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Table of Content

    Volume 11 Issue 11
    26 November 2006
    Progresses in studies on pharmacologic effects of ginsenosides
    WANG Hai-nan
    2006, 11(11):  1201-1206. 
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    Ginsenosides are major active ingredients of ginseng.The Pharmacologic effects of ginsenosides are various.The pharmacologic effects of individual ginsenoside have been studied deeply now, especially focusing on regulation of metabolism.In this article, we reviewed progresses in studies on pharmacologic effects of ginsenosides in recent years in the world, referring to nervous system, small intestinal transit, endocrine system, immune system, signal transduction, anti-aging, hemolysis,burn wound healing, synergy of anti-tumor, human sperm motility, drug metabolism enzyme and lowering plasma glucose.Furthermore, protopanaxadiol-type ginsenosides were compared with protopanaxatriol-type ginsenosides on the pharmacologic effects briefly.
    Advances in studies on population pharmacokinetics of antiepileptic drugs and CYP450 gene polymorphisms
    JIANG De-chun, BAI Xiang-rong, WANG Yu-qin, LI Lin
    2006, 11(11):  1207-1212. 
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    Antiepileptic drugs ( AEDs) should be used with individualized dsage regimens since they are metabolized by marked variability.It is an effective way to design individualized dosage regimens with population pharmacokinetic ( PPK) researching.There are lots of researches on PPK for antiepileptic drugs in the world, and many demographic features but genetic factors are analyzed in PPK models.CYP450 gene polymorphisms are important factors for interindividual variability.The latest advance of study for PPK is to analyze the effect on AEDs due to CYP450 gene polymorphisms, and to choose different initial doses according to gene polymorphisms.It will be valuable to facilitate individualized dosage regimen.However, one study indicates that the presently evaluated variant alleles in the CYP2C8, CYP3A4, CYP3A5 and ABCB1 genes did not explain the substantial interindividual variability in paclitaxel pharmacokinetics.Therefore,more deeply research should be done.
    Effect of cytokines on repairing myocardium in acute myocardial infarction
    SUN Chun-ling, HONG Hua-shan
    2006, 11(11):  1213-1218. 
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    The treatment modalities of stem cells repairing infarction myocardial include stem cell transplantation and mobilization.The inflammatory factors and cytokines play an important role in the process of repairing infracted myocardium.In this paper we will review the effect of cytokines on the process of stem cells mobilization,homing, proliferation and differentiation in after acute myocardium infraction.
    Muscarinic acetylcholine receptors-coupled M channels:a new drug target for neuropsychic diseases
    SONG Ming-ke, HU Guo-yuan, CHEN Hong-zhuan
    2006, 11(11):  1219-1224. 
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    The M-channel is a voltage-gated potassium channel , distributed in nervous system , playing a key role in controlling neuronal excitability.In brain , the transmitter acetylcholine increases neural activity by inhibiting M-channel via muscarinic acetylcholine receptors.This cholinergic excitation is important for alertness ,arousal , learning and memory.Mutations in M-channel genes result in epilepsy and deafness.M-channel activators are efficacious for treating epilepsy and neuropathic pain;conversely , its inhibitors are useful in improving symptoms of Alzheimer' s disease.Based on recent progress and findings , the M-channel has emerged as a promising drug target for treating neuropsychic diseases.
    Progress of “Cocktail” probe substrates approaches
    LIU Ying, JIAO Jian-jie, LOU Jian-shi
    2006, 11(11):  1225-1229. 
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    The method of simultaneous administration of several probe substrates is called “Cocktail” approaches.The objective of the article is to review the application of this technique in characterizing the activity of multiple drug-metabolizing enzymes and in clinical researches.This paper also shows Five-drug and Six-drug Cocktail set for evaluating in vivo activity of drug-metabolizing enzymes.
    Effect of Anshenbunao syruPon learning and memory and BDNF expression in hippocampus of sleePdeprivation rats
    WEI Hai-feng, YE Cui-fei, LI Chun-yang, DING Yue-xia, ZHAO Ning, LI Lin
    2006, 11(11):  1230-1233. 
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    AIM: To study the effects of An-Shen-Bu-Nao syruP(AS)on the learning and memory ability and BDNF expression in the hippocampus of sleePdeprivation(SD)rats.METHODS: 75 rats were divided into groups of control , control +AS (0.02 ml·kg-1), SD +distillated water (DW), SD +AS (0.02 ml·kg-1), and SD +AS (0.06 ml·kg-1).All rats were fed with AS or DW for 2 weeks , and they were subjected to sleePdeprivation for 4 days , then the passive avoidance was tested for learning and memory.Also the BDNF expression in the hippocampus was tested with western blot after sacrifice.RESULTS: Compared with the control rats , SD rats had the significantly reduced latency in passive avoidance test , showing the decreased learning and memory ability.SD combined with AS (0.06 ml·kg-1) rats showed significantly longer latency than the SD rats (P<0.05), indicating the better learning and memory ability than the sleePdeprivation rats ;BDNF expression was significantly higher in the rats of SD combined with AS (0.06 ml·kg-1)than the SD rats.CONCLUSION: An-Shen-Bu-Nao SyruPcan effectively improve the learning and memory ability of sleePdeprivation rats , and the enhancement of BDNF expression may contribute to this effect.
    Effect of gingkgolide combined with insulin treatment on learning ability of AD-like model rats
    WANG Xu-dong, PAN Ya, LI Qing-chun, LV Xin-rui, JIANG Nai-chang
    2006, 11(11):  1234-1238. 
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    AIM: To examine the effects of the gingkgolide combined with insulin treatment on the learning ability of the AD-like model rats and explore the possible mechanism of its effect.METHODS: The AD-like animal models were established by injection of okadaic acid( OA) in the hippocampal CA1 area, and pretreatment was administered by injecting insulin in the lateral brain ventricle and forced feeding with gingkgolides.The learning capability of the rats was examined by means of Morris water maze, and the expressions of neurofibrillary tangle(NFT) and glial fibrillary acidic protein ( GFAP) in the CA1 area were observed through Bielschowsky-dyeing and immunohistochemistry, respectively.RESULTS: The impaired learning ability of the rats in the gingkgolide combined with insulin grouPwas greatly improved compared with that in the grouPtreated with gingkgolide alone( P<0.05).Meanwhile, the expressions of GFAPand NFT in the CA1 area in the gingkgo grouPand gingkgo combined with insulin grouPwere significantly reduced,and even lower in the combined grouPthan in the gingkgo grouP( P<0.05).CONCLUSION: The gingkgolide combined with insulin treatment exerts a stronger improving effect on the learning ability of the AD-like model rats, possibly by reducing phosphorylation of Tau in neurons and inhibiting hyperplasia of the glial cells in the hippocampal CA1 area.
    Effect of tranilast on airway remodeling of experimental COPD rats
    ZHANG Wei, LIN Yong
    2006, 11(11):  1239-1242. 
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    AIM: To observe the effect of tranilast on experimental COPD rats in terms of airway remodeling.METHODS: Forty eight SD rats were divided into two groups in random:untreated model group, tranilast-treated grouP.Another eight rats were selected as control grouP.The COPD rat model was established by passive smoking and intratracheal instillation of lipopolysaccharide( LPS) and then treated with sterile saline or tranilast( 400 mg·kg-1·d-1 ) respectively.Eight rats in each grouPwere killed in 7th, 14th, 28th day after the beginning of proceeding.Bronchoalveolar lavage fluid ( BALF) was collected, and the total and differential cells were counted.The distribution and the ratio of type I to type III collagen in the lung tissue were determined using a sirius red polarizing microscopy morphometry method.Lung tissues were observed by hemotoxylin and eosin stain, then the image analysis were made.RESULTS: The total cells and the AM ratio in BALF of tranilasttreated grouPsignificantly decreased in comparison with those in model grouP( P<0.05) ;compared with control group, model grouPcollagen deposition increased and predominant type Ⅰ collagen presented in 28th day.Type Ⅰ collagen deposition in treated grouPwas lower than that in model grouPbut still higher than that in control grouP.Image analysis suggested that the airway wall thickness,the vessel thickness and the ratio of gland thickness airway wall thickness were significantly smaller than that in model grouP( P<0.05).CONCLUSION: Tranilast can lessen airway remodeling of COPD rat models through decreased the AM and type Ⅰ collagen deposition in the airway.
    Study on antitumor activity of allotri-tridecyl diethylamine in vitro and in vitro
    WANG Rui-xing, HUANG Xun-ru, WU Zhi-juan, LIN Jing, FANG Qiu-juan
    2006, 11(11):  1243-1247. 
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    AIM: To investigate antitumor effect of allotri-tridecyl diethylamine ( D-108) in vivo and in vitro.METHODS: The cytotoxic effects of D-108 on various tumor cell lines, human gingival fibroblast and marrow stromal cell cultured in vitro were determined with trypan blue dye exclusion test and MTT method.The acute toxicity of mice by administration of D-108 was evaluated by Bliss method.At a tolerable dose level, D-108 was administrated to treat transplanted solid tumor U14, and tumor weight inhibition was observed.Apoptosis morphological transformation of HL 60 cell induced by D-108 was detected by the Giemsa staining.RESULTS: The cytotoxic effects in vitro of D-108 on various tumor cell lines ( IC50:0.22 to 2.19 mg·L-1) were more powerful than both human gingival fibroblast and marrow stromal cell ( IC50:5.55 and 3.57 mg·L-1).LD50 of D-108 was 36.49 mg·kg-1 ( mice, i.g.).D-108 inhibited in vivo growth of implanted solid tumor U14 of mice effectually.The inhibition rate of tumor weight of D-108 ( 100mg·kg-1 ·d-1 i.g.) was 45.27 %.HL 60 cell appearance typical apoptosis morphological transformation induced by D-108.CONCLUSION: D-108 had obvious antitumor activity in vivo and in vitro and little toxicity.D-108 could induce the apoptosis of HL 60 cell.
    Protective effect of glycyrrhizin on acute cholestasis induced by alphanaphthylisothiocyanate in rats
    GUO Ji-qiang, DING Yu, LIAO Na, ZHAO Ying, ZHAI De-sheng, YANG Jin-nan, CHEN Xi-jing
    2006, 11(11):  1248-1252. 
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    AIM: To investigate the effects of glycyrrhizin(GL) and dexamethasone( DEX) on alpha-naphthylisothiocyanate( ANIT) induced acute cholestasis in rats.METHODS: Acute cholestasis in rats was induced by ANIT, and the effects of GL and DEX on acute cholestasis were examined by serology determination, histological assessment of hepatic injury and bile excretion experiments.RESULTS: The protection of DEX pretreatment was directed toward cholangiocytes rather than hepatocytes.Rats remedially treated with DEX 3 h after ANIT administration were not resistant to ANIT toxicity.Notably,remedial treatment with DEX 12 h after ANIT enhanced ANIT toxicity.However, GL attenuated both bile duct and hepatocyte damage induced by ANIT in the initial phase of impairment.CONCLUSION: GL exhibited better protection against ANIT-induced acute cholestasis than DEX.In the initial phase of impairment of acute cholestasis, the protection of GL maybe partially due to modifications of metabolism and excretion of ANIT and anti-inflammatory effect.
    Effect of shikonin on angiogenic ability of endothelial cells
    YUAN Ding-fen, DENG Hui, YAN Chun-lin, LIAO Kang-huang
    2006, 11(11):  1253-1255. 
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    AIM: To investigate the effect of shikonin on the endothelial cell and elucidate its anti-angiogenic mechanism.METHODS: MTT assay , cell migration assay and in vitro angiogenesis assay were explored to determine the effect of shikonin on the proliferation , migration and angiogenic ability of endothelial cells respectively.RESULTS: Shikonin can inhibit the angionenesis of endothelial cells in vitro.At 20 μmol·L-1 , the inhibition ratio of the proliferation , migration and angiogenic ability were 38.66 % ±0.05 %, 79.69 % ±0.03 % and 80.95 % ±0.05 % respectively.CONCLUSION: Shikonin can inhibit the angiogenesis through its effect on endothelial cell directly:the suppression of proliferation ,migration , angiogenic ability of endothelial cells.
    AQP4 deficiency alters regulative effects of estrogen on monoamine neurotransmitters
    LI Ping, ZHANG Jing, GAO Lin, FAN Yi, SUN Xiu-lan, DING Jian-hua, HU Gang
    2006, 11(11):  1256-1260. 
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    AIM: To investigate whether aquaporin-4(AQP4)participates in the regulative action of estrogen on neurotransmitters (NT).METHODS: The monoamine neurotransmitters were determined by high performance liquid chromatography (HPLC)in different brain regions of male AQP4-knockout CD1 mice and wild-type CD1 mice after they were intraperitoneally injected with different doses of estradiol.RESULTS: The contents of DA and 5-HT in the striatum and NE in the cortex of AQP4-knockout CD1 were significantly increased , and the concentrations of NE in the hippocampus and DA in the hypothalamus were decreased.Treatment with estradiol increased the contents of DA and 5-HT in the striatum and that of 5-HT in the hippocampus , decreased the levels of DA and 5-HT in the cerebrum, and also reduced the concentrations of DA and NE in the hypothalamus in wildtype mice.However , these changes were not found in AQP4-knockout mice.CONCLUSION: The deficiency of AQP4 in mice alters the regulative effects of estrogen on monoamine neurotransmitters , indicating that AQP4 participates in regulating metabolism of neurotransmitters.
    Screening potassium channel blocker with FRET-bases voltage sensor probes
    SUN Li-xin, LIAO Hong, YAN Ming, MA Yi-na, ZHANG Lu-yong
    2006, 11(11):  1261-1264. 
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    AIM: To establish high-throughput potassium channel assay using FRET-based voltage sensor probes (VSPs).METHODS: RBL-2H3 Cells , which endogenously express high level Kir channels , were loaded with CC2-DMPE and DiSBAC2(3).The fluorescence response ratio of 460 and 570 nm before and after addition of high K+ was then detected.The response ratio can be used to evaluate membrane potential changes.RESULTS: The assay is robust as indicated by a Z' factor larger than0.6.The throughput is in the range of 10 000 data points per day , which is significantly higher than many other methods presently available for potassium channel.In 102 compounds screened with VSPs , 11 compounds were found to change the fluorescence ratio dosedependently.CONCLUSION: The assay allows semiautomated screening of compounds for potassium channel activity on 384-well plates and is sufficiently rapid for testing a large number of compounds.
    Study on transport of 5-aminosalicylate in Caco-2, L-MDR1 and MRP2 cell monolayers
    XIN Hua-wen, Schwab Matthias, Klotz Ulrich
    2006, 11(11):  1265-1269. 
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    AIM: To investigate whether P-glycoprotein andMRP2 are involved in transport of 5-aminosalicylate( 5-ASA).METHODS: Permeability coefficients and transport rates of 5-ASA across Caco-2, L-MDR1 and MRP2 monolayers were measured.Trans epithelial transport of digoxin across Caco-2 monolayer with addition of 5-ASA was also studied.RESULTS: No differences of permeability coefficients and transport rates of 5-ASA at 5, 50 and 500 μmol·L-1between basal-to-apical and apical-to-basal direction were measurable across Caco-2,L-MDR1 and MRP2 monolayers ( P>0.05).Compared with control experiments, no significant differences were observed in basal-to-apical net transport and PapPof digoxin( 5 μmol·L-1) in the presence of 5-ASA ( 50μmol·L-1 -5 mmol·L-1) ( P>0.05).CONCLUSION: 5-ASA can not be regarded as a substrate of P-gPor MRP2.Inhibition or induction of P-glycoprotein by 5-ASA could be excluded.Further studies are needed to identify the nature of the involved active carrier system( s)in intestinal secretion of 5-ASA.
    Effect of simvastatin on non-neuronal M cholinoceptor of rabbit aorta endothelium with hyperlipemia
    LI Jun, WANG Qian, WANG Ru-huan, LONG Chao-liang, WANG Hai
    2006, 11(11):  1270-1274. 
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    AIM: To investigate the effect of simvastatin on non-neuronal M3 mRNA expression of rabbit aorta with hyperlipemia.METHODS: Hype rlipemia rabbit model was induced by high lipid diet.The simvastatin grouPwas treated with 5 mg·kg-1 everyday for 15 weeks.Endothelium dependent relaxation responses to acetylcholine( ACh) and non-endothelium dependent relaxation responses to nitroprusside ( SNP) of thoracic aortic rings were measured respectively.The M3 mRNA expression of aorta endothelium were tested by RT-PCR.RESULTS: Compared with the hyperlipemia group, simvastatin treatment significantly degraded the plasma lipid concentration,attenuated the inhibition of endothelium dependent relaxation induced by hyperlipemia and improved the mRNA expression of M3 in aorta endothelium.CONCLUSION: Simvastatin can reverse M3 mRNA expression of aorta endothelium reduced by hyperlipemia and improve the vasodilatory activity.
    Effect of triptolide on proliferation and apoptosis in A549 lung cancer cell
    SONG Lan, XU Zhao-jun, ZHANG Cai-ping, QIAO Xin-hui
    2006, 11(11):  1275-1278. 
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    AIM: To study the effect of triptolide on cell proliferation and apoptosis in A549 human lung cancer cell.METHODS: The effect of triptolide on cell viability in A549 cell was evaluated by MTT assay.Cell apoptosis was observed by flow cytometry and DNA ladder analysis.Activities of caspase-9 and caspase-3 were assayed with caspase colorimetric assay kit.RESULTS: Triptolide( eg., 0.5 -4.0 μg·ml-1)inhibited cell growth and induced apoptosis in a dose-dependent way at 24 h in A549 cells.The activation of caspase-9 and caspase-3 was significantly increased at 24 h in A549 cells when exposed to triptolide ( eg., 0.5 -4.0 μg·ml-1).CONCLUSION: Triptolide induces apoptosis in A549 cells partly through mitochondrial signal transduction pathway.
    Analysis on therapeutic effect of letrozole on abnormal ovulation
    LI Ping, RUAN Xiao-hong, GUO Jiang-hua, CHEN Xiao-yan, DENG Ai-min
    2006, 11(11):  1279-1284. 
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    AIM: To investigate and compare the therapeutic effect of letrozole on abnormal ovulation, and to investigate its indication and side effect.METHODS: 313 cases of abnormal ovulation who were treated for 871 treatment cycles were divided into 4 groups:anovulia without PCOS grouP( A) , PCOS grouP( B) , ovule ovulation( C) and LUFS ( D).They took letrozole 2.5 mg q.d.×5 d from menstruation stage 5th day and added HMG later.They were injected HCG 1 000 IU when average diameter of dominant follicle ≥18 μm or LH( +) in urine.The ovulation rates, pregnancy rates and abortion rates were compared among 4 groups.RESULTS: There were several cycles canceled in PCOS grouP( B) because there was OHSS or no dominant follicle.Dominant follicles rates were lower in grouPB than others.MFD was shorter in grouPC than others.The amount of MFD ≥15mm was more in grouPB than others.Pregnancy rates were higher for sinus ovarian follicle ≤8/side and less for MFD ≥15 mm.Early abortion rate was the highest in grouPC.All patients had bradymenorrhea, with 7 cycles in some patients having light gastrointestinal side effect.CONCLUSION: Letrozole can treat abnormal ovulation such as anovulia without PCOS.PCOS and LUFS can not improve the follicular development of ovule ovulation.The amount of sinus ovarian follicle before stimulated follicle can predict the sensitiveness of letrozole for PCOS.The time of stimulating follicle was best for 7 -13 days.There was slight side effect for letrozole.
    Effect of resveratrol on peripheral blood mononuclear cells oxidative DNA damage in type 2 diabetes mellitus patients in vitro
    JIANG Zhong, TANG Xu-lei
    2006, 11(11):  1285-1290. 
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    AIM: To explore the oxidant-antioxidant status and levels of mononuclear cells ( PBMCs) oxdative DNA damage in patients with type 2 diabetes mellitus( T2DM) , and to value the effect of resveratrol on peripheral blood mononuclear cells oxidative DNA damage in T2DM patients in vitro.METHODS: The DNA damages in PBMCs of 39 T2DM patients with vascular complication,and 29 T2DM patients without complication were detected by single cell gel electrophoresis ( the comet percentage).The levels of plasma total antioxidative capacity(TAC) , the contents of plasma malondialdehyde (MDA) and plasma thiol grouP( SH) were measured.The effect of resveratrol on DNA damage of T2DM patients were investigated in vitro.In addition, 26 healthy subjects were studied as a control grouP.RESULTS: The comet percentage of PBMCs and the contents of plasma MDA in T2DM patients without complication were all significantly higher than that in healthy controls ( P<0.01).The levels of plasma TAC and the contents of plasma thiol grouPin T2DM patients without complication were all remarkably lower than that in healthy controls ( all P<0.01).The comet percentage of PBMCs and the contents of plasma MDA in T2DM patients without complication were significantly lower than that in T2DM patients with vascular complication( P<0.05) , and the levels of plasma TAC in T2DM patients without complication were significantly higher than that in T2DM patients with vascular complication( P<0.05).There were positively correlations between the comet percentage of PBMCs and the contents of plasma MDA in T2DM patients without complication and T2DM patients with vascular complication( r =0.446, P<0.05 ;r =0.504, P<0.01) ;and there were nega-tively correlations between the comet percentage of PBMCs and the contents of plasma TAC in the two groups( r =-0.418, P<0.05 ;r =-0.399, P<0.05).The comet percentage of PBMCs of patients were reduced by 10μmol·L-1 resveratrol at 4 hours in vitro ( P<0.05).CONCLUSION: There are oxidant-antioxidant unbalance and oxidative DNA damage in T2DM patients, particularly in the patients with vascular complication.Oxidative stress is probably involved in pathogenesis of diabetic vascular complication.Resveratrol can reduce the oxdative DNA damage of PBMCs in patients with T2DM in vitro.Antioxidants supplementation may benefit the prevention of diabetic vascular complication.
    Effect of L-arginine on cardiac injury induced by adriamycin in rats
    SUN Sheng-tao, XU Yi-qun, WANG Yi-lin, PAN Xiao, ZHANG Qing-biao, ZHAO Hong-xiang, YANG Guan-ming
    2006, 11(11):  1291-1295. 
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    AIM: From the level of molecule, to study the effect of L-arginine ( L-Arg) on cardiac injury induced by adriamycin (ADM) in rats, and to explore the mechanism of increased content of nitric oxide (NO) with reduced activities of superoxide dismutase ( SOD) and glutathione peroxidase ( GPx).METHODS: Thirty-two Sprague-Dawley rats were randomly divided into four groups ( n =8, each):Control group, L-Arg group,ADM treated grouPand ADM combined with L-Arg grouP.Using biochemistry technique, we determined the contents of associated substance and activities of enzyme.Reverse transcription-polymerase chain reaction ( RTPCR) was used to analyze the expression of associated gene.RESULTS: Compared with ADM treated group, in ADM combined with L-Arg treated group, contents of malondialdehyde(MDA) and nitric oxide ( NO) in myocardium and activity of creatine kinase isoenzymic MB ( CKMB)in serum were significantly increased ( P<0.01).However, expressive levels of copper-zinc superoxide dismutase( Cu-Zn SOD) mRNA, manganese superoxide dismutase( Mn SOD) mRNA, GPxmRNA and activities of Mn SOD, Cu-Zn SOD and GPx were significantly reduced( P<0.01).CONCLUSION: L-Arg intensified cardiac injure.The mechanism may be related to increasing the content of NO in myocardium induced by ADM, and then NO intensified the reduced expressive levels of Mn SOD mRNA, Cu-Zn SOD mRNA and GPx mRNA induced by ADM, thereby intensified the reduced activities of Mn SOD, Cu-Zn SOD and GPx, resulting in intensified cardiac injure caused by the increased reactive oxygen species.
    Characteristics of sleep-wake cycles in mice lacking prostanoid DPreceptors
    MA Zhang-qing, HONG Zong-yuan
    2006, 11(11):  1296-1300. 
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    AIM: To investigate the effect of prostanoid DPreceptors ( DPR) on sleep-wake regulation in mice.METHODS: Under pentobarbital anesthesia,mice were chronically implanted with electroencephalogram( EEG) and electromyogram ( EMG) electrodes for polysomnographic recordings.The spontaneous sleep-wake cycles were monitored continuously by EEG/EMG recording system for 24 h beginning at 8 ∶; 00 P.m.and analyzed by SLEEPSIGN software in DPR knock out ( KO)and wild type (WT) mice.RESULTS: DPR-KO mice exhibited a similar circadian rhythm of sleep-wake cycles to WT mice.The amounts of rapid eye movement ( REM)sleePor non-REM ( NREM) sleePduring both the light and dark periods were identical between the DPR-KO and WT mice.Whereas, an increase in the episode number of wakefulness and a shortage in the duration of NREM sleePwere found in DPR-KO mice during the light period compared with WT mice.Moreover, DPR-KO mice showed lower activity in delta-wave component in NREM sleePand higher activity in theta-wave component in REM sleePthan WT mice.CONCLUSION: DPR plays a crucial role in mediating the prostaglandin D2-induced sleeP.Deficiency of DPR results in the low intensity and fragmented diurnal NREM sleePand the high vigilance REM sleep,with the normal circadian rhythm of sleePin mice.
    Use siRNA targeting gene c-Myc to inhibit cellular proliferation in human rectal cancer Colo320 cell line
    HUANG Hao, TU Xin, YU Nan-cai, LIU Qian, YI Yang-dong, MA Wei
    2006, 11(11):  1301-1304. 
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    AIM: To inhibit c-Myc gene expression in human rectal cancer cell line Colo320 by small interfering RNA ( siRNA) , and to provide a new method to study the role of c-Myc in Colo320 cell.METHODS: The c-Myc gene specific siRNA was designed according to its sequence and made by in vitro transcription.The c-Myc siRNA was transfected into Colo320 cell, and the cell was cultured for 48 to 96 hours before harvesting.c-Myc mRNA and protein level were monitored by using fluorescence real time reverse transcription polymerase chain reaction.Cellular proliferation activities were assayed by tetrazolium bromide (MTT) colorimetry and clone test.RESULTS: Compared with control group, there was a significant decrease in the c-Myc mRNA.Colo320 cells transfected with c-Myc siRNA had lower cellular proliferation than no-transfected Colo320 cells.CONCLUSION: Our results suggest that there exist RNA interference mechanism in Colo320 cell line, and the c-Myc siRNA can specifically inhibit the expression of c-Myc gene in Colo320 cells.RNA interference method provides a new way to study the role of c-Myc in cancer cell.
    Analysis of factors affecting on adverse drug reactions in 122 cases
    ZHAN San-hua, YUAN Kong-xian, LI Guo-zhong
    2006, 11(11):  1305-1308. 
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    AIM:To analyze factors affecting on adverse drug reactions ( ADRs) in 122 cases, in order to avoid and reduce occurrence of ADRs.METHODS: The cases of ADRs by the pharmacist and the clinical reports were collected, and then counted uPand analyzed.RESULTS: In 122 cases of ADRs, there were 11 severe cases, the others are ordinary.The most common clinical displays of ADRs were the lesion of skin and the append ants ( 50.82 %) , followed by the lesion of digestive system( 20.49 %) and nervous system responses( 18.03 %).Anti-infective drugs showed the highest proportion of ADRs, accounting for 61.48 % of the total.The affected patients ranged in age over 50 years( 34.42 %) and low age ( 21.32 %).The most of ADRs were induced by IV droP( 91.96 %).CONLUSION:For the child and the old man crowd clinical doctors must be prudent with the medicine, avoiding the unreasonable combination of the medications, use the anti-infective drugs reasonably and strengthen monitoring of its use, in order to reduce occurrence of ADRs.
    Plasma level of circulating endothelial cells in patients with early diabetic nephropathy and interventional treatment of ginkgo-damole injection
    HUANG Jing-ze, QIU Xiao-ping, WANG Jian
    2006, 11(11):  1309-1312. 
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    AIM: This study was undertaken to explore the relationshiPbetween urinary albumin excretion rate ( UAER) and plasma level of circulating endothelial cells( CEC) in patients with early diabetic nephropathy( EDN) and the interventional role of ginkgo-damole injection(GDI) on development of UAER in patients with EDN.METHODS: UAER and plasma level of CEC were measured in 65 cases with type 2 diabetes mellitus,and the relationshiPbetween them was analyzed.45 cases with diabetic nephropathy whose value of UAER is 30 -300 mg·d-1 were randomly divided into two groups.The 22 patients in the control grouPwere treated by routine method including decreasing blood sugar and controlling blood pressure.The 23 patients in the treated grouPwere treated with GDI 20 ml per day by intravenous dripping,with 2 weeks as one therapeutic course.The blood sugar,blood pressure, UAER and CEC in the two groups were observed and compared.RESULTS: Plasma level of CEC was markedly elevated in patients without albuminuria( SDM group) and patients with trace albuminuria( EDN group) when compared to the grouPof normal controls( NC group) ( P<0.01) , and plasma level of CEC in EDN grouPwas significantly higher than that in SDM( P<0.01).There was significant positive correlation between UAER and systolic blood pressure ( SBP) as well as CEC level ( P<0.01).After treatment with GDI,UAER and CEC level were obviously decreased in EDN grouP( P<0.01).There was significant positive correlation between change of UAER and that of CEC level ( P<0.001).However, those in the control grouPwere little changed.CONCLUSION: VEC injury may play an important role in the pathogenesis of diabetic nephropathy.GDI has protective function on early diabetic nephropathy by preventing VEC from being damaged.
    RelationshiPof plasma risperidone concentration and the efficacy in treatment of first-episode schizophrenia after a middle or low dosage risperidone adminstration
    WEI Chuan-mei, LIU Hui, GUO Rui-chen, FU Chong-ming
    2006, 11(11):  1313-1316. 
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    AIM: To study the efficacy and side effects of both middle and low doses of risperidone in the treatment of first-episode schizophrenia, and to investigate the relationshiPbetween plasma concentration of RSP, 9-OH-RSPand the efficacy or side effects occurred during RSPtreatment.METHODS: Compared the patients treated with middle dosage of risperidone ( groupB, 40 cases) and the other 42 cases ( groupA) that are treated with very low dosage of risperidone.RESULTS: Two groups were in statistical difference ( P<0.05) by itself.But there were no significant difference between grouPA and grouPB ( P<0.05).GrouPA took effect later than grouPB.Total scores of the treatment emergent symptom scale ( TESS) were significantly lower in grouPA than in grouPB.The plasma concentration of 9-OH-RSPand the active moiety ( RSP+9-OH-RSP) after one week' s administration of risperidone were higher in grouPB than that in grouPA ( P<0.05).CONCLUSION: This assay suggested that low dosage of risperidone is effective,safe and beneficial in the treatment of first-episode schizophrenia.
    Approach of compensation to subjects' impairment in clinical drug trial ( II)
    LIANG Wei-xiong
    2006, 11(11):  1317-1320. 
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    This issue analyzes the existing problems of the compensation to the subjects' impairment during clinical drug trial nowadays, giving discussion to the subjects of general principles of subjects' impairment compensation,the determination of compensation standard and the general procedure of compensation.