药物再利用方法在炎症性肠病治疗干预中的应用。

IF 1.3 Q4 PHARMACOLOGY & PHARMACY
Mohammad Aadil Bhat, Iqra Usman, Suneela Dhaneshwar
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引用次数: 0

摘要

以克罗恩病(CD)和溃疡性结肠炎(UC)为代表的炎症性肠病(IBD)是一种胃肠道慢性炎症性疾病,其特征是慢性复发性肠道炎症、腹痛、痉挛、食欲不振、疲劳、腹泻和体重减轻。尽管IBD的病因尚不清楚,但据信是基因和环境因素之间的相互作用,如肠道微生物群的失衡、饮食习惯的改变、极端不卫生的环境和不适当的免疫系统。由于对IBD病因缺乏了解,新型有效疗法的开发受到阻碍。目前的治疗方法包括使用氨基水杨酸盐、免疫抑制剂和皮质类固醇,这些药物可以有效控制症状、诱导和维持缓解、预防并发症、改变病程、提供多样化的治疗选择、展示生物疗法的进步并提高整体生活质量。然而,目前治疗的疗效被大量的副作用所掩盖,如体重减轻、情绪波动、皮肤问题、骨密度下降、更容易感染和血压升高。生物制品,如抗肿瘤坏死因子制剂,可以刺激某些个体的自身免疫反应,随着时间的推移,这种反应可能会降低药物的有效性,因此需要转向替代治疗。IBD患者对当前药物治疗的反应非常不同,这可能导致疾病发作,这突出表明迫切需要探索替代治疗方案,以满足开发高效、副作用更少的IBD新治疗策略的未满足需求。药物再利用是一种新的策略,将已经被证明对患者安全的现有药物重新部署用于治疗其他未经治疗的疾病。本叙述性综述的重点是潜在的候选药物,这些药物可以通过靶向和非靶向策略重新用于IBD的管理。它涵盖了它们的临床前、临床评估、作用机制和安全性,并预测了它们在IBD管理中的适当性。这篇综述对最有前景的再利用候选者提供了有用的见解,如抗炎和抗细胞凋亡的曲克芦丁,它已被发现可以改善DSS诱导的大鼠结肠炎,已经发现通过抗氧化和抗炎特性以及通过影响细胞凋亡和pyroptosis对DSS诱导的结肠炎具有显著改善作用的抗甾体酸药物二乙酰大黄酸。托吡酯是一种抗癫痫和抗惊厥药物,通过其细胞因子抑制作用,显著降低了啮齿类动物IBD实验模型中的整体病理生理和组织病理学事件。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Application of Drug Repurposing Approach for Therapeutic Intervention of Inflammatory Bowel Disease.

Inflammatory bowel disease (IBD), represented by Crohn's disease (CD) and ulcerative colitis (UC), is a chronic inflammatory disorder of the gastrointestinal tract (GIT) characterized by chronic relapsing intestinal inflammation, abdominal pain, cramping, loss of appetite, fatigue, diarrhoea, and weight loss. Although the etiology of IBD remains unclear, it is believed to be an interaction between genes, and environmental factors, such as an imbalance of the intestinal microbiota, changing food habits, an ultra-hygiene environment, and an inappropriate immune system. The development of novel effective therapies is stymied by a lack of understanding of the aetiology of IBD. The current therapy involves the use of aminosalicylates, immunosuppressants, and corticosteroids that can effectively manage symptoms, induce and sustain remission, prevent complications, modify the course of the disease, provide diverse treatment options, showcase advancements in biologic therapies, and enhance the overall quality of life. However, the efficacy of current therapy is overshadowed by a plethora of adverse effects, such as loss of weight, mood swings, skin issues, loss of bone density, higher vulnerability to infections, and elevated blood pressure. Biologicals, like anti-tumour necrosis factor agents, can stimulate an autoimmune response in certain individuals that may diminish the effectiveness of the medication over time, necessitating a switch to alternative treatments. The response of IBD patients to current drug therapy is quite varied, which can lead to disease flares that underlines the urgent need to explore alternative treatment option to address the unmet need of developing new treatment strategies for IBD with high efficacy and fewer adverse effects. Drug repurposing is a novel strategy where existing drugs that have already been validated safe in patients for the management of certain diseases are redeployed to treat other, unindicated diseases. The present narrative review focuses on potential drug candidates that could be repurposed for the management of IBD using on-target and off-target strategies. It covers their preclinical, clinical assessment, mechanism of action, and safety profiles, and forecasts their appropriateness in the management of IBD. The review presents useful insights into the most promising candidates for repurposing, like anti-inflammatory and anti-apoptotic troxerutin, which has been found to improve the DSS-induced colitis in rats, an antiosteoarthritic drug diacetylrhein that has been found to have remarkable ameliorating effects on DSS-induced colitis via anti-oxidant and anti- inflammatory properties and by influencing both apoptosis and pyroptosis. Topiramate, an antiepileptic and anticonvulsant drug, has remarkably decreased overall pathophysiological and histopathological events in the experimental model of IBD in rodents by its cytokine inhibitory action.

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