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Intestinal tract is an important organ for lowering serum uric acid in rats
The kidney was recognized as a dominant organ for uric acid excretion. The main aim of the study demonstrated intestinal tract was an even more important organ for serum uric acid (SUA) lowering. Sprague-Dawley rats were treated normally or with antibiotics, uric acid, adenine, or inosine of the sam...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5739491/ https://www.ncbi.nlm.nih.gov/pubmed/29267361 http://dx.doi.org/10.1371/journal.pone.0190194 |
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author | Yun, Yu Yin, Hua Gao, Zhiyi Li, Yue Gao, Tao Duan, Jinlian Yang, Rong Dong, Xianxiang Zhang, Lumei Duan, Weigang |
author_facet | Yun, Yu Yin, Hua Gao, Zhiyi Li, Yue Gao, Tao Duan, Jinlian Yang, Rong Dong, Xianxiang Zhang, Lumei Duan, Weigang |
author_sort | Yun, Yu |
collection | PubMed |
description | The kidney was recognized as a dominant organ for uric acid excretion. The main aim of the study demonstrated intestinal tract was an even more important organ for serum uric acid (SUA) lowering. Sprague-Dawley rats were treated normally or with antibiotics, uric acid, adenine, or inosine of the same molar dose orally or intraperitoneally for 5 days. Rat’s intestinal tract was equally divided into 20 segments except the cecum. Uric acid in serum and intestinal segment juice was assayed. Total RNA in the initial intestinal tract and at the end ileum was extracted and sequenced. Protein expression of xanthine dehydrogenase (XDH) and urate oxidase (UOX) was tested by Western blot analysis. The effect of oral UOX in lowering SUA was investigated in model rats treated with adenine and an inhibitor of uric oxidase for 5 days. SUA in the normal rats was 20.93±6.98 μg/ml, and total uric acid in the intestinal juice was 308.27±16.37 μg, which is two times more than the total SUA. The uric acid was very low in stomach juice, and attained maximum in the juice of the first segment (duodenum) and then declined all the way till the intestinal end. The level of uric acid in the initial intestinal tissue was very high, where XDH and most of the proteins associated with bicarbonate secretion were up-regulated. In addition, SUA was decreased by oral UOX in model rats. The results suggested that intestinal juice was an important pool for uric acid, and intestinal tract was an important organ for SUA lowering. The uric acid distribution was associated with uric acid synthesis and secretion in the upper intestinal tract, and reclamation in the lower. |
format | Online Article Text |
id | pubmed-5739491 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-57394912018-01-10 Intestinal tract is an important organ for lowering serum uric acid in rats Yun, Yu Yin, Hua Gao, Zhiyi Li, Yue Gao, Tao Duan, Jinlian Yang, Rong Dong, Xianxiang Zhang, Lumei Duan, Weigang PLoS One Research Article The kidney was recognized as a dominant organ for uric acid excretion. The main aim of the study demonstrated intestinal tract was an even more important organ for serum uric acid (SUA) lowering. Sprague-Dawley rats were treated normally or with antibiotics, uric acid, adenine, or inosine of the same molar dose orally or intraperitoneally for 5 days. Rat’s intestinal tract was equally divided into 20 segments except the cecum. Uric acid in serum and intestinal segment juice was assayed. Total RNA in the initial intestinal tract and at the end ileum was extracted and sequenced. Protein expression of xanthine dehydrogenase (XDH) and urate oxidase (UOX) was tested by Western blot analysis. The effect of oral UOX in lowering SUA was investigated in model rats treated with adenine and an inhibitor of uric oxidase for 5 days. SUA in the normal rats was 20.93±6.98 μg/ml, and total uric acid in the intestinal juice was 308.27±16.37 μg, which is two times more than the total SUA. The uric acid was very low in stomach juice, and attained maximum in the juice of the first segment (duodenum) and then declined all the way till the intestinal end. The level of uric acid in the initial intestinal tissue was very high, where XDH and most of the proteins associated with bicarbonate secretion were up-regulated. In addition, SUA was decreased by oral UOX in model rats. The results suggested that intestinal juice was an important pool for uric acid, and intestinal tract was an important organ for SUA lowering. The uric acid distribution was associated with uric acid synthesis and secretion in the upper intestinal tract, and reclamation in the lower. Public Library of Science 2017-12-21 /pmc/articles/PMC5739491/ /pubmed/29267361 http://dx.doi.org/10.1371/journal.pone.0190194 Text en © 2017 Yun et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Yun, Yu Yin, Hua Gao, Zhiyi Li, Yue Gao, Tao Duan, Jinlian Yang, Rong Dong, Xianxiang Zhang, Lumei Duan, Weigang Intestinal tract is an important organ for lowering serum uric acid in rats |
title | Intestinal tract is an important organ for lowering serum uric acid in rats |
title_full | Intestinal tract is an important organ for lowering serum uric acid in rats |
title_fullStr | Intestinal tract is an important organ for lowering serum uric acid in rats |
title_full_unstemmed | Intestinal tract is an important organ for lowering serum uric acid in rats |
title_short | Intestinal tract is an important organ for lowering serum uric acid in rats |
title_sort | intestinal tract is an important organ for lowering serum uric acid in rats |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5739491/ https://www.ncbi.nlm.nih.gov/pubmed/29267361 http://dx.doi.org/10.1371/journal.pone.0190194 |
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