Hypoglycemic, anti‐inflammatory, and neuroprotective potentials of crude methanolic extract from Acacia nilotica L. – results of an in vitro study

Author:

Rauf Abdur1,Ibrahim Muhammad1,Alomar Taghrid S.2,AlMasoud Najla2,Khalil Anees Ahmed3ORCID,Khan Muneeb4,Khalid Ahood3,Jan Muhammad Saeed5,Formanowicz Dorota6,Quradha Mohammed Mansour78ORCID

Affiliation:

1. Department of Chemistry University of Swabi Swabi, Anbar Khyber Pakhtunkhwa Pakistan

2. Department of Chemistry, College of Science Princess Nourah bint Abdulrahman University Riyadh Saudi Arabia

3. University Institute of Diet and Nutritional Sciences, Faculty of Allied Health Sciences The University of Lahore Lahore Pakistan

4. Department of Human Nutrition and Dietetics, Riphah College of Rehabilitation and Allied Health Sciences Riphah International University Lahore Pakistan

5. Department of Pharmacy Bacha Khan University Charsadda Khyber Pakhtunkhwa Pakistan

6. Chair and Department of Medical Chemistry and Laboratory Medicine Poznan University of Medical Sciences Poznan Poland

7. College of Education Seiyun University Seiyun Hadhramawt Yemen

8. Pharmacy Department, Medical Sciences Aljanad University for Science and Technology Taiz Yemen

Abstract

AbstractAcacia nilotica L., also known as babul, belonging to the Fabaceae family and the Acacia genus, is typically used for ornamental purposes and also as a medicinal plant found in tropical and subtropical areas. This plant is a rich source of bioactive compounds. The current study aimed to elucidate the hypoglycemic, anti‐inflammatory, and neuroprotective potential of A. nilotica's crude methanolic extract. The results of the in vitro antidiabetic assay revealed that methanolic extract of A. nilotica inhibited the enzyme α‐glucosidase (IC50: 33 μg mL−1) and α‐amylase (IC50: 17 μg mL−1) in a dose‐dependent manner. While in the anticholinesterase enzyme inhibitory assay, maximum inhibition was shown by the extract against acetylcholinesterase (AChE) (637.01 μg mL−1) and butyrylcholinesterase (BChE) (491.98 μg mL−1), with the highest percent inhibition of 67.54% and 71.50% at 1000 μg mL−1, respectively. This inhibitory potential was lower as compared to the standard drug Galantamine that exhibited 82.43 and 89.50% inhibition at the same concentration, respectively. Moreover, the methanolic extract of A. nilotica also significantly inhibited the activities of cyclooxygenase 2 (COX‐2) and 5‐lipoxygenase (5‐LOX) in a concentration‐dependent manner. The percent inhibitory activity of 5‐LOX and COX‐2 ranged from 42.47% to 71.53% and 43.48% to 75.22%, respectively. Furthermore, in silico, in vivo, and clinical investigations must be planned to validate the above‐stated bioactivities of A. nilotica.

Publisher

Wiley

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