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1.
Acta Pharmaceutica Sinica ; (12): 145-149, 2008.
Article in Chinese | WPRIM | ID: wpr-268155

ABSTRACT

Cajanus cajan L. is a natural plant, which contains a lot of potential active components. In the present study, we identified the effects of the stilbene extract from Cajanus cajan L. (sECC) on hepatic cholesterol metabolism in diet-induced (for 4 weeks) hyperlipidemic Kunming mice. All experimental mice were divided into 5 groups: control group, high lipid model group, sECC-treated with 200 or 100 mg kg(-1), and simvastatin (Sim, 12 mg kg(-1)) treated group. The mice were fed with fat and cholesterol-enriched chow except control mice that were fed with standard diet. The effects of sECC were investigated by monitoring serum and liver lipid profile (i. e. cholesterol homeostasis) in mice. To further explore the mechanism of sECC, hepatic cholesterol 7alpha-hydroxylase (CYP7A1) and low density lipoprotein (LDL) receptor expressions in cholesterol homeostasis were analyzed by reverse transcription PCR. After 4 weeks pretreatment, the mice in the high lipid model group showed markedly higher serum and hepatic lipid contents than control group (P< 0.01). Compared with high lipid model group, the increased serum and hepatic lipid contents were markedly attenuated by sECC (200 mg kg(-1)), the serum and hepatic total cholesterol were reduced by 31.5% and 22.7% (P<0.05), respectively. The triglyceride contents of serum and liver were also lowered by 23.0% and 14.4%, respectively. At the same times, serum LDL cholesterol decreased by 53.0% (P<0.01). The mRNA expressions of hepatic CYP7A1 and LDL-receptor were significantly enhanced in the mice administered with sECC (200 mg kg(-1)), whereas those expressions were suppressed by the fat and cholesterol-enriched diet. These data indicate that sECC reduces the atherogenic properties of dietary cholesterol in mice. It is indicated that expression enhancement of hepatic LDL-receptor and cholesterol 7alpha-hydroxylase may be responsible for the hypercholesterolemic effect.


Subject(s)
Animals , Male , Mice , Anticholesteremic Agents , Pharmacology , Body Weight , Cajanus , Chemistry , Cholesterol , Blood , Metabolism , Cholesterol 7-alpha-Hydroxylase , Genetics , Cholesterol, LDL , Blood , Drugs, Chinese Herbal , Pharmacology , Gene Expression Regulation , Hypercholesterolemia , Blood , Genetics , Metabolism , Pathology , Liver , Metabolism , Pathology , Organ Size , Plant Leaves , Chemistry , Plants, Medicinal , Chemistry , RNA, Messenger , Metabolism , Receptors, LDL , Genetics , Stilbenes , Pharmacology , Triglycerides , Blood , Metabolism
2.
Acta Pharmaceutica Sinica ; (12): 386-391, 2007.
Article in Chinese | WPRIM | ID: wpr-281888

ABSTRACT

The cajanine (longistylin A-2-carboxylic acid) is isolated and identified from extracts of Cajanus cajan L. (ECC) , which structure is similar to diethylstilbestrol. The regulation properties of the cajanine and other four extracts of Cajanus cajan L. (32-1, 35-1, 35-2, and 35-3) were tested in human osteoblast-like (HOS) TE85 cells and marrow-derived osteoclast-like cells. By using MTT assay to test the change of cell proliferation, 3H-proline incorporation to investigate the formation of collagen, and by measuring alkaline phosphatase (ALP) activity, bone formation in HOS TE85 cell was evaluated after pretreated for 48 hours. Bone marrow cells were cultured to examine the derivation of osteoclast cells (OLCs), which were stained with tartrate-resistant acid phosphatase (TRAP). The long term effect (pretreated for 18 days) on promoting mineralized bone-like tissue formation was tested by Alizarin red S staining in HOS TE85 cells. After the treatment with cajanine (1 x 10(-8) g x mL(-1)) for 48 hours, cell number increased significantly (57.7%). 3H-Proline incorporation also statistically increased (98.5%) in those cells. Significant change of ALP activity was also found (P < 0.01) in 35-1 and 35-3 treated cells (they were 66.2% and 82.4% in the concentration of 1 x 10(-8) g x mL(-1), respectively). The long term (18 days) effects of 32-1 and 35-3 on promoting mineralized bone-like tissue formation in HOS TE85 cell were obvious. There were much more red blots over the field of vision compared with that of control group. After the treatment of cajanine, derived-osteoclast cells appeared later and much less compared with control. The inhibition of cajanine was 22.8% while it was 37.9% in 32-1 treated cells in the dose of 1 x 10(-7) g x mL(-1). It is obvious that cajanine and ECCs promoted the osteoblast cells proliferation and mineralized bone-like tissue formation in HOS TE85 cells, while inhibited derivation of osteoclast cells. All of these suggested that cajanine has the estrogen-like action on osteoblast and osteoclast, which could be developed as anti-osteoporosis drugs.


Subject(s)
Animals , Humans , Rats , Alkaline Phosphatase , Metabolism , Bone Marrow Cells , Cell Biology , Bone Neoplasms , Metabolism , Pathology , Cajanus , Chemistry , Cell Line, Tumor , Cell Proliferation , Cells, Cultured , Collagen , Diethylstilbestrol , Pharmacology , Drugs, Chinese Herbal , Pharmacology , Osteoblasts , Osteoclasts , Cell Biology , Metabolism , Osteogenesis , Osteosarcoma , Pathology , Phytoestrogens , Pharmacology , Plant Leaves , Chemistry , Plants, Medicinal , Chemistry , Rats, Wistar
3.
Acta Pharmaceutica Sinica ; (12): 562-565, 2007.
Article in Chinese | WPRIM | ID: wpr-268597

ABSTRACT

The Cajanus cajan L. is a natural plant, which contains lots of potential active components. The effects of the stilbene extracts from Cajanus cajan L. (sECC) on ovariectomy (OVX)-induced bone loss in rats were identified. All experimental female rats were divided into 6 groups, i. e. sham-operated rats, OVX rats, 17beta-estradiol (E2)-treated rats, sECC-treated rats with three dosages, 50, 100, and 200 mg x kg(-1), separately. Two weeks after the operation, different dosage of sECC, E2 or deionized water were given to the 6 groups of rats, respectively for another 8 weeks through stomach. Then, all rats were killed. The body weight and uterus wet weight were measured. Contents of serum E2, follicle stimulating hormone (FSH), and luteinizing hormone (LH) were measured by radioimmunoassay. Femoral morphology was observed by HE stain. The results showed that there were no changes of the uterine weight and serum E2 concentration in sECC-treated rats compared with OVX rats. However, the serum FSH and LH concentrations reduced by 11.5% and 15.2% (P < 0.05), respectively. By HE staining, it is found that the 60% of the femur structure had been significantly improved in OVX rats treated with 200 mg x kg(-1) of sECC. The trabeculae were thicker and larger than that of OVX rats. It is clear that sECC improved femoral morphological structure and decreased FSH and LH contents without affecting serum E2 level and uterine weight in OVX rats. The results suggested that sECC had potential action in treatment of postmenopausal osteoporosis.


Subject(s)
Animals , Female , Rats , Body Weight , Cajanus , Chemistry , Drugs, Chinese Herbal , Pharmacology , Estradiol , Blood , Femur , Pathology , Follicle Stimulating Hormone , Blood , Luteinizing Hormone , Blood , Organ Size , Osteoporosis , Blood , Pathology , Ovariectomy , Plant Leaves , Chemistry , Plants, Medicinal , Chemistry , Rats, Wistar , Uterus , Pathology
4.
Chinese Journal of Gastrointestinal Surgery ; (12): 46-49, 2005.
Article in Chinese | WPRIM | ID: wpr-252468

ABSTRACT

<p><b>OBJECTIVE</b>To compare the diagnostic value of barium enema (BE), computed tomography (CT) and magnetic resonance imaging(MRI) in primary colorectal carcinoma.</p><p><b>METHODS</b>A total of 64 patients with suspected colorectal carcinoma received BE (n=39), spiral CT (n=31) and MRI (n=42). The detective results were compared with the surgical results.</p><p><b>RESULTS</b>Among 64 patients, 54 cases were pathologically proved as colorectal carcinoma. The diagnostic sensitivity of BE,CT and MRI was 96.9% ,96.2% and 97.1% ,and the overall accuracy was 92.3% 83.9 % and 90.5% respectively. The overall accuracy of CT and MRI for tumor T staging was 73.1% and 82.9% respectively.</p><p><b>CONCLUSION</b>BE can be considered as a primary approach for diagnosing colorectal carcinoma, CT and MRI be necessary diagnostic approaches. Combined BE with MRI is the best choice for diagnosing of colorectal carcinoma.</p>


Subject(s)
Adult , Aged , Aged, 80 and over , Female , Humans , Male , Middle Aged , Barium Sulfate , Colorectal Neoplasms , Diagnostic Imaging , Pathology , Enema , Magnetic Resonance Imaging , Neoplasm Staging , Sensitivity and Specificity , Tomography, Spiral Computed
5.
Acta Pharmaceutica Sinica ; (12): 272-275, 2003.
Article in Chinese | WPRIM | ID: wpr-251126

ABSTRACT

<p><b>AIM</b>To look for new active constituents from the aerial part of Cimicifuga foetida L.</p><p><b>METHODS</b>Various column chromatographic techniques were used for the isolation and purification of the principles. The structures were elucidated on the basis of spectral data and chemical evidences.</p><p><b>RESULTS</b>Five 9,19-cycloartane triterpenoid saponins and one sitosterol saponin were obtained and identified as cimifoetiside I [12 beta-hydroxycimigenol-3-O-beta-D-galactoyranoside, (1)], cimifoetiside II [(23R,24R) cimigenol-3-O-beta-D-galactopyranoside, (2)], cimigenol-3-O-beta-D-galactopyranoside (3), 12 beta-hydroxycimigenol-3-O-beta-D-xylopyranoside (4), 12 beta-hydroxycimigenol-3-O-alpha-L-arabinopyranoside (5), daucosterol (6).</p><p><b>CONCLUSION</b>Compounds 1 and 2 are new and compounds 4 and 5 were isolated from this plant for the first time.</p>


Subject(s)
Cimicifuga , Chemistry , Drugs, Chinese Herbal , Chemistry , Molecular Structure , Plant Components, Aerial , Chemistry , Plants, Medicinal , Chemistry , Sitosterols , Chemistry
6.
China Journal of Chinese Materia Medica ; (24): 135-138, 2003.
Article in Chinese | WPRIM | ID: wpr-266801

ABSTRACT

<p><b>OBJECTIVE</b>To find new active constituents from Rhizome of Cimicifuga foetida.</p><p><b>METHOD</b>Various column chromatographic techniques were employed for isolation and purification. The structures were elucidated on the basis of spectral and chemical evidences.</p><p><b>RESULT</b>Four triterpenoid compounds were isolated and identified as 7,8-didehydro-27-deoxyactein(1), 24-O-acetylshengmanol-3-O-beta-D-xyl (23R, 24R)[2], cimigenol(3), cimigenol-3-O-beta-D-xyl(4).</p><p><b>CONCLUSION</b>Compound 1 is a new compound, 2-4 were obtained from this medicinal material for the first time. The antiosteoporosis activity screening in vitro(by the method of SRB) indicates that Compounds 1, 2 and 4 can promote the proliferation for rat Osteoblastoma cell line (UMR106) at the concentration of 10(-9) kg.L-1.</p>


Subject(s)
Animals , Rats , Bone Neoplasms , Pathology , Cell Division , Cell Line, Tumor , Cimicifuga , Chemistry , Lanosterol , Chemistry , Pharmacology , Molecular Structure , Osteoblastoma , Pathology , Plants, Medicinal , Chemistry , Rhizome , Chemistry , Triterpenes , Chemistry , Pharmacology
7.
China Journal of Chinese Materia Medica ; (24): 230-232, 2003.
Article in Chinese | WPRIM | ID: wpr-266781

ABSTRACT

<p><b>OBJECTIVE</b>To find new active constituents from the aerial part of Cimicifuga foetida.</p><p><b>METHOD</b>Various column chromatographic techniques were used for the isolation and purification of the principles. The structures were elucidated on the basis of spectral data and chemical evidences.</p><p><b>RESULT</b>Four 9,19-cycloartane triterpenoid saponins were obtained and identified as Cimifoetiside III (25-anhydrocimigenol-3-O-beta-D-galactopyranoside, 1), 25-O-acetyl-cimigenol xylopyranoside (2), 25-O-acetyl-cimigenol galactopyranoside (3), 7 beta-hydrocimigenol xylopyranoside (4).</p><p><b>CONCLUSION</b>Compound 1 is new and compound 4 was isolated from this plant for the first time.</p>


Subject(s)
Cimicifuga , Chemistry , Galactosides , Chemistry , Lanosterol , Chemistry , Molecular Structure , Plant Components, Aerial , Chemistry , Plants, Medicinal , Chemistry , Saponins , Chemistry , Triterpenes , Chemistry
8.
Acta Pharmaceutica Sinica ; (12): 763-766, 2003.
Article in Chinese | WPRIM | ID: wpr-266608

ABSTRACT

<p><b>AIM</b>To seek for new bioactive constituents from the aerial parts of Cimicifuga dahurica.</p><p><b>METHODS</b>Various column chromatographic techniques were employed for the isolation and purification of the ingredients. The structures were elucidated on the basis of 1H, 13CNMR, 1H-1H COSY, HMQC, NOESY and HMBC spectra and chemical reactions.</p><p><b>RESULTS</b>Two cyclolanostanol xylosides, cimidahuside C and D were isolated from the EtOAc section of EtOH extracts.</p><p><b>CONCLUSION</b>Cimidahuside C(1) and D(2) are new triterpenoid xylosides.</p>


Subject(s)
Cimicifuga , Chemistry , Glycosides , Chemistry , Molecular Structure , Plant Components, Aerial , Chemistry , Plants, Medicinal , Chemistry , Triterpenes , Chemistry
9.
Acta Pharmaceutica Sinica ; (12): 117-120, 2002.
Article in Chinese | WPRIM | ID: wpr-343388

ABSTRACT

<p><b>AIM</b>To look for new active constituents from the aerial part of Cimicifuga foetida L.</p><p><b>METHODS</b>Various column chromatographic techniques were used for the isolation and purification of the ingredients. The structure were elucidated on the basis of spectral evidences and chemical reaction.</p><p><b>RESULTS</b>Five compounds were obtained and identified as 23-O-acetylshengmanol-3-O-alpha-L-arabinopyranoside (1), 23-O-acetylshengmanol-3-O-beta-D-xylopyranoside (2), 25-anhydrocimigenol-3-O-beta-D-xylopyranoside (3), cimigenol-3-O-alpha-L-arabinopyranoside (4), cimigenol-3-O-beta-D-xylopyranoside (5).</p><p><b>CONCLUSION</b>Compound 1 is a new compound, and compounds 2 and 4 were isolated from this plant for the first time.</p>


Subject(s)
Cimicifuga , Chemistry , Molecular Structure , Plant Stems , Chemistry , Plants, Medicinal , Chemistry , Saponins , Chemistry
10.
Acta Pharmaceutica Sinica ; (12): 535-538, 2002.
Article in Chinese | WPRIM | ID: wpr-251107

ABSTRACT

<p><b>AIM</b>To look for new active constituents from Chinese medicine "Sheng-ma", rhizome of Cimicifuga foetida L.</p><p><b>METHODS</b>The compounds were separated and purified by chromatography on silica gel and Sephadex LH-20. Their structures were determined by spectral analysis and chemical reaction.</p><p><b>RESULTS</b>Eight compounds were obtained and identified as cimicifugic acid (1), esculetin (2), caffeic acid methyl ester (3), 4-O-acetyl-caffeic acid (4), sinapic acid (5), caffeic acid (6), ferulic acid (7), isoferulic acid (8).</p><p><b>CONCLUSION</b>Compound 1 is a new compound, and compounds 2-7 were isolated from this plant for the first time.</p>


Subject(s)
Caffeic Acids , Chemistry , Cimicifuga , Chemistry , Coumaric Acids , Chemistry , Drugs, Chinese Herbal , Chemistry , Hydroxybenzoates , Chemistry , Molecular Conformation , Molecular Structure , Phenylacetates , Chemistry , Plants, Medicinal , Chemistry , Rhizome , Chemistry , Umbelliferones , Chemistry
11.
Virologica Sinica ; (4): 81-84, 2001.
Article in Chinese | WPRIM | ID: wpr-635224

ABSTRACT

Homology of three WSSV isolates, which were sampled from r epresentative maritime space of China: Tanghai isolate (Bo Bay of China), Ningbo isolate (East China Sea), Shenzhen isolate (South China Sea) was compared. Both of the genome RFLP patterns and the characteristic structural proteins SDS-PAG E electrophero grams showed that they were quite same. It suggested that they were the same ki nd of WSSV virus that caused explosive epidemic diseases of shrimps (EEDS) throu ghout southern and northern China. The same large PCR products achieved when usi ng the PCR primers from RV-PJ=PRDV (P. japonicus, Japan) and WSBV=PmNOBII I(P.monodon Taiwan, China) respectively to amplify the genome from P.chine nsis (Tanghai, China) with high fidelity Taq Polymerase. The sequence identiti es of WSSV from P. chinensis with those from RV-PJ=PRDV (P.japonicus, Japan) and WSBV=PmNOBIII (P.monodon Taiwan, China) are 97% and 100% respect ively, the results provided additional evidence that WSSV reported in different parts of the Asian and Pacific regions maybe quite the same or just different va riants of the same virus.

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