Peth J A, Kinnick T R, Youngblood E B, Tritschler H J, Henriksen E J
Muscle Metabolism Laboratory, Department of Physiology, University of Arizona College of Medicine, Tucson, Arizona 85721-0093, USA.
Am J Physiol Regul Integr Comp Physiol. 2000 Feb;278(2):R453-9. doi: 10.1152/ajpregu.2000.278.2.R453.
The purpose of this study was to assess the individual and interactive effects of the antioxidant alpha-lipoic acid (LPA) and the n-6 essential fatty acid gamma-linolenic acid (GLA) on insulin action in insulin-resistant obese Zucker rats. LPA, GLA, and a unique conjugate consisting of equimolar parts of LPA and GLA (LPA-GLA) were administered for 14 days at 10, 30, or 50 mg. kg body wt(-1). day(-1). Whereas LPA was without effect at 10 mg/kg, at 30 and 50 mg/kg it elicited 23% reductions (P < 0.05) in the glucose-insulin index (the product of glucose and insulin areas under the curve during an oral glucose tolerance test and an index of peripheral insulin action) that were associated with significant increases in insulin-mediated (2 mU/ml) glucose transport activity in isolated epitrochlearis (63-65%) and soleus (33-41%) muscles. GLA at 10 and 30 mg/kg caused 21-25% reductions in the glucose-insulin index and 23-35% improvements in insulin-mediated glucose transport in epitrochlearis muscle. The beneficial effects of GLA disappeared at 50 mg/kg. At 10 and 30 mg/kg, the LPA-GLA conjugate elicited 29 and 38% reductions in the glucose-insulin index. These LPA-GLA-induced improvements in whole body insulin action were accompanied by 28-63 and 38-57% increases in insulin-mediated glucose transport in epitrochlearis and soleus muscles and resulted from the additive effects of LPA and GLA. At 50 mg/kg, the metabolic improvements due to LPA-GLA were substantially reduced. In summary, these results indicate that the conjugate of the antioxidant LPA and the n-6 essential fatty acid GLA elicits significant dose-dependent improvements in whole body and skeletal muscle insulin action on glucose disposal in insulin-resistant obese Zucker rats. Moreover, these actions of LPA-GLA are due to the additive effects of its individual components.
本研究的目的是评估抗氧化剂α-硫辛酸(LPA)和n-6必需脂肪酸γ-亚麻酸(GLA)对胰岛素抵抗的肥胖Zucker大鼠胰岛素作用的个体及交互影响。以10、30或50 mg·kg体重⁻¹·天⁻¹的剂量给予LPA、GLA以及由等摩尔量的LPA和GLA组成的独特共轭物(LPA-GLA),持续14天。LPA在10 mg/kg时无作用,但在30和50 mg/kg时,可使葡萄糖-胰岛素指数(口服葡萄糖耐量试验期间葡萄糖和胰岛素曲线下面积的乘积,是外周胰岛素作用的一个指标)降低23%(P<0.05),这与离体肱三头肌(63 - 65%)和比目鱼肌(33 - 41%)中胰岛素介导的(2 mU/ml)葡萄糖转运活性显著增加有关。10和30 mg/kg的GLA可使葡萄糖-胰岛素指数降低21 - 25%,并使肱三头肌中胰岛素介导的葡萄糖转运提高23 - 35%。GLA在50 mg/kg时的有益作用消失。在10和30 mg/kg时,LPA-GLA共轭物可使葡萄糖-胰岛素指数分别降低29%和38%。这些由LPA-GLA引起的全身胰岛素作用改善伴随着肱三头肌和比目鱼肌中胰岛素介导的葡萄糖转运分别增加28 - 63%和38 - 57%,这是LPA和GLA的相加作用所致。在50 mg/kg时,LPA-GLA引起的代谢改善显著降低。总之,这些结果表明,抗氧化剂LPA与n-6必需脂肪酸GLA的共轭物可使胰岛素抵抗的肥胖Zucker大鼠在全身及骨骼肌胰岛素作用对葡萄糖处置方面产生显著的剂量依赖性改善。此外,LPA-GLA的这些作用是由于其各成分的相加作用。