TY - JOUR
T1 - Changes in blood pressure, urinary kallikrein, and urinary prostaglandin E2 in rats with streptozotocin-induced diabetes
AU - Hayashi, Matsuhiko
AU - Senba, Shigetoshi
AU - Saito, Ikuo
AU - Kitajima, Waichi
AU - Saruta, Takao
PY - 1983/5/1
Y1 - 1983/5/1
N2 - To reveal the mechanism of hypertension in diabetes mellitus, changes in blood pressure were measured in streptozotocin (STZ)-induced diabetes mellitus in male Wistar rats. Development of diabetes mellitus and elevation of blood pressure were observed in rats which received 60 mg/kg STZ, but not in rats which received 20 mg/kg STZ. In the rats which developed diabetes mellitus after STZ, the plasma renin activity, renal renin content, plasma aldosterone, and urinary kallikrein activity were all significantly reduced. The urinary excretion of prostaglandin E2 (PGE2) was significantly increased at 1 week after STZ in diabetic rats, but it gradually returned to control values and showed a tendency to decrease at 4 weeks after the treatment compared to the rats of the control groups. The pressor responsiveness to norepinephrine in the conscious unrestrained state in the STZ-induced diabetic rats was not remarkably changed compared to that of control rats. These results indicate that blood pressure gradually increases with the progress of diabetes. It is suggested that the changes in urinary excretion of PGE2 and urinary kallikrein activity may be related to the regulation of blood pressure in STZ-induced diabetic rats. On the other hand, it is considered unlikely that the reninangiotensin system and vascular responsiveness play an important role in the occurrence of hypertension in diabetes mellitus.
AB - To reveal the mechanism of hypertension in diabetes mellitus, changes in blood pressure were measured in streptozotocin (STZ)-induced diabetes mellitus in male Wistar rats. Development of diabetes mellitus and elevation of blood pressure were observed in rats which received 60 mg/kg STZ, but not in rats which received 20 mg/kg STZ. In the rats which developed diabetes mellitus after STZ, the plasma renin activity, renal renin content, plasma aldosterone, and urinary kallikrein activity were all significantly reduced. The urinary excretion of prostaglandin E2 (PGE2) was significantly increased at 1 week after STZ in diabetic rats, but it gradually returned to control values and showed a tendency to decrease at 4 weeks after the treatment compared to the rats of the control groups. The pressor responsiveness to norepinephrine in the conscious unrestrained state in the STZ-induced diabetic rats was not remarkably changed compared to that of control rats. These results indicate that blood pressure gradually increases with the progress of diabetes. It is suggested that the changes in urinary excretion of PGE2 and urinary kallikrein activity may be related to the regulation of blood pressure in STZ-induced diabetic rats. On the other hand, it is considered unlikely that the reninangiotensin system and vascular responsiveness play an important role in the occurrence of hypertension in diabetes mellitus.
KW - Experimental diabetes
KW - Experimental hypertension
KW - Kallikrein
KW - Prostaglandins
KW - Reninangiotensin system
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U2 - 10.1007/BF00508345
DO - 10.1007/BF00508345
M3 - Article
C2 - 6346111
AN - SCOPUS:0020598553
SN - 0028-1298
VL - 322
SP - 290
EP - 294
JO - Naunyn-Schmiedeberg's Archives of Pharmacology
JF - Naunyn-Schmiedeberg's Archives of Pharmacology
IS - 4
ER -