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. 2010 Mar 1;107(11):4813–4819. doi: 10.1073/pnas.0909422107

Fig. 4.

Fig. 4.

(A) Comparison of blood glucose levels in glucagon receptor null (Gcgr−/−) mice (□) and wild-type (Gcgr+/+) controls (•) after treatment with double-dose alloxan. (B) Comparison of severity of insulin deficiency in the alloxan-treated Gcgr−/− and Gcgr+/+ and nondiabetic Gcgr−/− and Gcgr+/+ controls based on plasma insulin levels and morphometric values for insulin-immunostained β-cells in pancreata. The results indicate no significant difference in residual insulin that could explain the absence of hyperglycemia in the alloxan-treated Gcgr−/− group. Nondiabetic, □; alloxan diabetic, ■.