Hikasa Y, Takase K, Ogasawara S
Department of Veterinary Surgery, School of Veterinary Medicine and Animal Sciences, Kitasato University, Aomori, Japan.
Am J Vet Res. 1989 Aug;50(8):1348-51.
Intramuscular injection of xylazine induced dose-dependent vomiting in cats (ED50 = 0.277 mg/kg); administration of standard dose of xylazine (2 mg/kg, 2 times the 100% emetic dose) induced vomiting in 100% of the cats studied. The xylazine-induced vomiting was antagonized by adrenoceptor antagonists possessing alpha 2-blocking activity, which were yohimbine, tolazoline, and phentolamine. Of these antagonists, yohimbine was the most effective; the maximal antagonistic effect was seen at 1 mg of yohimbine/kg, a dose at which the other drugs had little or no effect. At the doses studied, prazosin and phenoxybenzamine, adrenoceptor antagonists with alpha 1-blocking activity, did not prevent vomiting induced by xylazine. Beta-Adrenoceptor (propranolol), dopamine receptor (domperidone and chlorpromazine), a cholinoceptor (atropine), an opiate receptor (naloxone), and a histamine-receptor (diphenhydramine) antagonists, at the doses studied, did not prevent xylazine-induced vomiting. Pretreatment with 6-hydroxydopamine failed to prevent xylazine-induced vomiting. These results indicated that xylazine-induced vomiting in cats is mediated by alpha 2-adrenoceptors and suggested that the alpha 2-adrenoceptors mediating the vomiting attributable to xylazine may not be presynaptic alpha 2-receptors located on noradrenergic nerve terminals.
肌肉注射甲苯噻嗪可使猫出现剂量依赖性呕吐(半数有效剂量[ED50]=0.277毫克/千克);给予标准剂量的甲苯噻嗪(2毫克/千克,为100%催吐剂量的2倍)可使100%的受试猫发生呕吐。具有α2阻断活性的肾上腺素能受体拮抗剂,即育亨宾、妥拉唑啉和酚妥拉明,可拮抗甲苯噻嗪诱导的呕吐。在这些拮抗剂中,育亨宾最为有效;在1毫克/千克育亨宾时可观察到最大拮抗作用,此剂量下其他药物几乎没有或没有作用。在所研究的剂量下,具有α1阻断活性的肾上腺素能受体拮抗剂哌唑嗪和酚苄明不能预防甲苯噻嗪诱导的呕吐。在所研究的剂量下,β肾上腺素能受体拮抗剂(普萘洛尔)、多巴胺受体拮抗剂(多潘立酮和氯丙嗪)、胆碱能受体拮抗剂(阿托品)、阿片受体拮抗剂(纳洛酮)和组胺受体拮抗剂(苯海拉明)均不能预防甲苯噻嗪诱导的呕吐。用6-羟基多巴胺预处理不能预防甲苯噻嗪诱导的呕吐。这些结果表明,甲苯噻嗪诱导猫呕吐是由α2肾上腺素能受体介导的,提示介导甲苯噻嗪所致呕吐的α2肾上腺素能受体可能不是位于去甲肾上腺素能神经末梢的突触前α2受体。