TY - JOUR
T1 - RAesqeaurcheous extract of Piper sarmentosum decreases atherosclerotic lesions in high cholesterolemic experimental rabbits
AU - Amran, Adel A.
AU - Zakaria, Zaiton
AU - Othman, Faizah
AU - Das, Srijit
AU - Raj, Santhana
AU - Nordin, Nor Anita M.M.
N1 - Funding Information:
This work was supported by grant from the science fund grant from the Ministry of Science, Technology and Innovation. The authors wished to thank Uni-versiti Kebangsaan Malaysia for this study. The authors would also like to thanked Furley Marketing Sdn.Bhd. Malaysia for the plant extraction and Mrs Zanariyah for her technical assistance.
Publisher Copyright:
© 2010 Amran et al.
PY - 2010
Y1 - 2010
N2 - Background: Piper sarmentosum (P.s) has flavonoid component in its leaves which has antioxidative effect. To date, its effect on atherosclerosis has not been studied histologically. Aim: The study aimed to investigate the effect of P.s on atherosclerotic changes in hypercholesterolemic rabbits. Methods: Forty two male New Zealand white rabbits were divided into seven groups. C - control group fed normal rabbit chow, CH - cholesterol diet (1% cholesterol), W1 - 1% cholesterol with water extract of P.s (62.5 mg/kg), W2 - 1% cholesterol with water extract of P.s (125 mg/kg), W3 - 1% cholesterol with water extract of P.s (250 mg/kg), W4 - 1% cholesterol with water extract of P.s (500 mg/kg) and Smv - 1% cholesterol supplemented with simvistatin drug (1.2 mg/kg). All rabbits were treated for 10 weeks. Following 10 weeks of supplementation, the animals were sacrificed and the aortic tissue was taken for histological study. Results: Rabbits fed only with high cholesterol diet 1% cholesterol (CH) showed focal fatty streak lesions compared to the C group and 1% cholesterol supplemented with simvistatin drug (Smv) group. Atherosclerotic lesions in the 1% cholesterol group supplemented with P.s (500 mg/kg) i.e. W4 group showed significant reduction (30 ± 6.0%, p < 0.05) in fatty streak compared to the high cholesterol group (85.6 ± 4.1%) under Sudan IV stain. The atherosclerotic lesions under transmission electron microscope showed reduction in foam cells in the treatment groups compared to the CH groups. Conclusion: Administration of P.s extract has protective effect against atheroscleros.
AB - Background: Piper sarmentosum (P.s) has flavonoid component in its leaves which has antioxidative effect. To date, its effect on atherosclerosis has not been studied histologically. Aim: The study aimed to investigate the effect of P.s on atherosclerotic changes in hypercholesterolemic rabbits. Methods: Forty two male New Zealand white rabbits were divided into seven groups. C - control group fed normal rabbit chow, CH - cholesterol diet (1% cholesterol), W1 - 1% cholesterol with water extract of P.s (62.5 mg/kg), W2 - 1% cholesterol with water extract of P.s (125 mg/kg), W3 - 1% cholesterol with water extract of P.s (250 mg/kg), W4 - 1% cholesterol with water extract of P.s (500 mg/kg) and Smv - 1% cholesterol supplemented with simvistatin drug (1.2 mg/kg). All rabbits were treated for 10 weeks. Following 10 weeks of supplementation, the animals were sacrificed and the aortic tissue was taken for histological study. Results: Rabbits fed only with high cholesterol diet 1% cholesterol (CH) showed focal fatty streak lesions compared to the C group and 1% cholesterol supplemented with simvistatin drug (Smv) group. Atherosclerotic lesions in the 1% cholesterol group supplemented with P.s (500 mg/kg) i.e. W4 group showed significant reduction (30 ± 6.0%, p < 0.05) in fatty streak compared to the high cholesterol group (85.6 ± 4.1%) under Sudan IV stain. The atherosclerotic lesions under transmission electron microscope showed reduction in foam cells in the treatment groups compared to the CH groups. Conclusion: Administration of P.s extract has protective effect against atheroscleros.
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U2 - 10.1186/1476-511X-9-44
DO - 10.1186/1476-511X-9-44
M3 - Article
C2 - 20433693
AN - SCOPUS:77951611255
SN - 1476-511X
VL - 9
JO - Lipids in Health and Disease
JF - Lipids in Health and Disease
IS - 1
M1 - 44
ER -