Ekinci Akdemir Fazile Nur, Yildirim Serkan, Kandemir Fatih Mehmet, Küçükler Sefa, Eraslan Ersen, Güler Mustafa Can
Department of Nutrition and Dietetics, Faculty of Health Science, Ağrı İbrahim Çeçen University, Ağrı, Turkey.
Department of Pathology, Faculty of Veterinary, Atatürk University, Erzurum, Turkey.
Basic Clin Pharmacol Toxicol. 2025 Jan;136(1):e14121. doi: 10.1111/bcpt.14121.
Drug-induced organ toxicity is a significant health concern, with gentamicin known for its effective antibacterial properties but also severe side effects, particularly cytotoxicity in liver and kidney tissues. This current study observed the preventive role of baicalein and bergenin against hepatic and renal injuries caused by gentamicin in rats.
Thirty-two male Sprague Dawley rats were divided into four groups, namely, control, gentamicin (gentamicin 80 mg/kg/day), baicalein (gentamicin 80 mg/kg/day + baicalein 100 mg/kg/day) and bergenin (gentamicin 80 mg/kg/day + bergenin 100 mg/kg/day). Hepatotoxicity and nephrotoxicity were induced by giving gentamicin (80 mg/kg/day). We evaluated the biochemical markers, including alkaline phosphatase (ALP), urea, alanine transaminase (ALT), creatinine and aspartate transaminase (AST) levels, antioxidant enzymes, oxidative stress parameters and histopathological and immunohistochemical changes.
Gentamicin increased oxidative stress parameters and decreased antioxidant activity. The treatment with baicalein and bergenin significantly restored these markers.
Baicalein and bergenin significantly mitigated gentamicin-induced hepatic and renal toxicity by restoring biochemical markers, reducing oxidative stress and enhancing antioxidant enzyme activity. Histopathological and immunohistochemical analyses confirmed the protective effects of both compounds against organ damage. No statistically significant differences were observed between the two drugs for these parameters. These results suggest their potential as therapeutic agents to prevent gentamicin-induced organ toxicity.
药物性器官毒性是一个重大的健康问题,庆大霉素以其有效的抗菌特性而闻名,但也有严重的副作用,特别是对肝脏和肾脏组织的细胞毒性。本研究观察了黄芩苷和岩白菜素对庆大霉素所致大鼠肝、肾损伤的预防作用。
将32只雄性Sprague Dawley大鼠分为四组,即对照组、庆大霉素组(庆大霉素80mg/kg/天)、黄芩苷组(庆大霉素80mg/kg/天 + 黄芩苷100mg/kg/天)和岩白菜素组(庆大霉素80mg/kg/天 + 岩白菜素100mg/kg/天)。通过给予庆大霉素(80mg/kg/天)诱导肝毒性和肾毒性。我们评估了生化指标,包括碱性磷酸酶(ALP)、尿素、丙氨酸转氨酶(ALT)、肌酐和天冬氨酸转氨酶(AST)水平、抗氧化酶、氧化应激参数以及组织病理学和免疫组织化学变化。
庆大霉素增加了氧化应激参数并降低了抗氧化活性。黄芩苷和岩白菜素治疗显著恢复了这些指标。
黄芩苷和岩白菜素通过恢复生化指标、降低氧化应激和增强抗氧化酶活性,显著减轻了庆大霉素诱导的肝毒性和肾毒性。组织病理学和免疫组织化学分析证实了这两种化合物对器官损伤的保护作用。在这些参数上,两种药物之间未观察到统计学上的显著差异。这些结果表明它们作为预防庆大霉素诱导的器官毒性的治疗剂具有潜力。