Lucot J B, Crampton G H
J Pharmacol Exp Ther. 1986 May;237(2):450-5.
The possible role of the alpha-2 adrenoceptors in xylazine-induced vomiting and in motion sickness was investigated. Cats were divided into two groups according to motion sickness susceptibility and were observed after s.c. injections of xylazine. The incidence of vomiting increased with the dose, and at each dose, the high susceptibility group had a greater emetic incidence than the low susceptibility group. In another experiment with cats divided into two groups according to motion sickness susceptibility, s.c. administration of yohimbine effectively antagonized the xylazine-induced emesis in both susceptibility groups. The cats in the latter experiment were then challenged with a motion sickness stimulus, after s.c. pretreatment with yohimbine. Yohimbine failed to prevent motion sickness but did occasion an unexplained variability in the incidence of vomiting. These findings suggest that the emetic effect of xylazine results from stimulation of alpha-2 adrenoceptors but that these receptors are not fundamental to feline motion sickness. The fact that susceptibilities to xylazine-induced emesis and to motion sickness are correlated suggests a point of interaction other than the area postrema, which is known to be essential for xylazine-induced vomiting but not for motion sickness in the cat.
研究了α-2肾上腺素能受体在赛拉嗪诱发呕吐及晕动病中可能发挥的作用。根据晕动病易感性将猫分为两组,并在皮下注射赛拉嗪后进行观察。呕吐发生率随剂量增加而升高,且在每个剂量下,高易感性组的催吐发生率均高于低易感性组。在另一项根据晕动病易感性将猫分为两组的实验中,皮下注射育亨宾可有效拮抗两个易感性组中赛拉嗪诱发的呕吐。在后者实验中,给猫皮下注射育亨宾预处理后,再给予晕动病刺激。育亨宾未能预防晕动病,但确实导致呕吐发生率出现了无法解释的变化。这些发现表明,赛拉嗪的催吐作用源于α-2肾上腺素能受体的刺激,但这些受体对猫的晕动病并非至关重要。赛拉嗪诱发呕吐的易感性与晕动病易感性相关,这一事实表明存在一个除最后区之外的相互作用点,已知最后区对赛拉嗪诱发的呕吐至关重要,但对猫的晕动病并非如此。