Effect of insulin on whole body protein metabolism in children with type 1 diabetes

被引:9
作者
Caso, Giuseppe [1 ]
McNurlan, Margaret A. [1 ]
机构
[1] SUNY Stony Brook, Med Ctr, Dept Surg, Stony Brook, NY 11794 USA
关键词
children; insulin; protein degradation; protein synthesis; type; 1; diabetes; AMINO-ACID INFUSION; GROWING PUBERTAL CHILDREN; LEUCINE METABOLISM; ALBUMIN SYNTHESIS; SKELETAL-MUSCLE; ORAL NUTRIENTS; KINETICS; MELLITUS; RATS; AVAILABILITY;
D O I
10.1097/MCO.0b013e328333294d
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
Purpose of review Untreated type I diabetes (T1D) is associated with abnormalities in protein metabolism, leading to protein loss. These alterations can be particularly detrimental in children, affecting both normal growth and development. A better understanding of the effects of insulin on protein metabolism in children with T1D is essential for optimizing therapy and minimizing consequences of the disease. The aim of the present review is to outline the effects of insulin on whole body protein metabolism in T1D, focusing particularly on studies in children with T1D. Recent findings Whole body protein degradation and amino acid oxidation are enhanced in children with T1D. Insulin reduces the rates at which body proteins are degraded. Whole body protein synthesis is either unaffected or reduced by insulin, even when insulin is administered together with amino acids to prevent insulin-dependent hypoaminoacidemia. Provision of insulin with oral nutrients improves protein balance by inhibiting whole body protein degradation, but does not affect protein synthesis. Summary In children with T1D the anticatabolic effects of insulin on whole body protein metabolism are mainly exerted through a reduction in rates at which body proteins are degraded. Nutritional factors enhancing the anabolic effect of insulin need to be further elucidated.
引用
收藏
页码:93 / 96
页数:4
相关论文
共 28 条
[1]
RESPONSES OF PROTEIN-SYNTHESIS IN DIFFERENT SKELETAL-MUSCLES TO FASTING AND INSULIN IN RATS [J].
BAILLIE, AGS ;
GARLICK, PJ .
AMERICAN JOURNAL OF PHYSIOLOGY, 1991, 260 (06) :E891-E896
[2]
ATTENUATED RESPONSES OF MUSCLE PROTEIN-SYNTHESIS TO FASTING AND INSULIN IN ADULT FEMALE RATS [J].
BAILLIE, AGS ;
GARLICK, PJ .
AMERICAN JOURNAL OF PHYSIOLOGY, 1992, 262 (01) :E1-E5
[3]
BALLMER PE, 1995, J NUTR, V125, P512
[4]
INABILITY TO STIMULATE SKELETAL-MUSCLE OR WHOLE-BODY PROTEIN-SYNTHESIS IN TYPE-1 (INSULIN-DEPENDENT) DIABETIC-PATIENTS BY INSULIN-PLUS-GLUCOSE DURING AMINO-ACID INFUSION - STUDIES OF INCORPORATION AND TURNOVER OF TRACER L-[1-C-13]LEUCINE [J].
BENNET, WM ;
CONNACHER, AA ;
SMITH, K ;
JUNG, RT ;
RENNIE, MJ .
DIABETOLOGIA, 1990, 33 (01) :43-51
[5]
Effect of Insulin With Oral Nutrients on Whole-Body Protein Metabolism in Growing Pubertal Children With Type 1 Diabetes [J].
Braziuniene, Ieva ;
Garlick, Jeremy ;
Mileva, Izolda ;
Desikan, Vardhini ;
Wilson, Thomas A. ;
McNurlan, Margaret .
PEDIATRIC RESEARCH, 2009, 65 (01) :109-112
[6]
EFFECTS OF PUBERTY AND DIABETES ON METABOLISM OF INSULIN-SENSITIVE FUELS [J].
CAPRIO, S ;
CLINE, G ;
BOULWARE, S ;
PERMANENTE, C ;
SHULMAN, GI ;
SHERWIN, RS ;
TAMBORLANE, WV .
AMERICAN JOURNAL OF PHYSIOLOGY, 1994, 266 (06) :E885-E891
[7]
Response of albumin synthesis to oral nutrients in young and elderly subjects [J].
Caso, Giuseppe ;
Feiner, Joshua ;
Mileva, Izolda ;
Bryan, Leslie J. ;
Kelly, Patricia ;
Autio, Karen ;
Gelato, Marie C. ;
McNurlan, Margaret A. .
AMERICAN JOURNAL OF CLINICAL NUTRITION, 2007, 85 (02) :446-451
[8]
Protein metabolism in insulin-dependent diabetes mellitus [J].
Charlton, M ;
Nair, KS .
JOURNAL OF NUTRITION, 1998, 128 (02) :323S-327S
[9]
INSULIN-MEDIATED REDUCTION OF WHOLE-BODY PROTEIN BREAKDOWN - DOSE-RESPONSE EFFECTS ON LEUCINE METABOLISM IN POST-ABSORPTIVE MEN [J].
FUKAGAWA, NK ;
MINAKER, KL ;
ROWE, JW ;
GOODMAN, MN ;
MATTHEWS, DE ;
BIER, DM ;
YOUNG, VR .
JOURNAL OF CLINICAL INVESTIGATION, 1985, 76 (06) :2306-2311
[10]
THE EFFECT OF INSULIN INFUSION AND FOOD-INTAKE ON MUSCLE PROTEIN-SYNTHESIS IN POSTABSORPTIVE RATS [J].
GARLICK, PJ ;
FERN, M ;
PREEDY, VR .
BIOCHEMICAL JOURNAL, 1983, 210 (03) :669-676