Endothelin ETB Receptor-Mediated Astrocytic Activation: Pathological Roles in Brain Disorders

Int J Mol Sci. 2021 Apr 21;22(9):4333. doi: 10.3390/ijms22094333.

Abstract

In brain disorders, reactive astrocytes, which are characterized by hypertrophy of the cell body and proliferative properties, are commonly observed. As reactive astrocytes are involved in the pathogenesis of several brain disorders, the control of astrocytic function has been proposed as a therapeutic strategy, and target molecules to effectively control astrocytic functions have been investigated. The production of brain endothelin-1 (ET-1), which increases in brain disorders, is involved in the pathophysiological response of the nervous system. Endothelin B (ETB) receptors are highly expressed in reactive astrocytes and are upregulated by brain injury. Activation of astrocyte ETB receptors promotes the induction of reactive astrocytes. In addition, the production of various astrocyte-derived factors, including neurotrophic factors and vascular permeability regulators, is regulated by ETB receptors. In animal models of Alzheimer's disease, brain ischemia, neuropathic pain, and traumatic brain injury, ETB-receptor-mediated regulation of astrocytic activation has been reported to improve brain disorders. Therefore, the astrocytic ETB receptor is expected to be a promising drug target to improve several brain disorders. This article reviews the roles of ETB receptors in astrocytic activation and discusses its possible applications in the treatment of brain disorders.

Keywords: Alzheimer’s disease; ETB receptor; brain ischemia; endothelin; neuropathic pain; reactive astrocyte; traumatic brain injury.

Publication types

  • Review

MeSH terms

  • Alzheimer Disease / metabolism
  • Alzheimer Disease / physiopathology
  • Animals
  • Astrocytes / metabolism*
  • Astrocytes / physiology
  • Brain Diseases / metabolism*
  • Brain Diseases / physiopathology
  • Brain Injuries / metabolism
  • Brain Injuries / physiopathology
  • Brain Ischemia / metabolism
  • Brain Ischemia / physiopathology
  • Endothelin-1 / metabolism
  • Humans
  • Neuralgia / metabolism
  • Neuralgia / physiopathology
  • Receptor, Endothelin B / metabolism*
  • Receptor, Endothelin B / physiology

Substances

  • Endothelin-1
  • Receptor, Endothelin B