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. 2022 Jun 2;65(8):1375–1389. doi: 10.1007/s00125-022-05729-y

Fig. 5.

Fig. 5

Isolated A-IDE-KO islets show constitutive glucagon and insulin secretion. (a) Glucagon secreted by islets, isolated from control and A-IDE-KO mice, in response to low and high glucose (1 mmol/l glucose; 16 mmol/l glucose). (b) Glucagon secreted by isolated islets in response to insulin inhibition (in the presence of 1 mmol/l glucose). (c) Glucagon secreted by wild-type C57Bl/6J mouse islets treated with 10 μmol/l 6bK (selective IDE inhibitor) for 30 min, in response to low and high glucose. (d) Insulin secreted by isolated islets in response to low and high glucose. n = 17–21 islet batches. Data are presented as means ± SEM. *p<0.05 vs control 1 mmol/l glucose; †††p<0.001 vs control 16 mmol/l glucose; p<0.05 vs A-IDE-KO 16 mmol/l glucose. G, mmol/l glucose; INS, insulin