Genotoxic of co-codamol for human lymphocyte culture in vitro.

Sada Jasim Abdulameer, Anfal Izaldeen Alkateeb, Layth Ammar Chyad Al-Shammari
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Abstract

Co-codamol, a combination analgesic containing paracetamol and codeine phosphate, is widely used for pain relief, but its potential genotoxic effects on human lymphocytes remain largely unknown. This in vitro study investigates the genotoxic potential of co-codamol on cultured human lymphocytes by assessing cell viability, mitotic index (MI), chromosomal aberration frequency, and micronucleus (MN) formation. Lymphocytes were exposed to varying concentrations of co-codamol (0.02-0.12 mg/mL), and cytotoxicity was determined using the MTT assay. Results showed that co-codamol significantly reduced cell viability in a dose-dependent manner, with complete cell death at 0.12 mg/mL. The mitotic index was significantly decreased at higher concentrations, and a statistically significant increase in chromosomal aberrations and micronucleus formation was observed in treated lymphocytes compared to the control group (p < 0.05). These findings provide important evidence that co-codamol exhibits genotoxic potential in vitro, suggesting a potential risk of DNA damage associated with its use. Further in vivo investigations are warranted to assess the clinical relevance of these genotoxic effects and to elucidate the underlying mechanisms of toxicity.

co-codamol对人淋巴细胞体外培养的遗传毒性。
cocodamol是一种含有扑热息痛和磷酸可待因的复合镇痛药,广泛用于缓解疼痛,但其对人类淋巴细胞的潜在遗传毒性作用仍不清楚。本体外研究通过评估细胞活力、有丝分裂指数(MI)、染色体畸变频率和微核(MN)的形成,探讨了co-codamol对培养的人淋巴细胞的遗传毒性潜力。淋巴细胞暴露于不同浓度的co-codamol (0.02-0.12 mg/mL)中,使用MTT法测定细胞毒性。结果表明,co-codamol显著降低细胞活力,呈剂量依赖性,在0.12 mg/mL时细胞完全死亡。高浓度处理淋巴细胞有丝分裂指数显著降低,处理淋巴细胞染色体畸变和微核形成与对照组相比有统计学意义(p < 0.05)。这些发现提供了重要的证据,表明co-codamol在体外具有潜在的基因毒性,表明其使用可能导致DNA损伤。进一步的体内研究是必要的,以评估这些基因毒性作用的临床相关性,并阐明潜在的毒性机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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