Tsuchida Hisatoshi, Ohizumi Yasushi
Department of Pharmaceutical Molecular Biology, Graduate School of Pharmaceutical Sciences, Tohoku University, Aoba, Aramaki, Aoba-ku, Sendai 980-8578, Japan.
Eur J Pharmacol. 2003 Sep 5;477(1):53-8. doi: 10.1016/j.ejphar.2003.08.002.
The effects of (+)-nantenine on various pressor responses, recently reported exerting competitive antagonistic activity at the alpha1-adrenoceptor/5-hydroxytryptamine (5-HT)2A receptor, were examined in vivo. (+)-Nantenine (0.03-3 mg/kg) caused a dose-dependent inhibition of the pressor response to phenylephrine (alpha1-adrenoceptor agonist) or 5-HT (5-HT receptor agonist) in both anesthetized and pithed rats. The pressor response to UK 14304 (5-Bromo-N-[2-imidazolin-2-yl]-6-quinoxalinamine) (an alpha2-adrenoceptor agonist) was inhibited by (+)-nantenine (0.003-3 mg/kg) in pithed rats in a dose-dependent manner without affecting the angiotensin II-induced pressor response in anesthetized rats. The pressor response to sympathetic nerve stimulation was also inhibited by (+)-nantenine (0.3-3 mg/kg) in a dose-dependent manner. (+)-Nantenine (3 mg/kg) facilitated the norepinephrine release induced by sympathetic nerve stimulation in pithed rats. In the guinea pig vas deferens, the initial component of contractions induced by electrical field stimulation was enhanced by (+)-nantenine (1-30 microM) in a concentration-dependent manner, while the later component was inhibited by it. These data suggest that (+)-nantenine has antagonistic activities on alpha1-adrenoceptors, alpha2-adrenoceptors and 5-HT2A receptors in pithed rats.
最近有报道称(+)-南天竹碱对各种升压反应有影响,可在α1-肾上腺素能受体/5-羟色胺(5-HT)2A受体上发挥竞争性拮抗活性,本文对其进行了体内实验研究。在麻醉和脊髓横断大鼠中,(+)-南天竹碱(0.03 - 3毫克/千克)对去氧肾上腺素(α1-肾上腺素能受体激动剂)或5-羟色胺(5-HT受体激动剂)引起的升压反应产生剂量依赖性抑制。在脊髓横断大鼠中,(+)-南天竹碱(0.003 - 3毫克/千克)对UK 14304(5-溴-N-[2-咪唑啉-2-基]-6-喹喔啉胺)(一种α2-肾上腺素能受体激动剂)引起的升压反应产生剂量依赖性抑制,且不影响麻醉大鼠中血管紧张素II诱导的升压反应。(+)-南天竹碱(0.3 - 3毫克/千克)对交感神经刺激引起的升压反应也产生剂量依赖性抑制。在脊髓横断大鼠中,(+)-南天竹碱(3毫克/千克)促进了交感神经刺激诱导的去甲肾上腺素释放。在豚鼠输精管中,电场刺激诱导的收缩初始成分被(+)-南天竹碱(1 - 30微摩尔)浓度依赖性增强,而后期成分则被其抑制。这些数据表明,(+)-南天竹碱对脊髓横断大鼠的α1-肾上腺素能受体、α2-肾上腺素能受体和5-HT2A受体具有拮抗活性。