Langer G A
Basic Res Cardiol. 1985;80 Suppl 2:31-3.
Studies which focus on calcium (Ca) at the cellular surface indicate: Ca in the vascular and interstitial spaces is in rapid equilibrium with that bound within the sarcolemmal-glycocalyx complex of the cell. At [Ca]o of 1.0-1.5 mM 80-85% of this Ca is bound to phospholipid of the sarcolemmal bilayer and amounts to 500-700 mumoles/kg wet wt. tissue. Phospholipids of net anionic charge (phosphatidylserine, phosphatidylinositol) or zwitterionic structure (phosphatidylethanolamine) are likely to play a predominant role in the binding. Augmentation of net anionic charge (formation of phosphatidate by phospholipase D, addition of dodecylsulfate) of the sarcolemma augments Ca binding and is positively inotropic. Conversely, insertion of a cationic amphiphile (Polymyxin B, dodecyltrimethylamine) displaces Ca and is negatively inotropic. Augmentation of anionic Ca binding sites induces a significant increase of Na-Ca exchange in sarcolemmal vesicles which may contribute to the associated positive inotropy found in the intact myocardium.
聚焦于细胞表面钙(Ca)的研究表明:血管和间质空间中的Ca与结合在细胞肌膜-糖萼复合物内的Ca处于快速平衡状态。在细胞外钙浓度([Ca]o)为1.0 - 1.5 mM时,这种Ca的80 - 85%与肌膜双层的磷脂结合,相当于500 - 700微摩尔/千克湿重组织。带净负电荷的磷脂(磷脂酰丝氨酸、磷脂酰肌醇)或两性离子结构的磷脂(磷脂酰乙醇胺)可能在结合中起主要作用。肌膜净负电荷的增加(通过磷脂酶D形成磷脂酸、添加十二烷基硫酸盐)会增强Ca的结合,并具有正性肌力作用。相反,插入阳离子两亲物(多粘菌素B、十二烷基三甲基胺)会取代Ca,并具有负性肌力作用。阴离子Ca结合位点的增加会导致肌膜囊泡中钠-钙交换显著增加,这可能有助于在完整心肌中发现的相关正性肌力作用。