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. 2021 Apr 11;100(8):101182. doi: 10.1016/j.psj.2021.101182

Table 4.

Effect of dietary Fe source on DMT1 and FPN1 mRNA levels in small intestinal segments of broilers at 21 d of age.1

Fe source DMT1, RQ2,3
FPN1, RQ2,3
Duodenum3 Jejunum3 Ileum3 Pooled SE P value Duodenum3 Jejunum3 Ileum3 Pooled SE P value
Control 2.54Aa 0.60Ba 0.054C 0.362 <0.001 1.36Aa 0.65B 0.047C 0.129 <0.001
FeSO4๒7H2O 1.19Ab 0.25Bb 0.052C 0.133 <0.001 0.98Ab 0.32B 0.044C 0.062 <0.001
Fe-Met W 0.72Ab 0.31Bb 0.052C 0.013 <0.001 0.89Ab 0.41B 0.044C 0.063 <0.001
Fe-Pro M 0.84Ab 0.23Bb 0.055C 0.106 <0.001 0.79Ab 0.48B 0.042C 0.105 <0.001
Fe-Pro ES 0.79Ab 0.33Bb 0.051C 0.083 <0.001 0.75Ab 0.38B 0.041C 0.066 <0.001
Pooled SE 0.262 0.23 0.006 0.104 0.107 0.005
P-value <0.001 0.015 0.979 <0.001 0.253 0.929

a,bMeans within the same column lacking a common superscript differ (P < 0.02).

A,B,CMeans within the same row lacking a common superscript differ (P < 0.03).

1

Fe-Met W = Fe-Met with a weak chelation strength (Qf = 1.37), Fe-pro M = Fe proteinate with a moderate chelation strength (Qf = 43.6), Fe-pro ES = Fe proteinate with a extremely strong chelation strength (Qf = 8.59 × 103); DMT1 = divalent metal transporter 1; FPN1 = ferroportin 1; RQ = relative quantity.

2

The mRNA levels were calculated as the ratio of target gene mRNA to the geometric mean of GAPDH and β-action mRNA, and RQ = 2−ΔΔCT (CT = threshold cycle).

3

Data represent the means of 8 replicate cages (4 birds per cage; n = 8).