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Paracrine support of ovarian stimulation
Assisted reproductive technology has evolved on the back of blunderbuss ovarian stimulation regimes designed to maximize the number of oocytes recoverable for treatment purposes. However, oocyte ‘quality’ is finely programmed by local paracrine and autocrine signalling events during folliculogenesis...
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Published in: | Molecular human reproduction 2009-12, Vol.15 (12), p.843-850 |
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container_title | Molecular human reproduction |
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creator | Hillier, Stephen G. |
description | Assisted reproductive technology has evolved on the back of blunderbuss ovarian stimulation regimes designed to maximize the number of oocytes recoverable for treatment purposes. However, oocyte ‘quality’ is finely programmed by local paracrine and autocrine signalling events during folliculogenesis and can be adversely affected by inappropriate gonadotrophic stimulation. This brief review traces the full follicular lifespan—from initiation to ovulation—to identify gonadotrophin-responsive checkpoints likely to impact oocyte quality. It is argued that these might be targeted during controlled ovarian stimulation therapy to (i) increase responsiveness to FSH through follicular priming with LH or hCG, (ii) improve follicular synchrony and oocyte quality through conditioning with FSH and (iii) promote ‘gold standard’ pre-ovulatory maturation through follicular coasting with LH or hCG. It is concluded that whereas there can be no one-size-fits-all approach to ovarian stimulation, treatment regimes based on paracrine principles and tailored to personal needs will always be more likely to achieve the desired outcome. |
doi_str_mv | 10.1093/molehr/gap086 |
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However, oocyte ‘quality’ is finely programmed by local paracrine and autocrine signalling events during folliculogenesis and can be adversely affected by inappropriate gonadotrophic stimulation. This brief review traces the full follicular lifespan—from initiation to ovulation—to identify gonadotrophin-responsive checkpoints likely to impact oocyte quality. It is argued that these might be targeted during controlled ovarian stimulation therapy to (i) increase responsiveness to FSH through follicular priming with LH or hCG, (ii) improve follicular synchrony and oocyte quality through conditioning with FSH and (iii) promote ‘gold standard’ pre-ovulatory maturation through follicular coasting with LH or hCG. It is concluded that whereas there can be no one-size-fits-all approach to ovarian stimulation, treatment regimes based on paracrine principles and tailored to personal needs will always be more likely to achieve the desired outcome.</description><identifier>ISSN: 1360-9947</identifier><identifier>EISSN: 1460-2407</identifier><identifier>DOI: 10.1093/molehr/gap086</identifier><identifier>PMID: 19825856</identifier><language>eng</language><publisher>England: Oxford University Press</publisher><subject>Activins - metabolism ; Chorionic Gonadotropin - metabolism ; Female ; follicle development ; Follicle Stimulating Hormone - metabolism ; gonadotrophins ; Humans ; Inhibins - metabolism ; inhibins and activins ; Luteinizing Hormone - metabolism ; oocyte ; Oocytes - physiology ; Ovarian Follicle - cytology ; Ovarian Follicle - physiology ; ovary ; Ovulation Induction - methods ; Paracrine Communication ; Reproductive Techniques, Assisted</subject><ispartof>Molecular human reproduction, 2009-12, Vol.15 (12), p.843-850</ispartof><rights>The Author 2009. Published by Oxford University Press on behalf of the European Society of Human Reproduction and Embryology. All rights reserved. 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However, oocyte ‘quality’ is finely programmed by local paracrine and autocrine signalling events during folliculogenesis and can be adversely affected by inappropriate gonadotrophic stimulation. This brief review traces the full follicular lifespan—from initiation to ovulation—to identify gonadotrophin-responsive checkpoints likely to impact oocyte quality. It is argued that these might be targeted during controlled ovarian stimulation therapy to (i) increase responsiveness to FSH through follicular priming with LH or hCG, (ii) improve follicular synchrony and oocyte quality through conditioning with FSH and (iii) promote ‘gold standard’ pre-ovulatory maturation through follicular coasting with LH or hCG. It is concluded that whereas there can be no one-size-fits-all approach to ovarian stimulation, treatment regimes based on paracrine principles and tailored to personal needs will always be more likely to achieve the desired outcome.</description><subject>Activins - metabolism</subject><subject>Chorionic Gonadotropin - metabolism</subject><subject>Female</subject><subject>follicle development</subject><subject>Follicle Stimulating Hormone - metabolism</subject><subject>gonadotrophins</subject><subject>Humans</subject><subject>Inhibins - metabolism</subject><subject>inhibins and activins</subject><subject>Luteinizing Hormone - metabolism</subject><subject>oocyte</subject><subject>Oocytes - physiology</subject><subject>Ovarian Follicle - cytology</subject><subject>Ovarian Follicle - physiology</subject><subject>ovary</subject><subject>Ovulation Induction - methods</subject><subject>Paracrine Communication</subject><subject>Reproductive Techniques, Assisted</subject><issn>1360-9947</issn><issn>1460-2407</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><recordid>eNqFkEFLwzAYhoMobk6PXqU3d6lLmrRpjjqdE4YKGyJeQtIlGm2bmrSi_95Iix49fe_h4X0_HgCOETxDkOFZZUv14mbPooF5tgPGiGQwTgikuyHjkBkjdAQOvH-FENEkzffBCLE8hDQbg-m9cKJwplaR75rGujayOrIfwhlRR741VVeK1tj6EOxpUXp1NNwJ2CyuNvNlvLq7vpmfr-KCwKSN8xSzsJJJyBiSMMsJJFgyqlMstRRakYQoJCAhWkmipcQskTKFgkpCtxRPwGlf2zj73inf8sr4QpWlqJXtPKeYIExTmAQy7snCWe-d0rxxphLuiyPIf9TwXg3v1QT-ZGjuZKW2f_TgIgDTHrBd82_XsG18qz5_YeHeeEbDe3z5-MRv6eXDYk0v-Bp_AxP8faM</recordid><startdate>20091201</startdate><enddate>20091201</enddate><creator>Hillier, Stephen G.</creator><general>Oxford University Press</general><scope>BSCLL</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20091201</creationdate><title>Paracrine support of ovarian stimulation</title><author>Hillier, Stephen G.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c402t-85391726b0991b0684043b97f53bfbafe424e1a044feb4fbb392bb50a7b47d73</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Activins - metabolism</topic><topic>Chorionic Gonadotropin - metabolism</topic><topic>Female</topic><topic>follicle development</topic><topic>Follicle Stimulating Hormone - metabolism</topic><topic>gonadotrophins</topic><topic>Humans</topic><topic>Inhibins - metabolism</topic><topic>inhibins and activins</topic><topic>Luteinizing Hormone - metabolism</topic><topic>oocyte</topic><topic>Oocytes - physiology</topic><topic>Ovarian Follicle - cytology</topic><topic>Ovarian Follicle - physiology</topic><topic>ovary</topic><topic>Ovulation Induction - methods</topic><topic>Paracrine Communication</topic><topic>Reproductive Techniques, Assisted</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hillier, Stephen G.</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Molecular human reproduction</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hillier, Stephen G.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Paracrine support of ovarian stimulation</atitle><jtitle>Molecular human reproduction</jtitle><addtitle>Mol Hum Reprod</addtitle><date>2009-12-01</date><risdate>2009</risdate><volume>15</volume><issue>12</issue><spage>843</spage><epage>850</epage><pages>843-850</pages><issn>1360-9947</issn><eissn>1460-2407</eissn><abstract>Assisted reproductive technology has evolved on the back of blunderbuss ovarian stimulation regimes designed to maximize the number of oocytes recoverable for treatment purposes. However, oocyte ‘quality’ is finely programmed by local paracrine and autocrine signalling events during folliculogenesis and can be adversely affected by inappropriate gonadotrophic stimulation. This brief review traces the full follicular lifespan—from initiation to ovulation—to identify gonadotrophin-responsive checkpoints likely to impact oocyte quality. It is argued that these might be targeted during controlled ovarian stimulation therapy to (i) increase responsiveness to FSH through follicular priming with LH or hCG, (ii) improve follicular synchrony and oocyte quality through conditioning with FSH and (iii) promote ‘gold standard’ pre-ovulatory maturation through follicular coasting with LH or hCG. It is concluded that whereas there can be no one-size-fits-all approach to ovarian stimulation, treatment regimes based on paracrine principles and tailored to personal needs will always be more likely to achieve the desired outcome.</abstract><cop>England</cop><pub>Oxford University Press</pub><pmid>19825856</pmid><doi>10.1093/molehr/gap086</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Activins - metabolism Chorionic Gonadotropin - metabolism Female follicle development Follicle Stimulating Hormone - metabolism gonadotrophins Humans Inhibins - metabolism inhibins and activins Luteinizing Hormone - metabolism oocyte Oocytes - physiology Ovarian Follicle - cytology Ovarian Follicle - physiology ovary Ovulation Induction - methods Paracrine Communication Reproductive Techniques, Assisted |
title | Paracrine support of ovarian stimulation |
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