Selective mPGES-1 Inhibitor Ameliorated Adjuvant-Induced Arthritis in the Rat Model
Open Access
- 13 February 2024
- journal article
- research article
- Published by Wiley in Journal of Chemistry
- Vol. 2024, 1-8
Abstract
Endogenous prostaglandin E2 (PGE2) plays an important role in maintaining the homeostasis conditions. However, the overexpression of PGE2 in response to various inflammatory stimulations is an important target of anti-inflammatory drugs. Both inducible COX-2 (cyclooxygenase-2) and mPGES-1 (microsomal prostaglandin E2 synthase-1) enzymes are responsible for the inflammatory overexpressed PGE2 production. Among them, mPGES-1 is regarded as a more promising ideal target for anti-inflammatory drugs without the gastrointestinal and cardiovascular side effects. As our continuous research for the discovery of novel mPGES-1 inhibitors, we have characterized MPO-0144 as a selective mPGES-1 inhibitor with a selectivity index of >270 over COX-1 and >25 over COX-2, respectively. Herein, we evaluated the anti-inflammatory effect of MPO-0144 in an adjuvant-induced arthritis rat model. MPO-0144 attenuated the inflammatory responses without severe gastrointestinal side effects and organ toxicities. These overall data suggest a possibility that MPO-0144 downregulates PGE2 production by potent mPGES-1 and weak COX-2 inhibitory activities, thus attenuating the paw swelling in AIA (adjuvant-induced arthritis) rat models. MPO-0144 also exhibited favorable ADMET profiles. However, MPO-0144 did not show any inhibitory effects on human mPGES-1 enzyme at a high concentration. Therefore, MPO-0144 represents a valuable pharmacological tool for the study of regulation of inducible mPGES-1 in an inflammatory arthritis rat model.Keywords
Funding Information
- Ministry of Science, ICT and Future Planning (2022R1F1A1068898, 2020R1A5A2019413, RS-2021-DD120983)
- Korea Drug Development Fund (2022R1F1A1068898, 2020R1A5A2019413, RS-2021-DD120983)
- Ministry of Science and ICT, South Korea (2022R1F1A1068898, 2020R1A5A2019413, RS-2021-DD120983)
- Ministry of Trade, Industry and Energy (2022R1F1A1068898, 2020R1A5A2019413, RS-2021-DD120983)
- Ministry of Health and Welfare (2022R1F1A1068898, 2020R1A5A2019413, RS-2021-DD120983)
This publication has 33 references indexed in Scilit:
- Non-steroidal anti-inflammatory drugs (NSAIDs): A current insight into its molecular mechanism eliciting organ toxicitiesFood and Chemical Toxicology, 2023
- In vitro and in vivo neuroprotective effect of novel mPGES-1 inhibitor in animal model of Parkinson’s diseaseBioorganic & Medicinal Chemistry Letters, 2022
- Microsomal prostaglandin E2 synthase-1 and its inhibitors: Molecular mechanisms and therapeutic significancePharmacological Research, 2022
- Discovery of N-amido-phenylsulfonamide derivatives as novel microsomal prostaglandin E2 synthase-1 (mPGES-1) inhibitorsBioorganic & Medicinal Chemistry Letters, 2021
- A Multi‐step Virtual Screening Protocol for the Identification of Novel Non‐acidic Microsomal Prostaglandin E2 Synthase‐1 (mPGES‐1) InhibitorsChemMedChem, 2018
- GRC 27864, novel, microsomal prostaglandin E synthase-1 enzyme inhibitor: phase 1 study to evaluate safety, PK and biomarkers in healthy, adult subjectsOsteoarthritis and Cartilage, 2018
- Highly predictive and interpretable models for PAMPA permeabilityBioorganic & Medicinal Chemistry, 2017
- Rational design, synthesis and evaluation of chromone-indole and chromone-pyrazole based conjugates: Identification of a lead for anti-inflammatory drugEuropean Journal of Medicinal Chemistry, 2014
- Is there any association between imidapril hydrochloride stability profile under dry air conditions and cancer initiation?International Journal of Pharmaceutics, 2013
- Adverse Cardiovascular Effects of the CoxibsChemInform, 2005