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991.
T. Iwanaga †‡ A. McEuen† A. F. Walls† J. B. Clough† T. P. Keith§ S. Rorke† S. J. Barton† S. T. Holgate† J. W. Holloway † 《Clinical and experimental allergy》2004,34(7):1037-1042
BACKGROUND: Mast cell chymase has the potential to be an important mediator of inflammation and remodelling in the asthmatic lung. Previous studies have examined association between promoter polymorphism of the chymase gene (CMA1) and allergic phenotypes but the significance of this polymorphism is unclear. We have examined association of a CMA1 variant in relation to asthma in a large UK Caucasian family cohort. METHODS: A polymorphism of the CMA1 gene promoter (-1903G/A) was genotyped in 341 asthmatic families and in 184 non-asthmatic adults recruited from the UK PCR-RFLP based genotyping. Association with asthma diagnosis, atopy, specific and total IgE, and atopy and asthma severity was examined. RESULTS: Case-control studies did not reveal a significant difference in allele frequency between asthmatics and controls. A significant association was found between CMA1 genotypes and total IgE levels in subjects with self-reported eczema that remained significant after correction for multiple testing (median total serum IgE GG 297 kU/L, GA 144 kU/L, AA 48.4 kU/L, Pc=0.0032). CONCLUSION: These data suggest that CMA1 promoter polymorphism does not contribute to asthma susceptibility or severity but may be involved in regulating IgE levels in patients with eczema. 相似文献
992.
Christine N Vidal Rob Nicolson Timothy J DeVito Kiralee M Hayashi Jennifer A Geaga Dick J Drost Peter C Williamson Nagalingam Rajakumar Yihong Sui Rebecca A Dutton Arthur W Toga Paul M Thompson 《Neuropsychopharmacology》2006,60(3):218-225
BACKGROUND: Volumetric studies have reported reductions in the size of the corpus callosum (CC) in autism, but the callosal regions contributing to this deficit have differed among studies. In this study, a computational method was used to detect and map the spatial pattern of CC abnormalities in male patients with autism. METHODS: Twenty-four boys with autism (aged 10.0 +/- 3.3 years) and 26 control boys (aged 11.0 +/- 2.5 years) underwent a magnetic resonance imaging (MRI) scan at 3 Tesla. Total and regional areas of the CC were determined using traditional morphometric methods. Three-dimensional (3D) surface models of the CC were also created from the MRI scans. Statistical maps were created to visualize morphologic variability of the CC and to localize regions of callosal thinning in autism. RESULTS: Traditional morphometric methods detected a significant reduction in the total callosal area and in the anterior third of the CC in patients with autism; however, 3D maps revealed significant reductions in both the splenium and genu of the CC in patients. CONCLUSIONS: Statistical maps of the CC revealed callosal deficits in autism with greater precision than traditional morphometric methods. These abnormalities suggest aberrant connections between cortical regions, which is consistent with the hypothesis of abnormal cortical connectivity in autism. 相似文献
993.
994.
Tomáš Šimůnek Martin Štěrba Olga Popelová Michaela Adamcová Radomír Hrdina Vladimír Geršl 《Pharmacological reports : PR》2009,61(1):154-171
The risk of cardiotoxicity is the most serious drawback to the clinical usefulness of anthracycline antineoplastic antibiotics, which include doxorubicin (adriamycin), daunorubicin or epirubicin. Nevertheless, these compounds remain among the most widely used anticancer drugs. The molecular pathogenesis of anthracycline cardiotoxicity remains highly controversial, although the oxidative stress-based hypothesis involving intramyocardial production of reactive oxygen species (ROS) has gained the widest acceptance. Anthracyclines may promote the formation of ROS through redox cycling of their aglycones as well as their anthracycline-iron complexes. This proposed mechanism has become particularly popular in light of the high cardioprotective efficacy of dexrazoxane (ICRF-187). The mechanism of action of this drug has been attributed to its hydrolytic transformation into the iron-chelating metabolite ADR-925, which may act by displacing iron from anthracycline-iron complexes or by chelating free or loosely bound cellular iron, thus preventing site-specific iron-catalyzed ROS damage. However, during the last decade, calls for the critical reassessment of this “ROS and iron” hypothesis have emerged. Numerous antioxidants, although efficient in cellular or acute animal experiments, have failed to alleviate anthracycline cardiotoxicity in clinically relevant chronic animal models or clinical trials. In addition, studies with chelators that are stronger and more selective for iron than ADR-925 have also yielded negative or, at best, mixed outcomes. Hence, several lines of evidence suggest that mechanisms other than the traditionally emphasized “ROS and iron” hypothesis are involved in anthracycline-induced cardiotoxicity and that these alternative mechanisms may be better bases for designing approaches to achieve efficient and safe cardioprotection. 相似文献
995.
目的腹内侧前额叶皮质在随意运动的起始和控制、情感以及认知中具有重要作用。然而,黑质-纹状体通路变性后腹内侧前额叶皮质的神经活动和5-HT_(1A)受体的作用仍不清楚。本研究观察了6-羟基多巴胺(6- hydroxydopamine,6-OHDA)损毁黑质致密部(substantia nigra pars compacta,SNc)后大鼠腹内侧前额叶皮质神经活动的变化和体循环给予选择性5-HT_(1A)受体拮抗剂WAY-100635后神经元活动的改变。方法采用在体玻璃微电极细胞外记录方法,记录正常大鼠和SNc单侧损毁大鼠的腹内侧前额叶皮质神经元的活动。结果6-OHDA损毁SNc大鼠的腹内侧前额叶皮质神经元放电频率显著增加,放电形式没有明显改变。体循环给予WAY-100635 (0.1 mg/kg,i.v.)不改变正常大鼠腹内侧前额叶皮质神经元的平均放电频率和放电形式,而显著降低了SNc损毁大鼠前额叶皮质神经元的平均放电频率。结论黑质-纹状体通路的变性可导致腹内侧前额叶皮质神经活动增强,5-HT_(1A)受体拮抗剂WAY-100635可以抑制这种活动增强,提示可能存在腹内侧前额叶皮质5-HT_(1A)受体功能失调。 相似文献
996.
目的 探讨胃癌腹腔微转移情况的检测方法及意义。方法 手术中切除肿瘤前收集腹腔冲洗液,采用磁激活细胞分离术(MACS)对不同病理分期胃癌患者腹腔冲洗液中癌细胞进行富集并检测。分别标记带磁珠的细胞角蛋白(CK)抗体,经磁柱富集CK^+上皮细胞,用流式细胞仪检测其含量,并比较胃癌组与胃平滑肌瘤组(对照组)以及胃癌不同分期之间、磁富集前后CK^+上皮细胞含量的差异。结果 在未经MACS富集的标本中较少发现CK^+ CD45^-细胞;在富集后的标本中其含量在胃癌组与对照组有显著差异(41/50,1/10,P〈0.001);pTNMⅠ~Ⅱ期与Ⅲ~Ⅳ期之间(0.67%,3.42%,P〈0.001)差异有非常显著性。结论 MACS能有效地富集上皮来源细胞,提高上皮源细胞的检出率,并能反映腹腔游离癌细胞数量;上皮细胞数量与胃癌的存在及临床病理分期有关,其有利于判断肿瘤转移和预后并指导治疗。 相似文献
997.
钙池操纵的Ca~(2 )通道(store-operated Ca~(2 ) channels,SOC)是非兴奋细胞Ca~(2 )内流的主要通道之一,参与多种病理和生理过程,在钙信号通路的研究中,SOC的激活机制一直是人们关注的焦点之一,迄今为止,钙内流因子模型(Ca~(2 ) innux factor model,CIF model)和构象耦联模型fconformational coupling model)受到广泛关注.部分学者已经从很多不同类型的细胞中提取出CIF,并证实钙非依赖性的磷脂酶A_2(Ca~(2 )-independent phospholipase A_2,iPLA_2)作为CIF的底物,在某些类型细胞的SOC激活过程中发挥重要作用,并进一步提出了ER- CIF-iPLA_2-CaM-LysoPLs-SOC通路模型.瞬时受体电位(transient receptor potential,TRP)通道蛋白与1.4,5-磷酸肌醇受体(inositol 1,4,5 trisphosphate receptor,IP_3R)的结构连接作为构象耦联模型的基础已被广泛证实,随着对IP_3R,Ryanodine受体、肌动蛋白等在钙信号通路中所发挥作用的深入研究,构象耦联模型将得到不断补充和完善.SOC激活机制的破解,将对进一步完善非兴奋细胞的钙通道特性及其调节机制理论带来重大突破. 相似文献
998.
目的探讨不同方法治疗压疮的临床效果。方法将65例患者计Ⅱ~Ⅲ度溃疡84处按基本条件相当原则随机分成A、B、C三组,A组21例28处,伤口采用清创冲洗后,给予康惠尔水胶体敷料;B组23例30处,伤口采用湿润烧伤膏;C组21例26处,清创冲洗后,给予自制凡士林油纱敷料外敷溃疡面处。结果B组愈合率最高,且平均显效时间和愈合时间均较A、C两组明显缩短,且A、B组明显高于C组。结论采用清创冲洗后用湿润烧伤膏是治疗压疮较好的方法之一。 相似文献
999.
目的 研究彩色多普勒超声诊断房间隔缺损(ASD)的准确性。方法 回顾性分析经手术证实的64例ASD患者的超声检查结果并和手术结果对照。结果 64例患者中有1例三房心合并房间隔缺损畸形,1例合并右下肺静脉异位引流漏诊,术前超声正确诊断63例,定性诊断准确率达98.4%,有1例混合型定位不准确,定位准确率在98.4%,而且64例患者中超声检查结果显示在无合并其他畸形时房间缺损大小与右心系统扩大及肺动脉扩张呈正相关关系。结论 ASD是以右室容量超负荷为特征,彩色多普勒超声是诊断房间隔缺损的首选检查方法,并具有较高的准确性。 相似文献
1000.
对地衣芽孢杆菌(Bacilluslicheniformis)进行亚硝基胍和60Co诱变,获得一株γ PGA的高产菌株C9.γ PGA质量浓度由9.44g/L提高到19.76g/L,提高了109%.突变株传代10次,质量浓度保持基本稳定.通过正交试验和单因素试验对发酵培养基及发酵条件进行了优化.当发酵培养基中含柠檬酸12g/L、甘油80g/L、L 谷氨酸23g/L、氯化铵7g/L,pH7.0,装液量为50mL/250mL三角瓶,接种体积分数为5%时,37℃摇瓶发酵72h,γ PGA达到23.32g/L. 相似文献