Effect of reduced inspired oxygen on fetal growth and maternal glucose metabolism in rat pregnancy
The effect of prolonged exposure to a reduced fraction of inspired oxygen ([FiO 2] 0.17 for 3 days) on maternal glucose kinetics, placental glucose transporters GLUT1 and GLUT3, and fetal growth was examined in rat pregnancy. Arterial and venous catheters were placed 3 days before the study. [3- 3H]...
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Veröffentlicht in: | Metabolism, clinical and experimental clinical and experimental, 1999-06, Vol.48 (6), p.738-744 |
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creator | Saker, Firas Voora, Deepak M. Mahajan, Supriya D. Kiliç, Ílknur Ismail-Beigi, Faramarz Kalhan, Satish C. |
description | The effect of prolonged exposure to a reduced fraction of inspired oxygen ([FiO
2] 0.17 for 3 days) on maternal glucose kinetics, placental glucose transporters GLUT1 and GLUT3, and fetal growth was examined in rat pregnancy. Arterial and venous catheters were placed 3 days before the study. [3-
3H]glucose tracer and deuterium labeling of water were used to measure the rates of glucose turnover and gluconeogenesis (GNG), respectively. Glucose uptake by maternal tissues was measured using [
14C]2-deoxyglucose. Exposure to a reduced FiO
2 resulted in a significant decrease (mean ± SE) in fetal weight (room air, 4.02 ± 0.04 g; 0.17 FiO
2, 3.27 ± 0.6 g,
P < .02). There was a significant increase in the maternal-fetal glucose gradient (maternal-fetal glucose ratio: room air, 1.48 ± 0.11; 0.17 FiO
2, 2.26 ± 0.24,
P < .05), but there was no change in the maternal or fetal blood lactate concentration. No significant change in maternal blood pH was observed; however, a significant decrease in the blood partial pressure of O
2 (PO
2) occurred (room air, 97 ± 0.5 torr; 0.17 FiO
2, 81 ± 1.8) on day 3. There was no change in the rate of turnover of glucose or GNG in the maternal compartment, nor was there any effect on glucose uptake by the maternal tissues. Placental GLUT1 and GLUT3 mRNA were not different in the control or experimental animals. We conclude that a mild reduction in the FiO
2 for 3 days in rat pregnancy results in a significant fetal growth restriction that is not related to any observed alteration in maternal glucose metabolism. The lower glucose concentration in the fetal blood may be the consequence of an increase in fetal glucose metabolism, thereby resulting in an increased maternal-fetal gradient of glucose. |
doi_str_mv | 10.1016/S0026-0495(99)90173-7 |
format | Article |
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2] 0.17 for 3 days) on maternal glucose kinetics, placental glucose transporters GLUT1 and GLUT3, and fetal growth was examined in rat pregnancy. Arterial and venous catheters were placed 3 days before the study. [3-
3H]glucose tracer and deuterium labeling of water were used to measure the rates of glucose turnover and gluconeogenesis (GNG), respectively. Glucose uptake by maternal tissues was measured using [
14C]2-deoxyglucose. Exposure to a reduced FiO
2 resulted in a significant decrease (mean ± SE) in fetal weight (room air, 4.02 ± 0.04 g; 0.17 FiO
2, 3.27 ± 0.6 g,
P < .02). There was a significant increase in the maternal-fetal glucose gradient (maternal-fetal glucose ratio: room air, 1.48 ± 0.11; 0.17 FiO
2, 2.26 ± 0.24,
P < .05), but there was no change in the maternal or fetal blood lactate concentration. No significant change in maternal blood pH was observed; however, a significant decrease in the blood partial pressure of O
2 (PO
2) occurred (room air, 97 ± 0.5 torr; 0.17 FiO
2, 81 ± 1.8) on day 3. There was no change in the rate of turnover of glucose or GNG in the maternal compartment, nor was there any effect on glucose uptake by the maternal tissues. Placental GLUT1 and GLUT3 mRNA were not different in the control or experimental animals. We conclude that a mild reduction in the FiO
2 for 3 days in rat pregnancy results in a significant fetal growth restriction that is not related to any observed alteration in maternal glucose metabolism. The lower glucose concentration in the fetal blood may be the consequence of an increase in fetal glucose metabolism, thereby resulting in an increased maternal-fetal gradient of glucose.</description><identifier>ISSN: 0026-0495</identifier><identifier>EISSN: 1532-8600</identifier><identifier>DOI: 10.1016/S0026-0495(99)90173-7</identifier><identifier>PMID: 10381148</identifier><language>eng</language><publisher>New York, NY: Elsevier Inc</publisher><subject>Animals ; Biological and medical sciences ; Blood Glucose - metabolism ; Diseases of mother, fetus and pregnancy ; Embryonic and Fetal Development ; Female ; Fetus - metabolism ; Glucose Transporter Type 1 ; Glucose Transporter Type 3 ; Gynecology. Andrology. Obstetrics ; Hypoxia - blood ; Kinetics ; Lactic Acid - blood ; Medical sciences ; Monosaccharide Transport Proteins - metabolism ; Nerve Tissue Proteins ; Oxygen - blood ; Pregnancy ; Pregnancy, Animal - blood ; Pregnancy. Fetus. Placenta ; Rats ; Rats, Sprague-Dawley</subject><ispartof>Metabolism, clinical and experimental, 1999-06, Vol.48 (6), p.738-744</ispartof><rights>1999</rights><rights>1999 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c442t-3556b35bdc2ae52767b96e2fd4d5d06d09dd0b3946744c8777d2defbdc5ddf433</citedby><cites>FETCH-LOGICAL-c442t-3556b35bdc2ae52767b96e2fd4d5d06d09dd0b3946744c8777d2defbdc5ddf433</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0026049599901737$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=1863229$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/10381148$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Saker, Firas</creatorcontrib><creatorcontrib>Voora, Deepak M.</creatorcontrib><creatorcontrib>Mahajan, Supriya D.</creatorcontrib><creatorcontrib>Kiliç, Ílknur</creatorcontrib><creatorcontrib>Ismail-Beigi, Faramarz</creatorcontrib><creatorcontrib>Kalhan, Satish C.</creatorcontrib><title>Effect of reduced inspired oxygen on fetal growth and maternal glucose metabolism in rat pregnancy</title><title>Metabolism, clinical and experimental</title><addtitle>Metabolism</addtitle><description>The effect of prolonged exposure to a reduced fraction of inspired oxygen ([FiO
2] 0.17 for 3 days) on maternal glucose kinetics, placental glucose transporters GLUT1 and GLUT3, and fetal growth was examined in rat pregnancy. Arterial and venous catheters were placed 3 days before the study. [3-
3H]glucose tracer and deuterium labeling of water were used to measure the rates of glucose turnover and gluconeogenesis (GNG), respectively. Glucose uptake by maternal tissues was measured using [
14C]2-deoxyglucose. Exposure to a reduced FiO
2 resulted in a significant decrease (mean ± SE) in fetal weight (room air, 4.02 ± 0.04 g; 0.17 FiO
2, 3.27 ± 0.6 g,
P < .02). There was a significant increase in the maternal-fetal glucose gradient (maternal-fetal glucose ratio: room air, 1.48 ± 0.11; 0.17 FiO
2, 2.26 ± 0.24,
P < .05), but there was no change in the maternal or fetal blood lactate concentration. No significant change in maternal blood pH was observed; however, a significant decrease in the blood partial pressure of O
2 (PO
2) occurred (room air, 97 ± 0.5 torr; 0.17 FiO
2, 81 ± 1.8) on day 3. There was no change in the rate of turnover of glucose or GNG in the maternal compartment, nor was there any effect on glucose uptake by the maternal tissues. Placental GLUT1 and GLUT3 mRNA were not different in the control or experimental animals. We conclude that a mild reduction in the FiO
2 for 3 days in rat pregnancy results in a significant fetal growth restriction that is not related to any observed alteration in maternal glucose metabolism. The lower glucose concentration in the fetal blood may be the consequence of an increase in fetal glucose metabolism, thereby resulting in an increased maternal-fetal gradient of glucose.</description><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Blood Glucose - metabolism</subject><subject>Diseases of mother, fetus and pregnancy</subject><subject>Embryonic and Fetal Development</subject><subject>Female</subject><subject>Fetus - metabolism</subject><subject>Glucose Transporter Type 1</subject><subject>Glucose Transporter Type 3</subject><subject>Gynecology. Andrology. Obstetrics</subject><subject>Hypoxia - blood</subject><subject>Kinetics</subject><subject>Lactic Acid - blood</subject><subject>Medical sciences</subject><subject>Monosaccharide Transport Proteins - metabolism</subject><subject>Nerve Tissue Proteins</subject><subject>Oxygen - blood</subject><subject>Pregnancy</subject><subject>Pregnancy, Animal - blood</subject><subject>Pregnancy. Fetus. Placenta</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><issn>0026-0495</issn><issn>1532-8600</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1999</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkEtv1DAURi0EokPhJ4C8QBUsAn47XiFUFahUiQWwthz7ejBK4sFOoPPv8XRGwK4r61rnu4-D0HNK3lBC1dsvhDDVEWHkK2NeG0I17_QDtKGSs65XhDxEm7_IGXpS6w9CiNa9eozOKOE9paLfoOEqRvALzhEXCKuHgNNcd6kVON_utzDjPOMIixvxtuTfy3fs5oAnt0CZD3_j6nMFPDViyGOqU8vj4ha8K7Cd3ez3T9Gj6MYKz07vOfr24err5afu5vPH68v3N50Xgi0dl1INXA7BMweSaaUHo4DFIIIMRAViQiADN0JpIXyvtQ4sQGy8DCEKzs_RxbHvruSfK9TFTql6GEc3Q16rVaYXPRekgfII-pJrLRDtrqTJlb2lxB7k2ju59mDOGmPv5Frdci9OA9ZhgvBf6mizAS9PgKvejbG081P9x_WKM2Ya9u6IQbPxK0Gx1SeYm_um3S825HTPJn8AytuXfA</recordid><startdate>19990601</startdate><enddate>19990601</enddate><creator>Saker, Firas</creator><creator>Voora, Deepak M.</creator><creator>Mahajan, Supriya D.</creator><creator>Kiliç, Ílknur</creator><creator>Ismail-Beigi, Faramarz</creator><creator>Kalhan, Satish C.</creator><general>Elsevier 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>19990601</creationdate><title>Effect of reduced inspired oxygen on fetal growth and maternal glucose metabolism in rat pregnancy</title><author>Saker, Firas ; Voora, Deepak M. ; Mahajan, Supriya D. ; Kiliç, Ílknur ; Ismail-Beigi, Faramarz ; Kalhan, Satish C.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c442t-3556b35bdc2ae52767b96e2fd4d5d06d09dd0b3946744c8777d2defbdc5ddf433</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1999</creationdate><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Blood Glucose - metabolism</topic><topic>Diseases of mother, fetus and pregnancy</topic><topic>Embryonic and Fetal Development</topic><topic>Female</topic><topic>Fetus - metabolism</topic><topic>Glucose Transporter Type 1</topic><topic>Glucose Transporter Type 3</topic><topic>Gynecology. Andrology. Obstetrics</topic><topic>Hypoxia - blood</topic><topic>Kinetics</topic><topic>Lactic Acid - blood</topic><topic>Medical sciences</topic><topic>Monosaccharide Transport Proteins - metabolism</topic><topic>Nerve Tissue Proteins</topic><topic>Oxygen - blood</topic><topic>Pregnancy</topic><topic>Pregnancy, Animal - blood</topic><topic>Pregnancy. Fetus. Placenta</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Saker, Firas</creatorcontrib><creatorcontrib>Voora, Deepak M.</creatorcontrib><creatorcontrib>Mahajan, Supriya D.</creatorcontrib><creatorcontrib>Kiliç, Ílknur</creatorcontrib><creatorcontrib>Ismail-Beigi, Faramarz</creatorcontrib><creatorcontrib>Kalhan, Satish C.</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>Metabolism, clinical and experimental</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Saker, Firas</au><au>Voora, Deepak M.</au><au>Mahajan, Supriya D.</au><au>Kiliç, Ílknur</au><au>Ismail-Beigi, Faramarz</au><au>Kalhan, Satish C.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Effect of reduced inspired oxygen on fetal growth and maternal glucose metabolism in rat pregnancy</atitle><jtitle>Metabolism, clinical and experimental</jtitle><addtitle>Metabolism</addtitle><date>1999-06-01</date><risdate>1999</risdate><volume>48</volume><issue>6</issue><spage>738</spage><epage>744</epage><pages>738-744</pages><issn>0026-0495</issn><eissn>1532-8600</eissn><abstract>The effect of prolonged exposure to a reduced fraction of inspired oxygen ([FiO
2] 0.17 for 3 days) on maternal glucose kinetics, placental glucose transporters GLUT1 and GLUT3, and fetal growth was examined in rat pregnancy. Arterial and venous catheters were placed 3 days before the study. [3-
3H]glucose tracer and deuterium labeling of water were used to measure the rates of glucose turnover and gluconeogenesis (GNG), respectively. Glucose uptake by maternal tissues was measured using [
14C]2-deoxyglucose. Exposure to a reduced FiO
2 resulted in a significant decrease (mean ± SE) in fetal weight (room air, 4.02 ± 0.04 g; 0.17 FiO
2, 3.27 ± 0.6 g,
P < .02). There was a significant increase in the maternal-fetal glucose gradient (maternal-fetal glucose ratio: room air, 1.48 ± 0.11; 0.17 FiO
2, 2.26 ± 0.24,
P < .05), but there was no change in the maternal or fetal blood lactate concentration. No significant change in maternal blood pH was observed; however, a significant decrease in the blood partial pressure of O
2 (PO
2) occurred (room air, 97 ± 0.5 torr; 0.17 FiO
2, 81 ± 1.8) on day 3. There was no change in the rate of turnover of glucose or GNG in the maternal compartment, nor was there any effect on glucose uptake by the maternal tissues. Placental GLUT1 and GLUT3 mRNA were not different in the control or experimental animals. We conclude that a mild reduction in the FiO
2 for 3 days in rat pregnancy results in a significant fetal growth restriction that is not related to any observed alteration in maternal glucose metabolism. The lower glucose concentration in the fetal blood may be the consequence of an increase in fetal glucose metabolism, thereby resulting in an increased maternal-fetal gradient of glucose.</abstract><cop>New York, NY</cop><pub>Elsevier Inc</pub><pmid>10381148</pmid><doi>10.1016/S0026-0495(99)90173-7</doi><tpages>7</tpages></addata></record> |
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subjects | Animals Biological and medical sciences Blood Glucose - metabolism Diseases of mother, fetus and pregnancy Embryonic and Fetal Development Female Fetus - metabolism Glucose Transporter Type 1 Glucose Transporter Type 3 Gynecology. Andrology. Obstetrics Hypoxia - blood Kinetics Lactic Acid - blood Medical sciences Monosaccharide Transport Proteins - metabolism Nerve Tissue Proteins Oxygen - blood Pregnancy Pregnancy, Animal - blood Pregnancy. Fetus. Placenta Rats Rats, Sprague-Dawley |
title | Effect of reduced inspired oxygen on fetal growth and maternal glucose metabolism in rat pregnancy |
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