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ROLE OF THE DORSOMEDIAL HYPOTHALAMUS IN THE CARDIOVASCULAR RESPONSE TO STRESS
Author(s) -
DiMicco Joseph A.,
StotzPotter Elizabeth H.,
Monroe Amy J.,
Morin S Michelle
Publication year - 1996
Publication title -
clinical and experimental pharmacology and physiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.752
H-Index - 103
eISSN - 1440-1681
pISSN - 0305-1870
DOI - 10.1111/j.1440-1681.1996.tb02592.x
Subject(s) - microinjection , muscimol , kainate receptor , endocrinology , medicine , agonist , ampa receptor , nmda receptor , bicuculline , hypothalamus , glutamate receptor , chemistry , gabaa receptor , nbqx , receptor , kainic acid
SUMMARY 1. Disinhibition of the dorsomedial hypothalamus (DMH) in rats by local microinjection of GABA A receptor antagonists evokes behavioural and physiological changes resembling those seen in acute experimental stress. 2. Conversely, similar microinjection of muscimol, a potent agonist at inhibitory GABA A receptors, virtually abolishes stress‐induced increases in heart rate and arterial pressure. 3. Blockade of excitatory amino acid (EAA) receptors in the DMH also attentuates stress‐induced cardiovascular changes and microinjection of kainate, AMPA or NMDA at low doses elicits cardiovascular effects resembling those seen in stress. Paradoxically, injection of higher doses of NMDA or of glutamate into this region has no consistent effect. 4. The cardiovascular effects of bicuculline methiodide, a GABA A receptor antagonist, as well as those of NMDA and/or kainate were assessed after identical injection into either the DMH, the paraventricular nucleus (PVN) or the area between the two nuclei in both anaesthetized and conscious rats. For each agent, a similar pattern was seen, with the largest increases in heart rate and arterial pressure occurring after injection into the DMH and the smallest changes resulting from injection into the PVN. 5. In a parallel study, bilateral microinjection of muscimol into the DMH dramatically reduced air stress‐induced cardiovascular changes; similar injection into the area of the PVN had no effect, while injection into the area between the nuclei produced an intermediate effect. 6. Our findings suggest that activation of neurons in the region of the DMH mediates stress‐induced cardiovascular changes and that the activity of these neurons may be determined by the balance of tone at inhibitory GABA A receptors and EAA receptors.