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马洛替酯对四氯化碳诱导的大鼠肝损伤及胶原蓄积的预防作用。

Preventive effect of malotilate on carbon tetrachloride-induced liver damage and collagen accumulation in the rat.

作者信息

Ala-Kokko L, Stenbäck F, Ryhänen L

机构信息

Collagen Research Unit, Biocenter, Oulu, Finland.

出版信息

Biochem J. 1987 Sep 1;246(2):503-9. doi: 10.1042/bj2460503.

Abstract

Malotilate is a new drug suggested for use in chronic liver diseases. It is shown here to prevent liver damage caused by CCl4. The concomitant administration of malotilate with CCl4 significantly decreased hydroxyproline accumulation in the liver, liver prolyl 4-hydroxylase and liver and serum galactosylhydroxylysyl glucosyltransferase activities. However, it had no effect on the daily urinary hydroxyproline excretion or the hydroxyproline content of the skin, liver or lungs in normal young growing rats. It also had no specific inhibitory effect on hydroxyproline synthesis or secretion in fibroblast cultures, and did not affect the amount of procollagen-alpha 1(I)-specific mRNAs in these cultures. Thus it seems to have no direct inhibitory effect on collagen metabolism. In addition to inhibition of liver collagen accumulation, malotilate was also able to prevent the development of morphological changes in the liver such as focal necrosis, fatty infiltration and inflammatory changes. It also normalized almost completely the standard liver-function tests. It is possible that malotilate may prevent excessive collagen deposition by inhibiting the inflammation caused by CCl4-induced liver damage.

摘要

马洛替酯是一种被建议用于治疗慢性肝病的新药。本文显示它能预防四氯化碳所致的肝损伤。马洛替酯与四氯化碳同时给药可显著降低肝脏中羟脯氨酸的蓄积、肝脏脯氨酰4-羟化酶以及肝脏和血清半乳糖基羟赖氨酰葡糖基转移酶的活性。然而,它对正常生长发育的幼鼠每日尿羟脯氨酸排泄量或皮肤、肝脏及肺的羟脯氨酸含量没有影响。它对成纤维细胞培养物中羟脯氨酸的合成或分泌也没有特异性抑制作用,并且不影响这些培养物中前胶原-α1(I)特异性mRNA的量。因此,它似乎对胶原代谢没有直接抑制作用。除了抑制肝脏胶原蓄积外,马洛替酯还能够预防肝脏形态学变化的发生,如局灶性坏死、脂肪浸润和炎症改变。它还几乎完全使标准肝功能检查恢复正常。马洛替酯有可能通过抑制四氯化碳诱导的肝损伤所引起的炎症来预防过多的胶原沉积。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a4d0/1148302/4c241cac549e/biochemj00248-0247-a.jpg

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