Stimulus-dependent activation of c-Fos in neurons and glia in the rat cerebellum

The intent of the present study was to use chemical or electrical stimulation of cerebellar afferents to determine how different stimulation paradigms affect the pattern of activation of different populations of neurons in the cerebellar cortex. Specifically, we analyzed immediate changes in neuronal activity, identified neurons affected by different stimulation paradigms, and determined the time course over which neuronal activity is altered. In the present study, we used either systemic (harmaline) or electrical stimulation of the inferior cerebellar peduncle (10 and 40 Hz) to alter the firing rate of climbing and mossy fiber afferents to the rat cerebellum and an antibody made against the proto-oncogene, c-fos, as a marker to identify activated neurons and glia. In control animals, only a few scattered granule cells express nuclear Fos-like immunoreactivity. Although no other cells show Fos-like immunoreactivity in their nuclei, Purkinje cells express Fos-like immunoreactivity within their somatic and dendritic cytoplasm in control animals. Within 15 min of chemical or electrical stimulation, numerous granule and glial cells express Fos-like immunoreactivity in their nuclei. Cells in the molecular layer express Fos-like immunoreactivity following harmaline stimulation in a time and lobule specific manner; they do not appear to be activated in the electrical stimulation paradigm. Following harmaline injections, there is an initial loss of Fos-like immunoreactivity in the cytoplasm of Purkinje cells; 90 min later, nuclear staining is observed in a few scattered Purkinje cells. Following electrical stimulation, the cytoplasmic staining in Purkinje cells is enhanced; it is never present in the nucleus. Data derived from this study reveal cell-specific temporal and spatial patterns of c-Fos activation that is unique to each paradigm. Further, it reveals the presence of an activity dependent protein in the cytoplasm of Purkinje cell somata and dendrites.     

采用MDA-MB-231细胞膜进行表皮生长因子受体活性的检测

目的　探讨能否直接利用肿瘤细胞膜进行表皮生长因子受体 (Epidermalgrowthfactorreceptor,EGFR)催化活性检测。方法　首先筛选出EGFR基因表达水平相对较高的细胞株MDA MB 2 31,通过差速离心制备细胞膜 ,采用Westernblotting检测EGFR催化磷酸化的程度。结果　底物被磷酸化 ,加入特异性拮抗剂AG14 78后 ,磷酸化被抑制。结论　利用肿瘤细胞膜检测EGFR活性的设想是成立的 ,并且其方法简便、经济。     

VALUE AND LIMITATIONS OF SINUS NODE FUNCTION TE.ST BY ATRIAL PACING IN SICK SINUS SYNDROME DIAGNOSIS

In order to evaluate the significance of the sinus node function test by transvenous atrial pacing in the diagno,sis of sick sinus syndrome (SSS), sinus node recovery time (SRT), co]rrected sinus node recovery time (CSRT) and total atrio- sinus and sino-atrial conduction time (SACT) are observed in 69 patients including non-SSS group 39 cases and SSS group 30 cases. According to our data, we suggest criteria for sinus node dysfunction as follows. SRT>1,400 ms and/or A-V junctional esca.pe before sinus recovery and;or secondary pause, CSRT>560 ms. total SACT>300 ms. With l item abnormal, the false positive rat.e in the non-SSS group is 7.7c7。 and the false negative rate in the S.SS group 3.30i" with 2 items abnormal, the false positive rate in the non-SSS group Oi and the false negative rate in the SSS grOiup 6.7'70. Atropine test results are compared with that of atrial pacing, 95.8To and 84.2% are compatible with each other in these 2 groups. In order to cut the use of invasive technic to the minimum, we propose performing the atropine test first. Only in those with unexplainable test results should the trial pacing test. be resorted to..     

科技论文中通信作者和末位作者重要性的比较

【目的】 试图解决论文作者署名中通信作者与末位作者谁是最重要的作者的问题。【方法】 以Science期刊为研究对象,收集该刊论文的作者署名信息和作者贡献声明信息,提取贡献要素并进行规范化分类,结合作者贡献声明和作者署名位置、署名角色进行比较分析。【结果】 在论文作者署名位置的分布中,末位作者通常同时是通信作者。在论文研究中,通信作者往往比末位作者发挥更重要的作用。对于不是通信作者的末位作者,其对研究的贡献往往较低。【结论】 结合作者贡献声明能够合理地判断作者的重要性。学术界对于作者署名位置应该有更加统一的认识,建议在科技期刊中推行作者贡献声明政策,完善学术期刊作者贡献声明规范。     

皮下通道型胆囊肝胆管成形术治疗肝胆管结石 和胆管狭窄的临床研究

目的：总结皮下通道型胆囊肝胆管成形术的临床效果。方法：统计了1994年以来我院76例行STHG手术患者的适应症、临床效果及术后早期并发症。并选择同期实施的125 列行传统胆肠吻合（CJ）的患者进行对照。结果：STHG的手术适应症与传统胆肠吻合基本相同;STHG组患者的手术时间、住院时间、术中出血量明显少于CJ组,术后恢复良好,仅2例次并发症。结论;该术式既保存了胆囊及Oddi括约肌功能,又保证了胆汁的生理流向;防止了肠液的反,所以避免了消化功能紊乱,防止了反 流性胆管炎,对患者的影响小,是一种较为理想的治疗肝胆管结石和肝门胆管狭窄的术式。     

维生素D缺乏性晚发性佝偻病的骨密度研究

目的：探讨维生素D缺乏性晚发性佝偻病的骨密度变化;方法：采用病例对照研究方法。对640名学生进行问诊及体验,测定非优势侧尺挠骨中1／3交界处骨密度（BMD）,病例组检测骨碱性磷酸酶,拍摄腕部X光片,病例组与对照组同测血250HD3;结果：病例组骨密度显著低于对照组,病例组250HD3异常者显著低于对照组;结论：晚佝病是由于维生素D缺乏所至的骨量减少性疾病,日后影响峰值骨量的形成,并与成人期骨质疏松有密切的关系,骨密度检查对晚佝病有重要诊断价值。     

无呼吸道症状肺癌35例临床分析

目的：探讨完全无症状或无呼吸道症状肺癌的早期诊断。方法：随机抽取1995年2月至2001年3月经临床及病理诊断为肺癌的380例,其中“无症状”肺癌35例进行分析。结果：由于“无症状”肺癌的异位内分泌等作用,致使患者表现为神经科,骨科,皮肤科,消化科,内分泌科学等多学科病变。结论：为了提高“无症状”肺癌的早期确诊率,及早行胸片,CT片,支行镜等相关检查相当重要,定期体检对于早期发现肺癌有重要的意义。     

大鼠去势后胸腺变化的组织学及超微结构的观察

目的：探讨去势对大鼠胸腺淋巴细胞超微结构与细胞功能的影响。方法：分别于去势大鼠术后2周、4周、6周、8周后,取胸腺组织进行HE染色和透射电镜观察。结果：实验表明去势导致胸腺淋巴细胞结构坏死,或者细胞器严重受损。结论：去势后胸腺淋巴细胞形态和功能均受到损害。     

鸡贫血病毒VP 3基因的克隆及其体外凋亡诱导效应的研究

用PCR方法扩增了鸡贫血病毒标准株的vp3基因,并将其克隆于真核表达载体pcDNA3上,构建了重组体pcDNA-vp3.经酶切鉴定及测序分析表明,该片段和预期相符.在体外利用LipofectAMINETM介导的基因转染,将pc-DNA-vp3、pcDNA3分别转入肝癌细胞系HepG2和二倍体肝细胞系L-02中,转染后的RT-PCR结果证实vp3基因在细胞中得到了表达.同时利用筛选稳定表达细胞株的技术和原位细胞凋亡检测法,证明了鸡贫血病毒是以凋亡的方式诱导细胞死亡,并且只诱导癌细胞的凋亡,而不诱导正常或二倍体细胞死亡.表明鸡贫血病毒vp3基因很可能成为一种极具潜力的抗肿瘤生物制剂.