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Lactobacillus plantarum Lp3a improves functional constipation: evidence from a human randomized clinical trial and animal model

BACKGROUND: Functional constipation (FC) is a common gastrointestinal (GI) disorder characterized by symptoms of constipation without a clear physiologic or anatomic cause. Gut microbiome dysbiosis has been postulated to be a factor in the development of FC, and treatment with probiotic regimens, in...

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Autores principales: Zhang, Changliang, Zhang, Yu, Ma, Kai, Wang, Guangxian, Tang, Min, Wang, Runxin, Xia, Ziyue, Xu, Zhiyan, Sun, Miao, Bao, Xiaofeng, Gui, Hongxing, Wang, Hui
Formato: Online Artículo Texto
Lenguaje:English
Publicado: AME Publishing Company 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9011319/
https://www.ncbi.nlm.nih.gov/pubmed/35434041
http://dx.doi.org/10.21037/atm-22-458
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author Zhang, Changliang
Zhang, Yu
Ma, Kai
Wang, Guangxian
Tang, Min
Wang, Runxin
Xia, Ziyue
Xu, Zhiyan
Sun, Miao
Bao, Xiaofeng
Gui, Hongxing
Wang, Hui
author_facet Zhang, Changliang
Zhang, Yu
Ma, Kai
Wang, Guangxian
Tang, Min
Wang, Runxin
Xia, Ziyue
Xu, Zhiyan
Sun, Miao
Bao, Xiaofeng
Gui, Hongxing
Wang, Hui
author_sort Zhang, Changliang
collection PubMed
description BACKGROUND: Functional constipation (FC) is a common gastrointestinal (GI) disorder characterized by symptoms of constipation without a clear physiologic or anatomic cause. Gut microbiome dysbiosis has been postulated to be a factor in the development of FC, and treatment with probiotic regimens, including strains of Lactobacillus plantarum (L. plantarum), has demonstrated efficacy in managing symptoms. To further understand the role of L. plantarum in GI health, we conducted an animal study and a randomized, double-blind, placebo-controlled clinical trial to evaluate the effect of a specific sub-strain, Lp3a, on FC. METHODS: For the animal study, male Kunming mice were treated with doses of L. plantarum Lp3a ranging from 0.67 to 2.00 g/kg or an equivalent amount of placebo for 15 days prior to the induction of constipation via 20 mL/kg of 25% diphenoxylate solution. GI motility parameters including intestinal motion and stool amount were then assessed. In the human study, 120 patients with FC were randomized to treatment [L. plantarum Lp3a; 2×1.0×10(10 )(colony forming units; CFU) ×7 days] or control groups (n=60 each). The primary endpoint was survey information on FC signs/symptoms. Participants and observers were blinded to group allocation. A subset of 20 Lp3a treated patients underwent pre- and post-treatment 16 s ribosomal ribonucleic acid (rRNA) gene sequencing. Whole genome sequencing (WGS) of L. plantarum Lp3a was also performed. RESULTS: Lp3a-treated mice showed significantly improved intestinal motion, reduced time to first defecation, and increased stool amounts. Similarly, patients in the treatment group (n=59) reported significant improvements in FC signs/symptoms compared to controls (n=58; all P<0.05). Although 16 s rRNA sequencing revealed no significant variations between pre- and post-treatment samples, WGS of Lp3a itself revealed several biological pathways that may underlie the relief of FC symptoms in animals and humans, including methane and fatty acid metabolism and bile acid biosynthesis. CONCLUSIONS: We found that the use of the novel probiotic sub-strain, L. plantarum Lp3a, led to clinically significant improvements in FC in both mice and humans, and identified the potential biological mechanisms underlying this activity.
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spelling pubmed-90113192022-04-16 Lactobacillus plantarum Lp3a improves functional constipation: evidence from a human randomized clinical trial and animal model Zhang, Changliang Zhang, Yu Ma, Kai Wang, Guangxian Tang, Min Wang, Runxin Xia, Ziyue Xu, Zhiyan Sun, Miao Bao, Xiaofeng Gui, Hongxing Wang, Hui Ann Transl Med Original Article BACKGROUND: Functional constipation (FC) is a common gastrointestinal (GI) disorder characterized by symptoms of constipation without a clear physiologic or anatomic cause. Gut microbiome dysbiosis has been postulated to be a factor in the development of FC, and treatment with probiotic regimens, including strains of Lactobacillus plantarum (L. plantarum), has demonstrated efficacy in managing symptoms. To further understand the role of L. plantarum in GI health, we conducted an animal study and a randomized, double-blind, placebo-controlled clinical trial to evaluate the effect of a specific sub-strain, Lp3a, on FC. METHODS: For the animal study, male Kunming mice were treated with doses of L. plantarum Lp3a ranging from 0.67 to 2.00 g/kg or an equivalent amount of placebo for 15 days prior to the induction of constipation via 20 mL/kg of 25% diphenoxylate solution. GI motility parameters including intestinal motion and stool amount were then assessed. In the human study, 120 patients with FC were randomized to treatment [L. plantarum Lp3a; 2×1.0×10(10 )(colony forming units; CFU) ×7 days] or control groups (n=60 each). The primary endpoint was survey information on FC signs/symptoms. Participants and observers were blinded to group allocation. A subset of 20 Lp3a treated patients underwent pre- and post-treatment 16 s ribosomal ribonucleic acid (rRNA) gene sequencing. Whole genome sequencing (WGS) of L. plantarum Lp3a was also performed. RESULTS: Lp3a-treated mice showed significantly improved intestinal motion, reduced time to first defecation, and increased stool amounts. Similarly, patients in the treatment group (n=59) reported significant improvements in FC signs/symptoms compared to controls (n=58; all P<0.05). Although 16 s rRNA sequencing revealed no significant variations between pre- and post-treatment samples, WGS of Lp3a itself revealed several biological pathways that may underlie the relief of FC symptoms in animals and humans, including methane and fatty acid metabolism and bile acid biosynthesis. CONCLUSIONS: We found that the use of the novel probiotic sub-strain, L. plantarum Lp3a, led to clinically significant improvements in FC in both mice and humans, and identified the potential biological mechanisms underlying this activity. AME Publishing Company 2022-03 /pmc/articles/PMC9011319/ /pubmed/35434041 http://dx.doi.org/10.21037/atm-22-458 Text en 2022 Annals of Translational Medicine. All rights reserved. https://creativecommons.org/licenses/by-nc-nd/4.0/Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) .
spellingShingle Original Article
Zhang, Changliang
Zhang, Yu
Ma, Kai
Wang, Guangxian
Tang, Min
Wang, Runxin
Xia, Ziyue
Xu, Zhiyan
Sun, Miao
Bao, Xiaofeng
Gui, Hongxing
Wang, Hui
Lactobacillus plantarum Lp3a improves functional constipation: evidence from a human randomized clinical trial and animal model
title Lactobacillus plantarum Lp3a improves functional constipation: evidence from a human randomized clinical trial and animal model
title_full Lactobacillus plantarum Lp3a improves functional constipation: evidence from a human randomized clinical trial and animal model
title_fullStr Lactobacillus plantarum Lp3a improves functional constipation: evidence from a human randomized clinical trial and animal model
title_full_unstemmed Lactobacillus plantarum Lp3a improves functional constipation: evidence from a human randomized clinical trial and animal model
title_short Lactobacillus plantarum Lp3a improves functional constipation: evidence from a human randomized clinical trial and animal model
title_sort lactobacillus plantarum lp3a improves functional constipation: evidence from a human randomized clinical trial and animal model
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9011319/
https://www.ncbi.nlm.nih.gov/pubmed/35434041
http://dx.doi.org/10.21037/atm-22-458
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