氯吡格雷防治动脉粥样硬化缺血性疾病的研究进展

氯吡格雷防治动脉粥样硬化斑块破裂后血栓形成尤其是冠状动脉疾病及其经皮冠脉介入性治疗有了充足的临床试验证据,对于粥样斑块的形成和发展的相关依据正在进行,现就氯吡格雷全面预防和治疗动脉粥样硬化缺血性疾病的研究进展作一综述。     

超选择性动脉溶栓治疗急性缺血性脑卒中临床研究

目的评价超选择性动脉溶栓治疗急性缺血性脑卒中的疗效和安全性。方法选择2003年1月至2005年5月于本院进行超选择性动脉溶栓同时采用卒中登记方法收集的58例急性缺血性脑卒中患者,随访6个月,观察患者的预后。结果58例患者中并发脑出血6例(10．3%),其中症状性脑出血2例(3．4%)。1个月末、3个月末和6个月末分别死亡2例(3．4%)、4例(6．8%)和5例(9．3%)。3个月末和6个月未残疾或死亡例数分别为13例(22．4%)和9例(16．7%)。结论对选择的急性缺血性脑卒中患者进行超选择性动脉溶栓是有效和安全的。     

神经干细胞移植治疗缺氧缺血性脑损伤的实验研究

目的 研究神经干细胞移植治疗缺氧缺血性脑损伤的可行性。方法 取孕龄为12－16天的母鼠，从胎脑中分离神经细胞，进行培养、鉴定。用出生7天的SD大鼠的新生鼠制作缺氧缺血性脑损伤的动物模型，7天后接受神经干细胞移植（移植组，n＝16只），同时设置对照组，只注射磷酸缓冲液（对照组，n=8只），8－10周后，作Y迷宫实验检测大鼠的学习能力和记忆能力。取脑组织作免疫组织化学检查。结果 从大鼠胎脑中成功培养出神经干细胞，培养条件下呈悬浮状态生长，形成神经球，绝大多数的细胞表达神经干细胞的标志物神经巢蛋白（nestin）。接爱神经干细胞移植组大鼠的学习能力、记忆能力和对照组相比，有明显提高，差异具有显著性（P＜0.05）。接受神经干细胞移植大鼠组织中可见存活的移植细胞，并和宿主脑组织融合在一起。结论 在体外培养条件下，可从胎脑组织中培养出神经干细胞，移植到缺氧缺血性脑损伤大鼠脑内后，细胞与宿主的脑组织融合在一起，动物的学习、记忆能力有改善。移植神经干细胞是治疗缺氧缺知性脑损伤的有效方法之一。     

The self-traumatized perpetrator as a “transient mental illness”

Conceived of during the Vietnam war, the hypothesis that the perpetrators of atrocities could subsequently develop psychiatric disorders identical to those of their victims led to the emergence of a specific category: the self-traumatized perpetrator. While the United States was discovering that its soldiers had been involved in appallingly barbaric acts, psychiatry through the DSM-III post-traumatic stress disorder provided a more conciliatory response to the behavior of those veterans by shifting the political issue into the sphere of clinical debate. The author examines the origin, development and the subsequent exhaustion of this category from a strictly anthropological point of view. In this study, the category of self-traumatized perpetrator has been constructed on the basis of psychological knowledge and of various influencing external factors. In this sense, it can be viewed as transient category as far as psychiatric nosology is concerned, and is closely dependent on the outcome of the political and social issues that favored its emergence, and destined to disappear with them. In adopting the term coined by Ian Hacking, the author shows that the disorder observed in the case of the self-traumatized perpetrator is above all a “transient mental illness”     

新生儿缺氧缺血性脑病神经元烯醇化酶变化的研究

目的　探讨新生儿缺氧缺血性脑病时神经元烯醇化酶的变化,为HIE的诊断和治疗提供依据。方法　采用病历对照研究,将实验组分为三组:轻、中、重度HIE分别为2 1、4 9、8例;正常对照组73例。测定其血中神经元烯醇化酶的浓度变化。比较各组间检测指标的差异。结果　实验组NSE水平明显高于对照组,组间有显著性差异,P <0 .0 1:且实验组轻、中、重度间有显著性差异,P均<0 .0 5。结论　NSE水平与HIE的病情严重程度相关,是反映HIE严重程度比较客观的指标。     

The association of post-stroke neurological improvement with risk of subsequent deterioration due to stroke events

We sought to simultaneously confirm that substantial recovery at day 1 and day 7 after acute ischaemic stroke onset is associated with subsequent neurological deterioration in patients of the Acute Stroke Therapy by Inhibition of Neutrophils randomized clinical trial. Substantial recovery was assessed by improvement in the National Institutes of Health Stroke Score (NIHSS). Neurological deterioration was defined as any stroke event or NIHSS worsening from recovery assessment to day 90. After adjusting for age, t-PA and day 1 NIHSS, there was a non-significant tendency of substantial (pre-specified as 75%) recovery at day 1 to be associated with later deterioration [odds ratio (OR) 2.47; 95% CI, 0.95–6.50]. The corresponding OR for substantial (pre-defined as 65%) recovery at day 7 was 1.84 (0.85–3.96). Other thresholds for recovery were significantly associated with later deterioration: >50%, 80%, 90% and 100% for day 1 and >50%, 60%, 70%, 90% and 100% for day 7. The effect of recovery at day 1 was more important than that of later recovery. This study confirms the association between recovery and subsequent neurological deterioration and is the first to indicate the greater importance of acute recovery at day 1 in comparison with later recovery.     

降纤酶对进展性缺血性脑卒中预防作用的探讨

目的探讨降纤酶对进展性缺血性脑卒中的预防作用.方法将起病在72 h内的203例脑梗塞患者随机分成降纤酶治疗组及常规治疗组.降纤酶组在常规治疗的基础上加用降纤酶,治疗前后检测血液流变学各项指标,同时对进展性缺血性脑卒中患者的神经功能缺损进行评分.结果降纤酶组10例发生进展性缺血性脑卒中,常规治疗组24例,两组比较有显著性差异(P＜0.05);降纤酶组发生的进展性脑卒中的进展的严重程度比常规治疗组轻(P＜0.01);近期预后较常规治疗组好(P＜0.05);降纤酶治疗能明显降低血液流变学各项指标.结论降纤酶治疗能降低进展性缺血性脑卒中发生率,有利于进展性缺血性脑卒中患者神经功能的恢复.     

胃饲乙醇预处理诱导肝脏缺血耐受性的可行性探讨

目的探讨胃饲乙醇预处理对肝脏缺血再灌流损伤的影响,并初步评价其预处理的可行性。方法40%乙醇胃饲Wistar大鼠。分组:①大鼠36只,随机分6组:A组8g/kg、B组7g/kg、C组6g/kg、D组5g/kg、E组4g/kg、正常组0g/kg;以中毒症状及肝组织病理为指标,判定大鼠乙醇急性中毒剂量。②大鼠78只,随机分为4组:正常对照组(N)、单纯乙醇组(E)、单纯缺血组(ISCH)、胃饲乙醇预处理组(EPC);采用尾叶转流下的肝缺血模型,于再灌流3、6、12、24h留取标本。结果急性胃饲乙醇≤5g/kg预处理后,动物中毒症状轻,无死亡;乙醇预处理可以在一定程度上减轻肝脏90min的缺血再灌流损伤。结论适当剂量的乙醇胃饲预处理是一种安全的预处理措施,有望成为增强肝脏对缺血再灌流损伤耐受性的一种较好的预处理方式。     

Striatal cells containing the Ca2+-binding protein calretinin (protein 10) in ischemia-induced neuronal injury

The present study concerns the vulnerability of striatal interneurons immunopositive for the Ca²⁺-binding protein calretinin to ischemic neuronal injury. An immunohistochemical study was carried out on the striata of rats which had undergone transient middle cerebral artery occlusion. Two weeks after the ischemia, there was a marked reduction in the number of calretinin-positive neurons in the ipsilateral ischemic lesion, although the striatal interneurons positive for parvalbumin, which are a neuronal population distinct from the calretinin-immunoreactive cells in the striatum, were spared in the insulted areas. The present data indicate that the striatal calretinin-positive neurons are less resistant to transient ischemia, suggesting that there may exist vulnerability differences among the striatal interneurons in ischemia-induced neuronal injury.     

Flunarizine induces a transient loss of tyrosine hydroxylase immunoreactivity in nigrostriatal neurons

Neurotoxic effects of flunarizine (Fz), a selective calcium channel blocker, on the nigrostriatal dopamine system was investigated. Systemic injections of Fz to mice resulted in a transient loss of tyrosine hydroxylase (TH) immunoreactive nigrostriatal neurons without cell loss. TH immunoreactivity in these neurons was greatly reduced as rapidly as one day after drug administration (regardless of dosage used) and thereafter recovered in both dose- and time-dependent manners. Such a novel neurotoxic action of Fz may constitute a morphological substrate for reversible drug-induced parkinsonian signs described in recent clinical case reports.