Mohanakumar K P, Mitra N, Ganguly D K
Division of Pharmacology and Experimental Therapeutics, Indian Institute of Chemical Biology, Calcutta.
Neurosci Lett. 1990 Nov 27;120(1):91-3. doi: 10.1016/0304-3940(90)90175-9.
Studies were performed to bring out a serotoninergic involvement in physostigmine tremor, hitherto known to be working via the cholinergic system. 5-Hydroxytryptamine (5-HT) was estimated fluorimetrically after isolation on Sephadex G-10 and acetylcholinesterase (AChE) was assayed spectrophotometrically. The dose-dependent tremor was quantified by a double-blind study. No correlation (r = 0.01) existed between tremor and AChE inhibition since the non-tremoring dose of physostigmine caused the same degree of enzyme inhibition. An increase of 5-HT was found to be correlated (r = 0.59) with the duration and intensity of tremor. Cholinergic antagonists atropine (2 and 5 mg/kg, i.p.), scopolamine (0.5, 1.0, 2.0 mg/kg, i.p.) and mecamylamine (1 mg/kg, i.p.) failed to block the tremor while the 5-HT antagonists methysergide (5 mg/kg, i.v.) and cyproheptadine (10 and 30 mg/kg, s.c.) could afford more than 60% protection. These results suggest a serotoninergic rather than a cholinergic component in the genesis of physostigmine tremor.
进行了多项研究,以揭示血清素能系统在毒扁豆碱震颤中的作用,此前已知毒扁豆碱震颤是通过胆碱能系统起作用的。在通过葡聚糖凝胶G - 10分离后,采用荧光法测定5 - 羟色胺(5 - HT),并通过分光光度法测定乙酰胆碱酯酶(AChE)。通过双盲研究对剂量依赖性震颤进行了量化。震颤与AChE抑制之间不存在相关性(r = 0.01),因为毒扁豆碱的非震颤剂量引起的酶抑制程度相同。发现5 - HT的增加与震颤的持续时间和强度相关(r = 0.59)。胆碱能拮抗剂阿托品(2和5 mg/kg,腹腔注射)、东莨菪碱(0.5、1.0、2.0 mg/kg,腹腔注射)和美加明(1 mg/kg,腹腔注射)未能阻断震颤,而5 - HT拮抗剂甲基麦角新碱(5 mg/kg,静脉注射)和赛庚啶(10和30 mg/kg,皮下注射)可提供超过60%的保护。这些结果表明,在毒扁豆碱震颤的发生过程中,血清素能成分而非胆碱能成分起作用。