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1.
Article in English | MEDLINE | ID: mdl-22567032

ABSTRACT

This study investigated the antidepressant activity of ethanolic extract of U. lanosa Wallich var. appendiculata Ridsd (UL(EtOH)) for two-weeks administrations by using FST and TST on mice. In order to understand the probable mechanism of antidepressant-like activity of UL(EtOH) in FST and TST, the researchers measured the levels of monoamines and monoamine oxidase activities in mice brain, and combined the antidepressant drugs (fluoxetine, imipramine, maprotiline, clorgyline, bupropion and ketanserin). Lastly, the researchers analyzed the content of RHY in the UL(EtOH). The results showed that UL(EtOH) exhibited antidepressant-like activity in FST and TST in mice. UL(EtOH) increased the levels of 5-HT and 5-HIAA in cortex, striatum, hippocampus, and hypothalamus, the levels of NE and MHPG in cortex and hippocampus, the level of NE in striatum, and the level of DOPAC in striatum. Two-week injection of IMI, CLO, FLU and KET enhanced the antidepressant-like activity of UL(EtOH). UL(EtOH) inhibited the activity of MAO-A. The amount of RHY in UL(EtOH) was 17.12 mg/g extract. Our findings support the view that UL(EtOH) exerts antidepressant-like activity. The antidepressant-like mechanism of UL(EtOH) may be related to the increase in monoamines levels in the hippocampus, cortex, striatum, and hypothalamus of mice.

2.
J Ethnopharmacol ; 139(2): 558-65, 2012 Jan 31.
Article in English | MEDLINE | ID: mdl-22155390

ABSTRACT

ETHNOPHARMACOLOGICAL RELEVANCE: [corrected] In Taiwanese folk medicine, Davallia formosana is used to treat bone diseases, including osteoporosis. AIM: This study evaluated the anti-osteoporotic effect of ethanolic extract derived from Davallia formosana (DFE). MATERIALS AND METHODS: In this in vitro study, we investigated the inhibitory action of DFE on RANKL-stimulated osteoclastogenesis. The in vivo effects of DFE on bone metabolism were evaluated using ovariectomized (OVX) rats orally administered DFE (200, 500 mg/kg), alendronate (2.5 mg/kg, three times a week) or its vehicle for 12 weeks. RESULTS: This in vitro study demonstrated that DFE inhibited osteoclast differentiation, and also isolated the active component, (-)-epicatechin 3-O-ß-D-allopyranoside (ECAP). DFE did not affect the body or vaginal weight in OVX rats. The bone mineral density and bone calcium content in OVX rats were lower in the control group showing that DFE was able to prevent significant bone loss. In addition, the three point bending test and the microcomputer tomography scanning showed that DFE treatment enhanced bone strength and inhibited the deterioration of trabecular microarchitecture. In the biochemical assay, DFE decreased urinary deoxypyridinoline and calcium concentrations, but did not inhibit serum alkaline phosphatase activities, indicating that it ameliorated bone loss via inhibition of bone reabsorption. CONCLUSIONS: These results suggest that DFE may represent a useful remedy for the treatment of bone reabsorption diseases such as osteoporosis. In addition, ECAP could be used as a marker compound to control the quality of DFE.


Subject(s)
Bone Density Conservation Agents/pharmacology , Bone Remodeling/drug effects , Femur/drug effects , Osteoclasts/drug effects , Osteoporosis/prevention & control , Plant Extracts/pharmacology , Polypodiaceae , Alendronate/pharmacology , Alkaline Phosphatase/blood , Amino Acids/urine , Animals , Biomechanical Phenomena , Bone Density/drug effects , Bone Density Conservation Agents/chemistry , Bone Density Conservation Agents/isolation & purification , Calcium/urine , Catechin/pharmacology , Cell Differentiation/drug effects , Cell Line , Disease Models, Animal , Dose-Response Relationship, Drug , Female , Femur/diagnostic imaging , Femur/metabolism , Femur/pathology , Mice , Osteoclasts/metabolism , Osteoclasts/pathology , Osteoporosis/diagnostic imaging , Osteoporosis/etiology , Osteoporosis/metabolism , Osteoporosis/pathology , Ovariectomy , Plant Extracts/chemistry , Plant Extracts/isolation & purification , Plants, Medicinal , Polypodiaceae/chemistry , RANK Ligand/metabolism , Rats , Rats, Wistar , Rhizome , Solvents/chemistry , Time Factors , X-Ray Microtomography
3.
Am J Chin Med ; 38(3): 625-38, 2010.
Article in English | MEDLINE | ID: mdl-20503477

ABSTRACT

I-Tiao-Gung has long been used in the Kinmen area of Taiwan as an anti-inflammatory agent for the treatment of rheumatic illness. The roots of Flemingia lineata (FL), Flemingia macrophylla (FM) and Flemingia prostrata (FP) are also used as I-Tiao-Gung in the Taiwan markets. In the present study, we investigated the analgesic effect of aqueous extracts of Flemingia lineata (FL), Flemingia macrophylla (FM), and Flemingia prostrata (FP) by acetic acid-induced writhing response, formalin test, and the anti-inflammatory effect of FM, FL and FP by lambda-carrageenan-induced paw edema in mice. We also detected the changes in the activities of superoxide dismutase (SOD), glutathione reductase (GRx) and glutathione peroxidase (GPx) of liver in the lambda-carrageenan-induced paw edema in mice to investigate the anti-inflammatory mechanism of FL and FM. The results showed that FL and FM significantly inhibited the acetic acid-induced writhing response and formalin-induced licking time during the late phase (p < 0.001). FL and FM also significantly decreased the lambda-carrageenan-induced paw edema (p < 0.001). FL and FM significantly increased the GRx and GPx activities in the liver and decreased the levels of malondialdehyde (MDA) and nitric oxide (NO) in the edema paw (p < 0.001). These results indicated that FL and FM possessed analgesic and anti-inflammatory effects. The anti-inflammatory mechanism of FL and FM might be related to the decrease in the level of MDA in the edema paw via increasing the activities of GPx and GRx in the liver and decreasing the NO level in the edema paw.


Subject(s)
Analgesics/pharmacology , Anti-Inflammatory Agents/pharmacology , Fabaceae/chemistry , Plant Extracts/pharmacology , Animals , Carrageenan , Dose-Response Relationship, Drug , Edema/chemically induced , Edema/prevention & control , Fabaceae/classification , Glutathione Peroxidase/metabolism , Glutathione Reductase/metabolism , Hindlimb/drug effects , Hindlimb/metabolism , Hindlimb/pathology , Liver/drug effects , Liver/enzymology , Male , Malondialdehyde/metabolism , Mice , Mice, Inbred ICR , Nitric Oxide/metabolism , Pain Measurement , Phytotherapy , Plant Extracts/chemistry , Plant Roots/chemistry , Species Specificity , Superoxide Dismutase/metabolism , Treatment Outcome , Water/chemistry
4.
Am J Chin Med ; 32(1): 57-63, 2004.
Article in English | MEDLINE | ID: mdl-15154285

ABSTRACT

The influence of the aqueous crude extract of Glycine tomentella root (Leguminosae) on lipid metabolism was investigated in hyperlipidemic hamsters. It was found that the administration of the G. tomentella extract (GTE) leads to a decrease of high serum cholesterol and triglyceride levels induced by high-fat diet. The GTE also increased serum high-density lipoprotein (HDL) cholesterol and decreased serum low-density lipoprotein (LDL) cholesterol. The reduction of serum triglyceride levels was accompanied by a significant decrease in the hepatic triglyceride content, while the cholesterol content was not changed. The results indicate that GTE is definitely an anti-hyperlipidemic agent, at least, in animals.


Subject(s)
Fabaceae , Hyperlipidemias/prevention & control , Hypolipidemic Agents/pharmacology , Phytotherapy , Plant Extracts/pharmacology , Animals , Cholesterol/blood , Cholesterol, HDL/blood , Cholesterol, LDL/blood , Cricetinae , Dietary Fats , Hypolipidemic Agents/administration & dosage , Hypolipidemic Agents/therapeutic use , Male , Mesocricetus , Plant Extracts/administration & dosage , Plant Extracts/therapeutic use , Plant Roots , Triglycerides/blood
5.
Am J Chin Med ; 30(2-3): 235-43, 2002.
Article in English | MEDLINE | ID: mdl-12230012

ABSTRACT

The effect of oral administration of a 50% ethanol extract of Silene aprica (SA) on acute liver injury was examined in rats intoxicated with carbon tetrachloride (CCl4) and acetaminophen. The results indicated that SA protected the liver from CCl4- and acetaminophen-induced injury as judged by morphological and biochemical observations. An increase in both lipid peroxidation (LPO) and triglyceride concentrations occurred in the liver with CCl4 injection, SA administration significantly reduced these changes.


Subject(s)
Antioxidants/therapeutic use , Chemical and Drug Induced Liver Injury/prevention & control , Phytotherapy , Plant Extracts/therapeutic use , Silene , Acetaminophen , Alanine Transaminase/blood , Animals , Antioxidants/administration & dosage , Antioxidants/pharmacology , Aspartate Aminotransferases/blood , Carbon Tetrachloride , Dose-Response Relationship, Drug , Lipid Peroxidation/drug effects , Liver/drug effects , Liver/metabolism , Male , Plant Extracts/administration & dosage , Plant Extracts/pharmacology , Rats , Rats, Wistar
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