Estradiol reduces dendritic spine density in the ventral striatum of female Syrian hamsters

被引:56
|
作者
Staffend, Nancy A. [1 ]
Loftus, Caroline M. [1 ]
Meisel, Robert L. [1 ]
机构
[1] Univ Minnesota, Dept Neurosci, Minneapolis, MN 55455 USA
来源
BRAIN STRUCTURE & FUNCTION | 2011年 / 215卷 / 3-4期
基金
美国国家卫生研究院;
关键词
Estradiol; Nucleus accumbens; Caudate; Hippocampus; Spine density; Spine morphology; ESTROGEN-RECEPTOR-ALPHA; VENTROMEDIAL HYPOTHALAMIC NEURONS; METABOTROPIC GLUTAMATE RECEPTORS; NUCLEUS-ACCUMBENS; SYNAPTIC PLASTICITY; PREFRONTAL CORTEX; RAT; BETA; MODULATION; EXPERIENCE;
D O I
10.1007/s00429-010-0284-7
中图分类号
R602 [外科病理学、解剖学]; R32 [人体形态学];
学科分类号
100101 ;
摘要
Estradiol affects a variety of brain regions by modulating physiological and cellular functions as well as neuronal morphology. Within the striatum, estradiol is known to induce physiological and molecular changes, yet estradiol's effects on striatal dendritic morphology have not yet been evaluated. Using ballistic delivery of the lipophilic dye Dil to tissue sections, we were able to evaluate estradiol's effects on striatal morphology in female Syrian hamsters. We found that estradiol significantly decreased spine density within the nucleus accumbens core, with no effect in the nucleus accumbens shell or caudate. Interestingly, estradiol treatment caused a significant deconstruction of spines from more to less mature spine subtypes in both the nucleus accumbens core and shell regardless of changes in spine density. These results are significant in that they offer a novel mechanism for estradiol actions on a wide variety of nucleus accumbens functions such as motivation or reward as well as their pathological consequences (e.g. drug addiction).
引用
收藏
页码:187 / 194
页数:8
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