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1.
Neuroscience ; 166(2): 368-76, 2010 Mar 17.
Article in English | MEDLINE | ID: mdl-20045446

ABSTRACT

Adult neurogenesis occurs most notably in the subgranular zone (SGZ) of the hippocampal dentate gyrus and in the olfactory bulb (OB) where new neurons are generated from neural progenitors cells produced in the subventricular zone (SVZ) of the forebrain. As it is well known that gonadal steroid hormones, primarily estradiol, modulate neurogenesis in the hippocampus of adult female rodents, we wanted to determine whether estradiol would also affect the proliferation of progenitor cells in the SVZ and by consequence the rate of newly generated cells in the main OB. Thus a first group of adult female C57Bl6/J mice was ovariectomized and received a short term treatment with estradiol (single injection of 1 or 10 microg 17beta-estradiol or Silastic capsule of estradiol during 2 days) before receiving a single injection with BrdU to determine whether estradiol would modulate the cell proliferation in the SVZ. A second group of adult ovariectomized female mice was submitted to the same estradiol treatment before receiving four BrdU injections, and was sacrificed 21 days later to determine whether a modulation in cell proliferation actually leads to a modulation in the number of newborn cells in the main OB. We observed a decrease in cell proliferation in the SVZ following either dose of estradiol compared to the controls. Furthermore, 21 days after their generation in the SVZ, the number of BrdU labeled cells was also lower in the main OB, both in the granular and periglomerular cell layers of estradiol-treated animals. These results show that a short term treatment with estradiol actually downregulates cell proliferation leading to a decreased number of newborn cells in the OB.


Subject(s)
Cell Proliferation/drug effects , Estradiol/pharmacology , Lateral Ventricles/drug effects , Neurogenesis/drug effects , Olfactory Bulb/drug effects , Analysis of Variance , Animals , Cell Count , Cell Survival/drug effects , Estrogens/pharmacology , Female , Immunohistochemistry , Lateral Ventricles/physiology , Mice , Olfactory Bulb/physiology , Ovariectomy
2.
Neurosci Lett ; 421(2): 101-5, 2007 Jun 27.
Article in English | MEDLINE | ID: mdl-17566659

ABSTRACT

Previously [D.W. Wesson, M. Keller, Q. Douhard, M.J. Baum, J. Bakker, Enhanced urinary odor discrimination in female aromatase knockout mice, Horm. Behav. 49 (2006) 580-586] female aromatase knock out mice successfully learned to discriminate in a food-motivated go/no-go task between urinary volatiles from ovariectomized female mice treated with estradiol as opposed to estradiol plus progesterone whereas wild type females failed to learn this odor discrimination. We asked whether this behavioral difference is reflected in the ability of these two types of urinary volatiles to differentially stimulate Fos expression in juxtaglomerular cells (an index of glomerular activation) of the main olfactory bulb (MOB) in wild type versus ArKO female mice. Statistically significant differences in the profiles of MOB glomerular activation were seen in ovariectomized, estrogen-treated ArKO as well as WT female subjects following exposure to urinary volatiles from ovariectomized females given estradiol alone as opposed to estradiol plus progesterone. Therefore, previously observed differences between females of the two genotypes in their behavioral responses to these odors must reflect differential processing in more central segments of the olfactory pathway instead of in the MOB.


Subject(s)
Aromatase/deficiency , Discrimination, Psychological , Odorants , Olfactory Bulb , Sex Characteristics , Smell/physiology , Animals , Behavior, Animal , Discrimination, Psychological/physiology , Electronic Data Processing , Estrous Cycle/drug effects , Estrous Cycle/physiology , Female , Male , Mice , Mice, Inbred C57BL , Mice, Knockout , Olfactory Bulb/cytology , Olfactory Bulb/drug effects , Olfactory Bulb/physiology , Olfactory Pathways/drug effects , Olfactory Pathways/physiology , Oncogene Proteins v-fos/metabolism , Ovariectomy/methods
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