Dehghani Firoozabadi Mehdi, Nooralishahi Behrang, Rezaei-Tazangi Fatemeh
Tehran Heart Center, Cardiovascular Diseases Research Institute, Anesthesiology, Critical Care and Pain Research Center, Tehran University of Medical Science, Tehran, Iran.
Department of Anatomy, School of Medicine, Fasa University of Medical Sciences, Fasa, Iran.
Mol Pain. 2025 Jan-Dec;21:17448069251377460. doi: 10.1177/17448069251377460. Epub 2025 Aug 28.
Pain is an unpleasant sensory and emotional sensation about actual or possible tissue damage that can cause remarkable health and economic problems. For pain relief, analgesic drugs are commonly utilized; however, their prolonged use can cause different side effects from mild to severe stages. Therefore, discovering new and alternative choices for analgesic purposes is of importance. Hopeful evidence has shown that flavonoid compounds have various therapeutic and pharmacological potentials. Among these, silymarin, obtained from the milk thistle plant , has addressed its competence in medicine, as demonstrated by its capacity against metabolic diseases, malignancies, inflammatory-related disorders, and organ toxicities. In the recent decade, some documents have stated the analgesic influences of silymarin, especially in some pathological situations like rheumatoid arthritis and neuropathic pain. Also, there is promising information regarding the possible synergistic effects of silymarin and some pharmacological or bioactive compounds. For these reasons, this narrative literature review aims to summarize and discuss the analgesic abilities of this flavonoid agent in pathological and nonpathological conditions and its interactions with other drugs with a focus on the involved mechanisms.
疼痛是一种关于实际或潜在组织损伤的不愉快的感觉和情绪体验,会引发显著的健康和经济问题。为缓解疼痛,通常会使用镇痛药;然而,长期使用这些药物会导致从轻度到重度的不同副作用。因此,寻找新的镇痛替代选择至关重要。有希望的证据表明,黄酮类化合物具有多种治疗和药理潜力。其中,从水飞蓟植物中提取的水飞蓟素已证明其在医学上的功效,如对代谢性疾病、恶性肿瘤、炎症相关疾病和器官毒性的抵御能力。在最近十年中,一些文献阐述了水飞蓟素的镇痛作用,尤其是在类风湿性关节炎和神经性疼痛等一些病理情况下。此外,关于水飞蓟素与某些药理或生物活性化合物可能存在的协同作用也有令人期待的信息。基于这些原因,本叙述性文献综述旨在总结和讨论这种黄酮类药物在病理和非病理条件下的镇痛能力及其与其他药物的相互作用,并重点关注其中涉及的机制。