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Is vasopressin an important hypertensive hormone?
Hypertension (Dallas, Tex. : 1979)
|July 1, 1981
Summary
Arginine vasopressin (AVP) showed weak long-term hypertensive effects in dogs, especially when combined with angiotensin II or aldosterone. Acute AVP infusions caused temporary blood pressure changes, but sustained hypertension was minimal.
Area of Science:
- Cardiovascular Physiology
- Endocrinology
- Renal Physiology
Background:
- Arginine vasopressin (AVP) plays a role in blood pressure regulation.
- Understanding AVP's hypertensive potential is crucial for managing cardiovascular conditions.
- Existing research on AVP's chronic effects on blood pressure is limited.
Purpose of the Study:
- To quantitatively assess the hypertensive activity of chronic arginine vasopressin (AVP) infusion.
- To investigate AVP's effects in both normotensive and pre-hypertensive canine models.
- To compare AVP's impact on mean arterial pressure (MAP) under different hormonal conditions.
Main Methods:
- Chronic infusion of AVP at 140 and 560 microunits/kg/min in normotensive dogs.
- Chronic infusion of AVP in dogs with angiotensin II (AII) or aldosterone-induced hypertension.
- Continuous monitoring of mean arterial pressure (MAP) and daily fluid/electrolyte balance.
- Controlled daily saline infusion to all dogs.
Main Results:
- In normotensive dogs, AVP initially caused water retention and increased MAP, followed by diuresis and a decrease in MAP.
- In AII or aldosterone-hypertensive dogs, AVP infusion resulted in attenuated natriuresis and minimal or transient increases in MAP.
- Cessation of AVP in hypertensive models led to a transient drop in MAP, followed by fluid retention and return to baseline hypertension.
Conclusions:
- Chronic high plasma AVP levels exhibit weak long-term hypertensive effects, particularly in established hypertension models.
- AVP has pronounced acute effects on MAP but minimal sustained hypertensive impact.
- The interplay between AVP and other pressor systems (AII, aldosterone) significantly modulates AVP's hypertensive role.