Serum IGF-I levels and IGF-I gene splicing in muscle of healthy young males receiving rhGH

Abstract Objective Elevated growth hormone (GH) levels lead to increased circulating insulin-like growth factor-I (IGF-I), but the effects on localised muscle IGF-I splice variant expression is not known. The effects of rhGH administration, with or without an acute bout of high resistance exercise,...

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Veröffentlicht in:Growth hormone & IGF research 2009-02, Vol.19 (1), p.61-67
Hauptverfasser: Aperghis, Michael, Velloso, Cristiana P, Hameed, Mahjabeen, Brothwood, Theresa, Bradley, Lloyd, Bouloux, Pierre M.G, Harridge, Stephen D.R, Goldspink, Geoffrey
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container_end_page 67
container_issue 1
container_start_page 61
container_title Growth hormone & IGF research
container_volume 19
creator Aperghis, Michael
Velloso, Cristiana P
Hameed, Mahjabeen
Brothwood, Theresa
Bradley, Lloyd
Bouloux, Pierre M.G
Harridge, Stephen D.R
Goldspink, Geoffrey
description Abstract Objective Elevated growth hormone (GH) levels lead to increased circulating insulin-like growth factor-I (IGF-I), but the effects on localised muscle IGF-I splice variant expression is not known. The effects of rhGH administration, with or without an acute bout of high resistance exercise, were measured on serum IGF-I and on the mRNA levels of IGF-I splice variants in the vastus lateralis muscle of healthy young men. Design The study was a randomised double blind trial with a crossover design. Seven subjects were randomly assigned to a group receiving daily injections of rhGH (0.075 IU kg−1 day−1 ) or placebo for a two week period. Following a one month washout, the groups were reversed. Results Administration of rhGH increased circulating IGF-I from 31.8 ± 3.2 to 109 ± 5.4 nmol/L ( p < 0.05). There was no effect of the exercise bout. RNA was extracted from muscle biopsies obtained from exercised and non-exercised legs 2.5 h after the cessation of the exercise. Transcript expression was measured using Real-time QPCR. There was no effect of either exercise or rhGH administration on IGF-I 5′ (Class 1 or Class 2) or 3′ (IGF-IEa, or MGF) transcripts. Conclusion Although rhGH administration has an effect on liver IGF-I expression, as shown by increase in circulating IGF-I, muscle IGF-I expression is unaffected in young healthy subjects with normal GH profile. The findings contrast with those of a previous study in which GH deficient elderly men showed higher muscle IGF-I 3′ splice variant levels following rhGH administration with and without resistance training. Unlike in the liver, muscle Class1 and 2 IGF-I expression do not change significantly following administration of rhGH.
doi_str_mv 10.1016/j.ghir.2008.07.002
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The effects of rhGH administration, with or without an acute bout of high resistance exercise, were measured on serum IGF-I and on the mRNA levels of IGF-I splice variants in the vastus lateralis muscle of healthy young men. Design The study was a randomised double blind trial with a crossover design. Seven subjects were randomly assigned to a group receiving daily injections of rhGH (0.075 IU kg−1 day−1 ) or placebo for a two week period. Following a one month washout, the groups were reversed. Results Administration of rhGH increased circulating IGF-I from 31.8 ± 3.2 to 109 ± 5.4 nmol/L ( p &lt; 0.05). There was no effect of the exercise bout. RNA was extracted from muscle biopsies obtained from exercised and non-exercised legs 2.5 h after the cessation of the exercise. Transcript expression was measured using Real-time QPCR. There was no effect of either exercise or rhGH administration on IGF-I 5′ (Class 1 or Class 2) or 3′ (IGF-IEa, or MGF) transcripts. Conclusion Although rhGH administration has an effect on liver IGF-I expression, as shown by increase in circulating IGF-I, muscle IGF-I expression is unaffected in young healthy subjects with normal GH profile. The findings contrast with those of a previous study in which GH deficient elderly men showed higher muscle IGF-I 3′ splice variant levels following rhGH administration with and without resistance training. Unlike in the liver, muscle Class1 and 2 IGF-I expression do not change significantly following administration of rhGH.</description><identifier>ISSN: 1096-6374</identifier><identifier>EISSN: 1532-2238</identifier><identifier>DOI: 10.1016/j.ghir.2008.07.002</identifier><identifier>PMID: 18799338</identifier><language>eng</language><publisher>Scotland: Elsevier Ltd</publisher><subject>Adult ; Advanced Basic Science ; Alternative Splicing ; Class 2 ; Endocrinology &amp; Metabolism ; Exercise ; Growth hormone ; Human Growth Hormone - therapeutic use ; Humans ; IGF-I splice variants ; Insulin-Like Growth Factor I - genetics ; Insulin-Like Growth Factor I - metabolism ; Liver - metabolism ; Male ; Muscle class 1 ; Muscle, Skeletal - metabolism ; Recombinant Proteins - therapeutic use ; Young Adult</subject><ispartof>Growth hormone &amp; IGF research, 2009-02, Vol.19 (1), p.61-67</ispartof><rights>Elsevier Ltd</rights><rights>2008 Elsevier Ltd</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c409t-3c592045d11ada24366929b8f7bc16f6de0a7ebc106a06945c71588427c76f3c3</citedby><cites>FETCH-LOGICAL-c409t-3c592045d11ada24366929b8f7bc16f6de0a7ebc106a06945c71588427c76f3c3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.ghir.2008.07.002$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/18799338$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Aperghis, Michael</creatorcontrib><creatorcontrib>Velloso, Cristiana P</creatorcontrib><creatorcontrib>Hameed, Mahjabeen</creatorcontrib><creatorcontrib>Brothwood, Theresa</creatorcontrib><creatorcontrib>Bradley, Lloyd</creatorcontrib><creatorcontrib>Bouloux, Pierre M.G</creatorcontrib><creatorcontrib>Harridge, Stephen D.R</creatorcontrib><creatorcontrib>Goldspink, Geoffrey</creatorcontrib><title>Serum IGF-I levels and IGF-I gene splicing in muscle of healthy young males receiving rhGH</title><title>Growth hormone &amp; IGF research</title><addtitle>Growth Horm IGF Res</addtitle><description>Abstract Objective Elevated growth hormone (GH) levels lead to increased circulating insulin-like growth factor-I (IGF-I), but the effects on localised muscle IGF-I splice variant expression is not known. The effects of rhGH administration, with or without an acute bout of high resistance exercise, were measured on serum IGF-I and on the mRNA levels of IGF-I splice variants in the vastus lateralis muscle of healthy young men. Design The study was a randomised double blind trial with a crossover design. Seven subjects were randomly assigned to a group receiving daily injections of rhGH (0.075 IU kg−1 day−1 ) or placebo for a two week period. Following a one month washout, the groups were reversed. Results Administration of rhGH increased circulating IGF-I from 31.8 ± 3.2 to 109 ± 5.4 nmol/L ( p &lt; 0.05). There was no effect of the exercise bout. RNA was extracted from muscle biopsies obtained from exercised and non-exercised legs 2.5 h after the cessation of the exercise. Transcript expression was measured using Real-time QPCR. There was no effect of either exercise or rhGH administration on IGF-I 5′ (Class 1 or Class 2) or 3′ (IGF-IEa, or MGF) transcripts. Conclusion Although rhGH administration has an effect on liver IGF-I expression, as shown by increase in circulating IGF-I, muscle IGF-I expression is unaffected in young healthy subjects with normal GH profile. The findings contrast with those of a previous study in which GH deficient elderly men showed higher muscle IGF-I 3′ splice variant levels following rhGH administration with and without resistance training. Unlike in the liver, muscle Class1 and 2 IGF-I expression do not change significantly following administration of rhGH.</description><subject>Adult</subject><subject>Advanced Basic Science</subject><subject>Alternative Splicing</subject><subject>Class 2</subject><subject>Endocrinology &amp; Metabolism</subject><subject>Exercise</subject><subject>Growth hormone</subject><subject>Human Growth Hormone - therapeutic use</subject><subject>Humans</subject><subject>IGF-I splice variants</subject><subject>Insulin-Like Growth Factor I - genetics</subject><subject>Insulin-Like Growth Factor I - metabolism</subject><subject>Liver - metabolism</subject><subject>Male</subject><subject>Muscle class 1</subject><subject>Muscle, Skeletal - metabolism</subject><subject>Recombinant Proteins - therapeutic use</subject><subject>Young Adult</subject><issn>1096-6374</issn><issn>1532-2238</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kUFr2zAUx8VYWbu2X2CHodNudp8kW5JhDEZp00Chh3aXXYQiPyfKZDuT4kC-_WQSGOywkx56v___8HuEfGJQMmDybluuNz6WHECXoEoA_o5csVrwgnOh3-cZGllIoapL8jGlLQA0QlcfyCXTqmmE0Ffk5yvGqafLxWOxpAEPGBK1Q3v-WOOANO2Cd35YUz_QfkouIB07ukEb9psjPY5TXvU2YKIRHfrDjMbN4umGXHQ2JLw9v9fkx-PD2_1T8fyyWN5_fy5cBc2-EK5uOFR1y5htLa-ElA1vVrpTK8dkJ1sEqzDPIC3IpqqdYrXWFVdOyU44cU2-nHp3cfw9Ydqb3ieHIdgBxykZKbXikqsM8hPo4phSxM7sou9tPBoGZjZqtmY2amajBpTJRnPo87l9WvXY_o2cFWbg6wnI6vDgMZrkPA4OW5997E07-v_3f_sn7oIfvLPhFx4xbccpDtmeYSZxA-Z1vul8UtAADAQXfwBOzJo8</recordid><startdate>20090201</startdate><enddate>20090201</enddate><creator>Aperghis, Michael</creator><creator>Velloso, Cristiana P</creator><creator>Hameed, Mahjabeen</creator><creator>Brothwood, Theresa</creator><creator>Bradley, Lloyd</creator><creator>Bouloux, Pierre M.G</creator><creator>Harridge, Stephen D.R</creator><creator>Goldspink, Geoffrey</creator><general>Elsevier 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>20090201</creationdate><title>Serum IGF-I levels and IGF-I gene splicing in muscle of healthy young males receiving rhGH</title><author>Aperghis, Michael ; Velloso, Cristiana P ; Hameed, Mahjabeen ; Brothwood, Theresa ; Bradley, Lloyd ; Bouloux, Pierre M.G ; Harridge, Stephen D.R ; Goldspink, Geoffrey</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c409t-3c592045d11ada24366929b8f7bc16f6de0a7ebc106a06945c71588427c76f3c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Adult</topic><topic>Advanced Basic Science</topic><topic>Alternative Splicing</topic><topic>Class 2</topic><topic>Endocrinology &amp; Metabolism</topic><topic>Exercise</topic><topic>Growth hormone</topic><topic>Human Growth Hormone - therapeutic use</topic><topic>Humans</topic><topic>IGF-I splice variants</topic><topic>Insulin-Like Growth Factor I - genetics</topic><topic>Insulin-Like Growth Factor I - metabolism</topic><topic>Liver - metabolism</topic><topic>Male</topic><topic>Muscle class 1</topic><topic>Muscle, Skeletal - metabolism</topic><topic>Recombinant Proteins - therapeutic use</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Aperghis, Michael</creatorcontrib><creatorcontrib>Velloso, Cristiana P</creatorcontrib><creatorcontrib>Hameed, Mahjabeen</creatorcontrib><creatorcontrib>Brothwood, Theresa</creatorcontrib><creatorcontrib>Bradley, Lloyd</creatorcontrib><creatorcontrib>Bouloux, Pierre M.G</creatorcontrib><creatorcontrib>Harridge, Stephen D.R</creatorcontrib><creatorcontrib>Goldspink, Geoffrey</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>Growth hormone &amp; IGF research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Aperghis, Michael</au><au>Velloso, Cristiana P</au><au>Hameed, Mahjabeen</au><au>Brothwood, Theresa</au><au>Bradley, Lloyd</au><au>Bouloux, Pierre M.G</au><au>Harridge, Stephen D.R</au><au>Goldspink, Geoffrey</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Serum IGF-I levels and IGF-I gene splicing in muscle of healthy young males receiving rhGH</atitle><jtitle>Growth hormone &amp; IGF research</jtitle><addtitle>Growth Horm IGF Res</addtitle><date>2009-02-01</date><risdate>2009</risdate><volume>19</volume><issue>1</issue><spage>61</spage><epage>67</epage><pages>61-67</pages><issn>1096-6374</issn><eissn>1532-2238</eissn><abstract>Abstract Objective Elevated growth hormone (GH) levels lead to increased circulating insulin-like growth factor-I (IGF-I), but the effects on localised muscle IGF-I splice variant expression is not known. The effects of rhGH administration, with or without an acute bout of high resistance exercise, were measured on serum IGF-I and on the mRNA levels of IGF-I splice variants in the vastus lateralis muscle of healthy young men. Design The study was a randomised double blind trial with a crossover design. Seven subjects were randomly assigned to a group receiving daily injections of rhGH (0.075 IU kg−1 day−1 ) or placebo for a two week period. Following a one month washout, the groups were reversed. Results Administration of rhGH increased circulating IGF-I from 31.8 ± 3.2 to 109 ± 5.4 nmol/L ( p &lt; 0.05). There was no effect of the exercise bout. RNA was extracted from muscle biopsies obtained from exercised and non-exercised legs 2.5 h after the cessation of the exercise. Transcript expression was measured using Real-time QPCR. There was no effect of either exercise or rhGH administration on IGF-I 5′ (Class 1 or Class 2) or 3′ (IGF-IEa, or MGF) transcripts. Conclusion Although rhGH administration has an effect on liver IGF-I expression, as shown by increase in circulating IGF-I, muscle IGF-I expression is unaffected in young healthy subjects with normal GH profile. The findings contrast with those of a previous study in which GH deficient elderly men showed higher muscle IGF-I 3′ splice variant levels following rhGH administration with and without resistance training. Unlike in the liver, muscle Class1 and 2 IGF-I expression do not change significantly following administration of rhGH.</abstract><cop>Scotland</cop><pub>Elsevier Ltd</pub><pmid>18799338</pmid><doi>10.1016/j.ghir.2008.07.002</doi><tpages>7</tpages></addata></record>
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subjects Adult
Advanced Basic Science
Alternative Splicing
Class 2
Endocrinology & Metabolism
Exercise
Growth hormone
Human Growth Hormone - therapeutic use
Humans
IGF-I splice variants
Insulin-Like Growth Factor I - genetics
Insulin-Like Growth Factor I - metabolism
Liver - metabolism
Male
Muscle class 1
Muscle, Skeletal - metabolism
Recombinant Proteins - therapeutic use
Young Adult
title Serum IGF-I levels and IGF-I gene splicing in muscle of healthy young males receiving rhGH
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