Your browser doesn't support javascript.
Synthesis of N,N'-bis(1,5-dimethyl-2-phenyl-1,2-dihydro-3-oxopyrazol-4-yl) sebacamide that ameliorate osteoarthritis symptoms and improve bone marrow matrix structure and cartilage alterations induced by monoiodoacetate in the rat model: "Suggested potent anti-inflammatory agent against COVID-19".
Refat, M S; Hamza, R Z; Adam, Ama; Saad, H A; Gobouri, A A; Al-Salmi, F A; Altalhi, T; El-Megharbel, S M.
  • Refat MS; Department of Chemistry, Faculty of Science, 125895Taif University, Taif, Saudi Arabia.
  • Hamza RZ; Department of Chemistry, Faculty of Science, Port Said University, Port Said, Egypt.
  • Adam A; Department of Biology, Faculty of Science, 125895Taif University, Taif, Saudi Arabia.
  • Saad HA; Department of Zoology, Faculty of Science, 68799Zagazig University, Zagazig, Egypt.
  • Gobouri AA; Department of Chemistry, Faculty of Science, 125895Taif University, Taif, Saudi Arabia.
  • Al-Salmi FA; Department of Chemistry, Faculty of Science, 125895Taif University, Taif, Saudi Arabia.
  • Altalhi T; Department of Chemistry, Faculty of Science, 68799Zagazig University, Zagazig, Egypt.
  • El-Megharbel SM; Department of Chemistry, Faculty of Science, 125895Taif University, Taif, Saudi Arabia.
Hum Exp Toxicol ; 40(2): 325-341, 2021 Feb.
Article in English | MEDLINE | ID: covidwho-1067095
ABSTRACT
To assess the chondroprotective effect and influence of N,N'-bis(1,5-dimethyl-2-phenyl-1,2-dihydro-3-oxopyrazol-4-yl) sebacamide (dpdo) that was synthesized through the reaction of phenazone with sebacoyl chloride and screened for its biological activity especially as anti-arthritic and anti-inflammatory agent in a monoiodoacetate (MA)-induced experimental osteoarthritis (OA) model. Thirty male albino rats weighing "190-200 g" were divided randomly into three groups (10 each) control, MA-induced OA, and MA-induced OA + dpdo. In MA-induced OA rat, the tumor necrosis factor alpha, interleukin 6, C-reactive protein, rheumatoid factors, reactive oxygen species, as well as all the mitochondrial markers such as mitochondria membrane potential, swelling mitochondria, cytochrome c oxidase (complex IV), and serum oxidative/antioxidant status (malondialdehyde level and activities of myeloperoxidase and xanthine oxidase) are elevated. Also, the activity of succinate dehydrogenase (complex II), levels of ATP, the level of glutathione (GSH), and thiol were markedly diminished in the MA-induced OA group compared to the normal control rats. These findings showed that mitochondrial function is associated with OA pathophysiological alterations and high gene expressions of (IL-6, TNF-a, and IL-1b) and suggests a promising use of dpdo as potential ameliorative agents in the animal model of OA and could act as anti-inflammatory agent in case of severe infection with COVID-19. It is clearly appeared in improving the bone cortex and bone marrow in the treated group with the novel compound in histological and transmission electron microscopic sections which is a very important issue today in fighting severe infections that have significant effects on the blood indices and declining of blood corpuscles like COVID-19, in addition to declining the genotoxicity and inflammation induced by MA in male rats. The novel synthesized compound was highly effective in improving all the above mentioned parameters.
Subject(s)
Keywords

Full text: Available Collection: International databases Database: MEDLINE Main subject: Osteoarthritis / SARS-CoV-2 / COVID-19 Drug Treatment / Anti-Inflammatory Agents Type of study: Experimental Studies / Observational study / Randomized controlled trials Limits: Animals Language: English Journal: Hum Exp Toxicol Journal subject: Toxicology Year: 2021 Document Type: Article Affiliation country: 0960327120945779

Similar

MEDLINE

...
LILACS

LIS


Full text: Available Collection: International databases Database: MEDLINE Main subject: Osteoarthritis / SARS-CoV-2 / COVID-19 Drug Treatment / Anti-Inflammatory Agents Type of study: Experimental Studies / Observational study / Randomized controlled trials Limits: Animals Language: English Journal: Hum Exp Toxicol Journal subject: Toxicology Year: 2021 Document Type: Article Affiliation country: 0960327120945779