Nucleoside and Nucleotide Reverse Transcriptase Inhibitors Induce Aging by Inhibiting Telomerase Function

Shweta Singh, B. Sharma, N. J. Siddiqi
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Abstract

The telomeres existing at the end of the eukaryotic chromosome, play an important role in localization, pairing of homologous chromosomes during cell division and synapsis formation, while telomerase is involved in maintenance of the telomere length. The application of antiHIV-1 molecules particularly NRTIs have been shown to interfere with telomerase function thereby inducing aging processes. Since the application of these molecules has already indicated production of oxidative stress and toxicity in AIDS patients, their adverse impact on telomerase function may further worsen the situation. In addition, the negative influence of antiHIV-1 regimens on certain host factors involved in telomerase function may enhance aging. HAART changes the landscape of the disease by progressively decreasing the progression of HIV-1, but exerts prolonged adverse effects on the telomerase function. Though there is no exact information available on this issue, intensive efforts are needed to explore regulation of telomerase expression in HIV infected individuals and particularly those receiving antiretrovirals. DOI : 10.14302/issn.2324-7339.jcrhap-19-3070 Corresponding author: Bechan Sharma, Department of Biochemistry, University of Allahabad, Allahabad-211002, Uttar Pradesh, India, Cell:+91-9415715639, Email: bechansharma@gmail.com
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核苷和核苷酸逆转录酶抑制剂通过抑制端粒酶功能诱导衰老
端粒存在于真核生物染色体末端,在细胞分裂和突触形成过程中对同源染色体的定位、配对起重要作用,而端粒酶则参与端粒长度的维持。抗hiv -1分子特别是nrti的应用已被证明会干扰端粒酶的功能,从而诱导衰老过程。由于这些分子的应用已经表明了在艾滋病患者中产生氧化应激和毒性,它们对端粒酶功能的不利影响可能会进一步恶化这种情况。此外,抗hiv -1方案对参与端粒酶功能的某些宿主因子的负面影响可能会加速衰老。HAART通过逐步减少HIV-1的进展改变了疾病的格局,但对端粒酶功能产生了长期的不良影响。虽然在这个问题上没有确切的信息,但需要加紧努力探索艾滋病毒感染者,特别是接受抗逆转录病毒治疗的人的端粒酶表达的调节。DOI: 10.14302/issn.2324-7339。通讯作者:Bechan Sharma,印度阿拉哈巴德大学生物化学系,印度北方邦阿拉哈巴德211002,Cell:+91-9415715639, Email: bechansharma@gmail.com
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