Capsaicin: pharmacological applications and prospects for drug designing.

IF 2.8 4区 医学 Q2 PHARMACOLOGY & PHARMACY Journal of Pharmacy and Pharmacology Pub Date : 2024-12-09 DOI:10.1093/jpp/rgae150
Anshita Gupta, Renjil Joshi, Lokkanya Dewangan, Kamal Shah, Deependra Soni, Umesh K Patil, Nagendra Singh Chauhan
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Abstract

Objectives: A primary objective of this review is to summarize the evidence-based pharmacological applications of capsaicin, particularly its use to manage pain and treat various health conditions. A second goal of the review is to research how recent technological advances are improving the bioavailability and therapeutic index of capsaicin, as well as the development of novel capsaicin-mimetics that are able to enhance therapeutic responses in various human diseases.

Methods: In the review, numerous human clinical trials and preclinical studies are examined to determine how effective, safe, and optimal dosages of capsaicin can be used in pain management and therapeutic applications. Furthermore, it discusses capsaicin's mechanisms of action, specifically its interactions with the transient receptor potential vanilloid 1 (TRPV1) channel. As a result of this review, the potential of nanotechnology systems for bypassing the limits of capsaicin's pungency is discussed. The review takes into account individual factors such as pain tolerance and skin sensitivity.

Key findings: For topical applications, capsaicin is typically used in concentrations ranging from 0.025% to 0.1%, with higher concentrations being used under medical supervision for neuropathic pain. The formulation can come in the form of creams, gels, or patches, which provide sustained release over the course of time. A condition such as arthritis or neuropathy can be relieved with capsaicin as it depletes substance P from nerves. Neuropathy and osteoarthritis as well as musculoskeletal disorders have been treated successfully with this herbal medicine. A major mechanism through which capsaicin relieves pain is through activating TRPV1 channels, which induce calcium influx and neurotransmitter release. Additionally, it affects the transcription of genes related to pain modulation and inflammation, particularly when disease conditions or stress are present. There have been recent developments in technology to reduce capsaicin's pungency and improve its bioavailability, including nanotechnology.

Conclusions: It is proven that capsaicin is effective in pain management as well as a variety of therapeutic conditions because of its ability to deplete substance P and desensitize nerve endings. Although capsaicin is highly pungent and associated with discomfort, advancements in delivery technologies and the development of capsaicin-mimetics promise improved therapeutic outcomes. There is a great deal of complexity in the pharmacological action of capsaicin due to its interaction with TRPV1 channels and its ability to affect gene transcription. There is a need for further research and development in order to optimize capsaicin's clinical applications and to enhance its therapeutic index in a variety of human diseases.

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辣椒素:药理应用及药物设计展望。
目的:本综述的主要目的是总结辣椒素的循证药理学应用,特别是其在控制疼痛和治疗各种健康状况方面的应用。本综述的第二个目标是研究最近的技术进步如何提高辣椒素的生物利用度和治疗指数,以及能够增强各种人类疾病治疗反应的新型辣椒素模拟物的开发。方法:在回顾中,大量的人体临床试验和临床前研究进行了检查,以确定辣椒素在疼痛管理和治疗应用中的有效性,安全性和最佳剂量。此外,它还讨论了辣椒素的作用机制,特别是它与瞬时受体电位香草素1 (TRPV1)通道的相互作用。因此,本文讨论了纳米技术系统在克服辣椒素辛辣性限制方面的潜力。该审查考虑了个体因素,如疼痛耐受性和皮肤敏感性。主要发现:对于局部应用,辣椒素通常以0.025%至0.1%的浓度使用,在医疗监督下使用更高浓度用于神经性疼痛。配方可以是面霜、凝胶或贴片,在一段时间内提供持续释放。辣椒素可以减少神经中的P物质,从而缓解关节炎或神经病变等疾病。神经病变和骨关节炎以及肌肉骨骼疾病已经成功地治疗了这种草药。辣椒素缓解疼痛的主要机制是通过激活TRPV1通道,诱导钙流入和神经递质释放。此外,它还影响与疼痛调节和炎症相关的基因转录,特别是在疾病状况或压力存在时。最近在减少辣椒素的辛辣性和提高其生物利用度的技术上有了发展,包括纳米技术。结论:辣椒素具有消耗P物质和使神经末梢脱敏的能力,在疼痛管理和各种治疗条件下都是有效的。虽然辣椒素非常辛辣,并与不适有关,但递送技术的进步和辣椒素模拟物的发展有望改善治疗效果。由于辣椒素与TRPV1通道的相互作用及其影响基因转录的能力,其药理作用具有很大的复杂性。为了优化辣椒素的临床应用,提高其在多种人类疾病中的治疗指数,还需要进一步的研究和开发。
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
6.60
自引率
0.00%
发文量
91
审稿时长
3 months
期刊介绍: JPP keeps pace with new research on how drug action may be optimized by new technologies, and attention is given to understanding and improving drug interactions in the body. At the same time, the journal maintains its established and well-respected core strengths in areas such as pharmaceutics and drug delivery, experimental and clinical pharmacology, biopharmaceutics and drug disposition, and drugs from natural sources. JPP publishes at least one special issue on a topical theme each year.
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