Chávez E, Moreno-Sánchez R, Zazueta C, Rodríguez J S, Bravo C, Reyes-Vivas H
Departamento de Bioquímica, Instituto Nacional de Cardiología, Ignacio Chávez, México, DF, México.
J Bioenerg Biomembr. 1997 Dec;29(6):571-7. doi: 10.1023/a:1022483018482.
The role of inorganic phosphate as inhibitor of mitochondrial membrane permeability transition was studied. It is shown that in mitochondria containing a high phosphate concentration, i.e., 68 nmo/mg, Ca2+ did not activate the pore opening. Conversely, at lower levels of matrix phosphate, i.e., 38 nmol/mg, Ca2+ was able to induce subsequent pore opening. The inhibitory effect of phosphate was apparent in sucrose-based media, but it was not achieved in KCI media. The matrix free Ca2+ concentration and matrix pH were lowered by phosphate, but they were always higher in K+-media. In the absence of ADP, phosphate strengthened the inhibitory effect of cyclosporin A on carboxyatractyloside-induced Ca2+ efflux. Acetate was unable to replace phosphate in the induction of the aforementioned effects. It is concluded that phosphate preserves selective membrane permeability by diminishing the matrix free Ca2+ concentration.
研究了无机磷酸盐作为线粒体膜通透性转换抑制剂的作用。结果表明,在磷酸盐浓度较高(即68 nmo/mg)的线粒体中,Ca2+不会激活孔道开放。相反,在基质磷酸盐水平较低(即38 nmol/mg)时,Ca2+能够诱导随后的孔道开放。磷酸盐的抑制作用在蔗糖基培养基中很明显,但在KCI培养基中则无法实现。磷酸盐降低了基质游离Ca2+浓度和基质pH,但在K+培养基中它们总是更高。在没有ADP的情况下,磷酸盐增强了环孢素A对羧基苍术苷诱导的Ca2+外流的抑制作用。乙酸盐在诱导上述效应时无法替代磷酸盐。结论是磷酸盐通过降低基质游离Ca2+浓度来维持选择性膜通透性。