Nasu T
Department of Veterinary Pharmacology, Faculty of Agriculture, Yamaguchi University, Japan.
Experientia. 1995 Feb 15;51(2):113-6. doi: 10.1007/BF01929351.
Zn2+ in low concentrations (0.005-0.1 mM) inhibited the transient contractions in response to caffeine (25 mM) in a dose-dependent manner in smooth muscle of intact guinea-pig taenia caeci. At Zn2+ concentrations higher than 0.1 mM, caffeine did not elicit any response. After saponin-treatment of the fibres, which leaves the Ca2+ storage sites intact, caffeine contraction was completely inhibited by Zn2+ at a relatively low concentration (0.003 mM). However, in Triton-X-100-treated fibres, in which the Ca2+ release sites are destroyed, the contraction could be induced in the presence of Zn2+ by an increase in Ca2+. In conclusion, Zn2+ can block the intracellular Ca2+ release from caffeine-sensitive release sites in taenia caeci.
低浓度(0.005 - 0.1 mM)的Zn2+以剂量依赖的方式抑制了完整豚鼠盲肠带平滑肌对咖啡因(25 mM)的瞬时收缩。当Zn2+浓度高于0.1 mM时,咖啡因未引发任何反应。在用皂苷处理纤维后,Ca2+储存位点保持完整,较低浓度(0.003 mM)的Zn2+就能完全抑制咖啡因收缩。然而,在经Triton - X - 100处理的纤维中,Ca2+释放位点被破坏,增加Ca2+时在Zn2+存在的情况下仍可诱导收缩。总之,Zn2+可阻断盲肠带中对咖啡因敏感的释放位点的细胞内Ca2+释放。