Abstract |
Our previous studies have shown that female mice have less brain edema and better recovery in neurological deficits after intracerebral hemorrhage (ICH) and that 17β-estradiol treatment in male mice markedly reduces ICH-induced brain edema. In this study, we investigated the role of gender and the estrogen receptors (ERs) in iron-induced brain edema. There were three parts in this study: (1) either male or female mice received an injection of 10 μL FeCl2 (1 mM) into the right caudate; (2) females received an intracaudate injection of FeCl2 or saline with 1 μg of ICI 182,780 (antagonists of ERs) or vehicle; and (3) males were treated with the ER regulator tamoxifen (5 mg/kg subcutaneously) or vehicle 1 h after FeCl2 injection. Mice were euthanized 24 h later for brain edema determination. FeCl2 induced lower brain edema in females than in males. Co-injection of ICI 182,780 with FeCl2 aggravated iron-induced brain edema in female mice. ICI 182,780 itself did not induce brain edema at the dose of 1 μg. Tamoxifen treatment reduced FeCl2-induced brain edema in male mice. In conclusion, iron induced less brain edema in female mice than in males. ER modification can affect iron-induced brain edema.
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Authors | Qing Xie, Guohua Xi, Richard F Keep, Ya Hua |
Journal | Acta neurochirurgica. Supplement
(Acta Neurochir Suppl)
Vol. 121
Pg. 341-5
( 2016)
ISSN: 0065-1419 [Print] Austria |
PMID | 26463972
(Publication Type: Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't)
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Chemical References |
- Chlorides
- Estrogen Antagonists
- Estrogen Receptor Antagonists
- Iron Compounds
- Receptors, Estrogen
- Tamoxifen
- Fulvestrant
- Estradiol
- Iron
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Topics |
- Animals
- Brain
(drug effects, metabolism)
- Brain Edema
(chemically induced, metabolism)
- Caudate Nucleus
- Chlorides
(toxicity)
- Disease Models, Animal
- Estradiol
(analogs & derivatives, pharmacology)
- Estrogen Antagonists
(pharmacology)
- Estrogen Receptor Antagonists
(pharmacology)
- Female
- Fulvestrant
- Iron
- Iron Compounds
(toxicity)
- Male
- Mice
- Mice, Inbred C57BL
- Receptors, Estrogen
(antagonists & inhibitors, metabolism)
- Sex Factors
- Tamoxifen
(pharmacology)
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