Department of Pharmaceutical Sciences, Maharshi Dayanand University, Rohtak, Haryana, India.
School of Health Sciences, University of Petroleum and Energy Studies, Dehradun, Uttarakhand, India.
Inflammopharmacology. 2022 Aug;30(4):1153-1166. doi: 10.1007/s10787-022-01017-8. Epub 2022 Jul 8.
Traumatic brain injury (TBI) is an important global health concern that represents a leading cause of death and disability. It occurs due to direct impact or hit on the head caused by factors such as motor vehicles, crushes, and assaults. During the past decade, an abundance of new evidence highlighted the importance of inflammation in the secondary damage response that contributes to neurodegenerative and neurological deficits after TBI. It results in disruption of the blood-brain barrier (BBB) and initiates the release of macrophages, neutrophils, and lymphocytes at the injury site. A growing number of researchers have discovered various signalling pathways associated with the initiation and progression of inflammation. Targeting different signalling pathways (NF-κB, JAK/STAT, MAPKs, PI3K/Akt/mTOR, GSK-3, Nrf2, RhoGTPase, TGF-β1, and NLRP3) helps in the development of novel anti-inflammatory drugs in the management of TBI. Several synthetic and herbal drugs with both anti-inflammatory and neuroprotective potential showed effective results. This review summarizes different signalling pathways, associated pathologies, inflammatory mediators, pharmacological potential, current status, and challenges with anti-inflammatory drugs.
创伤性脑损伤(TBI)是一个重要的全球健康关注点,是导致死亡和残疾的主要原因之一。它是由于头部受到诸如机动车、挤压和攻击等因素的直接冲击或撞击而发生的。在过去的十年中,大量新证据强调了炎症在继发性损伤反应中的重要性,这种反应导致 TBI 后神经退行性和神经功能缺陷。它会破坏血脑屏障(BBB),并在损伤部位引发巨噬细胞、中性粒细胞和淋巴细胞的释放。越来越多的研究人员发现了与炎症的发生和进展相关的各种信号通路。针对不同的信号通路(NF-κB、JAK/STAT、MAPKs、PI3K/Akt/mTOR、GSK-3、Nrf2、RhoGTPase、TGF-β1 和 NLRP3)有助于开发新型抗炎药物来治疗 TBI。具有抗炎和神经保护潜力的几种合成药物和草药显示出了有效的结果。本综述总结了不同的信号通路、相关病理学、炎症介质、药理学潜力、现状和抗炎药物面临的挑战。