Abstract

This study was conducted to investigate the effect of different dietary ratios of 13 C to 12 C or 15 N to 14 N on their relative incorporation into tissues. Eighty male rats were used in two 21-day feeding trials in which they were fed diets with either high δ13C levels (δ13C = −13.89‰ and δ15N = 2.37‰ in experiment 1 and δ13C = −19.34‰ and δ15N = 4.73‰ in experiment 2) or low δ13C levels (δ13C = −17.90‰ and δ15N = 3.08‰ in experiment 1 and δ13C = −21.76‰ and δ15N = 0.53‰ in experiment 2), meanwhile, the dietary δ15N levels were designed to two ranks. Blood, liver, adipose and muscle tissues were collected on day 0, 3, 7, 14, and 21 for determination of 13 C, 12 C, 15 N and 14 N isotopes. Rat growth rate, antioxidant capacity and metabolic parameters were also assessed. The results indicate that adipose tissue tend to deplete 13 C before the stable isotopic ratios achieved final equilibrium. Therefore, feeds with different isotopic signatures had different incorporation rates into tissues. Low dietary 13 C levels decreased tissue δ13C values whereas high dietary 13 C levels did not alter tissue δ13C values during the 21-d experiment. Blood δ15N values were a reliable parameter in assessing the relative contribution of dietary nitrogen to tissues. This study revealed a relationship between dietary isotopic signatures and their incorporation rates into rat tissues. However, more studies are needed to illustrate the mechanism through which dietary isotopic ratios influence the extent of isotopic incorporation into the tissues.

Highlights

  • Use of stable isotopes has attracted a great deal of interest in physiological and metabolic research as many researchers are unwilling to use radioactive isotopes [1]

  • Since every feedstuff is characterized by its natural stable isotopic signature [4,5], the analysis of stable isotopes in tissues is proposed as a method to evaluate the relative contributions of nutrients from different feed sources to those deposited in tissues [6,7]

  • In trial 1, the activities of plasma glutamic-pyruvate transaminase (GPT), glutamic-oxaloacetic transaminase (GOT), total antioxidant capacity (T-AOC), superoxide dismutase (SOD), Glutathione peroxidase (GSH-Px), creatinine, total nitric oxide synthase (TNOS), inducible nitric oxide synthase (iNOS), plasma urea nitrogen and maleic dialdehyde (MDA) did not differ between rats fed the two dietary treatments

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Summary

Introduction

Use of stable isotopes has attracted a great deal of interest in physiological and metabolic research as many researchers are unwilling to use radioactive isotopes [1]. The stable isotopic analysis, which has been used as an important tool for so many years, is conducted to investigate the turnover and deposition of nutrients from the macroscopic view. Few studies have determined the effect of different dietary ratios of 13 C to 12 C or 15 N to 14 N on their relative incorporation into tissues If these discrimination factors are not fully understood, it is impossible to estimate the relative contributions of nutrients by using stable isotopic analysis. The present study was carried out to investigate the effect of dietary stable isotopic ratios on their isotopic discrimination in tissues by feeding rats diets providing high or low stable isotopic abundance

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