Suppr超能文献

天然产物作为通过抑制嘌呤能 P2X 受体的新型抗炎和镇痛化合物的来源。

Natural Products as a Source for New Anti-Inflammatory and Analgesic Compounds through the Inhibition of Purinergic P2X Receptors.

机构信息

Laboratory of Cellular Communication, Oswaldo Cruz Institute-FIOCRUZ, Rio de Janeiro 21040-360, Brazil.

出版信息

Pharmaceuticals (Basel). 2013 Apr 29;6(5):650-8. doi: 10.3390/ph6050650.

Abstract

Natural products have reemerged in traditional medicine as a potential source of new molecules or phytomedicines to help with health disorders. It has been established that members of the P2X subfamily, ATP-gated ion channels, are crucial to the inflammatory process and pain signalization. As such, several preclinical studies have demonstrated that P2X2R, P2X3R, P2X4R and P2X7R are promising pharmacological targets to control inflammatory and pain disorders. Several studies have indicated that natural products could be a good source of the new specific molecules needed for the treatment of diseases linked to inflammation and pain disorders through the regulation of these receptors. Herein, we discuss and give an overview of the applicability of natural products as a source to obtain P2X receptors (P2XR) selective antagonists for use in clinical treatment, which require further investigation.

摘要

天然产物在传统医学中重新兴起,成为寻找新分子或植物药以帮助治疗健康障碍的潜在来源。已经确定,P2X 亚家族成员,即 ATP 门控离子通道,对炎症过程和疼痛信号转导至关重要。因此,多项临床前研究表明,P2X2R、P2X3R、P2X4R 和 P2X7R 是控制炎症和疼痛障碍的有前途的药理学靶点。多项研究表明,天然产物可能是治疗与炎症和疼痛障碍相关疾病所需的新型特定分子的良好来源,这些疾病可通过调节这些受体来治疗。本文讨论并概述了天然产物作为获得用于临床治疗的 P2X 受体(P2XR)选择性拮抗剂的来源的适用性,这需要进一步研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c74f/3817725/9495f1e526bf/pharmaceuticals-06-00650-g001.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验