Department of Pharmacodynamics, Meiji Pharmaceutical University, 2-522-1 Noshio, Tokyo 204-8588, Japan.
Laboratory of Pharmacology, Kobe Pharmaceutical University, 4-19-1 Motoyama-Kita Higashinada, Kobe 668-8558, Japan.
Cells. 2023 Feb 24;12(5):719. doi: 10.3390/cells12050719.
Traumatic brain injury (TBI) is an intracranial injury caused by accidents, falls, or sports. The production of endothelins (ETs) is increased in the injured brain. ET receptors are classified into distinct types, including ET receptor (ET-R) and ET receptor (ET-R). ET-R is highly expressed in reactive astrocytes and upregulated by TBI. Activation of astrocytic ET-R promotes conversion to reactive astrocytes and the production of astrocyte-derived bioactive factors, including vascular permeability regulators and cytokines, which cause blood-brain barrier (BBB) disruption, brain edema, and neuroinflammation in the acute phase of TBI. ET-R antagonists alleviate BBB disruption and brain edema in animal models of TBI. The activation of astrocytic ET receptors also enhances the production of various neurotrophic factors. These astrocyte-derived neurotrophic factors promote the repair of the damaged nervous system in the recovery phase of patients with TBI. Thus, astrocytic ET-R is expected to be a promising drug target for TBI in both the acute and recovery phases. This article reviews recent observations on the role of astrocytic ET receptors in TBI.
创伤性脑损伤(TBI)是由事故、跌倒或运动引起的颅内损伤。在受伤的大脑中,内皮素(ET)的产生增加。ET 受体分为不同的类型,包括 ET 受体(ET-R)和 ET 受体(ET-R)。ET-R 在反应性星形胶质细胞中高度表达,并通过 TBI 上调。星形胶质细胞 ET-R 的激活促进向反应性星形胶质细胞的转化以及星形胶质细胞衍生的生物活性因子的产生,包括血管通透性调节剂和细胞因子,这会导致 TBI 急性期的血脑屏障(BBB)破坏、脑水肿和神经炎症。ET-R 拮抗剂可减轻 TBI 动物模型中的 BBB 破坏和脑水肿。星形胶质细胞 ET 受体的激活还增强了各种神经营养因子的产生。这些星形胶质细胞衍生的神经营养因子促进 TBI 患者恢复期受损神经系统的修复。因此,星形胶质细胞 ET-R 有望成为 TBI 急性和恢复期的有前途的药物靶点。本文综述了最近关于星形胶质细胞 ET 受体在 TBI 中的作用的观察结果。