Masugi F, Ogihara T, Saeki S, Otsuka A, Kumahara Y
Hypertension. 1985 Sep-Oct;7(5):742-6. doi: 10.1161/01.hyp.7.5.742.
The role of an endogenously occurring acetyl glyceryl ether phosphorylcholine (AGEPC) in blood pressure regulation was studied with an AGEPC antagonist in rats with hypertension of various etiologies. The hypotensive activity of an intravenously injected AGEPC was competitively suppressed by the intravenous infusion of 3-(N-n-octadecylcarbamoyloxy)-2-methoxypropyl-2-thiazolioethylphospha te (CV-3988) and was dose-dependent. The CV-3988 was infused intravenously into one- and two-kidney, one clip hypertensive, deoxycorticosterone-salt hypertensive, adrenal regeneration hypertensive, spontaneously hypertensive, and normotensive control rats. The increase in blood pressure caused by CV-3988 infusion in spontaneously hypertensive and normotensive control rats was significant (p less than 0.01 and p less than 0.001, respectively, at 60 min) compared with that caused by vehicle infusion. The increase was not seen in rats with secondary hypertension. In rats with two-kidney, one clip hypertension, the initial rapid decrease in blood pressure seen after unclipping was significantly (p less than 0.05) inhibited by CV-3988 infusion as compared with that by vehicle infusion. These results suggest that endogenous AGEPC may participate in the blood pressure regulation and pathophysiology of some forms of hypertension in rats.
采用AGEPC拮抗剂,对各种病因所致高血压大鼠体内内源性乙酰甘油醚磷酸胆碱(AGEPC)在血压调节中的作用进行了研究。静脉注射AGEPC的降压活性受到静脉输注3-(N-正十八烷基氨甲酰氧基)-2-甲氧基丙基-2-噻唑啉乙基磷酸酯(CV-3988)的竞争性抑制,且呈剂量依赖性。将CV-3988静脉输注到一侧肾脏和两侧肾脏单夹肾性高血压、脱氧皮质酮盐性高血压、肾上腺再生性高血压、自发性高血压大鼠以及正常血压对照大鼠体内。与输注溶媒相比,在自发性高血压大鼠和正常血压对照大鼠中,静脉输注CV-3988引起的血压升高在60分钟时具有显著性差异(分别为p<0.01和p<0.001)。继发性高血压大鼠未出现这种血压升高情况。在两侧肾脏单夹肾性高血压大鼠中,与输注溶媒相比,松开夹子后最初出现的血压快速下降受到CV-3988输注的显著抑制(p<0.05)。这些结果表明,内源性AGEPC可能参与大鼠某些类型高血压的血压调节和病理生理过程。