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Research Article

Antihyperlipidemic activity of Ichnocarpus frutescens in triton WR-1339-induced and high-fat diet animals

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Pages 1074-1081 | Received 30 Oct 2010, Accepted 20 Feb 2011, Published online: 18 May 2011

Figures & data

Chart 1.  Schematic representation of bioassay-guided fractionation of methanol extract of Ichnocarpus frutescens.

Chart 1.  Schematic representation of bioassay-guided fractionation of methanol extract of Ichnocarpus frutescens.

Figure 1.  Effect of Ichnocarpus frutescens methanol extract and fenofibrate on plasma lipid levels in triton induced hyperlipidemic rats. Values are mean ± SEM of six rats *p ≤ 0.01, **p ≤ 0.001. Normal control (Group 1), hyperlipidemic control (Group 2), hyperlipidemic + fenofibrate 65 mg/kg treated (Group 3), hyperlipidemic + methanol extract 100 mg/kg treated (Group 4), hyperlipidemic + methanol extract 200 mg/kg treated (Group 5), and hyperlipidemic + methanol extract 400 mg/kg treated (Group 6).

Figure 1.  Effect of Ichnocarpus frutescens methanol extract and fenofibrate on plasma lipid levels in triton induced hyperlipidemic rats. Values are mean ± SEM of six rats *p ≤ 0.01, **p ≤ 0.001. Normal control (Group 1), hyperlipidemic control (Group 2), hyperlipidemic + fenofibrate 65 mg/kg treated (Group 3), hyperlipidemic + methanol extract 100 mg/kg treated (Group 4), hyperlipidemic + methanol extract 200 mg/kg treated (Group 5), and hyperlipidemic + methanol extract 400 mg/kg treated (Group 6).

Table 1.  Effect of the methanol extract of I. frutescens on plasma lipid levels of high-fat diet induced hyperlipidemic rats.

Figure 2.  Effect of hot water soluble and hot water insoluble parts of methanol extract and fenofibrate on plasma lipid levels in triton-induced hyperlipidemic rats. Values are mean ± SEM of six rats **p ≤ 0.001. Normal control (Group 1), hyperlipidemic control (Group 2), hyperlipidemic + fenofibrate 200 mg/kg treated (Group 3), hyperlipidemic + hot water soluble part 200 mg/kg treated (Group 4), hyperlipidemic + hot water insoluble part 200 mg/kg treated (Group 5).

Figure 2.  Effect of hot water soluble and hot water insoluble parts of methanol extract and fenofibrate on plasma lipid levels in triton-induced hyperlipidemic rats. Values are mean ± SEM of six rats **p ≤ 0.001. Normal control (Group 1), hyperlipidemic control (Group 2), hyperlipidemic + fenofibrate 200 mg/kg treated (Group 3), hyperlipidemic + hot water soluble part 200 mg/kg treated (Group 4), hyperlipidemic + hot water insoluble part 200 mg/kg treated (Group 5).

Figure 3.  Effect of fractions of Ichnocarpus frutescens and fenofibrate on plasma lipid levels in triton induced hyperlipidemic rats. Values are mean ± SEM of six rats *p ≤ 0.01, **p ≤ 0.001. Normal control (Group 1), hyperlipidemic control (Group 2), hyperlipidemic + fenofibrate 200 mg/kg treated (Group 3), hyperlipidemic + hexane fraction 200 mg/kg treated (Group 4), hyperlipidemic + benzene fraction 200 mg/kg treated (Group 5), and hyperlipidemic + ethyl acetate fraction 200 mg/kg treated (Group 6), hyperlipidemic + acetone fraction 200 mg/kg treated (Group 7), hyperlipidemic + methanol fraction 200 mg/kg treated (Group 8).

Figure 3.  Effect of fractions of Ichnocarpus frutescens and fenofibrate on plasma lipid levels in triton induced hyperlipidemic rats. Values are mean ± SEM of six rats *p ≤ 0.01, **p ≤ 0.001. Normal control (Group 1), hyperlipidemic control (Group 2), hyperlipidemic + fenofibrate 200 mg/kg treated (Group 3), hyperlipidemic + hexane fraction 200 mg/kg treated (Group 4), hyperlipidemic + benzene fraction 200 mg/kg treated (Group 5), and hyperlipidemic + ethyl acetate fraction 200 mg/kg treated (Group 6), hyperlipidemic + acetone fraction 200 mg/kg treated (Group 7), hyperlipidemic + methanol fraction 200 mg/kg treated (Group 8).

Table 2.  Effect of the methanol extract of I. frutescens on the activities of biochemical parameters in high-fat diet induced hyperlipidemic rats.

Table 3.  Effect of I. frutescens fractions on plasma lipid levels in triton WR-1339-induced hyperlipidemic mice.

Table 4.  Effect of fraction 3 of Ichnocarpus frutescens and orlistat on fat excretion in feces of mice fed with high-fat diet.

Figure 4.  Effect of fraction 3 and orlistat on rat plasma Tg levels after oral administration of lipid emulsion. Values are mean ± SEM of six rats. *p ≤ 0.05 values deviate significantly from the high-fat diet control.

Figure 4.  Effect of fraction 3 and orlistat on rat plasma Tg levels after oral administration of lipid emulsion. Values are mean ± SEM of six rats. *p ≤ 0.05 values deviate significantly from the high-fat diet control.

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