Figure 1
From: GLP-1/Exendin-4 induces β-cell proliferation via the epidermal growth factor receptor

(A) Fasting glucose levels were increased in Cre+Ex−mice. This increase was not reversed by exendin-4 treatment (Cre+Ex+). (B) Glucose tolerance tests showed an enhanced ability to respond to a glucose load in control Cre− mice with exendin-4 treatment (Cre−Ex+). A defect in glucose tolerance was seen in Cre+Ex− mice that could not be salvaged with exendin-4 (Cre+Ex−). (C) β-cell mass was significantly increased in control mice as compared with Cre+ mice. (D) Insulin content mirrors β-cell mass. (E) Islet size was significantly increased in control mice after exendin-4 treatment (Cre−Ex+), as compared with Cre+Ex+ and Cre+Ex− mice. n = 5. All results were mean ± S.E. * #, p < 0.05, NS, no significance). (F) In vitro GSIS shows significantly increased insulin release in control mice with exendin-4 treatment (Cre−Ex+) at low and high glucose concentrations. At high glucose concentrations, there is significantly less insulin secretion in Cre+ mice, regardless of treatment with exendin-4, as compared to control Cre− mice.