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Evaluating the urate-lowering effects of different microbial fermented extracts in hyperuricemic models accompanied with a safety study

Uric acid (UA) is an end product of purine metabolism by the enzyme xanthine oxidase (XOD). Hyperuricemia is characterized by the accumulation of serum UA and is an important risk factor for gout and many chronic disorders. XOD inhibitors or uricase (catalyzes UA to the more soluble end product) can...

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Autores principales: Chen, Rong-Jane, Chen, Mei-Huei, Chen, Yen-Lin, Hsiao, Ching-Mao, Chen, Hsiu-Min, Chen, Siao-Jhen, Wu, Ming-Der, Yech, Yi-Jen, Yuan, Gwo-Fang, Wang, Ying-Jan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taiwan Food and Drug Administration 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9328828/
https://www.ncbi.nlm.nih.gov/pubmed/28911646
http://dx.doi.org/10.1016/j.jfda.2016.07.003
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author Chen, Rong-Jane
Chen, Mei-Huei
Chen, Yen-Lin
Hsiao, Ching-Mao
Chen, Hsiu-Min
Chen, Siao-Jhen
Wu, Ming-Der
Yech, Yi-Jen
Yuan, Gwo-Fang
Wang, Ying-Jan
author_facet Chen, Rong-Jane
Chen, Mei-Huei
Chen, Yen-Lin
Hsiao, Ching-Mao
Chen, Hsiu-Min
Chen, Siao-Jhen
Wu, Ming-Der
Yech, Yi-Jen
Yuan, Gwo-Fang
Wang, Ying-Jan
author_sort Chen, Rong-Jane
collection PubMed
description Uric acid (UA) is an end product of purine metabolism by the enzyme xanthine oxidase (XOD). Hyperuricemia is characterized by the accumulation of serum UA and is an important risk factor for gout and many chronic disorders. XOD inhibitors or uricase (catalyzes UA to the more soluble end product) can prevent these chronic diseases. However, currently available hypouricemic agents induce severe side effects. Therefore, we developed new microbial fermented extracts (MFEs) with substantial XOD inhibition activity from Lactobacillus (MFE-21) and Acetobacter (MFE-25), and MFE-120 with high uricase activity from Aspergillus. The urate-lowering effects and safety of these MFEs were evaluated. Our results showed that MFE-25 exerts superior urate-lowering effects in the therapeutic model. In the preventive model, both MFE-120 and MFE-25 significantly reduced UA. The results of the safety study showed that no organ toxicity and no treatment-related adverse effects were observed in mice treated with high doses of MFEs. Taken together, the results showed the effectiveness of MFEs in reducing hyperuricemia without systemic toxicity in mice at high doses, suggesting that they are safe for use in the treatment and prevention of hyperuricemia.
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spelling pubmed-93288282022-08-09 Evaluating the urate-lowering effects of different microbial fermented extracts in hyperuricemic models accompanied with a safety study Chen, Rong-Jane Chen, Mei-Huei Chen, Yen-Lin Hsiao, Ching-Mao Chen, Hsiu-Min Chen, Siao-Jhen Wu, Ming-Der Yech, Yi-Jen Yuan, Gwo-Fang Wang, Ying-Jan J Food Drug Anal Original Article Uric acid (UA) is an end product of purine metabolism by the enzyme xanthine oxidase (XOD). Hyperuricemia is characterized by the accumulation of serum UA and is an important risk factor for gout and many chronic disorders. XOD inhibitors or uricase (catalyzes UA to the more soluble end product) can prevent these chronic diseases. However, currently available hypouricemic agents induce severe side effects. Therefore, we developed new microbial fermented extracts (MFEs) with substantial XOD inhibition activity from Lactobacillus (MFE-21) and Acetobacter (MFE-25), and MFE-120 with high uricase activity from Aspergillus. The urate-lowering effects and safety of these MFEs were evaluated. Our results showed that MFE-25 exerts superior urate-lowering effects in the therapeutic model. In the preventive model, both MFE-120 and MFE-25 significantly reduced UA. The results of the safety study showed that no organ toxicity and no treatment-related adverse effects were observed in mice treated with high doses of MFEs. Taken together, the results showed the effectiveness of MFEs in reducing hyperuricemia without systemic toxicity in mice at high doses, suggesting that they are safe for use in the treatment and prevention of hyperuricemia. Taiwan Food and Drug Administration 2016-08-03 /pmc/articles/PMC9328828/ /pubmed/28911646 http://dx.doi.org/10.1016/j.jfda.2016.07.003 Text en © 2017 Taiwan Food and Drug Administration https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC-BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) ).
spellingShingle Original Article
Chen, Rong-Jane
Chen, Mei-Huei
Chen, Yen-Lin
Hsiao, Ching-Mao
Chen, Hsiu-Min
Chen, Siao-Jhen
Wu, Ming-Der
Yech, Yi-Jen
Yuan, Gwo-Fang
Wang, Ying-Jan
Evaluating the urate-lowering effects of different microbial fermented extracts in hyperuricemic models accompanied with a safety study
title Evaluating the urate-lowering effects of different microbial fermented extracts in hyperuricemic models accompanied with a safety study
title_full Evaluating the urate-lowering effects of different microbial fermented extracts in hyperuricemic models accompanied with a safety study
title_fullStr Evaluating the urate-lowering effects of different microbial fermented extracts in hyperuricemic models accompanied with a safety study
title_full_unstemmed Evaluating the urate-lowering effects of different microbial fermented extracts in hyperuricemic models accompanied with a safety study
title_short Evaluating the urate-lowering effects of different microbial fermented extracts in hyperuricemic models accompanied with a safety study
title_sort evaluating the urate-lowering effects of different microbial fermented extracts in hyperuricemic models accompanied with a safety study
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9328828/
https://www.ncbi.nlm.nih.gov/pubmed/28911646
http://dx.doi.org/10.1016/j.jfda.2016.07.003
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