Probiotic effects of Lacticaseibacillus rhamnosus 1155 and Limosilactobacillus fermentum 2644 on hyperuricemic rats

Hyperuricemia is the main cause of gout and involved in the occurrence of multiple diseases, such as hypertension, metabolic disorders and chronic kidney disease. Emerging evidence suggests that lactic acid bacteria (LAB) have shown the beneficial effects on the prevention or treatment of hyperurice...

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Main Authors: Yanjun Li, Jun Zhu, Guodong Lin, Kan Gao, Yunxia Yu, Su Chen, Lie Chen, Zuoguo Chen, Li Li
Format: Article
Language:English
Published: Frontiers Media S.A. 2022-09-01
Series:Frontiers in Nutrition
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fnut.2022.993951/full
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author Yanjun Li
Yanjun Li
Yanjun Li
Jun Zhu
Jun Zhu
Guodong Lin
Guodong Lin
Kan Gao
Kan Gao
Yunxia Yu
Yunxia Yu
Su Chen
Su Chen
Lie Chen
Lie Chen
Zuoguo Chen
Zuoguo Chen
Li Li
Li Li
author_facet Yanjun Li
Yanjun Li
Yanjun Li
Jun Zhu
Jun Zhu
Guodong Lin
Guodong Lin
Kan Gao
Kan Gao
Yunxia Yu
Yunxia Yu
Su Chen
Su Chen
Lie Chen
Lie Chen
Zuoguo Chen
Zuoguo Chen
Li Li
Li Li
author_sort Yanjun Li
collection DOAJ
description Hyperuricemia is the main cause of gout and involved in the occurrence of multiple diseases, such as hypertension, metabolic disorders and chronic kidney disease. Emerging evidence suggests that lactic acid bacteria (LAB) have shown the beneficial effects on the prevention or treatment of hyperuricemia. In this study, the urate-lowering effect of two LAB strains, Lacticaseibacillus rhamnosus 1155 (LR1155) and Limosilactobacillus fermentum 2644 (LF2644) on hyperuricemic rats were investigated. A hyperuricemic rat model was induced by the intragastric treatment of potassium oxonate, combined with a high purine diet. The oral administration of LR1155, LF2644, or a combination of LR1155 and LF2644 for 4 weeks significantly prevented the rise of the serum uric acid (UA) induced by hyperuricemia. LR1155 and LF2644 significantly elevated the fecal UA levels, increased the UA content and up-regulated gene expression of UA transporter, ATP-binding cassette subfamily G-2 (ABCG2), in colon and jejunum tissues, suggesting the accelerated UA excretion from the intestine. Besides, LR1155 significantly inhibited the activity of xanthine oxidase (XOD) in liver and serum, benefited the reduce of UA production. In addition, LF2644 strengthened the gut barrier functions through an up-regulation of the gene expressions for occluding and mucin2, accompanied with the reduced inflammatory indicators of lipopolysaccharide (LPS) and interleukin-1β (IL-1β) in hyperuricemic rat. Moreover, using 16s rDNA high-throughput sequencing of feces, LR1155 was shown to improve the hyperuricemia induced gut microbial dysbiosis. The genera Roseburia, Butyricicoccus, Prevotella, Oscillibacter, and Bifidobacterium may associate with the effect of LR1155 on microbiota in hyperuricemic rats. Collectively, the results indicated that LR1155 and LF2644 exhibit urate-lowering effects and could be used alone or in combination as a new adjuvant treatment for hyperuricemia.
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spelling doaj.art-55cd3481548140978dda11f0d8c8437b2022-12-22T03:48:50ZengFrontiers Media S.A.Frontiers in Nutrition2296-861X2022-09-01910.3389/fnut.2022.993951993951Probiotic effects of Lacticaseibacillus rhamnosus 1155 and Limosilactobacillus fermentum 2644 on hyperuricemic ratsYanjun Li0Yanjun Li1Yanjun Li2Jun Zhu3Jun Zhu4Guodong Lin5Guodong Lin6Kan Gao7Kan Gao8Yunxia Yu9Yunxia Yu10Su Chen11Su Chen12Lie Chen13Lie Chen14Zuoguo Chen15Zuoguo Chen16Li Li17Li Li18College of Biosystems Engineering and Food Science, Zhejiang University, Hangzhou, ChinaDepartment of Research and Development, Hangzhou Wahaha Group Co., Ltd., Hangzhou, ChinaKey Laboratory of Food and Biological Engineering of Zhejiang Province, Hangzhou, ChinaDepartment of Research and Development, Hangzhou Wahaha Group Co., Ltd., Hangzhou, ChinaKey Laboratory of Food and Biological Engineering of Zhejiang Province, Hangzhou, ChinaDepartment of Research and Development, Hangzhou Wahaha Group Co., Ltd., Hangzhou, ChinaKey Laboratory of Food and Biological Engineering of Zhejiang Province, Hangzhou, ChinaDepartment of Research and Development, Hangzhou Wahaha Group Co., Ltd., Hangzhou, ChinaKey Laboratory of Food and Biological Engineering of Zhejiang Province, Hangzhou, ChinaDepartment of Research and Development, Hangzhou Wahaha Group Co., Ltd., Hangzhou, ChinaKey Laboratory of Food and Biological Engineering of Zhejiang Province, Hangzhou, ChinaDepartment of Research and Development, Hangzhou Wahaha Group Co., Ltd., Hangzhou, ChinaKey Laboratory of Food and Biological Engineering of Zhejiang Province, Hangzhou, ChinaDepartment of Research and Development, Hangzhou Wahaha Group Co., Ltd., Hangzhou, ChinaKey Laboratory of Food and Biological Engineering of Zhejiang Province, Hangzhou, ChinaDepartment of Research and Development, Hangzhou Wahaha Group Co., Ltd., Hangzhou, ChinaKey Laboratory of Food and Biological Engineering of Zhejiang Province, Hangzhou, ChinaDepartment of Research and Development, Hangzhou Wahaha Group Co., Ltd., Hangzhou, ChinaKey Laboratory of Food and Biological Engineering of Zhejiang Province, Hangzhou, ChinaHyperuricemia is the main cause of gout and involved in the occurrence of multiple diseases, such as hypertension, metabolic disorders and chronic kidney disease. Emerging evidence suggests that lactic acid bacteria (LAB) have shown the beneficial effects on the prevention or treatment of hyperuricemia. In this study, the urate-lowering effect of two LAB strains, Lacticaseibacillus rhamnosus 1155 (LR1155) and Limosilactobacillus fermentum 2644 (LF2644) on hyperuricemic rats were investigated. A hyperuricemic rat model was induced by the intragastric treatment of potassium oxonate, combined with a high purine diet. The oral administration of LR1155, LF2644, or a combination of LR1155 and LF2644 for 4 weeks significantly prevented the rise of the serum uric acid (UA) induced by hyperuricemia. LR1155 and LF2644 significantly elevated the fecal UA levels, increased the UA content and up-regulated gene expression of UA transporter, ATP-binding cassette subfamily G-2 (ABCG2), in colon and jejunum tissues, suggesting the accelerated UA excretion from the intestine. Besides, LR1155 significantly inhibited the activity of xanthine oxidase (XOD) in liver and serum, benefited the reduce of UA production. In addition, LF2644 strengthened the gut barrier functions through an up-regulation of the gene expressions for occluding and mucin2, accompanied with the reduced inflammatory indicators of lipopolysaccharide (LPS) and interleukin-1β (IL-1β) in hyperuricemic rat. Moreover, using 16s rDNA high-throughput sequencing of feces, LR1155 was shown to improve the hyperuricemia induced gut microbial dysbiosis. The genera Roseburia, Butyricicoccus, Prevotella, Oscillibacter, and Bifidobacterium may associate with the effect of LR1155 on microbiota in hyperuricemic rats. Collectively, the results indicated that LR1155 and LF2644 exhibit urate-lowering effects and could be used alone or in combination as a new adjuvant treatment for hyperuricemia.https://www.frontiersin.org/articles/10.3389/fnut.2022.993951/fullhyperuricemialactic acid bacteriaurate-lowering effectintestinal excretionxanthine oxidaseABCG2
spellingShingle Yanjun Li
Yanjun Li
Yanjun Li
Jun Zhu
Jun Zhu
Guodong Lin
Guodong Lin
Kan Gao
Kan Gao
Yunxia Yu
Yunxia Yu
Su Chen
Su Chen
Lie Chen
Lie Chen
Zuoguo Chen
Zuoguo Chen
Li Li
Li Li
Probiotic effects of Lacticaseibacillus rhamnosus 1155 and Limosilactobacillus fermentum 2644 on hyperuricemic rats
Frontiers in Nutrition
hyperuricemia
lactic acid bacteria
urate-lowering effect
intestinal excretion
xanthine oxidase
ABCG2
title Probiotic effects of Lacticaseibacillus rhamnosus 1155 and Limosilactobacillus fermentum 2644 on hyperuricemic rats
title_full Probiotic effects of Lacticaseibacillus rhamnosus 1155 and Limosilactobacillus fermentum 2644 on hyperuricemic rats
title_fullStr Probiotic effects of Lacticaseibacillus rhamnosus 1155 and Limosilactobacillus fermentum 2644 on hyperuricemic rats
title_full_unstemmed Probiotic effects of Lacticaseibacillus rhamnosus 1155 and Limosilactobacillus fermentum 2644 on hyperuricemic rats
title_short Probiotic effects of Lacticaseibacillus rhamnosus 1155 and Limosilactobacillus fermentum 2644 on hyperuricemic rats
title_sort probiotic effects of lacticaseibacillus rhamnosus 1155 and limosilactobacillus fermentum 2644 on hyperuricemic rats
topic hyperuricemia
lactic acid bacteria
urate-lowering effect
intestinal excretion
xanthine oxidase
ABCG2
url https://www.frontiersin.org/articles/10.3389/fnut.2022.993951/full
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