Barth Z, Strauss J D, Heyder S, Van Eyk J, Wiesner R J, Rüegg J C
Department of Physiology II, University of Heidelberg, Germany.
Pflugers Arch. 1995 Jun;430(2):220-9. doi: 10.1007/BF00374653.
Skinned fibres from porcine ventricles exhibited a higher Ca2+ sensitivity (pCa50, i.e. -log10 Ca2+ concentration required for half-maximal activation, for force generation) than atrial fibres. The thiadiazinone derivative EMD 53998 increased Ca2+ sensitivity and Ca2+ efficacy in both preparations. The drug effect depended on the isoform of troponin (Tn). Using the vanadate method TnI and TnC could be partly extracted and replaced by foreign tropin or by the TnI subunit of added foreign troponins. We investigated the relationship between pCa and force development before and after replacement of TnI with foreign troponin (bovine ventricular troponin, cTn, or rabbit skeletal muscle troponin, sTn) in the presence and absence of EMD 53998. Substitution with bovine cTn increased Ca2+ sensitivity to a value characteristic of bovine ventricular skinned fibres (pCa50 = 5.4) and was further increased by EMD 53998. Substitution with sTn also increased Ca2+ sensitivity, but subsequent addition of EMD 53998 caused little further increase in Ca2+ sensitivity. Following extraction of TnI with vanadate, skinned fibres contracted in a Ca(2+)-independent manner and failed to relax at a pCa of 8. Relaxation could be induced, however, by bovine ventricular TnI and rabbit skeletal muscle recombinant TnI. This relaxation could be reversed by EMD 53998 (100 microM). The Ca(2+)-independent force of contracted fibres could also be depressed by a TnI inhibitory peptide, (cTnI 137-148) and, in addition, this effect was antagonized by EMD 53998.(ABSTRACT TRUNCATED AT 250 WORDS)
猪心室的去表皮纤维比心房纤维表现出更高的Ca2+敏感性(pCa50,即产生最大激活力一半时所需的-log10 Ca2+浓度)。噻二嗪酮衍生物EMD 53998在两种制剂中均增加了Ca2+敏感性和Ca2+效能。药物作用取决于肌钙蛋白(Tn)的同工型。使用钒酸盐法,TnI和TnC可部分被提取,并用外源肌钙蛋白或添加的外源肌钙蛋白的TnI亚基替代。我们研究了在有和没有EMD 53998的情况下,用外源肌钙蛋白(牛心室肌钙蛋白,cTn,或兔骨骼肌肌钙蛋白,sTn)替代TnI前后pCa与力发展之间的关系。用牛cTn替代可将Ca2+敏感性提高到牛心室去表皮纤维的特征值(pCa50 = 5.4),并且EMD 53998可进一步提高。用sTn替代也增加了Ca2+敏感性,但随后添加EMD 53998对Ca2+敏感性几乎没有进一步增加。用钒酸盐提取TnI后,去表皮纤维以Ca(2+)非依赖性方式收缩,并且在pCa为8时不能松弛。然而,牛心室TnI和兔骨骼肌重组TnI可诱导松弛。这种松弛可被EMD 53998(100 microM)逆转。收缩纤维的Ca(2+)非依赖性力也可被TnI抑制肽(cTnI 137 - 148)抑制,此外,这种作用被EMD 53998拮抗。(摘要截断于250字)