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Fetal brain sparing in a mouse model of chronic maternal hypoxia
Hypoxic stress is a common occurrence during human pregnancy, yet little is known about its effects on the fetal brain. This study examined the fetal hemodynamic responses to chronic hypoxia in an experimental mouse model of chronic maternal hypoxia (11% O2 from E14.5 to E17.5). Using high-frequency...
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Published in: | Journal of cerebral blood flow and metabolism 2019-06, Vol.39 (6), p.1172-1184 |
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container_title | Journal of cerebral blood flow and metabolism |
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creator | Cahill, Lindsay S Hoggarth, Johnathan Lerch, Jason P Seed, Mike Macgowan, Christopher K Sled, John G |
description | Hypoxic stress is a common occurrence during human pregnancy, yet little is known about its effects on the fetal brain. This study examined the fetal hemodynamic responses to chronic hypoxia in an experimental mouse model of chronic maternal hypoxia (11% O2 from E14.5 to E17.5). Using high-frequency Doppler ultrasound, we found fetal cerebral and ductus venosus blood flow were both elevated by 69% and pulmonary blood flow was decreased by 62% in the fetuses exposed to chronic hypoxia compared to controls. This demonstrates that brain sparing persists during chronic fetal hypoxia and is mediated by “streaming,” where highly oxygenated blood preferentially flows through the ductus venosus towards the cerebral circulation, bypassing the liver and the lungs. Consistent with these changes in blood flow, the fetal brain volume measured by MRI is preserved, while the liver and lung volumes decreased compared to controls. However, hypoxia exposed fetuses were rendered vulnerable to an acute hypoxic challenge (8% O2 for 3 min), demonstrating global blood flow decreases consistent with imminent fetal demise rather than elevated cerebral blood flow. Despite this vulnerability, there were no differences in adult brain morphology in the mice exposed to chronic maternal hypoxia compared to controls. |
doi_str_mv | 10.1177/0271678X17750324 |
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This study examined the fetal hemodynamic responses to chronic hypoxia in an experimental mouse model of chronic maternal hypoxia (11% O2 from E14.5 to E17.5). Using high-frequency Doppler ultrasound, we found fetal cerebral and ductus venosus blood flow were both elevated by 69% and pulmonary blood flow was decreased by 62% in the fetuses exposed to chronic hypoxia compared to controls. This demonstrates that brain sparing persists during chronic fetal hypoxia and is mediated by “streaming,” where highly oxygenated blood preferentially flows through the ductus venosus towards the cerebral circulation, bypassing the liver and the lungs. Consistent with these changes in blood flow, the fetal brain volume measured by MRI is preserved, while the liver and lung volumes decreased compared to controls. However, hypoxia exposed fetuses were rendered vulnerable to an acute hypoxic challenge (8% O2 for 3 min), demonstrating global blood flow decreases consistent with imminent fetal demise rather than elevated cerebral blood flow. 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This study examined the fetal hemodynamic responses to chronic hypoxia in an experimental mouse model of chronic maternal hypoxia (11% O2 from E14.5 to E17.5). Using high-frequency Doppler ultrasound, we found fetal cerebral and ductus venosus blood flow were both elevated by 69% and pulmonary blood flow was decreased by 62% in the fetuses exposed to chronic hypoxia compared to controls. This demonstrates that brain sparing persists during chronic fetal hypoxia and is mediated by “streaming,” where highly oxygenated blood preferentially flows through the ductus venosus towards the cerebral circulation, bypassing the liver and the lungs. Consistent with these changes in blood flow, the fetal brain volume measured by MRI is preserved, while the liver and lung volumes decreased compared to controls. However, hypoxia exposed fetuses were rendered vulnerable to an acute hypoxic challenge (8% O2 for 3 min), demonstrating global blood flow decreases consistent with imminent fetal demise rather than elevated cerebral blood flow. Despite this vulnerability, there were no differences in adult brain morphology in the mice exposed to chronic maternal hypoxia compared to controls.</description><subject>Animals</subject><subject>Blood Flow Velocity</subject><subject>Brain - diagnostic imaging</subject><subject>Brain - physiopathology</subject><subject>Cerebrovascular Circulation</subject><subject>Disease Models, Animal</subject><subject>Female</subject><subject>Fetal Hypoxia - physiopathology</subject><subject>Fetus - physiopathology</subject><subject>Hemodynamics</subject><subject>Magnetic Resonance Imaging</subject><subject>Mice</subject><subject>Original</subject><subject>Pregnancy</subject><subject>Ultrasonography - methods</subject><issn>0271-678X</issn><issn>1559-7016</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><recordid>eNp1UEtLxDAQDqK46-rdk_TopZpJm6a5iCK-QPCi4C1Ms9PdLm2zJl3Rf2-WVVHBy8zA95iZj7FD4CcASp1yoaBQ5XOcJc9EvsXGIKVOFYdim43XcLrGR2wvhAXnvMyk3GUjoSOS8XzMzq9pwDapPDZ9Epbom36WxBGTzq0CxTqlNnF1Yufe9Y1NOhzI91Eyf1-6twb32U6NbaCDzz5hT9dXj5e36f3Dzd3lxX1q8xKGlEjBVOfE6woJZaF0JcRUZBVAYXkmSyGKUmW5EKUlAGtB58AlctSAWVVnE3a28V2uqo6mlvrBY2uWvunQvxuHjfmN9M3czNyrKWSuQBfR4PjTwLuXFYXBdE2w1LbYU3zVgFZaFyWPV0wY31CtdyF4qr_XADfr4M3f4KPk6Od534KvpCMh3RACzsgs3GodYvjf8APok4sb</recordid><startdate>20190601</startdate><enddate>20190601</enddate><creator>Cahill, Lindsay S</creator><creator>Hoggarth, Johnathan</creator><creator>Lerch, Jason P</creator><creator>Seed, Mike</creator><creator>Macgowan, Christopher K</creator><creator>Sled, John G</creator><general>SAGE Publications</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>7X8</scope><scope>5PM</scope></search><sort><creationdate>20190601</creationdate><title>Fetal brain sparing in a mouse model of chronic maternal hypoxia</title><author>Cahill, Lindsay S ; Hoggarth, Johnathan ; Lerch, Jason P ; Seed, Mike ; Macgowan, Christopher K ; Sled, John G</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c481t-ee71d94e0fbaea5679b22d23b116c03582268734228ce11cc194105a0a91a3bf3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Animals</topic><topic>Blood Flow Velocity</topic><topic>Brain - diagnostic imaging</topic><topic>Brain - physiopathology</topic><topic>Cerebrovascular Circulation</topic><topic>Disease Models, Animal</topic><topic>Female</topic><topic>Fetal Hypoxia - physiopathology</topic><topic>Fetus - physiopathology</topic><topic>Hemodynamics</topic><topic>Magnetic Resonance Imaging</topic><topic>Mice</topic><topic>Original</topic><topic>Pregnancy</topic><topic>Ultrasonography - methods</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Cahill, Lindsay S</creatorcontrib><creatorcontrib>Hoggarth, Johnathan</creatorcontrib><creatorcontrib>Lerch, Jason P</creatorcontrib><creatorcontrib>Seed, Mike</creatorcontrib><creatorcontrib>Macgowan, Christopher K</creatorcontrib><creatorcontrib>Sled, John G</creatorcontrib><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><collection>PubMed Central (Full Participant titles)</collection><jtitle>Journal of cerebral blood flow and metabolism</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Cahill, Lindsay S</au><au>Hoggarth, Johnathan</au><au>Lerch, Jason P</au><au>Seed, Mike</au><au>Macgowan, Christopher K</au><au>Sled, John G</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Fetal brain sparing in a mouse model of chronic maternal hypoxia</atitle><jtitle>Journal of cerebral blood flow and metabolism</jtitle><addtitle>J Cereb Blood Flow Metab</addtitle><date>2019-06-01</date><risdate>2019</risdate><volume>39</volume><issue>6</issue><spage>1172</spage><epage>1184</epage><pages>1172-1184</pages><issn>0271-678X</issn><eissn>1559-7016</eissn><abstract>Hypoxic stress is a common occurrence during human pregnancy, yet little is known about its effects on the fetal brain. This study examined the fetal hemodynamic responses to chronic hypoxia in an experimental mouse model of chronic maternal hypoxia (11% O2 from E14.5 to E17.5). Using high-frequency Doppler ultrasound, we found fetal cerebral and ductus venosus blood flow were both elevated by 69% and pulmonary blood flow was decreased by 62% in the fetuses exposed to chronic hypoxia compared to controls. This demonstrates that brain sparing persists during chronic fetal hypoxia and is mediated by “streaming,” where highly oxygenated blood preferentially flows through the ductus venosus towards the cerebral circulation, bypassing the liver and the lungs. Consistent with these changes in blood flow, the fetal brain volume measured by MRI is preserved, while the liver and lung volumes decreased compared to controls. However, hypoxia exposed fetuses were rendered vulnerable to an acute hypoxic challenge (8% O2 for 3 min), demonstrating global blood flow decreases consistent with imminent fetal demise rather than elevated cerebral blood flow. Despite this vulnerability, there were no differences in adult brain morphology in the mice exposed to chronic maternal hypoxia compared to controls.</abstract><cop>London, England</cop><pub>SAGE Publications</pub><pmid>29271304</pmid><doi>10.1177/0271678X17750324</doi><tpages>13</tpages><oa>free_for_read</oa></addata></record> |
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source | Sage Journals Online; PubMed Central |
subjects | Animals Blood Flow Velocity Brain - diagnostic imaging Brain - physiopathology Cerebrovascular Circulation Disease Models, Animal Female Fetal Hypoxia - physiopathology Fetus - physiopathology Hemodynamics Magnetic Resonance Imaging Mice Original Pregnancy Ultrasonography - methods |
title | Fetal brain sparing in a mouse model of chronic maternal hypoxia |
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