Caloric restriction alters the feeding response of key metabolic enzyme genes

被引:88
作者
Dhahbi, JM
Mote, PL
Wingo, J
Rowley, BC
Cao, SX
Walford, RL
Spindler, SR [1 ]
机构
[1] Univ Calif Riverside, Dept Biochem, Riverside, CA 92521 USA
[2] Univ Calif Los Angeles, Sch Med, Dept Pathol, Los Angeles, CA 90024 USA
关键词
feeding; mice; glycolysis; gluconeogenesis; nitrogen metabolism;
D O I
10.1016/S0047-6374(01)00230-5
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Differential 'fuel usage' has been proposed as a mechanism for life-span extension by caloric restriction (CR). Here, we report the effects of CR, initiated after weaning, on metabolic enzyme gene expression 0, 1.5, 5, and 12 h after feeding of 24-month-old mice. Plasma glucose and insulin were reduced by similar to 20 and 80%. Therefore, apparent insulin sensitivity, as judged by the glucose to insulin ratio, increased 3.3-fold in CR mice. Phosphoenolpyruvate carboxykinase mRNA and activity were transiently reduced 1.5 h after feeding, but were 20-100% higher in CR mice at other times. Glucose-6-phosphatase mRNA was induced in CR mice and repressed in control mice before, and for 5 h following feeding. Feeding transiently induced glucokinase mRNA fourfold in control mice, but only slightly in CR mice. Pyruvate kinase and pyruvate dehydrogenase activities were reduced similar to 50% in CR mice at most times. Feeding induced glutaminase mRNA, and carbamyl phosphate synthetase I and glutamine synthase activity (and mRNA). They were each similar to twofold or higher in CR mice. These results indicate that in mice, CR maintains higher rates of gluconeogenesis and protein catabolism, even in the hours after feeding. The data are consistent with the idea that CR continuously promotes the turnover and replacement of extrahepatic proteins. (C) 2001 Elsevier Science Ireland Ltd. All rights reserved.
引用
收藏
页码:1033 / 1048
页数:16
相关论文
共 51 条
[1]   A POSSIBLE INVOLVEMENT OF VIP IN FEEDING-INDUCED SECRETION OF ACTH AND CORTICOSTERONE IN THE RAT [J].
ALEXANDER, LD ;
EVANS, K ;
SANDER, LD .
PHYSIOLOGY & BEHAVIOR, 1995, 58 (02) :409-413
[2]   Regulation of rat liver glucose-6-phosphatase gene expression in different nutritional and hormonal states - Gene structure and 5'-flanking sequence [J].
Argaud, D ;
Zhang, Q ;
Pan, WS ;
Maitra, S ;
Pilkis, SJ ;
Lange, AJ .
DIABETES, 1996, 45 (11) :1563-1571
[3]  
BHANDARI B, 1991, J BIOL CHEM, V266, P7784
[4]  
BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3
[5]   Calories and aging alter gene expression for gluconeogenic, glycolytic, and nitrogen-metabolizing enzymes [J].
Dhahbi, JM ;
Mote, PL ;
Wingo, J ;
Tillman, JB ;
Walford, RL ;
Spindler, SR .
AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM, 1999, 277 (02) :E352-E360
[6]   Caloric intake alters the efficiency of catalase mRNA translation in the liver of old female mice [J].
Dhahbi, JM ;
Tillman, JB ;
Cao, S ;
Mote, PL ;
Walford, RL ;
Spindler, SR .
JOURNALS OF GERONTOLOGY SERIES A-BIOLOGICAL SCIENCES AND MEDICAL SCIENCES, 1998, 53 (03) :B180-B185
[7]   The effects of dietary restriction on mitochondrial dysfunction in aging [J].
Feuers, RJ .
TOWARDS PROLONGATION OF THE HEALTHY LIFE SPAN: PRACTICAL APPROACHES TO INTERVENTION, 1998, 854 :192-201
[8]   EFFECT OF CHRONIC CALORIC RESTRICTION ON HEPATIC-ENZYMES OF INTERMEDIARY METABOLISM IN THE MALE FISCHER-344 RAT [J].
FEUERS, RJ ;
DUFFY, PH ;
LEAKEY, JA ;
TURTURRO, A ;
MITTELSTAEDT, RA ;
HART, RW .
MECHANISMS OF AGEING AND DEVELOPMENT, 1989, 48 (02) :179-189
[9]  
FEUERS RJ, 1990, PROG CLIN BIOL RES, V341, P177
[10]   ISOLATION AND CHARACTERIZATION OF THE MOUSE PYRUVATE DEHYDROGENASE-E1-ALPHA GENES [J].
FITZGERALD, J ;
HUTCHISON, WM ;
DAHL, HHM .
BIOCHIMICA ET BIOPHYSICA ACTA, 1992, 1131 (01) :83-90