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过氧化物酶体增殖物激活受体γ激动作用可改变生长激素对脂肪分解和胰岛素敏感性的影响。

Peroxisome proliferator-activated receptor gamma agonism modifies the effects of growth hormone on lipolysis and insulin sensitivity.

作者信息

Krag Morten B, Nielsen Søren, Guo Zengkui, Pedersen Steen B, Schmitz Ole, Christiansen Jens S, Jørgensen Jens O L

机构信息

Medical Department M, Aarhus University Hospital, Aarhus Sygehus, Aarhus C, Denmark.

出版信息

Clin Endocrinol (Oxf). 2008 Sep;69(3):452-61. doi: 10.1111/j.1365-2265.2008.03231.x. Epub 2008 Mar 10.

Abstract

CONTEXT

Peroxisome proliferator-activated receptor gamma (PPAR-gamma) agonists such as thiazolidinediones (TZDs) improve insulin sensitivity in type 2 diabetes mellitus (T2DM) through effects on fat metabolism whereas GH stimulates lipolysis and induces insulin resistance.

OBJECTIVE

To evaluate the impact of TZDs on fat metabolism and insulin sensitivity in subjects exposed to stable GH levels.

DESIGN

A randomized, placebo-controlled, double-blind parallel-group study including 20 GH-deficient patients on continued GH replacement therapy. The patients were studied before and after 12 weeks.

INTERVENTION

Patients received either pioglitazone 30 mg (N = 10) or placebo (N = 10) once daily for 12 weeks.

RESULTS

Adiponectin levels almost doubled during pioglitazone treatment (P = 0.0001). Pioglitazone significantly decreased basal free fatty acid (FFA) levels (P = 0.02) and lipid oxidation (P = 0.02). Basal glucose oxidation rate (P = 0.004) and insulin sensitivity (P = 0.03) improved in the patients who received pioglitazone treatment. The change in insulin-stimulated adiponectin level after pioglitazone treatment was positively correlated to the change in insulin-stimulated total glucose disposal (R = 0.69, P = 0.04).

CONCLUSION

The impact of GH on lipolysis and insulin sensitivity can be modified by administration of TZDs.

摘要

背景

过氧化物酶体增殖物激活受体γ(PPAR-γ)激动剂,如噻唑烷二酮类(TZDs),通过对脂肪代谢的作用改善2型糖尿病(T2DM)患者的胰岛素敏感性,而生长激素(GH)刺激脂肪分解并诱导胰岛素抵抗。

目的

评估TZDs对处于稳定GH水平的受试者脂肪代谢和胰岛素敏感性的影响。

设计

一项随机、安慰剂对照、双盲平行组研究,纳入20例接受持续GH替代治疗的GH缺乏患者。在12周前后对患者进行研究。

干预

患者每天接受一次30mg吡格列酮(N = 10)或安慰剂(N = 10),持续12周。

结果

吡格列酮治疗期间脂联素水平几乎翻倍(P = 0.0001)。吡格列酮显著降低基础游离脂肪酸(FFA)水平(P = 0.02)和脂质氧化(P = 0.02)。接受吡格列酮治疗的患者基础葡萄糖氧化率(P = 0.004)和胰岛素敏感性(P = 0.03)得到改善。吡格列酮治疗后胰岛素刺激的脂联素水平变化与胰岛素刺激的总葡萄糖处置变化呈正相关(R = 0.69,P = 0.04)。

结论

给予TZDs可改变GH对脂肪分解和胰岛素敏感性的影响。

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