...
首页> 外文期刊>Metabolism: Clinical and Experimental >Effects of free fatty acids on plasma resistin and insulin resistance in awake rats.
【24h】

Effects of free fatty acids on plasma resistin and insulin resistance in awake rats.

机译:游离脂肪酸对清醒大鼠血浆抵抗素和胰岛素抵抗的影响。

获取原文
获取原文并翻译 | 示例
           

摘要

Resistin has been postulated to play a role in obesity-related insulin resistance. To explore this possibility, we have investigated effects of acute euglycemic (5.2+/-0.1 mmol/L) hyperinsulinemia (96+/-8 microU/mL) with and without concurrent infusion of lipid plus heparin (to raise or lower plasma free fatty acid [FFA] levels) on glucose turnover and plasma resistin levels in alert rats. Plasma FFA concentrations increased during lipid/heparin (L/H) infusion (from 0.82 to 2.86 mmol/L, P<.001) and decreased (from 0.83 to 0.21 mmol/L, P<.001) in controls who were infused with insulin but not with L/H. L/H infusion reduced insulin suppression of endogenous glucose production by approximately 90% (from 28.9 to 3.1 mg. kg-1 . min-1, P<.001) and insulin-stimulated glucose uptake (glucose rate of disappearance) by 78% (from 30.8% to 6.9%, P<.001). Plasma resistin levels increased by 46% (from 39.9 to 58.4 microg/L, P<.05) during L/H infusion and did not change in controls (39.7 vs 39.3 microg/L). Plasma ghrelin levels decreased by 41% (from 892 to 584 ng/L, P<.05) in response to hyperinsulinemia, whereas concurrent L/H infusion had no additional effect on ghrelin levels (584+/-67 vs 548+/-82 ng/L). In summary, we found that FFA induced hepatic insulin resistance, and to a lesser extent, peripheral insulin resistance was associated with elevated plasma resistin levels. We conclude that FFA-induced release of resistin may contribute to the development of FFA-induced insulin resistance in rats.
机译:假设抵抗素在肥胖相关的胰岛素抵抗中起作用。为了探讨这种可能性,我们研究了急性和正常血糖(5.2 +/- 0.1 mmol / L)高胰岛素血症(96 +/- 8 microU / mL)的影响,有无同时输注脂质和肝素(升高或降低血浆游离脂肪)酸(FFA)水平对机敏大鼠的葡萄糖代谢和血浆抵抗素水平的影响。输注脂质/肝素(L / H)的对照组血浆中FFA浓度增加(从0.82至2.86 mmol / L,P <.001),而在接受脂质/肝素(L / H)的对照组中降低(从0.83至0.21 mmol / L,P <.001)胰岛素,但不使用L / H。 L / H输注将胰岛素对内源性葡萄糖产生的抑制作用降低了约90%(从28.9降低至3.1 mg。kg-1。min-1,P <.001),胰岛素刺激的葡萄糖摄取(葡萄糖消失率)降低了78% (从30.8%降至6.9%,P <.001)。在L / H输注期间,血浆抵抗素水平增加了46%(从39.9微克/升,从59.9微克/升,P <.05),并且在对照组中没有变化(39.7 vs 39.3微克/升)。响应高胰岛素血症,血浆生长素释放肽水平降低了41%(从892降至584 ng / L,P <.05),而同时进行L / H输注对生长素释放肽水平没有其他影响(584 +/- 67与548 +/- 82 ng / L)。总之,我们发现FFA诱导肝胰岛素抵抗,并且在较小程度上,外周胰岛素抵抗与血浆抵抗素水平升高相关。我们得出结论,FFA诱导的抵抗素释放可能有助于FFA诱导的大鼠胰岛素抵抗的发展。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号