Stress Induced Cortisol Release Depresses The Secretion of Testosterone in Patients With Type 2 Diabetes Mellitus.

IF 2.7 Q3 ENDOCRINOLOGY & METABOLISM Clinical Medicine Insights-Endocrinology and Diabetes Pub Date : 2023-01-03 eCollection Date: 2023-01-01 DOI:10.1177/11795514221145841
Safir Ullah Khan, Saba Jannat, Hadia Shaukat, Shiza Unab, Tanzeela, Maleeha Akram, Muhammad Nasir Khan Khattak, Monica Vizcara Soto, Muhammad Fiaz Khan, Amir Ali, Syed Shakeel Raza Rizvi
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Abstract

Background: Both hormonal and genetic data reveal that the stress hormone cortisol and its regulating genes may affect the level of testosterone in humans. It is uncertain whether type 2 diabetes mellitus would manifest similarly. Furthermore, a genetic strategy to screen out the stress system genes that may contribute to testosterone decline in humans is less understood.

Objectives: In this study, we aimed to elucidate the link between stress and testosterone levels, both hormonally and genetically.

Method: This study comprised 37 individuals with type 2 diabetes mellitus and 50 healthy individuals. For the analysis of hormones and the targeted genes, we used the RIA system and bioinformatics expertise.

Results: The patients had significantly elevated cortisol and lower testosterone readings, according to data from hormonal analyses. The bioinformatics approach reveals that SHBG was intracellularly suppressed by 2 defined stress system genes: FKB5 and CYP17. TCF4/TCF8, ATRX, and AR in skeletal muscle were inversely related to stress system genes. Furthermore, all testosterone regulated genes were positively linked with SHBG in the current study. A strong relationship between GNAS and PKA with CYP17 and FKBP5 reveals that the Gαs-cAMP/PKA signaling pathway may be one of the regulatory pathways through which the suppression of testosterone system genes happens. In conclusion, this study demonstrated that beyond stress, the key stress system genes might affect cortisol levels, which in turn affect testosterone figures via the Gαs-cAMP/PKA signaling pathway.

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压力诱导的皮质醇释放会抑制 2 型糖尿病患者睾酮的分泌
背景:荷尔蒙和遗传学数据显示,压力荷尔蒙皮质醇及其调节基因可能会影响人体睾酮的水平。目前还不确定 2 型糖尿病是否会有类似的表现。此外,筛选出可能导致人类睾酮下降的应激系统基因的遗传策略还不太清楚:在这项研究中,我们旨在从激素和基因两方面阐明压力与睾酮水平之间的联系:方法:这项研究包括 37 名 2 型糖尿病患者和 50 名健康人。在分析激素和目标基因时,我们使用了 RIA 系统和生物信息学专业知识:结果:根据激素分析的数据,患者的皮质醇明显升高,睾酮读数降低。生物信息学方法显示,SHBG 在细胞内受到 2 个确定的应激系统基因的抑制:FKB5和CYP17。骨骼肌中的 TCF4/TCF8、ATRX 和 AR 与应激系统基因成反比。此外,在本研究中,所有睾酮调控基因都与 SHBG 呈正相关。GNAS和PKA与CYP17和FKBP5之间的密切关系表明,Gαs-cAMP/PKA信号通路可能是抑制睾酮系统基因的调控途径之一。总之,这项研究表明,在应激之外,关键的应激系统基因可能会影响皮质醇水平,而皮质醇水平又会通过Gαs-cAMP/PKA信号通路影响睾酮含量。
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来源期刊
CiteScore
4.30
自引率
0.00%
发文量
15
审稿时长
8 weeks
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