Regulation of insulin secretion and expression of SUR1 gene by chronic exposure to free fatty acids in rat pancreatic beta cells.
- Author:
Li YUAN
1
;
Xiuling DENG
;
Lulu CHEN
;
Min ZHOU
Author Information
1. Department of Endocrinology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430022, China.
- Publication Type:Journal Article
- MeSH:
ATP-Binding Cassette Transporters;
biosynthesis;
genetics;
Animals;
Cells, Cultured;
Fatty Acids;
pharmacology;
Insulin;
secretion;
Islets of Langerhans;
drug effects;
physiology;
Male;
Potassium Channels;
biosynthesis;
genetics;
Potassium Channels, Inwardly Rectifying;
biosynthesis;
genetics;
RNA, Messenger;
biosynthesis;
genetics;
Rats;
Rats, Sprague-Dawley;
Receptors, Drug;
biosynthesis;
genetics;
Sulfonylurea Receptors
- From:
Journal of Huazhong University of Science and Technology (Medical Sciences)
2004;24(4):358-364
- CountryChina
- Language:English
-
Abstract:
To study the effects of free fatty acids on insulin secretion and expression of SUR1 gene in rat pancreatic B cells in vitro, and to explore the molecular mechanisms in lipotoxicity inducing insulin secretion dysfunction, pancreatic islet cells were isolated and digested from male SD rats. Purified islets were incubated with either 0.25 mmol/L palmitate or 0.125 mmol/L oleate for 48 h in vitro. Then islets were stimulated with either 5.6 mmol/L or 16.7 mmol/L glucose for 1 h. Insulin release was measured by using radioimmunoassay, and the expression of SUR1 gene mRNA was quantified by reserve transcription-polymerase chain reaction (RT-PCR). The islets exposed to both palmitate and oleate for 48 h showed an increased basal and a decreased glucose-indused insulin release as compared with control islets. Palmitate increased basal insulin secretion by 110% (P< 0.01), decreased glucose stimulated insulin secretion by 43% (P<0.01); while oleate increased basal insulin secretion by 80% (P<0.01) and decreased glucose stimulated insulin secretion by 32 % (P<0.05). RT-PCR showed that oleate significantly suppressed SUR1 gene expression by 64 % (P<0.01) as compared with the control group, while palmitate group manifested a light decrease of 15% (P>0.05) of SUR1 gene expression. Our results suggested that chronic exposure to free fatty acids of pancreatic beta cells inhibited glucose stimulated insulin secretion. Regulation of SUR1 gene expression may be involved in such effects, which may also be one of the molecular mechanisms in lipotoxocity inducing beta cells secretion dysfunction.
