Early feeding of carnivorous rainbow trout (Oncorhynchus mykiss) with a hyperglucidic diet during a short period:: effect on dietary glucose utilization in juveniles

被引:99
作者
Geurden, I.
Aramendi, M.
Zambonino-Infante, J.
Panserat, S. [1 ]
机构
[1] IFREMER, INRA, NuAGe, Nutr Aquaculture & Genom Res Unit,UMR A067,Nutr M, F-64310 St Pee Sur Nivelle, France
[2] IFREMER, Marine Fish Nutr Team, Plouzane, France
关键词
fish nutrition; nutritional programming; carbohydrate digestion; intestinal glucose transport; glucose metabolism;
D O I
10.1152/ajpregu.00444.2006
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Based on the concept of nutritional programming in higher vertebrates, we tested whether an acute hyperglucidic stimulus during early life could induce a long-lasting effect on carbohydrate utilization in carnivorous rainbow trout. The trout were fed a hyperglucidic diet (60% dextrin) at two early stages of development: either at first feeding Q days, stimulus 1) or after yolk absorption (5 days, stimulus 2). Before and after the hyperglucidic stimulus, they received a commercial diet until juvenile stage (> 10 g). Fish that did not experience the hyperglucidic stimuli served as controls. The short- and long-term effects of the stimuli were evaluated by measuring the expression of five key genes involved in carbohydrate utilization: a-amylase, maltase (digestion), sodium-dependent glucose cotransporter (SGLT1; intestinal glucose transport), and glucokinase and glucose-6-phosphatase, involved in the utilization and production of glucose, respectively. The hyperglucidic diet rapidly increased expressions of maltase, a-arrylase, and glucokinase in stimulus I fish and only of maltase in stimulus 2 fish, probably because of a lower plasticity at this later stage of development. In the final challenge test with juveniles fed a 25% dextrin diet, both digestive enzymes were upregulated in fish that had experienced the hyperglucidic stimulus at first feeding, confirming the possibility of modification of some long-term physiological functions in rainbow trout. In contrast, no persistent molecular adaptations were found for the genes involved in glucose transport or metabolism. In addition, growth and postprandial glycentia were unaffected by the stimuli. In summary, our data show that a short hyperglucidic stimulus during early trout life may permanently influence carbohydrate digestion.
引用
收藏
页码:R2275 / R2283
页数:9
相关论文
共 57 条
[1]   Programming into adulthood of islet adaptations induced by early nutritional intervention in the rat [J].
Aalinkeel, R ;
Srinivasan, M ;
Song, F ;
Patel, MS .
AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM, 2001, 281 (03) :E640-E648
[2]   A dietary intervention (high carbohydrate) during the neonatal period causes islet dysfunction in rats [J].
Aalinkeel, R ;
Srinivasan, M ;
Kalhan, SC ;
Laychock, SG ;
Patel, MS .
AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM, 1999, 277 (06) :E1061-E1069
[3]   KINETIC HETEROGENEITY OF NA-D-GLUCOSE COTRANSPORT IN TELEOST GASTROINTESTINAL-TRACT [J].
AHEARN, GA ;
BEHNKE, RD ;
ZONNO, V ;
STORELLI, C .
AMERICAN JOURNAL OF PHYSIOLOGY, 1992, 263 (05) :R1018-R1023
[4]   PROTEIN SPARING EFFECTS IN LARGE RAINBOW-TROUT, SALMO-GAIRDNERI [J].
BEAMISH, FWH ;
MEDLAND, TE .
AQUACULTURE, 1986, 55 (01) :35-42
[5]  
BEAUMONT A, 1994, DEVELOPMENT, P151
[6]   EFFECTS OF DIETARY CARBOHYDRATES AND OF THEIR MODE OF DISTRIBUTION ON GLYCEMIA IN RAINBOW-TROUT (SALMO-GAIRDNERI RICHARDSON) [J].
BERGOT, F .
COMPARATIVE BIOCHEMISTRY AND PHYSIOLOGY A-PHYSIOLOGY, 1979, 64 (04) :543-547
[7]   Hepatocyte nuclear factor-1α, GATA-4, and caudal related homeodomain protein Cdx2 interact functionally to modulate intestinal gene transcription -: Implication for the developmental regulation of the sucrose-isomaltase gene [J].
Boudreau, F ;
Rings, EHHM ;
van Wering, HM ;
Kim, RK ;
Swain, GP ;
Krasinski, SD ;
Moffett, J ;
Grand, RJ ;
Suh, ER ;
Traber, PG .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (35) :31909-31917
[8]   ADAPTATION OF THE EXOCRINE PANCREAS TO DIET [J].
BRANNON, PM .
ANNUAL REVIEW OF NUTRITION, 1990, 10 :85-105
[9]   Nutritional programming of adult disease [J].
Buckley, AJ ;
Jaquiery, AL ;
Harding, JE .
CELL AND TISSUE RESEARCH, 2005, 322 (01) :73-79
[10]  
Buddington RK, 1997, ACTA PHYSIOL SCAND, V161, P67