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PubMed1996

Hibernation enhances D-glucose uptake by intestinal brush border membrane vesicles in ground squirrels.

The ability to actively transport nutrients is maintained in intestinal tissues of hibernating ground squirrels compared with their active counterparts, and shows apparent upregulation in hibernators when transport rates are normalized to tissue mass. To identify the mechanisms responsible for the preservation of transport function during the extended fast of hibernation, we studied D-glucose uptake into jejunal brush border membrane vesicles prepared from active and hibernating 13-lined ground squirrels. Hibernators were without food and showing regular bouts of torpor for at least 6 weeks before sacrifice. Electron micrographs indicated similar microvillus heights of jejunal enterocytes in the two activity states, whereas microvillus density was slightly greater in the hibernators. Glucose uptake into brush border membrane vesicles was inversely related to medium osmolarity, indicating negligible binding of substrate to brush border membrane vesicles surfaces, and intravesicular spaces were similar in hibernating and active squirrels. Glucose uptake showed strong Na+ dependency in both groups, with equivalent overshoot values in the presence of Na+. Kinetic analysis revealed a significant increase in the maximal velocity of transport (Jmax) in hibernators (55.9 +/- 5.6 nmol.min-1. mg-1) compared with active squirrels (36.7 +/- 5.1 nmol.min-1. mg-1, P < 0.05), with no change in K(m). Thus, the structure and absorptive capacity of the intestinal brush border persists in fasted hibernators, and the increase in Jmax for glucose uptake during hibernation likely contributes to the enhanced Na(+)-dependent glucose absorption previously observed at the tissue level.

Animals↗
PubMed2001

Dietary fats and body lipid composition in relation to hibernation in free-ranging echidnas.

Laboratory studies have shown that high levels of dietary unsaturated fatty acids prolong torpor and lower body temperatures in hibernating herbivorous rodents, which may in turn improve winter survival. The importance of nutritional ecology in relation to hibernation in insectivorous hibernators is unknown. We therefore studied fatty acid composition of dietary insects and the depot fat of echidnas Tachyglossus aculeatus (Monotremata) during the pre-hibernation season and compared depot fat fatty acid composition before and after hibernation. Echidna depot fat fatty acid composition during the pre-hibernation season was almost identical to that of the most abundant prey species, the ant Iridomyrmex sp. Oleic acid (C18:1) was by far the most common fatty acid in both Iridomyrmex sp. (60%) and echidna depot fat (62%). After about 5 months of hibernation and an 18% loss of body mass, echidna fatty acid composition had changed significantly. The percentage of the monounsaturated oleic acid (C18:1) and palmitoleic acid (C16:1) had declined, whereas that of the saturated fatty acids (C12:0, C16:0, C18:0) and the polyunsaturated linoleic acid (C18:2) had increased. Our study suggests that, unlike herbivorous rodent hibernators, echidnas rely to a large extent on monounsaturated fatty acids as fuel for hibernation, reflecting the most common fatty acid in their food. Moreover, it appears that the high concentration of monounsaturated fatty acids compensates for the moderate availability of polyunsaturates and enables them to hibernate at low body temperatures.

Animals↗
PubMed1983

Evaluation of regeneration of nerve and reinnervation of skeletal muscle in the hibernating ground squirrel.

The retrograde transport of HRP was used to determine the status of axonal transport in the peroneal and sciatic nerves of hibernating and nonhibernating ground squirrels following crush of the peroneal nerve at 10 to 12 mm (SNS) or sciatic nerve at 33 to 35 mm (LNS) from its entrance into the extensor muscle. The ability of the proximal segment to reestablish axonal continuity and thus neuromuscular transmission was also studied. Two weeks to 3 months after nerve crush the extensor muscles were injected with HRP. We found that during hibernation no axonal transport across the site of crush was seen even after 3 months and that regeneration of the nerve during this period was minimal. Evidence of slight regeneration seen at 90 days could be due to periods of awaking of the animals during their natural hibernation cycle. In these animals HRP deposits were seen only in the nerve distal to crush, i.e., between crush site and muscle. In the nonhibernating squirrels, axoplasmic flow was reestablished at the site of injury as early as 2 weeks after crush, and HRP could be detected in the spinal cord in motoneurons of the ipsilateral ventral horn at spinal levels L3 to L5. In one hibernating animal the peroneal nerve was crushed at the distal site (SNS) and also the spinal cord was injured by dropping a weight. After nerve crush and the spinal cord injury the hibernating state could not be maintained and the animal stayed awake 22 days. The time course of regeneration of the nerve in that animal was similar to that seen in nonhibernating squirrels. After nerve crush in nonhibernating animals, reaction product was also found in sensory cell bodies of dorsal root ganglia as well as in terminals in the substantia gelatinosa of the spinal cord at the same levels. Thus, the axonal transport occurs in hibernating and non-hibernating squirrels in both sensory and motor nerve fibers. The extensor muscle fibers of the hibernating squirrels showed substantial membrane depolarization 90 days after crush. Action potentials from these fibers could be obtained from 15 to 35 days only through stimulating the nerve segment distal to the crush. Stimulation of the proximal nerve segment did not evoke muscle activity. These results demonstrate that nerve regeneration was nearly abolished during hibernation and that blockade of axonal transport continued across a region of nerve crush for the duration of the hibernating period.

Animals↗
PubMed2006

Circannual control of hibernation by HP complex in the brain.

Seasonal hibernation in mammals is under a unique adaptation system that protects organisms from various harmful events, such as lowering of body temperature (Tb), during hibernation. However, the precise factors controlling hibernation remain unknown. We have previously demonstrated a decrease in hibernation-specific protein (HP) complex in the blood of chipmunks during hibernation. Here, HP is identified as a candidate hormone for hibernation. In chipmunks kept in constant cold and darkness, HP is regulated by an individual free-running circannual rhythm that correlates with hibernation. The level of HP complex in the brain increases coincident with the onset of hibernation. Such HP regulation proceeds independently of Tb changes in constant warmth, and Tb decreases only when brain HP is increased in the cold. Blocking brain HP activity using an antibody decreases the duration of hibernation. We suggest that HP, a target of endogenously generated circannual rhythm, carries hormonal signals essential for hibernation to the brain.

Animals↗
PubMed2006

Seasonal changes in the intestinal immune system of hibernating ground squirrels.

Hibernation is associated with a prolonged fast (5-8 mo) which has the potential to affect intestinal immunity. We examined several aspects of the intestinal immune system in summer (non-hibernating) and hibernating ground squirrels. Peyer's patches were largely unaffected by hibernation, but numbers of intraepithelial lymphocytes (IEL) and lamina propria leukocytes (LPL) were greater in hibernators compared with summer. Hibernator IEL were less mature as demonstrated by low numbers of cells expressing activation-associated markers and co-receptors. Compared with summer, the percentage of B cells was higher and percentage of T cells was lower in the hibernator LPL. Hibernation was associated with greater mucosal levels of IFN-gamma, TNF-alpha, IL-10 and IL-4, but IL-6 and TGF-beta were unchanged. Mucosal IgA levels were greater in entrance and torpid hibernators compared with summer. The results suggest that modifications of the intestinal immune system during hibernation may help preserve gut integrity throughout the winter fast.

Animals↗
PubMed1998

Acetyl-CoA carboxylase control of fatty acid oxidation in hearts from hibernating Richardson's ground squirrels.

Although mammalian hibernators rely on stored body fat as a source of energy, direct measurement of energy substrate preference in heart tissue during hibernation, as well as potential mechanisms controlling fatty acid oxidation has not been examined. In order to determine whether an increase in fatty acid utilization occurs during hibernation, glucose and palmitate oxidation were measured in isolated working hearts from hibernating and non-hibernating Richardson's ground Squirrels. Hearts were perfused at either 37 degrees or 5 degrees C with perfusate containing 11 mM [U-14C]glucose and 1.2 mM [9,10-3H]palmitate, which allowed for direct measurement of both glucose oxidation (14CO2 production) and fatty acid oxidation (3H2O production). The contribution of fatty acid oxidation as a source of citric acid cycle acetyl-CoA was significantly greater in hearts from hibernating animals, compared to hearts from non-hibernating animals. Since acetyl-CoA carboxylase (ACC) regulates cardiac fatty acid oxidation (producing malonyl-CoA, a potent inhibitor of mitochondrial fatty acid uptake), we measured the activity and expression of ACC in these hearts. ACC activity was significantly decreased in hibernating ground squirrels, regardless of whether ACC was assayed at 37 degrees or 5 degrees C. This decrease in activity could not be explained by a change in the activity of 5'AMP-activated protein kinase, which can phosphorylate and inhibit ACC. Rather, the expression of the 280 kDa isoform of ACC (which predominates in cardiac muscle) was decreased in hearts from hibernating squirrel hearts. This suggests that a down regulation of ACC expression occurs as an adaptation for the increased utilization of fatty acid in hearts of hibernating ground squirrels.

Acetyl Coenzyme A↗
PubMed2000

Increased connexin43 gap junction protein in hamster cardiomyocytes during cold acclimatization and hibernation.

OBJECTIVE: The physiology of hibernation is characterized by dramatic reductions of heart rate, respiration, metabolism, blood pressure and body temperature and by resistance to ventricular fibrillation. Gap junctions in the heart provide low resistance pathways, facilitating electrical and metabolic coupling between cardiac muscle cells for coordinated action of the heart and tissue homeostasis. The conductance of these junctions, and therefore their function, is likely to be affected by the physiological changes that take place during hibernation. Our objective was to quantitate gap junction protein levels in cold acclimatization, hibernation and arousal. METHODS: We have used specific antibodies to connexins 43 and 40, in combination with confocal microscopy, to quantitatively analyze the expression of connexin protein in hamster (Mesocricetus auratus) left ventricles in four animal groups: normal controls at euthermy, cold controls (cold-exposed animals that did not undergo hibernation), hibernating animals and animals aroused from hibernation for 2 h. RESULTS: Connexin40 immunostaining was not detected in ventricular cardiomyocytes in any animal group but connexin43 was found in all groups. Connexin43 expression was significantly enhanced in hibernation and cold control ventricular cardiomyocytes. Total plaque area, numerical density and plaque size were higher in the cold controls and hibernating hamsters compared to normal controls and animals aroused from hibernation. CONCLUSION: It is possible that the increased size and number of connexin43 gap junction plaques in the cold controls may represent a compensatory response in order to maintain sufficient gap junction communication during physiological conditions that would reduce conductance. These changes may represent a mechanism by which the hamster avoids ventricular fibrillation during hibernation and arousal.

Adaptation, Physiological↗
PubMed1993

Sleep and mammalian hibernation: homologous adaptations and homologous processes?

Evidence from electroencephalographic, thermoregulatory and cellular neurophysiological studies suggests that sleep and hibernation may be homologous adaptations for energy conservation. However, despite the similarities between non-rapid eye movement (NREM) sleep and hibernation, the restorative function normally associated with slow wave sleep appears not to occur during hibernation, perhaps because of the low body temperature (Tb). Cellular neurophysiological studies also suggest that a bout of hibernation is not exclusively NREM sleep but is punctuated by periods of wakefulness. The entrance to hibernation involves both an inhibition of cortical activity and activation of hypothalamic regions, whereas the arousal from hibernation is primarily a hypothalamic function. Multiple neurochemical systems are affected by the arousal state change that occurs in hibernation, and a serotonergic-opiatergic interaction, in particular, may be important in regulating these events. Among regulated physiological systems affected by arousal state changes, the episodic respiration evident in hibernation shows striking similarities to the apneas observed during sleep in both humans and other mammals. Although the slight down-regulation of Tb and metabolism that accompanies the transition from wakefulness to NREM sleep may have served as a preadaptation for the evolution of hibernation among the mammals, increasing consideration must be given to the possibility that hibernation represents an arousal state distinct from any known normothermic arousal state.

Animals↗
PubMed1999

Sleep after arousal from hibernation is not homeostatically regulated.

Electroencephalographic slow-wave activity (SWA) in non-rapid eye movement (NREM) sleep is directly related to prior sleep/wake history, with high levels of SWA following extended periods of wake. Therefore, SWA has been thought to reflect the level of accumulated sleep need. The discovery that euthermic intervals between hibernation bouts are spent primarily in sleep and that this sleep is characterized by high and monotonically declining SWA has led to speculation that sleep homeostasis may play a fundamental role in the regulation of the timing of bouts of hibernation and periodic arousals to euthermia. It was proposed that because the SWA profile seen after arousal from hibernation is strikingly similar to what is seen in nonhibernating mammals after extended periods of wakefulness, that hibernating mammals may arouse from hibernation with significant accumulated sleep need. This sleep need may accumulate during hibernation because the low brain temperatures during hibernation may not be compatible with sleep restorative processes. In the present study, golden-mantled ground squirrels were sleep deprived during the first 4 h of interbout euthermia by injection of caffeine (20 mg/kg ip). We predicted that if the SWA peaks after bouts of hibernation reflected a homeostatic response to an accumulated sleep need, sleep deprivation should simply have displaced and possibly augmented the SWA to subsequent recovery sleep. Instead we found that after caffeine-induced sleep deprivation of animals just aroused from hibernation, the anticipated high SWA typical of recovery sleep did not occur. Similar results were found in a study that induced sleep deprivation by gentle handling (19). These findings indicate that the SWA peak immediately after hibernation does not represent homeostatic regulation of NREM sleep, as it normally does after prolonged wakefulness during euthermia, but instead may reflect some other neurological process in the recovery of brain function from an extended period at low temperature.

Animals↗
PubMed2001

[Hibernation--nature's model of resistance to ventricular fibrillation].

During hibernation, animals lower their body temperature to a few degrees above 0 degree C. This means that when entering and emerging from hibernation their body temperature passes through the critical level of +20 degrees C, a temperature region at which non-hibernating mammals develop circulatory arrest, usually due to ventricular fibrillation (VF). The hibernator heart is resistant to VF, not only that caused by hypothermia, but also VF as induced by local application of aconitine on the epicardium, and also by other factors which ordinarily cause VF in non-hibernators. Several mechanisms may explain the resistance to VF observed in the hibernator heart. The factors of greatest importance seem to be contrasting patterns of adrenergic innervation, divergent physico-chemical properties with a lower solidification point of lipids in the hibernator, distinct enzyme temperature activity curves seen in the hibernator, and differences in the handling of intracellular calcium, resulting in protection against calcium overload in the hibernator heart as compared with the non-hibernator heart.

Animals↗
PubMed1982

[14C]2-deoxyglucose uptake in ground squirrel brain during hibernation.

Autoradiographic patterns of [14C]2-deoxyglucose uptake are described throughout the brains of hibernating and euthermic ground squirrels. Autoradiographs of the brains of hibernating animals are generally homogeneous in comparison to euthermic animals; hence, the relative 2-deoxyglucose uptake (R2DGU) of gray to white matter for the majority of the 85 neural structures examined decreases during hibernation. Two categories of structures are identified as potentially important in hibernation: (1) structures that have the highest R2DGU during hibernation (cochlear nucleus, paratrigeminal nucleus, and superior colliculus) and (2) structures that undergo the least reduction in R2DGU in the transition from euthermia to hibernation (suprachiasmatic nucleus and lateral septal nucleus). The percentage of reduction in R2DGU that a structure undergoes in the transition from euthermia to hibernation is proportional to the R2DGU of that structure during euthermia. The suprachiasmatic, paratrigeminal, and cochlear nuclei undergo less of a reduction than would be predicted from this relationship and may be particularly important during hibernation. Sensory nuclei that receive primary afferent projections are among the structures with the highest R2DGU during hibernation. These metabolically active structures may be responsible for the sensitivity of the hibernator to environmental stimuli.

Animals↗
PubMedDate not supplied

[Biologically active substances in the tissues of hibernating animals].

It was supposed that the transitional period from euthermia to hibernation rather than the period of winter hibernation is optimal for the secretion of biologically active substances in rodent tissues. This hypothesis was tested in experiment. The maximal O2 consumption suppression was noted in mice after I. P. Injection of blood plasma from suslik Citellus undulatus at the beginning of its entering into hibernation. Low-molecular peptide fraction appearance in C. undulatus blood before hibernation was revealed by electrophoresis in gel and autoradiography. But its traces disappear by the end of bout. The endogenic inhibitory factor's maximal influence in early bout was shown by experiments with TRH and neoklotorphin (NKT). I.P. injections of these substances to C. undulatus were ineffective in the beginning of entering into hibernation, but clearly caused awakening after hibernation, has started. KT, being a fragment of NKT, inhibited suslik's heart rate when the awakening was provoked in the middle, but not in the end of bout. Possible transformation of biologically active substances in winter-hibernating rodents tissues is discussed. The KT "inhibitor" and NKT "stimulator" are supposed to pertain to the special type of regulatory peptides, that manage the hibernation cycle. One of the ways of inactivation of endogenic "hibernation trigger" is its removal from the organism with urine. The urine, taken from suslik immediately after hibernation proved to produce the greatest hypothermic effect on mice, I.P. injected with it.

Animals↗
PubMed1976

Protein metabolism in the black bear before and during hibernation.

During 3 to 5 months of hibernation, the American black bear does not defecate, urinate, or require food or water. Although the bear loses 15 to 25% of its body weight during this period, there is no significant change in its lean body mass. No net accumulation of the usual nitrogenous products of protein catabolism can be demonstrated in the dormant bear, and there is a decrease in urea production during hibernation. Because of these findings, it has been hypothesized that the black bear can alter its protein metabolism during hibernation by some unknown mechanism. During this study, the metabolis rate of protein turnover in four adult male black bears was measured before, during, and after hibernation, using 125I-labeled serum albumin from black bears as an indicator protein and 14C-labeled leucine as an indicator amino acid. For albumin during both phases, the disappearance rate of labeled albumin from serum was measured over 2 weeks and its turnover rate was calculated from these data. For [14C]leucine, the amino acid was injected during and after hibernation and its appearance in total proteins of plasma was measured. The results using labeled albumin revealed a threefold increase in turnover of protein during hibernation compared with protein turnover before hibernation. Leucine data supported these findings; more labeled leucine was incorporated in plasma proteins during hibernation than in the active state in spring. There were no significant changes in hematocrit, serum albumin concentration, thyroxin, or thyroxine-binding globulin between active and dormant periods, although triiodothyronine tended to decrease during hibernation. We speculate that increased protein turnover suggests a strongly acting protein-anabolic mechanism that would tend to compete with other catabolic pathways for amino acids. Another consequence of this increased protein turnover would be thermogenesis. This may have helped prevent any undue decrease in body temperature. It is notable that the body temperature of the dormant bear is appreciably higher than that of other hibernating animals.

Animals↗
PubMed1997

Hibernating myocardium: clinical and functional response to revascularisation.

OBJECTIVE: We assessed the effects of coronary bypass grafting on left ventricular (LV) function, exercise capacity and symptom profile in patients with LV impairment and evaluated the role of identifying myocardial hibernation in a prospective non-randomised study. METHODS: Of 120 patients screened, 47 patients with LV ejection fraction < 35% and three vessel coronary artery disease were studied. All underwent stress/redistribution and separate day rest/redistribution T1-201 imaging together with cine MRI at enrolment, and cine MRI at follow-up. Group 1, 30 patients undergoing bypass surgery, underwent symptom limited treadmill exercise testing with peak VO2 measurement, and symptom profile evaluation less than 3 months before, and 3-6 months after operation. Revascularisation was assessed by post-operative T1-201 imaging and repeat coronary angiography. Group 2, 17 patients treated on medical therapy alone underwent symptom profile assessment at enrolment and follow-up for those who survived. Segmental hibernation was defined as the equivalent of greater than 50% of maximal T1-201 uptake where wall motion was severely impaired on resting imaging. Patients were considered to be hibernating where two of nine LV segments fulfilled these criteria. RESULTS: In group 1, five patients died (17%), peri-or post-operatively, two defaulted and 23 attended follow-up studies. In group 2, three patients died prior to follow-up (18%). In the surgical group there was an increase in mean LVEF from 24.0 +/- 8% to 29.7 +/- 11% (P < 0.05) while in the medical group there was a fall from 25.7 +/- 10% to 20.6 +/- 8% (P < 0.05). In group 1, the mean NYHA dyspnoea grade improved from 2.7 to 1.4 while in the medical group it was unchanged, 2.6 to 2.5. In patients with myocardial hibernation identified pre-operatively, 18/19 (95%) improved LVEF after CABG compared with 2/4 (50%) of patients without hibernation. 17/19 (86%) patients with hibernation improved NYHA dyspnoea class compared with 2/4 (50%) of patients without. 60/93 (65%) of hibernating segments improved function after revascularisation while 47/53 (89%) hibernating segments showed no improvement on medical therapy alone. CONCLUSION: In patients with severe LV impairment with myocardial hibernation, coronary artery bypass grafting improves both global and regional systolic LV function, and symptom profile. Medical treatment of patients with LV impairment and myocardial hibernation does not improve LV contractile function or symptoms. Both surgical and medical therapy carry a high mortality rate.

Adult↗
PubMedDate not supplied

[Survival of dopaminergic neurons that were hibernated in vitro for seven days].

INTRODUCTION: The use of fresh foetal tissue in neurotransplants entails considerable problems of logistics that limit its clinical applicability, something that can be resolved by the development of optimal tissue storage procedures that do not affect in vivo viability and survival of dopamine. AIMS. To determine whether 7 days' hibernation affects the survival of mesencephalic tissue in vitro, and to compare it to fresh tissue. MATERIALS AND METHODS: The midbrains of rats were hibernated for 1, 3, 5 and 7 days at 4 degrees C. A cellular suspension was prepared for culture throughout a 7-day period. The number of TH+ cells present in the fresh and hibernated cultures was determined. RESULTS: The morphology of the hibernated and cultured dopaminergic neurons was very similar to that of the fresh cells. Comparing the viability of the hibernated and fresh cells did not reveal any significant differences. No significant differences between the numbers of TH+ neurons were observed at any of the hibernation times. The lowest rate of TH+ cell survival was reached at seven days' hibernation. Significant differences (p < 0.05) were found between the number of TH+ neurons for fresh and hibernated tissue. CONCLUSIONS: Hibernation at 4 degrees C for up to five days guarantees the survival of TH+ cells in vitro, but it is affected by longer times. This procedure could be considered useful for preserving human tissue in clinical transplant applications. These results refer to in vitro conditions; therefore, studies must be conducted to investigate the survival and functionality of hibernated and transplanted neurons in animal models to enable us to evaluate its applicability in neurorestorative therapy.

Animals↗
PubMed2003

Changes in hippocampal histamine receptors across the hibernation cycle in ground squirrels.

Hibernation is a physiological state characterized by a dramatic reduction in various functions, such as body temperature, heart rate, and metabolism. The hippocampus is thought to be important for regulation of the hibernation bout because it remains electrophysiologically active throughout this extremely depressed state. The question arises as to what neuronal influences act within the hippocampus during hibernation to sustain its activity. We hypothesized that histaminergic input might be an important contributor. Brain histamine is involved in functions relevant to hibernation, such as the regulation of diurnal rhythms, body temperature, and energy metabolism. Furthermore, we have previously shown that the histaminergic system appears to be activated during the hibernating state. In this study, we used receptor binding autoradiography, in situ hybridization, and GTP-gamma-S binding autoradiography to study changes in histamine receptors across the hibernation bout. We were able to demonstrate an increase in histamine H1 and H2 receptors in the hippocampus during hibernation, whereas the mRNA expression and receptor density of the inhibitory H3 receptor decreased. Histamine H3 receptors were shown to exhibit both histamine-activated and constitutive GTP-gamma-S-binding activity in the ground squirrel hippocampus, both of which decreased during hibernation, indicating a decrease in H3 receptor G-protein activation. Taken together, our results indicate that histamine may be involved in maintaining hibernation by sustaining hippocampal activity, possibly through H1 and H2 receptor activity and decreased inhibition by H3 receptors. The involvement of brain histamine, which is generally thought of as an arousal molecule, in maintaining a depressed state of the brain suggests a more general role for the amine in controlling arousal state.

Afferent Pathways↗
PubMed1975

Urea excretion in the hibernating Columbian ground squirrel (Spermophilus columbianus).

Hibernation was induced in Columbian ground squirrels by placing them in refrigerated cages equipped with urine-collection pans. On arousal, urine and blood were collected from each animal, which was then allowed to reenter hibernation. After several days the animal was sacrificed and bladder urine and another blood sample were taken. In addition, four active non-hibernating ground squirrels were placed in a cage at room temperature with neither food or water. Urine was collected at 9 and 26 hours and blood was collected at 0 and 26 hours. Although only seven of ten hibernating squirrels had a higher blood-urea level when sacrificed than during the previous arousal, the other three had very high levels in the arousal period and probably further excreted urea before entering hibernation. When total body urea was calculated on a body weight basis, all except one animal showed a greater level of urea during hibernation than in the previous arousal. During their period of dehydration, the non-hibernating summer squirrels showed a marked decrease in blood urea. The osmotic concentration of the urine from these squirrels was due less to urea than that excreted during arousal by hibernating squirrels. Thus, it appears that urea accumulates in the blood during hibernation and is excreted in the urine during arousal.

Animals↗
PubMed1988

Influence of photoperiod and gonadal steroids on hibernation in the European hamster.

Torpor was monitored daily in adult male and female European hamsters (Cricetus cricetus) induced to hibernate by exposure to a cold environment (6 degrees C). The effect of photoperiodic manipulations or administration of exogenous gonadal steroids was examined in gonadectomized or intact hamsters. 1. Gonadal regression occurred in all short day, but only in some long day, cold-exposed hamsters. Entry into hibernation was not observed until reproductive regression had occurred. Thus, gonadal atrophy appears to be a necessary precondition for hibernation. 2. Castrated hamsters in the short day cold condition showed a significantly greater incidence of torpor than those in the long day cold condition. Hence, photoperiod affected torpor independently of its effect on the gonadal cycle. 3. Testosterone, when administered via silastic capsules at near physiological levels, completely inhibited torpor in gonadectomized male and female hamsters hibernating in the short day cold condition. 4. In ovariectomized females, torpor was unaffected by progesterone treatment, but partially inhibited by estradiol. A greater inhibition of torpor was observed when estradiol-primed females were administered both estradiol and progesterone simultaneously. Thus, the effect of both hormones may be functionally comparable to that of the single testicular hormone. 5. Estradiol inhibited torpor to a greater extent in intact and ovariectomized female hamsters hibernating in long days than those in short days, suggesting an effect of photoperiod on responsiveness to estradiol. These results indicate an inverse relationship between the gonadal and hibernation cycles, and a probable role for gonadal steroids to influence the timing of the hibernation season. However, non-gonadal factors must also be involved in controlling hibernation, since photoperiod affected the incidence of torpor in gonadectomized animals and because hamsters were able to terminate hibernation in the absence of gonadal hormones.

Animals↗