Abstract |
The role of the endothelium-derived relaxing factor (EDRF), nitric oxide (NO), in the withdrawal-induced antihypertensive phenomenon (WAP) of arginine vasopressin (AVP) was studied in conscious unrestrained rats implanted with femoral arterial catheters for the measurement of arterial blood pressure. Cessation of a 3-h intravenous infusion of AVP (20 ng.kg-1.min-1) was followed by a large and long-lasting fall in mean arterial blood pressure below preinfusion control values in spontaneously hypertensive rats (SHR; -47.5 +/- 6.4 mmHg; 1 mmHg = 133.3 Pa) but not in normotensive Wistar-Kyoto (WKY) and Sprague-Dawley (SD) control rats. Chronic treatment of normotensive SD rats with the NO synthesis inhibitor, N omega-nitro-L-arginine (L-NNA; 0.5 g.L-1 in drinking water for 2 weeks), resulted in sustained hypertension. Similar to the SHR model, a large fall in blood pressure (-37.8 +/- 7.7 mmHg) was observed in this model of hypertension following cessation of the AVP infusion. In SHR, inhibition of NO synthesis with L-NNA (0.05 g.L-1 in drinking water for 2 weeks) failed to attenuate the fall in blood pressure following withdrawal of AVP. Chronic treatment with the NO precursor, L-arginine (L-Arg; 1.25 g.L-1 in drinking water for 2 weeks), did not affect the amplitude or the time course of the WAP in SHR. The results indicate that the L-Arg/NO pathway is not essential to the expression of the WAP to AVP in the SHR.
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Authors | R T Talom, J R McNeill |
Journal | Canadian journal of physiology and pharmacology
(Can J Physiol Pharmacol)
Vol. 75
Issue 7
Pg. 812-7
(Jul 1997)
ISSN: 0008-4212 [Print] Canada |
PMID | 9315348
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Antihypertensive Agents
- Enzyme Inhibitors
- Vasoconstrictor Agents
- Arginine Vasopressin
- Nitroarginine
- Nitric Oxide
- Arginine
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Topics |
- Animals
- Antihypertensive Agents
(pharmacology)
- Arginine
(pharmacology, physiology)
- Arginine Vasopressin
(pharmacology)
- Blood Pressure
(drug effects, physiology)
- Enzyme Inhibitors
(pharmacology)
- Hypertension
(drug therapy, metabolism)
- Male
- Nitric Oxide
(biosynthesis, physiology)
- Nitroarginine
(pharmacology)
- Rats
- Rats, Inbred SHR
- Rats, Inbred WKY
- Rats, Sprague-Dawley
- Substance Withdrawal Syndrome
(etiology, metabolism)
- Vasoconstrictor Agents
(pharmacology)
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