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A model of intrauterine infection and preterm delivery in mice

OBJECTIVE: Our purpose was to determine whether intrauterine bacterial inoculation leads to preterm delivery in mice. STUDY DESIGN: Fifty-four female CD-1 mice at 75% of the length of the gestational period (14.5 days) received either an intrauterine bacterial inoculum of 2 to 10 × 10 3 Escherichia...

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Published in:American journal of obstetrics and gynecology 1995-05, Vol.172 (5), p.1598-1603
Main Authors: Hirsch, Emmet, Saotome, Ichiko, Hirsch, David
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container_title American journal of obstetrics and gynecology
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creator Hirsch, Emmet
Saotome, Ichiko
Hirsch, David
description OBJECTIVE: Our purpose was to determine whether intrauterine bacterial inoculation leads to preterm delivery in mice. STUDY DESIGN: Fifty-four female CD-1 mice at 75% of the length of the gestational period (14.5 days) received either an intrauterine bacterial inoculum of 2 to 10 × 10 3 Escherichia coli ( n = 33), an intraperitoneal bacterial inoculum ( n = 7), or an intrauterine injection of a sterile solution ( n = 14). RESULTS: Delivery within 48 hours of surgery occurred in 91% of mice after intrauterine bacteria, in 0% after intraperitoneal bacteria, and in 7% after sterile intrauterine injection ( p < 0.001). Intrauterine bacterial inoculation produced systemic infection (i.e., recovery of organisms from culture of the heart) in 50% of animals post partum. Intraperitoneal bacteria and intrauterine saline solution injections resulted in systemic infection rates of 20% and 0%, respectively, 48 hours after surgery. Five of seven animals injected with bacteria into the uterus had histologic evidence of metritis, mild in all cases. Intrauterine bacterial inoculation resulted in induction of ribonucleic acid transcripts for tumor necrosis factor-α, interleukin-1α, interleukin-1β, and cyclooxygenase-2. CONCLUSIONS: Intrauterine inoculation with Escherichia coli in mice leads to preterm delivery and the local induction of factors known to be involved in human preterm labor with infection. The observation that intraperitoneal bacterial inoculation does not result in preterm delivery suggests that in this model labor is the product of a local (uterine) stimulus.
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STUDY DESIGN: Fifty-four female CD-1 mice at 75% of the length of the gestational period (14.5 days) received either an intrauterine bacterial inoculum of 2 to 10 × 10 3 Escherichia coli ( n = 33), an intraperitoneal bacterial inoculum ( n = 7), or an intrauterine injection of a sterile solution ( n = 14). RESULTS: Delivery within 48 hours of surgery occurred in 91% of mice after intrauterine bacteria, in 0% after intraperitoneal bacteria, and in 7% after sterile intrauterine injection ( p &lt; 0.001). Intrauterine bacterial inoculation produced systemic infection (i.e., recovery of organisms from culture of the heart) in 50% of animals post partum. Intraperitoneal bacteria and intrauterine saline solution injections resulted in systemic infection rates of 20% and 0%, respectively, 48 hours after surgery. Five of seven animals injected with bacteria into the uterus had histologic evidence of metritis, mild in all cases. Intrauterine bacterial inoculation resulted in induction of ribonucleic acid transcripts for tumor necrosis factor-α, interleukin-1α, interleukin-1β, and cyclooxygenase-2. CONCLUSIONS: Intrauterine inoculation with Escherichia coli in mice leads to preterm delivery and the local induction of factors known to be involved in human preterm labor with infection. The observation that intraperitoneal bacterial inoculation does not result in preterm delivery suggests that in this model labor is the product of a local (uterine) stimulus.</description><identifier>ISSN: 0002-9378</identifier><identifier>EISSN: 1097-6868</identifier><identifier>DOI: 10.1016/0002-9378(95)90503-0</identifier><identifier>PMID: 7538729</identifier><identifier>CODEN: AJOGAH</identifier><language>eng</language><publisher>Philadelphia, PA: Mosby, Inc</publisher><subject>Animals ; Biological and medical sciences ; Chi-Square Distribution ; cytokines ; Disease Models, Animal ; Diseases of mother, fetus and pregnancy ; Escherichia coli Infections - complications ; Escherichia coli Infections - metabolism ; Escherichia coli Infections - microbiology ; Female ; Gynecology. Andrology. Obstetrics ; Interleukin-1 - biosynthesis ; Intrauterine infection ; Medical sciences ; Mice ; Mice, Inbred Strains ; mouse ; Obstetric Labor, Premature - etiology ; Obstetric Labor, Premature - metabolism ; Pregnancy ; Pregnancy Complications, Infectious - metabolism ; Pregnancy Complications, Infectious - microbiology ; Pregnancy. Fetus. 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STUDY DESIGN: Fifty-four female CD-1 mice at 75% of the length of the gestational period (14.5 days) received either an intrauterine bacterial inoculum of 2 to 10 × 10 3 Escherichia coli ( n = 33), an intraperitoneal bacterial inoculum ( n = 7), or an intrauterine injection of a sterile solution ( n = 14). RESULTS: Delivery within 48 hours of surgery occurred in 91% of mice after intrauterine bacteria, in 0% after intraperitoneal bacteria, and in 7% after sterile intrauterine injection ( p &lt; 0.001). Intrauterine bacterial inoculation produced systemic infection (i.e., recovery of organisms from culture of the heart) in 50% of animals post partum. Intraperitoneal bacteria and intrauterine saline solution injections resulted in systemic infection rates of 20% and 0%, respectively, 48 hours after surgery. Five of seven animals injected with bacteria into the uterus had histologic evidence of metritis, mild in all cases. Intrauterine bacterial inoculation resulted in induction of ribonucleic acid transcripts for tumor necrosis factor-α, interleukin-1α, interleukin-1β, and cyclooxygenase-2. CONCLUSIONS: Intrauterine inoculation with Escherichia coli in mice leads to preterm delivery and the local induction of factors known to be involved in human preterm labor with infection. The observation that intraperitoneal bacterial inoculation does not result in preterm delivery suggests that in this model labor is the product of a local (uterine) stimulus.</description><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Chi-Square Distribution</subject><subject>cytokines</subject><subject>Disease Models, Animal</subject><subject>Diseases of mother, fetus and pregnancy</subject><subject>Escherichia coli Infections - complications</subject><subject>Escherichia coli Infections - metabolism</subject><subject>Escherichia coli Infections - microbiology</subject><subject>Female</subject><subject>Gynecology. Andrology. Obstetrics</subject><subject>Interleukin-1 - biosynthesis</subject><subject>Intrauterine infection</subject><subject>Medical sciences</subject><subject>Mice</subject><subject>Mice, Inbred Strains</subject><subject>mouse</subject><subject>Obstetric Labor, Premature - etiology</subject><subject>Obstetric Labor, Premature - metabolism</subject><subject>Pregnancy</subject><subject>Pregnancy Complications, Infectious - metabolism</subject><subject>Pregnancy Complications, Infectious - microbiology</subject><subject>Pregnancy. Fetus. Placenta</subject><subject>preterm delivery</subject><subject>Prostaglandin-Endoperoxide Synthases - biosynthesis</subject><subject>RNA - metabolism</subject><subject>Tumor Necrosis Factor-alpha - biosynthesis</subject><subject>Uterine Diseases - complications</subject><subject>Uterine Diseases - metabolism</subject><subject>Uterine Diseases - microbiology</subject><issn>0002-9378</issn><issn>1097-6868</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1995</creationdate><recordtype>article</recordtype><recordid>eNp9kE1LAzEURYMotVb_gcIsRHQx-pJpJsmmUIpfUHCj65BmXiAyHzWZFvrvzdjSpavwck_uC4eQawqPFGj5BAAsV4WQ94o_KOBQ5HBCxhSUyEtZylMyPiLn5CLG72Fkio3ISPBCCqbGZDbPmq7COutc5ts-mE2PwbeYBoe2912bmbbK1gHTfZMl0m8x7FKcNd7iJTlzpo54dTgn5Ovl-XPxli8_Xt8X82Vup5z1uXIwFRVaVkxpCUgtd1KuGJcgDMrCicLiCsEooFwyEGBApvWlkaAcBSgm5G7fuw7dzwZjrxsfLda1abHbRC0Ek5JRnsDpHrShizGg0-vgGxN2moIetOlBgh6caMX1nzY99N8c-jerBqvjo4OnlN8echOtqV0wrfXxiBW8LIGXCZvtMUwuth6DjtZja7HyIdnUVef__8cv1SeHWQ</recordid><startdate>19950501</startdate><enddate>19950501</enddate><creator>Hirsch, Emmet</creator><creator>Saotome, Ichiko</creator><creator>Hirsch, David</creator><general>Mosby, Inc</general><general>Elsevier</general><scope>IQODW</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>19950501</creationdate><title>A model of intrauterine infection and preterm delivery in mice</title><author>Hirsch, Emmet ; Saotome, Ichiko ; Hirsch, David</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c452t-9f047dec234160e1c5f88b25807ae83f73cebe0a901582070a08fec6a809f1003</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1995</creationdate><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Chi-Square Distribution</topic><topic>cytokines</topic><topic>Disease Models, Animal</topic><topic>Diseases of mother, fetus and pregnancy</topic><topic>Escherichia coli Infections - complications</topic><topic>Escherichia coli Infections - metabolism</topic><topic>Escherichia coli Infections - microbiology</topic><topic>Female</topic><topic>Gynecology. Andrology. Obstetrics</topic><topic>Interleukin-1 - biosynthesis</topic><topic>Intrauterine infection</topic><topic>Medical sciences</topic><topic>Mice</topic><topic>Mice, Inbred Strains</topic><topic>mouse</topic><topic>Obstetric Labor, Premature - etiology</topic><topic>Obstetric Labor, Premature - metabolism</topic><topic>Pregnancy</topic><topic>Pregnancy Complications, Infectious - metabolism</topic><topic>Pregnancy Complications, Infectious - microbiology</topic><topic>Pregnancy. Fetus. Placenta</topic><topic>preterm delivery</topic><topic>Prostaglandin-Endoperoxide Synthases - biosynthesis</topic><topic>RNA - metabolism</topic><topic>Tumor Necrosis Factor-alpha - biosynthesis</topic><topic>Uterine Diseases - complications</topic><topic>Uterine Diseases - metabolism</topic><topic>Uterine Diseases - microbiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hirsch, Emmet</creatorcontrib><creatorcontrib>Saotome, Ichiko</creatorcontrib><creatorcontrib>Hirsch, David</creatorcontrib><collection>Pascal-Francis</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>American journal of obstetrics and gynecology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hirsch, Emmet</au><au>Saotome, Ichiko</au><au>Hirsch, David</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A model of intrauterine infection and preterm delivery in mice</atitle><jtitle>American journal of obstetrics and gynecology</jtitle><addtitle>Am J Obstet Gynecol</addtitle><date>1995-05-01</date><risdate>1995</risdate><volume>172</volume><issue>5</issue><spage>1598</spage><epage>1603</epage><pages>1598-1603</pages><issn>0002-9378</issn><eissn>1097-6868</eissn><coden>AJOGAH</coden><abstract>OBJECTIVE: Our purpose was to determine whether intrauterine bacterial inoculation leads to preterm delivery in mice. STUDY DESIGN: Fifty-four female CD-1 mice at 75% of the length of the gestational period (14.5 days) received either an intrauterine bacterial inoculum of 2 to 10 × 10 3 Escherichia coli ( n = 33), an intraperitoneal bacterial inoculum ( n = 7), or an intrauterine injection of a sterile solution ( n = 14). RESULTS: Delivery within 48 hours of surgery occurred in 91% of mice after intrauterine bacteria, in 0% after intraperitoneal bacteria, and in 7% after sterile intrauterine injection ( p &lt; 0.001). Intrauterine bacterial inoculation produced systemic infection (i.e., recovery of organisms from culture of the heart) in 50% of animals post partum. Intraperitoneal bacteria and intrauterine saline solution injections resulted in systemic infection rates of 20% and 0%, respectively, 48 hours after surgery. Five of seven animals injected with bacteria into the uterus had histologic evidence of metritis, mild in all cases. Intrauterine bacterial inoculation resulted in induction of ribonucleic acid transcripts for tumor necrosis factor-α, interleukin-1α, interleukin-1β, and cyclooxygenase-2. CONCLUSIONS: Intrauterine inoculation with Escherichia coli in mice leads to preterm delivery and the local induction of factors known to be involved in human preterm labor with infection. The observation that intraperitoneal bacterial inoculation does not result in preterm delivery suggests that in this model labor is the product of a local (uterine) stimulus.</abstract><cop>Philadelphia, PA</cop><pub>Mosby, Inc</pub><pmid>7538729</pmid><doi>10.1016/0002-9378(95)90503-0</doi><tpages>6</tpages></addata></record>
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subjects Animals
Biological and medical sciences
Chi-Square Distribution
cytokines
Disease Models, Animal
Diseases of mother, fetus and pregnancy
Escherichia coli Infections - complications
Escherichia coli Infections - metabolism
Escherichia coli Infections - microbiology
Female
Gynecology. Andrology. Obstetrics
Interleukin-1 - biosynthesis
Intrauterine infection
Medical sciences
Mice
Mice, Inbred Strains
mouse
Obstetric Labor, Premature - etiology
Obstetric Labor, Premature - metabolism
Pregnancy
Pregnancy Complications, Infectious - metabolism
Pregnancy Complications, Infectious - microbiology
Pregnancy. Fetus. Placenta
preterm delivery
Prostaglandin-Endoperoxide Synthases - biosynthesis
RNA - metabolism
Tumor Necrosis Factor-alpha - biosynthesis
Uterine Diseases - complications
Uterine Diseases - metabolism
Uterine Diseases - microbiology
title A model of intrauterine infection and preterm delivery in mice
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