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    26 June 2011, Volume 1 Issue 3 Previous Issue    Next Issue

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    Antiproliferation Effects of Petasin on Human Neuroblastoma SK-N-SH Cells
    Cheng Yue-fang, Wang Cai-fang, Li Wen-jie, Lin Qing, Zhang Qi
    2011, 1 (3):  1-6. 
    Abstract ( 5527 )   PDF (4169KB) ( 2922 )  
    Objective: To study the antiproliferation effects of petasin on human neuroblastoma SK-N-SH cells and the possible mechanisms involved. Methods: The inhibitory effects of petasin on proliferation of tumor cells was detected by SRB assay; the effects of petasin on cell cycle arrest of SK-N-SH were measured by flow cytometry; the effects of apoptosis were examined by Hochest 33258 staining and flow cytometry and the phosphorylation of ERK1/2 of SK-N-SH was determined by western blotting. Results: Compared to that of other cancer cell lines such as SGC7901, SPC-A-1, SMMC 7721, Ec9706, SK-N-BE (2) and U251, the proliferation of SK-N-SH cells were strongly inhibited by petasin. After treated with petasin, the cell cycle of SK-N-SH arrested in G0/G1 phase, and there was no apoptosis detected either by Hoechst 33258 staining or by flow cytometry analysis. Finally, the phosphorylation of ERK1/2 was decreased by pretreatment with petasin in a dose-dependent way. Conclusion: Petasin is a potential anti-tumor of natural compounds, and shows the strong antiproliferation effect on SK-N-SH cells without inducing apoptosis. The inhibition of ERK1/2 phosphorylation might be involved in the antiproliferation effects of petasin.
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    Application of Uniform Design-High Throughput Screening in Research of Neuroprotective Effects of Five Ginsenoside and Notoginsenoside Components
    Song Zhi-bin, Zhang Dan-shen
    2011, 1 (3):  7-15. 
    Abstract ( 5013 )   PDF (2258KB) ( 3150 )  
    Objective: To evaluate the application of uniform design-high throughput screening technology for screening the active ingredients of traditional Chinese medicine. Methods: Weperformed uniform design compatibility study on four different saponin monomers ginsenoside Re, Rb1, Rg1, Rg3 and one notoginsenoside R1 each at six concentrations (1×10-4~1×10-9 mol·L-1), and their neuroprotective effects were assessed on the damaged nerve cells deprived of the serum. The obtained optimal combination of the ingredients from the above cell study was subjected to further animal tests for their pharmacological effects against the damages induced by cerebral ischemia reperfusion of mice model; the passive avoidance test, the hypoxia tolerance test were performed and the levels of aging-related enzymes in serum, brain and heart tissue were determined for assessing the effects of these ingredients. Results: The best combination samples (A11, A12, P5) obtained from cell screening experiment, have higher potency (cell survival ratio﹥90%) than any of five individual saponin monomers and vitamin E (the highest cell survival ratio was 78%) tested at a high concentration of 1×10-4 mol·L-1; these combinations significantly improved the learning and memory impairment induced by cerebral ischemia reperfusion injury, enhanced the hypoxia tolerance ability, increased the activity of superoxide dismutase, reduced the content of nitric oxide and maintained stability stable level of glutamic-pyruvic transaminase and lactic dehydrogenase (P<0.01~0.05). Conclusion: Uniform design compatibility and the traditional Chinese medicine compound compatibility have similarities. The best three combination samples obtained from five saponins by high-throughput screening show protective effect on cerebral ischemia reperfusion injury. Uniform design-high throughput screening technology is a reliable technology for massive potency screening of active ingredients of traditional Chinese medicine and compounds.
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    The Effects of Tenuigenin on Expression of nAChRα4 and PSD95 in Alzheimer’s Disease Model Rats
    Li Xiao-feng, Zhao Da-peng, Chen Shu-sha, Jing Wei, Li Xin-yi
    2011, 1 (3):  16-22. 
    Abstract ( 5487 )   PDF (9007KB) ( 2745 )  
    Objective: To investigate the effects and the underlying mechanisms of Tenuigenin on Alzheimer’s disease by observing the effects of Tenuigenin(TEN) on expression of nicotinic acetylcholine receptor subunit alpha-4 (nAChRα4) and postsynaptic density 95(PSD-95) in Alzheimer’s disease model rat. Methods: 32 male Wistar rats were divided randomly into four groups: control group,model group,12.5 mg·mL-1 dose TEN group and 37.5 mg·mL-1 dose TEN group. The rat model with Alzheimer’s disease was made by injecting ibotenic acid into Meynert basal nuclei of aging rat induced by D-gal.The expressions of nAChRα4 and PSD-95 in the hippocampus CA1 were measured by immunohistochemistry method. Results: Compared with the control group,the average gray-scale values of hippocampus CA1 nAChRα4 and PSD-95 in the model group were increased significantly and the average optical density was decreased obviously (P<0.01). Compared with the model group,the average gray-scale values in the hippocampus CA1 of 37.5 mg·mL-1 dose TEN group and 12.5 mg·mL-1 dose TEN group were obviously decreased and the average optical density was increased significantly (P<0.05). Meanwhile,the average gray-scale value within the hippocampus CA1 of 37.5 mg·mL-1 dose TEN group was significantly less than that in 12.5 mg·mL-1 dose TEN group,but more distinct than that on the average optical density aspect (P<0.01). Conclusion: TEN can dose-dependently increase the expression of CA1 area nAChRα4 and PSD-95 in Alzheimer’s disease model rats,which may partly explain the beneficial effects of TEN on cognitive function.
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    Antiemetic Effect and Mechanism of Small Pinelliae Decoction on Mink Vomit Model
    Ren Xu-ying,Mou Qun-fang,Luo Yi-ren,Wang Jue,Wang Yue,Zhang Fang
    2011, 1 (3):  23-26. 
    Abstract ( 5013 )   PDF (1160KB) ( 3169 )  
    Objective: To study the antiemetic effect of Small Pinelliae Decoction (SPD) and its mechanism. Methods: he active ingredients were extracted from TSPD(pinellia tuber:ginger=1:1) to make the granules. Cisplatin(7.5 mg·kg-1, ip) and apomorphine(1.6 mg·kg-1, ip) were used to prepare mink vomiting model. After 30 min of SPD (equivalent to 4.0, 1.0 g·kg-1 crude drug) ig. adminstration, minks were administered of cisplatin or morphine to study the inhibitory effect and mechanism of SPD on the two models of vomiting. Results: SPD could inhibit acute and delayed vomiting induced by cisplatin (within 72 h) in the minks, reduce the number of retching and vomiting(P<0.01), prolong the latency to vomit (P<0.01), and inhibit the expression of NK1 receptor in central (the area postrema) and peripheral (ileum tissue) tissues (P<0.05). SPD could also inhibit vomiting induced by apomorphine (within 6 h) (P<0.01), reduce significantly the ratio of vomiting (P<0.05) and did not affect the latency to vomit. Conclusion: SPD can inhibit vomiting induced by cisplatin and apomorphine, and its mechanism is related to the inhibition of central and peripheral NK1 receptor expression.
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    Comparative Study on Screening Acetylcholinesterase Inhibitors from Different Enzyme Sources
    Liu Jia-li, Yuan Yu-he, Chen Nai-hong
    2011, 1 (3):  27-30. 
    Abstract ( 4075 )   PDF (1169KB) ( 3264 )  
    Objective: To establish a reliable, fast, convenient and economical method of screening acetylcholinesterase inhibitors, and use it to screen acetylcholinesterase inhibitors from extracts of plants. Methods: Using the optimized Ellman method, we examined the inhibition effects of tacrine and huperzine on acetylcholinesterase enzyme from electric eel, human erythrocyte, rat hippocampus, striatum homogenate in 96-well plates under physiological pH value and temperature. The concentrations of AChE, substrate and DTNB, and reaction time were optimized. We also detected the inhibition effect of plant extracts on AChE. Results: Practical microassays for screening AChE inhibitors were successfully established by using AChEs mentioned above. The data analysis of screening results revealed that electric eel AChE possessed a high sensitivity to inhibitors, whereas human erythrocyte AChE shared high similarity with rat brain homogenate, on which the inhibitory effect of huperzine was superior to tacrine. However the plant extracts showed no inhibitory effect on AChE. Conclusion: The screening method established in this experiment is simple, fast, reliable and economical, and it can be used for pure compound screening.
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    Methods and Evaluation of Animal Models of Cerebral Ischemia and Cerebral Ischemia Reperfusion Injury
    Wang Shu, Zhang Li
    2011, 1 (3):  31-40. 
    Abstract ( 5232 )   PDF (1126KB) ( 6264 )  
    Cerebrovascular disease is a clinically common disease and frequently-occurring disease. The selection and application of reliable animal models are particularly important in studies for the prevention and treatment of cerebrovascular disease. The types, operation procedures of models, and characteristics of the global cerebral and focal cerebral ischemia and cerebral ischemia reperfusion injury in different animal models were discussed in detail in this paper. The improved Himori method (the model of cerebral ischemia reperfusion was produced in mice by temporarily obstructing bilateral common carotid arteries) and some key steps were especially presented in detail. The evaluation of the application characteristics of existing animal models will help to select the appropriate models of cerebral ischemia and cerebral ischemia reperfusion for studying cerebrovascular disease.
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    Mitochondria and Neurodegenerative Diseases
    Zhou Xiao-wen, Su Chao-fen, Luo Huan-min
    2011, 1 (3):  41-46. 
    Abstract ( 5038 )   PDF (1083KB) ( 4178 )  
    The neurodegenerative diseases are usually caused by the loss of the neurons and/or their myelin sheath, but the pathogenesis of these diseases are still indeterminate. Studies so far has proved that mitochondrial dysfunction and energy metabolism disorders are early pathological phenomena. This review concentrates on two of the most prevalent neurodegenerative diseases: Alzheimer’s disease (AD) and Parkinson’s disease (PD) and would be aimed to discuss the role of mitochondrial in pathogenesis of neurodegenerative diseases, providing new direction for further research.
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    High Temporal-spatial Resolution Neuroimaging Method Based on Reconstruction of MRI Scan Data with Optic-sensing Temporal Calibration
    Deng Liang, Shi Yi-Kai, Zhang Jun-Tian
    2011, 1 (3):  47-54. 
    Abstract ( 4437 )   PDF (2658KB) ( 3342 )  
    Functional magnetic resonance imaging is a powerful tool for biomedical imaging and neuroscience research. However, its practical utility is still rather limited due to poor spatial resolution, poor temporal resolution and low signal-to-noise ratio. In this paper, we proposed a new technique that enabled reconstruction of MRI scan data with optic collaborative sensing and realized high spatial resolution and high temporal resolution enhancement. For a specific task, a hemodynamic response in cortex related to neural activity could be scanned multiple times synchronized by optic sensing detection, and achieved time division coverage (TDC) of k-space data. Also, we presented a wavelength modulation spectroscopy with parametric exponential moving average (PEMA-WMS) method to realize real-time optic sensing in our proposed scheme. We illustrate the performance of this method with images of visual cortex functional imaging simulation with the Monte Carlo Modeling of light transport in pre-experimental MRI data phantom tissues.
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    Research Status of the Drugs Uesed in the Treatment of Affective Disorders Diseases
    XUE Zhan-xia, PENG Liang
    2011, 1 (3):  55-64. 
    Abstract ( 4610 )   PDF (1178KB) ( 3203 )  
    Affective disorders including depression (also known as unipolar depression) and bipolar disorder (unipolar depression),are the most common psychiatric disorders, which have high incidence ratio, high recurrence ratio, and is harmful to the society. Clinically, anti-unipolar depression drugs are mainly serotonin-specific reuptake inhibitors (SSRIs), fluoxetine as represented, and serotonin/norepinephrine dual reuptake inhibitor (SNRIs), duloxetine as represented. And lithium salts (Li+), valproate sodium, and carbamazepine are the three classical anti-bipolar drugs. At present, researches concerning these drugs propose following major mechanisms: ①The expression of cytosolic phospholipase A2 (cPLA2), extracellular-signal regulated kinases (ERK) and c-Fos and FosB is increased by SSRIs; ②Chronic administration of Fluoxetine could induce 5-HT2B receptor pre-mRNA editing, with the help of adenosine deaminase (ADAR2) activity; ③Lithium carbonate, carbamazepine, valproate sodium could upregulate the mRNA and protein of cPLA2a and induce alkalinization of cell. But the accurate pharmacological mechanisms of these drugs have not been fully elucidated and are needed to be further investigated.
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