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
Hauptverfasser: Mitchell, Bryan F, Taggart, Michael J
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container_issue 3
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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 Address for reprint requests and
doi_str_mv 10.1152/ajpregu.00153.2009
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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. 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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. 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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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