Goldstein D J, Kulakowski E C, Ropchak T G, Brown P, Keiser H R
Life Sci. 1987 Sep 14;41(11):1369-73. doi: 10.1016/0024-3205(87)90611-4.
CGP 6085 A, a specific 5-hydroxytryptamine (5-HT), serotonin uptake inhibitor, is also a potent hypotensive agent. Its depressor effect in the spontaneously hypertensive (SH) rats correlates well with its ability to inhibit serotonin uptake. Here we report that the effects of CGP 6085 A on arterial blood pressure were greatly reduced in rats pretreated with p-chlorophenylalanine (pCl-Phe), a specific depletor of serotonin. Moreover, in rats pretreated with the serotonin antagonist, methysergide, CGP 6085 A did not produce significant hypotension. We also found that centrally administered naloxone reverses the hypotensive effect of CGP 6085 A. These results provide further evidence for the existence of an important serotonin-opioid interaction in the mechanisms of arterial blood regulation in the rat.
CGP 6085 A是一种特异性的5-羟色胺(5-HT),即血清素摄取抑制剂,也是一种强效降压剂。它对自发性高血压(SH)大鼠的降压作用与其抑制血清素摄取的能力密切相关。在此我们报告,在用对氯苯丙氨酸(pCl-Phe,一种血清素特异性耗竭剂)预处理的大鼠中,CGP 6085 A对动脉血压的影响大大降低。此外,在用血清素拮抗剂美西麦角预处理的大鼠中,CGP 6085 A不会产生显著的低血压。我们还发现,中枢给予纳洛酮可逆转CGP 6085 A的降压作用。这些结果为大鼠动脉血压调节机制中存在重要的血清素-阿片样物质相互作用提供了进一步的证据。