Biol Reprod
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH
 QUICK SEARCH:   [advanced]


     


BOR - Papers in Press, published online ahead of print June 9, 2004.
Biol Reprod 2004, 10.1095/biolreprod.104.030023
This Article
Right arrow Full Text (Rapid PDF)
Right arrow All Versions of this Article:
71/4/1397    most recent
biolreprod.104.030023v1
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow Author home page(s):
Peter G. Smith
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Ting, A. Y.
Right arrow Articles by Smith, P. G.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Ting, A. Y.
Right arrow Articles by Smith, P. G.
Agricola
Right arrow Articles by Ting, A. Y.
Right arrow Articles by Smith, P. G.
Submitted April 29, 2004
Returned for revision May 20, 2004
Accepted May 27, 2004

Female Reproductive Tract


Estrogen Regulates Vaginal Sensory and Autonomic Nerve Density in the Rat

Alison Y. Ting , Audrey D. Blacklock , and Peter G. Smith *

* To whom correspondence should be addressed. E-mail: psmith{at}kumc.edu.

Abstract
Vaginal function is strongly influenced by reproductive hormone status. Vaginal dysfunction during menopause is generally assumed to occur because of diminished estrogen-mediated trophic support of vaginal target cells. However, peripheral neurons possess estrogen receptors and are potentially responsive to gonadal steroid hormones. In the present study, we investigated whether sensory and autonomic innervation of the vagina varies among rats during the estrus phase of the estrous cycle, following chronic ovariectomy, and after sustained estrogen replacement. Relative to rats in estrus, ovariectomized rats showed a 59% elevation in nerve density, as determined using the pan-neuronal marker PGP9.5. This increase persisted even after correcting for differences in vaginal tissue size, indicating true axonal proliferation after ovariectomy rather than changes secondary to altered volume. Increased total innervation after ovariectomy was attributable to increased densities of sympathetic nerves immunostained for tyrosine hydroxylase (70%), cholinergic parasympathetic nerves immunoreactive for vesicular acetylcholine transporter (93%), and calcitonin gene-related peptide-immunoreactive sensory nociceptor nerves (84%). Myelinated primary sensory innervation revealed by RT-97 immunoreactivity did not appear to be affected. Sustained 17{beta}-estradiol administration reduced innervation density to an extent comparable to that of estrus, implying that estrogen is the hormone mediating vaginal neuroplasticity. These findings indicate that some aspects of vaginal dysfunction during menopause may be attributable to changes in innervation. Increased sympathetic innervation may augment vasoconstriction and promote vaginal dryness, while sensory nociceptor axon proliferation may contribute to symptoms of pain, burning and itching associated with menopause and some forms of vulvodynia.

Key words: Estradiol • Neurotransmitters • Ovulatory cycle • Steroid hormones • Vagina


This article has been cited by other articles:


Home page
Endocr. Rev.Home page
R. H. Straub
The Complex Role of Estrogens in Inflammation
Endocr. Rev., August 1, 2007; 28(5): 521 - 574.
[Abstract] [Full Text] [PDF]


Home page
EndocrinologyHome page
M. A. Pessina, R. F. Hoyt Jr., I. Goldstein, and A. M. Traish
Differential Effects of Estradiol, Progesterone, and Testosterone on Vaginal Structural Integrity
Endocrinology, January 1, 2006; 147(1): 61 - 69.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH
Copyright © 2004 by the Society for the Study of Reproduction.