Histaminergic modulation of GABAergic transmission in rat ventromedial hypothalamic neurones
- 1 August 2001
- journal article
- Published by Wiley in The Journal of Physiology
- Vol. 534 (3) , 791-803
- https://doi.org/10.1111/j.1469-7793.2001.00791.x
Abstract
1. The ventromedial nucleus of the hypothalamus (VMH) is a key nucleus in the homeostatic regulation of neuroendocrine and behavioural functions. In mechanically dissociated rat VMH neurones with attached native presynaptic nerve endings, GABAergic spontaneous inhibitory postsynaptic currents (sIPSCs) were recorded using the nystatin perforated patch recording mode under voltage-clamp conditions. 2. Histamine reversibly inhibited the sIPSC frequency in a concentration-dependent manner without affecting the mean current amplitude. The selective histamine receptor type 3 (H(3)) agonist imetit (100 nM) mimicked this effect and it was completely abolished by the selective H(3) receptor antagonists clobenpropit (3 microM) and thioperamide (10 microM). 3. The GTP-binding protein inhibitor N-ethylmaleimide (10 microM) removed the histaminergic inhibition of GABAergic sIPSCs. 4. Elimination of external Ca(2+) reduced the GABAergic sIPSC frequency without affecting the distribution of current amplitudes. In this condition, the inhibitory effect of imetit on the sIPSC frequency completely disappeared, suggesting that the histaminergic inhibition requires extracellular Ca(2+). 5. The P/Q-type Ca(2+) channel blocker omega-agatoxin IVA (300 nM) attenuated the histaminergic inhibition of the GABAergic sIPSC frequency, but neither the N-type Ca(2+) channel blocker omega-conotoxin GVIA (3 microM) nor the L-type Ca(2+) channel blocker nicardipine (3 microM) was effective. 6. Activation of adenylyl cyclase with forskolin (10 microM) had no effect on histaminergic inhibition of the sIPSCs. 7. In conclusion, histamine inhibits spontaneous GABA release from presynaptic nerve terminals projecting to VMH neurones by inhibiting presynaptic P/Q-type Ca(2+) channels via a G-protein coupled to H(3) receptors and this may modulate the excitability of VMH neurones.Keywords
This publication has 46 references indexed in Scilit:
- On the mechanism of histaminergic inhibition of glutamate release in the rat dentate gyrusThe Journal of Physiology, 1999
- Special relationship of ?-aminobutyric acid to the ventromedial nucleus of the hypothalamus during embryonic developmentJournal of Comparative Neurology, 1999
- Mechanisms of modulation of voltage‐dependent calcium channels by G proteinsThe Journal of Physiology, 1998
- HYPOTHALAMIC AND MEDULLARY GABAAAND GABAb-ERGIC SYSTEMS DIFFERENTLY REGULATE SYMPATHETIC AND CARDIOVASCULAR SYSTEMSClinical and Experimental Pharmacology and Physiology, 1995
- Functional Significance of Steroid Modulation of GABAergic Neurotransmission: Analysis at the Behavioral, Cellular, and Molecular LevelsHormones and Behavior, 1995
- Organization of projections from the ventromedial nucleus of the hypothalamus: A Phaseolus vulgaris‐Leucoagglutinin study in the ratJournal of Comparative Neurology, 1994
- Nystatin Perforated Patch Recording and Its Applications to Analyses of Intracellular Mechanisms.The Japanese Journal of Physiology, 1994
- The effect of baclofen and somatostatin on neuronal activity in the rat ventromedial hypothalamic nucleus in vitroNeuropharmacology, 1992
- Histamine H3 receptor binding sites in rat brain membranes: modulations by guanine nucleotides and divalent cationsEuropean Journal of Pharmacology: Molecular Pharmacology, 1990
- Auto-inhibition of brain histamine release mediated by a novel class (H3) of histamine receptorNature, 1983