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51.
J. B. Payne R. A. Reinhardt M. P. Masada L. M. DuBois A. C. Allison 《Journal of periodontal research》1993,28(6):451-453
Gingival crevicular fluid (GCF) IL-8 and IL-1,1β levels were determined by sandwich enzyme-linked immunosorbent assays. Associations between IL-8 and IL-1β GCF levels, and between these cytokines and patient estrogen status were evaluated. IL-8 and IL-1β were detected more frequently and in higher amounts/30 s GCF sample in estrogen-deficient patients than in estrogensufficient patients. IL-8 and IL-1β GCF levels were significantly correlated. These lindings suggest that GCF IL-8 levels are associated with patient estrogen status and local IL-1β concentrations. 相似文献
52.
目的 探讨以顺铂为主的化疗方案加放疗对局部晚期非小细胞肺癌的疗效。方法 86例局部晚期非小细胞肺癌患随机分为治疗组及对照组各43例,放疗方案以CAP、EP、MVP或MOP,每人至少化疗两个周期,化疗后10~14天放射治疗,放疗采用^60Co外照射。结果 治疗组有效率83.7%,中位生存期14.5个月,对照组有效率67.4%,中位生存期10个月,两组不良反应为骨髓抑制、胃肠道反应。结论 以顺铂为主的化疗方案加放疗治疗局部晚期非小细胞肺癌的疗效较高,可提高肿瘤的局部控制率和延长生存期。 相似文献
53.
人膀胱癌T24细胞及其SCID小鼠移植瘤组织中KDR的表达 总被引:1,自引:1,他引:0
目的 检测KDR在人膀胱癌T24细胞及其SCID小鼠移植瘤组织中的表达。方法 常规培养T24细胞,建立荷人膀胱癌移植瘤SCID小鼠动物模型,使用抗KDR单克隆抗体,通过免疫荧光、免疫组化检测KDR在T24细胞及瘤体组织上的表达;结果 KDR在T24细胞及瘤体组织中均呈阳性表达。结论 本研究结果为进一步研究抗KDR单抗在荷T24细胞移植瘤动物体内分布及对瘤体生长的抑制效应奠定了实验基础。 相似文献
54.
A. Lecci F. Borsini L. Gragnani G. Volterra A. Meli 《Journal of neural transmission (Vienna, Austria : 1996)》1991,83(1-2):67-76
Summary Stress-induced hyperthermia (SIH), which is seen in the last mice removed from the cage, is a novel animal model sensitive to anxiolytic drugs. SIH is antagonized by CL 218872 (25 and 50 mg/kg, os), by tracazolate (5 and 7.5 mg/kg, ip) and by 2-AP-5 (50 and 100 mg/kg, ip). At higher dose, CL 218872 (100 mg/kg, os) and tracazolate (12.5 mg/kg, ip) lose their activity.PK 9084 (5–40 mg/kg, ip) and CGS 9896 (2–20 mg/kg, both ip and os) were also ineffective in preventing SIH. The anti-hyperthermic effect of CL 218872 (25 mg/kg) and tracazolate (7.5 mg/kg) was blocked by the benzodiazepine antagonist Ro 15–1788 (15 mg/kg). CGS 9896 (10 mg/kg, os) also reversed the effect of CL 218872 (25 mg/kg) on SIH.Differently from anxiolytics, MK-801 (0.5–1 mg/kg, os), PCP (2.5 mg/kg, ip) and d-amphetamine (10 mg/kg, ip) evoked hyperthermia in the first set of mice and prevented a further stress-induced rise of body temperature in the last set of mice. 相似文献
55.
袁柳明 《浙江中西医结合杂志》2007,17(1):35-36
我院自2001年1月-2005年12月,在常规综合治疗的基础上采用中药合654-2治疗重度黄疸型肝炎42例,疗效较满意,报道如下。 相似文献
56.
Isolation and characterization of a monoclonal anti-P30 antibody resistant mutant of Toxoplasma gondii 总被引:13,自引:0,他引:13
LLOYD H. KASPER 《Parasite immunology》1987,9(4):433-445
Of the possible iodine-labelled Toxoplasma gondii surface proteins, P30 (apparent Mr 30,000) is the principal one recognized by acute and convalescent anti-toxoplasma sera. This protein which comprises from 3 to 5% of the total parasite protein was used to raise a panel of parasiticidal monoclonal anti-P30 antibodies. One of these monoclonal antibodies was able to select a resistant mutant from a large population of chemically mutagenized wild-type P strain parasites. This mutant retained the wild type sensitivity to other non-P30 parasiticidal monoclonal antibodies as well as polyclonal anti-P30 rabbit sera. Analysis of surface radioiodinated wild type and mutant parasites showed that the mutant had a quantitative reduction in the amount of P30. A comparison of surface biotin labelled wild type and resistant parasites by two dimensional electrophoresis showed that the mutant lacked one and possibly two of several proteins that make up wild type P30. Western blot analysis indicated that the mutant was devoid of antigenically reactive P30. These findings further support the hypothesis that antigenic variants of T. gondii can be induced and may involve the major surface membrane antigens of the parasite. 相似文献
57.
目的观察氧化苦参碱对人胃癌SGC-7901细胞株体外增殖率的影响情况。方法噻唑蓝(MTT)比色测定法确定氧化苦参碱对胃癌SGC-7901细胞存活抑制作用。结果试验浓度下氧化苦参碱对SGC-7901细胞增殖抑制作用呈剂量依赖性,当浓度为12mg/ml时,对SGC-7901增殖的抑制率最大,达到87.63%。结论氧化苦参碱对人胃癌SGC-7901细胞的增殖具有明显的抑制作用。 相似文献
58.
翼腭窝的CT三维成像 总被引:2,自引:0,他引:2
目的:探讨CT三维成像评价翼腭窝解剖结构的价值。材料和方法:使用Philips Mx8000型多层CT检查仪对5个成人头颅标本进行准直1mm或0.5mm的容积采集,并将数据输入配套Mxview工作站(SGI02)进行三维重建处理,包括容积显示(VR)和三维正交多平面重建(MPR)。鼻腔内侧壁相关结构进行测量并与标本测量进行对比。结果:CT三维正交多平面重建图像可以十分清楚地显示翼腭窝结构及其6个通路结构,VR可以清楚、准确地显示鼻腔内侧壁结构,并均可以获得准确测量。结论:CT容积采集结合合理的三维重建可以直观、立体地显示翼腭窝解剖及其相关通连结构。 相似文献
59.
目的:观察足三里穴位注射654.2治疗婴幼儿秋冬季腹泻的疗效。方法:选择2月至2岁幼儿腹泻病例共284例,随机分为治疗组和对照组。治疗组146例采用足三里注射654-2 0.5-1.0mg/kg,同时口服补液盐;对照组138例使用补液、肌注病毒唑,口服庆大霉素及助消化剂。结果:治疗组治愈率93.2%,好转率4.1%,平均治愈时间2.49d;对照组治愈率57.9%,好转率31.6%,平均治愈时间4.55d。结论:足三里穴位注射654.2疗效显著,且简单易行、经济方便,可在临床推广使用。 相似文献
60.
Padmaja Yalamanchili Eric Wexler Megan Hayes Ming Yu Jody Bozek Mikhail Kagan Heike S. Radeke Michael Azure Ajay Purohit David S. Casebier Simon P. Robinson 《Journal of nuclear cardiology》2007,14(6):782-788
Background
BMS-747158-02 is a novel fluorine 18-labeled pyridazinone derivative designed for cardiac imaging. The uptake and retention
mechanisms of F-18 BMS-747158-02 in cardiac myocytes were studied in vitro, and the biodistribution of F-18 BMS-747158-02
was studied in vivo in mice.
Methods and Results
Fluorine 19 BMS-747158-01 inhibited mitochondrial complex I (MC-I) in bovine heart submitochondrial particles with an IC50 of 16.6±3 nmol/L that was comparable to the reference inhibitors of MC-1, rotenone, pyridaben, and deguelin (IC50 of 18.2±6.7 nmol/L, 19.8±2.6 nmol/L, and 23.1±1.5 nmol/L, respectively). F-18 BMS-747158-02 had high uptake in monolayers
of neonatal rat cardiomyocytes (10.3%±0.7% of incubated drug at 60 minutes) that was inhibited by 200 nmol/L of rotenone (91%±2%)
and deguelin (89%±3%). In contrast, an inactive pyridaben analog, P-0 (IC50 value>4 μmol/L in MC-1 assay), did not inhibit the binding of F-18 BMS-747158-02 in cardiomyocytes. Uptake and washout kinetics
for F-18 BMS-747158-02 in rat cardiomyocytes indicated that the time to half-maximal (t1/2) uptake was very rapid (approximately 35 seconds), and washout t1/2 for efflux of F-18 BMS-747158-02 was greater than 120 minutes. In vivo biodistribution studies in mice showed that F-18 BMS-747158-02
had substatial myocardial uptake (9.5%±0.5% of injected dose per gram) at 60 minutes and heart-to-lung and heart-to-liver
ratios of 14.1±2.5 and 8.3±0.5, respectively. Positron emission tomography imaging in the mouse allowed clear cardiac visualization
and demonstrated sustained myocardial uptake through 55 minutes.
Conclusions
F-18 BMS-747158-02 is a novel positron emission tomography cardiac tracer targeting MC-I in cardiomyocytes with rapid uptake
and slow washout. These characteristics allow fast and sustained accumulation in the heart. 相似文献