Lin Y H, Xu J H
Department of Pharmacology, Faculty of Pharmaceutical Sciences, Zhejiang Medical University, Hangzhou, China.
Zhongguo Yao Li Xue Bao. 1994 May;15(3):249-52.
4-Aminopyridine (4-AP) 1 mg.kg-1 sc at the scruff induced a licking response in mice. H1 receptor blockaders, such as diphenhydramine HCl (1, 10 mg.kg-1, sc at the scruff or 40 mg.kg-1, i.p.), chlorphenamine maleate (20 mg.kg-1, i.p.), and astemizole (2 mg.kg-1, i.g.), inhibited the licking response caused by 4-AP. Repeated injections of 4-AP (1 mg.kg-1) reduced the times of lick and the histamine content in the skin of injected site. 4-AP also promoted histamine release from incubated mouse peritoneal mast cells (PMC) in a dose-dependent manner. The results indicate that the licking response may originate from the histamine liberation of mast cells.
在小鼠颈部皮下注射1毫克/千克的4-氨基吡啶(4-AP)会引发舔舐反应。H1受体阻滞剂,如盐酸苯海拉明(1、10毫克/千克,颈部皮下注射或40毫克/千克,腹腔注射)、马来酸氯苯那敏(20毫克/千克,腹腔注射)和阿司咪唑(2毫克/千克,灌胃),可抑制由4-AP引起的舔舐反应。重复注射4-AP(1毫克/千克)可减少舔舐次数以及注射部位皮肤中的组胺含量。4-AP还以剂量依赖性方式促进培养的小鼠腹腔肥大细胞(PMC)释放组胺。结果表明,舔舐反应可能源于肥大细胞释放组胺。