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. Author manuscript; available in PMC: 2009 Dec 26.
Published in final edited form as: Cell. 2009 Jun 26;137(7):1225–1234. doi: 10.1016/j.cell.2009.04.022

Figure 2. Minipump delivery of bretazenil into the 4th ventricle is more efficacious than delivery into the 3rd ventricle.

Figure 2

(A) Percentage of initial body weight of DT-treated, AgrpDTR/+ mice in which bretazenil (75 ng/hr; 1/10th of the dosage used in Figure 1) or vehicle was chronically administered either subcutaneously (sc) or directly into the 3rd (3v) or 4th (4v) ventricle.

(B) Percentage of initial body weight of DT-treated, AgrpDTR/+ mice in which bretazenil (15 ng/hr; 1/50th of the dosage used in Figure 1) or vehicle was chronically administered directly into the 3rd or 4th ventricle. Note that abrupt withdrawal of bretazenil delivered into the 4th ventricle at Day 4 resulted in more profound decline of body weight than that was shown by the AgRP-ablated mice infused with vehicle; *, p < 0.01, ANOVA.

(C) Percentage of initial body weight of DT-treated, AgrpDTR/+ mice in which bretazenil (7.5 or 2.5 ng/hr, 1/100th or 1/300th of the dosage used in Figure 1, respectively) or vehicle was chronically administered directly into either the 3rd or 4th ventricle.

N = 6 - 8 for each group. Error bars represent the SEM.