Chatterjee K, Banerjee S K, Tiwari R, Mazumdar K, Bhattacharyya A, Chatterjee G C
Int J Vitam Nutr Res. 1981;51(3):254-65.
The influence of extraneous supplementation of L-ascorbic acid in chronic chlordane toxicity has been studied in rats. Oral administration of chlordane brings about a marked growth retardative effect, stimulates vitamin C synthesis in the system, elevates the vitamin C status of the liver and kidney tissues and also the urinary excretion. It inhibits the activities of acid and alkaline phosphatases, SDH and Mg2+-ATPase of both hepatic and renal tissues. The activities of serum and mitochondrial GOT, serum alkaline phosphatase, and glucose-6-phosphatase of both hepatic and renal tissues are markedly stimulated. The normal histological patterns of both liver and kidney tissues are grossly altered under chlordane toxicity condition. There occurs marked increase in the hepatic lipid composition. Supplementation of L-ascorbic acid in high doses to the chlordane treated rats can effectively counteract some of these alterations in respect of enzyme activities, morphological characteristics and of hepatic lipid composition.
已经在大鼠中研究了额外补充L-抗坏血酸对慢性氯丹毒性的影响。口服氯丹会产生明显的生长迟缓作用,刺激体内维生素C的合成,提高肝脏和肾脏组织的维生素C水平以及尿液排泄量。它会抑制肝脏和肾脏组织中酸性和碱性磷酸酶、SDH和Mg2+-ATP酶的活性。血清和线粒体GOT的活性、血清碱性磷酸酶以及肝脏和肾脏组织中葡萄糖-6-磷酸酶的活性均受到明显刺激。在氯丹毒性条件下,肝脏和肾脏组织的正常组织学模式发生了严重改变。肝脏脂质成分显著增加。给经氯丹处理的大鼠高剂量补充L-抗坏血酸可以有效抵消这些在酶活性、形态特征和肝脏脂质成分方面的改变。