Delbarre B, Delbarre G, Ferger A
Faculté de médecine, Tours.
Arch Mal Coeur Vaiss. 1990 Jul;83(8):1209-12.
The role of prostaglandins (PG) has been evoked in the mechanism of action of indapamide. Indeed, PG can act in the regulation of the blood pressure (BP) at different levels: vasodilatation, diuretic, natriuretic, antagonism of angiotensin II and vasopressin (VP), action on adrenergic system. To confirm this hypothesis, we studied the action of certain eicosanoids inhibitors on the antihypertensive action of indapamide in the SHR rat, anaesthetized with pentobarbital (40 mg/kg i.p.). Indapamide (3 mg/kg i.p.) induces significant decrease on BP over 60 min. Mepacrine (5 mg/kg i.p.), phospholipase A2 inhibitor, indomethacin (5 mg/kg i.p), cyclo-oxygenase inhibitor, and tranylcypromine (0,1 mg/kg i.p.), prostacyclin synthase inhibitor, antagonize the antihypertensive action of indapamide. In order to eliminate the importance of VP, we used Brattleboro rats (genetically depleted in VP): indapamide (3 mg/kg i.p.) maintains its hypotensive activity. To eliminate the role of kidney in PG synthesis, we have used cyclo-oxygenase extrarenal inhibitor (sulindac) and the bilateral nephrectomy. Sulindac (1,25 mg/kg i.p.) and the bilateral nephrectomy do not remove the hypotensive action of indapamide. These results, demonstrating the PG extrarenal role and probably that of PGI2, localized in the vascular wall, could explain part of the antihypertensive mechanism of indapamide.
前列腺素(PG)在吲达帕胺的作用机制中发挥了作用。实际上,PG可在不同水平调节血压(BP):血管舒张、利尿、排钠、拮抗血管紧张素II和血管加压素(VP)、作用于肾上腺素能系统。为证实这一假说,我们研究了某些类花生酸抑制剂对戊巴比妥(40mg/kg腹腔注射)麻醉的SHR大鼠中吲达帕胺降压作用的影响。吲达帕胺(3mg/kg腹腔注射)在60分钟内可使血压显著降低。氯喹(5mg/kg腹腔注射),磷脂酶A2抑制剂;吲哚美辛(5mg/kg腹腔注射),环氧化酶抑制剂;反苯环丙胺(0.1mg/kg腹腔注射),前列环素合成酶抑制剂,均可拮抗吲达帕胺的降压作用。为排除VP的影响,我们使用了遗传性VP缺乏的布拉特洛维大鼠:吲达帕胺(3mg/kg腹腔注射)仍保持其降压活性。为排除肾脏在PG合成中的作用,我们使用了肾外环氧化酶抑制剂(舒林酸)和双侧肾切除术。舒林酸(1.25mg/kg腹腔注射)和双侧肾切除术并未消除吲达帕胺的降压作用。这些结果表明PG的肾外作用以及可能位于血管壁的前列环素I2(PGI2)的作用,可能解释了吲达帕胺降压机制的一部分。