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Cystine supplementation sustains plasma mercaptalbumin levels in rats fed low-protein diets more effectively than methionine
We recently reported that dietary cystine maintained plasma mercaptalbumin levels in rats fed low-protein diets. The present study aimed to compare the influence of low-protein diets supplemented with cystine and methionine, which is another sulfur amino acid, on plasma mercaptalbumin levels in rats...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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the Society for Free Radical Research Japan
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8482384/ https://www.ncbi.nlm.nih.gov/pubmed/34616103 http://dx.doi.org/10.3164/jcbn.20-146 |
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author | Yano, Yukimi Maeda, Chihiro Kaneko, Ichiro Kobayashi, Yukiko Aoi, Wataru Kuwahata, Masashi |
author_facet | Yano, Yukimi Maeda, Chihiro Kaneko, Ichiro Kobayashi, Yukiko Aoi, Wataru Kuwahata, Masashi |
author_sort | Yano, Yukimi |
collection | PubMed |
description | We recently reported that dietary cystine maintained plasma mercaptalbumin levels in rats fed low-protein diets. The present study aimed to compare the influence of low-protein diets supplemented with cystine and methionine, which is another sulfur amino acid, on plasma mercaptalbumin levels in rats. Male Sprague–Dawley rats were fed a 20% soy protein isolate diet (control group), 5% soy protein isolate diet (low-protein group) or 5% soy protein isolate diet supplemented with either methionine (low-protein + Met group) or cystine (low-protein + Cyss group) for 1 week. The percentage of mercaptalbumin within total plasma albumin of the low-protein + Met group was significantly lower than that of the control and low-protein + Cyss groups. No significant differences in the mRNA levels of tumor necrosis factor-α, interleukin-6, interleukin-1β, and cyclooxygenase 2 in blood cells were observed between the low-protein + Met and low-protein + Cyss groups. Treatment with buthionine-(S,R)-sulfoximine, an inhibitor of glutathione synthesis, did not influence the percentage of mercaptalbumin within total plasma albumin in rats fed the low-protein diet supplemented with cystine. These results suggest that supplementation with cystine may be more effective than that with methionine to maintain plasma mercaptalbumin levels in rats with protein malnutrition. Cystine might regulate plasma mercaptalbumin levels via the glutathione-independent pathway. |
format | Online Article Text |
id | pubmed-8482384 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | the Society for Free Radical Research Japan |
record_format | MEDLINE/PubMed |
spelling | pubmed-84823842021-10-05 Cystine supplementation sustains plasma mercaptalbumin levels in rats fed low-protein diets more effectively than methionine Yano, Yukimi Maeda, Chihiro Kaneko, Ichiro Kobayashi, Yukiko Aoi, Wataru Kuwahata, Masashi J Clin Biochem Nutr Original Article We recently reported that dietary cystine maintained plasma mercaptalbumin levels in rats fed low-protein diets. The present study aimed to compare the influence of low-protein diets supplemented with cystine and methionine, which is another sulfur amino acid, on plasma mercaptalbumin levels in rats. Male Sprague–Dawley rats were fed a 20% soy protein isolate diet (control group), 5% soy protein isolate diet (low-protein group) or 5% soy protein isolate diet supplemented with either methionine (low-protein + Met group) or cystine (low-protein + Cyss group) for 1 week. The percentage of mercaptalbumin within total plasma albumin of the low-protein + Met group was significantly lower than that of the control and low-protein + Cyss groups. No significant differences in the mRNA levels of tumor necrosis factor-α, interleukin-6, interleukin-1β, and cyclooxygenase 2 in blood cells were observed between the low-protein + Met and low-protein + Cyss groups. Treatment with buthionine-(S,R)-sulfoximine, an inhibitor of glutathione synthesis, did not influence the percentage of mercaptalbumin within total plasma albumin in rats fed the low-protein diet supplemented with cystine. These results suggest that supplementation with cystine may be more effective than that with methionine to maintain plasma mercaptalbumin levels in rats with protein malnutrition. Cystine might regulate plasma mercaptalbumin levels via the glutathione-independent pathway. the Society for Free Radical Research Japan 2021-09 2021-04-07 /pmc/articles/PMC8482384/ /pubmed/34616103 http://dx.doi.org/10.3164/jcbn.20-146 Text en Copyright © 2021 JCBN https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives License (http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) ). |
spellingShingle | Original Article Yano, Yukimi Maeda, Chihiro Kaneko, Ichiro Kobayashi, Yukiko Aoi, Wataru Kuwahata, Masashi Cystine supplementation sustains plasma mercaptalbumin levels in rats fed low-protein diets more effectively than methionine |
title | Cystine supplementation sustains plasma mercaptalbumin levels in rats fed low-protein diets more effectively than methionine |
title_full | Cystine supplementation sustains plasma mercaptalbumin levels in rats fed low-protein diets more effectively than methionine |
title_fullStr | Cystine supplementation sustains plasma mercaptalbumin levels in rats fed low-protein diets more effectively than methionine |
title_full_unstemmed | Cystine supplementation sustains plasma mercaptalbumin levels in rats fed low-protein diets more effectively than methionine |
title_short | Cystine supplementation sustains plasma mercaptalbumin levels in rats fed low-protein diets more effectively than methionine |
title_sort | cystine supplementation sustains plasma mercaptalbumin levels in rats fed low-protein diets more effectively than methionine |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8482384/ https://www.ncbi.nlm.nih.gov/pubmed/34616103 http://dx.doi.org/10.3164/jcbn.20-146 |
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