The influence of probiotic diet and chondroitin sulfate administration on Ptgs2, Tgfb1 and Col2a1 expression in rat knee cartilage during monoiodoacetate-induced osteoarthritis.
Animals
Cartilage, Articular
/ drug effects
Chondroitin Sulfates
/ administration & dosage
Collagen Type II
/ biosynthesis
Cyclooxygenase 2
/ biosynthesis
Drug Evaluation, Preclinical
Food-Drug Interactions
Gene Expression Regulation
/ drug effects
Iodoacetic Acid
/ toxicity
Male
Microbiota
Osteoarthritis, Knee
/ chemically induced
Probiotics
/ therapeutic use
RNA, Messenger
/ biosynthesis
Rats
Transforming Growth Factor beta1
/ biosynthesis
Journal
Minerva medica
ISSN: 1827-1669
Titre abrégé: Minerva Med
Pays: Italy
ID NLM: 0400732
Informations de publication
Date de publication:
Oct 2019
Oct 2019
Historique:
pubmed:
3
4
2019
medline:
27
8
2019
entrez:
3
4
2019
Statut:
ppublish
Résumé
Osteoarthritis (OA) is a common worldwide disease induced by a wide range of biochemical processes, mainly inflammation and degradation of collagen. The aim of this study, was to describe the effect of a multistrain probiotic (PB) and chondroitin sulfate (CS), administered separately or in combination, on the expression of Ptgs2, Tgfb1 and Col2a1 during monoiodoacetate-induced OA in male rats. OA was induced in male rats by injecting monoiodoacetate in right hind knee. Therapeutic groups received 3 mg/kg of CS for 28 days and/or 1.4 g/kg of multistrain PB for 14 days. Knee cartilage were taken 30 days after monoiodoacetate injection. RNA was extracted and the expression of Ptgs2, Tgfb1 and Col2a1 were analyzed using SYBR Green 1-step real-time quantitative polymerase chain reaction. Induction of OA caused an upregulation in Ptgs2, Tgfb1 expression, and downregulation of Col2a1. Separate administration of PB and CS reduced Ptgs2 and Tgfb1 expressions. Their combined administration significantly decreased the expression of these pro-inflammatory cytokines, comparable to controls. Expression of Col2a1 showed similar behavior, with upregulation in therapeutic group with separate administration and the cumulative effects in case of co-administration. The multistrain PB diet may offer a perspective to improve the standard treatment of OA and, necessitates further investigation with clinical trials.
Sections du résumé
BACKGROUND
BACKGROUND
Osteoarthritis (OA) is a common worldwide disease induced by a wide range of biochemical processes, mainly inflammation and degradation of collagen. The aim of this study, was to describe the effect of a multistrain probiotic (PB) and chondroitin sulfate (CS), administered separately or in combination, on the expression of Ptgs2, Tgfb1 and Col2a1 during monoiodoacetate-induced OA in male rats.
METHODS
METHODS
OA was induced in male rats by injecting monoiodoacetate in right hind knee. Therapeutic groups received 3 mg/kg of CS for 28 days and/or 1.4 g/kg of multistrain PB for 14 days. Knee cartilage were taken 30 days after monoiodoacetate injection. RNA was extracted and the expression of Ptgs2, Tgfb1 and Col2a1 were analyzed using SYBR Green 1-step real-time quantitative polymerase chain reaction.
RESULTS
RESULTS
Induction of OA caused an upregulation in Ptgs2, Tgfb1 expression, and downregulation of Col2a1. Separate administration of PB and CS reduced Ptgs2 and Tgfb1 expressions. Their combined administration significantly decreased the expression of these pro-inflammatory cytokines, comparable to controls. Expression of Col2a1 showed similar behavior, with upregulation in therapeutic group with separate administration and the cumulative effects in case of co-administration.
CONCLUSIONS
CONCLUSIONS
The multistrain PB diet may offer a perspective to improve the standard treatment of OA and, necessitates further investigation with clinical trials.
Identifiants
pubmed: 30938133
pii: S0026-4806.19.06063-4
doi: 10.23736/S0026-4806.19.06063-4
doi:
Substances chimiques
COL2A1 protein, rat
0
Collagen Type II
0
RNA, Messenger
0
Tgfb1 protein, rat
0
Transforming Growth Factor beta1
0
Chondroitin Sulfates
9007-28-7
Cyclooxygenase 2
EC 1.14.99.1
Ptgs2 protein, rat
EC 1.14.99.1
Iodoacetic Acid
WF5188V710
Types de publication
Comparative Study
Journal Article
Langues
eng
Sous-ensembles de citation
IM