Lactobacillus fermentum CECT5716 prevents renal damage in the NZBWF1 mouse model of systemic lupus erythematosus.


Journal

Food & function
ISSN: 2042-650X
Titre abrégé: Food Funct
Pays: England
ID NLM: 101549033

Informations de publication

Date de publication:
24 Jun 2020
Historique:
pubmed: 28 5 2020
medline: 29 5 2021
entrez: 28 5 2020
Statut: ppublish

Résumé

The aim of this work was to evaluate whether the immune-modulatory bacterium Lactobacillus fermentum CECT5716 (LC40) protects the kidneys in a female mouse model of lupus with hypertension. Twenty-week-old female NZBWF1 (lupus) and NZW/LacJ (control) mice were treated with vehicle or LC40 (5 × 108 colony-forming units day-1) for 13 weeks. LC40 treatment reduced the increased plasma anti-dsDNA, endotoxemia, and high blood pressure in NZBWF1 mice. In parallel, LC40 also prevented alterations in kidney function parameters, measured by reduced creatinine and urea in urine excretion, and kidney injury, evaluated by albumin excretion in lupus mice. The main histological features found in the kidneys of lupus mice, such as glomerular, tubulointerstitial or vascular lesions present in the renal parenchyma, accompanied by immune-complex deposition and inflammatory infiltrates were also reduced by LC40. In addition, LC40 inhibited the increased levels of pro-inflammatory cytokines, NADPH oxidase activity and infiltration of Th17 and Th1 cells in the kidneys of NZBWF1 mice. Interestingly, no significant changes were observed in control mice treated with LC40. In conclusion, these results indicate that the consumption of LC40 can prevent the impairment of kidney function and damage, in part due to its capacity to reduce anti-dsDNA production and circulating levels of lipopolysaccharides, with the subsequent reduction of immune complex deposition, inflammation and oxidative stress. These results open new possibilities for the prevention of renal complications associated with hypertensive systemic lupus erythematosus by the chronic administration of the probiotic LC40.

Identifiants

pubmed: 32458936
doi: 10.1039/d0fo00578a
doi:

Substances chimiques

Cytokines 0
Transcription Factors 0
NADPH Oxidases EC 1.6.3.-

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

5266-5274

Auteurs

Néstor de la Visitación (N)

Department of Pharmacology, School of Pharmacy, University of Granada, Granada, Spain.

Iñaki Robles-Vera (I)

Department of Pharmacology, School of Pharmacy, University of Granada, Granada, Spain.

Marta Toral (M)

Gene Regulation in Cardiovascular Remodeling and Inflammation Group, Centro Nacional de Investigaciones Cardiovasculares (CNIC), Madrid, Spain. marta.toral@cnic.es and CIBERCV, Granada, Spain.

Francisco O'Valle (F)

Department of Pathology, School of Medicine, University of Granada, Granada, Spain and Instituto de Investigación Biosanitaria de Granada (Ibs.GRANADA), Granada, Spain.

Javier Moleon (J)

Department of Pharmacology, School of Pharmacy, University of Granada, Granada, Spain.

Manuel Gómez-Guzmán (M)

Department of Pharmacology, School of Pharmacy, University of Granada, Granada, Spain and Instituto de Investigación Biosanitaria de Granada (Ibs.GRANADA), Granada, Spain.

Miguel Romero (M)

Department of Pharmacology, School of Pharmacy, University of Granada, Granada, Spain and Instituto de Investigación Biosanitaria de Granada (Ibs.GRANADA), Granada, Spain.

Marcos Duarte (M)

Department of Pharmacology, School of Pharmacy, University of Granada, Granada, Spain.

Manuel Sánchez (M)

Department of Pharmacology, School of Pharmacy, University of Granada, Granada, Spain and Instituto de Investigación Biosanitaria de Granada (Ibs.GRANADA), Granada, Spain.

Rosario Jiménez (R)

Department of Pharmacology, School of Pharmacy, University of Granada, Granada, Spain and CIBERCV, Granada, Spain and Instituto de Investigación Biosanitaria de Granada (Ibs.GRANADA), Granada, Spain.

Juan Duarte (J)

Department of Pharmacology, School of Pharmacy, University of Granada, Granada, Spain and CIBERCV, Granada, Spain and Instituto de Investigación Biosanitaria de Granada (Ibs.GRANADA), Granada, Spain.

Articles similaires

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male
Humans Meals Time Factors Female Adult

Classifications MeSH