Increase in calcitonin gene related peptide (CGRP) and decrease in mast cells in dihydroepiandrosterone (DHEA)-induced polycystic rat ovaries

Citation
A. Krishna et al., Increase in calcitonin gene related peptide (CGRP) and decrease in mast cells in dihydroepiandrosterone (DHEA)-induced polycystic rat ovaries, ANAT EMBRYO, 203(5), 2001, pp. 375-382
Citations number
31
Categorie Soggetti
Cell & Developmental Biology
Journal title
ANATOMY AND EMBRYOLOGY
ISSN journal
03402061 → ACNP
Volume
203
Issue
5
Year of publication
2001
Pages
375 - 382
Database
ISI
SICI code
0340-2061(200105)203:5<375:IICGRP>2.0.ZU;2-F
Abstract
The polycystic ovary is reported to correspond with a high density in intra ovarian nerve fibers and their sympathetic hyperresponsiveness. Peptidergic nerves may also be involved in this process. An interaction between nerve fibers and mast cells is assumed because of nerve growth-factor production by mast cells. Here we investigated CGRP-positive nerve fibers and mast cel ls in polycystic ovaries induced in immature rats with dihydroepiandrostero ne (DHEA). The DHEA treated ovaries contained less corpora lutea than contr ols (mean +/- SEM: 4.3 +/-0.6 versus 11.3 +/-0.9, P >0.001) and less intact antral follicles (4.7 +/-0.7 versus 8.1 +/-1.1; P< 0.05) according to the histometric approach. By immunolabelling more CGRP-positive nerve fibers we re found in the DHEA treated ovaries than in controls (mean<plus/minus>SEM per one section: 23.2 +/-5.8 fibers versus 10.3 +/-0.9 and 171 +/- 44.7 var icosities versus 84 +/-9.5). This was confirmed by dot blot analysis, showi ng a significant higher CGRP signal intensity per microgram homogenized ova ries of the DHEA treated group compared to the untreated (P< 0.05). Toluidi ne-blue-stained mast cells populated the medulla in both groups, yet had st rikingly decreased in the DHEA treated ovaries (23.5<plus/minus>3.9 versus 89 +/-5.6, P< 0.005). Conclusion: the increase in CGRP-positive nerve fiber s and the decrease of toluidine-blue-stained mast cells points to an altere d neuroimmune function in DHEA-induced polycystic rat ovaries.