N-乙酰半胱氨酸预防达比加群引起的细胞毒性:体外研究

IF 0.7 4区 生物学 Q4 BIOLOGY
Özer Aylin, Gürpinar, Emre Kubat
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引用次数: 0

摘要

达比加群(Dabigatran,DBG)是一种口服直接凝血酶抑制剂,用于预防全身性栓塞和静脉血栓栓塞。达比加群的主要副作用是胃肠道不适。在本研究中,我们研究了 N-乙酰半胱氨酸(NAC)在体外环境中是否对达比加群诱导的细胞毒性有保护作用。在不含达比加群但含有 NAC 的培养基中检测 NAC 对细胞增殖和凋亡的影响。比较 DAB 和所有其他组,D 组的细胞存活率最低。然而,NAC I 组和 DBG-NAC I 组之间的差异无统计学意义,而与其他各组相比,差异有统计学意义。DBG 组的细胞形态变性,呈圆形,核凝缩。在其他稀释液中,细胞形态为健康的成纤维细胞形态。根据我们的研究结果,高浓度的 NAC 对 DBG 具有细胞保护作用,而中等或低浓度的 NAC 对细胞存活率没有有利影响。虽然在目前的研究中,同时使用适当剂量的 NAC 似乎能有效抑制达比加群的细胞毒性,但还需要进一步的实验和临床研究来证实我们的发现。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Prevention of dabigatran ınduced cytotoxicity by N-acetyl cysteine: An ın vitro study
Dabigatran (DBG) is an oral direct thrombin inhibitor used for prevention of systemic embolism and venous thromboembolism. The major side effect of DBG is gastrointestinal upset. In the present study, we have investigated whether N-acetyl cysteine (NAC) showed a protective effect on dabigatran-induced cytotoxicity in the in vitro setting. The medium not containing DBG but containing NAC were served to assay the effect of NAC on cell proliferation and apoptosis. Comparing DAB and all other groups, the cell viability was the lowest in the D group. However, there was no statistically significant difference between the NAC I and DBG-NAC I group, while the difference was statistically significant compared to all other groups. The cells in the DBG group showed a degenerative and round-shaped morphology with nuclear condensation. In other dilutions, the cell morphology was healthy with a fibroblastic morphology. Based on our study results, NAC at high concentrations exerts cytoprotective effects against DBG, while moderate or low concentrations have no favorable effect on cell viability of NAC. Although using concomitant NAC at appropriate doses appears to be effective agent against dabigatran cytotoxicity in the current study, further experimental and clinical studies are needed to confirm our findings.
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来源期刊
CiteScore
1.57
自引率
33.30%
发文量
84
审稿时长
6 months
期刊介绍: This journal, started in 1963, publishes full papers, notes and reviews in cell biology, molecular biology, genetic engineering, endocrinology, reproductive biology, immunology, developmental biology, comparative physiology, radiation biology, chronobiology, microbiology, pharmacology, toxicology and other biological fields including instrumentation and methodology. The papers having experimental design involving alteration and/or manipulation in biological system(s) providing insight into their functioning are considered for publication. Studies involving higher animals, human beings and of clinical nature are not encouraged for publication in the journal.
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