Landriscina C, Petragallo V, Morini P, Marcotrigiano G O
Laboratory of Biochemistry, Faculty of Veterinary Medicine, University of Bari, Italy.
Biochem Int. 1988 Aug;17(2):385-93.
The effect of hyper- and hypothyroidism on lipid peroxidation has been studied in rat liver microsomes under three different experimental conditions. Under none of these conditions was the formation of TBA-reactive substances affected by either of these two pathological states. On the contrary, with NADPH as the only peroxidation inducer, hydroperoxide concentration increased some three fold in microsomes from hyperthyroid rats, while a small decrease was measured in those from hypothyroid animals. Similarly, the activity of NADPH-cytochrome P-450 reductase was found to be 45.1% higher in hyperthyroid and 40.3% lower in hypothyroid microsomes. The possibility discussed here is that two distinct peroxidative mechanisms (of which one, NADPH-cytochrome P-450 reductase-dependent, is influenced by the thyroid hormone) can compete with each other for the substrate polyunsaturated fatty acids.
在三种不同实验条件下,研究了甲状腺功能亢进和减退对大鼠肝微粒体脂质过氧化的影响。在这些条件下,这两种病理状态均未影响TBA反应性物质的形成。相反,以NADPH作为唯一的过氧化诱导剂时,甲状腺功能亢进大鼠微粒体中的氢过氧化物浓度增加了约三倍,而甲状腺功能减退动物的微粒体中则有少量下降。同样,发现NADPH-细胞色素P-450还原酶的活性在甲状腺功能亢进的微粒体中高45.1%,在甲状腺功能减退的微粒体中低40.3%。这里讨论的可能性是,两种不同的过氧化机制(其中一种依赖NADPH-细胞色素P-450还原酶,受甲状腺激素影响)可能会相互竞争底物多不饱和脂肪酸。