1. Pancreatic glucose-dependent insulinotropic polypeptide (GIP) (1–30) expression is upregulated in diabetes and PEGylated GIP(1–30) can suppress the progression of low-dose-STZ-induced hyperglycaemia in mice
- Author
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Yukihiro Fujita, Masakazu Haneda, Yasutaka Takeda, Tsuyoshi Yanagimachi, Atsuko Abiko, Timothy J. Kieffer, Yuichi Makino, Kuralay Atageldiyeva, Yumi Takiyama, and Jun Honjo
- Subjects
Male ,0301 basic medicine ,endocrine system ,medicine.medical_specialty ,endocrine system diseases ,Endocrinology, Diabetes and Metabolism ,medicine.medical_treatment ,Gastric Inhibitory Polypeptide ,Peptide hormone ,Glucagon ,Streptozocin ,Alpha cell ,Diabetes Mellitus, Experimental ,Mice ,03 medical and health sciences ,Downregulation and upregulation ,Internal medicine ,Internal Medicine ,medicine ,Animals ,Hypoglycemic Agents ,Cell Proliferation ,Dipeptidyl-Peptidase IV Inhibitors ,geography ,geography.geographical_feature_category ,business.industry ,Insulin ,Body Weight ,Islet ,Streptozotocin ,Immunohistochemistry ,Peptide Fragments ,Mice, Inbred C57BL ,030104 developmental biology ,Endocrinology ,Hyperglycemia ,Beta cell ,business ,hormones, hormone substitutes, and hormone antagonists ,medicine.drug - Abstract
Glucose-dependent insulinotropic polypeptide (GIP) is a peptide hormone released from gut K cells. While the predominant form is GIP(1-42), a shorter form, GIP(1-30), is produced by pancreatic alpha cells and promotes insulin secretion in a paracrine manner. Here, we elucidated whether GIP(1-30) expression is modulated in mouse models of diabetes. We then investigated whether PEGylated GIP(1-30) can improve islet function and morphology as well as suppress the progression to hyperglycaemia in mice treated with low-dose streptozotocin (LD-STZ).We examined pancreatic GIP immunoreactivity in rodent diabetic models. We synthesised [D-Ala(2)]GIP(1-30) and modified the C-terminus with polyethylene glycol (PEG) to produce a dipeptidyl peptidase-4 (DPP-4)-resistant long-acting GIP analogue, [D-Ala(2)]GIP(1-30)-PEG. We performed i.p.GTT and immunohistochemical analysis in non-diabetic and LD-STZ diabetic mice, with or without administration of [D-Ala(2)]GIP(1-30)-PEG.Pancreatic GIP expression was concomitantly enhanced with alpha cell expansion in rodent models of diabetes. Treatment with DPP-4 inhibitor decreased both the GIP- and glucagon-positive areas and preserved the insulin-positive area in LD-STZ diabetic mice. Body weight was not affected by [D-Ala(2)]GIP(1-30)-PEG in LD-STZ or non-diabetic mice. Treatment with GIP significantly ameliorated chronic hyperglycaemia and improved glucose excursions in LD-STZ mice. Treatment with GIP also reduced alpha cell expansion in the islets and suppressed plasma glucagon levels compared with non-treated LD-STZ mice. Additionally, [D-Ala(2)]GIP(1-30)-PEG preserved beta cell area via inhibition of apoptosis in LD-STZ mice.Our data suggest that GIP(1-30) expression is upregulated in diabetes, and PEGylated GIP(1-30) can suppress the progression to STZ-induced hyperglycaemia by inhibiting beta cell apoptosis and alpha cell expansion.
- Published
- 2015