دورية أكاديمية

A new acyl derivative of sulfadimethoxine inhibits phagocyte oxidative burst and ameliorates inflammation in a mice model of zymosan-induced generalised inflammation.

التفاصيل البيبلوغرافية
العنوان: A new acyl derivative of sulfadimethoxine inhibits phagocyte oxidative burst and ameliorates inflammation in a mice model of zymosan-induced generalised inflammation.
المؤلفون: Baig TA; Dr. Panjwani Center for Molecular Medicine and Drug Research, International Center for Chemical and Biological Sciences, University of Karachi, Karachi, 75270, Pakistan., Haniffa HM; H.E.J. Research Institute of Chemistry, International Center for Chemical and Biological Sciences, University of Karachi, Karachi, 75270, Pakistan.; Department of Chemical Sciences, Faculty of Applied Sciences, South Eastern University, Sammanthurai, 32200, Sri Lanka., Siddiqui H; H.E.J. Research Institute of Chemistry, International Center for Chemical and Biological Sciences, University of Karachi, Karachi, 75270, Pakistan., Shah SF; Dr. Panjwani Center for Molecular Medicine and Drug Research, International Center for Chemical and Biological Sciences, University of Karachi, Karachi, 75270, Pakistan., Jabeen A; Dr. Panjwani Center for Molecular Medicine and Drug Research, International Center for Chemical and Biological Sciences, University of Karachi, Karachi, 75270, Pakistan. almas@iccs.edu.
المصدر: Inflammopharmacology [Inflammopharmacology] 2023 Dec; Vol. 31 (6), pp. 3303-3316. Date of Electronic Publication: 2023 Nov 16.
نوع المنشور: Journal Article
اللغة: English
بيانات الدورية: Publisher: Birkhäuser Country of Publication: Switzerland NLM ID: 9112626 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1568-5608 (Electronic) Linking ISSN: 09254692 NLM ISO Abbreviation: Inflammopharmacology Subsets: MEDLINE
أسماء مطبوعة: Publication: Basel ; Boston : Birkhäuser
Original Publication: Dordrecht, The Netherlands ; Norwell, MA, USA : Kluwer Academic Publishers, c1991-
مواضيع طبية MeSH: Sulfadimethoxine*/adverse effects , Sulfadimethoxine*/metabolism , Respiratory Burst*, Animals ; Mice ; Zymosan/pharmacology ; Inflammation/chemically induced ; Inflammation/drug therapy ; Inflammation/metabolism ; Anti-Inflammatory Agents/therapeutic use ; Cytokines/metabolism ; NF-kappa B/metabolism ; Phagocytes/metabolism ; Disease Models, Animal ; Nitric Oxide/metabolism ; Lipopolysaccharides/pharmacology
مستخلص: Chronic inflammation and oxidative stress play a pivotal role in the pathophysiology of most challenging illnesses, including cancer, Alzheimer's, cardiovascular and autoimmune diseases. The present study aimed to investigate the anti-inflammatory potential of a new sulfadimethoxine derivative N-(4-(N-(2,6-dimethoxypyrimidin-4-yl) sulfamoyl) phenyl) dodecanamide (MHH-II-32). The compound was characterised by applying 1 H-, 13 C-NMR, EI-MS and HRFAB-MS spectroscopic techniques. The compound inhibited zymosan-induced oxidative bursts from whole blood phagocytes and isolated polymorphonuclear cells with an IC 50 value of (2.5 ± 0.4 and 3.4 ± 0.3 µg/mL), respectively. Furthermore, the inhibition of nitric oxide with an IC 50 (3.6 ± 2.2 µg/mL) from lipopolysaccharide-induced J774.2 macrophages indicates its in vitro anti-inflammatory efficacy. The compound did not show toxicity towards normal fibroblast cells. The observational findings, gross anatomical analysis of visceral organs and serological tests revealed the non-toxicity of the compound at the highest tested intraperitoneal (IP) dose of 100 mg/kg in acute toxicological studies in Balb/c mice. The compound treatment (100 mg/kg) (SC) significantly (P < 0.001) downregulated the mRNA expression of inflammatory markers TNF-α, IL-1β, IL-2, IL-13, and NF-κB, which were elevated in zymosan-induced generalised inflammation (IP) in Balb/c mice while upregulated the expression of anti-inflammatory cytokine IL-10, which was reduced in zymosan-treated mice. No suppressive effect was observed at the dose of 25 mg/kg. Ibuprofen was taken as a standard drug. The results revealed that the new acyl derivative of sulfadimethoxine has an immunomodulatory effect against generalised inflammatory response with non-toxicity both in vitro and in vivo, and has therapeutic potential for various chronic inflammatory illnesses.
(© 2023. The Author(s), under exclusive licence to Springer Nature Switzerland AG.)
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معلومات مُعتمدة: NRPU-8263 Higher Education Commision, Pakistan
فهرسة مساهمة: Keywords: Anti-inflammatory; Cytokines; Nitric oxide; Oxidative burst; Sulfadimethoxine; Zymosan
المشرفين على المادة: 9010-72-4 (Zymosan)
30CPC5LDEX (Sulfadimethoxine)
0 (Anti-Inflammatory Agents)
0 (Cytokines)
0 (NF-kappa B)
31C4KY9ESH (Nitric Oxide)
0 (Lipopolysaccharides)
تواريخ الأحداث: Date Created: 20231116 Date Completed: 20231204 Latest Revision: 20231204
رمز التحديث: 20240628
DOI: 10.1007/s10787-023-01372-0
PMID: 37971604
قاعدة البيانات: MEDLINE
الوصف
تدمد:1568-5608
DOI:10.1007/s10787-023-01372-0