Are animal models relevant to key aspects of human parturition?
1 Departments of Obstetrics & Gynecology and Physiology, Heritage Medical Research Centre, University of Alberta, Edmonton, Alberta, Canada; and 2 Institute of Cellular Medicine, Newcastle University, Newcastle-upon-Tyne, United Kingdom Submitted 13 March 2009 ; accepted in final form 9 June 200...
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Veröffentlicht in: | American journal of physiology. Regulatory, integrative and comparative physiology integrative and comparative physiology, 2009-09, Vol.297 (3), p.R525-R545 |
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container_title | American journal of physiology. Regulatory, integrative and comparative physiology |
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creator | Mitchell, Bryan F Taggart, Michael J |
description | 1 Departments of Obstetrics & Gynecology and Physiology, Heritage Medical Research Centre, University of Alberta, Edmonton, Alberta, Canada; and 2 Institute of Cellular Medicine, Newcastle University, Newcastle-upon-Tyne, United Kingdom
Submitted 13 March 2009
; accepted in final form 9 June 2009
ABSTRACT
Preterm birth remains the most serious complication of pregnancy and is associated with increased rates of infant death or permanent neurodevelopmental disability. Our understanding of the regulation of parturition remains inadequate. The scientific literature, largely derived from rodent animal models, suggests two major mechanisms regulating the timing of parturition: the withdrawal of the steroid hormone progesterone and a proinflammatory response by the immune system. However, available evidence strongly suggests that parturition in the human has significantly different regulators and mediators from those in most of the animal models. Our objectives are to critically review the data and concepts that have arisen from use of animal models for parturition and to rationalize the use of a new model. Many animal models have contributed to advances in our understanding of the regulation of parturition. However, we suggest that those animals dependent on progesterone withdrawal to initiate parturition clearly have a limitation to their translation to the human. In such models, a linear sequence of events (e.g., luteolysis, progesterone withdrawal, uterine activation, parturition) gives rise to the concept of a "trigger" mechanism. Conversely, we propose that human parturition may arise from the concomitant maturation of several systems in parallel. We have termed this novel concept "modular accumulation of physiological systems" (MAPS). We also emphasize the urgency to determine the precise role of the immune system in the process of parturition in situations other than intrauterine infection. Finally, we accentuate the need to develop a nonprimate animal model whose physiology is more relevant to human parturition. We suggest that the guinea pig displays several key physiological characteristics of gestation that more closely resemble human pregnancy than do currently favored animal models. We conclude that the application of novel concepts and new models are required to advance translational research in parturition.
progesterone withdrawal; modular accumulation of physiological systems; uterine activation; cervical ripening
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doi_str_mv | 10.1152/ajpregu.00153.2009 |
format | Article |
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Submitted 13 March 2009
; accepted in final form 9 June 2009
ABSTRACT
Preterm birth remains the most serious complication of pregnancy and is associated with increased rates of infant death or permanent neurodevelopmental disability. Our understanding of the regulation of parturition remains inadequate. The scientific literature, largely derived from rodent animal models, suggests two major mechanisms regulating the timing of parturition: the withdrawal of the steroid hormone progesterone and a proinflammatory response by the immune system. However, available evidence strongly suggests that parturition in the human has significantly different regulators and mediators from those in most of the animal models. Our objectives are to critically review the data and concepts that have arisen from use of animal models for parturition and to rationalize the use of a new model. Many animal models have contributed to advances in our understanding of the regulation of parturition. However, we suggest that those animals dependent on progesterone withdrawal to initiate parturition clearly have a limitation to their translation to the human. In such models, a linear sequence of events (e.g., luteolysis, progesterone withdrawal, uterine activation, parturition) gives rise to the concept of a "trigger" mechanism. Conversely, we propose that human parturition may arise from the concomitant maturation of several systems in parallel. We have termed this novel concept "modular accumulation of physiological systems" (MAPS). We also emphasize the urgency to determine the precise role of the immune system in the process of parturition in situations other than intrauterine infection. Finally, we accentuate the need to develop a nonprimate animal model whose physiology is more relevant to human parturition. We suggest that the guinea pig displays several key physiological characteristics of gestation that more closely resemble human pregnancy than do currently favored animal models. We conclude that the application of novel concepts and new models are required to advance translational research in parturition.
progesterone withdrawal; modular accumulation of physiological systems; uterine activation; cervical ripening
Address for reprint requests and other correspondence: B. F. Mitchell, 220 Heritage Medical Research Centre, Univ. of Alberta, Edmonton, Alberta, Canada T6G 2S2 (e-mail: brymitch{at}ualberta.ca )</description><identifier>ISSN: 0363-6119</identifier><identifier>EISSN: 1522-1490</identifier><identifier>DOI: 10.1152/ajpregu.00153.2009</identifier><identifier>PMID: 19515978</identifier><identifier>CODEN: AJPRDO</identifier><language>eng</language><publisher>United States: American Physiological Society</publisher><subject>Animals ; Births ; Cervical Ripening ; Female ; Gestational Age ; Guinea Pigs ; Humans ; Immune System - physiology ; Laboratory animals ; Mice ; Models, Animal ; Myometrium - metabolism ; Myometrium - physiology ; Parturition - blood ; Parturition - physiology ; Pregnancy ; Progesterone ; Progesterone - blood ; Rabbits ; Rats ; Rodents ; Sheep ; Signal Transduction ; Species Specificity ; Uterine Contraction</subject><ispartof>American journal of physiology. Regulatory, integrative and comparative physiology, 2009-09, Vol.297 (3), p.R525-R545</ispartof><rights>Copyright American Physiological Society Sep 2009</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c432t-c1859b0ebf67d6c88e918a5564b265aaccf39f2c08220642bd32fac2e1c78c8e3</citedby><cites>FETCH-LOGICAL-c432t-c1859b0ebf67d6c88e918a5564b265aaccf39f2c08220642bd32fac2e1c78c8e3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>315,782,786,3041,27931,27932</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19515978$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Mitchell, Bryan F</creatorcontrib><creatorcontrib>Taggart, Michael J</creatorcontrib><title>Are animal models relevant to key aspects of human parturition?</title><title>American journal of physiology. Regulatory, integrative and comparative physiology</title><addtitle>Am J Physiol Regul Integr Comp Physiol</addtitle><description>1 Departments of Obstetrics & Gynecology and Physiology, Heritage Medical Research Centre, University of Alberta, Edmonton, Alberta, Canada; and 2 Institute of Cellular Medicine, Newcastle University, Newcastle-upon-Tyne, United Kingdom
Submitted 13 March 2009
; accepted in final form 9 June 2009
ABSTRACT
Preterm birth remains the most serious complication of pregnancy and is associated with increased rates of infant death or permanent neurodevelopmental disability. Our understanding of the regulation of parturition remains inadequate. The scientific literature, largely derived from rodent animal models, suggests two major mechanisms regulating the timing of parturition: the withdrawal of the steroid hormone progesterone and a proinflammatory response by the immune system. However, available evidence strongly suggests that parturition in the human has significantly different regulators and mediators from those in most of the animal models. Our objectives are to critically review the data and concepts that have arisen from use of animal models for parturition and to rationalize the use of a new model. Many animal models have contributed to advances in our understanding of the regulation of parturition. However, we suggest that those animals dependent on progesterone withdrawal to initiate parturition clearly have a limitation to their translation to the human. In such models, a linear sequence of events (e.g., luteolysis, progesterone withdrawal, uterine activation, parturition) gives rise to the concept of a "trigger" mechanism. Conversely, we propose that human parturition may arise from the concomitant maturation of several systems in parallel. We have termed this novel concept "modular accumulation of physiological systems" (MAPS). We also emphasize the urgency to determine the precise role of the immune system in the process of parturition in situations other than intrauterine infection. Finally, we accentuate the need to develop a nonprimate animal model whose physiology is more relevant to human parturition. We suggest that the guinea pig displays several key physiological characteristics of gestation that more closely resemble human pregnancy than do currently favored animal models. We conclude that the application of novel concepts and new models are required to advance translational research in parturition.
progesterone withdrawal; modular accumulation of physiological systems; uterine activation; cervical ripening
Address for reprint requests and other correspondence: B. F. Mitchell, 220 Heritage Medical Research Centre, Univ. of Alberta, Edmonton, Alberta, Canada T6G 2S2 (e-mail: brymitch{at}ualberta.ca )</description><subject>Animals</subject><subject>Births</subject><subject>Cervical Ripening</subject><subject>Female</subject><subject>Gestational Age</subject><subject>Guinea Pigs</subject><subject>Humans</subject><subject>Immune System - physiology</subject><subject>Laboratory animals</subject><subject>Mice</subject><subject>Models, Animal</subject><subject>Myometrium - metabolism</subject><subject>Myometrium - physiology</subject><subject>Parturition - blood</subject><subject>Parturition - physiology</subject><subject>Pregnancy</subject><subject>Progesterone</subject><subject>Progesterone - blood</subject><subject>Rabbits</subject><subject>Rats</subject><subject>Rodents</subject><subject>Sheep</subject><subject>Signal Transduction</subject><subject>Species Specificity</subject><subject>Uterine Contraction</subject><issn>0363-6119</issn><issn>1522-1490</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpdkE1L7DAUhoMoOn78AReX4MJdx-SkSZOViFw_QBBE1yHNnM50btv0Ju2V-fdWZ7iCq7M4z_vy8hByztmccwlXbt1HXI5zxrgUc2DM7JHZ9ICM54btkxkTSmSKc3NEjlNaM8ZykYtDcsSN5NIUekaubyJS19Wta2gbFtgkGrHBf64b6BDoH9xQl3r0Q6KhoquxdR3tXRzGWA916K5PyUHlmoRnu3tC3u5-v94-ZE_P94-3N0-ZzwUMmedampJhWaliobzWaLh2Uqq8BCWd874SpgLPNABTOZQLAZXzgNwX2msUJ-Ry29vH8HfENNi2Th6bxnUYxmRVIY3mCibw4ge4DmPspm0WwBRGgzITBFvIx5BSxMr2cVIQN5Yz--nW7tzaL7f20-0U-rVrHssWF9-RncwJyLbAql6u3uuItl9tUh2asNz8L5w2WGFfJEjxAcEWhlQ</recordid><startdate>20090901</startdate><enddate>20090901</enddate><creator>Mitchell, Bryan F</creator><creator>Taggart, Michael J</creator><general>American Physiological Society</general><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>7QP</scope><scope>7QR</scope><scope>7TS</scope><scope>7U7</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>P64</scope><scope>7X8</scope></search><sort><creationdate>20090901</creationdate><title>Are animal models relevant to key aspects of human parturition?</title><author>Mitchell, Bryan F ; Taggart, Michael J</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c432t-c1859b0ebf67d6c88e918a5564b265aaccf39f2c08220642bd32fac2e1c78c8e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Animals</topic><topic>Births</topic><topic>Cervical Ripening</topic><topic>Female</topic><topic>Gestational Age</topic><topic>Guinea Pigs</topic><topic>Humans</topic><topic>Immune System - physiology</topic><topic>Laboratory animals</topic><topic>Mice</topic><topic>Models, Animal</topic><topic>Myometrium - metabolism</topic><topic>Myometrium - physiology</topic><topic>Parturition - blood</topic><topic>Parturition - physiology</topic><topic>Pregnancy</topic><topic>Progesterone</topic><topic>Progesterone - blood</topic><topic>Rabbits</topic><topic>Rats</topic><topic>Rodents</topic><topic>Sheep</topic><topic>Signal Transduction</topic><topic>Species Specificity</topic><topic>Uterine Contraction</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Mitchell, Bryan F</creatorcontrib><creatorcontrib>Taggart, Michael J</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Physical Education Index</collection><collection>Toxicology Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>American journal of physiology. Regulatory, integrative and comparative physiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Mitchell, Bryan F</au><au>Taggart, Michael J</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Are animal models relevant to key aspects of human parturition?</atitle><jtitle>American journal of physiology. Regulatory, integrative and comparative physiology</jtitle><addtitle>Am J Physiol Regul Integr Comp Physiol</addtitle><date>2009-09-01</date><risdate>2009</risdate><volume>297</volume><issue>3</issue><spage>R525</spage><epage>R545</epage><pages>R525-R545</pages><issn>0363-6119</issn><eissn>1522-1490</eissn><coden>AJPRDO</coden><abstract>1 Departments of Obstetrics & Gynecology and Physiology, Heritage Medical Research Centre, University of Alberta, Edmonton, Alberta, Canada; and 2 Institute of Cellular Medicine, Newcastle University, Newcastle-upon-Tyne, United Kingdom
Submitted 13 March 2009
; accepted in final form 9 June 2009
ABSTRACT
Preterm birth remains the most serious complication of pregnancy and is associated with increased rates of infant death or permanent neurodevelopmental disability. Our understanding of the regulation of parturition remains inadequate. The scientific literature, largely derived from rodent animal models, suggests two major mechanisms regulating the timing of parturition: the withdrawal of the steroid hormone progesterone and a proinflammatory response by the immune system. However, available evidence strongly suggests that parturition in the human has significantly different regulators and mediators from those in most of the animal models. Our objectives are to critically review the data and concepts that have arisen from use of animal models for parturition and to rationalize the use of a new model. Many animal models have contributed to advances in our understanding of the regulation of parturition. However, we suggest that those animals dependent on progesterone withdrawal to initiate parturition clearly have a limitation to their translation to the human. In such models, a linear sequence of events (e.g., luteolysis, progesterone withdrawal, uterine activation, parturition) gives rise to the concept of a "trigger" mechanism. Conversely, we propose that human parturition may arise from the concomitant maturation of several systems in parallel. We have termed this novel concept "modular accumulation of physiological systems" (MAPS). We also emphasize the urgency to determine the precise role of the immune system in the process of parturition in situations other than intrauterine infection. Finally, we accentuate the need to develop a nonprimate animal model whose physiology is more relevant to human parturition. We suggest that the guinea pig displays several key physiological characteristics of gestation that more closely resemble human pregnancy than do currently favored animal models. We conclude that the application of novel concepts and new models are required to advance translational research in parturition.
progesterone withdrawal; modular accumulation of physiological systems; uterine activation; cervical ripening
Address for reprint requests and other correspondence: B. F. Mitchell, 220 Heritage Medical Research Centre, Univ. of Alberta, Edmonton, Alberta, Canada T6G 2S2 (e-mail: brymitch{at}ualberta.ca )</abstract><cop>United States</cop><pub>American Physiological Society</pub><pmid>19515978</pmid><doi>10.1152/ajpregu.00153.2009</doi></addata></record> |
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subjects | Animals Births Cervical Ripening Female Gestational Age Guinea Pigs Humans Immune System - physiology Laboratory animals Mice Models, Animal Myometrium - metabolism Myometrium - physiology Parturition - blood Parturition - physiology Pregnancy Progesterone Progesterone - blood Rabbits Rats Rodents Sheep Signal Transduction Species Specificity Uterine Contraction |
title | Are animal models relevant to key aspects of human parturition? |
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