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DOI: 10.1055/s-0030-1269896
© Georg Thieme Verlag KG Stuttgart · New York
Morphofunctional Alterations in Endocrine Pancreas of Short- and Long-term Dexamethasone-treated Rats
Publication History
received 13.08.2010
accepted 22.11.2010
Publication Date:
10 January 2011 (online)
![](https://www.thieme-connect.de/media/hmr/201104/lookinside/thumbnails/10.1055-s-0030-1269896-1.jpg)
Abstract
Long-term dexamethasone therapy may induce peripheral insulin resistance (IR), which in turn elicits increased beta-cell function and proliferation. However, whether such adaptive compensations occur during short-term treatment with dexamethasone is unclear. Here, we compared morphofunctional parameters in endocrine pancreas after short- and long-term dexamethasone administration. Groups of rats received daily i. p. injection of 1 mg/kg b. w. dexamethasone for 1 (DEX-1), 3 (DEX-3), or 5 consecutive days (DEX-5), whilst control rats were saline-treated (CTL). Despite the absence of apparent IR in DEX-1 rats, this group exhibited increased circulating insulin levels and glucose-stimulated insulin secretion (GSIS), compared to the CTL group (p<0.05). Evident IR as well as marked hyperinsulinemia and GSIS, as judged by the static and dynamic insulin secretion values, were observed in DEX-3 and DEX-5 rats (p<0.05). GSIS in islets cultured with 1 μM dexamethasone was lower compared to the control (p<0.05). Marked increases in beta-cell proliferation were observed in DEX-3 and DEX-5 rats, compared to CTL and DEX-1 rats (p<0.05). The alterations observed in DEX-3 rats were more pronounced in DEX-5 rats, which also exhibited a higher content of islet Cdk4 and Cd2 proteins, compared to the CTL group (p<0.05). We conclude that short-term dexamethasone treatment (DEX-1) induces an increase in beta-cell function that does not require the presence of discernible IR. As the treatment continues, the IR develops rapidly, and increased insulin secretion as well as beta-cell hyperplasia is demanded for the appropriate maintenance of glucose homeostasis.
Key words
beta-cell proliferation - dexamethasone - glucocorticoid - insulin secretion - insulin resistance - short- and long-term treatment
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Correspondence
A. Rafacho
Departamento de Ciências
Fisiológicas
Centro de Ciências Biológicas
–CCB
Universidade Federal de Santa
Catarina (UFSC)
88040-900 Florianópolis SC
Brazil
Phone: +55/48/3721 9444
Fax: +55/48/3721 9672
Email: rafacho@ccb.ufsc.br