The peri‐microvascular edema in hippocampal CA1 area in a rat model of sepsis

Encephalopathy is a common complication of sepsis. However, little is known about the morphological changes that occur in the brain during sepsis. In this study, fecal peritonitis was induced in Wistar rats, which had been monitored for 4 h before their brains were removed and samples from the CA1 area taken. In addition to higher blood pressure with a decreasing pattern and a significant drop in rectal temperature, an increased heart rate and marked respiratory failure were observed. The tissue was investigated and compared with corresponding hippocampal samples taken from sham‐operated and not operated control groups. Significantly more peri‐microvascular edema was found in the hippocampal CA1 area in the septic group. The percentages of the peri‐microvascular edema were 158.57 ± 3.6%, 122.84 ± 1.5% and 120.24 ± 1.9% in the fecal peritonitis group, sham‐operated and not operated control groups, respectively. The results may suggest that the edema observed around the microvessels may participate in the pathogenesis of the septic encephalopathy probably by causing in the microvascular permeability characteristics.     

联合测定子宫内膜异位症患者血清中EMAb及CA125的临床评价

目的：对联合测定子宫内膜异位症（内异症）患者血清中ＥＭＡｂ及ＣＡ１２５进行临床评价。方法：采取内异症１０９例术前（内异症组）和健康妇女３０例（对照组）空腹静脉血，用酶联免疫吸附法（ＥＬＩＳＡ）测定两组血清中ＥＭＡｂ水平；用放射免疫法（ＲＩＡ）测定血清中ＣＡ１２５水平。结果：内异症组ＥＭＡｂ阳性率为６３．３０％，对照组为１０％，两组差异有显著性（Ｐ＜０．０５）。内异症各期及子宫腺肌病间ＥＭＡｂ阳性率差异无显著性（Ｐ＞０．０５）。内异症组血清ＣＡ１２５水平平均为７０．７０±１６．６２Ｕ／ｍｌ，对照组为１５．３８±５．３２Ｕ／ｍｌ，两组差异有显著性。如以ＣＡ１２５≥３５Ｕ／ｍｌ为阳性界值，则内异症组阳性率为８０．２３％，对照组为６．６６％。单独测定ＥＭＡｂ诊断内异症的敏感性为６３．３０％，特异性为９０％；单独测定ＣＡ１２５诊断内异症的敏感性为８０．２３％、特异性为９３．３３％。如以两者均阳性为诊断标准，则敏感性为５７．８０％，特异性为１００％；如以其中之一阳性为诊断标准，则敏感性为９１．７４％，特异性为８３．３３％。结论：测定内异症患者血清中ＥＭＡｂ及ＣＡ１２５水平对内异症有较好的辅助诊断价值，联合测定ＥＭＡｂ及?     

尖锐湿疣患者人乳头瘤病毒的基因分型

目的 探索尖锐湿疣患者人乳头瘤病毒的基因分型。方法 PCR方法检测HPV6／11型、HPV16／18型DNA。结果 检测尖锐湿疣患者100例，对其中35例进行组织活检，阳性检出率为91．4％(32／35)，阳性检出中，HPV6／11型26例(81．2％)，HPV16／18型3例(9．4％)，HPV6／11 HPV16／18型3例(9．4％)；对其中65例进行宫颈抹片检测，阳性检出率为92．3％(60／65)，阳性检出中，HPV6／11型41例(68．3％)，HPV16／18型12例(20．0％)，HPV6／11 HPV16／18型7例(11．7％)。结论 尖锐湿疣患者人乳头瘤病毒感染以HPV6／11型为主，HPV16／18型在宫颈处感染率高于其它处组织。     

运用多普勒超声心动图技术对染色体三体异常小鼠胚胎心脏发育的研究

对２０个１６三体染色体异常小鼠胚胎进行了多普勒超声心动图研究。胎龄从１０天至１５天。９例发现流入道返流波型，６例发现流出道返流波型。１２０例染色体正常胚胎无一例发现返流波型。１６三体小鼠模型作为先天性心脏病研究的理想模型，本文首次提供了对此类模型胚胎血液动力学研究的非创伤性监测方法。     

顺铂联合足叶乙甙治疗原发灶未明转移癌的临床观察

目的　观察顺铂 (DDP)联合足叶乙甙 (VP -16 )治疗原发灶未明转移癌 (MUO)的疗效。方法　 10例MUO患者均采用EP方案 :DDP 30mg m2 第 1～ 3天 ,足叶乙甙 (VP -16 ) 6 0mg m2 第 1～ 5天 ,2 8天为一周期。结果　 10例中 4例达到完全缓解(CR)为 40 %,3例部分缓解 (PR)为 30 %,2例稳定 (SD)为 2 0 %,1例进展 (PD)为 10 %。结论　顺铂联合足叶乙甙对原发灶未明转移癌有较好的疗效 ,且毒副反应可以耐受。     

胃粘膜癌变过程中P1 6、CyclinD1的表达

目的：探讨Ｐ１６、ＣｙｃｌｉｎＤ１的表达在胃癌发生发展中的作用。方法：采用免疫组化Ｓ－Ｐ法。结果：在胃粘膜癌变过程中，Ｐ１６阳性表达率逐渐下降，其中异型增生和胃癌组Ｐ１６阳性表达率明显低于慢性浅表性胃炎组（Ｐ　＜０．０５）；ＣｙｃｌｉｎＤ１阳性表达率逐渐增高，其中肠化生、异型增生和胃癌组ＣｙｃｌｉｎＤ１阳性表达率明显高于慢性浅表性胃炎组（Ｐ　＜０．０５）。在胃癌中，Ｐ１６阳性表达率与胃癌分期和分化程度有关，ＣｙｃｌｉｎＤ１的阳性表达率与之无关。结论：Ｐ１６表达缺失和ＣｙｃｌｉｎＤ１异常表达是胃癌发生过程中一个较早的分子事件，且Ｐ１６表达缺失与胃癌进展和恶性程度有关。     

CA的治疗和护理

目的 探讨对CA的最佳治疗方案及有效护理措施.方法 采取二氧化碳激光联合重组人白介素100万u局部疣体基地部注射和20万u臀部皮下注射治疗CA,根据病人实际情况给予一般性病护理措施、支持性心理治疗和健康教育.结果 675例CA患者386例一次性治愈,137例二次治愈,71例三次治愈,27例三次以上治愈,54例失访,总治愈率为92.0%,三个月后复发106例,复发率为17.1%.结论 采用本法治疗CA是一种简便、安全、不留疤痕、行之有效的方法.     

Impaired spatial working and reference memory in segmental trisomy (Ts65Dn) mice

To evaluate the cognitive phenotype of the segmental trisomy 16 (Ts65Dn) mouse, a model of Down Syndrome (DS, trisomy 21), we assessed spatial working and reference memory using a 12-arm radial maze (RAM). Ts65Dn mice made a greater number of reference memory errors across trials compared to control mice. Both genotypes showed improvement across trials, although improvement was slower in Ts65Dn mice. Ts65Dn mice also made a greater number of working memory errors on the RAM, and in contrast to control mice, did not improve across trials, always performing at near-chance levels. These results provide evidence for both spatial working and reference memory deficits in Ts65Dn mice, characteristics of cognitive dysfunction.     

Effect of nilvadipine on the voltage-dependent Ca channels in rat hippocampal CA1 pyramidal neurons

Effects of nilvadipine on the low- and high-voltage activated Ca²⁺ currents (LVA and HVA I_Ca, respectively) were compared with other organic Ca²⁺ antagonists in acutely dissociated rat hippocampal CA1 pyramidal neurons. The inhibitory effects of nilvadipine, amlodipine and flunarizine on LVA I_Ca were concentration- and use-dependent. The apparent half-maximum inhibitory concentrations (IC₅₀s) at every 1- and 30-s stimulation were 6.3×10⁻⁷ M and 1.8×10⁻⁶ M for flunarizine, 1.9×10⁻⁶ M and 7.6×10⁻⁶ M for nilvadipine, and 4.0×10⁻⁶ M and 8.0×10⁻⁶ M for amlodipine, respectively. Thus, the strength of the use-dependence was in the sequence of nilvadipine>flunarizine>amlodipine. Nilvadipine also inhibited the HVA I_Ca in a concentration-dependent manner with an IC₅₀ of 1.5×10⁻⁷ M. The hippocampal CA1 neurons were observed to have five pharmacologically distinct HVA Ca²⁺ channel subtypes consisting of L-, N-, P-, Q- and R-types. Nilvadipine selectively inhibited the L-type Ca²⁺ channel current which comprised 34% of the total HVA I_Ca. On the other hand, amlodipine non-selectively inhibited the HVA Ca²⁺ channel subtypes. These results suggest that the inhibitory effect of nilvadipine on the neuronal Ca²⁺ influx through both LVA and HVA L-type Ca²⁺ channels, in combination with the cerebral vasodilatory action, may prevent neuronal damage during ischemia.