Obesity is associated with intestine dysbiosis and is characterized by a low-grade inflammatory status, which affects vascular function. In the present study, we evaluated the effects of a probiotic with immunomodulatory properties, Lactobacillus coryniformis CECT5711, in obese mice fed on an HFD (high-fat diet). The probiotic treatment was given for 12 weeks, and it did not affect the weight evolution, although it reduced basal glycaemia and insulin resistance. L. coryniformis administration to HFD-induced obese mice induced marked changes in microbiota composition and reduced the metabolic endotoxaemia as it decreased the LPS (lipopolysaccharide) plasma level, which was associated with a significant improvement in gut barrier disruption. Furthermore, it lowered TNFα (tumour necrosis factor α) expression in liver, improving the inflammatory status, and thus the glucose metabolism. Additionally, the probiotic reversed the endothelial dysfunction observed in obese mice when endothelium- and NO (nitric oxide)-dependent vasodilatation induced by acetylcholine in aortic rings was studied. It also restored the increased vessel superoxide levels observed in obese mice, by reducing NADPH oxidase activity and increasing antioxidant enzymes. Moreover, chronic probiotic administration for 2 weeks also improved endothelial dysfunction and vascular oxidative stress induced by in vivo administration of LPS in control mice fed on a standard chow diet. The results of the present study demonstrate an endothelial-protective effect of L. coryniformis CECT5711 in obese mice by increasing NO bioavailability, suggesting the therapeutic potential of this gut microbiota manipulation to prevent vasculopathy in obesity.
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Research Article|
March 10 2014
The probiotic Lactobacillus coryniformis CECT5711 reduces the vascular pro-oxidant and pro-inflammatory status in obese mice
Marta Toral;
Marta Toral
1
*Department of Pharmacology, School of Pharmacy, University of Granada, Granada, Spain
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Manuel Gómez-Guzmán;
Manuel Gómez-Guzmán
1
*Department of Pharmacology, School of Pharmacy, University of Granada, Granada, Spain
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Rosario Jiménez;
Rosario Jiménez
*Department of Pharmacology, School of Pharmacy, University of Granada, Granada, Spain
†Instituto de Investigación Biosanitaria de Granada, Granada, Spain
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Miguel Romero;
Miguel Romero
*Department of Pharmacology, School of Pharmacy, University of Granada, Granada, Spain
†Instituto de Investigación Biosanitaria de Granada, Granada, Spain
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Manuel Sánchez;
Manuel Sánchez
*Department of Pharmacology, School of Pharmacy, University of Granada, Granada, Spain
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María Pilar Utrilla;
María Pilar Utrilla
†Instituto de Investigación Biosanitaria de Granada, Granada, Spain
‡CIBER-EHD, Department of Pharmacology, Center for Biomedical Research, University of Granada, Granada, Spain
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Natividad Garrido-Mesa;
Natividad Garrido-Mesa
‡CIBER-EHD, Department of Pharmacology, Center for Biomedical Research, University of Granada, Granada, Spain
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María Elena Rodríguez-Cabezas;
María Elena Rodríguez-Cabezas
†Instituto de Investigación Biosanitaria de Granada, Granada, Spain
‡CIBER-EHD, Department of Pharmacology, Center for Biomedical Research, University of Granada, Granada, Spain
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Mónica Olivares;
Mónica Olivares
§Research Department of Biosearch, Granada, Spain
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Julio Gálvez;
Julio Gálvez
†Instituto de Investigación Biosanitaria de Granada, Granada, Spain
‡CIBER-EHD, Department of Pharmacology, Center for Biomedical Research, University of Granada, Granada, Spain
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Juan Duarte
*Department of Pharmacology, School of Pharmacy, University of Granada, Granada, Spain
†Instituto de Investigación Biosanitaria de Granada, Granada, Spain
Correspondence: Dr Juan Duarte (email [email protected]).
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Publisher: Portland Press Ltd
Received:
July 01 2013
Revision Received:
January 07 2014
Accepted:
January 10 2014
Accepted Manuscript online:
January 10 2014
Online ISSN: 1470-8736
Print ISSN: 0143-5221
© The Authors Journal compilation © 2014 Biochemical Society
2014
Clin Sci (Lond) (2014) 127 (1): 33–45.
Article history
Received:
July 01 2013
Revision Received:
January 07 2014
Accepted:
January 10 2014
Accepted Manuscript online:
January 10 2014
Citation
Marta Toral, Manuel Gómez-Guzmán, Rosario Jiménez, Miguel Romero, Manuel Sánchez, María Pilar Utrilla, Natividad Garrido-Mesa, María Elena Rodríguez-Cabezas, Mónica Olivares, Julio Gálvez, Juan Duarte; The probiotic Lactobacillus coryniformis CECT5711 reduces the vascular pro-oxidant and pro-inflammatory status in obese mice. Clin Sci (Lond) 1 July 2014; 127 (1): 33–45. doi: https://doi.org/10.1042/CS20130339
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