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睾酮通过上调雄性小鼠肝脏中雄激素受体和半胱氨酸亚磺酸脱羧酶的表达来增强牛磺酸的合成。

Testosterone enhances taurine synthesis by upregulating androgen receptor and cysteine sulfinic acid decarboxylase expressions in male mouse liver.

作者信息

Zhang Di, Fan Jingjing, Liu Hui, Qiu Guobin, Cui Sheng

机构信息

College of Veterinary Medicine, Yangzhou University, Yangzhou, People's Republic of China.

Jiangsu Co-innovation Center for Prevention and Control of Important Animal Infectious Diseases and Zoonoses, Yangzhou University, Yangzhou, People's Republic of China.

出版信息

Am J Physiol Gastrointest Liver Physiol. 2023 Apr 1;324(4):G295-G304. doi: 10.1152/ajpgi.00076.2022. Epub 2023 Feb 7.

Abstract

Taurine is an end-product of cysteine metabolism, whereas cysteine dioxygenase (CDO) and cysteine sulfinate decarboxylase (CSAD) are key enzymes regulating taurine synthesis. Sex steroids, including estrogens and androgens, are associated with liver physiopathological processes; however, we still do not know whether taurine and sex steroids interact in regulating liver physiology and hepatic diseases, and whether there are sex differences, although our recent study shows that the estrogen is involved in regulating taurine synthesis in mouse liver. The present study was thus proposed to identify whether 17-β-estradiol and testosterone (T) play their roles by regulating CDO and CSAD expression and taurine synthesis in male mouse liver. Our results demonstrated that testosterone did not have a significant influence on CDO expression but significantly enhanced CSAD, androgen receptor (AR) expressions, and taurine levels in mouse liver, cultured hepatocytes, and HepG2 cells, whereas these effects were abrogated by AR antagonist flutamide. Furthermore, our results showed that testosterone increased CSAD-promoter-luciferase activity through the direct interaction of the AR DNA binding domain with the CSAD promoter. These findings first demonstrate that testosterone acts as an important factor to regulate sulfur amino acid metabolism and taurine synthesis through AR/CSAD signaling pathway. In addition, the in vivo and in vitro experiments showed that 17-β-estradiol has no significant effects on liver CSAD expression and taurine synthesis in male mice and suggest that the effects of sex steroids on the taurine synthesis in mouse liver have sex differences. These results are crucial for understanding the physiological functions of taurine/androgen and their interacting mechanisms in the liver. This study demonstrates that testosterone functions to enhance taurine synthesis by interacting with androgen receptor and binding to cysteine sulfinate decarboxylase () promoter zone. Whereas estrogen has no significant effects either on liver CSAD expression or taurine synthesis in male mice and suggests that the effects of sex steroids on taurine synthesis in the liver have gender differences. These new findings are the potential for establishing effective protective and therapeutic strategies for liver diseases.

摘要

牛磺酸是半胱氨酸代谢的终产物,而半胱氨酸双加氧酶(CDO)和半胱氨酸亚磺酸脱羧酶(CSAD)是调节牛磺酸合成的关键酶。包括雌激素和雄激素在内的性类固醇与肝脏生理病理过程相关;然而,尽管我们最近的研究表明雌激素参与调节小鼠肝脏中的牛磺酸合成,但我们仍然不知道牛磺酸和性类固醇在调节肝脏生理和肝脏疾病方面是否相互作用,以及是否存在性别差异。因此,本研究旨在确定17-β-雌二醇和睾酮(T)是否通过调节雄性小鼠肝脏中CDO和CSAD的表达以及牛磺酸合成来发挥作用。我们的结果表明,睾酮对小鼠肝脏、培养的肝细胞和HepG2细胞中的CDO表达没有显著影响,但显著增强了CSAD、雄激素受体(AR)的表达以及牛磺酸水平,而这些作用被AR拮抗剂氟他胺消除。此外,我们的结果表明,睾酮通过AR DNA结合结构域与CSAD启动子的直接相互作用增加了CSAD启动子-荧光素酶活性。这些发现首次证明,睾酮是通过AR/CSAD信号通路调节含硫氨基酸代谢和牛磺酸合成的重要因素。此外,体内和体外实验表明,17-β-雌二醇对雄性小鼠肝脏CSAD表达和牛磺酸合成没有显著影响,这表明性类固醇对小鼠肝脏中牛磺酸合成的影响存在性别差异。这些结果对于理解牛磺酸/雄激素的生理功能及其在肝脏中的相互作用机制至关重要。本研究表明,睾酮通过与雄激素受体相互作用并结合半胱氨酸亚磺酸脱羧酶()启动子区域来增强牛磺酸合成。而雌激素对雄性小鼠肝脏CSAD表达或牛磺酸合成均无显著影响,这表明性类固醇对肝脏中牛磺酸合成的影响存在性别差异。这些新发现为建立有效的肝脏疾病保护和治疗策略提供了潜力。

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