Abstract:
The investigation was carried out for isolation and characterization of the possible phytochemical compounds of leaves of
Hyophorbe verschaffeltii and determination of its antioxidant activity. The air dried leaves of
Hyophorbe verschaffeltii were extracted with 70% methanol. The chromatographic investigation for aqueous fraction lead to isolation of five compounds by Column chromatography, thin layer chromatography (TLC), Preparative thin layer chromatography (PTLC) and paper chromatography. The isolated compounds were identified by spectroscopic techniques as
1H-NMR and
13C-NMR. The 70% methanolicrnextract was assayed for its antioxidant activity in
vivo by CCl
4-induced hepatic injury technique and levels of serum liver enzymes Alanine aminotransferase (ALT) and Aspartate aminotransferase (AST) were determined, also Oxidative Damage Markers as superoxide dismutase (SOD) and malondialdehyde (MDA) in liver tissue were studied.
Hyophorbe verschaffeltii (Arecaceae) afforded aqueous fraction from which five compounds Quercetin (compound H-1), Quercetin 7, 3', 4' trimethoxy (compound H-4), Luteolin (compound H-5), Cannigenin (compound H-2) and Brisbagenin (compound H-3) were identified for the first time. The
H. verschaffeltii extract (200mg/kg) showed a remarkable hepatoprotective and antioxidant activity against CCl
4-induced hepatotoxicity as judged from the serum marker enzymes and antioxidant levels in liver tissues.CCl
4-induced a significant rise in ALT, AST, MDA and reduction in SOD level. Treatment of rats with
H. verschaffeltii extract (200mg/kg) significantly (
P<0.001) decrease serum liverrnenzymes ALT and AST against CCl
4-treated rats. Also the
H. verschaffeltii extract showed significant (
P<0.001) elevation of SOD level by 124.7 % as compared to control group and the CCl
4 intoxicated group treated with
H.verschaffeltii showed significant and efficient decline in the level of MDA (
P<0.001) compared to CCl
4 group by 40.25%.
Hyophorbe verschaffeltii have the free radicle scavenging activity that controls the CC
4-induced oxidative stress in liver tissue and capable of boosting the intracellular antioxidant capabilities.