Rittenhouse P A, Bakkum E A, Van de Kar L D
Department of Pharmacology, Stritch School of Medicine, Loyola University-Chicago.
J Pharmacol Exp Ther. 1991 Oct;259(1):58-65.
DOI [(+/-)-1-(2,5-dimethoxy-4-iodophenyl)-2-aminopropane HCI] is a serotonin (5-HT1C/5-HT2) agonist, with potent cardiovascular effects. The purpose of the present studies was to determine the identity and location of the 5-HT receptor subtype(s) mediating the renin and blood pressure responses to DOI. Injection (i.p.) of DOI to conscious male rats elevated plasma renin activity in a dose-dependent manner. The 5-HT1C/5-HT2 antagonist ritanserin completely blocked the DOI-induced increase in plasma renin activity. In order to distinguish the 5-HT2- from the 5-HT1C- mediated effect of DOI, spiperone was administered before DOI. Low doses of spiperone (0.01 and 0.1 mg/kg, s.c.) significantly reduced the renin response to DOI. Because spiperone has a higher affinity for 5-HT2 than 5-HT1C receptors, these data suggest that DOI stimulates renin secretion through 5-HT2 receptors. To separate central from peripheral 5-HT receptors, we injected DOI into rats pretreated with saline or xylamidine, a 5-HT2 antagonist which does not cross the blood-brain barrier. Xylamidine produced a shift to the right and suppression of the maximal effect of DOI on plasma renin activity, suggesting a role for peripheral 5-HT2 receptors in the effect of DOI. On the other hand, i.c.v. administration of DOI, using doses lower than the peripherally effective doses, caused a significant elevation of plasma renin activity at 200 micrograms/kg. These experiments suggest that DOI's elevation of plasma renin activity has both peripheral and central sites of action.(ABSTRACT TRUNCATED AT 250 WORDS)
DOI[(±)-1-(2,5-二甲氧基-4-碘苯基)-2-氨基丙烷盐酸盐]是一种血清素(5-HT1C/5-HT2)激动剂,具有强大的心血管效应。本研究的目的是确定介导肾素和血压对DOI反应的5-HT受体亚型的身份和位置。向清醒的雄性大鼠腹腔注射DOI可使血浆肾素活性呈剂量依赖性升高。5-HT1C/5-HT2拮抗剂利坦色林完全阻断了DOI诱导的血浆肾素活性升高。为了区分DOI由5-HT2介导的效应和由5-HT1C介导的效应,在注射DOI之前给予了螺哌隆。低剂量的螺哌隆(0.01和0.1毫克/千克,皮下注射)显著降低了对DOI的肾素反应。由于螺哌隆对5-HT2受体的亲和力高于对5-HT1C受体的亲和力,这些数据表明DOI通过5-HT2受体刺激肾素分泌。为了区分中枢和外周5-HT受体,我们将DOI注射到用生理盐水或赛拉米定预处理的大鼠体内,赛拉米定是一种不能穿过血脑屏障的5-HT2拮抗剂。赛拉米定使DOI对血浆肾素活性的最大效应向右偏移并受到抑制,表明外周5-HT2受体在DOI的效应中起作用。另一方面,以低于外周有效剂量的剂量脑室内注射DOI,在剂量为200微克/千克时可使血浆肾素活性显著升高。这些实验表明,DOI使血浆肾素活性升高具有外周和中枢作用部位。(摘要截短于250字)