首页> 外文期刊>Metabolism: Clinical and Experimental >Insulin regulation of free fatty acid kinetics in adult cystic fibrosis patients with impaired glucose tolerance.
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Insulin regulation of free fatty acid kinetics in adult cystic fibrosis patients with impaired glucose tolerance.

机译:葡萄糖调节受损的成年囊性纤维化患者的胰岛素调节游离脂肪酸动力学。

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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-(3)H]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) mumol/L, P = .9] and palmitate flux [CF = 114 +/- 11 (100, 72 to 171); control = 105 +/- 12 (106, 54 to 182) mumol/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) mumol/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) mumol/min] than controls: [24 +/- 2 (23, 17 to 34) mumol/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.
机译:囊性纤维化(CF)患者在抑制肝葡萄糖生成和蛋白水解方面具有胰岛素抵抗性,但尚未研究胰岛素对脂肪游离脂肪酸(FFA)释放的影响。 [11,10-(3)H]棕榈酸酯动力学在11名稳定的糖耐量受损(IGT)成人CF患者和9名正常对照受试者中进行了测量。基线血浆棕榈酸酯浓度[CF = 99 +/- 13(中位数74,范围65至187);控制= 88 +/- 9(88,46至138)mumol / L,P = 0.9]和棕榈酸酯通量[CF = 114 +/- 11(100,72至171);对照组= 105 +/- 12(106,54至182)mumol / min,P = 0.9]在CF患者和对照组之间没有差异。但是,在正常胰岛素钳夹过程中,向餐后生理水平注入胰岛素时,CF患者的棕榈酸酯浓度往往较高:CF = 18 +/- 3(13,10至47),对照= 12 +/- 1(11, 8至18)mumol / L,P = 0.08。高胰岛素血症期间较高的棕榈酸酯浓度似乎是由于对脂肪组织棕榈酸酯释放的抑制作用降低,因为CF受试者的平均棕榈酸酯通量比对照组高32%[32 +/- 5(26,17至66)mumol / min]: [24 +/- 2(23,17至34)摩尔/分钟],P = 0.20。与正常对照组相比,CF患者在胰岛素诱导的血浆棕榈酸酯浓度和通量抑制方面存在更大的异质性。总之,在临床上稳定的患有IGT的CF患者中,胰岛素抑制脂解存在缺陷,类似于CF中对氨基酸和葡萄糖代谢的描述。脂解作用的这种定量差异可能解释了胰岛素诱导的CF中肝葡萄糖生成的抑制作用不足,并且可能是对能量需求增加的代谢适应。

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