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Astrocytes mediate protective actions of estrogenic compounds after traumatic brain injury

  • Cynthia Martin-Jiménez
  • , Diana Milena Gaitán-Vaca
  • , Natalia Areiza
  • , Valentina Echeverria
  • , Ghulam Md Ashraf
  • , Janneth González
  • , Amirhossein Sahebkar
  • , Luis Miguel Garcia-Segura
  • , George E. Barreto
  • Universidad Javeriana
  • Universidad San Sebastián
  • VA Medical Center
  • King Fahd Medical Research Center
  • Mashhad University of Medical Sciences
  • Instituto Cajal, CSIC
  • Instituto de Salud Carlos III

Research output: Contribution to journalReview articlepeer-review

35 Scopus citations

Abstract

Traumatic brain injury (TBI) is a serious public health problem. It may result in severe neurological disabilities and in a variety of cellular metabolic alterations for which available therapeutic strategies are limited. In the last decade, the use of estrogenic compounds, which activate protective mechanisms in astrocytes, has been explored as a potential experimental therapeutic approach. Previous works have suggested estradiol (E2) as a neuroprotective hormone that acts in the brain by binding to estrogen receptors (ERs). Several steroidal and nonsteroidal estrogenic compounds can imitate the effects of estradiol on ERs. These include hormonal estrogens, phytoestrogens and synthetic estrogens, such as selective ER modulators or tibolone. Current evidence of the role of astrocytes in mediating protective actions of estrogenic compounds after TBI is reviewed in this paper. We conclude that the use of estrogenic compounds to modulate astrocytic properties is a promising therapeutic approach for the treatment of TBI.

Original languageEnglish
Pages (from-to)142-160
Number of pages19
JournalNeuroendocrinology
Volume108
Issue number2
DOIs
StatePublished - 01 Feb 2019

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • Astrocytes
  • Estrogenic compounds
  • Neuroprotection
  • Traumatic brain injury

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