Volume 2,Issue 1,2010 Table of Contents

  • Display Type:
  • Text List
  • Abstract List
  • 1  Strategies for Revitalization of Traditional Medicine
    MUKHERJEE Pulok K PITCHAIRAJAN Venkatesh MURUGAN Venkatesh SIVASANKARAN Ponnusankar KHAN Yaseen
    2010, 2(1):1-15. DOI: 10.3969/j.issn.1674-6384.2010.01.001
    [Abstract](2586) [HTML](0) [PDF 398.82 K](4902)
    Abstract:
    Traditional medicine (TM) plays an inevitable role in drug discovery and development. Most of the therapeutically useful molecules used in the present day are inspired from TM. Herbal drugs are the oldest forms of medicines used for the treatment of various ailments and the TM of every country has a long history of their usage. To develop more data on their quality, safety, and efficacy, so also to improve the consumer’s need of modern days several thrust areas of research are to be focused on the development of TM. Based on the above concept, a paradigm shift is required for the revitalization of TM. These facts along with the modern scientific approaches, molecular tools, and strategies make it necessary for TM to be revitalized. Confluencing several strategies with the technological and scientific developments including pharmacogenomics, nutrigenomics, system biology, and related approaches, the scientific potential of TM can be explored further with international coordination and collaborations.
    2  Relationship between DNA Barcoding and Chemical Classification of Salvia Medicinal Herbs
    HAN Jian-ping LIU Chang LI Min-hui SHI Lin-chun SONG Jing-yuan YAO Hui PANG Xiao-hui CHEN Shi-lin
    2010, 2(1):16-29. DOI: 10.3969/j.issn.1674-6384.年份.期.第几篇文章
    [Abstract](2214) [HTML](0) [PDF 855.39 K](4977)
    Abstract:
    Objective To make the identification of medicinal herbs in Salvia L. quickly and accurately. Methods In this work, DNA barcoding and chemical fingerprint were compared for the identification of herbs in Salvia L. First, the nucleotide sequences of the internal transcribed spacer region two amplified from 48 medicinal plants in Salvia L., and three other groups of medicinal plants in Lamiaceae were sequenced. A molecular phylogeny was constructed using the minimum evolution and maximum parsimony methods according to their sequence diversity. Second, the water-solution bioactive components and lipid soluble components were tested by HPLC. Then a chemical phylogeny was built using HPLC fingerprint data. Comparing the molecular and chemical phylogenetic trees revealed many similarities. Results DNA barcoding was sequencing based and could therefore provide more accurate results within a shorter time especially in large-scale studies. Conclusion The results show that ITS2 region is a novel DNA barcode for the authentication of the species in Salvia L. This is the first work to show the relationship between DNA barcoding and chemical components.
    3  Toxicological Assessment of Trans-resveratrol
    ZENG Jian-guo HU Yi-xiu ZHANG Xiang-qian
    2010, 2(1):30-40. DOI: 10.3969/j.issn.1674-6384.2010.01.003
    [Abstract](1767) [HTML](0) [PDF 237.09 K](2586)
    Abstract:
    Objective To evaluate toxicity and safety of trans-resveratrol (t-RSV). Methods For assays of acute toxicity, genetic toxicity, and sub-chronic toxicity, Ames test, mice bone marrow erythrocyte micronucleus, and mice sperm abnormality were performed. Results In the acute oral toxicity tests, maximum tolerable dose (15 g/kg) in male and female Kunming mice showed no toxicological signs. For 90-d feeding of t-RSV at dosage range of 167–500 mg/(kg?d) in both male and female Sprague-Dawley rats, no noticeable toxicological effects were observed. Conclusion T-RSV has no acute toxicity and no genotoxicity, no harmful effects on the human body at the tested dosage range and thus resveratrol is safe for human consumption.
    4  Transformation of Compound K from Saponins in Leaves of Panax notoginseng by Immobilized β-Glucanase
    DONG Hui-juan JIANG Bin-hui HAN Ying GENG Yong ZHAO Yu-qing
    2010, 2(1):41-47. DOI: 10.3969/j.issn.1674-6384.2010.01.004
    [Abstract](1501) [HTML](0) [PDF 402.35 K](2596)
    Abstract:
    Objective To prepare an active anti-tumor component, compound K (C-K), from saponins in leaves of Panax notoginseng (SLPN) using immobilized β-glucanase. Methods Two entrapments, alginate gel-1 (Alg 1) and alginate gel-2 (Alg 2), were evaluated for their ability to immobilize β-glucanase. The amount and purity of C-K obtained from the transformation process were analyzed by HPLC, and the immobilizing parameters were optimized. Results β-Glucanase can be immobilized and reused with either of the entrapment. However, using Alg 1 resulted in higher enzyme activity than Alg 2. The optimal concentration of the immobilized enzyme was 10%; The optimal crosslinking time was 4–6 h; and the optimal concentration of the crosslinking agent was 6%–7%. Conclusion Immobilized β-glucanase shows sustained enzyme activity, good ethanol tolerance, and was reusable for the preparation of C-K from SLPN.
    5  Effects of Astragaloside Ⅳ Derivative on Heart Failure in Rats
    WANG Wei-ting ZHAO Zhuan-you HAN Ying-mei XU Wei-ren TANG Li-da
    2010, 2(1):48-53. DOI: 10.3969/j.issn.1674-6384.2010.01.005
    [Abstract](1661) [HTML](0) [PDF 106.21 K](2835)
    Abstract:
    Objective Astragaloside Ⅳ derivative (ASId) is one of Astragaloside Ⅳ (ASI) derivatives with higher water-solubility and may have more druggability than ASI. The present study aims at observing the effects of ASId on cardiovascular parameters in chronic heart failure in rats. Methods Using echocardiographic and haemodynamic measurements, the effects of ASId on congestive heart failure (CHF) induced by ligation of the left coronary artery in rats were investigated. Results ASId iv 0.5, 1.0, and 2.0 mg/(kg?d) attenuated the decline of ejection fraction. The peak derivatives of the left ventricle (LV) pressure (dp/dt) in ASId treated groups were significantly increased. Both LV volumes in diastole and in systole were decreased significantly after ASId treatment, accompanied with a trend towards normalization of relative wall thickness at end-systole. ASId 0.5, 1.0, and 2.0 mg/(kg?d) attenuated the increase of LV systolic and diastolic wall stress. ASId treatment also inhibited compensatory hypertrophy of depressed heart. Conclusion ASId could improve cardiac functions and inhibite compensatory hypertrophy and LV remodelling, which suggests the possibility of ASId as a new therapeutic drug for the treatment of CHF.
    6  Influence of Different Extraction and Purification Methods on Astragalus Polysaccharides and Pharmacological Evaluation
    YANG Yi-fang FENG Jing-qian XU Hai-yan PENG Dan-ming HU Jian-ping
    2010, 2(1):54-61. DOI: 10.3969/j.issn.1674-6384.2010.01.006
    [Abstract](1829) [HTML](0) [PDF 194.40 K](2083)
    Abstract:
    Objective To clarify the influence on component and pharmacological action of Astragalus polysaccharides (APS) as complementary therapeutic agents prepared by different extraction and purification techniques. Methods Components of APS prepared by different extraction and purification techniques were analyzed, and these APS were used for synergy and attenuation of chemotherapy, radiotherapy treatment with H22 liver cancer and Lewis lung cancer of tumor-bearing mice, and also used for the regulation of immune function to immunosuppression mice. Results Experimental data were analyzed by means of statistical method to get pharmaco-result: A3 (extracted by microwave assistance and purified by membrane separation) > A4 (extracted by refluxing and purified by membrane separation) > A1 (extracted by refluxing and no purification) ≈ A2 (extracted by microwave assistance and no purification). There were no significant differences on pharmacodynamic action between A1 and A2. However, compared with A1 and A2, it was worth noting that A3 and A4 exhibited good pharmacodynamic action. Then A3-in and A4-in, the samples in dialyzer after dialysis, were separated and purified to get homogeneous APS, which were the principal constituents of APS in dialyzer, with the molecular weight (Mw) of 7669 and 14 142 determined by HPGPC, respectively. The average Mw of APS outside of the dialyzer, A3-out was 3102 and A4-out 3256, which were the main compositions of A3 and A4, accounted for 79.63% and 53.92%, respectively. Conclusion APS with Mw about 5000 Da exhibit better antitumor effect and immunological activity. Refluxing, microwave assistance extractions, and membrane enrichment techniques bring different cases on Mw distribution, components and pharmacodynamic action, and obviously exhibit relationship among component, Mw distribution, and pharmacological action.
    7  A New Steroidal Glycoside from Roots of Cynanchum auriculatum
    YIN Min FENG Xu CHEN Yu WANG Ming XIA Bing DONG Yun-fa
    2010, 2(1):62-64. DOI: 10.3969/j.issn.1674-6384.2010.01.007
    [Abstract](1498) [HTML](0) [PDF 0.00 Byte](219)
    Abstract:
    Abstract: Objective To study the chemical constituents of Cynanchum auriculatum. Methods Two steroidal glycosides were purified by column chromatography and their structures were elucidated by spectroscopic analysis. Results and Conclusion Compound 1 is a new steroidal glycoside, named kidjoranin-3-O-β-D-cymaropyranoside. Compound 2 is isolated from this plant for the first time.
    8  Chemical Constituents of Ganoderma resinaceum
    DING Ping QIU Jin-ying LIANG Ying-jiao
    2010, 2(1):65-67. DOI: 10.3969/j.issn.1674-6384.2010.01.008
    [Abstract](1187) [HTML](0) [PDF 0.00 Byte](230)
    Abstract:
    Abstract: Objective To study the chemical constituents of Ganoderma resinaceum. Methods Chemical constituents were isolated and purified by silica gel column, Sephadex LH-20, and ODS column chromatography. The structures were identified by means of physicochemical and spectral data. Results From the CHCl3 part of the fruiting bodies of this material, eight compounds were isolated. Their structures were determined to be ergosterol (1), β-sitosterol (2), ganoderic acid E (3), ganoderic acid G (4), ganoderic acid C2 (5), ganoderic acid B (6), ganoderic acid A (7), and lucidenic acid A (8). Conclusion All the compounds were obtained from this fungus for the first time.
    9  Regulation of Fengxiaofang on Expression of Gene Gob-5 in Asthmatic Mice
    BAI Gen-ben LIU Yang LI You-lin MA Xiao-xin YAN Shi FAN Chang-zheng GUO Ya-hong
    2010, 2(1):68-71. DOI: 10.3969/j.issn.1674-6384.2010.01.009
    [Abstract](1520) [HTML](0) [PDF 0.00 Byte](211)
    Abstract:
    Abstract: Objective To observe the regulation of Fengxiaofang on the expression of gene Gob-5 in ovalbumin-challenged asthmatic mice. Methods The murine model of allergic asthma established by ovalbumin was used. The model mice were treated experimentally with Fengxiaofang and Dexamethasone as a positive control. The quantitive expression of gene Gob-5 in lung of mice was detected by real-time quantitative PCR. Results The expression of gene Gob-5 in lung of mice was down-regulated by Fengxiaofang. In the experiment, there were no significant differences between the one-fold or ten-fold dosage groups and the normal control group. Gene Gob-5 expression in five-fold dosage was significantly lower than that in the normal control group. Conclusion Fengxiaofang has the effect of lowering the expression of gene Gob-5 which maybe related to the potency on asthmatic disease.
    10  Inhibition of Celastrus orbiculatus Extracts on VEGF Expression in Hepatoma Cells of Mice
    QIAN Ya-yun LIU Yan-qing
    2010, 2(1):72-76. DOI: 10.3969/j.issn.1674-6384.2010.01.010
    [Abstract](1059) [HTML](0) [PDF 0.00 Byte](227)
    Abstract:
    Abstract: Objective To discuss the antitumor mechanism preliminarily by observing effects of Celastrus orbiculatus extracts (COE) on vascular endothelial growth factor (VEGF) mRNA and protein expression in hepatoma (Hepa1-6) cells of mice. Methods Hepa1-6 cells were treated with COE at different nontoxic concentration (0, 10, 20, 40, 80, and 160 μg/mL) for 16 h. The mRNA and protein expressions of VEGF were detected by reverse transcription-PCR and Western Blotting, respectively. Results COE significantly inhibited VEGF expression at both mRNA and protein levels in a dose-dependent manner. Conclusion COE can inhibit VEGF expression in Hepa1-6 cells, therefore suggest that VEGF could be chosen as an therapeutic target for COE in the context of cancer chemoprevention and anticancer therapy.

    Current Issue


    Volume , No.

    Table of Contents

    Archive

    Volume

    Issue

    Most Read

    Most Cited

    Most Downloaded

    WeChat

    Mobile website