 on gene expression of thermosensitive TRP ion channels in the hypothalamus. Comparison with the effect of cooling. Bull. Exp. Biol. Med. 2018, 166, 188–191. [Google Scholar] [CrossRef]
  50. Kozyreva, T.V.; Evtushenko, A.A.; Voronova, I.P.; Khramova, G.M.; Kozaruk, V.P. Effects of acute cooling on expression of genes for thermosensitive TRP ion channels in the hypothalamus. Neurosci. Behav. Physiol. 2019, 49, 804–808. [Google Scholar] [CrossRef]
  51. Kunert-Keil, C.; Bisping, F.; Kruger, J.; Brinkmeier, H. Tissue-specific expression of TRP channel genes in the mouse and its variation in three different mouse strains. BMC Genom. 2006, 7, 159. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  52. Wang, X.P.; Yu, X.; Yan, X.J.; Lei, F.; Chai, Y.S.; Jiang, J.F.; Yuan, Z.Y.; Xing, D.M.; Du, L.J. TRPM8 in the negative regulation of TNFalpha expression during cold stress. Sci. Rep. 2017, 7, 45155. [Google Scholar] [CrossRef] [PubMed]
  53. Pereira, I.; Mendes, S.J.; Pereira, D.M.; Muniz, T.F.; Colares, V.L.; Monteiro, C.R.; Martins, M.M.; Grisotto, M.A.; Monteiro-Neto, V.; Monteiro, S.G.; et al. Transient receptor potential ankyrin 1 channel expression on peripheral blood leukocytes from rheumatoid arthritic patients and correlation with pain and disability. Front. Pharmacol. 2017, 8, 53. [Google Scholar] [CrossRef] [Green Version]
  54. Billeter, A.T.; Galbraith, N.; Walker, S.; Lawson, C.; Gardner, S.A.; Sarojini, H.; Galandiuk, S.; Polk, H.C., Jr. TRPA1 mediates the effects of hypothermia on the monocyte inflammatory response. Surgery 2015, 158, 646–654. [Google Scholar] [CrossRef] [PubMed]
  55. Bertin, S.; Aoki-Nonaka, Y.; Lee, J.; de Jong, P.R.; Kim, P.; Han, T.; Yu, T.; To, K.; Takahashi, N.; Boland, B.S.; et al. The TRPA1 ion channel is expressed in CD4+ T cells and restrains T-cell-mediated colitis through inhibition of TRPV1. Gut 2017, 66, 1584–1596. [Google Scholar] [CrossRef]
  56. Sahoo, S.S.; Majhi, R.K.; Tiwari, A.; Acharya, T.; Kumar, P.S.; Saha, S.; Kumar, A.; Goswami, C.; Chattopadhyay, S. Transient receptor potential ankyrin1 channel is endogenously expressed in T cells and is involved in immune functions. Biosci. Rep. 2019, 39. [Google Scholar] [CrossRef] [Green Version]
  57. Stokes, A.; Wakano, C.; Koblan-Huberson, M.; Adra, C.N.; Fleig, A.; Turner, H. TRPA1 is a substrate for de-ubiquitination by the tumor suppressor CYLD. Cell Signal. 2006, 18, 1584–1594. [Google Scholar] [CrossRef]
  58. Nagata, K.; Duggan, A.; Kumar, G.; Garcia-Anoveros, J. Nociceptor and hair cell transducer properties of TRPA1, a channel for pain and hearing. J. Neurosci. 2005, 25, 4052–4061. [Google Scholar] [CrossRef] [Green Version]
  59. Sawada, Y.; Hosokawa, H.; Hori, A.; Matsumura, K.; Kobayashi, S. Cold sensitivity of recombinant TRPA1 channels. Brain Res. 2007, 1160, 39–46. [Google Scholar] [CrossRef]
  60. Koppelkamm, A.; Vennemann, B.; Lutz-Bonengel, S.; Fracasso, T.; Vennemann, M. RNA integrity in post-mortem samples: Influencing parameters and implications on RT-qPCR assays. Int. J. Legal. Med. 2011, 125, 573–580. [Google Scholar] [CrossRef]
  61. Osterloh, M.; Bohm, M.; Kalbe, B.; Osterloh, S.; Hatt, H. Identification and functional characterization of TRPA1 in human myoblasts. Pflugers Arch. 2016, 468, 321–333. [Google Scholar] [CrossRef]
  62. Chung, S.; Baumlin, N.; Dennis, J.S.; Moore, R.; Salathe, S.F.; Whitney, P.L.; Sabater, J.; Abraham, W.M.; Kim, M.D.; Salathe, M. Electronic cigarette vapor with nicotine causes airway mucociliary dysfunction preferentially via TRPA1 receptors. Am. J. Respir. Crit. Care Med. 2019, 200, 1134–1145. [Google Scholar] [CrossRef] [Green Version]
  63. Shigetomi, E.; Tong, X.; Kwan, K.Y.; Corey, D.P.; Khakh, B.S. TRPA1 channels regulate astrocyte resting calcium and inhibitory synapse efficacy through GAT-3. Nat. Neurosci. 2011, 15, 70–80. [Google Scholar] [CrossRef] [Green Version]
  64. Wu, S.W.; Lindberg, J.E.; Peters, J.H. Genetic and pharmacological evidence for low-abundance TRPV3 expression in primary vagal afferent neurons. Am. J. Physiol. Regul. Integr. Comp. Physiol. 2016, 310, R794–R805. [Google Scholar] [CrossRef] [Green Version]
  65. Jin, C.; Kim, S.; Kang, H.; Yun, K.N.; Lee, Y.; Zhang, Y.; Kim, Y.; Kim, J.Y.; Han, K. Shank3 regulates striatal synaptic abundance of Cyld, a deubiquitinase specific for Lys63-linked polyubiquitin chains. J. Neurochem. 2019, 150, 776–786. [Google Scholar] [CrossRef]
  66. Kheradpezhouh, E.; Choy, J.M.C.; Daria, V.R.; Arabzadeh, E. TRPA1 expression and its functional activation in rodent cortex. Open Biol. 2017, 7. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  67. Sun, B.; Bang, S.I.; Jin, Y.H. Transient receptor potential A1 increase glutamate release on brain stem neurons. Neuroreport 2009, 20, 1002–1006. [Google Scholar] [CrossRef]
  68. Yokoyama, T.; Ohbuchi, T.; Saito, T.; Sudo, Y.; Fujihara, H.; Minami, K.; Nagatomo, T.; Uezono, Y.; Ueta, Y. Allyl isothiocyanates and cinnamaldehyde potentiate miniature excitatory postsynaptic inputs in the supraoptic nucleus in rats. Eur. J. Pharmacol. 2011, 655, 31–37. [Google Scholar] [CrossRef]
  69. Bud Craig, A.D. Central neural substrates involved in temperature discrimination, thermal pain, thermal comfort, and thermoregulatory behavior. Handb. Clin. Neurol. 2018, 156, 317–338. [Google Scholar] [CrossRef] [PubMed]
  70. Nagashima, K. Central mechanisms for thermoregulation in a hot environment. Ind. Health 2006, 44, 359–367. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  71. Gentry, C.; Andersson, D.A.; Bevan, S. TRPA1 mediates the hypothermic action of acetaminophen. Sci. Rep. 2015, 5, 12771. [Google Scholar] [CrossRef] [Green Version]
  72. Matsuda, K.; Arkwright, P.D.; Mori, Y.; Oikawa, M.A.; Muko, R.; Tanaka, A.; Matsuda, H. A rapid shift from chronic hyperoxia to normoxia induces systemic anaphylaxis via transient receptor potential ankyrin 1 channels on mast cells. J. Immunol. 2020, 205, 2959–2967. [Google Scholar] [CrossRef] [PubMed]
  73. Matsuo, T.; Isosaka, T.; Hayashi, Y.; Tang, L.; Doi, A.; Yasuda, A.; Hayashi, M.; Lee, C.Y.; Cao, L.; Kutsuna, N.; et al. Thiazoline-related innate fear stimuli orchestrate hypothermia and anti-hypoxia via sensory TRPA1 activation. Nat. Commun. 2021, 12, 2074. [Google Scholar] [CrossRef]
  74. Hayes, M.R.; Leichner, T.M.; Zhao, S.; Lee, G.S.; Chowansky, A.; Zimmer, D.; De Jonghe, B.C.; Kanoski, S.E.; Grill, H.J.; Bence, K.K. Intracellular signals mediating the food intake-suppressive effects of hindbrain glucagon-like peptide-1 receptor activation. Cell Metab. 2011, 13, 320–330. [Google Scholar] [CrossRef] [Green Version]
  75. Robson, M.J.; Quinlan, M.A.; Margolis, K.G.; Gajewski-Kurdziel, P.A.; Veenstra-VanderWeele, J.; Gershon, M.D.; Watterson, D.M.; Blakely, R.D. p38alpha MAPK signaling drives pharmacologically reversible brain and gastrointestinal phenotypes in the SERT Ala56 mouse. Proc. Natl. Acad. Sci. USA 2018, 115, E10245–E10254. [Google Scholar] [CrossRef] [Green Version]
  76. Zhang, Z.; DiVittorio, J.R.; Joseph, A.M.; Correa, S.M. The effects of estrogens on neural circuits that control temperature. Endocrinology 2021, 162. [Google Scholar] [CrossRef]
  77. Pakai, E.; Tekus, V.; Zsiboras, C.; Rumbus, Z.; Olah, E.; Keringer, P.; Khidhir, N.; Matics, R.; Deres, L.; Ordog, K.; et al. The neurokinin-1 receptor contributes to the early phase of lipopolysaccharide-induced fever via stimulation of peripheral cyclooxygenase-2 protein expression in mice. Front. Immunol. 2018, 9, 166. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  78. Linkous, C.A.; Huang, C.; Fowler, J.R. UV photochemical oxidation of aqueous sodium sulfide to produce hydrogen and sulfur. J. Photochem. Photobiol. A Chem. 2004, 168, 153–160. [Google Scholar] [CrossRef]
  79. Palkovits, M.; Graf, L.; Hermann, I.; Borvendeg, J.; Acs, Z.; Lang, T. Regional distribution of enkephalins, endorphins and ACTH in the central nervous system of rats determined by radioimmunoassay. In Endorphins’78; Graf, L., Palkovits, M., Ronai, A.Z., Eds.; Akademiai Kiado: Budapest, Hungary, 1978; pp. 187–195. [Google Scholar]
  80. Paxinos, G.; Franklin, K.B.J. The Mouse Brain in Stereotaxic Coordinates; Academic Press: San Diego, CA, USA, 2001. [Google Scholar]
  81. Ali, A.; Syed, S.M.; Jamaluddin, M.F.B.; Colino-Sanguino, Y.; Gallego-Ortega, D.; Tanwar, P.S. Cell lineage tracing identifies hormone-regulated and Wnt-responsive vaginal epithelial stem cells. Cell Rep. 2020, 30, 1463–1477.e1467. [Google Scholar] [CrossRef] [PubMed]
  82. Morikawa, M.; Mitani, Y.; Holmborn, K.; Kato, T.; Koinuma, D.; Maruyama, J.; Vasilaki, E.; Sawada, H.; Kobayashi, M.; Ozawa, T.; et al. The ALK-1/SMAD/ATOH8 axis attenuates hypoxic responses and protects against the development of pulmonary arterial hypertension. Sci. Signal. 2019, 12, eaay4430. [Google Scholar] [CrossRef] [PubMed]
  83. Garami, A.; Steiner, A.A.; Romanovsky, A.A. Fever and hypothermia in systemic inflammation. Handb. Clin. Neurol. 2018, 157, 565–597. [Google Scholar] [CrossRef]
  84. Bhatia, M.; Gaddam, R.R. Hydrogen sulfide in inflammation: A novel mediator and therapeutic target. Antioxid. Redox Signal. 2021, 34, 1368–1377. [Google Scholar] [CrossRef] [PubMed]
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Figure 1. Colonic temperature and oxygen consumption (VO2) responses of C57BL/6 mice to Na2S (doses indicated) and saline administered i.c.v. The changes in colonic temperature (a form of deep Tb) are shown in the upper panel, while the changes in VO2 (an indicator of thermogenesis) are depicted in the lower panel. Here and in Figures 2–5, n is the number of animals in each experimental group.
Figure 1. Colonic temperature and oxygen consumption (VO2) responses of C57BL/6 mice to Na2S (doses indicated) and saline administered i.c.v. The changes in colonic temperature (a form of deep Tb) are shown in the upper panel, while the changes in VO2 (an indicator of thermogenesis) are depicted in the lower panel. Here and in Figures 2–5, n is the number of animals in each experimental group.
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Figure 2. Blood flow intensity changes in the lumbar back-skin of anesthetized C57BL/6 mice in response to Na2S (dose indicated) and saline administered i.c.v.
Figure 2. Blood flow intensity changes in the lumbar back-skin of anesthetized C57BL/6 mice in response to Na2S (dose indicated) and saline administered i.c.v.
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Figure 3. Colonic temperature response of C57BL/6 mice to Na2S (dose indicated) and saline administered i.p.
Figure 3. Colonic temperature response of C57BL/6 mice to Na2S (dose indicated) and saline administered i.p.
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Figure 4. Colonic temperature and VO2 responses of C57BL/6 mice to GYY4137 (dose indicated) and saline administered i.c.v. Note that in the bottom graph the number of saline-treated mice is only 7, because in one of the animals the VO2 data could not be collected due to technical difficulties.
Figure 4. Colonic temperature and VO2 responses of C57BL/6 mice to GYY4137 (dose indicated) and saline administered i.c.v. Note that in the bottom graph the number of saline-treated mice is only 7, because in one of the animals the VO2 data could not be collected due to technical difficulties.
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Figure 5. Colonic temperature (upper panel) and VO2 (lower panel) responses to Na2S (A) and colonic temperature responses to GYY4137 (B) administered i.c.v. (doses indicated) in Trpa1+/+ and Trpa1−/− mice.
Figure 5. Colonic temperature (upper panel) and VO2 (lower panel) responses to Na2S (A) and colonic temperature responses to GYY4137 (B) administered i.c.v. (doses indicated) in Trpa1+/+ and Trpa1−/− mice.
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Figure 6. RNAscope in situ hybridization in the mouse brain for Trpa1 mRNA. Representative confocal images of (A) the medial preoptic area (MPO), (B) the dorsomedial hypothalamic area (DMH), (C) the lateral parabrachial nucleus (LPB), (D) the rostral raphe pallidus nucleus (rRPa). Note the low number of Trpa1 mRNA transcripts (red) in all areas as also shown in higher magnification insets representing the respective boxed areas (A–D). Positive control staining for Ppib mRNA (red) in the cortex (E) and negative control staining for the bacterial dabP mRNA (red) in the same cortical area (F). Cell nuclei were counterstained with DAPI (blue). Scale bar: 50 µm for all images.
Figure 6. RNAscope in situ hybridization in the mouse brain for Trpa1 mRNA. Representative confocal images of (A) the medial preoptic area (MPO), (B) the dorsomedial hypothalamic area (DMH), (C) the lateral parabrachial nucleus (LPB), (D) the rostral raphe pallidus nucleus (rRPa). Note the low number of Trpa1 mRNA transcripts (red) in all areas as also shown in higher magnification insets representing the respective boxed areas (A–D). Positive control staining for Ppib mRNA (red) in the cortex (E) and negative control staining for the bacterial dabP mRNA (red) in the same cortical area (F). Cell nuclei were counterstained with DAPI (blue). Scale bar: 50 µm for all images.
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Table
Table 1. Primers used to amplify target loci for RT-qPCR.
Table 1. Primers used to amplify target loci for RT-qPCR.
Gene Amplified
(Mus Musculus)		Nucleotide Sequence of PrimerPrimer TypeProduct Length in bpNCBI RefSeq
Trpa1ATCCAAATAGACCCAGGCACGsense101NM_177781.5
CAAGCATGTGTCAATGTTTGGTACTantisense
GapdhTTCACCACCATGGAGAAGGCsense237NM_001289726.1
GGCATGGACTGTGGTCATGAantisense
ActbCTGTATGCCTCTGGTCGTACsense214NM_007393.5
TGATGTCACGCACGATTTCCantisense
Table
Table 2. RNAscope probes and applied dilutions.
Table 2. RNAscope probes and applied dilutions.
Probes (Mus Musculus)Catalog NumberFluorophoresDilution
Trpa1400211TSA Plus Cyanine 31:750
3-plex Negative Control Probe320871TSA Plus Fluorescein, Cyanine 3 and 51:750
3-plex Positive Control Probe320881TSA Plus Fluorescein, Cyanine 3 and 51:750
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Olah, E.; Rumbus, Z.; Kormos, V.; Tekus, V.; Pakai, E.; Wilson, H.V.; Fekete, K.; Solymar, M.; Kelava, L.; Keringer, P.; et al. The Hypothermic Effect of Hydrogen Sulfide Is Mediated by the Transient Receptor Potential Ankyrin-1 Channel in Mice. Pharmaceuticals 2021, 14, 992. https://doi.org/10.3390/ph14100992

AMA Style

Olah E, Rumbus Z, Kormos V, Tekus V, Pakai E, Wilson HV, Fekete K, Solymar M, Kelava L, Keringer P, et al. The Hypothermic Effect of Hydrogen Sulfide Is Mediated by the Transient Receptor Potential Ankyrin-1 Channel in Mice. Pharmaceuticals. 2021; 14(10):992. https://doi.org/10.3390/ph14100992

Chicago/Turabian Style

Olah, Emoke, Zoltan Rumbus, Viktoria Kormos, Valeria Tekus, Eszter Pakai, Hannah V. Wilson, Kata Fekete, Margit Solymar, Leonardo Kelava, Patrik Keringer, and et al. 2021. "The Hypothermic Effect of Hydrogen Sulfide Is Mediated by the Transient Receptor Potential Ankyrin-1 Channel in Mice" Pharmaceuticals 14, no. 10: 992. https://doi.org/10.3390/ph14100992

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