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The Roles of Anandamide, Fatty Acid Amide Hydrolase, and Leukemia Inhibitory Factor on the Endometrium during the Implantation Window

BACKGROUND/AIMS: We investigated the role of the endocannabinoid system (ECS) in the endometrium of unexplained infertility (UI) patients, and effect of anandamide (AEA) on leukemia inhibitory factor (LIF). METHODS: Patients were divided into UI and control groups. Endometrium samples were collected...

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Autores principales: Cui, Na, Wang, Changyan, Zhao, Zhiming, Zhang, Jie, Xu, Yueming, Yang, Yang, Hao, Guimin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5650704/
https://www.ncbi.nlm.nih.gov/pubmed/29085337
http://dx.doi.org/10.3389/fendo.2017.00268
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author Cui, Na
Wang, Changyan
Zhao, Zhiming
Zhang, Jie
Xu, Yueming
Yang, Yang
Hao, Guimin
author_facet Cui, Na
Wang, Changyan
Zhao, Zhiming
Zhang, Jie
Xu, Yueming
Yang, Yang
Hao, Guimin
author_sort Cui, Na
collection PubMed
description BACKGROUND/AIMS: We investigated the role of the endocannabinoid system (ECS) in the endometrium of unexplained infertility (UI) patients, and effect of anandamide (AEA) on leukemia inhibitory factor (LIF). METHODS: Patients were divided into UI and control groups. Endometrium samples were collected at the midluteal phase. Levels of cannabinoid type 1 (CB1), fatty acid amide hydrolase (FAAH), and LIF were examined. LIF productions were measured after AEA, CB1 antagonist AM251, and CB2 antagonist AM630 stimulation. RESULTS: Rates of available embryo, successful implantation and pregnancy, and the endometrial thickness of UI group were significantly lower than control, suggesting uterine receptivity was decreased in UI group. FAAH and LIF levels were significantly decreased, whereas endometrial CB1 was slightly increased in UI group. LIF production was promoted by low amount of AEA administration (1–10 μM), while the promotion was reduced by higher concentration of AEA (50 μM). LIF levels were decreased by AM251 or AM630, compared with AEA alone. Expressions of FAAH and LIF were closely associated with uterus receptivity and implantation rate of UI patients. Different concentrations of AEA could stimulate dynamic changes in LIF production. CONCLUSION: Our data indicated the important role of the ECS in human fertility, which may promote new strategies for successful implantation and treatments for reproductive diseases.
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spelling pubmed-56507042017-10-30 The Roles of Anandamide, Fatty Acid Amide Hydrolase, and Leukemia Inhibitory Factor on the Endometrium during the Implantation Window Cui, Na Wang, Changyan Zhao, Zhiming Zhang, Jie Xu, Yueming Yang, Yang Hao, Guimin Front Endocrinol (Lausanne) Endocrinology BACKGROUND/AIMS: We investigated the role of the endocannabinoid system (ECS) in the endometrium of unexplained infertility (UI) patients, and effect of anandamide (AEA) on leukemia inhibitory factor (LIF). METHODS: Patients were divided into UI and control groups. Endometrium samples were collected at the midluteal phase. Levels of cannabinoid type 1 (CB1), fatty acid amide hydrolase (FAAH), and LIF were examined. LIF productions were measured after AEA, CB1 antagonist AM251, and CB2 antagonist AM630 stimulation. RESULTS: Rates of available embryo, successful implantation and pregnancy, and the endometrial thickness of UI group were significantly lower than control, suggesting uterine receptivity was decreased in UI group. FAAH and LIF levels were significantly decreased, whereas endometrial CB1 was slightly increased in UI group. LIF production was promoted by low amount of AEA administration (1–10 μM), while the promotion was reduced by higher concentration of AEA (50 μM). LIF levels were decreased by AM251 or AM630, compared with AEA alone. Expressions of FAAH and LIF were closely associated with uterus receptivity and implantation rate of UI patients. Different concentrations of AEA could stimulate dynamic changes in LIF production. CONCLUSION: Our data indicated the important role of the ECS in human fertility, which may promote new strategies for successful implantation and treatments for reproductive diseases. Frontiers Media S.A. 2017-10-16 /pmc/articles/PMC5650704/ /pubmed/29085337 http://dx.doi.org/10.3389/fendo.2017.00268 Text en Copyright © 2017 Cui, Wang, Zhao, Zhang, Xu, Yang and Hao. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Endocrinology
Cui, Na
Wang, Changyan
Zhao, Zhiming
Zhang, Jie
Xu, Yueming
Yang, Yang
Hao, Guimin
The Roles of Anandamide, Fatty Acid Amide Hydrolase, and Leukemia Inhibitory Factor on the Endometrium during the Implantation Window
title The Roles of Anandamide, Fatty Acid Amide Hydrolase, and Leukemia Inhibitory Factor on the Endometrium during the Implantation Window
title_full The Roles of Anandamide, Fatty Acid Amide Hydrolase, and Leukemia Inhibitory Factor on the Endometrium during the Implantation Window
title_fullStr The Roles of Anandamide, Fatty Acid Amide Hydrolase, and Leukemia Inhibitory Factor on the Endometrium during the Implantation Window
title_full_unstemmed The Roles of Anandamide, Fatty Acid Amide Hydrolase, and Leukemia Inhibitory Factor on the Endometrium during the Implantation Window
title_short The Roles of Anandamide, Fatty Acid Amide Hydrolase, and Leukemia Inhibitory Factor on the Endometrium during the Implantation Window
title_sort roles of anandamide, fatty acid amide hydrolase, and leukemia inhibitory factor on the endometrium during the implantation window
topic Endocrinology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5650704/
https://www.ncbi.nlm.nih.gov/pubmed/29085337
http://dx.doi.org/10.3389/fendo.2017.00268
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