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首页> 外文期刊>American Journal of Physiology >Akt1 kinase and dynamics of insulin resistance in denervated muscles in vivo.
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Akt1 kinase and dynamics of insulin resistance in denervated muscles in vivo.

机译:Akt1激酶和失神经肌肉体内胰岛素抵抗的动态。

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Basal and insulin-stimulated activity of Akt1 kinase and uptake of 2-deoxy-D-glucose (2-DG) were measured in soleus (slow-twitch) and plantaris (fast-twitch) muscles of rats at 1 and 3 days after sectioning the sciatic nerve in one hindlimb of the animals. At 1 day after surgery, the insulin-stimulated activity of Akt1 kinase in denervated soleus and plantaris muscles remained unchanged, but the insulin-stimulated 2-DG uptake by these muscles was reduced by 71 and 61%, respectively, compared with the corresponding muscles of the contralateral sham (control) hindlimb. At 3 days, the insulin-stimulated activity of Akt1 kinase in the denervated soleus and plantaris muscles was 86 and 71% lower, respectively, than in their sham counterparts. At this time point, the denervated soleus muscles showed no increase in 2-DG uptake in response to insulin. In contrast, the denervated plantaris muscle exhibited the same absolute level of insulin-stimulated 2-DG uptake as the sham plantaris muscle; however, the insulin-induced increment in 2-DG uptake was reduced by 60%, whereas basal 2-DG uptake was increased by 251% compared with the sham plantaris muscle. None of the denervated muscles showed a decrease in the abundance of Akt1 kinase. The results demonstrate that the causes of insulin resistance in denervated muscles are dependent on time after surgery. Initially, they involve only mechanisms downstream of Akt1 kinase (day 1), whereas at day 3 they also involve mechanisms upstream of, and including, Akt1 kinase.
机译:在切片后1天和3天,测量比目鱼肌(慢肌)和plant肌(快肌)中Akt1激酶的基础和胰岛素刺激活性以及2-脱氧-D-葡萄糖(2-DG)的摄取动物后肢的坐骨神经。术后1天,神经失常的比目鱼肌和plant肌中Akt1激酶的胰岛素刺激活性保持不变,但是与相应的肌肉相比,这些肌肉的胰岛素刺激的2-DG摄取分别降低了71%和61%。对侧假肢(对照)的后肢。在第3天,神经失常的比目鱼肌和足底肌中Akt1激酶的胰岛素刺激活性分别比假手术者低86和71%。在这个时间点上,神经失常的比目鱼肌显示对胰岛素的2-DG摄取没有增加。相反,失神经的plant肌表现出与假plant肌相同的胰岛素刺激的2-DG摄取绝对水平。然而,与假plant肌相比,胰岛素诱导的2-DG摄取增加减少了60%,而基础2-DG摄取增加了251%。失神经的肌肉均未显示Akt1激酶丰度降低。结果表明,失神经肌肉中胰岛素抵抗的原因取决于手术后的时间。最初,它们仅涉及Akt1激酶下游的机制(第1天),而在第3天,它们还涉及Akt1激酶上游的机制,包括Akt1激酶。

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