The molecular mechanisms underlying anti‐inflammatory effects of galangin in different diseases

Author:

Hassanein Emad H. M.1ORCID,Abd El‐Maksoud Mostafa S.2,Ibrahim Islam M.2,Abd‐alhameed Esraa K.3,Althagafy Hanan S.4,Mohamed Nesma M.56,Ross Samir A.78ORCID

Affiliation:

1. Department of Pharmacology and Toxicology, Faculty of Pharmacy Al‐Azhar University Asyut Egypt

2. Faculty of Pharmacy Al‐Azhar University Asyut Egypt

3. Department of Pharmacology and Toxicology, Faculty of Pharmacy Beni‐Suef University Beni Suef Egypt

4. Department of Biochemistry, Faculty of Science University of Jeddah Jeddah Saudi Arabia

5. Department of Pharmacognosy, Faculty of Pharmacy Assiut University Asyut Egypt

6. Department of Pharmacognosy, Faculty of Pharmacy Badr University in Assiut Asyut Egypt

7. National Center for Natural Products Research, Research Institute of Pharmaceutical Sciences, School of Pharmacy The University of Mississippi University Mississippi USA

8. Department of BioMolecular Sciences, Division of Pharmacognosy, School of Pharmacy University of Mississippi University Mississippi USA

Abstract

AbstractWhen used as an alternative source of drugs to treat inflammation‐associated diseases, phytochemicals with anti‐inflammatory properties provide beneficial impacts. Galangin is one of the most naturally occurring flavonoids. Galangin has many biological activities, such as anti‐inflammatory, antioxidant, antiproliferative, antimicrobial, anti‐obesity, antidiabetic, and anti‐genotoxic activities. We observed that galangin was well tolerated and positively impacted disease underlying inflammation for the renal, hepatic, central nervous system, cardiovascular, gastrointestinal system, skin, and respiratory disorders, as well as ulcerative colitis, acute pancreatitis, retinopathy, osteoarthritis, osteoporosis, and rheumatoid arthritis. Galangin anti‐inflammatory effects are mediated mainly by suppressing p38 mitogen‐activated protein kinases, nuclear factor‐kappa B, and nod‐like receptor protein 3 signals. These effects are confirmed and supported by molecular docking. Clinical translational research is required to accelerate the bench‐to‐bedside transfer and determine whether galangin can be utilised as a safe, natural source of pharmaceutical anti‐inflammatory medication for humans.

Publisher

Wiley

Subject

Pharmacology

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