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  • 1
    Publication Date: 2002-08-06
    Description: Excessive caloric intake is thought to be sensed by the brain, which then activates thermogenesis as a means of preventing obesity. The sympathetic nervous system, through beta-adrenergic receptor (betaAR) action on target tissues, is likely the efferent arm of this homeostatic mechanism. To test this hypothesis, we created mice that lack the three known betaARs (beta-less mice). beta-less mice on a Chow diet had a reduced metabolic rate and were slightly obese. On a high-fat diet, beta-less mice, in contrast to wild-type mice, developed massive obesity that was due entirely to a failure of diet-induced thermogenesis. These findings establish that betaARs are necessary for diet-induced thermogenesis and that this efferent pathway plays a critical role in the body's defense against diet-induced obesity.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Bachman, Eric S -- Dhillon, Harveen -- Zhang, Chen-Yu -- Cinti, Saverio -- Bianco, Antonio C -- Kobilka, Brian K -- Lowell, Bradford B -- New York, N.Y. -- Science. 2002 Aug 2;297(5582):843-5.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Medicine, Division of Endocrinology, Beth Israel Deaconess Medical Center and Harvard Medical School, 99 Brookline Avenue, Boston, MA 02215, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/12161655" target="_blank"〉PubMed〈/a〉
    Keywords: Adipose Tissue, Brown/drug effects/metabolism ; Animals ; Basal Metabolism/drug effects ; Body Temperature/drug effects ; Body Weight/drug effects/genetics ; *Diet ; Dietary Fats/administration & dosage/pharmacology ; Energy Intake ; Female ; Homeostasis/drug effects ; Immunohistochemistry ; Male ; Mice ; Mice, Knockout ; Obesity/blood/genetics/*metabolism/prevention & control ; Oxygen Consumption/drug effects ; Phenotype ; Receptors, Adrenergic, beta/genetics/*metabolism ; *Signal Transduction/drug effects ; Sympathetic Nervous System/drug effects/physiology ; Thermogenesis/genetics/*physiology
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 2
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    American Association for the Advancement of Science (AAAS)
    Publication Date: 2005-01-22
    Description: Maintenance of normal blood glucose levels depends on a complex interplay between the insulin responsiveness of skeletal muscle and liver and glucose-stimulated insulin secretion by pancreatic beta cells. Defects in the former are responsible for insulin resistance, and defects in the latter are responsible for progression to hyperglycemia. Emerging evidence supports the potentially unifying hypothesis that both of these prominent features of type 2 diabetes are caused by mitochondrial dysfunction.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Lowell, Bradford B -- Shulman, Gerald I -- R01 DK040936/DK/NIDDK NIH HHS/ -- New York, N.Y. -- Science. 2005 Jan 21;307(5708):384-7.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Medicine, Beth Israel Deaconess Medical Center, 99 Brookline Avenue, Harvard Medical School, Boston, MA 02215, USA. blowell@bidmc.harvard.edu〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/15662004" target="_blank"〉PubMed〈/a〉
    Keywords: Adenosine Triphosphate ; Animals ; Diabetes Mellitus, Type 2/*physiopathology ; Fatty Acids/metabolism ; Gene Expression Regulation ; Glucose/metabolism ; Humans ; Hyperglycemia/physiopathology ; Insulin/secretion ; Insulin Resistance ; Ion Channels ; Islets of Langerhans/cytology/*physiology/secretion ; Liver/metabolism ; Membrane Transport Proteins/genetics/metabolism ; Mitochondria/*physiology ; Mitochondrial Proteins/genetics/metabolism ; Models, Biological ; Muscle, Skeletal/metabolism ; Obesity/physiopathology ; Oxidation-Reduction ; Oxidative Phosphorylation ; Superoxides/metabolism ; Transcription Factors/metabolism
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 3
    Publication Date: 2012-06-05
    Description: Neural activity during development critically shapes postnatal wiring of the mammalian brain. This is best illustrated by the sensory systems, in which the patterned feed-forward excitation provided by sensory organs and experience drives the formation of mature topographic circuits capable of extracting specific features of sensory stimuli. In contrast, little is known about the role of early activity in the development of the basal ganglia, a phylogenetically ancient group of nuclei fundamentally important for complex motor action and reward-based learning. These nuclei lack direct sensory input and are only loosely topographically organized, forming interlocking feed-forward and feed-back inhibitory circuits without laminar structure. Here we use transgenic mice and viral gene transfer methods to modulate neurotransmitter release and neuronal activity in vivo in the developing striatum. We find that the balance of activity between the two inhibitory and antagonist pathways in the striatum regulates excitatory innervation of the basal ganglia during development. These effects indicate that the propagation of activity through a multi-stage network regulates the wiring of the basal ganglia, revealing an important role of positive feedback in driving network maturation.〈br /〉〈br /〉〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3367801/" target="_blank"〉〈img src="https://static.pubmed.gov/portal/portal3rc.fcgi/4089621/img/3977009" border="0"〉〈/a〉   〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3367801/" target="_blank"〉This paper as free author manuscript - peer-reviewed and accepted for publication〈/a〉〈br /〉〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Kozorovitskiy, Yevgenia -- Saunders, Arpiar -- Johnson, Caroline A -- Lowell, Bradford B -- Sabatini, Bernardo L -- F31 NS074842/NS/NINDS NIH HHS/ -- F31 NS074842-02/NS/NINDS NIH HHS/ -- NS046579/NS/NINDS NIH HHS/ -- R01 DK089044/DK/NIDDK NIH HHS/ -- R01 NS046579/NS/NINDS NIH HHS/ -- R01 NS046579-09/NS/NINDS NIH HHS/ -- T32 MH020017/MH/NIMH NIH HHS/ -- Howard Hughes Medical Institute/ -- England -- Nature. 2012 May 13;485(7400):646-50. doi: 10.1038/nature11052.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Howard Hughes Medical Institute, Department of Neurobiology, Harvard Medical School, 220 Longwood Ave, Boston, Massachusetts 02115, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/22660328" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Basal Ganglia/cytology/*embryology/*physiology ; Cerebral Cortex/cytology/physiology ; Feedback, Physiological ; Female ; Male ; Mice ; Mice, Transgenic ; Models, Neurological ; Neostriatum/cytology/*embryology/*physiology ; Neural Inhibition ; Neural Pathways/*physiology ; Synapses/*metabolism ; Thalamus/cytology/physiology ; Vesicular Inhibitory Amino Acid Transport Proteins/deficiency/genetics/metabolism ; gamma-Aminobutyric Acid/secretion
    Print ISSN: 0028-0836
    Electronic ISSN: 1476-4687
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
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  • 4
    Publication Date: 2012-01-20
    Description: Dopamine has a central role in motivation and reward. Dopaminergic neurons in the ventral tegmental area (VTA) signal the discrepancy between expected and actual rewards (that is, reward prediction error), but how they compute such signals is unknown. We recorded the activity of VTA neurons while mice associated different odour cues with appetitive and aversive outcomes. We found three types of neuron based on responses to odours and outcomes: approximately half of the neurons (type I, 52%) showed phasic excitation after reward-predicting odours and rewards in a manner consistent with reward prediction error coding; the other half of neurons showed persistent activity during the delay between odour and outcome that was modulated positively (type II, 31%) or negatively (type III, 18%) by the value of outcomes. Whereas the activity of type I neurons was sensitive to actual outcomes (that is, when the reward was delivered as expected compared to when it was unexpectedly omitted), the activity of type II and type III neurons was determined predominantly by reward-predicting odours. We 'tagged' dopaminergic and GABAergic neurons with the light-sensitive protein channelrhodopsin-2 and identified them based on their responses to optical stimulation while recording. All identified dopaminergic neurons were of type I and all GABAergic neurons were of type II. These results show that VTA GABAergic neurons signal expected reward, a key variable for dopaminergic neurons to calculate reward prediction error.〈br /〉〈br /〉〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3271183/" target="_blank"〉〈img src="https://static.pubmed.gov/portal/portal3rc.fcgi/4089621/img/3977009" border="0"〉〈/a〉   〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3271183/" target="_blank"〉This paper as free author manuscript - peer-reviewed and accepted for publication〈/a〉〈br /〉〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Cohen, Jeremiah Y -- Haesler, Sebastian -- Vong, Linh -- Lowell, Bradford B -- Uchida, Naoshige -- F32 DK078478/DK/NIDDK NIH HHS/ -- F32 DK078478-01/DK/NIDDK NIH HHS/ -- P30 DK046200/DK/NIDDK NIH HHS/ -- P30 DK046200-08/DK/NIDDK NIH HHS/ -- P30 DK057521/DK/NIDDK NIH HHS/ -- P30 DK057521-01/DK/NIDDK NIH HHS/ -- R01 DK075632/DK/NIDDK NIH HHS/ -- R01 DK075632-01/DK/NIDDK NIH HHS/ -- R01 DK075632-02/DK/NIDDK NIH HHS/ -- R01 DK075632-03/DK/NIDDK NIH HHS/ -- R01 DK075632-04/DK/NIDDK NIH HHS/ -- R01 DK075632-05/DK/NIDDK NIH HHS/ -- R01 DK075632-06/DK/NIDDK NIH HHS/ -- R01 DK075632-07/DK/NIDDK NIH HHS/ -- R01 DK089044/DK/NIDDK NIH HHS/ -- R01 DK089044-01/DK/NIDDK NIH HHS/ -- Howard Hughes Medical Institute/ -- England -- Nature. 2012 Jan 18;482(7383):85-8. doi: 10.1038/nature10754.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Molecular and Cellular Biology, Center for Brain Science, Harvard University, Cambridge, Massachusetts 02138, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/22258508" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Cues ; Dopamine/metabolism ; Dopaminergic Neurons/*metabolism ; GABAergic Neurons/*metabolism ; Male ; Mice ; Mice, Inbred C57BL ; Odors/analysis ; Principal Component Analysis ; *Punishment ; *Reward ; Rhodopsin/metabolism ; Ventral Tegmental Area/*cytology/*physiology ; gamma-Aminobutyric Acid/metabolism
    Print ISSN: 0028-0836
    Electronic ISSN: 1476-4687
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
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  • 5
    Publication Date: 2014-02-04
    Description: Hunger is a hard-wired motivational state essential for survival. Agouti-related peptide (AgRP)-expressing neurons in the arcuate nucleus (ARC) at the base of the hypothalamus are crucial to the control of hunger. They are activated by caloric deficiency and, when naturally or artificially stimulated, they potently induce intense hunger and subsequent food intake. Consistent with their obligatory role in regulating appetite, genetic ablation or chemogenetic inhibition of AgRP neurons decreases feeding. Excitatory input to AgRP neurons is important in caloric-deficiency-induced activation, and is notable for its remarkable degree of caloric-state-dependent synaptic plasticity. Despite the important role of excitatory input, its source(s) has been unknown. Here, through the use of Cre-recombinase-enabled, cell-specific neuron mapping techniques in mice, we have discovered strong excitatory drive that, unexpectedly, emanates from the hypothalamic paraventricular nucleus, specifically from subsets of neurons expressing thyrotropin-releasing hormone (TRH) and pituitary adenylate cyclase-activating polypeptide (PACAP, also known as ADCYAP1). Chemogenetic stimulation of these afferent neurons in sated mice markedly activates AgRP neurons and induces intense feeding. Conversely, acute inhibition in mice with caloric-deficiency-induced hunger decreases feeding. Discovery of these afferent neurons capable of triggering hunger advances understanding of how this intense motivational state is regulated.〈br /〉〈br /〉〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3955843/" target="_blank"〉〈img src="https://static.pubmed.gov/portal/portal3rc.fcgi/4089621/img/3977009" border="0"〉〈/a〉   〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3955843/" target="_blank"〉This paper as free author manuscript - peer-reviewed and accepted for publication〈/a〉〈br /〉〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Krashes, Michael J -- Shah, Bhavik P -- Madara, Joseph C -- Olson, David P -- Strochlic, David E -- Garfield, Alastair S -- Vong, Linh -- Pei, Hongjuan -- Watabe-Uchida, Mitsuko -- Uchida, Naoshige -- Liberles, Stephen D -- Lowell, Bradford B -- F32 DK078478/DK/NIDDK NIH HHS/ -- F32 DK089710/DK/NIDDK NIH HHS/ -- K08 DK071561/DK/NIDDK NIH HHS/ -- P30 DK046200/DK/NIDDK NIH HHS/ -- P30 DK057521/DK/NIDDK NIH HHS/ -- P30 DK57521/DK/NIDDK NIH HHS/ -- P30 HD018655/HD/NICHD NIH HHS/ -- R01 DK071051/DK/NIDDK NIH HHS/ -- R01 DK075632/DK/NIDDK NIH HHS/ -- R01 DK089044/DK/NIDDK NIH HHS/ -- R01 DK096010/DK/NIDDK NIH HHS/ -- R01 MH095953/MH/NIMH NIH HHS/ -- R01 MH101207/MH/NIMH NIH HHS/ -- R37 DK053477/DK/NIDDK NIH HHS/ -- England -- Nature. 2014 Mar 13;507(7491):238-42. doi: 10.1038/nature12956. Epub 2014 Feb 2.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉1] Division of Endocrinology, Diabetes and Metabolism, Department of Medicine, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, Massachusetts 02215, USA [2] Diabetes, Endocrinology and Obesity Branch, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, Maryland 20892, USA (M.J.K.); National Institute on Drug Abuse, National Institutes of Health, Baltimore, Maryland 21224, USA (M.J.K.); Cardiovascular and Metabolic Diseases, Pfizer, 610 Main Street, Cambridge, Massachusetts 02139, USA (B.P.S.); Division of Pediatric Endocrinology, Departments of Pediatrics, University of Michigan, Ann Arbor, Michigan 48105, USA (D.P.O.); Cardiovascular and Metabolic Diseases, Novartis Institutes for BioMedical Research, 100 Technology Square, Cambridge, Massachusetts 02139, USA (L.V.). [3]. ; Division of Endocrinology, Diabetes and Metabolism, Department of Medicine, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, Massachusetts 02215, USA. ; 1] Division of Endocrinology, Diabetes and Metabolism, Department of Medicine, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, Massachusetts 02215, USA [2] Diabetes, Endocrinology and Obesity Branch, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, Maryland 20892, USA (M.J.K.); National Institute on Drug Abuse, National Institutes of Health, Baltimore, Maryland 21224, USA (M.J.K.); Cardiovascular and Metabolic Diseases, Pfizer, 610 Main Street, Cambridge, Massachusetts 02139, USA (B.P.S.); Division of Pediatric Endocrinology, Departments of Pediatrics, University of Michigan, Ann Arbor, Michigan 48105, USA (D.P.O.); Cardiovascular and Metabolic Diseases, Novartis Institutes for BioMedical Research, 100 Technology Square, Cambridge, Massachusetts 02139, USA (L.V.). ; 1] Department of Cell Biology, Harvard Medical School, Boston, Massachusetts 02115, USA [2] Program in Neuroscience, Harvard Medical School, Boston, Massachusetts 02115, USA. ; 1] Division of Endocrinology, Diabetes and Metabolism, Department of Medicine, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, Massachusetts 02215, USA [2] Center for Integrative Physiology, University of Edinburgh, Edinburgh EH8 9XD, UK. ; Division of Pediatric Endocrinology, Departments of Pediatrics, University of Michigan, Ann Arbor, Michigan 48105, USA. ; Center for Brain Science, Department of Molecular and Cellular Biology, Harvard University, 16 Divinity Avenue, Cambridge, Massachusetts 02138, USA. ; 1] Program in Neuroscience, Harvard Medical School, Boston, Massachusetts 02115, USA [2] Center for Brain Science, Department of Molecular and Cellular Biology, Harvard University, 16 Divinity Avenue, Cambridge, Massachusetts 02138, USA. ; 1] Division of Endocrinology, Diabetes and Metabolism, Department of Medicine, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, Massachusetts 02215, USA [2] Program in Neuroscience, Harvard Medical School, Boston, Massachusetts 02115, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/24487620" target="_blank"〉PubMed〈/a〉
    Keywords: Agouti-Related Protein/deficiency/*metabolism ; Animals ; Appetite/drug effects/physiology ; Arcuate Nucleus of Hypothalamus/cytology/metabolism ; Brain Mapping ; Cell Tracking ; Clozapine/analogs & derivatives/pharmacology ; Dependovirus/genetics ; Eating/drug effects/physiology ; Female ; Food Deprivation ; Hunger/drug effects/*physiology ; Integrases/metabolism ; Male ; Mice ; Neural Pathways/drug effects/*physiology ; Neuronal Plasticity/drug effects/physiology ; Neurons/drug effects/*metabolism ; Neurons, Afferent/drug effects/metabolism ; Paraventricular Hypothalamic Nucleus/cytology/*physiology ; Peptide Fragments/deficiency/metabolism ; Pituitary Adenylate Cyclase-Activating Polypeptide/metabolism ; Rabies virus/genetics ; Satiety Response/physiology ; Thyrotropin-Releasing Hormone/metabolism
    Print ISSN: 0028-0836
    Electronic ISSN: 1476-4687
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
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  • 6
    Publication Date: 2007-06-09
    Description: Forming distinct representations of multiple contexts, places, and episodes is a crucial function of the hippocampus. The dentate gyrus subregion has been suggested to fulfill this role. We have tested this hypothesis by generating and analyzing a mouse strain that lacks the gene encoding the essential subunit of the N-methyl-d-aspartate (NMDA) receptor NR1, specifically in dentate gyrus granule cells. The mutant mice performed normally in contextual fear conditioning, but were impaired in the ability to distinguish two similar contexts. A significant reduction in the context-specific modulation of firing rate was observed in the CA3 pyramidal cells when the mutant mice were transferred from one context to another. These results provide evidence that NMDA receptors in the granule cells of the dentate gyrus play a crucial role in the process of pattern separation.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉McHugh, Thomas J -- Jones, Matthew W -- Quinn, Jennifer J -- Balthasar, Nina -- Coppari, Roberto -- Elmquist, Joel K -- Lowell, Bradford B -- Fanselow, Michael S -- Wilson, Matthew A -- Tonegawa, Susumu -- G0501146/Medical Research Council/United Kingdom -- MH62122/MH/NIMH NIH HHS/ -- P50-MH58880/MH/NIMH NIH HHS/ -- New York, N.Y. -- Science. 2007 Jul 6;317(5834):94-9. Epub 2007 Jun 7.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Picower Institute for Learning and Memory, RIKEN-MIT Neuroscience Research Center, Department of Biology and Department of Brain and Cognitive Sciences, Massachusetts Institute of Technology, Cambridge, MA 02139, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/17556551" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Behavior, Animal ; Conditioning (Psychology) ; Cues ; Dentate Gyrus/cytology/*physiology ; Discrimination (Psychology) ; Excitatory Postsynaptic Potentials ; Fear ; Hippocampus/cytology/*physiology ; Learning/*physiology ; Maze Learning ; Memory/*physiology ; Mice ; Mice, Knockout ; *Neuronal Plasticity ; *Pattern Recognition, Physiological ; Perforant Pathway ; Pyramidal Cells/physiology ; Receptors, N-Methyl-D-Aspartate/genetics/*physiology ; Recombination, Genetic ; Synaptic Transmission
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 7
    Publication Date: 2016-03-24
    Description: Instinctive reactions to danger are critical to the perpetuation of species and are observed throughout the animal kingdom. The scent of predators induces an instinctive fear response in mice that includes behavioural changes, as well as a surge in blood stress hormones that mobilizes multiple body systems to escape impending danger. How the olfactory system routes predator signals detected in the nose to achieve these effects is unknown. Here we identify a specific area of the olfactory cortex in mice that induces stress hormone responses to volatile predator odours. Using monosynaptic and polysynaptic viral tracers, we found that multiple olfactory cortical areas transmit signals to hypothalamic corticotropin-releasing hormone (CRH) neurons, which control stress hormone levels. However, only one minor cortical area, the amygdalo-piriform transition area (AmPir), contained neurons upstream of CRH neurons that were activated by volatile predator odours. Chemogenetic stimulation of AmPir activated CRH neurons and induced an increase in blood stress hormones, mimicking an instinctive fear response. Moreover, chemogenetic silencing of AmPir markedly reduced the stress hormone response to predator odours without affecting a fear behaviour. These findings suggest that AmPir, a small area comprising 〈5% of the olfactory cortex, plays a key part in the hormonal component of the instinctive fear response to volatile predator scents.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Kondoh, Kunio -- Lu, Zhonghua -- Ye, Xiaolan -- Olson, David P -- Lowell, Bradford B -- Buck, Linda B -- Howard Hughes Medical Institute/ -- England -- Nature. 2016 Apr 7;532(7597):103-6. doi: 10.1038/nature17156. Epub 2016 Mar 21.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Howard Hughes Medical Institute, Basic Sciences Division, Fred Hutchinson Cancer Research Center, 1100 Fairview Avenue North, Seattle, Washington 98109, USA. ; Division of Endocrinology, Diabetes and Metabolism, Department of Medicine, Beth Israel Deaconess Medical Center and Harvard Medical School, Boston, Massachusetts 02115, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/27001694" target="_blank"〉PubMed〈/a〉
    Keywords: Adrenocorticotropic Hormone/blood ; Animals ; Corticosterone/blood ; Corticotropin-Releasing Hormone/blood/metabolism ; Escape Reaction ; Fear ; Female ; Hippocampus/cytology/physiology ; Hormones/blood/*metabolism ; Instinct ; Male ; Mice ; Neurons/metabolism ; Odors/*analysis ; Olfactory Cortex/*anatomy & histology/cytology/*physiology ; *Olfactory Pathways ; Olfactory Perception/physiology ; *Predatory Behavior ; Smell/*physiology ; *Stress, Psychological ; Telencephalon/anatomy & histology/cytology/physiology
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    Electronic ISSN: 1476-4687
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
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  • 8
    Publication Date: 2001-12-26
    Print ISSN: 0027-8424
    Electronic ISSN: 1091-6490
    Topics: Biology , Medicine , Natural Sciences in General
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  • 9
    Publication Date: 2010-04-05
    Print ISSN: 0027-8424
    Electronic ISSN: 1091-6490
    Topics: Biology , Medicine , Natural Sciences in General
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  • 10
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