Thirst Is Associated with Suppression of Habenula Output and Active Stress Coping: Is there a Role for a Non-canonical Vasopressin-Glutamate Pathway?
Author(s) -
Limei Zhang,
Vito S. Hernández,
Erika VázquezJuárez,
Freya K. Chay,
Rafael A. Barrio
Publication year - 2016
Publication title -
frontiers in neural circuits
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.036
H-Index - 61
ISSN - 1662-5110
DOI - 10.3389/fncir.2016.00013
Subject(s) - neuroscience , thirst , habenula , glutamatergic , gabaergic , vasopressin , optogenetics , glutamate receptor , premovement neuronal activity , hypothalamus , lateral hypothalamus , biology , psychology , central nervous system , endocrinology , biochemistry , receptor , inhibitory postsynaptic potential
Water-homeostasis is a fundamental physiological process for terrestrial life. In vertebrates, thirst drives water intake, but the neuronal circuits that connect the physiology of water regulation with emotional context are poorly understood. Vasopressin (VP) is a prominent messenger in this circuit, as well as L-glutamate. We have investigated the role of a VP circuit and interaction between thirst and motivational behaviors evoked by life-threatening stimuli in rats. We demonstrate a direct pathway from hypothalamic paraventricular VP-expressing, glutamatergic magnocellular neurons to the medial division of lateral habenula (LHbM), a region containing GABAergic neurons. In vivo recording and juxtacellular labeling revealed that GABAergic neurons in the LHbM had locally branching axons, and received VP-positive axon terminal contacts on their dendrites. Water deprivation significantly reduced freezing and immobility behaviors evoked by innate fear and behavioral despair, respectively, accompanied by decreased Fos expression in the lateral habenula. Our results reveal a novel VP-expressing hypothalamus to the LHbM circuit that is likely to evoke GABA-mediated inhibition in the LHbM, which promotes escape behavior during stress coping.
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