Endothelin systems in the brain: Involvement in pathophysiological responses of damaged nerve tissues

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Abstract

In addition to their potent vasoconstriction effects, endothelins (ETs) show multiple actions in various tissues including the brain. The brain contains high levels of ETs, and their production is stimulated in many brain disorders. Accumulating evidence indicates that activation of brain ET receptors is involved in several pathophysiological responses in damaged brains. In this article, the roles of brain ET systems in relation to brain disorders are reviewed. In the acute phase of stroke, prolonged vasospasm of cerebral arteries and brain edema occur, both of which aggravate brain damage. Studies using ET antagonists show that activation of ET A receptors in the brain vascular smooth muscle induces vasospasm after stroke. Brain edema is induced by increased activity of vascular permeability factors, such as vascular endothelial growth factor and matrix metalloproteinases. Activation of ET B receptors stimulates astrocytic production of these permeability factors. Increases in reactive astrocytes are observed in neurodegenerative diseases and in the chronic phase of stroke, where they facilitate the repair of damaged nerve tissues by releasing neurotrophic factors. ETs promote the induction of reactive astrocytes through ET B receptors. ETs also stimulate the production of astrocytic neurotrophic factors. Recent studies have shown high expression of ET B receptors in neural progenitors. Activation of ET B receptors in neural progenitors promotes their proliferation and migration, suggesting roles for ET B receptors in neurogenesis. Much effort has been invested in the pursuit of novel drugs to induce protection or repair of damaged nerve tissues. From these studies, the pharmacological significance of brain ET systems as a possible target of neuroprotective drugs is anticipated.

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APA

Koyama, Y. (2013, August). Endothelin systems in the brain: Involvement in pathophysiological responses of damaged nerve tissues. Biomolecular Concepts. https://doi.org/10.1515/bmc-2013-0004

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