Estrogen protects primary cortical neurons from glutamate toxicity

Neurosci Lett. 1996 Jul 5;212(1):13-6. doi: 10.1016/0304-3940(96)12760-9.

Abstract

The gonadal steroid estrogen has been shown to affect neuronal growth, differentiation and survival. We examined the ability of estrogen to protect primary cortical neurons from toxicity induced by the excitatory neurotransmitter glutamate. In these experiments, a 24-h pretreatment with 15 and 50 nM 17 beta-estradiol significantly reduced cellular lactate dehydrogenase (LDH) release from primary cortical neurons, indicating that neurons treated with 17 beta-estradiol were protected from a toxic glutamate exposure. Pretreatment with related steroids such as progesterone, dihydrotestosterone, dexamethasone or cholesterol did not significantly decrease LDH release. The anti-estrogen tamoxifen blocked the protective effects of 17 beta-estradiol suggesting that a classical steroid hormone receptor may be involved in the mechanism subserving estrogen neuroprotection during glutamate toxicity.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Anti-Inflammatory Agents / pharmacology
  • Cell Death / drug effects
  • Cerebral Cortex / cytology*
  • Cholesterol / pharmacology
  • Dexamethasone / pharmacology
  • Dihydrotestosterone / pharmacology
  • Dose-Response Relationship, Drug
  • Estradiol / pharmacology*
  • Estrogen Antagonists / pharmacology
  • Glutamic Acid / toxicity*
  • Neurons / cytology
  • Neurons / drug effects*
  • Neuroprotective Agents / pharmacology
  • Rats
  • Receptors, Estrogen / antagonists & inhibitors
  • Sensitivity and Specificity
  • Tamoxifen / pharmacology

Substances

  • Anti-Inflammatory Agents
  • Estrogen Antagonists
  • Neuroprotective Agents
  • Receptors, Estrogen
  • Dihydrotestosterone
  • Tamoxifen
  • Glutamic Acid
  • Estradiol
  • Dexamethasone
  • Cholesterol