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4-氨基吡啶、咖啡因和奎宁对蟾蜍离体腹直肌作用的比较。

A comparison of the actions of 4-aminopyridine, caffeine and quinine on the toad isolated rectus abdominis muscle.

作者信息

Savage A O

机构信息

Department of Pharmacology and Therapeutics, College of Medicine, University of Ibadan, Nigeria.

出版信息

Comp Biochem Physiol C Comp Pharmacol Toxicol. 1989;92(1):27-33. doi: 10.1016/0742-8413(89)90197-7.

Abstract
  1. 4-Aminopyridine (4-AP)-induced contractures have been compared with those evoked by caffeine and quinine on the toad rectus abdominis muscle. 2. All three compounds produced slowly-developing sustained contractures. The time to half maximal contracture and relaxation was significantly longer for 4-AP than for caffeine or quinine. 3. Verapamil and manganese inhibited 4-AP, caffeine and quinine-induced contractures. 4. Ca2+-free-EGTA Ringer and procaine severely inhibited caffeine and quinine responses, but 4-AP contractures were relatively unaffected. 5. In depolarizing (100 mM K+) Ringer solution, caffeine and quinine responses were reduced to 6-9% of their controls. 4-AP responses were reduced by about 25%. 6. It is concluded that in the toad rectus muscle, 4-AP-induced contractures differ from those produced by caffeine and quinine, and appear to rely mainly on the release of intracellular located Ca2+, while caffeine and quinine are considered to act predominantly on plasma membrane sites.
摘要
  1. 已将4-氨基吡啶(4-AP)诱导的挛缩与咖啡因和奎宁在蟾蜍腹直肌上诱发的挛缩进行了比较。2. 这三种化合物均产生缓慢发展的持续性挛缩。4-AP达到最大挛缩和松弛一半的时间比咖啡因或奎宁明显更长。3. 维拉帕米和锰抑制4-AP、咖啡因和奎宁诱导的挛缩。4. 无钙-EGTA林格液和普鲁卡因严重抑制咖啡因和奎宁反应,但4-AP挛缩相对未受影响。5. 在去极化(100 mM钾离子)林格液中,咖啡因和奎宁反应降低至对照的6-9%。4-AP反应降低约25%。6. 得出结论,在蟾蜍肌肉中,4-AP诱导的挛缩与咖啡因和奎宁产生的挛缩不同,似乎主要依赖于细胞内Ca2+的释放,而咖啡因和奎宁被认为主要作用于质膜部位。

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