PMID- 8847648 OWN - NLM STAT- MEDLINE DCOM- 19961023 LR - 20220309 IS - 0022-3751 (Print) IS - 1469-7793 (Electronic) IS - 0022-3751 (Linking) VI - 489 ( Pt 2) IP - Pt 2 DP - 1995 Dec 1 TI - Synaptic control of rat supraoptic neurones during osmotic stimulation of the organum vasculosum lamina terminalis in vitro. PG - 567-77 AB - 1. The effects of osmotic or electrical stimulation of the organum vasculosum lamina terminalis (OVLT) were examined during intracellular recordings (32 degrees C) obtained from ninety-five supraoptic nucleus magnocellular neurosecretory cells (MNCs) in superfused explants of rat hypothalamus. 2. Brief (10-20 s) applications of hypertonic and hypotonic solutions to the area of the OVLT caused prolonged (> 1 min) increases and decreases, respectively, in electrical activity in seventy of seventy-four trials performed on neurones with membrane potentials near spike threshold (approximately -55 mV). Changes in firing frequency were related to changes in external osmolality in a dose-dependent manner between 275 and 355 mosmol kg-1. 3. When 30 s periods recorded immediately before, and 30 s following, the application of an osmotic stimulus were examined, the frequency of spontaneous EPSPs (sEPSPs) was related in a dose-dependent manner to the osmolality of the solution superfusing the OVLT region. The increased EPSP frequency was maintained and did not adapt if the osmolality of the medium was raised for periods of > 10 min. In contrast, the frequency of spontaneous IPSPs (sIPSPs) was virtually unaffected by changes in external osmotic pressure. 4. Osmotically evoked changes in MNC firing were strongly correlated with accompanying changes in the frequency of sEPSPs (slope, 0.9; correlation coefficient (r) = 0.7), but not sIPSPs (r = 0.2), suggesting that changes in firing rate following osmotic stimulation of the OVLT are selectively mediated by changes in synaptic excitation. 5. In the presence of bicuculline (5-10 microM), electrical stimulation of the OVLT evoked fast EPSPs in forty-seven of forty-eight MNCs tested. These responses were reversibly reduced by application of 20-40 microM kynurenic acid (n = 3) or 20-40 microM 6-cyano-7-nitroquinoxaline-2,3-dione (CNQX; n = 11). Similarly, bath application of CNQX (n = 3) or kynurenic acid (n = 4) reversibly abolished the excitatory response of supraoptic neurones following hypertonic stimulation of the OVLT. 6. Brief (10-15 s) applications of gamma-aminobutyric acid (GABA) over the OVLT reversibly abolished increases in sEPSP frequency and action potential firing rate evoked by hyperosmotic stimulation of the OVLT. In the presence of GABA, the rates of sEPSP and sIPSP frequency were reduced to 37 +/- 10 and 44 +/- 13% (means +/- S.E.M.), respectively, of those observed under isotonic conditions (295 mosmol kg-1). 7. These results suggest that inhibitory and excitatory pathways originating from neurones located within the OVLT are tonically active under resting osmotic conditions in rat hypothalamic explants. Osmotically evoked changes in MNC firing, however, are selectively mediated through increases or decreases in the intensity of the excitatory component of OVLT-derived inputs. FAU - Richard, D AU - Richard D AD - Centre for Research in Neuroscience, Montreal General Hospital, Canada. FAU - Bourque, C W AU - Bourque CW LA - eng PT - Journal Article PT - Research Support, Non-U.S. Gov't PL - England TA - J Physiol JT - The Journal of physiology JID - 0266262 RN - 56-12-2 (gamma-Aminobutyric Acid) RN - Y37615DVKC (Bicuculline) SB - IM MH - Animals MH - Bicuculline/pharmacology MH - Electric Stimulation MH - Evoked Potentials/*physiology MH - Hypothalamus/*physiology MH - In Vitro Techniques MH - Male MH - Osmolar Concentration MH - Rats MH - Supraoptic Nucleus/*physiology MH - Synaptic Transmission/physiology MH - gamma-Aminobutyric Acid/pharmacology PMC - PMC1156780 EDAT- 1995/12/01 00:00 MHDA- 1995/12/01 00:01 PMCR- 1995/12/01 CRDT- 1995/12/01 00:00 PHST- 1995/12/01 00:00 [pubmed] PHST- 1995/12/01 00:01 [medline] PHST- 1995/12/01 00:00 [entrez] PHST- 1995/12/01 00:00 [pmc-release] AID - 10.1113/jphysiol.1995.sp021073 [doi] PST - ppublish SO - J Physiol. 1995 Dec 1;489 ( Pt 2)(Pt 2):567-77. doi: 10.1113/jphysiol.1995.sp021073.