CART Regulates Islet Hormone Secretion and Is Expressed in the β-Cells of Type 2 Diabetic Rats
- 1Department of Experimental Medical Science, Division of Diabetes, Metabolism, and Endocrinology, Lund University, Lund, Sweden
- 2Yerkes National Primate Research Center of Emory University, Atlanta, Georgia
- Address correspondence and reprint requests to Nils Wierup, PhD, Lund University, Department of Experimental Medical Science, Division of Diabetes, Metabolism, and Endocrinology, BMC F10, 22 184, Lund, Sweden. E-mail: nils.wierup{at}med.lu.se
Abstract
Cocaine- and amphetamine-regulated transcript (CART) is an anorexigenic peptide widely expressed in the central, peripheral, and enteric nervous systems. CART is also expressed in endocrine cells, including β-cells during rat development and δ-cells of adult rats. We examined the effect of CART 55–102 on islet hormone secretion, using INS-1(832/13) cells and isolated rat islets. In addition, islet CART expression was examined in two rat models of type 2 diabetes: Goto-Kakizaki (GK) rats and dexamethasone (DEX)-treated rats. At high glucose, CART potentiated cAMP-enhanced insulin secretion via the cAMP/protein kinase A-dependent pathway. In the absence of cAMP-elevating agents, CART was without effect on INS-1 cells but modestly inhibited secretion of insulin, glucagon, and somatostatin from isolated islets. CART was markedly upregulated in the β-cells of both diabetes models. Thus, in DEX-treated rats, islet CART mRNA expression, and the number of CART-immunoreactive β-cells were 10-fold higher than in control rats. In GK rats, the relative number of CART-expressing β-cells was 30-fold higher than in control rats. We conclude that CART is a regulator of islet hormone secretion and that CART is upregulated in the β-cells of type 2 diabetic rats.
- CART, cocaine- and amphetamine-regulated transcript
- DEX, dexamethasone
- GLP-1, glucagon-like peptide-1
- GSIS, glucose-stimulated insulin secretion
- HBSS, HEPES-buffered saline solution
- IBMX, isobutyl-methylxanthine
- PKA, protein kinase A
- PP, pancreatic polypeptide
- TEM, transmission electron microscope
Footnotes
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- Accepted October 28, 2005.
- Received November 11, 2004.
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