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41.
Z M Huang D Thewke Q Q Gong D Schlichter W D Wicks 《Brain research. Molecular brain research》1991,11(3-4):309-319
Transient transfection of pLB2CAT constructs bearing short synthetic oligonucleotides derived either from the tyrosine hydroxylase (TH) promoter or other sources was used to examine functional cAMP regulatory element (CRE) activity in a variety of cell lines. The region containing only the putative TH CRE was found to be as or more effective in conferring cAMP responsiveness onto pLB2CAT (which employs the TK promoter) than the immediate 272 bp region of the TH promoter. Increases in CAT activity of 10- to 20-fold were observed in JEG-3 cells with a single insert of the TH CRE region (-31 to -54) in pLB2CAT, and the presence of a second insert generated only a modest further increase. This construct also responded to cAMP in 4 other cell lines tested but the degree of increase was less dramatic. Inserts containing the consensus 8 bp CRE motif embedded in other natural or artificial contexts served generally as weak functional CREs in all cell lines tested. In vitro analysis revealed that a specific protein-DNA complex apparently containing a single protein with a MW of 45-50 kDa was formed equally well with JEG-3 cell nuclear extract and CRE-bearing-TH and other fragments which produced dramatically different cAMP effects in vivo. These results suggest specificity in the effects of cAMP on different CREs which are dictated by contextual differences. 相似文献
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目的 对胸腰段脊柱脊髓,马尾神经损伤患者的外科治疗及几种内固定方法的疗效进行探讨。方法 对166例患者的治疗进行回顾分析。该组患者中椎体爆裂性骨折37例,椎体压缩骨折超二分之一109例,椎体骨折脱位14例,多节段或跳跃骨折6例,脊髓损伤按Frankel分级,A级59例,B级46例,C级42例,D级19例,治疗采用后路减压复位122例,前路减压复位,髂骨植骨融合44例。结果 术后123例获3-18个月随访,随访患者中随4例RF钉断裂,5例Harrington上钩脱落,6例棍断裂,其余患者内固定稳固,脊髓,马尾神经恢复,除35例仍为A级外,余脊髓神经功能恢复1-3个级别。结论 各种不同内固定可保持或增强脊柱的稳定,胸腰段脊柱脊髓损伤的外科治疗应根据骨折类型,脊髓及马尾神经损伤程度选择手术入路及内固定材料。 相似文献
45.
选择性环氧化酶—2抑制剂的研究现状及应用评价 总被引:3,自引:1,他引:2
选择性环氧化酶(COX)-2抑制剂可有效地治疗炎症,同时避免或减轻由于抑制COX-1而导致的毒副作用。有乐观的临床应用前景,但其不良反应亦不容忽视,寻找临床评价好的选择性COX-2抑制剂是当前非甾体类抗类药物研究的重点。 相似文献
46.
The effects of intracellular Ca2+ (Ca2+i) on K+ currents in hippocampal cells were examined using acutely isolated cells obtained from adult guinea pigs. Whole-cell voltage-clamp recordings were carried out in a configuration that allowed a continuous perfusion of the intracellular medium. Recording media were made to block inward currents and allowed selective activation of K(+)-dependent outward currents. Voltage-dependent outward currents consisted of an initial rapidly decaying component followed by a sustained component. The time constant of decay of the transient current was about 25 msec, and previous studies (Numann et al., 1987) showed that the kinetic and pharmacological properties of this current closely resembled the A current recorded in invertebrate neurons (Connor and Stevens, 1971; Thompson, 1982). Intracellular perfusion of hippocampal cells with a solution containing elevated Ca2+ (about 4.5 x 10(-4) M) elicited outward currents at the holding potential (-45 to -55 mV) and produced changes in voltage-dependent K+ currents. The transient outward current (IA) activated by depolarization was suppressed with increases in Ca2+i. Delayed, sustained K+ currents were greatly potentiated. Data also showed that, among the 3 effects elicited by Ca2+i, suppression of IA was most sensitive to Ca2+i elevation. Previous results (Numann et al., 1987) showed that IA had a lower threshold (about -45 mV) than sustained currents (about -40 mV). By using low levels of depolarization (-40 mV), IA can be selectively activated, and the suppressive effect of Ca2+i on IA was confirmed on the kinetically isolated IA.(ABSTRACT TRUNCATED AT 250 WORDS) 相似文献
47.
Therapy of human cervical carcinoma with monoclonal antibody-Pseudomonas exotoxin conjugates. 总被引:1,自引:0,他引:1
Pseudomonas exotoxin A (PE) linked to the F(ab')2 fragment of 1H10, a murine monoclonal antibody recognizing a carbohydrate epitope of a glycoconjugate expressed on the surface of human cervical carcinoma tumor cells, was evaluated for in vitro and in vivo activity. PE can kill cells by ADP-ribosylating elongation factor 2 thus inhibiting protein synthesis. Disulfide- as well as thioether-linked immunotoxins (1H10-PE) killed cervical carcinoma cells in vitro and were 20-160 times more inhibitory to target than to control cells. Cell killing was antibody mediated as demonstrated by the reduction of 1H10-PE growth inhibition to target CaSki cells by free 1H10 F(ab')2. In addition, a control antibody immunotoxin was nontoxic to CaSki cells. Thioether-linked 1H10-PE administered either i.v. or i.p. suppressed the growth of established solid s.c. cervical carcinoma tumors xenografted in nude mice for over 30 days. Treatment with antibody alone or a control immunotoxin had no significant effect on tumor growth. Administration of immunotoxin i.p. was associated with less toxicity than administration i.v., but i.v. injections were more effective at suppressing the growth of established solid tumors. 相似文献
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Xiaoguang Chen Yi Li Lei Wang Mark Katakowski Lijie Zhang Jieli Chen Yongxian Xu Subhash C. Gautam Michael Chopp 《Neuropathology》2002,22(4):275-279
Intravenous administration of human bone marrow stromal cells (hMSCs) after middle cerebral artery occlusion (MCAo) in rats provides functional benefit. We tested the hypothesis that these functional benefits are derived in part from hMSC production of growth and trophic factors. Quantitative sandwich enzyme‐linked immunosorbent assay (ELISA) of hMSCs cultured with normal and MCAo brain extracts were performed. hMSCs cultured in supernatant derived from ischemic brain extracts increased production of brain‐derived neurotrophic factor (BDNF), nerve growth factor (NGF), vascular endothelial growth factor (VEGF) and hepatocyte growth factor (HGF). These neurotrophins and angiogenic growth factors increased in a post‐ischemia time‐dependent manner. The hMSC capacity to increase expression of growth and trophic factors may be the key to the benefit provided by transplanted hMSCs in the ischemic brain. 相似文献
50.
烹调油烟致大小鼠肺癌的实验研究 总被引:1,自引:0,他引:1
[目的]了解烹调油烟(cooking oil fumes,COF)的动物致癌性。[方法]采用动式染毒法给Balb/c小鼠(雌雄各半)吸入COF浓度为9.09、20.65、38.85mg/m^3,染毒1次/1~2d,30min/次,共150次,计8个月;SD大鼠(雌雄各半)吸入COF浓度为6、88、15.06、35.33mg/m^3,染毒1次/2d,30min/次,共191次,计12.5个月。分别制备COF慢性中毒动物模型;两实验均设空白对照组,吸入与实验组相同温度的清洁空气。[结果]COF诱发Balb/c小鼠实验组肺癌总发生率为18、95%(29/153),低、中、高浓度组肺癌发生率分别为15.09%、20、00%和22.00%,与对照组差异均有显著性。但低、中、高三组间差异无显著性(P〉0.05);COF诱发SD大鼠肺癌总发生率为9、10%(9/99),低、中、高浓度组肺癌发生率分别为6.45%、8.57%、12.12%,高浓度组肺癌发生率高于对照组(P〈0.05)。各性别组间肺癌发生率的差别无显著性(P〉0.05)。[结论]COF可以诱导Balb/c小鼠和SD大鼠肺癌,诱发的肺癌主要为肺腺癌(小鼠28/29,大鼠7/9),余为小细胞肺癌。 相似文献