Val'dman A V, Medvedev O S, Rozhanskaia N I
Biull Eksp Biol Med. 1981 Nov;92(11):560-2.
Antagonism between cardiovascular effects of clonidin (10-30 micrograms/kg) and naloxon (0.15-1.0 mg/kg) was studied on anesthetized spontaneously hypertensive rats (SHR) as compared to Wistar Kyoto (WKY) rats and on awake cats. Naloxon was shown to completely block the clonidin hypotensive effect in SHR and cats and to partially block it in WKY rats. In some experiments, naloxon was administered after the blockade of peripheral M-cholinoreceptors by metacin (2 mg/kg). In these experiments naloxon evoked elevation of blood pressure, cardiac output and heart rate (in cats). It is concluded that the opioid link participates in the development of clonidin-evoked bradycardia and hypotension both in hypertensive and in normotensive animals.
研究了可乐定(10 - 30微克/千克)和纳洛酮(0.15 - 1.0毫克/千克)对麻醉的自发性高血压大鼠(SHR)、Wistar Kyoto(WKY)大鼠以及清醒猫心血管效应的拮抗作用。结果表明,纳洛酮可完全阻断SHR和猫体内可乐定的降压作用,而在WKY大鼠中则部分阻断该作用。在一些实验中,在通过美他环素(2毫克/千克)阻断外周M - 胆碱受体后给予纳洛酮。在这些实验中,纳洛酮引起血压、心输出量和心率升高(在猫中)。结论是,阿片类物质环节参与了高血压和正常血压动物中可乐定诱发的心动过缓和低血压的发生。