Effect of aging on the sensitivity of growth hormone secretion to insulin-like growth factor-I negative feedback
To determine the effect of aging on the suppression of GH secretion by insulin-like growth factor (IGF)-I, we studied 11 healthy young adults (6 men, 5 women, mean +/- SD: 25.2 +/- 4.6 yr old; body mass index 23.7 +/- 1.8 kg/m2) and 11 older adults (6 men, 5 women, 69.5 +/- 5.8 yr old; body mass ind...
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description | To determine the effect of aging on the suppression of GH secretion by insulin-like growth factor (IGF)-I, we studied 11 healthy young adults (6 men, 5 women, mean +/- SD: 25.2 +/- 4.6 yr old; body mass index 23.7 +/- 1.8 kg/m2) and 11 older adults (6 men, 5 women, 69.5 +/- 5.8 yr old; body mass index 24.2 +/- 2.5 kg/m2). Saline (control) or recombinant human IGF-I (rhIGF-I) (2 h baseline then, in sequence, 2.5 h each of 1, 3, and 10 micrograms/kg.h) was infused iv during the last 9.5 h of a 40.5-h fast; serum glucose was clamped within 15% of baseline. Baseline serum GH concentrations (mean +/- SE: 3.3 +/- 0.7 vs. 1.9 +/- 0.5 micrograms/L, P = 0.02) and total IGF-I concentrations (219 +/- 15 vs. 103 +/- 19 micrograms/L, P < 0.01) were higher in the younger subjects. In both age groups, GH concentrations were significantly decreased by 3 and 10 micrograms/kg.h, but not by 1 microgram/kg.h rhIGF-I. The absolute decrease in GH concentrations was greater in young than in older subjects during the 3 and 10 micrograms/kg.h rhIGF-I infusion periods, but both young and older subjects suppressed to a similar GH level during the last hour of the rhIGF-I infusion (0.78 +/- 0.24 microgram/L and 0.61 +/- 0.16 microgram/L, respectively). The older subjects had a greater increase above baseline in serum concentrations of both total (306 +/- 24 vs. 244 +/- 14 micrograms/L, P = 0.04) and free IGF-I (8.5 +/- 1.4 vs. 4.2 +/- 0.6 micrograms/L, P = 0.01) than the young subjects during rhIGF-I infusion, and their GH suppression expressed in relation to increases in both total and free serum IGF-I concentrations was significantly less than in the young subjects. We conclude that the ability of exogenous rhIGF-I to suppress serum GH concentrations declines with increasing age. This suggests that increased sensitivity to endogenous IGF-I negative feedback is not a cause of the decline in GH secretion that occurs with aging. |
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M ; HARTMAN, M. L ; PEZZOLI, S. S ; HARRELL, F. E ; HINTZ, R. L ; ALBERTI, K. G. M. M ; THORNER, M. O</creator><creatorcontrib>CHAPMAN, I. M ; HARTMAN, M. L ; PEZZOLI, S. S ; HARRELL, F. E ; HINTZ, R. L ; ALBERTI, K. G. M. M ; THORNER, M. O</creatorcontrib><description>To determine the effect of aging on the suppression of GH secretion by insulin-like growth factor (IGF)-I, we studied 11 healthy young adults (6 men, 5 women, mean +/- SD: 25.2 +/- 4.6 yr old; body mass index 23.7 +/- 1.8 kg/m2) and 11 older adults (6 men, 5 women, 69.5 +/- 5.8 yr old; body mass index 24.2 +/- 2.5 kg/m2). Saline (control) or recombinant human IGF-I (rhIGF-I) (2 h baseline then, in sequence, 2.5 h each of 1, 3, and 10 micrograms/kg.h) was infused iv during the last 9.5 h of a 40.5-h fast; serum glucose was clamped within 15% of baseline. Baseline serum GH concentrations (mean +/- SE: 3.3 +/- 0.7 vs. 1.9 +/- 0.5 micrograms/L, P = 0.02) and total IGF-I concentrations (219 +/- 15 vs. 103 +/- 19 micrograms/L, P < 0.01) were higher in the younger subjects. In both age groups, GH concentrations were significantly decreased by 3 and 10 micrograms/kg.h, but not by 1 microgram/kg.h rhIGF-I. The absolute decrease in GH concentrations was greater in young than in older subjects during the 3 and 10 micrograms/kg.h rhIGF-I infusion periods, but both young and older subjects suppressed to a similar GH level during the last hour of the rhIGF-I infusion (0.78 +/- 0.24 microgram/L and 0.61 +/- 0.16 microgram/L, respectively). The older subjects had a greater increase above baseline in serum concentrations of both total (306 +/- 24 vs. 244 +/- 14 micrograms/L, P = 0.04) and free IGF-I (8.5 +/- 1.4 vs. 4.2 +/- 0.6 micrograms/L, P = 0.01) than the young subjects during rhIGF-I infusion, and their GH suppression expressed in relation to increases in both total and free serum IGF-I concentrations was significantly less than in the young subjects. We conclude that the ability of exogenous rhIGF-I to suppress serum GH concentrations declines with increasing age. This suggests that increased sensitivity to endogenous IGF-I negative feedback is not a cause of the decline in GH secretion that occurs with aging.</description><identifier>ISSN: 0021-972X</identifier><identifier>EISSN: 1945-7197</identifier><identifier>DOI: 10.1210/jc.82.9.2996</identifier><identifier>PMID: 9284733</identifier><identifier>CODEN: JCEMAZ</identifier><language>eng</language><publisher>Bethesda, MD: Endocrine Society</publisher><subject>3-Hydroxybutyric Acid ; Adult ; Aging - physiology ; Biological and medical sciences ; Blood Glucose - analysis ; Development. Metamorphosis. Moult. Ageing ; Dose-Response Relationship, Drug ; Fatty Acids, Nonesterified - blood ; Feedback ; Female ; Fundamental and applied biological sciences. Psychology ; Glucose - pharmacology ; Human Growth Hormone - antagonists & inhibitors ; Human Growth Hormone - blood ; Human Growth Hormone - secretion ; Humans ; Hydroxybutyrates - blood ; Infusions, Intravenous ; Insulin - blood ; Insulin-Like Growth Factor I - metabolism ; Insulin-Like Growth Factor I - pharmacology ; Male ; Osmolar Concentration ; Recombinant Proteins ; Vertebrates: anatomy and physiology, studies on body, several organs or systems</subject><ispartof>The journal of clinical endocrinology and metabolism, 1997-09, Vol.82 (9), p.2996-3004</ispartof><rights>1997 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c315t-b317299ad090fedc5296803ab12ef3009330f124421c112fc1a189454d5236be3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>315,782,786,27933,27934</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=2802225$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/9284733$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>CHAPMAN, I. M</creatorcontrib><creatorcontrib>HARTMAN, M. L</creatorcontrib><creatorcontrib>PEZZOLI, S. S</creatorcontrib><creatorcontrib>HARRELL, F. E</creatorcontrib><creatorcontrib>HINTZ, R. L</creatorcontrib><creatorcontrib>ALBERTI, K. G. M. M</creatorcontrib><creatorcontrib>THORNER, M. O</creatorcontrib><title>Effect of aging on the sensitivity of growth hormone secretion to insulin-like growth factor-I negative feedback</title><title>The journal of clinical endocrinology and metabolism</title><addtitle>J Clin Endocrinol Metab</addtitle><description>To determine the effect of aging on the suppression of GH secretion by insulin-like growth factor (IGF)-I, we studied 11 healthy young adults (6 men, 5 women, mean +/- SD: 25.2 +/- 4.6 yr old; body mass index 23.7 +/- 1.8 kg/m2) and 11 older adults (6 men, 5 women, 69.5 +/- 5.8 yr old; body mass index 24.2 +/- 2.5 kg/m2). Saline (control) or recombinant human IGF-I (rhIGF-I) (2 h baseline then, in sequence, 2.5 h each of 1, 3, and 10 micrograms/kg.h) was infused iv during the last 9.5 h of a 40.5-h fast; serum glucose was clamped within 15% of baseline. Baseline serum GH concentrations (mean +/- SE: 3.3 +/- 0.7 vs. 1.9 +/- 0.5 micrograms/L, P = 0.02) and total IGF-I concentrations (219 +/- 15 vs. 103 +/- 19 micrograms/L, P < 0.01) were higher in the younger subjects. In both age groups, GH concentrations were significantly decreased by 3 and 10 micrograms/kg.h, but not by 1 microgram/kg.h rhIGF-I. The absolute decrease in GH concentrations was greater in young than in older subjects during the 3 and 10 micrograms/kg.h rhIGF-I infusion periods, but both young and older subjects suppressed to a similar GH level during the last hour of the rhIGF-I infusion (0.78 +/- 0.24 microgram/L and 0.61 +/- 0.16 microgram/L, respectively). The older subjects had a greater increase above baseline in serum concentrations of both total (306 +/- 24 vs. 244 +/- 14 micrograms/L, P = 0.04) and free IGF-I (8.5 +/- 1.4 vs. 4.2 +/- 0.6 micrograms/L, P = 0.01) than the young subjects during rhIGF-I infusion, and their GH suppression expressed in relation to increases in both total and free serum IGF-I concentrations was significantly less than in the young subjects. We conclude that the ability of exogenous rhIGF-I to suppress serum GH concentrations declines with increasing age. This suggests that increased sensitivity to endogenous IGF-I negative feedback is not a cause of the decline in GH secretion that occurs with aging.</description><subject>3-Hydroxybutyric Acid</subject><subject>Adult</subject><subject>Aging - physiology</subject><subject>Biological and medical sciences</subject><subject>Blood Glucose - analysis</subject><subject>Development. Metamorphosis. Moult. Ageing</subject><subject>Dose-Response Relationship, Drug</subject><subject>Fatty Acids, Nonesterified - blood</subject><subject>Feedback</subject><subject>Female</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Glucose - pharmacology</subject><subject>Human Growth Hormone - antagonists & inhibitors</subject><subject>Human Growth Hormone - blood</subject><subject>Human Growth Hormone - secretion</subject><subject>Humans</subject><subject>Hydroxybutyrates - blood</subject><subject>Infusions, Intravenous</subject><subject>Insulin - blood</subject><subject>Insulin-Like Growth Factor I - metabolism</subject><subject>Insulin-Like Growth Factor I - pharmacology</subject><subject>Male</subject><subject>Osmolar Concentration</subject><subject>Recombinant Proteins</subject><subject>Vertebrates: anatomy and physiology, studies on body, several organs or systems</subject><issn>0021-972X</issn><issn>1945-7197</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1997</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNo9kEFr3DAUhEVJSTZpb70GdAg91Vu9J3ttHUNI20CglxZ6E7L8tKuNV9pI2oT8-9pkk9Mcvo-BGca-gFgCgvi-tcsOl2qJSq0-sAWouqlaUO0JWwiBUKkW_52x85y3QkBdN_KUnSrs6lbKBdvfOke28Oi4Wfuw5jHwsiGeKWRf_JMvLzNbp_hcNnwT0y6GmdpExc9u5D7kw-hDNfoHehOdsSWm6o4HWpuphrgjGnpjHz6xj86MmT4f84L9_XH75-ZXdf_7593N9X1lJTSl6iW00yAzCCUcDbZBteqEND0gOSmEklI4wLpGsADoLBjopuX10KBc9SQv2NfX3n2KjwfKRe98tjSOJlA8ZN0qbFayFpP47VW0KeacyOl98juTXjQIPR-st1Z3qJWeD570y2Pvod_R8C4fH5341ZGbbM3okgnW53cNO4GIjfwPy9CDaw</recordid><startdate>19970901</startdate><enddate>19970901</enddate><creator>CHAPMAN, I. M</creator><creator>HARTMAN, M. L</creator><creator>PEZZOLI, S. S</creator><creator>HARRELL, F. E</creator><creator>HINTZ, R. L</creator><creator>ALBERTI, K. G. M. M</creator><creator>THORNER, M. O</creator><general>Endocrine Society</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>19970901</creationdate><title>Effect of aging on the sensitivity of growth hormone secretion to insulin-like growth factor-I negative feedback</title><author>CHAPMAN, I. M ; HARTMAN, M. L ; PEZZOLI, S. S ; HARRELL, F. E ; HINTZ, R. L ; ALBERTI, K. G. M. M ; THORNER, M. O</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c315t-b317299ad090fedc5296803ab12ef3009330f124421c112fc1a189454d5236be3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1997</creationdate><topic>3-Hydroxybutyric Acid</topic><topic>Adult</topic><topic>Aging - physiology</topic><topic>Biological and medical sciences</topic><topic>Blood Glucose - analysis</topic><topic>Development. Metamorphosis. Moult. Ageing</topic><topic>Dose-Response Relationship, Drug</topic><topic>Fatty Acids, Nonesterified - blood</topic><topic>Feedback</topic><topic>Female</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Glucose - pharmacology</topic><topic>Human Growth Hormone - antagonists & inhibitors</topic><topic>Human Growth Hormone - blood</topic><topic>Human Growth Hormone - secretion</topic><topic>Humans</topic><topic>Hydroxybutyrates - blood</topic><topic>Infusions, Intravenous</topic><topic>Insulin - blood</topic><topic>Insulin-Like Growth Factor I - metabolism</topic><topic>Insulin-Like Growth Factor I - pharmacology</topic><topic>Male</topic><topic>Osmolar Concentration</topic><topic>Recombinant Proteins</topic><topic>Vertebrates: anatomy and physiology, studies on body, several organs or systems</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>CHAPMAN, I. M</creatorcontrib><creatorcontrib>HARTMAN, M. L</creatorcontrib><creatorcontrib>PEZZOLI, S. S</creatorcontrib><creatorcontrib>HARRELL, F. E</creatorcontrib><creatorcontrib>HINTZ, R. L</creatorcontrib><creatorcontrib>ALBERTI, K. G. M. M</creatorcontrib><creatorcontrib>THORNER, M. O</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 clinical endocrinology and metabolism</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>CHAPMAN, I. M</au><au>HARTMAN, M. L</au><au>PEZZOLI, S. S</au><au>HARRELL, F. E</au><au>HINTZ, R. L</au><au>ALBERTI, K. G. M. M</au><au>THORNER, M. O</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Effect of aging on the sensitivity of growth hormone secretion to insulin-like growth factor-I negative feedback</atitle><jtitle>The journal of clinical endocrinology and metabolism</jtitle><addtitle>J Clin Endocrinol Metab</addtitle><date>1997-09-01</date><risdate>1997</risdate><volume>82</volume><issue>9</issue><spage>2996</spage><epage>3004</epage><pages>2996-3004</pages><issn>0021-972X</issn><eissn>1945-7197</eissn><coden>JCEMAZ</coden><abstract>To determine the effect of aging on the suppression of GH secretion by insulin-like growth factor (IGF)-I, we studied 11 healthy young adults (6 men, 5 women, mean +/- SD: 25.2 +/- 4.6 yr old; body mass index 23.7 +/- 1.8 kg/m2) and 11 older adults (6 men, 5 women, 69.5 +/- 5.8 yr old; body mass index 24.2 +/- 2.5 kg/m2). Saline (control) or recombinant human IGF-I (rhIGF-I) (2 h baseline then, in sequence, 2.5 h each of 1, 3, and 10 micrograms/kg.h) was infused iv during the last 9.5 h of a 40.5-h fast; serum glucose was clamped within 15% of baseline. Baseline serum GH concentrations (mean +/- SE: 3.3 +/- 0.7 vs. 1.9 +/- 0.5 micrograms/L, P = 0.02) and total IGF-I concentrations (219 +/- 15 vs. 103 +/- 19 micrograms/L, P < 0.01) were higher in the younger subjects. In both age groups, GH concentrations were significantly decreased by 3 and 10 micrograms/kg.h, but not by 1 microgram/kg.h rhIGF-I. The absolute decrease in GH concentrations was greater in young than in older subjects during the 3 and 10 micrograms/kg.h rhIGF-I infusion periods, but both young and older subjects suppressed to a similar GH level during the last hour of the rhIGF-I infusion (0.78 +/- 0.24 microgram/L and 0.61 +/- 0.16 microgram/L, respectively). The older subjects had a greater increase above baseline in serum concentrations of both total (306 +/- 24 vs. 244 +/- 14 micrograms/L, P = 0.04) and free IGF-I (8.5 +/- 1.4 vs. 4.2 +/- 0.6 micrograms/L, P = 0.01) than the young subjects during rhIGF-I infusion, and their GH suppression expressed in relation to increases in both total and free serum IGF-I concentrations was significantly less than in the young subjects. We conclude that the ability of exogenous rhIGF-I to suppress serum GH concentrations declines with increasing age. This suggests that increased sensitivity to endogenous IGF-I negative feedback is not a cause of the decline in GH secretion that occurs with aging.</abstract><cop>Bethesda, MD</cop><pub>Endocrine Society</pub><pmid>9284733</pmid><doi>10.1210/jc.82.9.2996</doi><tpages>9</tpages></addata></record> |
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subjects | 3-Hydroxybutyric Acid Adult Aging - physiology Biological and medical sciences Blood Glucose - analysis Development. Metamorphosis. Moult. Ageing Dose-Response Relationship, Drug Fatty Acids, Nonesterified - blood Feedback Female Fundamental and applied biological sciences. Psychology Glucose - pharmacology Human Growth Hormone - antagonists & inhibitors Human Growth Hormone - blood Human Growth Hormone - secretion Humans Hydroxybutyrates - blood Infusions, Intravenous Insulin - blood Insulin-Like Growth Factor I - metabolism Insulin-Like Growth Factor I - pharmacology Male Osmolar Concentration Recombinant Proteins Vertebrates: anatomy and physiology, studies on body, several organs or systems |
title | Effect of aging on the sensitivity of growth hormone secretion to insulin-like growth factor-I negative feedback |
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