Development of Anti-Inflammatory Drug from Crataeva Nurvala: In Silico and In Vitro Approach

IF 0.8 Q3 Pharmacology, Toxicology and Pharmaceutics Journal of Pharmacy and Bioallied Sciences Pub Date : 2024-04-01 DOI:10.4103/jpbs.jpbs_594_23
K. Nithin Krishna, Kalaiselvi Krishnamoorthy, V. Veeraraghavan, Selvaraj Jayaraman
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Abstract

ABSTRACT Crataeva nurvala, a medicinal plant with potential therapeutic properties, offers a promising avenue for the development of novel anti-inflammatory drugs. This study adopted a combined in silico and in vitro approach to investigate the anti-inflammatory potential of compounds derived from Crataeva nurvala. In the in silico phase, virtual screening and molecular docking analyses were conducted to identify bioactive compounds from Crataeva nurvala that could interact with key inflammatory targets. Subsequently, selected compounds were synthesized and subjected to in vitro experimentation. Cellular models were employed to assess the anti-inflammatory effects of Crataeva nurvala-derived compounds, focusing on the modulation of pro-inflammatory cytokine levels and the underlying signaling pathways. Virtual screening and molecular docking led to the identification of several bioactive compounds with favorable interactions with inflammatory targets. In the in vitro experiments, treatment with Crataeva nurvala-derived compounds resulted in a significant reduction in pro-inflammatory cytokine production. Moreover, the compounds exhibited the ability to modulate inflammatory signaling pathways, further substantiating their anti-inflammatory potential. This study not only contributes to the development of effective anti-inflammatory drugs but also underscores the value of harnessing natural sources such as Crataeva nurvala for therapeutic interventions in inflammatory disorders. The dual-phase strategy presented here provides a robust framework for anti-inflammatory drug discovery and validation.
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从 Crataeva Nurvala 中开发抗炎药物:硅学和体外方法
摘要 Crataeva nurvala 是一种具有潜在治疗特性的药用植物,它为新型抗炎药物的开发提供了一种前景广阔的途径。本研究采用了硅学和体外相结合的方法来研究从 Crataeva nurvala 中提取的化合物的抗炎潜力。 在硅学阶段,研究人员通过虚拟筛选和分子对接分析,从 Crataeva nurvala 中发现了能与关键炎症靶点相互作用的生物活性化合物。随后,合成了选定的化合物并进行了体外实验。采用细胞模型来评估 Crataeva nurvala 衍生化合物的抗炎作用,重点是调节促炎细胞因子水平和潜在的信号通路。 通过虚拟筛选和分子对接,确定了几种与炎症靶点具有良好相互作用的生物活性化合物。在体外实验中,用 Crataeva nurvala 衍生的化合物处理可显著减少促炎细胞因子的产生。此外,这些化合物还表现出调节炎症信号通路的能力,进一步证实了它们的抗炎潜力。 这项研究不仅有助于开发有效的抗炎药物,还强调了利用 Crataeva nurvala 等天然资源对炎症性疾病进行治疗干预的价值。本文介绍的双阶段策略为抗炎药物的发现和验证提供了一个强有力的框架。
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
CiteScore
1.50
自引率
0.00%
发文量
275
审稿时长
34 weeks
期刊介绍: Journal of Pharmacy And Bioallied Sciences is a Quarterly multidisciplinary open access biomedical journal. Journal of Pharmacy And Bioallied Sciences is an international medium of interaction between scientist, academicians and industrial personnel’s.JPBS is now offial publication of OPUBS.
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