Uptake of manganese from manganese–lysine complex in the primary rat intestinal epithelial cells |
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Authors: | H. Zhang E. R. Gilbert K. Zhang X. Ding Y. Luo J. Wang Q. Zeng S. Bai |
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Affiliation: | 1. Animal Nutrition Institute, Sichuan Agricultural University Ya'an, Sichuan, China;2. Department of Animal and Poultry Sciences, Virginia Tech University, Blacksburg, VA, USA |
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Abstract: | This study was conducted to compare the differences of the uptake of Mn from Mn–lysine complex (MnLys) and MnSO4 and to determine the potential mechanisms of the uptake of Mn from MnLys. We first established the primary rat intestinal epithelial cell culture model and used it to determine the uptake of Mn from different Mn sources. The MnLys increased (p < 0.001) Mn uptake when compared to MnSO4. The uptake of Mn decreased (p < 0.05) with added Fe concentration increasing in the medium regardless of Mn source. The MnLys decreased (p < 0.01) Mn2+ efflux transporter ferroportin 1 (FPN1) mRNA level, but did not influence (p > 0.06) Mn2+ influx transporter DMT1 mRNA expression when compared to MnSO4. The results above indicated that the increase of Mn accumulation for MnLys at least partly was due to the decrease of Mn efflux by reduced FPN1 expression. The N‐ethylmaleimide, as an l ‐lysine transport system y+ inhibitor, decreased (p < 0.001) the uptake of Mn from MnLys, but did not affect (p > 0.10) the uptake of Mn from MnSO4. The cycloheximide, as an l ‐lysine transport system b0,+ activator, increased (p < 0.001) the uptake of Mn from MnLys, whereas also did not influence the uptake of Mn from MnSO4. The MnLys increased (p < 0.01) the system y+ member cationic amino acid transporter (CAT) 1, and system b0,+ components rBAT and b0,+AT mRNA expression when compared to MnSO4. These results suggested that the uptake of Mn from MnLys complex might be transported by CAT1 and system b0,+, which was different from ionized Mn2+ uptake pathway. In conclusion, the uptake of MnLys complex not only might be absorbed as Mn2+, but also appeared to be transported through CAT1 and system b0,+ in the primary rat intestinal epithelial cells. |
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Keywords: | manganese– lysine complex uptake intestinal epithelial cells |
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