Buntai Medical and Diagnostic Laboratories, Osogbo, Nigeria; Reproductive Biology and Toxicology Research Laboratories, Oasis of Grace Hospital, Osogbo, Osun State, Nigeria.
Reproductive Biology and Toxicology Research Laboratories, Oasis of Grace Hospital, Osogbo, Osun State, Nigeria; Department of Morbid Anatomy, Obafemi Awolowo University Teaching Hospital Complex (OAUTHC), Ile-Ife, Osun State, Nigeria.
Biomed Pharmacother. 2021 May;137:111309. doi: 10.1016/j.biopha.2021.111309. Epub 2021 Jan 30.
Anti-Koch and HAART have been shown to independently induce toxicity to the liver and kidney, albeit available data are few and inconsistent. The present study evaluates the impact of Anti-Koch and HAART, when administered singly and in combination, on hepatic and renal status, and the possible role of adenine deaminase (ADA)/xanthine oxidase (XO) pathway. Anti-Koch and HAART administration were observed to independently impair hepatic and renal functions, diminish glutathione content, and substantially increase lipid peroxidation (MDA) and nitrogen reactive specie (NO). Coherently, these drugs caused significant accumulation of polymorphonuclear leucocytes, up-regulated ADA/XO signaling, increased uric acid production, and enhanced DNA fragmentation in the liver and kidney. Anti-Koch treatment did not significantly alter hepatic and renal levels of nitric oxide nor induce DNA fragmentation in the kidney. Co-administration of anti-Koch and HAART aggravated the observed biochemical alterations. Findings from the histopathological studies of the liver and renal tissues were in agreement with observed biochemical alterations. In conclusion, this report is the first to reveal that anti-Koch and HAART, when administered singly or in combination, attenuate glutathione content and elevate uric acid production in the liver and kidney via upregulation of ADA/XO signaling with resultant oxidative and nitrosative stress, and increased DNA fragmentation.
抗-Koch 和高效抗逆转录病毒治疗(HAART)已被证明可独立诱导肝和肾毒性,尽管可用数据很少且不一致。本研究评估了抗-Koch 和 HAART 单独和联合使用对肝肾功能的影响,以及腺嘌呤脱氨酶(ADA)/黄嘌呤氧化酶(XO)途径的可能作用。抗-Koch 和 HAART 的给药被观察到独立地损害肝和肾功能,降低谷胱甘肽含量,并显著增加脂质过氧化(MDA)和氮反应性物质(NO)。一致地,这些药物导致多形核白细胞大量积累,上调 ADA/XO 信号,增加尿酸生成,并增强肝和肾中的 DNA 片段化。抗-Koch 治疗并未显著改变肝和肾中的一氧化氮水平,也未在肾中诱导 DNA 片段化。抗-Koch 和 HAART 的联合给药加重了观察到的生化变化。肝和肾组织的组织病理学研究结果与观察到的生化变化一致。总之,本报告首次揭示,抗-Koch 和 HAART 单独或联合使用时,通过上调 ADA/XO 信号导致氧化和硝化应激以及 DNA 片段化增加,从而降低肝和肾中的谷胱甘肽含量并升高尿酸生成。