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Localisation and function of the endocannabinoid system in the human ovary.

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posted on 2012-10-24, 09:00 authored by Mona R. El-Talatini, Anthony H. Taylor, Janine C. Elson, Laurence Brown, Allan C. Davidson, Justin C. Konje
Background Although anandamide (AEA) had been measured in human follicular fluid and is suggested to play a role in ovarian follicle and oocyte maturity, its exact source and role in the human ovary remains unclear. Methods and Findings Immunohistochemical examination of normal human ovaries indicated that the endocannabinoid system was present and widely expressed in the ovarian medulla and cortex with more intense cannabinoid receptor 2 (CB2) than CB1 immunoreactivity in the granulosa cells of primordial, primary, secondary, tertiary follicles, corpus luteum and corpus albicans. The enzymes, fatty acid amide hydrolase (FAAH) and N-acyclphosphatidylethanolamine-phospholi​paseD (NAPE-PLD), were only found in growing secondary and tertiary follicles and corpora lutea and albicantes. The follicular fluid (FF) AEA concentrations of 260 FF samples, taken from 37 infertile women undergoing controlled ovarian hyperstimulation for in vitro fertilisation and intracytoplasmic sperm injection with embryo transfer, were correlated with ovarian follicle size (P = 0.03). Significantly higher FF AEA concentrations were also observed in mature follicles (1.43±0.04 nM; mean±SEM) compared to immature follicles (1.26±0.06 nM), P = 0.0142 and from follicles containing morphologically assessed mature oocytes (1.56±0.11 nM) compared to that containing immature oocytes (0.99±0.09 nM), P = 0.0011. ROC analysis indicated that a FF AEA level of 1.09 nM could discriminate between mature and immature oocytes with 72.2% sensitivity and 77.14% specificity, whilst plasma AEA levels and FF AEA levels on oocyte retrieval day were not significantly different (P = 0.23). Conclusions These data suggest that AEA is produced in the ovary, is under hormonal control and plays a role in folliculogenesis, preovulatory follicle maturation, oocyte maturity and ovulation.

Funding

This work was supported in part by a British United Provident Association (BUPA) grant, generous funding from Perkin-Elmer, with additional funding provided from the Miscellaneous Research Income of the Endocannabinoid Research Group, University of Leicester.

History

Citation

PLoS ONE, 2009, 4 (2), pp. e4579-e4579

Published in

PLoS ONE

Publisher

Public Library of Science

issn

1932-6203

Copyright date

2009

Available date

2012-10-24

Publisher version

http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0004579

Language

eng

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