Drug-Induced Gingival Enlargement: A Comparative Study on the Effect of Phenytoin, Gabapentin, and Cyclosporin on Gingival Fibroblast Cells.

IF 2.4 4区 生物学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY
K M Veena, V Mohammed Hasil, Prashanth Shenoy, R Abhijna Ballal, Sanath Kumar Shetty
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Abstract

Drug-induced gingival enlargement (DIGE) is an abnormal overgrowth that may occur as a side effect in some patients when calcium channel blockers, immunosuppressants, or anticonvulsants are taken. The prevalence of DIGE was shown to be 70% for phenytoin (30% for other anticonvulsant medicines) and 50-80% for cyclosporine. The usage of these medications is increasing as new indications emerge. These drugs act through a common mechanism of action at the cellular level by inhibiting intracellular calcium influx. DIGE is characterized by the presence of varied quantities of inflammatory infiltrates, primarily plasma cells, and an excessive build-up of extracellular matrix like-collagen. Fibroblasts, the cells responsible for collagen synthesis, may become hyperactive, leading to the excessive production of collagen fibers. This increased collagen content can result in the enlargement of gingival tissues. As collagen deposits increase, it hinders normal oral care routines, masticatory processes, and esthetics. In this study, we compared the cytotoxicity of phenytoin, gabapentin, and cyclosporine on gingival fibroblast cells using the methyl thiazolyl-tetrazolium assay to understand their effect on gingival fibroblast cells. Phenytoin had the greatest half-maximal inhibitory concentration (IC50) with a value of 305.78 µg/ml, followed by gabapentin with a value of 260.44 µg/ml and cyclosporin with a value of 243.79 µg/ml. Understanding the cytotoxic thresholds of these medications is essential for improving patient outcomes and minimizing the incidence of gingival enlargement in those requiring long-term therapy. According to the study, cytotoxicity increases along with medication concentration. These findings will assist medical professionals in selecting the drug that poses the least risk of adverse effects on gingival health, ultimately guiding more informed prescribing practices.

药物诱发的牙龈增生:苯妥英、加巴喷丁和环孢素对牙龈成纤维细胞影响的比较研究
药物性牙龈肿大(DIGE)是一种异常的过度生长,在一些患者服用钙通道阻滞剂、免疫抑制剂或抗惊厥药时可能作为副作用发生。苯妥英的DIGE患病率为70%(其他抗惊厥药物为30%),环孢素为50-80%。随着新的适应症的出现,这些药物的使用也在增加。这些药物在细胞水平上通过抑制细胞内钙流入的共同作用机制起作用。DIGE的特征是存在不同数量的炎症浸润,主要是浆细胞,以及细胞外基质如胶原蛋白的过度积累。负责胶原合成的成纤维细胞可能变得过度活跃,导致胶原纤维的过量产生。胶原蛋白含量的增加会导致牙龈组织的扩大。随着胶原蛋白沉积的增加,它会妨碍正常的口腔护理程序、咀嚼过程和美学。在这项研究中,我们比较了苯妥英、加巴喷丁和环孢素对牙龈成纤维细胞的细胞毒性,采用甲基噻唑四氮唑实验来了解它们对牙龈成纤维细胞的影响。苯妥英的半最大抑制浓度(IC50)最高,为305.78µg/ml,其次是加巴喷丁,为260.44µg/ml,环孢素为243.79µg/ml。了解这些药物的细胞毒性阈值对于改善患者预后和减少那些需要长期治疗的牙龈扩大的发生率至关重要。根据这项研究,细胞毒性随着药物浓度的增加而增加。这些发现将帮助医疗专业人员选择对牙龈健康不利影响风险最小的药物,最终指导更明智的处方实践。
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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来源期刊
Molecular Biotechnology
Molecular Biotechnology 医学-生化与分子生物学
CiteScore
4.10
自引率
3.80%
发文量
165
审稿时长
6 months
期刊介绍: Molecular Biotechnology publishes original research papers on the application of molecular biology to both basic and applied research in the field of biotechnology. Particular areas of interest include the following: stability and expression of cloned gene products, cell transformation, gene cloning systems and the production of recombinant proteins, protein purification and analysis, transgenic species, developmental biology, mutation analysis, the applications of DNA fingerprinting, RNA interference, and PCR technology, microarray technology, proteomics, mass spectrometry, bioinformatics, plant molecular biology, microbial genetics, gene probes and the diagnosis of disease, pharmaceutical and health care products, therapeutic agents, vaccines, gene targeting, gene therapy, stem cell technology and tissue engineering, antisense technology, protein engineering and enzyme technology, monoclonal antibodies, glycobiology and glycomics, and agricultural biotechnology.
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