Antisense drug targeting with VEGF mRNA designed by computer aid and inhibitory effects on K562 cell line in vitro     

FEI Jia  ZHANG Huan 《园艺学报》2003,19(5):645-648

AIM:The effective antisense sequences targeted VEGF mRNA with computer software would be screened and designed, and effect of them on growth K562 cells and protein expression of VEGF were studied with experiments.METHODS:Seven antisense sequences were selected and synthesized, which consisted of 18-20 deoxynucleotide acid and were modified with phosphorothioate, according to principle of low free energy of overall △G₃₇ Overall. Cell growth was assayed by trypan blue dye exclusion assay and level of VEGF protien in the media was determined by ELISA.RESULTS:Six of seven sequences were capable of inhibing growth of K562 cells and downregulating the VEGF protein expression significantly, compared with Scrambed control group. It was found that there was a close correlation between low level of overall △G₃₇ and antisense effectiveness (r=0.887,P<0.01).CONCLUSION:VEGF mRNA antisense oliogdeoxynucleotides, which were designed by computer software of RNAstructure, were able to inhibit growth of K562 and its protein expression. The VEGF mRNA may be new target attached by drugs. At same time, the computer aided design is useful methods to obtain the effective antisense.  相似文献   

杂草对灭生性除草剂百草枯的抗性问题   总被引：4，自引：0，他引：4  

张宏军  贾富勤  张佳  李晓晶 《农药科学与管理》2003,24(12):26-29

本文综述了百草枯抗性杂草的发生、发展情况以及抗性机理方面的报道，并就抗性杂草的治理提出几点建议。  相似文献   

Inhibitory effects of LDL-ACM complex on subcutaneous implanted tumors in nude mice()     

JIANG An-li  KANG Lu-dong  ZHAO Chun-hua  BI Wen-xiang  HU Xiao-yan  KONG Feng  XU Song-de 《园艺学报》2003,19(1):55-58

AIM: In order to evaluate the applicable value of LDL as a targeted vehicle for chemotherapeutic agents, we investigated and compared the inhibitory effects of LDL-ACM complex and free ACM on nude mice's subcutaneous implanted tumors derived from gastric cancer cell lines, SGC-7901 and NKM-45. METHODS: LDL-ACM complex was prepared and the tumor model of nude mice was established by subcutaneous implantation of SGC-7901 and NKM-45. Then, the groups of nude mice developed subcutaneous implanted tumors were received either LDL-ACM complex or free ACM. Subsequently, the tumor size, weight and leukemia cell counts were measured and the rates of tumor-inhibition and the survival were compared among the groups. RESULTS: The inhibitory effects of LDL-ACM complex on the tumors, especially on SGC-7901 implanted tumors were much more obvious than that of free ACM. It was also indicated that the action of LDL-ACM complex was mediated by LDL receptor. CONCLUSION: These results showed that LDL-ACM complex had significant inhibitory effects on the implanted tumors and the effect might be mediated by LDL receptor.  相似文献   

The mechanisms of pathophysiological vasodilation or vascular hyporesponse     

KAI Li  HU De-yao  LIU Liang-ming 《园艺学报》2003,19(1):130-133

In some pathophysiological processes such as severe shock, the patients and animal experimental models fail to respond to pressor medicine. Vascular hyporesponse or vasodilation is one of the key problems in treatment of these patents. Although considerable progress had been made in recent years, the precise mechanisms of vascular contractile hyporeactivity have not been completely elucidated. A number of studies indicate that vascular hyporesponse or vasodilation correlate with many factors. In this review, the possible mechanisms about vascular hyporesponse or vasodilation during shock and other pathphysiolgoical processes were discussed.  相似文献   

Effect of hemin on the expression of heme oxygenase-1 in rat vascular smooth muscle cells     

HU Chang-xing  MA Ye-xin  FU Du-guan  REN Peng 《园艺学报》2003,19(11):1493-1496

  相似文献   

Rat urotensin-II-induced main pulmonary artery contractions are mediated by MAPK     

CHEN Shao-xian  XUE Bi-cheng  GONG Yong-sheng  FAN Xiao-fang  HU Liang-gang  CHEN Yan-fan  WANG Liang-xing 《园艺学报》2003,19(10):1365-1368

AIM: To investigate rat Urotensin-II(rat U-II)-induced vasoconstriction of rat main pulmonary arteries and the role of mitogen-activated protein kinase(MAPK). METHODS: The main pulmonary artery was dissected from the male Sprague-Dawley rats and artery ring width was 3-4 mm. Concentration-response curves were generated to rat U-II(0.03 nmol/L-30 nmol/L).Inhibitor of MAPK, PD 98059(0.1 μmol/L-10 μmol/L) were added into the medium after rat U-II(30 nmol/L)induced vasoconstriction had reached plateau to construct the relaxant concentration-response curves and their EC₅₀ and E_max. RESULTS：Rat U-II was a potent vasoconstrictor of isolated rat main pulmonary arteries [EC₅₀=7.95±0.40, E_max=(14.28±6.34)% of the response to 60 mmol/L KCl]; PD 98059 caused concentration-dependent relaxations of rat U-II precontracted arteries [EC₅₀=5.91±0.45, E_max=(81.39±13.65)%]. CONCLUSION: Rat U-II was a potent vasoconstrictor of rat main pulmonary arteries and this response was mediated through MAPK.  相似文献   

库布齐沙漠穿沙公路沙害综合防治技术   总被引：20，自引：4，他引：20  

胡春元  杨茂  杨存良  刘永茂  蒋有则  张润焕 《干旱区资源与环境》2002,16(3):71-77

库布齐穿沙公路修建在库布齐沙漠高大的流动沙丘区 ,风沙流侵袭与沙丘整体前移埋压公路是主要沙害形式。现有防沙措施是沙障保护下的人工植被及天然植被相结合的综合防护体系 ,固沙及阻沙效益明显。目前要解决的是尽快形成公路两侧稳定的植被群落 ,以保证公路的长期畅通  相似文献   

组氨醇脱氢酶抑制剂的研究动态     

胡利明  李学恕  刘钊杰 《农药学学报》2002,4(3):1-5

组氨醇脱氢酶(HDH)是组氨酸生物合成过程中最后两步反应的催化酶。对组氨醇脱氢酶的结构、催化机理、组氨醇脱氢酶抑制剂等方面的研究动态进行了较为详细的综述。  相似文献   

1-(1-苯基-1,2,4-三氮唑-3-氧代乙酰氧基)烃基膦酸酯的合成与植物生长调节活性   总被引：1，自引：0，他引：1  

贺红武  孟利平  胡利明  刘钊杰 《农药学学报》2002,4(3):14-18

合成了一系列新的1-(1-苯基-1, 2, 4-三氮唑-3-氧代乙酰氧基) 烃基膦酸酯, 并测定了它们对小麦和黄瓜的植物生长调节活性。结果表明, 在100 Lg/g 时, 所有化合物对小麦芽鞘的生长具有抑制作用, 而在10 Lg/g时化合物6a、6g 对黄瓜显示了较高的促生长活性。  相似文献   

新型取代氨基(或芳氧)磺酰基苯氧丙酸酯的合成及其除草活性   总被引：3，自引：0，他引：3  

胡方中  吕凯  任雪玲  陈彬 《农药学学报》2002,4(4):17-22

由α-苯氧基丙酸酯出发,合成了取代氨基(或芳氧)磺酰基苯氧丙酸酯,并测定了它们的除草活性。所有的化合物均经1H NMR和元素分析确证,初步的生测结果表明上述化合物具有一定的除草活性。  相似文献