姬松茸多糖的抗炎作用

[目的 ]观察姬松茸多糖的抗炎作用 .[方法 ]制作二甲苯所致小鼠耳急性炎症模型、角叉菜胶所致大鼠关节肿胀模型、小鼠棉球肉芽肿亚急性炎症模型和大鼠佐剂关节炎模型 ,给予 4 0 ,80 ,16 0mg/kg的姬松茸多糖 .[结果 ]姬松茸多糖明显抑制上述各类型炎症反应 .[结论 ]姬松茸多糖具有抗炎作用 .     

大鼠脑内儿茶酚胺类递质及其代谢物的同时提取及反向高效液相测定法

目的建立一种操作简便、高效的测定脑组织中去甲肾上腺素(NA)、肾上腺素(AD)、多巴胺(DA)、3,4二羟基苯乙酸(DOPAC)及高香草酸(HVA)的方法,为有关药物作用机理的研究提供实验手段.方法以有机溶剂提取,高效液相色谱--电化学检测器(HPLC-EC)测定大鼠纹状体、皮质、下丘脑NA、AD、DA、DOPAC及HVA的含量.结果测得NA、AD、DA、DOPAC及HVA的绝对回收率依次分别为:80.3%±12.4%,86.5%±14.3%,90.3%±12.1%,89.5%±17.2%、87.6%±[13].2%.线性范围0.2～20ng,批内与批间变异系数分别小于8%及10%.结论该方法具有简便、迅速、回收率较高的特点,便于实验室应用.     

家兔急性周围型肺栓塞影像模型的制备

目的探讨用可吸收性明胶海绵制作家兔急性肺栓塞(PE)影像模型的可行性。方法20只实验组家兔随机分成5组,采用明胶海绵栓子经股静脉插管制成急性PE的动物模型。栓塞后行肺动脉造影检查,栓塞后2h、24h、3d、7d、14d(A、B、C、D、E组)分批处死家兔,解剖肺动脉并观察栓塞区肺组织病理变化。对照组2只注入生理盐水,分别于第7天,14天处死。结果20只实验组家兔1只麻醉意外死亡,19只制备模型后成活,模型制备成功率95%。肺动脉造影显示46支叶及段肺动脉栓塞。肺动脉解剖共发现栓子65个,栓塞动脉50支。A组肺体积肿胀,色深红,镜下观察见肺组织充血。B组、C组、D组、E组中15只家兔肺表面呈苍白色、暗红色、黑色或苍白色区内见黑色坏死区,另外1只仅见肺体积肿大,肺颜色无变化,E组1只第3天左侧发生气胸,肺萎缩;光镜下观察肺组织水肿、淤血、出血、坏死,炎性细胞浸润,肺泡含气减少,肺泡支架结构破坏,E组2例栓塞区见肺组织机化,栓子周围有血小板血栓和/或混合血栓形成。对照组2只家兔肺部仅见少量炎性细胞浸润。结论用明胶海绵作为栓塞物制备家兔急性肺栓塞模型,其方法简便、成功率高,为肺栓塞影像学研究提供了一种较好的实验模型。     

茂名石化公司社区居民的慢性病调查及饮食建议

目的　探究成人肥胖与高血压、糖尿病的关系 ,并给予饮食方面的建议。方法　抽样调查。在社区内抽样 2 891名居民 (2 0～ 74岁 ,曾在三个生活小区之一居住 5年以上者 ) ,分析其患肥胖及其他相关因素。结果　肥胖症及超体重率分别为 4 . 0 1%、2 2 . 97%。经标准化后肥胖症发生率为 3 2 3% (男 3 .0 5 % ,女3. 4 2 % ) ,超体重率为 19. 5 5 % (男 2 2 . 4 2 % ,女 16 . 5 % )。而且 ,所有肥胖人群中发生高血压和糖尿病的危险百分率分别是 1 70、2 13。结论　在茂名石油公司社区成人超体重和患肥胖症的情况是严峻的 ,适当的营养和合理的膳食干预是减少高血压、糖尿病等慢性病发病率的有效措施之一。     

Closed to reason: time for accountability for the International Narcotic Control Board

For more than two decades, the International Narcotic Control Board (INCB) has tried to stop harm reduction and its HIV prevention programs. This posture is based on a fundamental misunderstanding of their responsibilities and of drug addiction itself – i.e. as a public health and clinical care matter made criminal by decree. A recent focal point for the Board's action has been rejecting the use of supervised injection facilities to reduce morbidity and mortality of drug injectors. They single out individual countries and attempt to bully them into rejecting such programs under the banner of the United Nations (falsely) and in the name of international treaties. Their unrelenting and unjustified badgering of signatories to the international treaties that established the INCB is not only unjustified; it is an affront to one of the core purposes of the Board itself: to ensure adequate medical supplies and safe use of controlled substances. The INCB's ill-conceived obsession with intravenousaddiction as a crime flies in the face of the medical view and policies of the World Health Organization and the universally endorsed principles of the General Assembly of the United Nations.     

睾丸微石症2例报告及文献复习

目的:认识睾丸微石症(TM)的临床意义和诊断方法。方法:回顾性报告2例TM病例的临床资料,结合文献进行讨论。结果:2例分别因左精索静脉曲张和附睾炎就诊的患者行阴囊超声检查时发现睾丸内散在多发点状强回声,如针尖样,1～2mm,后无声影。分别诊断为局部TM、左精索静脉曲张和TM,左附睾炎。甲胎蛋白、人绒毛膜促性腺激素、乳酸脱氢酶和睾酮等检查均正常。对睾丸微石症未做特殊处置,随访6～8个月,体检和睾丸瘤标未见异常,阴囊超声睾丸图像无特征性改变。结论:TM是一种少见、无明显临床症状、相对稳定的疾病。多因阴囊其他疾病行超声检查时偶然发现,其是否属于癌前病变尚有争议,但是定期随访和阴囊超声检查是必要的。     

血管紧张素对增生性瘢痕成纤维细胞纤维连接蛋白合成的影响

目的：探讨血管紧张素Ⅱ（AngⅡ）及其Ⅰ型、Ⅱ型受体阻断剂和钙调神经磷酸激酶（CaN）的阻滞利环胞素A（CsA）对增生性瘢痕来源的成纤维细胞纤维连接蛋白mRNA和蛋白表达的作用。方法：体外分离培养增生性瘢痕成纤维细胞，分别将一定浓度的AngⅡ（10^-9～10^-5mmol／L），和AngⅡ10^-6mmol／L加上不同阻滞剂losartan、PD123319、环胞素A（浓度均为10^-5mmol／L）加入细胞培养液中刺激48h，分别采用逆转录聚合酶链反应（RT—PCR）及Westernblot印迹方法检测增生性瘢痕成纤维细胞纤维连接蛋白（FN）的mRNA及蛋白表达。结果：体外成功地培养增生性瘢痕成纤维细胞。经AngⅡ刺激48h后，FN mRNA和蛋白表达量明显增高，增高程度与AngⅡ浓度呈正比；加入losaartan和环胞素A后，FN原mRNA和蛋白表达量较单用AngⅡ组下降，而加入PD123319后，FNmRNA和蛋白表达量较单用AngⅡ组无明显改变。结论：AngⅡ可促增生性瘢痕成纤维细胞的FN合成，可能在增生性瘢痕的发展过程中起重要作用，该作用主要通过AngⅡ的Ⅰ型受体介导完成，该作用可能与CaN信号通路有关。     

经股动脉导管药盒系统植入术的并发症分析

目的研究经股动脉途径植入导管药盒系统导致并发症的原因,进一步提高其临床应用的价值。方法对76例中晚期恶性肿瘤采用经股动脉途径植入导管药盒系统,定期或不定期经皮经药盒灌注化疗和栓塞,总结其并发症。结果发生并发症13例,发生率为17.1%(13/76)。包括留置导管尖端移位4例,靶动脉闭塞2例,迟发出血2例,留置导管堵塞1例,切口延期愈合1例,药盒外露1例,留置导管与药盒分离1例,靶动脉假性动脉瘤形成1例。结论经皮股动脉途径导管药盒系统植入术的并发症只要处理得当,是可以控制的。本技术不失为一种安全可靠的治疗手段,值得临床应用。     

不同浓度5-溴脱氧尿嘧啶核苷标记山羊骨髓基质干细胞的体外研究

Objective To explore the feasibility of labeling and tracing in vitro goat bone marrow mesenchymal stem cells (BMSCs) by bromodeoxyuridine (BrdU) on the basis of investigation of its optimal concentration, incubating time and cytotoxicity. Methods A healthy goat, aged 10 months old, male, weighing 32 kg, was used in this study. Bone marrow was aspirated. BMSCs were isolated and cultured using the adherence method in vitro. The fourth passage of BMSCs (P4) were incubated with BrdU at 5, 10, 15, 20 μmol/L as 5, 10, 15, 20 μmol/L BMSC groups. Cells were not labeled by BrdU as negative control. The following parameters were measured: induction, differentiation and determination of goat BMSCs; the optimal mass concentration and incubation time of 5-BrdU labeling; cell positive rate at 12, 24, 48 and 72 hours in each group using immunofluoreseenee; the cell survival rate after various concentrations of BrdU ladling by trypan-blue exclusion. Results The morphology of the primary and passage goat BMSCs was fusiform in shape. Goat BMSCs could differentiate into osteoblasts and chondrocytes following induction. BMSC nucleus showed green fluorescence under fluorescence microscope after being labeled by BrdU. The mean labeling rate increased with the increase in the concentration and incubation time of BrdU, and reached to (93.32± 3.25)% after incubation in 15 μmol/L, BrdU for 48 hours. There were no significant differences between 15 μmol/L BrdU for 72 hours, 20 μmol/L BrdU for 48 hours and 72 hours (P > 0.05), or between the other groups or time points (P < 0.05). The labeling rate of the blank control group was 0. The cell survival rate was all above 90% (P > 0.05). Conclusions BrdU can be used as a labeling marker for goat BMSCs. When the concentration is 15 μmol/L and the incubation time is 48 hours, the optimal labeling effect can be achieved. Goat BMSCs labeled with BrdU is of high efficiency and safety.