2-((3-(chloromethyl) benzoyl) oxy) benzoic acid suppresses NF-κB expression in the kidneys and lungs of LPS-Induced BALB/C mice

Kuncoro, Foe, Philipus, Karel, Martha, Ervina, Yudy, Tjahjono, Hendy, Wijaya, Novita, Bernadette Dian, Wiyanto, Putri, Claritta Angelina, Regis, Partana, Fransiskus, Michelle, Angelina, Sianty, Dewi, Yesery, Esar, Senny, Wuryanto, Hadinugroho, Hevi, Wihadmadyatami and Caroline, Caroline (2025) 2-((3-(chloromethyl) benzoyl) oxy) benzoic acid suppresses NF-κB expression in the kidneys and lungs of LPS-Induced BALB/C mice. Journal of Advanced Pharmaceutical Technology and Research, 16 (3). pp. 163-168. ISSN pISSN: 22314040, eISSN: 09762094

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Abstract

Sepsis, a life‑threatening systemic inflammatory condition, is a leading cause of mortality worldwide. Its pathophysiology involves the activation of nuclear factor kappa beta (NF‑κB), which promotes the release of proinflammatory cytokines. Acetylsalicylic acid (ASA), a widely used nonsteroidal anti‑inflammatory drug, inhibits NF‑κB but poses risks of peptic ulcer disease and nephrotoxicity. This study evaluates the efficacy of 2‑((3‑(chloromethyl)benzoyl)oxy)benzoic acid (3‑CH Cl), a novel salicylate derivative, in reducing NF‑κB expression in the kidneys and lungs of lipopolysaccharide (LPS)‑induced septic BALB/C mice. Mice were divided into four groups: untreated, LPS only, LPS + ASA (60 mg/kg BW), and LPS + 3‑CH © 2025 Journal of Advanced Pharmaceutical Technology & Research | Published by Wolters Kluwer-Medknow 22 Cl (60 mg/kg BW). NF‑κB expression was assessed via immunohistochemistry. LPS significantly increased NF‑κB expression in both renal and pulmonary tissues compared to controls (P < 0.0001). While ASA treatment reduced NF‑κB levels (P < 0.0001), 3‑CH Cl demonstrated superior suppression in the renal cortex, renal medulla, and alveolar regions (P < 0.05). In addition, 3‑CH 22 Cl alleviated hypothermia in septic mice, comparable to ASA. Given its enhanced anti‑inflammatory efficacy and reduced gastrointestinal risk, 3‑CH Cl presents a promising alternative to ASA for sepsis‑related inflammation management. Further studies are warranted to explore its clinical applications.

Item Type: Article
Uncontrolled Keywords: 3‑CH Cl, acetylsalicylic acid, immunohistochemistry, inflammation, lipopolysaccharide, NF‑κB
Subjects: Pharmacy
Divisions: Journal Publication
Depositing User: F.X. Hadi
Date Deposited: 01 Oct 2025 04:29
Last Modified: 01 Oct 2025 04:29
URI: https://repositori.ukwms.ac.id/id/eprint/44555

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