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. 2015 Jun 11;10(6):e0129644. doi: 10.1371/journal.pone.0129644

Fig 1. Administration of ZAG increases basal glucose uptake.

Fig 1

Differentiated SGBS adipocytes (A) and LiSa-2 adipocytes (B) were cultured for 24 hours with or without 25 μg/ml ZAG. Glucose uptake was measured during the final 10 min by incorporation of labelled 2-deoxyglucose into the cells. Results are the mean±SEM of 3–4 independent experiments performed in triplicate. (C) Gene expression of GLUT1, GLUT3 and GLUT4 in SGBS and (D) LiSa-2 adipocytes treated or not with ZAG was analyzed by quantitative real time PCR (qPCR). Data are presented as mean±SEM (n = 3). *, P < 0.01 vs control.