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地塞米松介导的PGC-1α和内脂素下调调节小鼠睾丸中的睾酮合成和抗氧化系统。

Dexamethasone mediated downregulation of PGC-1α and visfatin regulates testosterone synthesis and antioxidant system in mouse testis.

作者信息

Annie Lalrawngbawli, Gurusubramanian Guruswami, Kumar Roy Vikas

机构信息

Department of Zoology, Mizoram University, Aizawl, Mizoram 796 004, India.

Department of Zoology, Mizoram University, Aizawl, Mizoram 796 004, India.

出版信息

Acta Histochem. 2019 Feb;121(2):182-188. doi: 10.1016/j.acthis.2018.12.004. Epub 2018 Dec 19.

Abstract

Dexamethasone, a synthetic glucocorticoid has been used as an immunosuppressive and anti-inflammatory and affects reproduction. It has been suggested that testicular steroidogenesis involves PGC-1α and visfatin as key regulators. Previous studies have shown that dexamethasone down-regulates PGC-1α and visfatin expression in muscle and mammary epithelial cells respectively. However, the effect of dexamethasone on testicular visfatin and PGC-1α expressions has not been investigated. The aims of the present study were to investigate the effect of dexamethasone, on the expression of PGC-1α, visfatin and antioxidant enzymes activities in mouse testis. The results of the present study showed that dexamethasone treatment significantly decreased the expression of visfatin and PGC-1α in mice testis, along with significant decreased in testicular antioxidant enzymes activates. Further, dexamethasone treatment also significantly increased the testicular lipid peroxidation and decreased testosterone synthesis. The dexamethasone induced changes in PGC-1α and visfatin in the testis were significantly correlated with changes in serum testosterone concentrations and antioxidant enzymes activities. Thus, dexamethasone induced testicular toxicity may involve the PGC-1α and visfatin as important molecules to exhibit its effects.

摘要

地塞米松,一种合成糖皮质激素,已被用作免疫抑制剂和抗炎剂,并影响生殖。有人提出,睾丸类固醇生成涉及PGC-1α和内脂素作为关键调节因子。先前的研究表明,地塞米松分别下调肌肉和乳腺上皮细胞中PGC-1α和内脂素的表达。然而,地塞米松对睾丸内脂素和PGC-1α表达的影响尚未得到研究。本研究的目的是研究地塞米松对小鼠睾丸中PGC-1α、内脂素表达和抗氧化酶活性的影响。本研究结果表明,地塞米松处理显著降低了小鼠睾丸中内脂素和PGC-1α的表达,同时睾丸抗氧化酶活性也显著降低。此外,地塞米松处理还显著增加了睾丸脂质过氧化并降低了睾酮合成。地塞米松诱导的睾丸中PGC-1α和内脂素的变化与血清睾酮浓度和抗氧化酶活性的变化显著相关。因此,地塞米松诱导的睾丸毒性可能涉及PGC-1α和内脂素作为重要分子来发挥其作用。

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