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Glucocorticoids induce corticosteroid-binding globulin biosynthesis by immature mouse liver and kidney
Marked changes in mouse corticosteroid-binding globulin (CBG) gene expression in the liver and kidney occur postnatally. To study the influence of glucocorticoids on the initiation of mouse CBG biosynthesis in these tissues during the first two weeks after birth, we administered dexamethasone (0.5 μ...
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Published in: | The Journal of steroid biochemistry and molecular biology 1997-02, Vol.60 (3), p.163-169 |
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description | Marked changes in mouse corticosteroid-binding globulin (CBG) gene expression in the liver and kidney occur postnatally. To study the influence of glucocorticoids on the initiation of mouse CBG biosynthesis in these tissues during the first two weeks after birth, we administered dexamethasone (0.5 μg/g body wt/day) to 4- and 11-day-old pups for three days. This resulted in higher serum CBG and hepatic CBG mRNA levels in animals, irrespective of their ages. Higher relative amounts of CBG mRNA in the kidneys of 14-day-old pups after three days of dexamethasone treatment coincided with higher amounts of intact and proteolytically cleaved CGB in their urine, and both are indicative of increased CGB production by the developing renal tubules. When an additional group of 11-day-old pups (
n = 4) was treated with 0.25 μg dexamethasone/g body weight per day for five days, this also resulted in significantly higher levels of serum CBG (
P < 0.01), hepatic CBG mRNA (
P < 0.01) and renal CBG mRNA (
P < 0.05), compared to littermates treated with the oil vehicle alone. In contrast, serum CBG levels progressively decreased in adult female mice during five days of treatment with 0.5 μg dexamethasone/g body weight per day. Taken together, these data indicate that glucocorticoids induce murine CBG gene expression in the immature liver and kidney, and support the concept that the effects of glucocorticoids on CBG gene expression are developmentally stage-specific. |
doi_str_mv | 10.1016/S0960-0760(96)00181-1 |
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n = 4) was treated with 0.25 μg dexamethasone/g body weight per day for five days, this also resulted in significantly higher levels of serum CBG (
P < 0.01), hepatic CBG mRNA (
P < 0.01) and renal CBG mRNA (
P < 0.05), compared to littermates treated with the oil vehicle alone. In contrast, serum CBG levels progressively decreased in adult female mice during five days of treatment with 0.5 μg dexamethasone/g body weight per day. Taken together, these data indicate that glucocorticoids induce murine CBG gene expression in the immature liver and kidney, and support the concept that the effects of glucocorticoids on CBG gene expression are developmentally stage-specific.</description><identifier>ISSN: 0960-0760</identifier><identifier>EISSN: 1879-1220</identifier><identifier>DOI: 10.1016/S0960-0760(96)00181-1</identifier><identifier>PMID: 9191973</identifier><language>eng</language><publisher>Oxford: Elsevier Ltd</publisher><subject>Adrenals. Interrenals ; Adrenocortical hormones. Regulation ; Age Factors ; Animals ; Biological and medical sciences ; Blotting, Western ; Body Weight ; Dexamethasone - pharmacology ; Female ; Fundamental and applied biological sciences. Psychology ; Gene Expression ; Glucocorticoids - pharmacology ; Kidney - metabolism ; Liver - metabolism ; Male ; Mice ; Mice, Inbred BALB C ; Pilot Projects ; RNA, Messenger - analysis ; Sex Factors ; Transcortin - biosynthesis ; Transcortin - genetics ; Transcortin - urine ; Vertebrates: endocrinology</subject><ispartof>The Journal of steroid biochemistry and molecular biology, 1997-02, Vol.60 (3), p.163-169</ispartof><rights>1997</rights><rights>1997 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c389t-b433ee8c04c10b586bd01befb7a08cfa97597250251c51dec3c3d8bfdcfb70203</citedby><cites>FETCH-LOGICAL-c389t-b433ee8c04c10b586bd01befb7a08cfa97597250251c51dec3c3d8bfdcfb70203</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=2676543$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/9191973$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Zhao, Xian-Feng</creatorcontrib><creatorcontrib>Scrocchi, Louise A.</creatorcontrib><creatorcontrib>Hammond, Geoffrey L.</creatorcontrib><title>Glucocorticoids induce corticosteroid-binding globulin biosynthesis by immature mouse liver and kidney</title><title>The Journal of steroid biochemistry and molecular biology</title><addtitle>J Steroid Biochem Mol Biol</addtitle><description>Marked changes in mouse corticosteroid-binding globulin (CBG) gene expression in the liver and kidney occur postnatally. To study the influence of glucocorticoids on the initiation of mouse CBG biosynthesis in these tissues during the first two weeks after birth, we administered dexamethasone (0.5 μg/g body wt/day) to 4- and 11-day-old pups for three days. This resulted in higher serum CBG and hepatic CBG mRNA levels in animals, irrespective of their ages. Higher relative amounts of CBG mRNA in the kidneys of 14-day-old pups after three days of dexamethasone treatment coincided with higher amounts of intact and proteolytically cleaved CGB in their urine, and both are indicative of increased CGB production by the developing renal tubules. When an additional group of 11-day-old pups (
n = 4) was treated with 0.25 μg dexamethasone/g body weight per day for five days, this also resulted in significantly higher levels of serum CBG (
P < 0.01), hepatic CBG mRNA (
P < 0.01) and renal CBG mRNA (
P < 0.05), compared to littermates treated with the oil vehicle alone. In contrast, serum CBG levels progressively decreased in adult female mice during five days of treatment with 0.5 μg dexamethasone/g body weight per day. Taken together, these data indicate that glucocorticoids induce murine CBG gene expression in the immature liver and kidney, and support the concept that the effects of glucocorticoids on CBG gene expression are developmentally stage-specific.</description><subject>Adrenals. Interrenals</subject><subject>Adrenocortical hormones. Regulation</subject><subject>Age Factors</subject><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Blotting, Western</subject><subject>Body Weight</subject><subject>Dexamethasone - pharmacology</subject><subject>Female</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Gene Expression</subject><subject>Glucocorticoids - pharmacology</subject><subject>Kidney - metabolism</subject><subject>Liver - metabolism</subject><subject>Male</subject><subject>Mice</subject><subject>Mice, Inbred BALB C</subject><subject>Pilot Projects</subject><subject>RNA, Messenger - analysis</subject><subject>Sex Factors</subject><subject>Transcortin - biosynthesis</subject><subject>Transcortin - genetics</subject><subject>Transcortin - urine</subject><subject>Vertebrates: endocrinology</subject><issn>0960-0760</issn><issn>1879-1220</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1997</creationdate><recordtype>article</recordtype><recordid>eNqFkE1r3DAQhkVoSTcfPyGgQyntwe3IXlvWqYTQpoVAD23PQhqNE7W2lEp2YP99tVmz1zAHwTvPjIaHsSsBHwWI7tNPUB1UIDt4r7oPAKIXlThhG9FLVYm6hldsc0TesLOc_wBA0wh5yk6VKCWbDRtuxwUjxjR7jN5l7oNbkPia5JlSiStbYh_u-f0Y7TL6wK2PeRfmB8o-c7vjfprMvCTiU1wy8dE_UeImOP7Xu0C7C_Z6MGOmy_U9Z7-_fvl18626-3H7_eb6rsKmV3Nlt01D1CNsUYBt-846EJYGKw30OBglWyXrFupWYCscYYON6-3gsCBQQ3PO3h32Pqb4b6E868lnpHE0gcphWiqQIKAuYHsAMcWcEw36MfnJpJ0WoPd-9bNfvZenVaef_WpR5q7WDxY7kTtOrUJL_-3aNxnNOCQT0OcjVneya7d77PMBoyLjyVPSGT0FJOcT4axd9C8c8h_XzZnW</recordid><startdate>19970201</startdate><enddate>19970201</enddate><creator>Zhao, Xian-Feng</creator><creator>Scrocchi, Louise A.</creator><creator>Hammond, Geoffrey L.</creator><general>Elsevier Ltd</general><general>Elsevier Science</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>19970201</creationdate><title>Glucocorticoids induce corticosteroid-binding globulin biosynthesis by immature mouse liver and kidney</title><author>Zhao, Xian-Feng ; Scrocchi, Louise A. ; Hammond, Geoffrey L.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c389t-b433ee8c04c10b586bd01befb7a08cfa97597250251c51dec3c3d8bfdcfb70203</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1997</creationdate><topic>Adrenals. Interrenals</topic><topic>Adrenocortical hormones. Regulation</topic><topic>Age Factors</topic><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Blotting, Western</topic><topic>Body Weight</topic><topic>Dexamethasone - pharmacology</topic><topic>Female</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Gene Expression</topic><topic>Glucocorticoids - pharmacology</topic><topic>Kidney - metabolism</topic><topic>Liver - metabolism</topic><topic>Male</topic><topic>Mice</topic><topic>Mice, Inbred BALB C</topic><topic>Pilot Projects</topic><topic>RNA, Messenger - analysis</topic><topic>Sex Factors</topic><topic>Transcortin - biosynthesis</topic><topic>Transcortin - genetics</topic><topic>Transcortin - urine</topic><topic>Vertebrates: endocrinology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Zhao, Xian-Feng</creatorcontrib><creatorcontrib>Scrocchi, Louise A.</creatorcontrib><creatorcontrib>Hammond, Geoffrey L.</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>The Journal of steroid biochemistry and molecular biology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zhao, Xian-Feng</au><au>Scrocchi, Louise A.</au><au>Hammond, Geoffrey L.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Glucocorticoids induce corticosteroid-binding globulin biosynthesis by immature mouse liver and kidney</atitle><jtitle>The Journal of steroid biochemistry and molecular biology</jtitle><addtitle>J Steroid Biochem Mol Biol</addtitle><date>1997-02-01</date><risdate>1997</risdate><volume>60</volume><issue>3</issue><spage>163</spage><epage>169</epage><pages>163-169</pages><issn>0960-0760</issn><eissn>1879-1220</eissn><abstract>Marked changes in mouse corticosteroid-binding globulin (CBG) gene expression in the liver and kidney occur postnatally. To study the influence of glucocorticoids on the initiation of mouse CBG biosynthesis in these tissues during the first two weeks after birth, we administered dexamethasone (0.5 μg/g body wt/day) to 4- and 11-day-old pups for three days. This resulted in higher serum CBG and hepatic CBG mRNA levels in animals, irrespective of their ages. Higher relative amounts of CBG mRNA in the kidneys of 14-day-old pups after three days of dexamethasone treatment coincided with higher amounts of intact and proteolytically cleaved CGB in their urine, and both are indicative of increased CGB production by the developing renal tubules. When an additional group of 11-day-old pups (
n = 4) was treated with 0.25 μg dexamethasone/g body weight per day for five days, this also resulted in significantly higher levels of serum CBG (
P < 0.01), hepatic CBG mRNA (
P < 0.01) and renal CBG mRNA (
P < 0.05), compared to littermates treated with the oil vehicle alone. In contrast, serum CBG levels progressively decreased in adult female mice during five days of treatment with 0.5 μg dexamethasone/g body weight per day. Taken together, these data indicate that glucocorticoids induce murine CBG gene expression in the immature liver and kidney, and support the concept that the effects of glucocorticoids on CBG gene expression are developmentally stage-specific.</abstract><cop>Oxford</cop><pub>Elsevier Ltd</pub><pmid>9191973</pmid><doi>10.1016/S0960-0760(96)00181-1</doi><tpages>7</tpages></addata></record> |
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subjects | Adrenals. Interrenals Adrenocortical hormones. Regulation Age Factors Animals Biological and medical sciences Blotting, Western Body Weight Dexamethasone - pharmacology Female Fundamental and applied biological sciences. Psychology Gene Expression Glucocorticoids - pharmacology Kidney - metabolism Liver - metabolism Male Mice Mice, Inbred BALB C Pilot Projects RNA, Messenger - analysis Sex Factors Transcortin - biosynthesis Transcortin - genetics Transcortin - urine Vertebrates: endocrinology |
title | Glucocorticoids induce corticosteroid-binding globulin biosynthesis by immature mouse liver and kidney |
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