芦丁:一种镇痛类黄酮。

IF 4.6 2区 医学 Q2 IMMUNOLOGY
Inflammopharmacology Pub Date : 2025-03-01 Epub Date: 2025-02-17 DOI:10.1007/s10787-025-01671-8
Fatemeh Forouzanfar, Toktam Sahranavard, Aristidis Tsatsakis, Mehrdad Iranshahi, Ramin Rezaee
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引用次数: 0

摘要

芦丁(维生素P或芦丁苷)是一种柑橘类黄酮苷,对不同器官的健康有益,可以对抗各种疾病,包括炎症和疼痛。大部分芦丁的治疗效果都归功于它的抗氧化和抗炎特性。本文综述了芦丁镇痛作用的研究进展,并对芦丁的作用机制进行了综述。研究了芦丁对链脲佐菌素诱导的糖尿病、慢性收缩性损伤以及奥沙利铂、福尔马林、醋酸和谷氨酸诱导的小鼠或大鼠伤害性疼痛的缓解作用。根据文献,芦丁的镇痛作用是通过增强抗氧化库、降低炎症细胞因子(如肿瘤坏死因子α (TNF-α)和白细胞介素-1β)水平、抑制环氧化酶-2 (COX-2)和诱导型一氧化氮合酶(iNOS)的表达以及调节MAPK、NF-κB和Nrf-2/HO-1信号传导来诱导的。芦丁镇痛活性的临床前研究结果是有希望的,然而,其安全性需要更彻底的调查,并应进行临床试验以评估其对人体的镇痛作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Rutin: a pain-relieving flavonoid.

Rutin (vitamin P or rutoside) is a citrus flavonoid glycoside that has shown beneficial health effects in different organs against various conditions including inflammation and pain. The majority of rutin therapeutic benefits are ascribed to its antioxidant and anti-inflammatory properties. This review article discusses studies that investigated pain-relieving activity of rutin and summarizes the reported mechanisms of action. Rutin pain-relieving effect has been studied in streptozotocin-induced diabetes, chronic constriction injury, and oxaliplatin-, formalin-, acetic acid- and glutamate-induced nociception in mice or rats. Based on the literature, rutin analgesic effects are induced through potentiation of antioxidant arsenal, reduction of inflammatory cytokines (e.g., Tumor necrosis factor alpha (TNF-α) and interleukin-1β) levels, suppression of cyclooxygenase-2 (COX-2) and inducible nitric oxide synthase (iNOS) expressions and modulation of MAPK, NF-κB and Nrf-2/HO-1 signaling. Preclinical findings on rutin pain-relieving activity are promising, however, its safety profile needs to be more thoroughly investigated and clinical trials should be conducted to assess its analgesic effects in humans.

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来源期刊
Inflammopharmacology
Inflammopharmacology IMMUNOLOGYTOXICOLOGY-TOXICOLOGY
CiteScore
8.00
自引率
3.40%
发文量
200
期刊介绍: Inflammopharmacology is the official publication of the Gastrointestinal Section of the International Union of Basic and Clinical Pharmacology (IUPHAR) and the Hungarian Experimental and Clinical Pharmacology Society (HECPS). Inflammopharmacology publishes papers on all aspects of inflammation and its pharmacological control emphasizing comparisons of (a) different inflammatory states, and (b) the actions, therapeutic efficacy and safety of drugs employed in the treatment of inflammatory conditions. The comparative aspects of the types of inflammatory conditions include gastrointestinal disease (e.g. ulcerative colitis, Crohn''s disease), parasitic diseases, toxicological manifestations of the effects of drugs and environmental agents, arthritic conditions, and inflammatory effects of injury or aging on skeletal muscle. The journal has seven main interest areas: -Drug-Disease Interactions - Conditional Pharmacology - i.e. where the condition (disease or stress state) influences the therapeutic response and side (adverse) effects from anti-inflammatory drugs. Mechanisms of drug-disease and drug disease interactions and the role of different stress states -Rheumatology - particular emphasis on methods of measurement of clinical response effects of new agents, adverse effects from anti-rheumatic drugs -Gastroenterology - with particular emphasis on animal and human models, mechanisms of mucosal inflammation and ulceration and effects of novel and established anti-ulcer, anti-inflammatory agents, or antiparasitic agents -Neuro-Inflammation and Pain - model systems, pharmacology of new analgesic agents and mechanisms of neuro-inflammation and pain -Novel drugs, natural products and nutraceuticals - and their effects on inflammatory processes, especially where there are indications of novel modes action compared with conventional drugs e.g. NSAIDs -Muscle-immune interactions during inflammation [...]
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