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AJP - Regulatory, Integrative and Comparative Physiology, Vol 256, Issue 5 1076-R1083, Copyright © 1989 by American Physiological Society
ARTICLES |
S. M. Gardiner, A. M. Compton and T. Bennett
Department of Physiology and Pharmacology, Medical School, Queen's Medical Centre, Nottingham, United Kingdom.
Regional hemodynamic responses to subcutaneous injection of hyperoncotic polyethylene glycol (PEG) were assessed in Long-Evans (i.e., normal) and Brattleboro [i.e., arginine vasopressin (AVP)-deficient] rats with chronically implanted, pulsed Doppler probes. The results were compared with saline-injected time controls. PEG injection elicited an early (30 min) selective mesenteric vasoconstriction in Long-Evans rats; 4-5 h after PEG the mesenteric vasoconstriction was greater in Long-Evans than in Brattleboro rats, but the renal and hindquarters vasoconstrictions were similar in both strains. There was a transient mesenteric vasodilatation [with no change in blood pressure (BP)] in Long-Evans rats given an antagonist of the V1-receptor actions of AVP 5 h after PEG. In the presence of the AVP antagonist, Long-Evans rats showed a marked dependence on the vasoconstrictor actions of the renin-angiotensin system for the maintenance of BP, similar to Brattleboro rats. Both strains also showed marked hypotensive responses to inhibition of sympathoadrenal activity (with pentolinium). Hence, AVP has clear-cut hemodynamic effects after PEG administration, but its role is not indispensable.
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