Threonine affects intestinal function, protein synthesis and gene expression of TOR in Jian carp (Cyprinus carpio var. Jian)

PLoS One. 2013 Jul 26;8(7):e69974. doi: 10.1371/journal.pone.0069974. Print 2013.

Abstract

This study aimed to investigate the effects of threonine (Thr) on the digestive and absorptive ability, proliferation and differentiation of enterocytes, and gene expression of juvenile Jian carp (Cyprinus carpio var. Jian). First, seven isonitrogenous diets containing graded levels of Thr (7.4-25.2 g/kg diet) were fed to the fishes for 60 days. Second, enterocyte proliferation and differentiation were assayed by culturing enterocytes with graded levels of Thr (0-275 mg/l) in vitro. Finally, enterocytes were cultured with 0 and 205 mg/l Thr to determine protein synthesis. The percent weight gain (PWG), specific growth rate, feed intake, feed efficiency, protein retention value, activities of trypsin, lipase and amylase, weights and protein contents of hepatopancreas and intestine, folds heights, activities of alkaline phosphatase (AKP), γ- glutamyl transpeptidase and Na(+)/K(+)-ATPase in all intestinal segments, glutamate-oxaloacetate transaminase (GOT) and glutamate-pyruvate transaminase (GPT) activities in hepatopancreas, and 4E-BP2 gene expression in muscle, hepatopancreas and intestinal segments were significantly enhanced by Thr (p<0.05). However, the plasma ammonia concentration and TOR gene expression decreased (p<0.05). In vitro, Thr supplement significantly increased cell numbers, protein content, the activities of GOT, GPT, AKP and Na(+)/K(+)-ATPase, and protein synthesis rate of enterocytes, and decreased LDH activity and ammonia content in cell medium (p<0.05). In conclusion, Thr improved growth, digestive and absorptive capacity, enterocyte proliferation and differentiation, and protein synthesis and regulated TOR and 4E-BP2 gene expression in juvenile Jian carp. The dietary Thr requirement of juvenile Jian carp was 16.25 g/kg diet (51.3 g/kg protein) based on quadratic regression analysis of PWG.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Ammonia / blood
  • Animals
  • Carps / blood
  • Carps / physiology*
  • Cell Differentiation
  • Cell Proliferation
  • Cells, Cultured
  • Digestion
  • Enterocytes / cytology
  • Enterocytes / metabolism
  • Fish Proteins / genetics*
  • Fish Proteins / metabolism
  • Gene Expression Regulation
  • Intestines / physiology
  • Protein Biosynthesis
  • TOR Serine-Threonine Kinases / genetics*
  • TOR Serine-Threonine Kinases / metabolism
  • Threonine / metabolism*

Substances

  • Fish Proteins
  • Threonine
  • Ammonia
  • TOR Serine-Threonine Kinases

Grants and funding

This research was financially supported by National Science Foundation of China (30871926) (http://www.nsfc.gov.cn/Portal0/default152.htm), Program for New Century Excellent Talents in University of Ministry of Education of China (NCET-08-0905) (http://www.moe.edu.cn/publicfiles/business/htmlfiles/moe/A08/index.html) and National Department Public Benefit Research Foundation (Agriculture) of China (201003020) (http://www.moa.gov.cn/). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.