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Effects of Different Methionine Sources on Methionine Metabolism in the IPEC-J2 Cells
As one of the essential amino acids, methionine (Met) plays an important role in biological events such as methylation and antioxidant properties besides its function in protein synthesis. Different Met sources have been used in animal production, but their effects on Met metabolic pathways are not...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6662248/ https://www.ncbi.nlm.nih.gov/pubmed/31380429 http://dx.doi.org/10.1155/2019/5464906 |
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author | Zuo, Fangrui Gu, Qiongyao Li, Shengqing Wei, Hongkui Peng, Jian |
author_facet | Zuo, Fangrui Gu, Qiongyao Li, Shengqing Wei, Hongkui Peng, Jian |
author_sort | Zuo, Fangrui |
collection | PubMed |
description | As one of the essential amino acids, methionine (Met) plays an important role in biological events such as methylation and antioxidant properties besides its function in protein synthesis. Different Met sources have been used in animal production, but their effects on Met metabolic pathways are not well understood. In the present study, we investigated the effects of different Met sources (L-Met, DL-Met, DL-2-hydroxy-4-(methylthio)butanoic acid (DL-HMTBA), and DL-methionyl-DL-methionine (DL-MM)) on the metabolism of Met in small intestinal porcine epithelial cell line (IPEC-J2) and the contents of extracellular Met sources. The results showed that concentrations of intracellular Met, S-adenosylmethionine (SAM), S-adenosylhomocysteine (SAH), and the ratio of SAM to SAH in the DL-HMTBA group were significantly lower than that in other Met source groups, while the content of 5-methyltetrahydrofolate (5-MTHF) was significantly higher. Moreover, the mRNA levels of MAT2A, AHcy, CBS, MTHFR, and MTR in the DL-HMTBA group were significantly higher than those in other Met source groups. Further study showed that the total content of extracellular Met sources was highest in the DL-HMTBA group, followed by DL-MM group, followed by L-Met and DL-Met groups. These results demonstrated that DL-HMTBA mainly affects the transmethylation and remethylation of Met and it can promote the trans-sulfur metabolism of Met when compared with other Met sources. In addition, most DL-HMTBA and a small amount of DL-MM can escape the intestinal first-pass metabolism and then provide more extracellular Met sources than L-Met and DL-Met. Therefore, this study can provide a theoretical basis for the selection of Met sources in livestock. |
format | Online Article Text |
id | pubmed-6662248 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Hindawi |
record_format | MEDLINE/PubMed |
spelling | pubmed-66622482019-08-04 Effects of Different Methionine Sources on Methionine Metabolism in the IPEC-J2 Cells Zuo, Fangrui Gu, Qiongyao Li, Shengqing Wei, Hongkui Peng, Jian Biomed Res Int Research Article As one of the essential amino acids, methionine (Met) plays an important role in biological events such as methylation and antioxidant properties besides its function in protein synthesis. Different Met sources have been used in animal production, but their effects on Met metabolic pathways are not well understood. In the present study, we investigated the effects of different Met sources (L-Met, DL-Met, DL-2-hydroxy-4-(methylthio)butanoic acid (DL-HMTBA), and DL-methionyl-DL-methionine (DL-MM)) on the metabolism of Met in small intestinal porcine epithelial cell line (IPEC-J2) and the contents of extracellular Met sources. The results showed that concentrations of intracellular Met, S-adenosylmethionine (SAM), S-adenosylhomocysteine (SAH), and the ratio of SAM to SAH in the DL-HMTBA group were significantly lower than that in other Met source groups, while the content of 5-methyltetrahydrofolate (5-MTHF) was significantly higher. Moreover, the mRNA levels of MAT2A, AHcy, CBS, MTHFR, and MTR in the DL-HMTBA group were significantly higher than those in other Met source groups. Further study showed that the total content of extracellular Met sources was highest in the DL-HMTBA group, followed by DL-MM group, followed by L-Met and DL-Met groups. These results demonstrated that DL-HMTBA mainly affects the transmethylation and remethylation of Met and it can promote the trans-sulfur metabolism of Met when compared with other Met sources. In addition, most DL-HMTBA and a small amount of DL-MM can escape the intestinal first-pass metabolism and then provide more extracellular Met sources than L-Met and DL-Met. Therefore, this study can provide a theoretical basis for the selection of Met sources in livestock. Hindawi 2019-07-16 /pmc/articles/PMC6662248/ /pubmed/31380429 http://dx.doi.org/10.1155/2019/5464906 Text en Copyright © 2019 Fangrui Zuo et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Zuo, Fangrui Gu, Qiongyao Li, Shengqing Wei, Hongkui Peng, Jian Effects of Different Methionine Sources on Methionine Metabolism in the IPEC-J2 Cells |
title | Effects of Different Methionine Sources on Methionine Metabolism in the IPEC-J2 Cells |
title_full | Effects of Different Methionine Sources on Methionine Metabolism in the IPEC-J2 Cells |
title_fullStr | Effects of Different Methionine Sources on Methionine Metabolism in the IPEC-J2 Cells |
title_full_unstemmed | Effects of Different Methionine Sources on Methionine Metabolism in the IPEC-J2 Cells |
title_short | Effects of Different Methionine Sources on Methionine Metabolism in the IPEC-J2 Cells |
title_sort | effects of different methionine sources on methionine metabolism in the ipec-j2 cells |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6662248/ https://www.ncbi.nlm.nih.gov/pubmed/31380429 http://dx.doi.org/10.1155/2019/5464906 |
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