Feto-Placental 11beta-hydroxysteroid dehydrogenase2 activity affect fetal growth
Project/Area Number |
24591596
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Research Category |
Grant-in-Aid for Scientific Research (C)
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Allocation Type | Multi-year Fund |
Section | 一般 |
Research Field |
Embryonic/Neonatal medicine
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Research Institution | Asahikawa Medical College |
Principal Investigator |
NAGAYA Ken 旭川医科大学, 医学部, 講師 (80396382)
|
Project Period (FY) |
2012-04-01 – 2016-03-31
|
Project Status |
Completed (Fiscal Year 2015)
|
Budget Amount *help |
¥5,200,000 (Direct Cost: ¥4,000,000、Indirect Cost: ¥1,200,000)
Fiscal Year 2014: ¥2,080,000 (Direct Cost: ¥1,600,000、Indirect Cost: ¥480,000)
Fiscal Year 2013: ¥1,560,000 (Direct Cost: ¥1,200,000、Indirect Cost: ¥360,000)
Fiscal Year 2012: ¥1,560,000 (Direct Cost: ¥1,200,000、Indirect Cost: ¥360,000)
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Keywords | 胎児発育 / 11βハイドロキシステロイド脱水素酵素 / 胎児胎盤発育 / 胎児副腎機能 / 11βHSD2 |
Outline of Final Research Achievements |
Feto-Placental 11 β HSD2 controls glucocorticoid disclosure to fetus. We investigated the influence by which these give it to fetus growth. Placental HSD11B2 mRNA was employed as a placental 11βHSD2 activity. Although urinal cortisone/cortisol metabolism ratio(u-F/E) didn't correlate with placental HSD11B2 mRNA, we thought that u-F/E could estimate fetal 11βHSD2 activity. The placental HSD11B2 mRNA in SGA infants was significantly low compared with AGA infants. And, The placental HSD11B2 mRNA was correlated with SDS of the birth weight and birth head circumference respectively. u-F/E in SGA infants was significantly low compared with AGA infants. However, there was no correlation between urine F/E and fetal growth. These relations were admitted in girls.
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Report
(5 results)
Research Products
(1 results)