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Name OZAWA Hitoshi

Title

Immunocytochemical analysis of sex differences in calcitonin gene-related peptide in the rat dorsal root ganglion, with special reference to estrogen and its receptor

Author

YM Yang,H Ozawa,HP Lu,K Yuri,S Hayashi,K Nihonyanagi,M Kawata

Sole or Joint Author

 

Journal

BRAIN RESEARCH

Publisher

ELSEVIER SCIENCE BV

All Volumes

 

All Pages

 

Volume

791

Number

1-2

Starting Page

35

Ending Page

42

Publication Date

1998-04

Refereed Paper

Not refereed

Invited Paper

Not invited

Language

English

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ISSN

 

ID:DOI

10.1016/S0006-8993(98)00021-3

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URL

Description

Previous studies have shown that the calcitonin gene-related peptide (CGRP) immunoreactivity in the central nervous system (CNS) of adult rats is sexually dimorphic and regulated by sex steroid. In the present study, we used immunocytochemistry to investigate the sex difference in CGRP-immunoreactive (IR) neurons in rat dorsal root ganglia (DRG). The numbers of CGRP-IR neurons at the cervical, lumbar and sacral levels in the female rats were significantly lower than those of the male rats. We also found that the number of CGRP-IR neurons at the lumbar level was increased in ovariectomized (OVX) rats, but was decreased in estradiol (E-2)-treated rats (OVX + E-2). A large number of estrogen receptor (ER)-IR neurons at the lumbar level were found in the female rats, and its number was greater than that in the male rats. We also investigated the change in the number of ER-IR neurons of OVX rats after estrogen treatment. The number of ER-IR neurons in the OVX + E-2 rats was consistent with that of the intact female rats, but was significantly increased in the OVX rats. As shown by a double-labeling immunocytochemical method, over 80% of the CGRP-IR neurons at the lumbar level showed ER immunoreactivity in the female, OVX and OVX + E-2 rats, compared to only about 46% in the male rats. These results indicate that there is a gender difference in CGRP expression in the rat DRG, and that this CGRP expression might be downregulated by estrogen (at least in part) through its receptor. (C) 1998 Elsevier Science B.V.

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