Insulin regulation of free fatty acid kinetics in adult cystic fibrosis patients with impaired glucose tolerance.
Insulin regulation of free fatty acid kinetics in adult cystic fibrosis patients with impaired glucose tolerance.
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胰岛素对糖耐量受损成人囊性纤维化患者游离脂肪酸动力学的调节。
DOI:
10.1016/j.metabol.2004.06.015
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发表时间:
2004
期刊:
影响因子:
--
通讯作者:
Jensen,MichaelD
中科院分区:
文献类型:
--
作者:
Moran,Antoinette;Basu,Rita;Milla,Carlos;Jensen,MichaelD
Cystic fibrosis (CF) patients are insulin-resistant with regards to suppression of hepatic glucose production and proteolysis, but the effect of insulin on adipose free fatty acid (FFA) release has not been studied. [9,10-3H]palmitate kinetics were measured in 11 stable adult CF patients with impaired glucose tolerance (IGT) and 9 normal control subjects. Baseline plasma palmitate concentrations [CF = 99 ± 13 (median 74, range 65 to 187); control = 88 ± 9 (88, 46 to 138) μmol/L, P = .9] and palmitate flux [CF = 114 ± 11 (100, 72 to 171); control = 105 ± 12 (106, 54 to 182) μmol/min, P = 0.9] were not different between CF patients and controls. During a euglycemic clamp with infusion of insulin to physiologic postprandial levels, however, palmitate concentrations tended to be higher in CF patients: CF = 18 ± 3 (13, 10 to 47), control = 12 ± 1 (11, 8 to 18) μmol/L, P = 0.08. The higher palmitate concentrations during hyperinsulinemia appeared to be due to reduced suppression of adipose tissue palmitate release, because mean palmitate flux was 33% greater in CF subjects [32 ± 5 (26, 17 to 66) μmol/min] than controls: [24 ± 2 (23, 17 to 34) μmol/min], P = .20. There was considerably greater heterogeneity in insulin-induced suppression of plasma palmitate concentration and flux in CF patients compared to normal control subjects. In summary, a defect in insulin suppression of lipolysis was seen in clinically stable CF patients with IGT, similar to what has been described in CF for amino acid and glucose metabolism. This quantitative difference in lipolysis may account for inadequate insulin-induced suppression of hepatic glucose production in CF, and may be a metabolic adaptation to increased energy needs.
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DOI:
10.1172/jci113733
发表时间:
1988-10
期刊:
The Journal of clinical investigation
影响因子:
--
作者:
H. F. Stames;R. S. Warren;M. Jeevanandam;J. Gabrilove;W. Larchian;H. Oettgen;Murray F. Brennan
通讯作者:
H. F. Stames;R. S. Warren;M. Jeevanandam;J. Gabrilove;W. Larchian;H. Oettgen;Murray F. Brennan
DOI:
--
发表时间:
1993
期刊:
International journal of obesity and related metabolic disorders : journal of the International Association for the Study of Obesity
影响因子:
--
作者:
Murgatroyd Pr;Prakash Shetty;Andrew M. Prentice
通讯作者:
Andrew M. Prentice
DOI:
10.1210/jcem.79.1.8027259
发表时间:
1994
期刊:
The Journal of clinical endocrinology and metabolism
影响因子:
--
作者:
Austin,A;Kalhan,SC;Orenstein,D;Nixon,P;Arslanian,S
通讯作者:
Arslanian,S
影响因子:
8.2
作者:
M. Greenfield;O. Kolterman;J. Olefsky;G. Reaven
通讯作者:
G. Reaven
DOI:
--
发表时间:
1992
期刊:
Nutrition (Burbank, Los Angeles County, Calif.)
影响因子:
--
作者:
Hasselgren,PO;Fischer,JE
通讯作者:
Fischer,JE