Bousquet P, Feldman J, Schwartz J
Life Sci. 1984 Jul 23;35(4):373-80. doi: 10.1016/0024-3205(84)90647-7.
Blood pressure was studied in pentobarbital anesthetized rats and cats after central administration of ouabain. Intracerebroventricular (i.c.v.) injections caused a classical biphasic effect, a short lasting hypotension followed by a hypertensive phase. When injected directly into the nucleus reticularis lateralis region (NRL), ouabain (0.01-2 micrograms/kg) caused a dose-dependent pressor effect. In the same region, kryptofix 221, a sodium complexing agent, produced a fall in blood pressure. Moreover, central administration of ouabain prevented the hypotensive effect of i.v. clonidine whereas the central hypotensive effect of muscimol was not affected. It is concluded that sodium movements play an important role in the blood pressure regulation within the NRL region. We also report here that ouabain antagonizes the hypotensive effect of clonidine suggesting that sodium movement might be the essential link of this action.
在戊巴比妥麻醉的大鼠和猫中,研究了中枢给予哇巴因后的血压情况。脑室内(i.c.v.)注射产生了典型的双相效应,先是短暂的低血压,随后是高血压阶段。当直接注射到外侧网状核区域(NRL)时,哇巴因(0.01 - 2微克/千克)产生剂量依赖性升压效应。在同一区域,钠络合剂环糊精221可使血压下降。此外,中枢给予哇巴因可阻止静脉注射可乐定的降压作用,而蝇蕈醇的中枢降压作用不受影响。得出的结论是,钠转运在NRL区域的血压调节中起重要作用。我们在此还报告,哇巴因拮抗可乐定的降压作用,提示钠转运可能是这一作用的关键环节。