Kentish J C
Department of Pharmacology, United Medical School, St. Thomas' Hospital, London, U.K.
Pflugers Arch. 1991 Oct;419(3-4):310-8. doi: 10.1007/BF00371112.
Possible interactions between the effects of pH and phosphate (Pi) on the maximum force development of cardiac myofibrils were investigated in rat skinned trabeculae in solutions of different pH (7.4-6.2) and [Pi] (where [] denote concentration). At pH 7.0 there was an inverse linear relationship between force and log [Pi] over the [Pi] range 0.2-20 mM; its slope (-0.46/decade) was twice that found previously for skeletal muscle [21]. Acidosis depressed force substantially, but the relative change of force was unaffected by Pi addition (0, 5, 20 mM); there was no evidence for the synergism between acidosis and Pi that would be expected if some of the inhibition by acidosis was due to protonation of Pi to the putative inhibitory form, H2PO4-. It was taken into account that even without Pi addition, there was enough Pi inside the muscle from various sources to produce significant changes in [H2PO4-] as the pH was varied. The results suggest that H+ and Pi inhibit maximum force development of cardiac myofibrils independently, by different mechanisms. From this it is argued that H+ and Pi may be released at different steps in the crossbridges cycle. In the myocardium Pi and H+ probably exert tonic inhibitory influences on cardiac myofibrils under all conditions.
在不同pH值(7.4 - 6.2)和磷酸盐(Pi)浓度([]表示浓度)的溶液中,对大鼠去表皮小梁心肌肌原纤维最大力发展过程中pH值和Pi效应之间可能的相互作用进行了研究。在pH 7.0时,在0.2 - 20 mM的Pi浓度范围内,力与log [Pi]之间呈反线性关系;其斜率(-0.46/十倍)是先前在骨骼肌中发现的斜率的两倍[21]。酸中毒显著降低了力,但力的相对变化不受添加Pi(0、5、20 mM)的影响;没有证据表明酸中毒和Pi之间存在协同作用,而如果酸中毒的某些抑制作用是由于Pi质子化形成假定的抑制形式H2PO4-,则预期会有这种协同作用。考虑到即使不添加Pi,随着pH值的变化,肌肉内部来自各种来源的Pi也足以使[H2PO4-]产生显著变化。结果表明,H+和Pi通过不同机制独立抑制心肌肌原纤维的最大力发展。由此认为,H+和Pi可能在横桥循环的不同步骤释放。在心肌中,Pi和H+可能在所有条件下对心肌肌原纤维施加张力抑制作用。