Increased levels of free fatty acids in fasted mice stimulate in vivo β-cell electrical activity

被引:16
作者
Fernandez, J [1 ]
Valdeolmillos, M [1 ]
机构
[1] Univ Miguel Hernandez, Inst Neurociencias, E-03550 Alicante, Spain
关键词
D O I
10.2337/diabetes.47.11.1707
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The electrical activity of pancreatic beta-cells in 48-h fasted mice has been recorded in vivo. Their electrical activity is exceedingly high at low levels of blood glucose when compared with control animals. For example, at a blood glucose concentration of 4.5 mmol/l, at which beta-cells are permanently hyperpolarized in control animals, fasted animals show continuous spiking activity. In fasted animals, hyperpolarization only occurs at glycemias below 2.2 mmol/l. As in fed animals, the electrical activity in fasted mice can be decreased or suppressed by the injection of diazoxide, indicating the participation of K-ATP channels. The treatment of fasted animals with nicotinic acid, an inhibitor of lipolysis, produces a decrease in the levels of free fatty acids (FFAs) and a decrease in electrical activity, thereby restoring the dose-response curve for glucose in fasted animals to values close to those found in fed animals. Conversely, the injection of palmitic acid produces an increase in electrical activity without a change in blood glucose. These results point to FFAs as important regulators of electrical activity during fasting in vivo. They also indicate a dissociation of electrical activity and insulin release in fasted animals, since an increase in electrical activity is not associated with increased insulin secretion.
引用
收藏
页码:1707 / 1712
页数:6
相关论文
共 38 条
[1]   GLUCOSE INDUCES CLOSURE OF SINGLE POTASSIUM CHANNELS IN ISOLATED RAT PANCREATIC BETA-CELLS [J].
ASHCROFT, FM ;
HARRISON, DE ;
ASHCROFT, SJH .
NATURE, 1984, 312 (5993) :446-448
[2]  
ASHCROFT FM, 1992, INSULIN MOL BIOL PAT, P97
[3]  
Atwater I., 1989, MOL CELLULAR BIOL DI, V1, P49
[4]   ROLE OF PLASMA FREE FATTY-ACIDS IN CONTROL OF INSULIN-SECRETION IN MAN [J].
BALASSE, EO ;
OOMS, HA .
DIABETOLOGIA, 1973, 9 (02) :145-151
[5]   Role of fatty acids in the pathogenesis of insulin resistance and NIDDM [J].
Boden, G .
DIABETES, 1997, 46 (01) :3-10
[6]   Evidence for an anaplerotic malonyl-CoA pathway in pancreatic beta-cell nutrient signaling [J].
Brun, T ;
Roche, E ;
AssimacopoulosJeannet, F ;
Corkey, BE ;
Kim, KH ;
Prentki, M .
DIABETES, 1996, 45 (02) :190-198
[7]   ADAPTATION OF GLYCOLYTIC-ENZYMES - GLUCOSE USE AND INSULIN RELEASE IN RAT PANCREATIC-ISLETS DURING FASTING AND REFEEDING [J].
BURCH, PT ;
TRUS, MD ;
BERNER, DK ;
LEONTIRE, A ;
ZAWALICH, KC ;
MATSCHINSKY, FM .
DIABETES, 1981, 30 (11) :923-928
[8]   MORE DIRECT EVIDENCE FOR A MALONYL-COA-CARNITINE PALMITOYLTRANSFERASE-I INTERACTION AS A KEY EVENT IN PANCREATIC BETA-CELL SIGNALING [J].
CHEN, SY ;
OGAWA, A ;
OHNEDA, M ;
UNGER, RH ;
FOSTER, DW ;
MCGARRY, JD .
DIABETES, 1994, 43 (07) :878-883
[9]   INTRACELLULAR ATP DIRECTLY BLOCKS K+ CHANNELS IN PANCREATIC B-CELLS [J].
COOK, DL ;
HALES, CN .
NATURE, 1984, 311 (5983) :271-273
[10]  
CORKEY BE, 1989, J BIOL CHEM, V264, P21608