Ben-Zvi Z, Hurwitz A
Eur J Pharmacol. 1987 Jun 4;137(2-3):191-6. doi: 10.1016/0014-2999(87)90222-6.
The effects of alpha 2-adrenoceptor agonists on sulfobromophthalein (BSP) disposition in mice were studied. It was found that agents with both central and peripheral activities (clonidine, guanabenz, B-HT 920 and methyldopa) as well as peripherally acting alpha 2-adrenoceptor agonists (para amino-clonidine and St 91) inhibited sulfobromophthalein disposition in the mouse, and also caused substantial hypothermia. The effects of these agonists were inhibited by yohimbine, a specific alpha 2-antagonist, except for those of para amino-clonidine where only partial reversal was achieved. The effects of clonidine on BSP disposition were also reversed by piperoxan but not by the alpha 1-adrenoceptor antagonists, prazosin and phenoxybenzamine, nor by the beta-blocker, propranolol. These results suggest that, in mice, peripheral alpha 2-adrenoceptors are involved in the effects of the alpha-agonists on BSP disposition.
研究了α2-肾上腺素能受体激动剂对小鼠磺溴酞钠(BSP)代谢的影响。发现具有中枢和外周活性的药物(可乐定、胍那苄、B-HT 920和甲基多巴)以及外周作用的α2-肾上腺素能受体激动剂(对氨基可乐定和St 91)均抑制小鼠的磺溴酞钠代谢,且还引起明显体温过低。除对氨基可乐定仅部分被逆转外,这些激动剂的作用均被特异性α2-拮抗剂育亨宾抑制。可乐定对BSP代谢的作用也被哌罗克生逆转,但未被α1-肾上腺素能受体拮抗剂哌唑嗪和酚苄明逆转,也未被β-阻滞剂普萘洛尔逆转。这些结果表明,在小鼠中,外周α2-肾上腺素能受体参与α-激动剂对BSP代谢的作用。