Disease-Modifying Potential of Metformin and Alendronate in an Experimental Mouse Model of Osteoarthritis

Osteoarthritis (OA) is the most common degenerative joint disease causing progressive damages of the cartilage and subchondral bone, synovial inflammation, and severe pain. Despite the complex pathomorphological changes that occur in OA, the approach to different forms of OA is standardized. The glo...

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Main Authors: Lyudmila Belenska-Todorova, Sevdalina Nikolova Lambova, Stela Stoyanova, Elenka Georgieva, Tsvetelina Batsalova, Dzhemal Moten, Desislava Kolchakova, Balik Dzhambazov
Format: Article
Language:English
Published: MDPI AG 2021-08-01
Series:Biomedicines
Subjects:
Online Access:https://www.mdpi.com/2227-9059/9/8/1017
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spelling doaj-d01cfd3368114d31805fb7f73968b89b2021-08-26T13:33:10ZengMDPI AGBiomedicines2227-90592021-08-0191017101710.3390/biomedicines9081017Disease-Modifying Potential of Metformin and Alendronate in an Experimental Mouse Model of OsteoarthritisLyudmila Belenska-Todorova0Sevdalina Nikolova Lambova1Stela Stoyanova2Elenka Georgieva3Tsvetelina Batsalova4Dzhemal Moten5Desislava Kolchakova6Balik Dzhambazov7Faculty of Medicine, Sofia University “St. Kliment Ohridski”, 1407 Sofia, BulgariaDepartment of Propaedeutics of Internal Diseases, Faculty of Medicine, Medical University of Plovdiv, 4002 Plovdiv, BulgariaDepartment of Developmental Biology, Plovdiv University “Paisii Hilendarski”, 4000 Plovdiv, BulgariaDepartment of Developmental Biology, Plovdiv University “Paisii Hilendarski”, 4000 Plovdiv, BulgariaDepartment of Developmental Biology, Plovdiv University “Paisii Hilendarski”, 4000 Plovdiv, BulgariaDepartment of Developmental Biology, Plovdiv University “Paisii Hilendarski”, 4000 Plovdiv, BulgariaDepartment of Developmental Biology, Plovdiv University “Paisii Hilendarski”, 4000 Plovdiv, BulgariaDepartment of Developmental Biology, Plovdiv University “Paisii Hilendarski”, 4000 Plovdiv, BulgariaOsteoarthritis (OA) is the most common degenerative joint disease causing progressive damages of the cartilage and subchondral bone, synovial inflammation, and severe pain. Despite the complex pathomorphological changes that occur in OA, the approach to different forms of OA is standardized. The global results from pharmacological treatment are not satisfactory. Hence, this study aimed to explore the effects of metformin, alendronate, and their combination on OA development and progression in mice with collagenase-induced osteoarthritis (CIOA). Female ICR (CD-2) mice were randomized to five groups: control group, CIOA untreated, CIOA + metformin, CIOA + alendronate, and CIOA + metformin + alendronate. OA was induced by the intra-articular (i.a.) injection of collagenase. OA phenotype was analyzed by flow cytometry (bone marrow cell differentiation), ELISA (serum levels of the adipokines leptin and resistin), and histology (pathological changes of the knee joint). Treatment with metformin, alendronate, or their combination inhibited the expression of RANK and RANKL on osteoblasts and osteoclasts obtained by ex vivo cultivation of bone marrow cells in mineralization or osteoclastogenic media. In addition, metformin treatment was effective for the attenuation of fibroblast differentiation, but not of mesenchymal stem cells (MSCs), while alendronate had an opposite effect. The combination of metformin and alendronate had a suppressive effect on both MSCs and fibroblasts differentiation. Treatment with metformin, alendronate, and their combination decreased serum concentrations of leptin and resistin in the chronic phase of arthritis. The histopathological examination showed that compared with the untreated CIOA group (OA score 9), the groups treated with metformin (OA score 4) or alendronate (OA score 6) had lower scores for cartilage changes. Metformin combined with alendronate significantly decreased the degree of cartilage degeneration (OA score 2), suggesting that this combination might be a useful approach for the treatment of OA patients.https://www.mdpi.com/2227-9059/9/8/1017osteoarthritismouse modelmetforminbisphosphonatetreatmentosteoclastogenesis
collection DOAJ
language English
format Article
sources DOAJ
author Lyudmila Belenska-Todorova
Sevdalina Nikolova Lambova
Stela Stoyanova
Elenka Georgieva
Tsvetelina Batsalova
Dzhemal Moten
Desislava Kolchakova
Balik Dzhambazov
spellingShingle Lyudmila Belenska-Todorova
Sevdalina Nikolova Lambova
Stela Stoyanova
Elenka Georgieva
Tsvetelina Batsalova
Dzhemal Moten
Desislava Kolchakova
Balik Dzhambazov
Disease-Modifying Potential of Metformin and Alendronate in an Experimental Mouse Model of Osteoarthritis
Biomedicines
osteoarthritis
mouse model
metformin
bisphosphonate
treatment
osteoclastogenesis
author_facet Lyudmila Belenska-Todorova
Sevdalina Nikolova Lambova
Stela Stoyanova
Elenka Georgieva
Tsvetelina Batsalova
Dzhemal Moten
Desislava Kolchakova
Balik Dzhambazov
author_sort Lyudmila Belenska-Todorova
title Disease-Modifying Potential of Metformin and Alendronate in an Experimental Mouse Model of Osteoarthritis
title_short Disease-Modifying Potential of Metformin and Alendronate in an Experimental Mouse Model of Osteoarthritis
title_full Disease-Modifying Potential of Metformin and Alendronate in an Experimental Mouse Model of Osteoarthritis
title_fullStr Disease-Modifying Potential of Metformin and Alendronate in an Experimental Mouse Model of Osteoarthritis
title_full_unstemmed Disease-Modifying Potential of Metformin and Alendronate in an Experimental Mouse Model of Osteoarthritis
title_sort disease-modifying potential of metformin and alendronate in an experimental mouse model of osteoarthritis
publisher MDPI AG
series Biomedicines
issn 2227-9059
publishDate 2021-08-01
description Osteoarthritis (OA) is the most common degenerative joint disease causing progressive damages of the cartilage and subchondral bone, synovial inflammation, and severe pain. Despite the complex pathomorphological changes that occur in OA, the approach to different forms of OA is standardized. The global results from pharmacological treatment are not satisfactory. Hence, this study aimed to explore the effects of metformin, alendronate, and their combination on OA development and progression in mice with collagenase-induced osteoarthritis (CIOA). Female ICR (CD-2) mice were randomized to five groups: control group, CIOA untreated, CIOA + metformin, CIOA + alendronate, and CIOA + metformin + alendronate. OA was induced by the intra-articular (i.a.) injection of collagenase. OA phenotype was analyzed by flow cytometry (bone marrow cell differentiation), ELISA (serum levels of the adipokines leptin and resistin), and histology (pathological changes of the knee joint). Treatment with metformin, alendronate, or their combination inhibited the expression of RANK and RANKL on osteoblasts and osteoclasts obtained by ex vivo cultivation of bone marrow cells in mineralization or osteoclastogenic media. In addition, metformin treatment was effective for the attenuation of fibroblast differentiation, but not of mesenchymal stem cells (MSCs), while alendronate had an opposite effect. The combination of metformin and alendronate had a suppressive effect on both MSCs and fibroblasts differentiation. Treatment with metformin, alendronate, and their combination decreased serum concentrations of leptin and resistin in the chronic phase of arthritis. The histopathological examination showed that compared with the untreated CIOA group (OA score 9), the groups treated with metformin (OA score 4) or alendronate (OA score 6) had lower scores for cartilage changes. Metformin combined with alendronate significantly decreased the degree of cartilage degeneration (OA score 2), suggesting that this combination might be a useful approach for the treatment of OA patients.
topic osteoarthritis
mouse model
metformin
bisphosphonate
treatment
osteoclastogenesis
url https://www.mdpi.com/2227-9059/9/8/1017
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