Central activation of the A1 adenosine receptor in fed mice recapitulates only some of the attributes of daily torpor
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Mice enter bouts of daily torpor, drastically reducing metabolic rate, core body temperature (T b), and heart rate (HR), in response to reduced caloric intake. Because central adenosine activation has been shown to induce a torpor-like state in the arctic ground squirrel, and blocking the adenosine-1 (A1) receptor prevents daily torpor, we hypothesized that central activation of the A1 adenosine receptors would induce a bout of natural torpor in mice. To test the hypothesis, mice were subjected to four different hypothermia bouts: natural torpor, forced hypothermia (FH), isoflurane-anesthesia, and an intracerebroventricular injection of the selective A1 receptor agonist N6-cyclohexyladenosine (CHA). All conditions induced profound hypothermia. T b fell more rapidly in the FH, isoflurane-anesthesia, and CHA conditions compared to torpor, while mice treated with CHA recovered at half the rate of torpid mice. FH, isoflurane-anesthesia, and CHA-treated mice exhibited a diminished drop in HR during entry into hypothermia as compared to torpor. Mice in all conditions except CHA shivered while recovering from hypothermia, and only FH mice shivered substantially while entering hypothermia. Circulating lactate during the hypothermic bouts was not significantly different between the CHA and torpor conditions, both of which had lower than baseline lactate levels. Arrhythmias were largely absent in the FH and isoflurane-anesthesia conditions, while skipped beats were observed in natural torpor and periodic extended (>1 s) HR pauses in the CHA condition. Lastly, the hypothermic bouts showed distinct patterns of gene expression, with torpor characterized by elevated hepatic and cardiac Txnip expression and all other hypothermic states characterized by elevated c-Fos and Egr-1 expression. We conclude that CHA-induced hypothermia and natural torpor are largely different physiological states.
KeywordsTorpor Hibernation Adenosine Hypothermia Targeted temperature management
Targeted temperature management is perhaps one of the most promising new treatments for patients suffering from acute bouts of toxicity, ischemia, or myocardial infarction (Gordon 2001; Group 2002; Yenari and Han 2012; Scirica 2013; Ahmad et al. 2014). However, humans respond to exogenous cooling by generating heat to mitigate cooling. The thermoregulatory responses elicited by exogenous cooling such as shivering, brown fat activation, and vasoconstriction via the sympathetic nervous system (SNS) might lessen the benefits of targeted temperature management. In contrast, many small mammals and birds naturally lower core body temperature (T b) as they enter bouts of torpor. Despite decades of research into both peripheral compounds and central brain pathways involved in a torpor bout, our understanding of the mechanism of induction and arousal from torpor is still rudimentary (Bouma et al. 2011).
Adenosine, a ubiquitous nucleoside and purinergic signaling molecule, has garnered recent attention as a potential torpor mediator. Adenosine is involved in thermoregulation, energy signaling, and sleep (Fredholm et al. 2011). Centrally, adenosine inhibits GABA release in the arcuate nucleus (ARC) of the hypothalamus through the adenosine A1 and A2 receptors (Chen and van den Pol 1997). The ARC is essential for entry into torpor and acts as a center of integration for hunger and satiety signals from the periphery (Gluck et al. 2006; Pelz et al. 2008; Minor et al. 2009). Additionally, central levels of adenosine relay peripheral energy levels as minor fluctuations in ATP levels cause large perturbations on adenosine levels (Dunwiddie and Masino 2001). Furthermore, adenosine plays a role in controlling sleep (Bjorness and Greene 2009), and long-term electroencephalogram recordings of hibernating ground squirrels revealed that bouts of torpor are entered through a sleep state (Walker et al. 1977; Heller and Ruby 2004).
In addition to the correlative evidence listed above, experimental evidence of manipulating adenosine signaling suggests the involvement of adenosine in mediating a pathway for torpor induction. For example, peripheral administration of adenosine (or adenosine receptor agonists) causes a drop in T b, MR, and HR in animals that utilize torpor and those that do not (Miller and Hsu 1992; Anderson et al. 1994; Swoap et al. 2007; Yang et al. 2007; Olson et al. 2013; Jinka et al. 2015). Similarly, central administration of cyclohexyladenosine (CHA), an A1 adenosine receptor-specific agonist or adenosine monophosphate (AMP), causes a fall in T b (Jinka et al. 2011; Muzzi et al. 2013; Tupone et al. 2013). Importantly, central administration of the non-selective adenosine receptor antagonist 8-sulfophenyltheophylline into torpid mice, or the A1 receptor-specific antagonist 8-cyclopenthyltheophylline into torpid hamsters, causes a return to normothermia from a bout of torpor (Bruns et al. 1983; Tamura et al. 2005; Iliff and Swoap 2012). What is not known, however, is whether CHA initiates a bout of natural torpor and not just unregulated hypothermia.
Due to the diverse inhibitory and sleep-promoting effects of central A1 adenosine receptors, the necessity of adenosine signaling during entry into torpor, and the known hypothermic response to A1 adenosine receptor activation, we hypothesized that central administration of CHA would induce entry into torpor in mice. Our objective was to characterize the physiological fingerprints of four hypothermic states at multiple levels to distinguish between a natural torpid state and unregulated hypothermia. We measured physiological changes in HR, HR variability, rate of T b changes, shivering, circulating metabolites, and gene expression during natural bouts of torpor and during acute central injections of CHA. Further, we used isoflurane-anesthesia and forced hypothermia (FH) as additional points of comparison because they impose hypothermia on the organism when used in targeted temperature management in humans (Group 2002; Scirica 2013; Ahmad et al. 2014).
Materials and methods
All experiments were approved by the Williams College Institutional Animal Care and Use Committee and were performed in accordance with the guidelines described by the US National Institutes of Health Guide for the Care and Use of Laboratory Animals. C57Bl/6 J female mice were ordered pre-cannulated from Taconic Biosciences (Hudson, NY) with a guide cannula implanted into the lateral ventricle of the mouse. The mice were singly housed with Teklad sani-chip bedding (Envigo #7090) at 22 °C, except during forced hypothermia, with a 12 h dark/light cycle. Food and water were provided ad libitum in all conditions except torpor.
Electrocardiogram radiotelemeter implantation
All telemeter implantations were performed at Williams College. Mice were initially anesthetized under 5% isoflurane in oxygen and then transferred to 2% isoflurane in oxygen through a nose cone. A small midline incision of the peritoneum revealed the body cavity into which a sterilized radiotelemeter was placed (TA10ETAF-20; Data Sciences International, St Paul, MN). This telemeter provides an electrocardiogram (ECG), T b, and activity. The ribs of the telemeter were sutured with a non-absorbable suture (5 − 0 Ethilon; Johnson & Johnson, New Brunswick, NJ) to the peritoneum in order to hold the telemeter in place. The skin was further separated from the peritoneum both ventral-laterally and ventral-medially up to the shoulder in order to place the ECG leads in approximately a Lead II configuration. The peritoneum was closed with additional sutures. The skin was closed with 7-mm wound clips (Reflex Clips; Fine Science Tools, Foster City, CA) and dressed with a triple antibiotic ointment. The mice were allowed to recover for at least 10 days before experimental testing.
Body temperature (T b), ECG, and locomotor activity were sampled for a period of 10 s once per minute. All outputs from the ECG radiotelemeters were collected through receiver pads and D.S.I. acquisition software. The data were subsequently analyzed by D.S.I. analysis software or Ponemah analysis software. HR was calculated from ECG traces. Shivering was quantified using the Ponemah software by enabling the “noise” feature as we have shown previously (Maher et al. 2015).
A total of 26 mice were used in the current study. Physiological data were collected on at least five mice for each condition. However, not every mouse experienced each condition. The four experimental conditions were natural torpor, FH, isoflurane-anesthesia, and CHA. After any one intervention, mice were allowed to recover for 3–7 days before further testing to allow for sufficient time to re-establish circadian rhythms (1 day) and normal food intake (2 days post caloric restriction). To account for potential residual effects of previous treatments in our analysis, a random crossover design was used. To achieve a bout of natural torpor, mice were calorically restricted to 70% of standard chow per day, administered at the onset of the dark phase. After a bout of torpor (approximately 2–3 days post-initiation of caloric restriction), the mice were fed ad libitum. For forced hypothermia, mice were anesthetized for 20 s under 5% isoflurane in oxygen and placed in a restrainer (Product RSTR551; Kent Scientific). The restrainer was subsequently placed resting in between two diagonally oriented ice packs with the animal’s tail touching the packs (0–4 °C) at an ambient temperature of 13 °C. After T b reached approximately 21 °C, mice were placed in their home cages unrestrained and recovery was monitored. For anesthesia, mice were anesthetized at a T a of 22 °C under 2% isoflurane in oxygen in an anesthesia chamber. After T b reached approximately 28 °C, mice were placed in their home cages and recovery was monitored. For CHA treatment, CHA (Sigma Chemical, St. Louis, MO) was dissolved in 25% cyclodextrin (Sigma Chemical) solution in sterile saline. A 24-cm-long PE50 polyethylene tubing (Plastics One, Roanoke, VA) with a 2.3 mm injector attached (Plastics One, Roanoke, VA) was prefilled with a CHA solution or vehicle (25% cyclodextrin in sterile saline). Fifty pmol in 2 µL of CHA solution or 2 µL of vehicle was administered over a 1-min period. The injector was left in the guide cannula for 3 min. All CHA injections were performed during the first two hours of the light phase, in accordance with the natural circadian rhythm of torpor. Mice were injected and monitored in their home cages until they fully aroused. The mice spontaneously aroused from the CHA injection without provocation from the experimenter or a warming of the ambient temperature.
Blood lactate levels were measured from the tail vein using a commercially available lactate meter (http://www.lactate.com). Lactate was measured before the bout of hypothermia and when T b was approximately 30 °C.
Mice were euthanized under brief exposure to isoflurane-anesthesia when T b was approximately 30 °C across all conditions (natural torpor n = 6, FH n = 6, isoflurane-anesthesia n = 4, CHA n = 5). Control naïve, euthermic mice were also euthanized (n = 5). Liver and heart were removed (hearts were not removed in the isoflurane-anesthesia condition), quick frozen in liquid nitrogen, and stored at −80 °C. Total RNA was extracted from liver and heart samples with an RNeasy mini kit (Qiagen). After extraction, RNA was stored at −80 °C. mRNA in the total RNA pool was converted to cDNA using a RT2 first-strand kit (Qiagen) and stored at −20 °C. A RT2 Profiler PCR array for the mouse hypoxia signaling pathway (Qiagen PAMM-032Z) was used for qRT-PCR (Bio Rad CFX96). Cycle numbers were normalized to the average of five housekeeping genes (beta actin, beta 2 microglobulin, glyceraldehyde dehydrogenase, beta glucuronidase, and HSP90ab1). qRT-PCR was performed in duplicate. Each sample included a no-reverse transcriptase control and a no-template control. Relative changes in gene expression were calculated using the 2−ΔΔCt method.
Data are reported as mean ± SE. Statistical tests were performed using IBM SPSS v21. Univariate ANOVAs followed by Tukey post-hoc tests were performed. A p value of less than 0.05 was accepted as statistically significant.
To test the hypothesis that central administration of CHA engages the physiological processes involved in caloric restriction (CR)-induced torpor in mice and to assess the differences between CHA-induced hypothermia and other hypothermic states, mice were subjected to four conditions: CR-induced torpor, FH, isoflurane-anesthesia, and central CHA injection. Behaviorally, changes in the posture of the mice were observed in CR-induced torpor and central CHA-injected mice. CR-induced torpid animals reduced exposed body surface area by curling over and remaining motionless for the entirety of the bout. Central CHA-injected mice and isoflurane-anesthetized mice tended to be splayed across the cage floor. All four conditions showed a drop in T b, and associated drop in HR (Fig. 1a). Vehicle injection caused no change in T b (data not shown).
Mice in natural torpor exhibited a complex relationship between T b and HR (Fig. 1b), as observed previously in mice and hamsters (Mertens, Stiedl et al. 2008, Swoap and Gutilla 2009). The T b/HR relationship in CR-induced torpor shown in Fig. 1b can be divided into four periods (labeled 1–4): initially, HR decreased with little change in T b, T b decreased with a gradual slowing of HR, and then these two phases were reversed. HR increased with little change in T b and finally T b returned to baseline with a gradual quickening of HR. The T b/HR relationship in the FH, isoflurane-anesthesia, and CHA conditions was qualitatively different from the T b/HR relationship in CR-induced torpor (Fig. 1b). For FH-treated mice, the fall in HR during T b cooling tracked the rise in HR during T b warming. In isoflurane-anesthetized mice, HR did not decrease as much during cooling as it did in CR-induced torpor. In CHA-treated mice, the fall in HR with decreasing T b was similar to that of FH-treated mice. The difference in HR at 30 °C during recovery from hypothermia and the HR at 30 °C during descent into hypothermia showed a diminished drop in HR in all three conditions relative to CR-induced torpor (Fig. 1c).
During entry into hypothermia, torpor showed a significantly slower maximum rate of T b decline compared to FH, isoflurane-anesthesia, and CHA (Fig. 2). FH exhibited the fastest decrease in T b (p < 0.05). The rate of decline in T b after CHA injection was threefold greater than that observed in natural torpor (−0.62 ± 0.13 vs. −0.18 ± 0.02 °C/min, respectively; p < 0.05). During recovery from hypothermia, there was no difference in the rate of T b increase between torpor, FH, and isoflurane-anesthesia. However, CHA exhibited a significantly slower maximal rate of recovery as compared to torpor and FH (0.29 ± 0.06 vs. 0.43 ± 0.03 and 0.53 ± 0.04 °C/min, respectively; p < 0.05).
Shivering was approximated by quantifying the noise on ECG tracings (Fig. 3). Torpid mice exhibited periodic bouts of shivering during entry into torpor and while they maintained a low T b. As they recovered, torpid mice shivered vigorously. In contrast, FH mice shivered consistently throughout the hypothermic bout, both during cooling and rewarming. Anesthetized mice did not shiver while under isoflurane-anesthesia, but did so vigorously once they were removed from the anesthesia chamber. CHA mice showed minimal shivering throughout the bout.
As we have shown previously (Swoap and Iliff 2012), mice had significantly lower lactate levels during torpor compared to baseline lactate levels (0.53 ± 0.15 mM vs. 1.93 ± 0.13 mM, respectively; p < 0.05) (Fig. 4). Torpid mice also showed significantly lower lactate levels compared to FH mice (3.67 ± 0.25 mM) and anesthetized mice (5.50 ± 0.54 mM); and FH and anesthetized mice showed significantly higher lactate levels compared to baseline. There was no significant difference in circulating lactate levels between CHA-treated mice (0.84 ± 0.19 mM) and torpid mice.
Disparate cardiovascular responses to the hypothermic bouts were further uncovered by analysis of ECG tracings. Both torpid and CHA mice often exhibited asystoles, which were not found in FH or anesthetized mice (Fig. 3b). Torpid mice regularly skipped single beats, whereas the asystoles seen in the CHA condition were often much longer. These differences in asystoles between hypothermic bouts can be visualized by Poincare plots, which graph adjacent interbeat intervals (IBIs) against each other (Fig. 5). Skipped beats characteristic of torpor appeared symmetric around the line of identity (Fig. 5a), while the longer pauses between beats in CHA-treated mice were asymmetric (black arrow in Fig. 5d). P-waves were not found during the longer pauses in the CHA condition, suggesting sinus arrest. The number of events where any single IBI was three times longer than the preceding IBI was determined throughout the entire bout of hypothermia in all four conditions. These events were not observed in FH or anesthetized mice. In CR-induced bouts of torpor, these events occurred 5 ± 3 times per bout, whereas these events occurred a significantly greater number of times (129 ± 18) during a bout of CHA-induced hypothermia. No other types of arrhythmias were detected in the analyses.
Steady-state mRNA levels in the heart and liver from mice in each condition, as assessed by qRT-PCR arrays, showed unique patterns of gene expression (Fig. 6). Four genes in the liver and heart—Txnip, c-Fos, Egr1, and Hif1a—showed distinct expression patterns in the hypothermic bouts. Torpor was characterized by upregulated Txnip both in the liver and the heart. The only other condition that exhibited elevated Txnip mRNA was FH in the liver. In contrast, c-Fos and Egr1 were induced in the liver and heart of mice in all hypothermic conditions tested except during natural torpor. Hif1a was only modestly induced in the liver of FH, while in the heart, Hif1a was modestly decreased only in CHA. None of the other mRNAs on the PCR array were significantly different among the groups. A full listing of those mRNAs can be found at this website (https://www.qiagen.com/ch/shop/pcr/primer-sets/rt2-profiler-pcr-arrays/?catno=PAMM-032Z#geneglobe).
We had hypothesized that administration of an A1 receptor agonist would recapitulate the physiological changes that occur during a bout of caloric restriction-induced torpor in the mouse based on the conclusions of previous experiments, including (1) central administration of CHA in the rat (Tupone et al. 2013) or the arctic ground squirrel (Jinka et al. 2011) causes a fall in HR, metabolic rate and T b and (2) antagonizing the adenosine receptor before (Iliff and Swoap 2012) or during a bout of torpor (Tamura et al. 2005; Iliff and Swoap 2012) prevents torpor entry or induces arousal, respectively. However, the data in the current study do not support the initial hypothesis that central administration of CHA induces a natural bout of daily torpor in mice. Similar to previous reports in the arctic ground squirrel and rat (Jinka et al. 2011; Tupone et al. 2013), T b and HR decreased significantly in the mouse due to injection of CHA in the lateral ventricle (Fig. 1). The mode of CHA administration in the current set of experiments is important. Because cells outside of the brain express adenosine receptors, it is important to acknowledge the possibility that the CHA-injected ICV could cross the blood–brain barrier into the periphery. However, the dosage that we used here (50 pmol) is vanishingly small relative to the dosage of peripheral adenosine that influences T b in mice (~0.0005 vs. 100 mg/kg, respectively). Based on multiple lines of evidence, the hypothermia induced by CHA injection into the lateral ventricle has physiological characteristics that are distinct from the hypothermia observed during a natural bout of torpor.
HR dynamics differed between conditions at two levels: (1) the relationship between HR and T b and (2) HR pauses. The T b/HR loop observed in natural torpor has been seen previously (Morhardt 1970; Milsom et al. 1999; Swoap and Gutilla 2009), and similar loops have been observed between T b/metabolic rate and T b/QT interval of the ECG (Mertens et al. 2008; Geiser et al. 2014). The breadth of the T b/HR loop is driven by the autonomic nervous system, with the parasympathetic nervous system (PNS) dominating during entry into torpor and the sympathetic nervous system (SNS) active during exit from torpor (Milsom et al. 1999). T b/HR loop in FH mice has almost no breadth, suggesting that the autonomic influence on HR is nearly the same during entry and exit into hypothermia. The T b/HR loops in isoflurane-anesthetized mice were intermediate in their breadth as has been seen previously (Morhardt 1970), consistent with the finding that isoflurane depresses the SNS but has little effect on the PNS (Constantinides et al. 2011). We show here that CHA causes a drop in HR before a drop in T b, but the resulting T b/HR loop has diminished breadth as compared to natural torpor. Others have shown similar relationships with oxygen consumption, carbon dioxide production, and HR, as these all fall before T b when arctic ground squirrels or rats are injected ICV with CHA (Jinka et al. 2011; Tupone et al. 2013). The diminished breadth in the CHA condition (Fig. 1) shown here is important because it suggests that injection of CHA did not fully involve the ANS for HR control. Specifically, entry into hypothermia did not reduce HR in the CHA condition as deeply as in the natural torpor condition, resulting in a smaller difference in HR during entry and exit from hypothermia (Fig. 1c). Because the slowed HR during entry into torpor is mediated through elevated PNS activity, it seems that the PNS is not fully engaged during entry into hypothermia induced by CHA. However, this hypothesis requires further study with pharmacological methods to manipulate ANS control of HR during induced hypothermia.
One distinctive cardiovascular feature of natural torpor in mammals is the appearance of skipped beats, particularly during entry into torpor (Lyman and O’Brien 1963; Milsom et al. 1999). Administration of atropine, a muscarinic antagonist, causes the disappearance of the skipped beats during a natural bout of torpor, suggesting that the skipped beats are mediated via the PNS (Milsom et al. 1999). While the current study observed skipped beats in natural torpor, no HR pauses or skipped beats were observed in either FH or isoflurane-anesthesia, demonstrating a lack of the torpor-specific PNS action in these two models of hypothermia. Mice given CHA exhibited long, asymmetric HR pauses that required a 2–3 beat recovery period to return to the HR before the pause (see Fig. 3b tracing and open arrow in Fig. 5). Rats also exhibit HR pauses/skipped beats in response to central CHA administration that then disappear with the administration of atropine after CHA (Tupone et al. 2013). This suggests that the long pauses between beats in rats in response to central CHA are mediated by the PNS. Administration of atropine during CHA-induced hypothermia in mice in the current study was not performed, so the mechanism of sinus pauses herein remains unknown. However, the HR of CHA-treated mice is higher than the HR of torpid mice at all T bs during descent into hypothermia, suggesting that if the PNS activity is elevated in CHA treatment (lowering heart rate), it is not elevated nearly as much as it is during a torpor bout. Hence, the mechanism of the sinus pauses in the mouse given ICV CHA is unknown, and we speculate that they may be a result of altered autonomic activity.
The CHA-induced hypothermic bout had a faster fall in Tb during entrance into hypothermia compared to natural torpor (Fig. 2). This elevated rate of descent into hypothermia could be a result of faster metabolic inhibition by CHA relative to natural torpor, increased heat loss with CHA relative to natural torpor (e.g., the tail artery vasoconstriction that occurs in natural torpor may be impaired or absent with CHA) or some combination of the two. In addition, the CHA-treated mice recovered from hypothermia more slowly than the other groups (Fig. 2). CHA-treated mice rarely shivered and this lack of shivering likely contributed to the slower Tb recovery (Fig. 3). The lack of shivering with central CHA administration has also been seen in the rat (Tupone et al. 2013). The mechanism of shivering inhibition by CHA is not clear, although this could be an advantage for this compound in targeted temperature management, where current protocols for humans utilize anti-shivering agents (Group 2002; Scirica 2013). Further, the slowed rate of rewarming from CHA administration may be due to the inability to sympathetically activate brown fat pads. Indeed, mice deficient in UCP1 recover from torpor bouts at about half the rate of wild-type mice (Oelkrug et al. 2011).
As discussed above, the autonomic nervous system is important at several stages of the torpor bout. The PNS is active during entrance into torpor which slows HR and leads to asystoles. Vasoconstriction of vessels feeding peripheral tissues such as the tail is induced via the SNS during the torpor bout, slowing the rate of heat loss. SNS activity increases HR and heat production from brown fat in a UCP1-dependent way during arousal, influencing the rate of heat gain during arousal. Further, we (Swoap et al. 2006; Swoap and Weinshenker 2008) and others (Braulke and Heldmaier 2010) have shown the absolute requirement for a functional SNS for entry into torpor, whereas blocking PNS activity with atropine does not impact the likelihood of torpor bouts in the hamster (Braulke and Heldmaier 2010). Given that CHA-induced hypothermia resulted in (1) an elevated hypothermic HR relative to natural torpor, (2) entrance into hypothermia at a faster rate than natural torpor, and (3) arousal from hypothermia at a slower rate than natural torpor, it seems that CHA-administered ICV at this dose does not fully capture the modulation of the autonomic nervous system throughout a natural torpor bout.
The third line of evidence utilized for assessment of hypothermia was circulating lactate. Elevated circulating lactate is traditionally believed to be caused by respiring tissues that turn to anaerobic metabolism during hypoxia and hypoperfusion. Hypoxia in the mouse is associated with elevated levels of circulating adenosine (Dunwiddie and Masino 2001), and thus there may be a link between hypoxia, adenosine, and hypothermia. In both natural torpor and CHA-induced hypothermia, however, the lactate levels were lower than baseline (Fig. 4), suggesting that neither of these models evoked global hypoxia. Indeed, the low circulating lactate level in the CHA condition indicates either an active suppression of metabolism or increased utilization of lactate, or both. The lack of shivering observed in this study in mice injected with CHA, combined with previous data showing that CHA in the rat decreases brown adipose heat production, EMG activity, and CO2 production, suggests a suppression of metabolic rate as the reason for low lactate levels (Tupone et al. 2013). The high lactate levels during FH may be at least partially explained by the vigorous shivering exhibited by these mice due to SNS activation during descent into hypothermia.
The fourth level of interrogation of the hypothermic state was the analysis of hepatic and cardiac steady-state mRNA levels using a “mouse-hypoxia” PCR array. The vast majority of the analyzed hypoxia-related mRNAs was unchanged among any of the states (data not shown). Hypoxia inducible factor 1-alpha (Hif1a) is a transcription factor involved in the cellular response to hypoxic conditions that plays an important role in the metabolic switch between oxidative phosphorylation and anaerobic metabolism. It was expected that Hif1a would be upregulated in hypothermic states due to the decreased blood flow to tissues, particularly with isoflurane-anesthesia and FH as both of these states lead to elevated circulating lactate levels. However, Hif1a was only moderately induced in the liver of FH mice. Two genes that distinguished torpid from non-torpid hypothermic states were c-Fos and Egr1. These transcription factors are both early response genes, where the former is a proto-oncogene and the latter is part of the MAP kinase pathway, and are markers of increased cellular activity. The mRNAs for both of these genes were robustly activated in the heart and liver of FH, isoflurane-anesthesia, and CHA-treated mice, yet not induced in natural torpor (Fig. 6). In contrast, thioredoxin interacting protein (Txnip) was upregulated only in the liver and heart of torpid mice and the liver of FH mice. Txnip regulates cellular redox by binding and inhibiting the action of the thioredoxin protein, which results in the accumulation of reactive oxygen species. This gene was previously found to be induced in the hypothalamus, white and brown adipose tissue, and liver of torpid mice and Siberian hamsters (Hand et al. 2013). Based on their results, these authors suggested that Txnip is involved in regulating energy expenditure during torpor.
In conclusion, this study robustly replicates and extends to mice the observation that CHA induces hypothermia, while further investigating cardiovascular and biochemical characteristics during this induced hypothermic state. The data herein suggest that CHA-induced hypothermia in fed mice captured some of the aspects of natural torpor, but missed others, notably the HR dynamics of natural torpor. However, we tested only a single dose of CHA, 50 pmol, which was based on two previous publications (weight adjusted for rats and arctic ground squirrels), that also published only a single dose of CHA ICV (Jinka et al. 2011; Tupone et al. 2013). A more comprehensive dose response study might help to fully illuminate the influence that CHA might have on the suite of coordinated physiological responses in the mouse. Also, only female mice were tested in the current study, and thus extrapolation of our findings to male mice should be taken with caution. Administering CHA to a mouse with a genotype that is unable to undergo daily torpor, such as a dbh−/− mouse (Swoap et al. 2006) or a mouse with an ablated ARC (Gluck et al. 2006), might definitively distinguish between the two states. Further, we recognize the potential for off-target effects of CHA, such as phosphorylation, and subsequent desensitization of delta opioid receptors (Cheng et al. 2010), which may be relevant as delta opioid receptors may be involved in hypothermia/torpor (Borlongan et al. 2009). Future experiments should use specific knock-out mice or combine CHA with a specific A1-antagonist to rule out effects mediated by targets other than the A1-receptor. It is important to note that CHA was administered to mice in the fed condition in the current study, whereas natural torpor was achieved through caloric restriction. Others have shown an increased sensitivity to CHA in the fasted state in rats (Jinka et al. 2010). Hence, it may be possible that CHA requires another signal induced by caloric restriction to fully recapitulate the physiological and behavioral aspects of natural torpor. The mode of administration, namely through an indwelling catheter in the lateral ventricle of the brain and not peripherally, suggests that adenosine receptor agonists can function at regions within the brain. Given the dosage used in the current study, 50 pmol, and the mode of administration (ICV), it is highly unlikely that CHA was acting at peripheral sites (i.e., heart and vasculature).
It is very likely that the central signal that initiates fasting-induced torpor is actually a combination of signals that arise from a calorically restricted state. Indeed, circulating satiety hormone levels, such as leptin, have been implicated in the torpor pathway as torpor can be inhibited in ob/ob mice through leptin administration (Gavrilova et al. 1999). While CHA injection appears not to induce a natural torpor state, it is important to note that (1) despite the arrhythmias in CHA-injected mice, no mice died as a result of the CHA and (2) administration of this compound may have therapeutic potential, as rats subjected to cardiac arrest showed decreased neuronal cell death and increased survival after CHA IP injection (Miller and Hsu 1992; Jinka et al. 2015).
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