TY - JOUR
T1 - In-vitro scavenging activity and acute toxicity study of methanol leaves extract and fractions of Lophira lanceolata Tiegh. Ex Keay(Ochnaceae) in rats
AU - Oussou, Jean Baptiste N.
AU - Asiedu-Gyekye, Isaac J.
AU - Yapo, Adou F.
AU - N’Guessan, Benoit B.
AU - Amoateng, Patrick
AU - Kouakou, Leandre K.
AU - Asante, Isaac K.
AU - Ehile, Etienne E.
N1 - Publisher Copyright:
© 2016, Advanced Research Journals. All rights reserved.
PY - 2016
Y1 - 2016
N2 - Petroleum ether, dichloromethane, ethyl acetate, butanol and water fractions were prepared from the methanol extract of the plant. The scavenging activity of DPPH (2,2-Diphenyl-1-picrylhydrazyl), the total phenolic (TPC) and total flavonoid (TFC)contents of the extract and fractions were determined by spectrophotometrical methods using gallic acid (GA) and quercetin (Qu) as reference antioxidant. The fifty percent inhibitory concentration (IC50),fifty percent effective concentration (EC50) and the antiradical power (ARP) were determined for all extract and fractions. An acute toxicity study using a single oral dose of 5000 mg/kg of the ethyl acetate fraction of the plant was conducted in female Albino rats following the OECD(420) Guidelines. Blood samples were collected for hematological and biochemical analysis. Histopathological examinations of the heart, kidney and liver were performed. The results showed that the ethylacetate fraction of L lanceolata had the highest free radical scavenging activity of DPPH (IC50=1,43;EC50= 0.07 and ARP= 14,28)and also contain the highest amount of total phenols (14,4±0,02mg of GA equivalent/g of plant fraction) and total flavonoids (93,3±0,04mg of Qu equivalent/g of plant fraction)as compared to other fractions and ascorbic acid (IC50=5,82;EC50= 3.44; ARP=3,44). The hematological parameters and the lipid profile didn’t show any major change compared to the control group. However, a significant increase of aspartate aminotransferase (AST, p<0.001) and alanine aminotransferase (ALT, p<0.001) showed that the ethyl acetate fraction of the methanol extract of L. lanceolata leaves might not totally be safe for consumption, in the conditions of our experiment.
AB - Petroleum ether, dichloromethane, ethyl acetate, butanol and water fractions were prepared from the methanol extract of the plant. The scavenging activity of DPPH (2,2-Diphenyl-1-picrylhydrazyl), the total phenolic (TPC) and total flavonoid (TFC)contents of the extract and fractions were determined by spectrophotometrical methods using gallic acid (GA) and quercetin (Qu) as reference antioxidant. The fifty percent inhibitory concentration (IC50),fifty percent effective concentration (EC50) and the antiradical power (ARP) were determined for all extract and fractions. An acute toxicity study using a single oral dose of 5000 mg/kg of the ethyl acetate fraction of the plant was conducted in female Albino rats following the OECD(420) Guidelines. Blood samples were collected for hematological and biochemical analysis. Histopathological examinations of the heart, kidney and liver were performed. The results showed that the ethylacetate fraction of L lanceolata had the highest free radical scavenging activity of DPPH (IC50=1,43;EC50= 0.07 and ARP= 14,28)and also contain the highest amount of total phenols (14,4±0,02mg of GA equivalent/g of plant fraction) and total flavonoids (93,3±0,04mg of Qu equivalent/g of plant fraction)as compared to other fractions and ascorbic acid (IC50=5,82;EC50= 3.44; ARP=3,44). The hematological parameters and the lipid profile didn’t show any major change compared to the control group. However, a significant increase of aspartate aminotransferase (AST, p<0.001) and alanine aminotransferase (ALT, p<0.001) showed that the ethyl acetate fraction of the methanol extract of L. lanceolata leaves might not totally be safe for consumption, in the conditions of our experiment.
KW - Acute toxicity
KW - Antioxidant activity
KW - Biochemistry
KW - Hematology
KW - Histopathology
KW - Lophira lanceolata
UR - http://www.scopus.com/inward/record.url?scp=85019523983&partnerID=8YFLogxK
U2 - 10.5138/09750185.1855
DO - 10.5138/09750185.1855
M3 - Article
AN - SCOPUS:85019523983
SN - 0975-0185
VL - 8
SP - 411
EP - 421
JO - International Journal of Phytomedicine
JF - International Journal of Phytomedicine
IS - 3
ER -