Open Access DRIVERset
Vol 3 No 2 (2026): African Journal of Biochemistry and Molecular Biology Research

Phytochemical and Anti-Sickling Properties of Aqueous Extract of Pennisetum purpureum Schumach (Elephant Grass) Shoots

Onwubiko U. I. (Unknown)
Imo C. (Unknown)
Onwubiko G. N. (Unknown)
Boyi R.N (Unknown)
Dawoye Y. (Unknown)
Galadima A. O. (Unknown)
Sanusi A. (Unknown)
Solomon J. E. (Unknown)



Article Info

Publish Date
06 Jun 2026

Abstract

Sickle cell disease remains a major haematological disorder associated with haemoglobin S polymerization and erythrocyte sickling, highlighting the need to explore plant-derived compounds with potential anti-sickling activity. This study aimed to determine the anti-sickling potential of the aqueous extract of young shoots of Pennisetum purpureum using microscopy after 2% sodium metabisulphite-induced sickling of sickle red blood cells. The findings showed that Pennisetum purpureum extract significantly reversed many sickled cells to normal-shaped cells, with the percentage reversal depending on both concentration and exposure time. At 250 μg/mL, sickle cell reversal was 88.82% at 0 min, 86.09% at 30 min, and 85.19% at 60 min, whereas the control without extract showed no reversal. At 500 μg/mL, the reversal percentages were 80.14% at 0 min, 92.27% at 30 min, and 90.51% at 60 min. At 1000 μg/mL, reversal increased from 79.13% at 0 min to 94.82% at 30 min and 96.50% at 60 min. Phytochemical analysis indicated the presence of aromatic and alkylic compounds, including quercetin, epicatechin, resveratrol, vanillic acid, ellagic acid, and kaempferol. These compounds may contribute to anti-sickling activity through hydrophobic interactions that interfere with haemoglobin S polymerization and stabilize the hydrophobic erythrocyte lipid bilayer membrane. This study contributes to phytomedicine and sickle cell research by demonstrating the potential of Pennisetum purpureum young shoot extract as a source of bioactive compounds with anti-sickling properties, although further biochemical, toxicological, and clinical validation is required.

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