首页> 外文期刊>The journals of gerontology.Series A. Biological sciences and medical sciences >Aging elevates basal adenosine monophosphate-activated protein kinase (AMPK) activity and eliminates hypoxic activation of AMPK in mouse liver.
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Aging elevates basal adenosine monophosphate-activated protein kinase (AMPK) activity and eliminates hypoxic activation of AMPK in mouse liver.

机译:衰老提高了小鼠肝脏中基础磷酸腺苷单磷酸激活的蛋白激酶(AMPK)的活性,并消除了AMPK的低氧激活。

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Despite the central role of adenosine monophosphate-activated protein kinase (AMPK) in the cellular stress response, it is unknown whether age-related changes in AMPK activity play a role in the diminished stress tolerance that is characteristic of aging. To address this question, we determined in the mouse liver how normal aging affects 1) basal AMPK activity, and 2) the degree to which AMPK activity is increased by in vivo hypoxia. We found that the basal activity of AMPK alpha1, but not alpha2, was higher in livers from 24-month-old mice compared to those from 5-month-old mice. Furthermore, while hypoxia elevated AMPK alpha1 and alpha2 activities in livers from 5-month-old mice, hypoxia failed to increase the activity of either isoform of AMPK in 24-month-old mice. These findings suggest that age-associated changes in hepatic AMPK activity may play a role in the physiological changes that occur in the liver with normal aging.
机译:尽管腺苷单磷酸激活的蛋白激酶(AMPK)在细胞应激反应中起着中心作用,但未知与年龄相关的AMPK活性变化是否在降低以衰老为特征的应激耐受性中起作用。为了解决这个问题,我们确定了小鼠肝脏中正常衰老如何影响1)基础AMPK活性,以及​​2)体内缺氧增加AMPK活性的程度。我们发现,与5个月大的小鼠相比,24个月大的小鼠的肝脏中AMPK alpha1而不是alpha2的基础活性更高。此外,尽管缺氧会提高5个月大小鼠肝脏中AMPK alpha1和alpha2的活性,但缺氧并不能增加24个月大小鼠中AMPK任一同工型的活性。这些发现表明,与肝脏衰老相关的肝脏AMPK活性变化可能在正常衰老肝脏中发生的生理变化中起作用。

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