Erin A N, Gorbunov N V, Brusovanik V I, Tyurin V A, Prilipko L L
Brain Res. 1986 Nov 19;398(1):85-90. doi: 10.1016/0006-8993(86)91253-9.
Using fluorescent and ESR-spin probes, the effects of phospholipases A2, C and D on rat brain synaptosomal membranes were investigated. It was shown that the exposure of synaptosomal membranes to phospholipases A2, C and D results in their depolarization and an increase of the negative surface potential. In the case of phospholipases A2 and C, these changes are associated with a decrease of the microviscosity of the membrane lipid bilayer. alpha-Tocopherol stabilizes synaptosomal membranes against the damaging action of the phospholipases. This stabilization consists in the reconstitution of the transmembrane potential and an increase of microviscosity of the phospholipase-treated membranes. The stabilizing effect of alpha-tocopherol is due to the binding of phospholipid hydrolysis products, but not to the inhibition of phospholipases. The observed stabilization of synaptosomal membranes by alpha-tocopherol is regarded as a possible mechanism of biological action of vitamin E on biomembranes.
运用荧光和电子自旋共振(ESR)探针,研究了磷脂酶A2、C和D对大鼠脑突触体膜的影响。结果表明,突触体膜暴露于磷脂酶A2、C和D会导致其去极化以及表面负电位增加。在磷脂酶A2和C的作用下,这些变化与膜脂双层微黏度的降低有关。α-生育酚可稳定突触体膜,使其免受磷脂酶的破坏作用。这种稳定作用表现为跨膜电位的恢复以及磷脂酶处理过的膜微黏度的增加。α-生育酚的稳定作用归因于其对磷脂水解产物的结合,而非对磷脂酶的抑制。观察到的α-生育酚对突触体膜的稳定作用被认为是维生素E对生物膜发挥生物学作用的一种可能机制。