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药物重定位方法在炎症性肠病治疗干预中的应用。

Application of Drug Repurposing Approach for Therapeutic Intervention of Inflammatory Bowel Disease.

机构信息

Department of Pharmacology, Amity Institute of Pharmacy, Lucknow, Amity University Uttar Pradesh, UP, Noida, India.

Department of Pharmaceutical Chemistry, Amity Institute of Pharmacy, Amity University Maharashtra, Mumbai, Maharashtra, India.

出版信息

Curr Rev Clin Exp Pharmacol. 2024;19(3):234-249. doi: 10.2174/0127724328245156231008154045.

Abstract

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.

摘要

炎症性肠病(IBD),包括克罗恩病(CD)和溃疡性结肠炎(UC),是一种胃肠道(GIT)慢性炎症性疾病,其特征为慢性复发的肠道炎症、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,但人们认为它是基因与环境因素(如肠道微生物失衡、饮食习惯改变、过度卫生环境和不合适的免疫系统)相互作用的结果。由于对 IBD 的病因缺乏了解,新型有效疗法的发展受到了阻碍。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、改变疾病进程、提供多种治疗选择、展示生物疗法的进展、并提高整体生活质量。然而,目前的治疗方法存在大量不良反应,如体重减轻、情绪波动、皮肤问题、骨密度降低、更容易感染和血压升高,这使得其疗效黯然失色。生物制剂,如抗肿瘤坏死因子制剂,可能会在某些个体中引发自身免疫反应,从而随着时间的推移降低药物的有效性,因此需要转为替代治疗。IBD 患者对现有药物治疗的反应差异很大,这可能导致疾病发作,凸显出迫切需要探索替代治疗方案,以满足开发高效低不良反应的 IBD 新治疗策略的未满足需求。药物再利用是一种新策略,即将已经在患者中验证用于治疗某些疾病的安全药物重新用于治疗其他未指明的疾病。本综述重点介绍了使用靶向和非靶向策略,可通过药物再利用用于治疗 IBD 的潜在药物候选物。它涵盖了它们的临床前和临床评估、作用机制和安全性概况,并预测了它们在 IBD 管理中的适用性。该综述为重新利用最有前途的候选药物提供了有用的见解,如具有抗炎和抗细胞凋亡作用的曲克芦丁,已被发现可改善大鼠 DSS 诱导的结肠炎;具有抗骨关节炎作用的二乙酰rhein,已被发现通过抗氧化和抗炎特性以及影响细胞凋亡和细胞焦亡,对 DSS 诱导的结肠炎具有显著的改善作用;抗癫痫和抗惊厥药物托吡酯,通过其细胞因子抑制作用,可显著降低 IBD 实验模型中啮齿动物的整体生理病理和组织病理事件。

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