Anti-Inflammatory and Anti-Diabetic Activity of Ferruginan, a Natural Compound from Olea ferruginea

Author:

Rauf Abdur1ORCID,Rashid Umer2,Shah Zafar Ali1,Rehman Gauhar3ORCID,Bashir Kashif4,Jamil Johar5,Iftikhar 1,Rahman Abdur3ORCID,Alsahammari Abdulrahman6ORCID,Alharbi Metab6,Al-Shahrani Abdulmajeed7,Ribaudo Giovanni8ORCID

Affiliation:

1. Department of Chemistry, University of Swabi, Swabi, Anbar 23430, Pakistan

2. Department of Chemistry, COMSATS University Islamabad, Abbottabad Campus, Islamabad 22060, Pakistan

3. Department of Zoology, Abdul Wali Khan University, Mardan 23200, Pakistan

4. Department of Health and Biological Sciences, Abasyn University, Peshawar 25000, Pakistan

5. Department of Microbiology, University of Swabi, Swabi, Anbar 23430, Pakistan

6. Department of Pharmacology and Toxicology, College of Pharmacy, King Saud University, P.O. Box 2455, Riyadh 11451, Saudi Arabia

7. Laboratory Department, Almadah General Hospital, Ministry of Health, Riyadh 10336, Saudi Arabia

8. Dipartimento di Medicina Molecolare e Traslazionale, Università Degli Studi di Brescia, Viale Europa 11, 25123 Brescia, Italy

Abstract

Inflammation is a complex response of the human organism and relates to the onset of various disorders including diabetes. The current research work aimed at investigating the anti-inflammatory and anti-diabetic effects of ferruginan, a compound isolated from Olea ferruginea. Its in vitro anti-inflammatory activity was determined by using the heat-induced hemolysis assay, while the anti-diabetic effect of the compound was studied by the yeast cell glucose uptake assay. Ferruginan exhibited a maximum of 71.82% inhibition of inflammation and also increased the uptake of glucose by yeast cells by up to 74.96% at the highest tested concentration (100 µM). Moreover, ferruginan inhibited α-amylase dose-dependently, by up to 75.45% at the same concentration. These results indicated that ferruginan possesses promising anti-inflammatory and anti-diabetic properties in vitro, even if at high concentrations. To provide preliminary hypotheses on the potentially multi-target mechanisms underlying such effects, docking analyses were performed on α-amylase and on various molecular targets involved in inflammation such as 5′-adenosine monophosphate-activated protein kinase (AMPK, PDB ID 3AQV), cyclooxygenase (COX-1, PDB ID 1EQG, and COX-2, 1CX2), and tumor necrosis factor alpha (TNF-α, PDB ID 2AZ5). The docking studies suggested that the compound may act on α-amylase, COX-2, and AMPK.

Funder

Researchers Supporting Project

King Saud University, Riyadh, Saudi Arabia

Publisher

MDPI AG

Subject

Process Chemistry and Technology,Chemical Engineering (miscellaneous),Bioengineering

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