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丁基羟基茴香醚可有效抑制大鼠和人类的2型11β-羟基类固醇脱氢酶。

Butylated Hydroxyanisole Potently Inhibits Rat and Human 11β-Hydroxysteroid Dehydrogenase Type 2.

作者信息

Li Linxi, Wu Ying, Wu Xiaolong, Wang Huang, Bai Yanfang, Wang Xiudi, Akingbemi Benson T, Huang Ping, Ge Ren-Shan

机构信息

Center of Scientific Research, The Second Affiliated Hospital and Yuying Children's Hospital of Wenzhou Medical University, Wenzhou, Zhejiang, PR China.

出版信息

Pharmacology. 2016;97(1-2):10-7. doi: 10.1159/000441034. Epub 2015 Nov 14.

Abstract

Butylated hydroxyanisole (BHA) is a widely used antioxidant for food preservation. 11β-hydroxysteroid dehydrogenases, isoforms 1 (HSD11B1) and 2 (HSD11B2) have been demonstrated to be the regulators of the local level of active glucocorticoid, which has a broad range of physiological actions. In this study, the potency of BHA was tested for the inhibition of HSD11B1 and HSD11B2 in rat and human tissues. BHA showed potent inhibition of HSD11B2 with the half maximal inhibitory concentration calculated at 13.99 and 69.25 µmol/l for the rat and human, respectively. Results showed that BHA competitively inhibited HSD11B2 when a steroid substrate was used. However, it served as a mixed inhibition factor when the cofactor NAD+ was used. In contrast, the potency of BHA to inhibit both rat and human HSD11B1 was diminished, with the concentration of 100 μmol/l causing no inhibitory effect on the isoform. In conclusion, we observed that BHA is a selective inhibitor of HSD11B2, implying that this agent may cause excessive glucocorticoid action in local tissues such as kidney and placentas.

摘要

丁基羟基茴香醚(BHA)是一种广泛用于食品保鲜的抗氧化剂。11β-羟基类固醇脱氢酶同工型1(HSD11B1)和同工型2(HSD11B2)已被证明是局部活性糖皮质激素水平的调节因子,糖皮质激素具有广泛的生理作用。在本研究中,测试了BHA对大鼠和人体组织中HSD11B1和HSD11B2的抑制效力。BHA对HSD11B2表现出强效抑制作用,大鼠和人体的半数最大抑制浓度分别计算为13.99和69.25μmol/L。结果表明,当使用类固醇底物时,BHA竞争性抑制HSD11B2。然而,当使用辅因子NAD+时,它作为一种混合抑制因子。相比之下,BHA抑制大鼠和人体HSD11B1的效力减弱,100μmol/L的浓度对该同工型没有抑制作用。总之,我们观察到BHA是HSD11B2的选择性抑制剂,这意味着该药物可能在肾脏和胎盘等局部组织中导致糖皮质激素作用过度。

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