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1.
Biol Pharm Bull ; 35(11): 1907-13, 2012.
Article in English | MEDLINE | ID: mdl-23123463

ABSTRACT

Hyperlipidemia is a major contributor for atherosclerosis and hypolipidemic drugs such as statin are highly prescribed to treat elevated lipid level in plasma. Rubus coreanus, which is widely cultivated in south eastern Asia, have been reported to show significant cholesterol lowering action in hyperlipidemic subjects. Our objective was to determine the cellular effect of Rubus coreanus extract (RCE) on cholesterol biosynthesis in human hepatic cells (HepG2) and to elucidate the molecular mechanism by which it causes change in cholesterol metabolism. RCE treatment lowered cholesterol biosynthesis as well as secretion from HepG2 cells. This effect was associated with lowering the release of apolipoproteins from hepatic cells. RCE treatment also showed an increase in phosphorylation of foxhead box protein 01 (FoXo-1) and 5-adenosine monophosphate-activated protein kinase (AMPK), thus lowering expression of phosphoenolpyruvate carboxykinase (PEPCK) and G6Pase, which might be a major pathway for cholesterol biosynthesis inhibition. Apart from this; RCE also lowered sterol regulatory element-binding protein-1 (SREBP-1) expression in HepG2 cells, showing a long term regulation of cholesterol biosynthesis activity. These results indicate that one of the anti-hyperlipidemic actions of RCE is due to inhibition of cholesterol biosynthesis in hepatic cells and provides first documentation of a hypolipidemic bio-molecular action of Rubus coreanus.


Subject(s)
Cholesterol/metabolism , Fatty Acids/metabolism , Hypolipidemic Agents/pharmacology , Plant Extracts/pharmacology , Rosaceae , AMP-Activated Protein Kinases/metabolism , Apolipoprotein A-I/metabolism , Apolipoproteins B/metabolism , Forkhead Box Protein O1 , Forkhead Transcription Factors/metabolism , Glucose-6-Phosphatase/metabolism , Hep G2 Cells , Humans , Hypolipidemic Agents/analysis , Liver/cytology , Liver/metabolism , Plant Extracts/analysis , Protein Serine-Threonine Kinases/metabolism , Solvents/chemistry , Sterol Regulatory Element Binding Protein 1/metabolism , Water/chemistry
2.
J Agric Food Chem ; 50(13): 3765-7, 2002 Jun 19.
Article in English | MEDLINE | ID: mdl-12059157

ABSTRACT

Mosquito larvicidal activity of Piper longum fruit-derived materials against the fourth-instar larvae of Aedes aegypti was examined. A crude methanol extract of P. longum fruits was found to be active against the larvae, and the hexane fraction of the methanol extract showed a strong larvicidal activity of 100% mortality. The biologically active component of P. longum fruits was characterized as pipernonaline by spectroscopic analyses. The LC(50) value of pipernonaline was 0.25 mg/L. The toxicity of pipernonaline is comparable to that of pirimiphos-methyl as a mosquito larvicide. In tests with available components derived from P. longum, no activity was observed with piperettine, piperine, or piperlongumine.


Subject(s)
Aedes , Alkaloids/isolation & purification , Fruit/chemistry , Insecticides/isolation & purification , Piperaceae/chemistry , Piperidines , Plant Extracts/chemistry , Aedes/growth & development , Alkaloids/chemistry , Animals , Insecticides/chemistry , Larva , Methanol
3.
Am J Chin Med ; 40(5): 967-78, 2012.
Article in English | MEDLINE | ID: mdl-22928828

ABSTRACT

Oxidized low-density lipoprotein (oxLDL) contributes to atherosclerosis in part by being taken up into macrophages via scavenger receptors and leading to foam cell formation. Herbal compounds that have been used to treat blood stasis (a counterpart of atherosclerosis) for centuries include extracts of medicinal plants in the Rosaceae and Leguminosae families. In this study, we investigated the effect of the unripe Rubus coreanus (Korean black raspberry) fruit extract on oxLDL uptake by murine macrophage cells. In the presence of Rubus coreanus extract (RCE), Dil-labeled oxLDL uptake was inhibited in a dose-dependent manner. SP600125, a specific JNK inhibitor, inhibited the uptake of Dil-oxLDL into macrophages. RCE also inhibited JNK phosphorylation in a time- and dose-dependent manner in macrophages treated with oxLDL. These results indicate that among the mitogen-activated protein kinases, JNK phosphorylation is inhibited by RCE, which is likely the mechanism underlying the RCE-induced inhibition of oxLDL uptake by macrophages.


Subject(s)
Atherosclerosis/metabolism , JNK Mitogen-Activated Protein Kinases/metabolism , Lipoproteins, LDL/metabolism , Macrophages/drug effects , Plant Extracts/pharmacology , Rosaceae , Animals , Atherosclerosis/drug therapy , Dose-Response Relationship, Drug , Foam Cells/drug effects , Foam Cells/metabolism , Fruit , Macrophages/metabolism , Mice , Phosphorylation , Phytotherapy
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