Analysis of gene expression profile of multidrug resistant MCF/DOX cell line after benflumetol derivative LY980503 treatment

AIM:To investigate the effect of LY980503(a benflumetol derivative)on multidrug resistance of tumor cell line using DNA microarray.METHODS:Total RNA was extracted from multidrug resistant MCF/DOX cell line. cDNA microarray containing 320 cDNAs was used to detect the gene expression profile.RESULTS:9 down-regulated genes and 1 up-regulated gene were identified after multidrug resistant MCF/DOX cells were treated with LY980503.CONCLUSION:LY980503 can effectively reverse the resistance of MCF/DOX to DOX in vitro by adjusting the expression of multi-genes.     

Bcl-2 antisense oligodeoxynucleotide increases the sensitivity of HL60 and K562 cells to daunorubicin

AIM:To investigate whether the bcl-2 antisense oligonucleotide increases the sensitivity of HL60 and K562 cell lines to daunorubicin.METHODS:IC50 for HL60 and K562 was determined with MTT method, the expression levels of Bcl-2 protein were assayed by immunofluorescence using fluoresce isothiocyanate labeling. In addition, apoptosis was detected by morphological observation and flow cytometric analysis of DNA fragmentation.RESULTS:It was found that the two oligonucleotides directed against the coding region and the translation initiation of bcl-2 mRNA, combined respectively with daunorubicin, inhibited expression of bcl-2 protein, increased apoptosis in HL60 and K562 cells, and decreased IC50 of daunorubicin significantly (P＜0.05). Compared to the antisense oligonucleotide directed against the translation initiation of bcl-2 mRNA, the antisense oligonucleotide directed against the coding region showed stronger effects in the aspects of increasing the sensitivity of HL60 cells to daunorubicin (P＜0.05).CONCLUSIONS:These two antisense sequences in the translation initiation and the coding region of bcl-2 mRNA increased the sensitivity of HL60 and K562 cell lines to daunorubicin in a sequence-specific manner.     

Effect of antifibrotic herb serum on rat hepatic stellate cell proliferation and collagen synthesis

AIM: To investigate the effect of Chinese herbs, Ganxianfang(GXF), on rat hepatic stellate cells (HSC) proliferation and collagen synthesis. METHODS: Two types of herb serum, portal venous serum and circumferential venous serum, were prepared from rats infused intragastrically with 16, 8, 4 times adult dose of GXF decoction. HSC isolated from rat liver were processed with the above sera in vitro. Then we mensurated the radioactivity of HSC admixed with [[³H]H]proline and [[³H]H]thymine to judge the effect on proliferation and collagen synthesis of HSC. RESULTS: Both two types of serum collected 0.5, 1, 2 h after intragastrical infusion inhibited HSC proliferation (P＜0.05), and the serum collected 1 h after intragastrical infusion had the strongest effect (P＜0.05). Portal serum decreasea collagen synthesis (P＜0.05), but circumferential serum had no effect (P＞0.05). CONCLUSION: Inhibition of HSC proliferation and decrease of collagen synthesis may contribute to the GXF antifibrotic action.     

中国和欧盟动物源性产品中药物残留限量差异性分析(一)

将中国和欧盟动物源性产品中药物残留标准进行了对比,同时结合TBT/SPS预警数据库,找出二者差异性,并提出了改进建议。     

副猪嗜血杆菌病病原的分离鉴定与药敏试验

对1例临床、病理剖检症状疑似副猪嗜血杆菌病进行实验室诊断,最后确诊其病原为副猪嗜血杆菌。经药敏试验显示,副猪嗜血杆菌对氨苄青霉素、卡那霉素、庆大霉素等药物敏感。     

江苏地区小麦赤霉病菌种群检测与抗药性分析

本研究旨在检测江苏地区小麦赤霉病菌的种群组成与对传统杀菌剂单剂的抗性严重度。以江苏溧阳、通州和盐城地区小麦赤霉病菌子囊孢子为试材,鉴定其优势种群,检测对多菌灵、戊唑醇和咪鲜胺的抗性。结果表明：江苏地区小麦赤霉病菌株中全部检测到亚细亚镰孢,是绝对优势种群;禾谷镰孢占比最高是溧阳地区的14%,最低是通州地区的8%,平均占比为11.33%,显著低于亚细亚镰孢占比;江苏地区小麦赤霉病菌对多菌灵的抗性频率介于26.3%~54.5%;未检测到戊唑醇和咪鲜胺具有抗性的赤霉菌株。综上,江苏地区小麦赤霉病菌优势种群是亚细亚镰孢,其对多菌灵单剂已产生严重抗性,未发现对戊唑醇和咪鲜胺产生抗性。     

莫桑比克鳗鲡养殖生物学主要特性研究

对莫桑比克鳗鲡（Anguillamor morata）玻璃鳗经形态学鉴定品种后,开展了主要养殖生物学特性研究。耐受高温和低温分别为39℃和7℃,适宜生存水温15℃～33℃;耐受盐度与水温相关,水温30℃致死盐度2．9％,适宜盐度小于1．1％,20℃致死盐度2．7％,适宜盐度小于1．8％,10℃致死盐度2．1％,适宜盐度小于2．0％;耐受pH值与水温相关,30℃致死pH值分别为3．5和11．0,适宜pH值6．0—7．0,20℃致死pH值分别为4．0和11．0,适宜pH值6．0～8．0,10℃致死pH值分别为3．5和10．5,适宜pH值5．5—8．5。常用药物S高聚碘、二氧化氯、三氯异氰尿酸、苯扎溴铵、溴氯海因、甲醛、敌百虫的安全浓度高于或接近常用浓度,硫酸铜、溴氰菊脂乳油、氯氰菊脂、甲苯咪唑的安全浓度低于常用浓度。水体中非离子态氨的安全浓度为2．51mg／L,亚硝酸氮的安全浓度为55．12mg／L。     

动物源性食品中尼卡巴嗪残留量的测定

动物产品中的尼卡巴嗪药物残留已被我国及美国、日本、欧盟等国家和地区列为重点检测内容,其最大残留量为0．01mg／kg-0．2mg／kg不等。为探讨合适的检测方法,本文对国内外相关尼卡巴嗪的分析检测方法的优缺点做了分析和比较,并重点介绍了动物源性食品中尼卡巴嗪残留量检测的高效液相色谱法（HPLC）和高效液相色谱-质谱联用（HPLC-MS）法。运用这两种方法进行检测,其最低检测限可达到10μg／kg甚至0．5μg／kg,基本上符合现有相关标准的限量要求。     

一株感染深水网箱养殖许氏平鲉的病原菌分离与鉴定

2016年7月,山东省长岛县深水网箱养殖许氏平鲉(Sebastes schlegeli)暴发严重皮肤溃疡症。作者对病鱼进行病原菌分离。通过形态学观察、常规生理生化试验、gyrB和16S rDNA基因克隆测序等方法对分离菌株进行鉴定。在病灶溃疡处分离到一株绝对优势菌BZ01,该菌株在TSB固体培养基上呈半透明菌落,在TCBS选择性培养基上菌落呈绿色。透射电镜观察为短棒状,具有单根极生鞭毛。人工回接感染证明,该菌株对许氏平鲉具有较强的致病力,可以引起皮肤溃疡等症状,且与自然感染症状一致,其LD₅₀为2.07×10~6 CFU/ml。通过gyrB和16S rDNA基因序列测定并构建系统发育树显示,菌株BZ01与弧菌属同源性最高,并在系统发育树中与轮虫弧菌(Vibrio rotiferianus)聚为一枝,结合形态及生理生化表型测定结果,将该菌株鉴定为轮虫弧菌(V.rotiferianus)。药敏试验结果显示,该菌株对四环素类、喹诺酮类、香豆素类、肽酰转移酶类高度敏感,而对大环内酯类、多肽类、磺胺类、β-内酰胺类、氨基糖苷类中度敏感或不敏感。     

Reversing effect of naringin on cisplatin resistance in human lung cancer A549/DDP cells

AIM: To investigate the effect of naringin (NRG) on cisplatin (DDP) resistance in human lung cancer A549/DDP cells and its possible mechanism. METHODS: A549/DDP cells were cultured in vitro and treated with NRG and/or DDP at different concentrations for 24 h, and then the cell viability were measured by CCK-8 assay. The combination index (CI) of NRG and DDP were analyzed by Chou-Talalay method. The apoptosis rate was analyzed by flow cytometry. Western blot was performed to detect the protein levels of P-glycoprotein (P-gp), multidrug resistance-associated protein 1 (MRP1), p-Akt, CXC chemokine receptor 4 (CXCR4), cleaved caspase-3, Bcl-2 and Bax.RESULTS: The protein levels of P-gp, MRP1, p-Akt and CXCR4 in the A549/DDP cells were higher than those in the A549 cells (P<0.05). The cell viability was remarkably reduced in a dose-dependent manner when A549/DDP cells were exposed to NRG and/or DDP (P<0.05), and the IC₅₀ values of NRG and DDP were 36.92 μmol/L and 129.77 μmol/L, respectively. When the inhibition rate exceeded 15%, NRG in combination with DDP produced a synergistic effect (CI<1). Combination treatment with NRG and DDP significantly induced apoptosis (P<0.05), up-regulated the protein levels of cleaved caspase-3 and Bax, and down-regulated the protein level of Bcl-2 (P<0.05). Meanwhile, NRG remarkably down-regulated the protein levels of P-gp, MRP1, p-Akt and CXCR4 in a dose-dependent manner (P<0.05). CONCLUSION: NRG may enhance the sensibility of A549/DDP cells to DDP most likely via up-regulating the protein level of Bax and down-regulating the protein levels of Bcl-2, P-gp, MRP1, p-Akt and CXCR4.