Barriviera M L, Hasson-Voloch A
Instituto de Biofísica Carlos Chagas Filho da Universidade Federal do Rio de Janeiro, Brasil.
Z Naturforsch C J Biosci. 1996 Nov-Dec;51(11-12):883-92. doi: 10.1515/znc-1996-11-1218.
The effect of denervation on the lipid metabolism and on the activity of (Na+ - K+)ATPase isoforms from the membrane fraction P3, which corresponds to the innervated electrocyte membrane, was evaluated. On a discontinuous sucrose gradient, normal P3 membranes exhibit a bimodal ("a" and "b bands) distribution of the (Na+ - K+)ATPase activity, which upon denervation changes to an unimodal ("c" band) distribution. Using these fractions, which have a higher (Na+ - K+)ATPase activity, we characterized the lipids at the hydrophobic protein surface boundary, (i.e., the bulk lipids that surround the protein). The results confirm that these lipids consist of phospholipids and cholesterol. The quantitative composition of the phospholipids is similar for both isoform fractions obtained from the discontinuous gradient of normal membranes, with phosphatidylcholine, phosphatidylethanolamine and phosphatidylserine representing about 90% of the total phospholipids. Sphingomyelin, phosphatidylinositol, diphosphatidylglycerol and phosphatidic acid were in the minority. However, in the single band obtained after denervation, the three major phospholipid components decreased to 70% of the total, and a significant increase in the other phospholipids and in cholesterol was observed. The high cholesterol content of the denervated fraction may confer membrane stabilization, as it is likely to cause a decrease in the membrane fluidity and consequently in the enzyme activity.
评估了去神经支配对脂质代谢以及来自膜组分P3(对应于受神经支配的电细胞的膜)的(Na + - K +)ATP酶同工型活性的影响。在不连续蔗糖梯度上,正常的P3膜呈现出(Na + - K +)ATP酶活性的双峰(“a”和“b”带)分布,而去神经支配后则变为单峰(“c”带)分布。利用这些具有较高(Na + - K +)ATP酶活性的组分,我们对疏水蛋白表面边界处的脂质(即围绕蛋白的大量脂质)进行了表征。结果证实这些脂质由磷脂和胆固醇组成。从正常膜的不连续梯度获得的两种同工型组分的磷脂定量组成相似,磷脂酰胆碱、磷脂酰乙醇胺和磷脂酰丝氨酸约占总磷脂的90%。鞘磷脂、磷脂酰肌醇、二磷脂酰甘油和磷脂酸占少数。然而,去神经支配后获得的单带中,三种主要磷脂成分降至总磷脂的70%,并且观察到其他磷脂和胆固醇显著增加。去神经支配组分中高胆固醇含量可能赋予膜稳定性,因为它可能导致膜流动性降低,进而导致酶活性降低。