Targeting Some Key Metalloproteinases by Nano-Naringenin and <i>Amphora coffeaeformis</i> as a Novel Strategy for Treatment of Osteoarthritis in Rats

Osteoarthritis (OA) represents the highest degenerative disorder. Because cartilage erosion is a common pathological alteration in OA, targeting some key metalloproteinases such as MMP-3, ADAMTS-5 besides their inhibitor TIMP-3 by natural products, could be an effective strategy to protect against o...

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Main Authors: Nema S. Shaban, Abeer M. Radi, Mohamed A. Abdelgawad, Mohammed M. Ghoneim, Rasha Hamed Al-Serwi, Randa M. Hassan, Eman T. Mohammed, Rania A. Radi, Fatma M. Halfaya
Format: Article
Language:English
Published: MDPI AG 2023-02-01
Series:Pharmaceuticals
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Online Access:https://www.mdpi.com/1424-8247/16/2/260
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author Nema S. Shaban
Abeer M. Radi
Mohamed A. Abdelgawad
Mohammed M. Ghoneim
Rasha Hamed Al-Serwi
Randa M. Hassan
Eman T. Mohammed
Rania A. Radi
Fatma M. Halfaya
author_facet Nema S. Shaban
Abeer M. Radi
Mohamed A. Abdelgawad
Mohammed M. Ghoneim
Rasha Hamed Al-Serwi
Randa M. Hassan
Eman T. Mohammed
Rania A. Radi
Fatma M. Halfaya
author_sort Nema S. Shaban
collection DOAJ
description Osteoarthritis (OA) represents the highest degenerative disorder. Because cartilage erosion is a common pathological alteration in OA, targeting some key metalloproteinases such as MMP-3, ADAMTS-5 besides their inhibitor TIMP-3 by natural products, could be an effective strategy to protect against osteoarthritis. Forty female Wister rats were categorized into five equal groups. Control, osteoarthritic (OA) (monosodium iodoacetate (MIA) 2 mg/50 µL saline, single intra-articular injection), OA+ indomethacin (2 mg/kg/daily/orally), OA+ nano-naringenin (25 mg/kg/daily/orally), and OA+ <i>Amphora coffeaeformis</i> (772 mg/kg/daily/orally). Treatments were initiated on the 8th day after osteoarthritis induction and continued for 28 days thereafter. Finally, blood and knee joint samples were collected from all rats for biochemical and histopathological evaluations. The current study showed that MIA induced oxidative stress, which resulted in changes in the inflammatory joint markers associated with increased right knee diameter and higher clinical scores for lameness. <i>Amphora coffeaeformis</i> followed by nano-naringenin exhibited a potential anti-arthritic activity by reducing the concentrations of serum MMP-3, ADAMTS-5, and joint MDA and increasing the levels of serum TIMP-3 and joint GSH, similar to indomethacin. The histopathological results confirmed these outcomes. In conclusion, <i>Amphora coffeaeformis</i> and nano-naringenin can be considered as natural therapeutic agents for osteoarthritis owing to their antioxidant and anti-inflammatory activities.
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spelling doaj.art-a99017631f2e46fd8ec5d3c05db9e5ca2023-11-16T22:37:12ZengMDPI AGPharmaceuticals1424-82472023-02-0116226010.3390/ph16020260Targeting Some Key Metalloproteinases by Nano-Naringenin and <i>Amphora coffeaeformis</i> as a Novel Strategy for Treatment of Osteoarthritis in RatsNema S. Shaban0Abeer M. Radi1Mohamed A. Abdelgawad2Mohammed M. Ghoneim3Rasha Hamed Al-Serwi4Randa M. Hassan5Eman T. Mohammed6Rania A. Radi7Fatma M. Halfaya8Department of Pharmacology, Faculty of Veterinary Medicine, Beni-Suef University, Beni-Suef 62511, EgyptDepartment of Pharmacology, Faculty of Veterinary Medicine, Beni-Suef University, Beni-Suef 62511, EgyptDepartment of Pharmaceutical Chemistry, College of Pharmacy, Jouf University, Aljouf 72341, Saudi ArabiaDepartment of Pharmacy Practice, College of Pharmacy, AlMaarefa University, Ad Diriyah 13713, Saudi ArabiaDepartment of Basic Dental Sciences, College of Dentistry, Princess Nourah bint Abdulrahman University, Riyadh 11671, Saudi ArabiaDepartment of Cytology and Histology, Faculty of Veterinary Medicine, Beni-Suef University, Beni-Suef 62511, EgyptDepartment of Biochemistry and Chemistry of Nutrition, Faculty of Veterinary Medicine, Beni-Suef University, Beni-Suef 62511, EgyptDepartment of Biochemistry and Chemistry of Nutrition, Faculty of Veterinary Medicine, Beni-Suef University, Beni-Suef 62511, EgyptDepartment of Surgery, Anesthesiology and Radiology, Faculty of Veterinary Medicine, Beni-Suef University, Beni-Suef 62511, EgyptOsteoarthritis (OA) represents the highest degenerative disorder. Because cartilage erosion is a common pathological alteration in OA, targeting some key metalloproteinases such as MMP-3, ADAMTS-5 besides their inhibitor TIMP-3 by natural products, could be an effective strategy to protect against osteoarthritis. Forty female Wister rats were categorized into five equal groups. Control, osteoarthritic (OA) (monosodium iodoacetate (MIA) 2 mg/50 µL saline, single intra-articular injection), OA+ indomethacin (2 mg/kg/daily/orally), OA+ nano-naringenin (25 mg/kg/daily/orally), and OA+ <i>Amphora coffeaeformis</i> (772 mg/kg/daily/orally). Treatments were initiated on the 8th day after osteoarthritis induction and continued for 28 days thereafter. Finally, blood and knee joint samples were collected from all rats for biochemical and histopathological evaluations. The current study showed that MIA induced oxidative stress, which resulted in changes in the inflammatory joint markers associated with increased right knee diameter and higher clinical scores for lameness. <i>Amphora coffeaeformis</i> followed by nano-naringenin exhibited a potential anti-arthritic activity by reducing the concentrations of serum MMP-3, ADAMTS-5, and joint MDA and increasing the levels of serum TIMP-3 and joint GSH, similar to indomethacin. The histopathological results confirmed these outcomes. In conclusion, <i>Amphora coffeaeformis</i> and nano-naringenin can be considered as natural therapeutic agents for osteoarthritis owing to their antioxidant and anti-inflammatory activities.https://www.mdpi.com/1424-8247/16/2/260<i>Amphora coffeaeformis</i>nano-naringeninmetalloproteinasesrat MIA-osteoarthritis model
spellingShingle Nema S. Shaban
Abeer M. Radi
Mohamed A. Abdelgawad
Mohammed M. Ghoneim
Rasha Hamed Al-Serwi
Randa M. Hassan
Eman T. Mohammed
Rania A. Radi
Fatma M. Halfaya
Targeting Some Key Metalloproteinases by Nano-Naringenin and <i>Amphora coffeaeformis</i> as a Novel Strategy for Treatment of Osteoarthritis in Rats
Pharmaceuticals
<i>Amphora coffeaeformis</i>
nano-naringenin
metalloproteinases
rat MIA-osteoarthritis model
title Targeting Some Key Metalloproteinases by Nano-Naringenin and <i>Amphora coffeaeformis</i> as a Novel Strategy for Treatment of Osteoarthritis in Rats
title_full Targeting Some Key Metalloproteinases by Nano-Naringenin and <i>Amphora coffeaeformis</i> as a Novel Strategy for Treatment of Osteoarthritis in Rats
title_fullStr Targeting Some Key Metalloproteinases by Nano-Naringenin and <i>Amphora coffeaeformis</i> as a Novel Strategy for Treatment of Osteoarthritis in Rats
title_full_unstemmed Targeting Some Key Metalloproteinases by Nano-Naringenin and <i>Amphora coffeaeformis</i> as a Novel Strategy for Treatment of Osteoarthritis in Rats
title_short Targeting Some Key Metalloproteinases by Nano-Naringenin and <i>Amphora coffeaeformis</i> as a Novel Strategy for Treatment of Osteoarthritis in Rats
title_sort targeting some key metalloproteinases by nano naringenin and i amphora coffeaeformis i as a novel strategy for treatment of osteoarthritis in rats
topic <i>Amphora coffeaeformis</i>
nano-naringenin
metalloproteinases
rat MIA-osteoarthritis model
url https://www.mdpi.com/1424-8247/16/2/260
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