Estrogen treatment and gonadal function in the regulation of lipoprotein lipase

Lipoprotein lipase (LPL) activity was measured in adipose tissue, heart and diaphragm in Sprague-Dawley rats after estrogen therapy or orchiectomy. Enzyme activity was measured by incubation of tissue fragments with a triolein emulsion in the presence of serum and heparin. In confirmation of other w...

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Veröffentlicht in:Atherosclerosis 1976-09, Vol.24 (3), p.491-499
Hauptverfasser: Wilson, D.E., Flowers, C.M., Carlile, S.I., Udall, K.S.
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container_end_page 499
container_issue 3
container_start_page 491
container_title Atherosclerosis
container_volume 24
creator Wilson, D.E.
Flowers, C.M.
Carlile, S.I.
Udall, K.S.
description Lipoprotein lipase (LPL) activity was measured in adipose tissue, heart and diaphragm in Sprague-Dawley rats after estrogen therapy or orchiectomy. Enzyme activity was measured by incubation of tissue fragments with a triolein emulsion in the presence of serum and heparin. In confirmation of other work, depression of adipose tissue LPL followed estradiol treatment in pharmacologic or near-physiologic doses. Cardiac and diaphragmatic muscle LPL were increased. Estrogen-treated male animals showed growth retardation. However, they gained weight steadily and did not show significant differences in serum insulin, glucose or d-β-hydroxybutyrate. The effects of estradiol in male animals were reversed by sequential fasting and re-feeding. At times during growth and aging in normal female rats, adipose tissue activity was decreased while cardiac and skeletal muscle activities were increased relative to males of the same age or body weight. Castration of male rats failed to reproduce the effect of estrogens on tissue lipoprotein lipase. These in vitro data suggest that exogenous estrogens may shift the flux of triglyceride fatty acids from storage in the adipose organ toward incorporation by muscle. These, and other data, raise the possibility that physiological estrogen secretion exerts a tonic influence over the synthesis and ultimate destination of triglyceride fatty acids.
doi_str_mv 10.1016/0021-9150(76)90141-6
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Enzyme activity was measured by incubation of tissue fragments with a triolein emulsion in the presence of serum and heparin. In confirmation of other work, depression of adipose tissue LPL followed estradiol treatment in pharmacologic or near-physiologic doses. Cardiac and diaphragmatic muscle LPL were increased. Estrogen-treated male animals showed growth retardation. However, they gained weight steadily and did not show significant differences in serum insulin, glucose or d-β-hydroxybutyrate. The effects of estradiol in male animals were reversed by sequential fasting and re-feeding. At times during growth and aging in normal female rats, adipose tissue activity was decreased while cardiac and skeletal muscle activities were increased relative to males of the same age or body weight. Castration of male rats failed to reproduce the effect of estrogens on tissue lipoprotein lipase. 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Enzyme activity was measured by incubation of tissue fragments with a triolein emulsion in the presence of serum and heparin. In confirmation of other work, depression of adipose tissue LPL followed estradiol treatment in pharmacologic or near-physiologic doses. Cardiac and diaphragmatic muscle LPL were increased. Estrogen-treated male animals showed growth retardation. However, they gained weight steadily and did not show significant differences in serum insulin, glucose or d-β-hydroxybutyrate. The effects of estradiol in male animals were reversed by sequential fasting and re-feeding. At times during growth and aging in normal female rats, adipose tissue activity was decreased while cardiac and skeletal muscle activities were increased relative to males of the same age or body weight. Castration of male rats failed to reproduce the effect of estrogens on tissue lipoprotein lipase. These in vitro data suggest that exogenous estrogens may shift the flux of triglyceride fatty acids from storage in the adipose organ toward incorporation by muscle. These, and other data, raise the possibility that physiological estrogen secretion exerts a tonic influence over the synthesis and ultimate destination of triglyceride fatty acids.</description><subject>17β-Estradiol</subject><subject>Adipose Tissue - drug effects</subject><subject>Adipose Tissue - enzymology</subject><subject>Aging</subject><subject>Animals</subject><subject>Castration</subject><subject>Diaphragm - drug effects</subject><subject>Diaphragm - enzymology</subject><subject>Estradiol - analogs &amp; derivatives</subject><subject>Estradiol - pharmacology</subject><subject>Estrogens</subject><subject>Fasting-re-feeding</subject><subject>Growth</subject><subject>Heart - drug effects</subject><subject>Kinetics</subject><subject>Lipoprotein lipase</subject><subject>Lipoprotein Lipase - metabolism</subject><subject>Male</subject><subject>Myocardium - enzymology</subject><subject>Organ Specificity</subject><subject>Rats</subject><subject>Testosterone - analogs &amp; derivatives</subject><subject>Testosterone - pharmacology</subject><subject>Triglycerides</subject><issn>0021-9150</issn><issn>1879-1484</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1976</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kMtOwzAQRS3EqxT-oIusECwCduI4zgYJVeUhVeoG1pZjT4pRahfbQeLvcUnVJasZzb1zR3MQmhF8RzBh9xgXJG9IhW9qdttgQknOjtCE8LrJCeX0GE0OlnN0EcInxpjWhJ-h06YmJeUTtFqE6N0abBY9yLgBGzNpdbZ2VmrZZ91gVTTOZiY5PiDzsB56-TdxXdabrdt6FyGpqZcBLtFJJ_sAV_s6Re9Pi7f5S75cPb_OH5e5okUR8xaXlQINsmM1ZbygtKwophJUTVsOupFKNlphVhQVw1VZNhRoRQlnBOsWoJyi6zE3nf8aIESxMUFB30sLbgiClxXBvCHJSEej8i4ED53YerOR_kcQLHYYxY6R2DESNRN_GAVLa7N9_tBuQB-WRm5JfhhlSD9-G_AiKAM2vWQ8qCi0M__n_wIlR4F4</recordid><startdate>197609</startdate><enddate>197609</enddate><creator>Wilson, D.E.</creator><creator>Flowers, C.M.</creator><creator>Carlile, S.I.</creator><creator>Udall, K.S.</creator><general>Elsevier Ireland Ltd</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></search><sort><creationdate>197609</creationdate><title>Estrogen treatment and gonadal function in the regulation of lipoprotein lipase</title><author>Wilson, D.E. ; Flowers, C.M. ; Carlile, S.I. ; Udall, K.S.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c422t-b035cedeaf6746824435404aec74b8ed9aca9dc062256053394e45418610dbee3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1976</creationdate><topic>17β-Estradiol</topic><topic>Adipose Tissue - drug effects</topic><topic>Adipose Tissue - enzymology</topic><topic>Aging</topic><topic>Animals</topic><topic>Castration</topic><topic>Diaphragm - drug effects</topic><topic>Diaphragm - enzymology</topic><topic>Estradiol - analogs &amp; derivatives</topic><topic>Estradiol - pharmacology</topic><topic>Estrogens</topic><topic>Fasting-re-feeding</topic><topic>Growth</topic><topic>Heart - drug effects</topic><topic>Kinetics</topic><topic>Lipoprotein lipase</topic><topic>Lipoprotein Lipase - metabolism</topic><topic>Male</topic><topic>Myocardium - enzymology</topic><topic>Organ Specificity</topic><topic>Rats</topic><topic>Testosterone - analogs &amp; derivatives</topic><topic>Testosterone - pharmacology</topic><topic>Triglycerides</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wilson, D.E.</creatorcontrib><creatorcontrib>Flowers, C.M.</creatorcontrib><creatorcontrib>Carlile, S.I.</creatorcontrib><creatorcontrib>Udall, K.S.</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><jtitle>Atherosclerosis</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wilson, D.E.</au><au>Flowers, C.M.</au><au>Carlile, S.I.</au><au>Udall, K.S.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Estrogen treatment and gonadal function in the regulation of lipoprotein lipase</atitle><jtitle>Atherosclerosis</jtitle><addtitle>Atherosclerosis</addtitle><date>1976-09</date><risdate>1976</risdate><volume>24</volume><issue>3</issue><spage>491</spage><epage>499</epage><pages>491-499</pages><issn>0021-9150</issn><eissn>1879-1484</eissn><abstract>Lipoprotein lipase (LPL) activity was measured in adipose tissue, heart and diaphragm in Sprague-Dawley rats after estrogen therapy or orchiectomy. Enzyme activity was measured by incubation of tissue fragments with a triolein emulsion in the presence of serum and heparin. In confirmation of other work, depression of adipose tissue LPL followed estradiol treatment in pharmacologic or near-physiologic doses. Cardiac and diaphragmatic muscle LPL were increased. Estrogen-treated male animals showed growth retardation. However, they gained weight steadily and did not show significant differences in serum insulin, glucose or d-β-hydroxybutyrate. The effects of estradiol in male animals were reversed by sequential fasting and re-feeding. At times during growth and aging in normal female rats, adipose tissue activity was decreased while cardiac and skeletal muscle activities were increased relative to males of the same age or body weight. Castration of male rats failed to reproduce the effect of estrogens on tissue lipoprotein lipase. These in vitro data suggest that exogenous estrogens may shift the flux of triglyceride fatty acids from storage in the adipose organ toward incorporation by muscle. These, and other data, raise the possibility that physiological estrogen secretion exerts a tonic influence over the synthesis and ultimate destination of triglyceride fatty acids.</abstract><cop>Ireland</cop><pub>Elsevier Ireland Ltd</pub><pmid>971348</pmid><doi>10.1016/0021-9150(76)90141-6</doi><tpages>9</tpages></addata></record>
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ispartof Atherosclerosis, 1976-09, Vol.24 (3), p.491-499
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source Elsevier ScienceDirect Journals Complete - AutoHoldings; MEDLINE
subjects 17β-Estradiol
Adipose Tissue - drug effects
Adipose Tissue - enzymology
Aging
Animals
Castration
Diaphragm - drug effects
Diaphragm - enzymology
Estradiol - analogs & derivatives
Estradiol - pharmacology
Estrogens
Fasting-re-feeding
Growth
Heart - drug effects
Kinetics
Lipoprotein lipase
Lipoprotein Lipase - metabolism
Male
Myocardium - enzymology
Organ Specificity
Rats
Testosterone - analogs & derivatives
Testosterone - pharmacology
Triglycerides
title Estrogen treatment and gonadal function in the regulation of lipoprotein lipase
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