子痫颅脑CT表现及与临床关系

目的分析子痫颅脑CT表现及与临床相关性。方法18例子痫患者均行颅脑CT平扫,其中3例行增强扫描,8例进行CT复查。结果14例患者显示脑白质内广泛低密度水肿区,枕叶脑白质累及为主,并多伴有额叶、顶叶受侵。4例表现为脑内局限性低密度区,2例合并脑出血,呈散在小斑片状分布。结论CT是子痫脑内病灶较好的影像检查手段,既可发现早期病灶,又可评价预后。     

The expression of somatostatin receptors 1 and 2 in benign,pre‐malignant and malignant laryngeal lesions

The expression of somatostatin receptors 1 and 2 in benign, pre‐malignant and malignant laryngeal lesions The role of chemotherapy in squamous cell carcinoma of the larynx has not been clearly defined. Whilst toxic chemotherapy regimes may confer a marginal improvement in survival, surgery and radiotherapy remain the mainstay of treatment. Somatostatin is a naturally occurring peptide, which exerts antiproliferative and antiangiogenic effects via five membrane‐bound receptor subtypes. The expression of somatostatin receptor subtypes (SSTRs) 1 and 2 was studied in benign, pre‐malignant and malignant laryngeal specimens. Epithelial expression of SSTR1 was detected in 4/6 (67%) Reinke's oedema, 5/6 (83%) pre‐malignant and 8/12 (67%) malignant specimens, with virtually no stromal or vascular expression. High levels of epithelial SSTR2 expression were noted in all Reinke's oedema specimens, compared with low‐to‐moderate levels in only 2/6 (33%) pre‐malignant and 3/12 (25%) malignant specimens (P < 0.01). This ‘loss’ of epithelial SSTR2 expression may provide a growth advantage in pre‐malignant and malignant laryngeal lesions. Vascular expression of SSTR2 was ubiquitous in all groups, with scant stromal expression. Overall, most (>80%) pre‐malignant and malignant laryngeal specimens expressed at least one of the two SSTR subtypes studied. Somatostatin analogues may have a therapeutic role in squamous cell carcinoma of the larynx.     

基础医学教师课堂教学质量评价

为了了解本科教师的教学质量和教学效果 ,教学专家和学生评价了 14 7位基础医学教师。结果显示 ,讲师以上职称教师的教学质量明显好于初级职称教师 (P<0 .0 5 ) ,高级职称教师教学的科学性、艺术性和思想性明显好于讲师和助教 (P<0 .0 5 )。文章还对教学中存在的问题和对策进行了讨论。     

Pre‐conditioning activates adenosine utilization in a cost‐effective way during myocardial ischaemia

During pre‐conditioning the interstitial concentration of adenosine, in contrast to lactate, presents a die‐away curve‐pattern for every successive episode of ischaemia. This die‐away pattern might not necessarily be attributed to diminished adenosine production. The present study was undertaken to investigate whether pre‐conditioning alters the metabolic turnover of adenosine as observed by the lactate production during ischaemia. Interstitial levels of metabolites in pre‐conditioned (n=21) and non‐preconditioned (n=21) porcine hearts were monitored with microdialysis probes inserted in both ischaemic and non‐ischaemic tissue in an open chest heart model. Three subgroups perturbated with either plain microdialysis buffer (control), buffer containing adenosine (375 μM ), or buffer containing deoxyadenosine (375 μM ) were studied. All animals were subjected to 90 min of equilibrium microdialysis before 40 min of regional myocardial ischaemia and 120 min of reperfusion. Pre‐conditioning consisted of four repetitive episodes of 10 min of ischaemia and 20 min of reperfusion. Significantly higher levels of inosine and lactate were found in the ischaemic tissue of the pre‐conditioned subgroup receiving adenosine (P < 0.05) compared with the other two subgroups receiving deoxyadenosine and plain buffer, respectively. This difference was only valid for pre‐conditioned ischaemic myocardium, and hence equal amounts of inosine and lactate were produced in the non‐preconditioned ischaemic myocardium regardless of the presence of adenosine or deoxyadenosine. In the non‐ischaemic myocardium baseline levels of metabolites were measured in all subgroups. Pre‐conditioning favoured degradation of exogenous adenosine to inosine successively ending up in enhanced lactate production. This was probably because of the involvement of the hexose monophosphate pathway in the pre‐conditioned ischaemic myocardium. This route may therefore be supplementary in energy metabolism as a metabolic flow can be started by adenosine ending up in lactate without initial adenosine 5′‐triphosphate (ATP) investment. Utilization of adenosine in this way may also explain the successive die‐away pattern of adenosine seen in consecutive pre‐conditioning cycles.     

梗死前心绞痛对急性心肌梗死溶栓-再灌注的影响

目的 :探讨梗死前心绞痛与急性心肌梗死溶栓 再灌注的关系。方法 :对 2 7例梗死前 1周内有不稳定性心绞痛和 2 5例梗死前无心绞痛的患者进行比较。 2组基础临床情况相匹配。梗死范围大小根据血清酶和∑R、NQ来估计 ,冠脉再通时间以抬高最明显的ST段迅速下降达 5 0 %为准。结果 :溶栓后 30min内梗死前心绞痛组 33%冠脉再通 ,而梗死前无心绞痛组没有 1例再通 (P <0 0 0 5 ) ;6 0min内再通率分别为 5 9%和 36 % (P <0 0 0 5 ) ;再通时间分别为 (49± 16 )min和 (6 9± 19)min(P <0 0 5 )。在梗死前心绞痛组 ,反映梗死范围大小的血清酶均明显低 ,而∑R相对较高 ,NQ数目相对较少 (均P <0 0 5 )。结论 :梗死前心绞痛组溶栓效果较好 ,梗死范围较小 ,梗死前反复心绞痛可作为对溶栓治疗敏感的预测指标。     

全麻诱导前预注芬太尼“先发镇痛”效应临床研究

目的：探讨全麻预注芬太尼的先发镇痛效应。／方法：选择40例择期全麻病人,随机分成试验组与对照组（n=20例）,术前常规用药,试验组诱导前用芬太尼5ug/kg,对照组将芬太尼改切皮后静注,术中麻醉维持相同,手术结束后病人自然清醒。术后有镇痛药使用意愿者均使用哌替啶镇痛。结果：两组病人一般情况及芬太尼总用量无显著性差异（P＞0．05）,试验组初次使用镇痛药时间明显延长（P＜0．01）,用药次数及剂量也显著少于对照组（P＜0．01）,试验组术后仅7（35％）例使用派替啶,而对照组使用哌替啶者达15（75％）例,两组差异性显著（P＜0．05）,结论：全麻前预注芬太尼具有良好的先发镇痛效应。     

子痫发生相关因素的探讨

目的 探讨与子痫发生相关的临床因素。方法 回顾５年间孕产妇妊高征中先兆子痫的发生情况,探讨产前检查、妊高征的程度、硫酸镁用量与子痫发生的关系,并对子痫的先兆症状及其出现时进行分析。结果 子痫发生率占财期孕产女的０．５６％（５１／９１０１）,占妊高征的８．３３％（５１／６２）。产前检查次数与子亲的发生明显相关,中、重度妊高征中子痫的发生率较高,硫酸镁日用量小于１５ｇ时子痫的发生率升高明显。轻度妊高征     

自发性高血压大鼠左心室肥厚与血压、心肌局部血管紧张素Ⅱ的关系

目的 研究自发性高血压大鼠(SHR)左心室肥厚与血压、心肌局部血管紧张素Ⅱ的关系。方法 取SHR(n=40)及正常对照组WKY(n=41),分为4周龄、8周龄、12周龄、24周龄及36周龄组．测收缩压、体重,左心室重量及用放免法测定心肌局部血管紧张素(AⅡ)含量,并进行两两线性相关分析。结果 通过对5个年龄段的SHR和WKY的收缩压、左心室重与体重比(LVM／BW)及心肌局部AⅡ含量的测定结果发现三者之间存在相关性,其中AⅡ与心肌肥厚有明显相关性。结论 血压与AⅡ在SHR大鼠的左心室肥厚中起着重要作用。     

盐酸芬氟拉明对映体的柱前衍生物GC法分析

以ω－莰烷酰氯为衍生试剂,采用柱前衍生化ＧＣ法,成功地分析了盐酸芬氟拉明、金刚乙胺和盐酸氯胺酮。光谱分析确证了芬氟拉明酰胺衍生物的结构,优化了盐酸芬氟拉明酰胺衍生物的结构,优化了盐酸芬氟拉明衍生条件,建立了盐酸花氟拉明的内标法定量分析方法。