<p>Explants from SD (A) or Zucker rats (B, C) were pre-treated or not with L-NAME (1 mmol/L) or AG490 (10 µmol/L) for 30 min, then exposed or not to either leptin (10 µg/L), SNAP (1 mmol/L) or IFN-γ (50 µg/L) for 2 h in KRB medium containing 2% BSA and [1-<sup>14</sup>C]-pyruvate. Glyceroneogenic flux was measured by the [1-<sup>14</sup>C]-pyruvate incorporation into neutral lipids. Each value represents the mean ± SEM, (n = 4) *, <i>P</i><0.01 <i>vs</i>. control; <sup>a </sup><i>P</i><0.01 <i>vs.</i> leptin-treated explants. (C) Representative autoradiogram of a western blot performed on WAT cytosolic proteins from Zucker rats reveals total NOS III and its Ser<sup>1179</sup> phosphorylated form.</p
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