Your browser doesn't support javascript.
loading
Role and mechanism of rosiglitazone on the impairment of insulin secretion induced by free fatty acids on isolated rat islets / 中华医学杂志(英文版)
Chinese Medical Journal ; (24): 574-580, 2006.
Article in English | WPRIM | ID: wpr-267082
ABSTRACT
<p><b>BACKGROUND</b>Prolonged exposure of pancreatic beta-cells to fatty acids increases basal insulin secretion but inhibits glucose-stimulated insulin secretion. Rosiglitazone is a new antidiabetic agent of the thiazolidinediones. However, the relationship between thiazolidinediones and insulin secretion is highly controversial. The aim of this study is to explore the effect and mechanism of rosiglitazone on insulin secretion of islets under chronic exposure to free fatty acids (FFA).</p><p><b>METHODS</b>Pancreatic islets were isolated from the pancreata of male Sprague-Dawley rats by the collagenase digestion and by the dextran gradient centrifugation method. The purified islets were cultured in the presence or absence of rosiglitazone and palmitate for 48 hours. The insulin secretion was measured by radioimmunoassay. The mRNA level of peroxisome proliferator-activated receptor gamma, uncoupling protein 2 (UCP-2) and insulin were determined by real-time polymerase chain reaction (PCR). The cell cytotoxicity assay was measured by cell counting kit-8.</p><p><b>RESULTS</b>Islets exposed to elevated palmitate for 48 hours showed an increased basal and a decreased glucose-stimulated insulin secretion (P < 0.01). The mRNA level of UCP-2 was increased by 3.7 fold in the 0.5 mmol/L concentration of palmitate. When islets were cultured with palmitate (0.5 mmol/L) in the presence of rosiglitazone (1.0 micromol/L), both basal and glucose-stimulated insulin secretion reversed to a pattern of control islets (P < 0.05, P < 0.01). The addition of rosiglitazone in the culture medium decreased the mRNA level of UCP-2 by 2.2 fold, having a statistically significant difference (P < 0.05) as compared with islets cultured with palmitate alone. The cell viability was not affected.</p><p><b>CONCLUSION</b>The protective effects of rosiglitazone on insulin secretion of isolated pancreatic islets under chronic exposure to palmitate might be mediated through the downregulation of UCP-2 expression.</p>
Subject(s)
Full text: Available Index: WPRIM (Western Pacific) Main subject: Membrane Transport Proteins / Pharmacology / RNA, Messenger / Cell Survival / Gene Expression Regulation / Islets of Langerhans / Rats, Sprague-Dawley / Bodily Secretions / Reverse Transcriptase Polymerase Chain Reaction / Mitochondrial Proteins Limits: Animals Language: English Journal: Chinese Medical Journal Year: 2006 Type: Article

Similar

MEDLINE

...
LILACS

LIS

Full text: Available Index: WPRIM (Western Pacific) Main subject: Membrane Transport Proteins / Pharmacology / RNA, Messenger / Cell Survival / Gene Expression Regulation / Islets of Langerhans / Rats, Sprague-Dawley / Bodily Secretions / Reverse Transcriptase Polymerase Chain Reaction / Mitochondrial Proteins Limits: Animals Language: English Journal: Chinese Medical Journal Year: 2006 Type: Article