HEPATOPROTECTIVE ACTIVITY OF CHRYSOPHYLLUM ALBIDUM AGAINST CARBON TETRACHLORIDE INDUCED HEPATIC DAMAGE IN RATS

The leaf extract of Chrysophyllum albidum was studied for hepatoprotective activity against rats with induced liver damage by carbon tetrachloride (CCl4). The rats were divided into five groups of eight rats per group. Animals of group A served as normal and were given only vehicle (distilled water) for 7 days. Animals of group B (positive control) were administered with vehicle on the first four days, and with the vehicle and CCl4 on the fifth, sixth and seventh day. The animals of groups C, D and E were respectively administered with 500, 1000 and 1500 mg/kg of extract & distilled water for the first four days, and with distilled water, extract and CCl4 on the last three days. Animals were subsequently anaesthetized and blood samples were collected for alanine amino transferase (ALT), aspartate amino transferase (AST), alkaline phosphatase (ALP), total bilirubin, total protein and albumin assays; liver organ was isolated and processed for histopathological studies. The results showed that the levels of AST, ALT, ALP and total bilirubin were significantly higher in rats treated with CCl4 indicating liver injury, while these parameters were reduced significantly (p < 0.05) after treatment of rats with the extract. The hepatoprotective activity of C. albidum was also supported by histopathological studies of liver tissue. The liver tissue of rats in the group treated with CCl4 showed marked centrilobular fatty degeneration and necrosis while the groups treated with plant extract showed signs of protection against this toxicant as evidenced by the absence of necrosis

Biochemical, haematological and histopathological studies of extract of Ageratum conyzoides L. in Sprague Dawley rats

This study was conducted to evaluate the safety potential of the leaf extract of Ageratum conyzoides Linnaeus in Sprague Dawley (SD) rats using biochemical, haematological and histological indices of toxicity. Four groups of seven male SD rats per group were used for the study. To group A was administered 0.25% CMC-Na/ kg body weight and was used as the control group, while groups B, C and D were respectively administered with 500, 1000 and 1500 mg/kg body weight of the ethanolic leaf extract of A. conyzoides by gastric intubation for 14 days. Animals were subsequently anaesthetized, blood samples were collected for biochemical and haematological assays; organs were isolated and weighed, while the liver, kidney and spleen were processed for histopathological studies. Aspartate amino transferase, lactate dehydrogenase, creatine kinase and alkaline phosphatase were significantly (p < 0.05) reduced in the groups treated with 1000 and 1500 mg/kg body weight of the extract. Furthermore, there was a significant (p < 0.05) elevation in white blood cell count, mean platelet volume and % platelet distribution width. Histopathological studies indicated various degrees of hepatocellular necrosis in all the treated groups accompanied by significant increases in the weight of liver and spleen. The results showed that the ethanolic leaf extract of A. conyzoides significantly alters the biomarkers of cardiac and skeletal muscle disorders, and higher doses could induce liver cell injury

Antioxidant activities of the leaves of Chrysophyllum Albidum G.

Chrysophyllum albidum G. is a tropical plant and commonly found in Nigeria. It belongs to the sapotaceae family and used in folklore in the treatment of yellow fever, malaria, diarrhea, vaginal and dermatological infections. The study was aimed at investigating the antioxidant properties of this plant by employing the in vitro and in vivo experimental models. The effect of DPPH free radical scavenging activity on the fractions of petroleum ether, ethanol, butanol, ethylacetate, and water of C. albidum was determined. The ethyl acetate fraction was purified in colunm chromatography to obtain myricetin rhamnoside. Structure elucidation was done by NMR and mass spectroscopic techniques. Furthermore, ethanol extract was administered to five groups of eight rats per group. The animals in the normal group were administered with vehicle alone for 7 days. The positive control animals were given vehicle on the first four days, and with the vehicle and hepatotoxin (CCl4) on the fifth, sixth and seventh day. The animals in the treatment category were respectively administered with 500, 1000 and 1500 mg/kg b.w. of extract &amp; distilled water for the first four days, and with distilled water, extract and CCl4 on the last three days. Animals were subsequently anaesthetized and blood samples were collected for catalase (CAT), malondialdehyde (MDA), reduced gluthathione (GSH) and superoxide dismutase (SOD) assays. The petroleum ether fraction showed the least antiradical activity (4057.5 ± 809.6 g/kg) while ethyl ether exhibited the highest activity (414.4 ± 92.0 g/kg). Myricetin rhamnoside also exhibited an excellent radical scavenging activity (314.1 ± 60.2) which was comparable to the positive control. Result from animal study showed that C. albidum exhibited significant (p &lt; 0.05) differences on the activity of CAT, MDA and GSH. The plant could therefore be employed as sources of natural antioxidant boosters and for the treatment of some oxidative stress disorders in which free radicals are implicated