Effects of Arginine Vasopressin on the Renal Function in Spontaneously Hypertensive Rats

Spontaneously Hypertensive Rat에서 Arginine Vasopressin의 신장효과

  • Kim, Jong-Hun (Department of General Surgery, Jeonbug National University Medical School) ;
  • Cho, Kyung-Woo (Department of Physiology, Jeonbug National University Medical School) ;
  • Yun, Young-Yi (Department of Physiology, Jeonbug National University Medical School)
  • 김종훈 (전북대학교 의과대학 일반외과학교실) ;
  • 조경우 (전북대학교 의과대학 생리학교실) ;
  • 윤영의 (전북대학교 의과대학 생리학교실)
  • Published : 1987.12.30

Abstract

There have been reports on the aberration of the control mechanisms of the blood pressure, hormone secretion, and renal functions in spontaneously hypertensive rats (SHR). However, the contribution of the renin-angiotensin system in the maintenance of high blood pressure in SHR is still controversial. Recently, it has been reported that the negative feedback short loop control mechanism of the renin-angiotensin system may be changed in SHR. In the present experiment, it was attempted to explore the possible alterations in the effect of arginine vasopressin (AVP) on the renal function in SHR. Experiments have been done in anesthetized SHR as well as in normotensive Wistar and Sprague-Dawley rats as control groups. Pharmacologic doses of AVP (10-13 mU/rat/10 min) decreased urine volume, excreted amount of creatinine and para-amino-hippuric acid. No differences in these parameters was observed between normotensive and hypertensive rats. AVP increased sodium and potassium excretion, but the responses in SHR were suppressed as compared with normotensive rats. Intravenous infusion of AVP also increased blood pressure in normotensive and hypertensive rats and a vasopressor effect of AVP was attenuated in SHR. There was a positive correlation between the changes in blood pressure and excreted amount of sodium during AVP infusion. These data suggest that the attenuated natriuretic effect of intravenous infusion of AVP may be due to a difference in renal tubular responsiveness to AVP but not due to a difference in vasopressor responsiveness.

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