Acute and Subacute Toxicity of Aspilia Africana Leaves

This study was designed to evaluate the toxicity of the aqueous extract of Aspilia africana leaves. Oral doses of 500 mg/kg and 1000 mg/kg were administered for 28 days to rats after every 2 days for sub-acute toxicity. For acute toxicity; 5 doses of 2; 4; 8; 12 and 16g/Kg body weight were investigated in mice. The control groups consisted of mice or rats administered with distilled water. The signs of toxicity fluctuated lightly from one mammal to another throughout the experiment. The liver; kidneys and heart weight of rats revealed no significant differences between the test groups and the control. The results indicated that the medium lethal dose (LD50) was found to be greater in females than males with an average of 6.6g/Kg body weight for both sexes. Regardless of the significant differences observed at certain points in some biochemical parameters (ALT; AST; ALP; Creatinine and Glutathione); none showed any linear dose responsiveness. On the other hand; most of the parameters investigated were found to be gender dependent. These results suggested that A Africana can be classified among substances with low toxicity

Acute and subacute toxicity of aspilia africana leaves

This study was designed to evaluate the toxicity of the aqueous extract of Aspilia africana leaves. Oral doses of 500 mg/kg and 1000 mg/kg were administered for 28 days to rats after every 2 days for sub-acute toxicity. For acute toxicity; 5 doses of 2; 4; 8; 12 and 16g/Kg body weight were investigated in mice. The control groups consisted of mice or rats administered with distilled water. The signs of toxicity fluctuated lightly from one mammal to another throughout the experiment. The liver; kidneys and heart weight of rats revealed no significant differences between the test groups and the control. The results indicated that the medium lethal dose (LD50) was found to be greater in females than males with an average of 6.6g/Kg body weight for both sexes. Regardless of the significant differences observed at certain points in some biochemical parameters (ALT; AST; ALP; Creatinine and Glutathione); none showed any linear dose responsiveness. On the other hand; most of the parameters investigated were found to be gender dependent. These results suggested that A Africana can be classified among substances with low toxicity

Evaluation of Antimicrobial Activity of the Stem Bark of Cylicodiscus Gabunensis (Mimosaceae)

Ethyl acetate (EA) extract of the stem bark of Cylicodiscus gabunensis (CG) was analysed phytochemically and evaluated for its antimicrobial activity against 17 pathogenic species isolated from patient: Escherichia coli; Klebsiella pneumoniae; Shigella dysenteriae; Shigella flexneri; Morganella morganii; Proteus vulgaris; Proteus mirabilis ; Salmonella typhi; Citrobacter freundii; Enterobacter cloacae; Enterobacter agglomerans; Staphylococcus aureus; Streptococcus feacalis; Pseudomonas aeruginosa; Bacillus cereus T; Candida albicans and Candida glabrata. Flavonoids; saponins; tannins; polyphenols; coumarins; triterpenes and/or sterols and reducing sugars were detected in the (EA) extract of CG. The best MIC and MBC values for the microorganisms sensitive to the extract were 0.00078 and 0.00315 mg/ml respectively. The greater and remarkable antimicrobial activity of the (EA) extract of CG was recorded with Staphylococcus aureus; Proteus vulgaris and Bacillus cereus T. These results provide a rationalization for the traditional use of this plant for the treatment of infections diseases

Acute and subacute toxicities of hydroethanolic extract of the ripe fruits of solatium torvum sw. (solanaceae).

Acute and subacute toxicity of the hydro-ethanolic extract of the ripe fruit of Solanum torvum Sw. was studied by force-feeding albino Wistar rats following the European Community and WHO toxicity guidelines. The results of the acute toxicity study indicated the median lethal dose (LD50; as I9g/kg body weight after 48 hours of treatment, and the significant variation (P < 0.05) of serum aspartate aminotransferase (AST), alanine aminotransferase (ALT), total proteins (TP), total bilirubin (TBil), and creatinine at doses of 16–20g/kg body weight. These results also indicated significant variation of the liver alkaline phosphatase (ALP), AST, ALT, TP, glutathione (GSH), and malondialdehyde (MDA) at higher doses. The results of the subacute toxicity study showed significant variation in the body weight, but no modification (P < 0.05) of blood and liver parameters compared to the control group. In both acute and subacute toxicity, histological studies revealed that there were no major pathological changes of the liver and kidneys in treated rats. The results show that this extract is not highly toxic, but consumption of higher doses beyond 16g/kg could cause liver injury. Moderate consumption of small doses up to Ig/kg twice a week for 6 weeks appeared safe.