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多酚作为脊髓损伤中疼痛和炎症的潜在治疗方法。

Polyphenols as Potential Therapeutics for Pain and Inflammation in Spinal Cord Injury.

作者信息

Iqubal Ashif, Ahmed Musheer, Iqubal Mohammad K, Pottoo Faheem H, Haque Syed E

机构信息

Department of Pharmacology, School of Pharmaceutical Education and Research, Jamia Hamdard, New Delhi- 110062, India.

Department of Pharmaceutics, School of Pharmaceutical Education and Research, Jamia Hamdard, New Delhi-110062, India.

出版信息

Curr Mol Pharmacol. 2021;14(5):714-730. doi: 10.2174/1874467213666201223111743.

Abstract

Spinal cord injury (SCI) and associated pain and inflammation caused by trauma or infection are serious health care issues world-wide. The various inflammatory, redox-sensitive and apoptotic events are contributing factors, but altered neuronal function, axonal degeneration, activated microglia, endothelial cells, astrocytes, fibroblasts, pericytes, Schwann cells, and meningeal cells are major players in its pathogenesis. Further, monocytes and neutrophil infiltration get recruited and facilitate the release of chemokines, cytokines, and other mediators of inflammation. This event leads to the production of different amino acids, neuropeptides kinin, prostaglandins, prostacyclin, thromboxane, leukotrienes, bradykinin, histamine, matrix metal proteinases, and serotonin that stimulate nerve endings and manifest the inflammation and pain processes, etc. Arachidonic acid (AA), NF-kB, NLRP3 inflammasome, and nitric oxide pathways along with P2X7 receptor and ion channel transient receptor potential (TRP) vanilloid are some of the recently explored targets for modulation of pain and inflammation in SCI. Till now, NSAIDs, opioids, antidepressants, anticonvulsants, NMDA antagonists, α2-adrenergic agonists, and GABA-receptor agonists are used for the management of these pathological conditions. However, these drugs are associated with various side effects. Additionally, the number of available animal models for SCI has enhanced the understanding of the complex pathological mechanisms involved in the generation of chronic inflammatory pain in SCI. These findings enable us to identify and validate several potent natural analgesic-anti-inflammatory drug candidates with minimal side effects. However, these compounds have been studied in preclinical models and shown promising results, but no clinical studies have been performed. Therefore, a detailed exploration of these natural compounds is important for bringing them from bench to bedside.

摘要

脊髓损伤(SCI)以及由创伤或感染引起的相关疼痛和炎症是全球范围内严重的医疗保健问题。各种炎症、氧化还原敏感和凋亡事件都是促成因素,但神经元功能改变、轴突退化、活化的小胶质细胞、内皮细胞、星形胶质细胞、成纤维细胞、周细胞、雪旺细胞和脑膜细胞是其发病机制中的主要参与者。此外,单核细胞和中性粒细胞浸润被募集并促进趋化因子、细胞因子和其他炎症介质的释放。这一事件导致不同氨基酸、神经肽激肽、前列腺素、前列环素、血栓素、白三烯、缓激肽、组胺、基质金属蛋白酶和5-羟色胺的产生,这些物质刺激神经末梢并表现出炎症和疼痛过程等。花生四烯酸(AA)、核因子-κB(NF-κB)、NLRP3炎性小体和一氧化氮途径以及P2X7受体和离子通道瞬时受体电位(TRP)香草酸受体是最近探索的用于调节脊髓损伤中疼痛和炎症的一些靶点。到目前为止,非甾体抗炎药、阿片类药物、抗抑郁药、抗惊厥药、N-甲基-D-天冬氨酸(NMDA)拮抗剂、α2-肾上腺素能激动剂和γ-氨基丁酸(GABA)受体激动剂被用于治疗这些病理状况。然而,这些药物都伴有各种副作用。此外,现有的脊髓损伤动物模型数量增加了对脊髓损伤中慢性炎性疼痛产生所涉及的复杂病理机制的理解。这些发现使我们能够识别和验证几种副作用最小的强效天然镇痛抗炎候选药物。然而,这些化合物仅在临床前模型中进行了研究并显示出有前景的结果,但尚未进行临床研究。因此,对这些天然化合物进行详细探索对于将它们从实验室应用到临床至关重要。

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