Amygdalar glutamatergic neuronal systems play a key role on the hibernating state of hamsters
© Alò et al; licensee BioMed Central Ltd. 2011
Received: 8 July 2010
Accepted: 20 January 2011
Published: 20 January 2011
Excitatory transmitting mechanisms are proving to play a critical role on neuronal homeostasis conditions of facultative hibernators such as the Syrian golden hamster. Indeed works have shown that the glutamatergic system of the main olfactory brain station (amygdala) is capable of controlling thermoregulatory responses, which are considered vital for the different hibernating states. In the present study the role of amygdalar glutamatergic circuits on non-hibernating (NHIB) and hibernating (HIB) hamsters were assessed on drinking stimuli and subsequently compared to expression variations of some glutamatergic subtype mRNA levels in limbic areas. For this study the two major glutamatergic antagonists and namely that of N-methyl-D-aspartate receptor (NMDAR), 3-(+)-2-carboxypiperazin-4-yl-propyl-1-phosphonate (CPP) plus that of the acid α-amine-3-hydroxy-5-metil-4-isoxazol-propionic receptor (AMPAR) site, cyano-7-nitro-quinoxaline-2,3-dione (CNQX) were infused into the basolateral amygdala nucleus. Attempts were made to establish the type of effects evoked by amygdalar glutamatergic cross-talking processes during drinking stimuli, a response that may corroborate their major role at least during some stages of this physiological activity in hibernators.
From the behavioral results it appears that the two glutamatergic compounds exerted distinct effects. In the first case local infusion of basolateral complexes (BLA) with NMDAR antagonist caused very great (p < 0.001) drinking rhythms while moderately increased feeding (p < 0.05) responses during arousal with respect to moderately increased drinking levels in euthermics. Conversely, treatment with CNQX did not modify drinking rhythms and so animals spent more time executing exploratory behaviors. These same antagonists accounted for altered glutamatergic transcription activities as displayed by greatly reduced GluR1, NR1 and GluR2 levels in hippocampus, ventromedial hypothalamic nucleus (VMN) and amygdala, respectively, plus a great (p < 0.01) up-regulation of GluR2 in VMN of hibernators.
We conclude that predominant drinking events evoked by glutamatergic mechanisms, in the presence of prevalently down regulated levels of NR1/2A of some telencephalic and hypothalamic areas appear to constitute an important neuronal switch at least during arousal stage of hibernation. The establishment of the type of glutamatergic subtypes that are linked to successful hibernating states, via drinking stimuli, may have useful bearings toward sleeping disorders.
The participation of the amygdala (AMY) in a growing number of neuroprotective functions is making this telencephalic limbic area a key site for many physiological activities such as hibernation. AMY is composed of spatially contiguous plus anatomically interconnected nuclei i.e. basolateral (BLA) and cortico-medial complexes . It influences a number of emotional and mnemonic features, especially through extensive visceral (hypothalamus and olfactory lobes) and autonomic-somatomotor connections [2–4]. Interestingly, these connections seem to control the induction of rapid eye movement (REM) as well as the awaking state via the suppression of glutamate (Glu) excitatory signals [5, 6]. At date, satiety states controlled by BLA plus its anatomical connections to the hypothalamus (HTH), hippocampus (HIP) and cortex (COR) have largely pointed to HIP as a main limbic switch controlling feeding habits . This type of control seems to strongly rely on some classes of glutamatergic receptor subunits such as N-methyl-D-aspartate receptor (NMDAR) subtypes (NR1, NR2A-D, NR3) of the ionotropic Glu family, which have shown to modulate a large amount of activities ranging from development, synaptic plasticity to mnemonic neuronal processes events [7–10]. In the case of the other class of ionotropic Glu receptor, the α-amino-3-hydroxi-5-methyl-4 isoxazole receptor (AMPAR) is a homo- or hetero-oligomeric site composed of GluRA-GluRD (or GluR1-GluR4) subunits, which are responsible for the majority of fast excitatory synaptic transmission. In addition, recent reports have demonstrated that these subtypes are not only actively involved with plasticity activities of learning and memory processes, but also with the induction of spontaneous locomotor behaviors in rats [11, 12].
It is largely known that the glutamatergic neuronal system is composed of two principal classes of receptor complexes. A first class consisting of NMDAR subtypes (NR1, NR2A-D, NR3) of the ionotropic Glu family is involved in a large amount of activities ranging from mnemonic processes to excitotoxicity events occurring during cerebral ischemia and neurodegenerative disorders such as Parkinson's and Huntington's diseases as well as epilepsy and neuropathic pain disorders [7–10]. The AMPAR family is responsible for the majority of fast excitatory synaptic transmission activities . Previously, studies have highlighted a key NR1,2 blocking type of event on some neurotransmission activities while NR3 seems to be more specific for the excitatory events of other receptor systems such as glycine receptor [13, 14]. In particular, NMDAR dynamic membrane trafficking seems to exert a critical role on feeding habits of the Arctic ground squirrel very probably through the elicitation of taste centers during the entrance stage of hibernation [15–17].
For this study hibernation, which is a well known physiological phenomenon leading to hypothermia and thus the survival of animals under extraordinary stressful conditions constitutes a major and valuable experimental paradigm . Indeed during the different states of this physiological condition a neuroprotective program with adaptive homeostatic mechanisms is activated [19, 20]. Interestingly, the 8 day hibernating cycle features a torpor bout that is interrupted by brief spontaneous pre-arousal sessions followed by an arousal period (last four days of hibernation) so that the different states are characterized by a decrease in body temperature with short periods of inter-bout euthermy [21, 22]. It is noteworthy that our rodent model i.e. the Syrian golden hamster (Mesocricetus auratus) is a permissive hibernating rodent characterized by peculiar brain vascular properties and this may have strong bearings on the necessity of maintaining a constant hypothalamic osmoregulation state throughout the wake-sleep cycle of rodents [15, 23]. Hence on the basis of the above information it was the aim of the present study to define the type of BLA-dependent Glu neurochemical mechanisms responsible for overall molecular cross-talking mechanisms operating on both drinking plus feeding behaviors of hibernators . In addition the behavioral effects were also related to expression variations of NMDAR and AMPAR subtypes in key limbic areas such as AMY, HTH, HIP and COR that may exert a key switching ON/OFF role of hibernation. These results could be a good starting point for corroborating the precise role of BLA on water consumption with interesting bearings regarding their neurocircuitry activities of some limbic areas occurring in occasion of sleeping episodes since the increase of extracellular fluid appears to exert a stimulatory effect, above all during the arousal state [15, 22, 24, 25].
Animals and stereotaxic surgery
Animal maintenance and all experimental procedures were carried out in accordance with Guide for Care and Use of Laboratory Animals issued by the European Communities Council Directive of 24 November 1986 (86/609/EEC). Efforts were made to minimize animal suffering and reduce the number of specimens used.
Motor and feeding behaviors
For the present study our permissive facultative hibernating hamster, which regularly undergoes bouts of torpor enabled us to examine frequent neuronal changes evoked throughout the entire 8 days hibernating cycle . In a first part, euthermic animals were maintained on a photoperiod of 12-h/12-h light/dark cycle (lights on at 0700 h) at a temperature of 25°C. Other hamsters (hibernators) were maintained on a 8:16 h light/dark cycle at a temperature of approximately 8°C, due to its permissive hibernating capability allowing them to frequently enter and exit from this physiological state . Both animal groups either received a NMDAR (n = 8) or AMPAR (n = 8) antagonist and compared to controls (n = 8) of their respective physiological states prior to behavioral analyses. In this case, three observation sessions consisting of morning (10 a.m.), early (2 p.m.) and late (6 p.m.) afternoon were carried out in which drinking and feeding behaviors were estimated during two 1/2 h observations for each session. The amount of food and water, given ad libitum that was consumed during the "lights on cycle" of this period was evaluated.
Food and water consumption were determined for both euthermic phase and hibernating bouts by estimating the daily amount of rodent chow pellets and water consumed in an interval of four-one half hour observations conducted during the above indicated times. These values were based on previously weighed pellets per day for the entire torpor stage (3rd to 5th day) of the hibernators plus the registration of the precise water volume given to all animals and subtracting the quantities of chow and water not consumed (controlling that no water leakage occurred).
The time spent executing feeding and drinking behaviors were also monitored with respect to the typical motor behaviors, i.e. raising of back, circling during the total hibernation period starting at day 0 and continuing up to the entire 8 day cycle. In this same session the volume of water consumed during the last four days of hibernation, which coincide with the two days prior and to the two days of arousal was estimated according to the same observation modality as above. Moreover, drinking rhythms were compared to behavioral motor activities during the same above observation interval of the last four days of hibernation. From such evaluations, water volume estimated during the entire behavioral observations turned out to be a useful indicator to further establish the percentage of water intake during different days of torpor state.
During the entire behavioral sessions the time spent by all animals in the different motor behaviors plus the amount of chow pellets and water consumed, along with the amount being lost in the litter was recorded during the three different observation sessions (morning, noon and afternoon) with a NV-VS7 Panasonic video camera (Tokyo, Japan).
At the end of the behavioral observations (6 p.m.) that coincided with the last of the three and eight treatment doses for euthermics and hibernators, respectively, the brain was removed and stored at -40°C for neuroanatomic and molecular studies. For verification purposes, a series of 20 μm sections deriving from euthermics were stained with thionin in order to establish the position of the cannula. Subsequently, the sequence of NR1 and NR2A was determined from the total RNA extracted from the whole brain of euthermic hamsters (n = 4) using TRI reagent dissolved in DEPC-water. Reverse transcription (RT) reaction was performed using 2 μg total RNA with RETROscript kit at 44°C for 1 h after template denaturation at 75°C for 3 min. Then PCR was carried out on the different dilutions of cDNA obtained by RT using the following coupled primers as described by Chowanadisai et al. : NR1 forward primer (5'ccaggctgtgcgggacaac a3') and NR1 reverse primer (5'tggaggccagggtggaggtg3') binding to position 2419-2438 and 2933-2914, respectively, of Rattus norvegicus sequence (NM_ 017010); NR2A forward primer (5'ccacactgcccatgaacaggaa cc3') and NR2A reverse primer (5'ggctcccatacaagttgccc tcca3') binding to position 3488-3511 and 3982-3959, respectively, of Rattus norvegicus sequence ( NM_ 012573). PCR was performed with the following programs: NR1 - initial incubation at 94°C for 2', amplification was carried out for 33 cycles at 94°C for 30'', at 59°C for 30'', at 72°C for 1' while the last primer extension step was at 72°C for 2'; NR2A - initial incubation at 94°C for 2', amplication phase for 34 cycles at 94°C for 30'', 55°C for 30'', 72°C for 1' and the last extension step at 72°C for 2'. Subsequently, amplified products (approximately 10 μl volume) were separated on 1.5% agarose gel and visualized by ethidium-bromide staining under UV illumination.
Transcription activity of NMDAR and AMPAR subtypes
Synthetic oligonucleotide probes were designed from the sequences of the above PCR products: the antisense probes were complementary to the encoding sequences of bp 2367-2412 for NR1 and bp 3644-3689 for NR2A of the mature protein for NR1 (5'agtaaccacgccctcagcgtaagtactatggcttgggtacagaag3') and NR2A (5'attgtaaagtggcctgagtaggtgg gcagattagaaaggcaactt3'). For GluR1 and GluR2 probes, due to comparable results of mice probes being applied to other animal models, neuronal expression capacities of these AMPAR subtypes were also done using probes specific for mouse . The antisense probes were complementary to the encoding sequences of bp 1959-2003 for GluR1 and bp 1919-1963 for GluR2 of the mature protein for GluR1 (5'gtcactggttgtctgatctcgtccttcttcaaactcttcactgtg3') and GluR2 (5'ttcactactttgtgtttctcttcac tttcaaattcctcagtgtg3'), respectively.
Afterwards, in situ hybridization was carried out on hamster brain sections using antisense and sense probes labeled by 3'-tailing with digoxigenin-11-dUTP (DIG) according to the instructions supplied by DIG oligonucleotide tailing kit. The preparation of the probe was done via its incubation at 37°C for 30 min and stopped with 0.2 M EDTA pH 8.0. Probe concentration was determined by quantification against known standards on Hybond N+ filters. Then posterior brain sections (10 μm) of euthermic (n = 8) and hibernating (n = 8) hamsters treated with antagonists of NMDAR and AMPAR with respect to their controls (n = 8) were incubated with 100 ng of antisense probe in 100 μl of hybridization solution for overnight in situ hybridization at 50°C in a humidified chamber as previously reported . Nonspecific hybridization was obtained on slides incubated with the sense probe. For immunological detection, sections were cover-slipped for 45' with PBS buffer containing 2% normal sheep serum and 0.3% Triton X100. Then an anti-digoxigenin alkaline phosphatase antibody 1:100 was added for 2 h at room temperature and the alkaline phosphatase color reaction buffer (NBT/BCIP) was added to sections and incubated for 72 h in a humidified dark chamber. At the end of this time, reaction was blocked by a solution of Tris-HCl 100 nM plus EDTA 1 mM. Neuronal hybridization signals of these posterior brain areas that include AMY, HTH, HIP and COR areas were viewed at a bright-field Dialux EB 20 microscope (Leitz) under a phase contrast objective (40X). Transcriptional activity was evaluated using a Panasonic Telecamera (Canon Objective Lens FD 50 mm, 1:3.5) attached to a Macintosh computer-assisted image analyzer system by running an Image software of NIH.
The changes induced by the two NMDAR and AMPAR antagonists on feeding and drinking behaviors plus on motor behaviors were evaluated by a two-way repeated measures for Analysis Of Variance (ANOVA) and differences were established by using Scheffe's post hoc comparison test or Newman-Keul's multiple range post hoc test when there was a significant p-value ≤ 0.05. The mRNA transcript levels (mean ± s.e.m.) of NMDAR (NR1 + NR2A) and of AMPAR (GluR1 + GluR2) expressing neurons were compared among non-hibernating and hibernating hamsters treated with Glu antagonists with respect to their controls, by using ANOVA followed by Newman-Keul's multiple range post hoc test when p value ≤ 0.05.
Feeding and drinking behaviors
In order to analyze the expression of NR1 and NR2A subunits in hamster brain, RT-PCR methods were performed by using a pair of primers that in the rat brain featured only one amplification product at 500 bp, which is similar to that obtained in the euthermic adult hamster for both subunits . In the case of GluR1 and GluR2 probes, those designed from mice sequences, due to comparable results with other animal models were used for the present study.
Influence of CPP and CNQX on AMPAR plus NMDAR expression differences
In this first study, the prevalent role of AMPAR and NMDAR subtypes on drinking behavior turned out to be a determining driving stimulus for the arousal state of our hibernating hamster model. Previous works have shown that ambient conditions like photoperiod, temperature and food shortage are among the major factors regulating the transition from euthermic to torpor state and then to arousal of permissive hibernators [29, 33]. Dense glutamate receptors levels in the different AMY subnuclei, above all in BLA complex, plus HIP and HTH sites corroborate the importance of glutamatergic neuroreceptors in hibernating rodents . Hence, while the infusion of BLA with NMDAR antagonist tends to strongly favor increased drinking bouts, it seems to account for less motor activity especially during the last two days of hibernation that coincide with arousal state. As a consequence, it appears that the main NMDAR actions of limbic areas during hibernation are aimed at satisfying some of the major physiological states via glutamatergic neuronal mechanisms [22, 35]. The fact that elevated drinking frequencies resulted in euthermics and above all in hibernators following infusion of BLA with CPP point to this AMY NMDAR site as a favorable target for such a vital function. This relationship is in line with lesions AMY failing to increase feeding bouts, which strengthens the failure of hamsters to display any eating stimuli aside prior to awakening state (6th-7th day) in which CPP-treated hibernators displayed moderately significant increases of feeding intervals . Moreover, such a relationship tends to fit well with HTH stressors accounting for blocked hunger stimuli despite the presence of food sources and so hibernators do not show any desire of eating during torpor while such an action is deactivated during the arousal state . In this context, projections of BLA glutamatergic fibers towards the lateral HTH area, which form part of the historical feeding circuit linked to initiation of eating bouts, suggests that its topographically pivotal position exerts a key switching role not only for hunger state, but above all for drinking rhythms during arousal phase. Thus the induction of drinking behavior in hibernators by NMDAR signals may constitute a first major BLA stimuli responsible for the release of osmotic factors directly or indirectly via the activation, among other, of vasopressin [1, 38, 39] that could in turn lead to the promotion of the arousal state in hamsters.
We next checked to establish which specific BLA glutamatergic subtype(s) was involved with increased drinking rates. From the altered NMDAR expression levels of CPP-treated hamsters accounting for modified drinking bouts, it seems that this subtype in various limbic areas is responsible for such modifications. A strong up-regulation of NR1 mRNA levels was reported for telencephalic areas such as COR of euthermics while a strong down-regulation of NR2A levels characterized both this brain area and AMY of non-hibernating hamsters. In the case of hibernators, a moderate down-regulation was instead registered for VMN NR1 levels, while an inverted pattern was typical of the AMY and HIP. These results appear to support a NR1- and NR2A/2B-dependent facilitation of drinking motivation, which is in agreement with enhanced licking motivational stimuli being related to a rapid activity-dependent redistribution of HTH synaptic and extra-synaptic NMDAR domains . Interestingly, such a feature seems to rely on the cross-talking of BLA with other regions as shown by the infusion of this AMY complex with NMDAR antagonists evoking increased motor behaviors plus a reduction of feeding bouts probably via interactions with other telencephalic areas like the nucleus accumbens, which controls food seeking and intake [40, 41].
It is worthy to note that while the disruption of the tonic inhibitory component of BLA excitatory NMDAR mechanisms seems to preferentially control drinking rhythms, AMPAR signals appeared to be instead responsible for the induction of exploratory type of locomotor behaviors in our hibernating rodent [42, 43]. This condition tends to be confirmed, aside by HTH AMPAR neuronal cues accounting mostly for the induction of feeding behaviors and consequently a greater body mass in hibernators, by CNQX in other brain areas like COR and HIP promoting exploratory type of behaviors [44–47]. Now, the fact that neuronal NMDAR activities modify drinking frequencies, especially during hibernating bouts should be of no surprise since moderately significant down-regulated NR1 expressing neurons were typical of key HTH areas such as VMN while a strong reduction of GluR1 mRNAs characterized Ce and Or-Py. Consequently, CPP-dependent behavior and neuronal expression relationships appear to be attributed to the blocking of exploratory stimulus via the inhibition of silent neurons (GluR1 and NR1), at least during hibernation. Conversely, their activation during arousal might serve as a driving stimulus for the promotion of exploratory activities . Indeed altered brain water homeostasis during this physiological state, leading to the shrinkage of cerebral cells seem to be typical of hypoxic metabolic processes and so may very well contribute, along with the inhibition of GluR1 and NR1 activities to the triggering of hyperphagic and drinking responses prior to arousal [25, 49, 50]. Furthermore, a synergic interaction of NMDAR and AMPAR sites during the ischemic episodes of arousal favorably support plasticity events via an interaction of NR1/2B with GluR1-dependent phosphorylative mechanisms that have been recently proposed for their therapeutic values against white matter diseases . On the other hand such a feature may be also tightly linked to the influences of other neuronal systems and namely the GABAergic system since interneuron signaling of a vast number of encephalic fields are involved with GABAAR-related glutamatergic plasticity events  and this type of relationship may constitute interesting future research prospects.
The results of present study have shown for the first time that glutamatergic neuroreceptor system to play a key role on vital physiological activities of the facultative hibernating golden hamster during the different states of hibernation. In particular, it seems that the down regulatory activities of NR1/2A account for the activation of the arousal state through drinking stimuli, which are in line with the influence of NMDAR excitatory system towards the promotion of the different hibernating states in the Arctic ground squirrel . Curiously, it was glutamatergic cross-talking activities of BLA eliciting drinking and not eating stimuli that resulted to be a very strong switching "on" mechanism for the induction of the arousal state. Now, because ischemic risks are at a peak in the waking state of hamsters due to very low body food storages, like in the arousal thermogenesis phase, makes this permissive facultative hibernating rodent a good model for studying neurodegenerative and neuroprotection events during such a critical physiological state [22, 32, 51].
acid α-amino-3-idrossi-5-metil-4-isoxazol-propionic receptor
glutamatergic type 1 receptor
glutamatergic type 2 receptor
ventromedial hypothalamic nucleus
NR2A-D, NR3: N-methyl-D-aspartate receptor subtypes
rapid eye movement
Polymerase chain reaction
ethylene diamine tetraacetic acid
phosphate buffer solution
alkaline phosphatase color reaction buffer
Analysis Of Variance
hippocampal oriens-pyramidalis layer
lateral amygdala nucleus
hypothalamic ventromedial nucleus
hippocampal dentate gyrus
amygdalar central nucleus
This study was co-financed by MIUR (Italian University Research Ministry).
- Petrovich GD, Canteras NS, Swanson LW: Combinatorial amygdalar inputs to hippocampal domains and hypothalamic behavior systems. Brain Res Rev. 2001, 38: 247-289. 10.1016/S0165-0173(01)00080-7.View ArticlePubMedGoogle Scholar
- Anderson AK: Feeling emotional: the amygdala links emotional perception and experience. Soc Cogn Affect Neurosci. 2007, 2: 71-72. 10.1093/scan/nsm022.PubMed CentralView ArticleGoogle Scholar
- Packard MG: Anxiety, cognition, and habit: A multiple memory systems perspective. Brain Res. 2009, 1293: 121-128. 10.1016/j.brainres.2009.03.029.View ArticlePubMedGoogle Scholar
- Sah P, Faber ES, Lopez DA, Power J: The amygdaloid complex: anatomy and physiology. Physiol Rev. 2003, 83: 803-834.View ArticlePubMedGoogle Scholar
- Deboer T, Sanford LD, Ross RJ, Morrison AR: Effects of electrical stimulation in the amygdala on ponto-geniculo-occipital waves in rats. Brain Res. 1998, 793: 305-400. 10.1016/S0006-8993(98)00178-4.View ArticlePubMedGoogle Scholar
- Feinberg I, Schoepp DD, Hsieh KC, Darchia N, Campbell G: The metabotropic Glutamate (mGLU)2/3 Receptor Antagonist LY341495 [2S-2-Amino-2 (1S,2S-2-carboxycyclopropyl-1-yl)-3(xanth-9-yl)propanoic Acid] Stimulates Waking and Fast Electroencephalogram Power and Blocks the Effects of the mGLU2/3 Receptor Agonist LY379268 [(ÿ-)-2-Oxa-4aminobicyclo[3.1.0]hexane-4,6-dicarboxylate] in rats. J Pharmacol Exp Therap. 2005, 312: 826-833. 10.1124/jpet.104.076547.View ArticleGoogle Scholar
- Yamakura T, Shimoji K: Subunit-and site-specific pharmacology of the NMDA receptor channel. Prog Neurobiol. 1999, 50: 279-298. 10.1016/S0301-0082(99)00007-6.View ArticleGoogle Scholar
- Paoletti P, Neyton J: NMDA receptor subunits: function and pharmacology. Curr Op Pharmacol. 2007, 7: 39-47. 10.1016/j.coph.2006.08.011.View ArticleGoogle Scholar
- Riedel G, Platt B, Micherau J: Glutammate receptor function in learning and memory. Behav Brain Res. 2003, 140: 1-47. 10.1016/S0166-4328(02)00272-3.View ArticlePubMedGoogle Scholar
- Rosin DL, Bates TA, Skaper SD: Excitatory aminoacid induced oligodendrocyte cell death in vitro: receptor-dependent and-independent mechanisms. J Neurochem. 2004, 90: 1173-1185. 10.1111/j.1471-4159.2004.02584.x.View ArticlePubMedGoogle Scholar
- Rose CR, Konnerth A: NMDA receptor-mediated Na+ signals in spines and dendrites. J Neurosci. 2001, 21: 4207-4214.PubMedGoogle Scholar
- O'Neill MF, Sanger G, Ornstein PL, Osborne DJ, Woodhouse SM: Locomotor activity detects subunits-selective effects of agonists and decahydroisoquinoline antagonists at AMPA/kainic acid ionotropic glutamate receptors in adult rats. Psychopharmacol. 2005, 179: 181-188.View ArticleGoogle Scholar
- Cavara NA, Orth A, Hollmann M: Effects of NR1 splicing on NR1/NR3-type excitatory glycine receptors. BMC Neurosci. 2009, 10: 32-10.1186/1471-2202-10-32.PubMed CentralView ArticlePubMedGoogle Scholar
- Neyton J, Paoletti P: Relating NMDA Receptor Function to Receptor Subunit Composition: Limitations of the Pharmacological Approach. J Neurosci. 2006, 26: 1331-1333. 10.1523/JNEUROSCI.5242-05.2006.View ArticlePubMedGoogle Scholar
- Zhao HW, Ross AP, Christian SL, Buchholz JN, Drew KL: Decreased NR1 phosphorylation and decreased NMDAR function in hibernating Arctic ground squirrels. J Neurosci Res. 2006, 84: 291-298. 10.1002/jnr.20893.PubMed CentralView ArticlePubMedGoogle Scholar
- Yasoshima Y, Morimoto T, Yamamoto T: Different disruptive effects on the acquisition and expression of conditioned taste aversion by blockades of amygdalar ionotropic and metabotropic glutamatergic receptor subtypes in rats. Brain Res. 2000, 869: 15-24. 10.1016/S0006-8993(00)02397-0.View ArticlePubMedGoogle Scholar
- Popov VI, Ignat'ev DA, Lindemann B: Ultrastructure of taste receptor cells in active and hibernating ground squirrels. J Electron Microsc. 1999, 48: 957-969.View ArticleGoogle Scholar
- Van Breukelen F, Martin SL: Invited review: molecular adaptations in mammalian hibernators: unique adaptations or generalized responses?. J Appl Physio. 2002, 92: 2640-2647.View ArticleGoogle Scholar
- Epperson LE, Martin SL: Quantitative assessment of ground squirrel mRNA levels in multiple stages of hibernation. Physiological Genomics. 2002, 10: 93-102.View ArticlePubMedGoogle Scholar
- Facciolo RM, Alò R, Granata T, Canonaco A, Dessì Fulgheri F, Canonaco M: Protective success of some neurosignaling systems during hibernation. Kerala India: Research SignPos. Edited by: Canonaco M, Facciolo RM. 2007, 273-91. Evolutionary Molecular Strategies and Plasticity.Google Scholar
- Geiser F: Metabolic rate and body temperature reduction during hibernation and daily torpor. Annu Rev Physiol. 2004, 66: 239-274. 10.1146/annurev.physiol.66.032102.115105.View ArticlePubMedGoogle Scholar
- Drew KL, Buck CL, Barnes BM, Christian SL, Rasley BT, Harris MB: Central nervous system regulation of mammalian hibernation: implications for metabolic suppression and ischemia tolerance. J Neurochem. 2007, 102: 1713-1726. 10.1111/j.1471-4159.2007.04675.x.PubMed CentralView ArticlePubMedGoogle Scholar
- Luppi M, Martelli D, Amici R, Baracchi F, Cerri M, Dentico D, Perez E, Zamboni G: Hypothalamic osmoregulation is manteined across the wake-sleep cycle in the rat. J Sleep Res. 2010, 19: 394-399. 10.1111/j.1365-2869.2009.00810.x.View ArticlePubMedGoogle Scholar
- Stenzel-Poore M, Stevens SL, Xiong Z, Lessov NS, Harrington CA, Mori M, Meller R, Rosenzweig H, Tobar E, Shaw T: Effect of ischaemic preconditioning on genomic response to cerebral ischemia: similarity to neuroprotective strategies in hibernation and hypoxia-tolerant states. Lancet. 2003, 362: 1028-1037. 10.1016/S0140-6736(03)14412-1.View ArticlePubMedGoogle Scholar
- Magariños AM, McEwen BS, Saboureau M, Pevet P: Rapid and reversibile changes in intrahippocampal connectivity during the course of hibernation in European hamsters. Proc Natl Acad Sci. 2006, 103: 18775-18780.PubMed CentralView ArticlePubMedGoogle Scholar
- Osborne PG, Hashimoto M: Mammalian cerebral metabolism and amino acid neurotransmission during hibernation. J Neurochem. 2008, 106: 1888-1899.PubMedGoogle Scholar
- Vajnerova O, Brozek G: The effect of direct administration of drugs into the licking generator in rats. Behav Brain Res. 2002, 136: 211-216. 10.1016/S0166-4328(02)00133-X.View ArticlePubMedGoogle Scholar
- Nürnberger F, Pleschka K, Masson-Pévet M, Pévet P: The somatostatin system of the brain and hibernation in the European hamster (Cricetus cricetus). Cell Tis Res. 1997, 288: 441-447.View ArticleGoogle Scholar
- Madeo M, Granata T, Facciolo RM, Tripepi S, Canonaco M: Feeding differences in puberal and aged golden hamsters (Mesocricetus auratus) are related to specific cerebral expression pattern of histamine subtype 3 receptor. Behav Neurosci. 2006, 120: 1235-1241. 10.1037/0735-7044.120.6.1235.View ArticlePubMedGoogle Scholar
- Giuffrida R, Musumeci S, D'Antoni S, Bonaccorso CM, Giuffrida-Stella AM, Oostra B, Catania MV: A reduced number of metabotropic glutamate subtype 5 receptor are associated with costitutive homer proteins in a mouse model of Fragile X syndrome. J Neurosci. 2005, 25: 8908-8916. 10.1523/JNEUROSCI.0932-05.2005.View ArticlePubMedGoogle Scholar
- Canonaco M, Madeo M, Alò R, Giusi G, Granata T, Carelli A, Facciolo RM: The histaminergic signaling system exerts a neuroprotective role against neurodegenerative-induced processes in the hamster. J Pharmacol Exp Ther. 2005, 315: 188-195. 10.1124/jpet.105.088153.View ArticlePubMedGoogle Scholar
- Chowanadisai W, Kelleher SL, Lönnerdal B: Maternal zinc deficiency reduces NMDA receptor expression in neonatal rat brain, which persists into early adulthood. J Neurochem. 2005, 94: 510-9. 10.1111/j.1471-4159.2005.03246.x.View ArticlePubMedGoogle Scholar
- Carey HV, Andrews MT, Martin SL: Mammalian hibernation: cellular and molecular responses to depressed metabolism and low temperature. Physiol Rev. 2003, 83: 1153-1181.View ArticlePubMedGoogle Scholar
- Stanley BG, Willett VL, Donias HW, Dee MG, Duva MA: Lateral hypothalamic NMDA receptors and glutamate as physiological mediators of eating and weight control. Am J Physiol. 1996, 270: 443-449.Google Scholar
- Duva MA, Tomkins EM, Moranda LM, Kaplan R, Sukhaseum A, Jimenez A, Stanley BG: Reverse microdialysis of N-methyl-Daspartic acid into the lateral hypothalamus of rats: effects on feeding and other behaviors. Brain Res. 2001, 921: 122-132. 10.1016/S0006-8993(01)03108-0.View ArticlePubMedGoogle Scholar
- Holland PC, Petrovich GD, Gallagher M: The effects of amygdala lesions on conditioned stimulus-potentiated eating in rats. Physiol Behav. 2002, 76: 117-129. 10.1016/S0031-9384(02)00688-1.View ArticlePubMedGoogle Scholar
- Bratincsák A, McMullen D, Miyake S, Tóth ZE, Hallenbeck JM, Palkovits M: Spatial and temporal activation of brain regions in hibernation: c-fos expression during the hibernation bout in thirteen-lined ground squirrel. J Comp Neurol. 2007, 504: 443-58.View ArticleGoogle Scholar
- Elmquist JK, Elias CF, Saper CB: From lesions to leptin: hypothalamic control of food intake and body weight. Neuron. 1999, 22: 221-232. 10.1016/S0896-6273(00)81084-3.View ArticlePubMedGoogle Scholar
- Hrabovszky E, Csapo AK, Kallo I, Wilheim T, Turi GF, Liposits ZS: Localization and osmotic regulation of vesicular glutamate transporter-2 in magnocellular neurons of the rat hypothalamus. Neurochem Int. 2006, 48: 753-761. 10.1016/j.neuint.2005.12.013.View ArticlePubMedGoogle Scholar
- Wenthold RJ, Prybylowski K, Standley S, Sans N, Petralia RS: Trafficking of NMDA receptors. Annu Rev Pharmacol Toxicol. 2003, 43: 335-358. 10.1146/annurev.pharmtox.43.100901.135803.View ArticlePubMedGoogle Scholar
- Baldwin AE, Holahan MR, Sadeghian K, Kelley AE: N-methyl-Daspartate receptor-dependent plasticity within a distributed corticostriatal network mediates appetitive instrumental learning. Behav Neurosci. 2000, 114: 1-15. 10.1037/0735-7044.114.1.84.View ArticleGoogle Scholar
- Mead NA, Brown G, Le Merrer J, Stephens DN: Effects of delection of gria1 or gria2 genes encoding glutamatergic AMPA-receptor subunits on place preference conditioning in mice. Psycopharmacology. 2004, 179: 164-171. 10.1007/s00213-004-2071-8.View ArticleGoogle Scholar
- Vekovischeva OY, Aitta-Aho T, Echenko O, Kankaanpää A, Seppälä T, Honkanen A, Sprengel R, Korpi ER: Reduced aggression in AMPA-type glutamate receptor Glu-A subunit-deficient mice. Genes Brain Behav. 2004, 3: 253-265. 10.1111/j.1601-1848.2004.00075.x.View ArticlePubMedGoogle Scholar
- Kelley AE: Ventral striatal control of appetitive motivation: role in ingestive behavior and reward-related learning. Neurosci Biobehav Rev. 2004, 27: 765-776. 10.1016/j.neubiorev.2003.11.015.View ArticlePubMedGoogle Scholar
- Maletínská L, Toma RS, Pirnik Z, Kiss A, Slaninová J, Haluzík M, Zelezná B: Effect of cholecystokinin on feeding is attenuated in monosodium glutamate obese mice. Regul Pept. 2006, 136: 58-63.View ArticlePubMedGoogle Scholar
- Romanelli P, Di Matteo L, Cobellis G, Varriale B, Menegazzi M, Gironi Carnevale UA, Ruocco LA, Sadile AG: Transcription factor expression, RNA synthesis and NADPH-diaphorase across the rat brain and exposure to spatial novelty. Behav Brain Res. 2007, 184: 91-100. 10.1016/j.bbr.2007.06.021.View ArticlePubMedGoogle Scholar
- Du J, Creson TK, Wu LJ, Ren M, Gray NA, Falke C, Wei Y, Wang Y, Blumenthal R, Yuan RMV, Chen G, Zhuo M, Manji HK: The role of hippocampal GluR1 and GluR2 receptors in manic-like behavior. J Neurosci. 2008, 28: 68-79. 10.1523/JNEUROSCI.3080-07.2008.PubMed CentralView ArticlePubMedGoogle Scholar
- Yamaguchi K, Yamada T: Involvement of anteroventral third ventricular AMPA/kainate receptors in both hyperosmotic and hypovolemic AVP secretion in conscious rats. Brain Res Bull. 2006, 71: 183-92. 10.1016/j.brainresbull.2006.09.002.View ArticlePubMedGoogle Scholar
- Barros RC, Zimmer ME, Branco LG, Milsom WK: Hypoxic metabolic response of the golden-mantled ground squirrel. J Appl Physiol. 2001, 91: 603-612.PubMedGoogle Scholar
- Bakiri Y, Hamilton NB, Káradóttir R, Attwell D: Testing NMDA receptor block as a therapeutic strategy for reducing ischaemic damage to CNS white matter. Glia. 2008, 56: 233-240. 10.1002/glia.20608.PubMed CentralView ArticlePubMedGoogle Scholar
- Ross AP, Christian SL, Zhao HW, Drew KL: Persistent tolerance to oxygen and nutrient deprivation and N-methyl-D-aspartate in cultured hippocampal slices from hibernating Arctic ground squirrel. J Cereb Blood Flow Metab. 2006, 26: 1148-1156.PubMedGoogle Scholar
- De Lima AD, Gieseler A, Voigt T: Relationship between GABAergic interneurons migration and early neocortical network activity. Dev Neurobiol. 2009, 69: 105-123. 10.1002/dneu.20696.View ArticlePubMedGoogle Scholar