EFFECTS OF LONG-TERM VASOPRESSIN RECEPTOR STIMULATION ON MEDULLARY BLOOD-FLOW AND ARTERIAL-PRESSURE

Citation
Aw. Cowley et al., EFFECTS OF LONG-TERM VASOPRESSIN RECEPTOR STIMULATION ON MEDULLARY BLOOD-FLOW AND ARTERIAL-PRESSURE, American journal of physiology. Regulatory, integrative and comparative physiology, 44(5), 1998, pp. 1420-1424
Citations number
22
Categorie Soggetti
Physiology
ISSN journal
03636119
Volume
44
Issue
5
Year of publication
1998
Pages
1420 - 1424
Database
ISI
SICI code
0363-6119(1998)44:5<1420:EOLVRS>2.0.ZU;2-7
Abstract
Studies were carried out using instrumented unanesthetized rats to det ermine the longterm effects of arginine vasopressin (AVP) and a specif ic vasopressin V-1 receptor agonist (V(1)AG; [Phe(2), Ile(3), Orn(8)]- vasopressin) on the renal medullary blood flow and arterial blood pres sure. It was hypothesized that the hypertension observed with chronic medullary infusion of a V1 receptor agonist may be associated with a s ustained reduction of blood flow, whereas infusion of AVP may fail to produce a sustained reduction of blood flow and thereby be unable to p roduce hypertension. Uninephrectomized Sprague-Dawley rats were prepar ed with implanted renal cortical and medullary optical fibers for dail y measurements of cortical and medullary blood flow using laser-Dopple r flowmetry techniques. An implanted renal medullary interstitial infu sion catheter delivered either AVP or a specific V1AG at a dose of 2 n g . kg(-1). min(-1) over a period of 5 days. The V(1)AG produced no ch ange of cortical blood flow but a chronic 35% reduction of medullary b lood flow (P < 0.05) and mild hypertension (11 +/- 4 mmHg, P < 0.05). AVP produced only an initial, nonsignificant 1- to 2-day reduction of medullary blood flow (-13%) and failed to raise arterial pressure sign ificantly. We conclude that a sustained V1AG response is necessary to achieve a chronic reduction of medullary blood flow and hypertension. The present data are consistent with the idea that chronic stimulation of V-2 receptors by AVP offsets the vasoconstrictor and hypertension actions of AVP-induced stimulation of medullary V1 receptors.