PMID- 11701134 OWN - NLM STAT- MEDLINE DCOM- 20020115 LR - 20190614 IS - 0006-8993 (Print) IS - 0006-8993 (Linking) VI - 919 IP - 2 DP - 2001 Nov 23 TI - Regional haemodynamic responses to activation of the medial prefrontal cortex depressor region. PG - 221-31 AB - Electrical or chemical stimulation of the medial prefrontal cortex (MPFC) produces depressor and sympathoinhibitory responses. To characterise the MPFC depressor response more fully, we determined the regional haemodynamic changes which occurred in response to stimulation of the MPFC. In halothane-anaesthetised rats, we recorded arterial blood pressure and renal, superior mesenteric, and iliac arterial vascular conductance using miniaturised Doppler flow probes. Electrical stimulation of the MPFC (50-100 microA) was used to map the location of the depressor region. Increases in vascular conductance (or increases in blood flow) were recorded from the renal (+2.3+/-0.5 kHz/mmHgx10(3)), mesenteric (+4.4+/-0.4 kHz/mmHgx10(3)), and iliac (+8.3+/-1.0 kHz/mmHgx10(3)) vascular beds in response to stimulation of the MPFC depressor region coinciding with the ventral infralimbic (IL) and dorsal peduncular (DP) cortical areas. Similar responses were obtained after microinjection of the chemical excitant L-glutamate (n=3, 100 nl, 100 mM), indicating that the responses were due to excitation of cell bodies and not due to axons traversing the area. Administration of the nitric oxide synthesis inhibitor N(G)-nitro-L-arginine methyl ester (L-NAME, 25 micromol/kg, i.v., n=5) significantly reduced the MPFC depressor response (51%, 12.5+/-1.2 to 6.1+/-2.5 mmHg). The increases in conductance in the hindquarter and mesenteric vascular beds were significantly reduced after L-NAME treatment (mesenteric by 77%, iliac by 70%), but there was no significant reduction of renal flow (35%). These observations indicate that the depressor region of the MPFC is localised to ventral regions (IL and DP) and that the depressor response is mediated by increased conductance in the hindquarters and mesenteric vascular beds. Furthermore, the depressor response may be mediated, in part, by release of nitric oxide in these vascular beds. FAU - Owens, N C AU - Owens NC AD - Department of Medicine, Clinical Pharmacology and Therapeutics Unit, Austin and Repatriation Medical Centre, University of Melbourne, Heidelberg, Victoria, Australia. FAU - Verberne, A J AU - Verberne AJ LA - eng PT - Journal Article PT - Research Support, Non-U.S. Gov't PL - Netherlands TA - Brain Res JT - Brain research JID - 0045503 RN - 0 (Enzyme Inhibitors) RN - 31C4KY9ESH (Nitric Oxide) RN - 3KX376GY7L (Glutamic Acid) RN - V55S2QJN2X (NG-Nitroarginine Methyl Ester) SB - IM MH - Animals MH - Blood Pressure/drug effects/*physiology MH - Efferent Pathways/drug effects/*physiology MH - Electric Stimulation MH - Enzyme Inhibitors/pharmacology MH - Glutamic Acid/metabolism/pharmacology MH - Iliac Artery/drug effects/physiology MH - Male MH - NG-Nitroarginine Methyl Ester/pharmacology MH - Neural Inhibition/drug effects/physiology MH - Nitric Oxide/*metabolism MH - Prefrontal Cortex/drug effects/*physiology MH - Rats MH - Rats, Sprague-Dawley MH - Reflex/drug effects/physiology MH - Regional Blood Flow/drug effects/*physiology MH - Splanchnic Circulation/drug effects/physiology MH - Sympathetic Nervous System/drug effects/*physiology MH - Vasodilation/drug effects/*physiology EDAT- 2001/11/10 10:00 MHDA- 2002/01/16 10:01 CRDT- 2001/11/10 10:00 PHST- 2001/11/10 10:00 [pubmed] PHST- 2002/01/16 10:01 [medline] PHST- 2001/11/10 10:00 [entrez] AID - S0006-8993(01)03017-7 [pii] AID - 10.1016/s0006-8993(01)03017-7 [doi] PST - ppublish SO - Brain Res. 2001 Nov 23;919(2):221-31. doi: 10.1016/s0006-8993(01)03017-7.