Abstract

ABSTRACTThe present study was performed to investigate the roles of anterior intestine in the postprandial glucose homeostasis of the omnivorous Genetically Improved Farmed Tilapia (GIFT). Sub-adult fish (about 173 g) were sampled at 0, 1, 3, 8 and 24 h post feeding (HPF) after 36 h of food deprivation, and the time course of changes in intestinal glucose transport, glycolysis, glycogenesis and gluconeogenesis at the transcription and enzyme activity level, as well as plasma glucose contents, were analyzed. Compared with 0 HPF (fasting for 36 h), the mRNA levels of both ATP-dependent sodium/glucose cotransporter 1 and facilitated glucose transporter 2 increased during 1-3 HPF, decreased at 8 HPF and then leveled off. These results indicated that intestinal uptake of glucose and its transport across the intestine to blood mainly occurred during 1-3 HPF, which subsequently resulted in the increase of plasma glucose level at the same time. Intestinal glycolysis was stimulated during 1-3 HPF, while glucose storage as glycogen was induced during 3-8 HPF. Unexpectedly, intestinal gluconeogenesis (IGNG) was also strongly induced during 1-3 HPF at the state of nutrient assimilation. The mRNA abundance and enzyme activities of glutamic-pyruvic and glutamic-oxaloacetic transaminases increased during 1-3 HPF, suggesting that the precursors of IGNG might originate from some amino acids. Taken together, it was concluded that the anterior intestine played an important role in the regulation of postprandial glucose homeostasis in omnivorous tilapia, as it represented significant glycolytic potential and glucose storage. It was interesting that postprandial IGNG was stimulated by feeding temporarily, and its biological significance remains to be elucidated in fish.

Highlights

  • Besides liver and kidney, small intestine is identified as the third gluconeogenic organ to contribute to endogenous glucose production (EGP) in the post-absorptive or fasting state of mammals (Croset et al, 2001; Mithieux et al, 2004a)

  • The mRNA level of intestinal sglt1 rather than glut2 increased in response to a glucose load (Kirchner et al, 2008; Polakof et al, 2010)

  • The mRNA level of glut1 was not changed with feeding time (P>0.05), glut2 mRNA abundance increased by 4.61-5.54 times during 1-3 h post feeding (HPF) (P

Read more

Summary

Introduction

Small intestine is identified as the third gluconeogenic organ to contribute to endogenous glucose production (EGP) in the post-absorptive or fasting state of mammals (Croset et al, 2001; Mithieux et al, 2004a). IGNG is not modified with low dietary protein reception in the carnivorous rainbow trout (Oncorhynchus mykiss) (Kirchner et al, 2005) Both in vivo and in vitro data prove that a regulation of IGNG by insulin, glucose, lactate or amino acid changes is absent in rainbow trout (Polakof et al, 2010). It seems that the role of IGNG in glucose homeostasis and its regulatory mechanisms between fish and mammals might be very different

Methods
Results
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call