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Gunn大鼠中的药物结合作用:尿苷二磷酸葡萄糖醛酸基转移酶和尿苷二磷酸葡萄糖基转移酶活性降低,甘氨酸-N-酰基转移酶活性增加。

Drug conjugation in Gunn rats: reduced UDP-glucuronosyl transferase and UDP-glucosyl transferase activities with increased glycine-N-acyltransferase activity.

作者信息

Marniemi J, Vainio H, Parkki M

出版信息

Pharmacology. 1975;13(6):492-501. doi: 10.1159/000136943.

Abstract

Glucuronyl, glucosyl, glutathione, glycine conjugations and epoxide hydration were studied in livers of Wistar and Gunn rats. The activities of bilirubin UDP-glucuronosyl transferase and UDP-glucosyl transferase were reduced in microsomes of homozygous and heterozygous Gunn rats compared to Wistar rats (over 90 and 55-65%, respectively). Conjugation of 4-methylumbelliferone by UDP-glucuronosyl transferase was also reduced (30-35%) in Gunn rats. Treatment of microsomes in vitro with membrane perturbating agents increased the measurable activities but did not change the activity relationships between Wistar and Gunn rats. Microsomal epoxide hydrase and soluble glutathione-S-epoxide transferase activities occurred in Gunn rats at the Wistar level, but mitochondrial glycine-N-acyltransferase activity was elevated in homozygous and heterozygous Gunn rats (66 and 47%, respectively). The reciprocal velocity plots of UDP-glucuronosyl transferase activity were similarly concave in Gunn and Wistar rats.

摘要

对Wistar大鼠和Gunn大鼠的肝脏进行了葡萄糖醛酸基、葡萄糖基、谷胱甘肽、甘氨酸结合反应以及环氧化物水化作用的研究。与Wistar大鼠相比,纯合子和杂合子Gunn大鼠微粒体中胆红素UDP - 葡萄糖醛酸基转移酶和UDP - 葡萄糖基转移酶的活性降低(分别超过90%和55 - 65%)。Gunn大鼠中UDP - 葡萄糖醛酸基转移酶对4 - 甲基伞形酮的结合反应也降低了(30 - 35%)。用膜扰动剂体外处理微粒体可提高可测量的活性,但并未改变Wistar大鼠和Gunn大鼠之间的活性关系。Gunn大鼠微粒体环氧化物水解酶和可溶性谷胱甘肽 - S - 环氧化物转移酶的活性与Wistar大鼠相当,但纯合子和杂合子Gunn大鼠的线粒体甘氨酸 - N - 酰基转移酶活性升高(分别为66%和47%)。Gunn大鼠和Wistar大鼠中UDP - 葡萄糖醛酸基转移酶活性的倒数速度图同样呈凹形。

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