Khandoudi N, Guo A C, Chesnais M, Feuvray D
Laboratoire de Physiologie Cellulaire, URA CNRS 1121, Université Paris-XI, Orsay, France.
Cardiovasc Res. 1993 Mar;27(3):447-52. doi: 10.1093/cvr/27.3.447.
The aim was to examine contractile properties of skinned cardiac fibres from rats with streptozotocin induced diabetes and to compare the effects of two agents, caffeine and 2,3-butanedione monoxime (BDM), on myocardial contractile characteristics of normal and diabetic cardiac fibres.
Small fibre bundles dissected from papillary muscles of the left ventricle were chemically skinned by exposure to Triton X-100. The tension-pCa (pCa = -log10 [Ca2+]) relationships were determined under isometric conditions.
In skinned fibres from diabetic rats maximum Ca2+ activated force was unchanged in comparison with normal rats, but a significant, though small, increase in the Ca2+ sensitivity [pCa for one half maximal activation (pCa50)] of contraction was shown. Caffeine (5-20 mM) increased Ca2+ sensitivity in a dose dependent manner and to the same extent in the two groups of preparations. Up to 10 mM caffeine, maximum force was not affected. On the other hand, BDM (2 and 5 mM) decreased Ca2+ sensitivity in both normal and diabetic fibres, but the rightward shift of the tension-pCa relationship induced by BDM was more pronounced in diabetic than in normal fibres: pCa50 was 5.55(SEM 0.02), 5.51(0.01), and 5.46(0.01) in normal fibres, and 5.62(0.01), 5.51(0.02), and 5.45(0.02) in diabetic fibres for 0, 2, and 5 mM BDM, respectively. Maximum tension was similarly decreased by BDM in the two groups of fibres.
(1) No change is induced by diabetes in the site of action of caffeine; (2) some drugs that affect myofilament Ca2+ sensitivity, such as BDM, may act differently in diabetic and control myocardium.
研究链脲佐菌素诱导的糖尿病大鼠的去表皮心肌纤维的收缩特性,并比较咖啡因和2,3-丁二酮一肟(BDM)这两种药物对正常和糖尿病心肌纤维心肌收缩特性的影响。
从左心室乳头肌中分离出小纤维束,通过暴露于 Triton X-100进行化学去表皮处理。在等长条件下测定张力-pCa(pCa = -log10 [Ca2+])关系。
与正常大鼠相比,糖尿病大鼠的去表皮纤维中最大Ca2+激活力没有变化,但收缩的Ca2+敏感性[半数最大激活的pCa(pCa50)]有显著(尽管很小)增加。咖啡因(5 - 20 mM)以剂量依赖方式增加Ca2+敏感性,且在两组制剂中增加程度相同。高达10 mM咖啡因时,最大力不受影响。另一方面,BDM(2和5 mM)降低了正常和糖尿病纤维中的Ca2+敏感性,但BDM引起的张力-pCa关系的右移在糖尿病纤维中比在正常纤维中更明显:对于0、2和5 mM BDM,正常纤维中的pCa50分别为5.55(标准误0.02)、5.51(0.01)和5.46(0.01),糖尿病纤维中分别为5.62(0.01)、5.51(0.02)和5.45(0.02)。两组纤维中BDM均同样降低了最大张力。
(1)糖尿病对咖啡因的作用位点无影响;(2)一些影响肌丝Ca2+敏感性的药物,如BDM,在糖尿病和对照心肌中的作用可能不同。