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. Author manuscript; available in PMC: 2018 Oct 11.
Published in final edited form as: Neuron. 2017 Oct 11;96(2):461–475.e5. doi: 10.1016/j.neuron.2017.09.043

Figure 8. AgRP neurons are epistatic to leptin's effect on food intake.

Figure 8

(A) Schematic of experiments in (B-D). Optogenetic stimulation of AgRP neurons in ad libitum fed WT and ob/ob mice prior to (prestim) or during (costim) food availability. Blue indicates the timing of laser stimulation.

(B) Cumulative food intake by ob/ob mice after no stimulation (black), 60 min pre-stimulation (red), or during 60 min co-stimulation (blue). Traces represent mean ± SEM (n = 6-10 mice per group).

(C) Quantification of food intake from (B).

(D) Raster plots showing feeding pattern in individual mice from (B and C).

(E) Schematic of experiments in (F-H). Optogenetic stimulation of AgRP neurons in ad libitum fed, ob/ob mice during chronic vehicle or leptin infusion by mini-osmotic pumps. Stimulation occurred prior to (prestim) or during (costim) food availability as in (A).

(F) Bodyweight change in ob/ob mice 3 days after implantation of a mini-osmotic pump infusing vehicle (gray, n = 6 mice) or leptin (red, n = 7 mice)

(G) Quantification of food intake by ad libitum fed ob/ob mice from (F) receiving chronic vehicle (gray) or leptin (red) infusion after no stimulation, 60 min pre-stimulation, or during 60 min co-stimulation.

(H) Raster plots showing feeding pattern in individual mice from (G).

(C, F, G) ■ denotes individual mice. Bars represent mean ± SEM. *P < 0.05, **P < 0.01, ***P < 10-3. (D and H) Each row represents a single trial from a different animal and each point indicates consumption of a 0.02 g pellet.

See also Figure S7.