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5,5'-二苯基乙内酰脲对甲状腺切除大鼠肝细胞溶质苹果酸酶和线粒体α-甘油磷酸脱氢酶活性的影响。

Effect of 5,5'-diphenylhydantoin on the activities of hepatic cytosol malic enzyme and mitochondrial alpha-glycerophosphate dehydrogenase in athyreotic rats.

作者信息

Mann D N, Kumara-Siri M H, Surks M I

出版信息

Endocrinology. 1983 May;112(5):1732-8. doi: 10.1210/endo-112-5-1732.

Abstract

Since 5,5'-diphenylhydantoin (DPH) decreases specific nuclear receptor binding of T3, the possibility that DPH might affect thyroid activity was examined by measurement of the activity of rat hepatic cytosol malic enzyme (ME) and mitochondrial alpha-glycerophosphate dehydrogenase (alpha-GPD) after DPH administration. Groups of athyreotic rats, prepared by thyroidectomy and 131I administration, were injected with vehicle (V), DPH, T3, or a combined dose of DPH and T3 for 48 h. The rats were then killed, and liver fractions were prepared for the measurement of ME and alpha-GPD activities. Compared with the V group, DPH treatment resulted in a significant increase in mean ME activity in four experiments; the mean ME activity for all studies was 2.2-fold greater than that of the V group (P less than 0.001). A significant increase in mean alpha-GPD activity was not observed in DPH-treated rats. T3 treatment resulted in a mean 31.5-fold increase in ME activity and a 10.9-fold increase in alpha-GPD activity. The magnitude of T3 induction of both enzymes was substantially attenuated by simultaneous injection of DPH, to 54-66% of the activity induced by T3 alone (P less than 0.001). Pair-feeding a T3-injected group and the DPH plus T3 group did not result in a decrease in the activity of either enzyme. Moreover, the observed changes did not appear to result from alterations in enzyme determinations or from significant changes in cytosol or mitochondrial protein concentration, cytosol T3, or plasma glucose. Although DPH-induced changes in the fractional rate of enzyme metabolism cannot be excluded, it is possible that changes in enzyme activities observed after DPH injection resulted from an interaction between DPH and the nuclear T3 receptor. If so, based on the effects observed in the present studies, DPH might be classified as a partial thyroid agonist.

摘要

由于5,5'-二苯基乙内酰脲(DPH)会降低T3与特异性核受体的结合,因此通过在给予DPH后测量大鼠肝细胞溶质苹果酸酶(ME)和线粒体α-甘油磷酸脱氢酶(α-GPD)的活性,来研究DPH是否可能影响甲状腺活性。通过甲状腺切除术和给予131I制备的无甲状腺大鼠组,分别注射赋形剂(V)、DPH、T3或DPH与T3的联合剂量,持续48小时。然后处死大鼠,制备肝脏组分以测量ME和α-GPD活性。与V组相比,在四项实验中,DPH处理导致平均ME活性显著增加;所有研究的平均ME活性比V组高2.2倍(P小于0.001)。在DPH处理的大鼠中未观察到平均α-GPD活性显著增加。T3处理导致ME活性平均增加31.5倍,α-GPD活性增加10.9倍。同时注射DPH可使T3对这两种酶的诱导幅度大幅降低,降至单独T3诱导活性的54 - 66%(P小于0.001)。对注射T3的组和DPH加T3组进行配对喂食,并未导致两种酶的活性降低。此外,观察到的变化似乎不是由酶测定的改变或细胞溶质或线粒体蛋白浓度、细胞溶质T3或血浆葡萄糖的显著变化引起的。虽然不能排除DPH诱导的酶代谢分数率变化,但DPH注射后观察到的酶活性变化可能是由于DPH与核T3受体之间的相互作用。如果是这样,根据本研究中观察到的效应,DPH可能被归类为部分甲状腺激动剂。

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