Uncovering the Therapeutic Potential of Phosphocreatine in Diabetic Retinopathy: Mitigating Mitochondrial Dysfunction and Apoptosis via JAK2/STAT3 Signaling Pathway

IF 2.8 4区 医学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY Journal of Molecular Neuroscience Pub Date : 2024-01-17 DOI:10.1007/s12031-023-02175-2
Eskandar Qaed, Eman Alyafeai, Ahmed Al-Maamari, Mohamed Y. Zaky, Marwan Almoiliqy, Bandar Al-Hamyari, Abdullah Qaid, Saeed Yafei, Waleed Aldahmash, Mueataz A. Mahyoub, Fuhan Wang, Le Kang, Zeyao Tang, Jianbin Zhang
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Abstract

Diabetic retinopathy (DR) stands as a prevalent complication of diabetes mellitus, causing damage to the delicate retinal capillaries and potentially leading to visual impairment. While the exact underlying cause of DR remains elusive, compelling research suggests that mitochondrial energy deficiency and the excessive generation of reactive oxygen species (ROS) play pivotal roles in its pathogenesis. Recognizing that controlling hyperglycemia alone fails to reverse the defects in retinal mitochondria induced by diabetes, current strategies seek to restore mitochondrial function as a means of safeguarding against DR. To address this pressing issue, a comprehensive study was undertaken to explore the potential of phosphocreatine (PCr) in bolstering mitochondrial bioenergetics and providing protection against DR via modulation of the JAK2/STAT3 signaling pathway. Employing rat mitochondria and RGC-5 cells, the investigation meticulously assessed the impact of PCr on ROS production, mitochondrial membrane potential, as well as the expression of crucial apoptotic and JAK2/STAT3 signaling pathway proteins, utilizing cutting-edge techniques such as high-resolution respirometry and western blotting. The remarkable outcomes revealed that PCr exerts a profound protective influence against DR by enhancing mitochondrial function and alleviating diabetes-associated symptoms and biochemical markers. Notably, PCr administration resulted in an upregulation of antiapoptotic proteins, concomitant with a downregulation of proapoptotic proteins and the JAK2/STAT3 signaling pathway. These significant findings firmly establish PCr as a potential therapeutic avenue for combating diabetic retinopathy. By augmenting mitochondrial function and exerting antiapoptotic effects via the JAK2/STAT3 signaling pathway, PCr demonstrates promising efficacy both in vivo and in vitro, particularly in counteracting the oxidative stress engendered by hyperglycemia. In summary, our study sheds light on the potential of PCr as an innovative therapeutic strategy for diabetic retinopathy. By bolstering mitochondrial function and exerting protective effects via the modulation of the JAK2/STAT3 signaling pathway, PCr holds immense promise in ameliorating the impact of DR in the face of oxidative stress induced by hyperglycemia.

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揭示磷酸肌酸在糖尿病视网膜病变中的治疗潜力:通过 JAK2/STAT3 信号通路缓解线粒体功能障碍和细胞凋亡
糖尿病视网膜病变(DR)是糖尿病的一种常见并发症,会对脆弱的视网膜毛细血管造成损害,并可能导致视力损伤。虽然糖尿病视网膜病变的确切病因仍然难以捉摸,但令人信服的研究表明,线粒体能量缺乏和活性氧(ROS)的过度生成在其发病机制中起着关键作用。由于认识到仅控制高血糖无法逆转糖尿病诱导的视网膜线粒体缺陷,目前的策略寻求恢复线粒体功能作为预防 DR 的一种手段。为了解决这个紧迫的问题,我们开展了一项综合研究,探索磷酸肌酸(PCr)通过调节 JAK2/STAT3 信号通路增强线粒体生物能并提供抗 DR 保护的潜力。这项研究利用大鼠线粒体和 RGC-5 细胞,采用高分辨率呼吸测定法和 Western 印迹法等尖端技术,细致评估了 PCr 对 ROS 生成、线粒体膜电位以及关键凋亡蛋白和 JAK2/STAT3 信号通路蛋白表达的影响。研究结果表明,PCr 能增强线粒体功能,减轻糖尿病相关症状和生化指标,从而对 DR 产生深远的保护作用。值得注意的是,服用 PCr 可上调抗凋亡蛋白,同时下调促凋亡蛋白和 JAK2/STAT3 信号通路。这些重要发现坚定地确立了 PCr 作为防治糖尿病视网膜病变的潜在治疗途径的地位。通过增强线粒体功能并通过 JAK2/STAT3 信号通路发挥抗凋亡作用,PCr 在体内和体外都表现出了良好的疗效,尤其是在对抗高血糖引起的氧化应激方面。总之,我们的研究揭示了 PCr 作为糖尿病视网膜病变创新治疗策略的潜力。PCr 可增强线粒体功能,并通过调节 JAK2/STAT3 信号通路发挥保护作用,因此在面对高血糖诱导的氧化应激时,PCr 在改善 DR 的影响方面大有可为。
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来源期刊
Journal of Molecular Neuroscience
Journal of Molecular Neuroscience 医学-神经科学
CiteScore
6.60
自引率
3.20%
发文量
142
审稿时长
1 months
期刊介绍: The Journal of Molecular Neuroscience is committed to the rapid publication of original findings that increase our understanding of the molecular structure, function, and development of the nervous system. The criteria for acceptance of manuscripts will be scientific excellence, originality, and relevance to the field of molecular neuroscience. Manuscripts with clinical relevance are especially encouraged since the journal seeks to provide a means for accelerating the progression of basic research findings toward clinical utilization. All experiments described in the Journal of Molecular Neuroscience that involve the use of animal or human subjects must have been approved by the appropriate institutional review committee and conform to accepted ethical standards.
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