PHOSPHATE-DEPLETION IMPAIRS LEUCINE-INDUCED INSULIN-SECRETION

被引:0
作者
OH, HY
FADDA, GZ
SMOGORZEWSKI, M
LIOU, HH
MASSRY, SG
机构
[1] UNIV SO CALIF,SCH MED,DIV NEPHROL,LOS ANGELES,CA 90033
[2] UNIV SO CALIF,SCH MED,DEPT MED,LOS ANGELES,CA
来源
JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY | 1994年 / 5卷 / 05期
关键词
PHOSPHATE DEPLETION; INSULIN SECRETION; LEUCINE; ALPHA-KETOGLUTARATE; GLUTAMATE DEHYDROGENASE;
D O I
暂无
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Phosphate depletion (PD) in vivo causes a sundry of abnormalities in pancreatic islets including a rise in cytosolic calcium, low ATP content, reduced Ca2+ ATPase and Na+-K+ ATPase activity, and impaired insulin secretion in response to glucose or potassium. L-Leucine is a strong secretagogue that triggers insulin secretion by deamination to alpha-ketoisocaproic acid (KIC) and the subsequent metabolism of the latter to ATP and by the activation of glutamate dehydrogenase (GLDH), which acts on glutamate to generate alpha-ketoglutarate, the metabolism of which results in ATP production. The generation of ATP triggers events that lead to insulin secretion. It is not known whether PD impairs leucine-induced insulin secretion, and the cellular derangements that are involved in such an abnormality are not defined. These issues were studied in PD rats and in pair-weighed normal animals as controls. D-leucine uptake by islets from PD rats is normal, but both leucine- and KIC-induced insulin secretions are impaired and the activity of branched-chain keto acid dehydrogenase, which facilitates the metabolism of KIC, is reduced. Both leucine and 2-aminobicyclo (2-2-1) haptene failed to stimulate GLDH and to augment the generation of alpha-ketoglutarate in the islets of PD rats. Also, the concentration of basal alpha-ketoglutarate was significantly higher in the islets of PD rats, suggesting that its metabolism is impaired. In addition, the activity of glutaminase is significantly reduced, an abnormality that would result in decreased production of glutamate, the substrate for GLDH. The data show that PD impairs leucine-induced insulin secretion. This derangement is due to impairment in the leucine-alpha-ketoisocaproic acid pathway as well as in the leucine-GLDH-alpha-ketoglutarate-glutaminase pathway. The results support the notion that PD is associated with a generalized failure of the pancreatic islets to respond to the three main secretagogues of insulin, i.e., glucose, potassium, and amino acids.
引用
收藏
页码:1259 / 1265
页数:7
相关论文
共 28 条
[1]   EFFECTS OF 2-KETOISOCAPROATE ON INSULIN RELEASE AND SINGLE POTASSIUM CHANNEL ACTIVITY IN DISPERSED RAT PANCREATIC BETA-CELLS [J].
ASHCROFT, FM ;
ASHCROFT, SJH ;
HARRISON, DE .
JOURNAL OF PHYSIOLOGY-LONDON, 1987, 385 :517-529
[2]   IMPAIRED ENERGY-METABOLISM IN RAT MYOCARDIUM DURING PHOSPHATE-DEPLETION [J].
BRAUTBAR, N ;
BACZYNSKI, R ;
CARPENTER, C ;
MOSER, S ;
GEIGER, P ;
FINANDER, P ;
MASSRY, SG .
AMERICAN JOURNAL OF PHYSIOLOGY, 1982, 242 (06) :F699-F704
[3]   IMPAIRED ENERGY-METABOLISM IN SKELETAL-MUSCLE DURING PHOSPHATE-DEPLETION [J].
BRAUTBAR, N ;
CARPENTER, C ;
BACZYNSKI, R ;
KOHAN, R ;
MASSRY, SG .
KIDNEY INTERNATIONAL, 1983, 24 (01) :53-57
[4]   EFFECTS OF LEUCINE ON INSULIN-SECRETION AND BETA-CELL MEMBRANE-POTENTIAL IN MOUSE ISLETS OF LANGERHANS [J].
BROUWER, AE ;
CARROLL, PB ;
ATWATER, IJ .
PANCREAS, 1991, 6 (02) :221-228
[5]   INTRACELLULAR ATP DIRECTLY BLOCKS K+ CHANNELS IN PANCREATIC B-CELLS [J].
COOK, DL ;
HALES, CN .
NATURE, 1984, 311 (5983) :271-273
[6]   VERAPAMIL CORRECTS ABNORMAL-METABOLISM OF PANCREATIC-ISLETS AND INSULIN-SECRETION IN PHOSPHATE-DEPLETION [J].
FADDA, GZ ;
HAJJAR, SM ;
ZHOU, XJ ;
MASSRY, SG .
ENDOCRINOLOGY, 1992, 130 (01) :193-202
[7]   ON THE MECHANISM OF IMPAIRED INSULIN-SECRETION IN CHRONIC-RENAL-FAILURE [J].
FADDA, GZ ;
HAJJAR, SM ;
PERNA, AF ;
ZHOU, XJ ;
LIPSON, LG ;
MASSRY, SG .
JOURNAL OF CLINICAL INVESTIGATION, 1991, 87 (01) :255-261
[8]  
FADDA GZ, 1991, P SOC EXP BIOL MED, V198, P742
[9]  
GOLD LM, 1977, J LAB CLIN MED, V89, P559
[10]  
GYLFE E, 1976, ACTA DIABETOL LAT, V13, P20, DOI 10.1007/BF02591577