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. Author manuscript; available in PMC: 2012 Feb 2.
Published in final edited form as: Cell Metab. 2011 Feb 2;13(2):183–194. doi: 10.1016/j.cmet.2011.01.008

Figure 1. Brain insulin suppresses whole body lipolysis.

Figure 1

(A) Experimental protocol of the euglycemic clamp studies of SD rats. ICV or MBH insulin infusions were performed during basal insulin clamps (1 mU · kg−1 · min−1) and compared to rats subjected to hyperinsulinemic clamps (3 mU · kg−1 · min−1), while glycerol and glucose fluxes were determined through tracer dilution techniques. (B, C) Ra glycerol during basal (B) and clamped (C) conditions (n ≥ 3 per group). (D) Change of plasma NEFA levels compared to baseline during the 6 hr infusion protocol. Arrowhead marks the start of the clamp at time point 120 min (n ≥ 4 per group). (E) AUC of Fig. 1D comparing vehicle to ICV and MBH insulin infused rats prior to the start of the clamp study (time point -120 to 120 min, n ≥ 4 per group). (F) Plasma insulin levels during baseline (time point −120 to 120 min pre-clamp period) and the clamp (120 to 240 min, n ≥ 6 per group). (G, H, I) Plasma glucagon, leptin and adiponectin levels of MBH vehicle and insulin infused rats at baseline and the clamp (n ≥ 6). All error bars are s.e.m.; * P < 0.05, ** P < 0.01, *** P < 0.001 versus vehicle + 1 mU · kg−1 · min−1 clamp group if not otherwise indicated. # P < 0.05 versus vehicle + 3 mU· kg−1 · min−1 clamp group. (See also Fig. S1)