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 |
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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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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><identifier>ISSN: 0021-9150</identifier><identifier>EISSN: 1879-1484</identifier><identifier>DOI: 10.1016/0021-9150(76)90141-6</identifier><identifier>PMID: 971348</identifier><language>eng</language><publisher>Ireland: Elsevier Ireland Ltd</publisher><subject>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</subject><ispartof>Atherosclerosis, 1976-09, Vol.24 (3), p.491-499</ispartof><rights>1976</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c422t-b035cedeaf6746824435404aec74b8ed9aca9dc062256053394e45418610dbee3</citedby><cites>FETCH-LOGICAL-c422t-b035cedeaf6746824435404aec74b8ed9aca9dc062256053394e45418610dbee3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/0021-9150(76)90141-6$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3548,27923,27924,45994</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/971348$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Wilson, D.E.</creatorcontrib><creatorcontrib>Flowers, C.M.</creatorcontrib><creatorcontrib>Carlile, S.I.</creatorcontrib><creatorcontrib>Udall, K.S.</creatorcontrib><title>Estrogen treatment and gonadal function in the regulation of lipoprotein lipase</title><title>Atherosclerosis</title><addtitle>Atherosclerosis</addtitle><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.</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 & 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 & 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 & 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 & 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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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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