Huang Y, He Z H, Li Y X
Laboratory of Cardiovascular Physiology, Hunan Medical University, Changsha, China.
Zhongguo Yao Li Xue Bao. 1997 May;18(3):234-7.
To explore the possible mechanisms underlying the positive inotropic effect of MCI-154.
Skinned fibers with disrupted or preserved sarcoplasmic reticulum (SR) were prepared by saponin 500 or 50 mg.L-1. The tension-pCa relationship and pCa50 of saponin (500 mg.L-1)-skinned fibers were taken as the indices of Ca2+ sensitivity of contractile proteins. The amplitude of caffeine-induced contracture was an index of Ca2+ release from SR in saponin (50 mg.L-1)-skinned fibers.
MCI-154 directly enhances the Ca2+ sensitivity of contractile protein but has little effect on Ca2+ release from SR in rat skinned cardiac fibers.
探讨MCI-154正性肌力作用的可能机制。
用500或50mg·L-1皂角苷制备肌浆网(SR)破坏或保留的去皮肤纤维。以皂角苷(500mg·L-1)去皮肤纤维的张力-pCa关系和pCa50作为收缩蛋白Ca2+敏感性指标。咖啡因诱导的挛缩幅度是皂角苷(50mg·L-1)去皮肤纤维中SR释放Ca2+的指标。
1)MCI-154(0.1mmol·L-1)对收缩蛋白有Ca2+增敏作用。与对照值5.54(5.30-5.79)相比,pCa50增加到5.84(5.54-6.14)(P<0.01,n=8)。Hill系数n降低0.29(P<0.01,n=8);2)在SR保留的制剂中,MCI-154未产生挛缩。MCI-154处理前后咖啡因诱导的挛缩无变化(P>0.05,n=4)。
MCI-154直接增强收缩蛋白的Ca2+敏感性,但对大鼠去皮肤心脏纤维中SR释放Ca2+的影响较小。