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成年大鼠甲状腺功能减退对脑膜流动性、脂质含量及组成的影响。

Effect of hypothyroidism induced in adult rats on brain membrane fluidity and lipid content and composition.

作者信息

Tacconi M T, Cizza G, Fumagalli G, Sarzi Sartori P, Salmona M

机构信息

Istituto di Ricerche Farmacologiche Mario Negri, Milano, Italy.

出版信息

Res Commun Chem Pathol Pharmacol. 1991 Jan;71(1):85-103.

PMID:2024067
Abstract

This study was designed to establish whether fluidity and lipid composition of brain membranes were affected by hypothyroidism, in the hope of clarifying the mechanism through which thyroid hormone deficiency might influence nerve cell functions. Rats were made hypothyroid by injections of PTU (dissolved in 0.005 M NaOH, 50 mg/kg, ip, daily for 28 days). Membrane fluidity, cholesterol (chol) and phospholipids (PL) content, and PL and their fatty acid composition were measured in plasma, erythrocyte plasma membranes, liver microsomes and brain subcellular fractions. P2 pellets from brains of hypothyroid animals were less fluid than those of euthyroid ones; subcellular fractionation showed that mitochondrial membranes were responsible for the rigidity observed. Similar changes were found in erythrocyte "ghosts". The reduced fluidity seemed to be related more to alterations in the ratios between phosphatidylcholine, sphingomyelin and phosphatidylethanolamine, than to those of chol/PL, protein/PL or fatty acid unsaturation index. The well known alteration in hypothyroidism-induced desaturase activity, which in peripheral tissue leads to a reduction of 20:4n-6 and to an increase in its precursors (18:2n-6 and 20:3n-6), is barely detectable in brain membranes. Only in phosphatidylcholine of synaptosomes and myelin did slight changes in percentages of the n-6 family fatty acids result in a significant alteration of 20:4n-6/20:3n-6 ratios.

摘要

本研究旨在确定甲状腺功能减退是否会影响脑膜的流动性和脂质组成,以期阐明甲状腺激素缺乏可能影响神经细胞功能的机制。通过注射丙硫氧嘧啶(PTU,溶于0.005 M氢氧化钠,50 mg/kg,腹腔注射,每日一次,共28天)使大鼠甲状腺功能减退。测定了血浆、红细胞质膜、肝微粒体和脑亚细胞组分中的膜流动性、胆固醇(chol)和磷脂(PL)含量,以及PL及其脂肪酸组成。甲状腺功能减退动物脑的P2沉淀比甲状腺功能正常动物的流动性更低;亚细胞分级分离表明,线粒体膜是观察到的刚性的原因。在红细胞“血影”中也发现了类似的变化。流动性降低似乎更多地与磷脂酰胆碱、鞘磷脂和磷脂酰乙醇胺之间比例的改变有关,而不是与chol/PL、蛋白质/PL或脂肪酸不饱和指数的改变有关。甲状腺功能减退引起的去饱和酶活性的众所周知的改变,在外周组织中导致20:4n-6减少及其前体(18:2n-6和20:3n-6)增加,在脑膜中几乎检测不到。仅在突触体和髓磷脂的磷脂酰胆碱中,n-6家族脂肪酸百分比的轻微变化导致20:4n-6/20:3n-6比例的显著改变。

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