RGD Reference Report - Activation of AMPK is essential for AICAR-induced glucose uptake by skeletal muscle but not adipocytes. - Rat Genome Database

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Activation of AMPK is essential for AICAR-induced glucose uptake by skeletal muscle but not adipocytes.

Authors: Sakoda, H  Ogihara, T  Anai, M  Fujishiro, M  Ono, H  Onishi, Y  Katagiri, H  Abe, M  Fukushima, Y  Shojima, N  Inukai, K  Kikuchi, M  Oka, Y  Asano, T 
Citation: Sakoda H, etal., Am J Physiol Endocrinol Metab 2002 Jun;282(6):E1239-44.
RGD ID: 625764
Pubmed: PMID:12006353   (View Abstract at PubMed)
DOI: DOI:10.1152/ajpendo.00455.2001   (Journal Full-text)

5-Aminoimidazole-4-carboxamide ribonucleoside (AICAR) reportedly activates AMP-activated protein kinase (AMPK) and stimulates glucose uptake by skeletal muscle cells. In this study, we investigated the role of AMPK in AICAR-induced glucose uptake by 3T3-L1 adipocytes and rat soleus muscle cells by overexpressing wild-type and dominant negative forms of the AMPKalpha2 subunit by use of adenovirus-mediated gene transfer. Overexpression of the dominant negative mutant had no effect on AICAR-induced glucose transport in adipocytes, although AMPK activation was almost completely abolished. This suggests that AICAR-induced glucose uptake by 3T3-L1 adipocytes is independent of AMPK activation. By contrast, overexpression of the dominant negative AMPKalpha2 mutant in muscle markedly suppressed both AICAR-induced glucose uptake and AMPK activation, although insulin-induced uptake was unaffected. Overexpression of the wild-type AMPKalpha2 subunit significantly increased AMPK activity in muscle but did not enhance glucose uptake. Thus, although AMPK activation may not, by itself, be sufficient to increase glucose transport, it appears essential for AICAR-induced glucose uptake in muscle.

Objects referenced in this article
Gene Prkaa2 protein kinase AMP-activated catalytic subunit alpha 2 Rattus norvegicus

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