胃癌患者血清肝细胞生长因子的检测及意义

Objective To explore the clinical significance of serum HGF level changes in gastric cancer pa-tients. Methods 60 cases of patients who operatied and clinicopathological confirmed gastric cancer, were detected serum HGF level by enzyme linked immunosorbent assay(ELISA) .40 cases were administered radical gastrectomy,20 cases of patients who had distant metastasis and loss operative chance were detected 7 days and 3 months preopera-tive,postoperative serum HGF level respectively. At the same time 40 cases of chronic gastritis patients and 40 cases of healthy examination people were selected as control group. Results Serum HGF level in patients with gastric canc-er was significantly higher than that of chronic gastritis and normal controls(P <0. 01). The serum HGF level of pa-tients with tumor vascular invasion significantly increased(P <0. 05). The patients with lymph node metastasis,serum HGF level was significantly higher than that patients with no lymph node metastasis(P <0. 05). The serum HGF level of patients with liver metastasis was significantly higher than that patients with no liver metastasis(P <0. 05). The se-rum HGF level of gastric cancer patients whose maximum diameter of the tumor ≥3cm were significantly higher than that maximum diameter of the tumor <3cm(P<0. 05). According to TNM staging of gastric cancer,the serum HGF level of Ⅰ phase and Ⅱ phase patients were significantly lower than that Ⅲ phase and Ⅳ phase patients(P <0.05).The serum HGF level of gastric cancer patients had no significant correlation with sex ,age and histological type(P <0.05). The serum HGF level of 40 cases of patients who were 1 week after surgery were significantly decreased,the patients who were 3 months after surgery were more obvious(P <0. 05 and P <0. 001). Conclusion HGF may play an important role in gastric cancer occurrence and development. The detection of serum HGF level can become an im-portant index for monitoring the degree of gastric cancer and prognosis of patients.     

Puerarin blocks Na~+ current in rat ventricular myocytes

AIM: To study the effect of puerarin (Pue) on Na~+ channel in rat ventricular myocytes. METHODS: Whole-cell patch-clamp technique was applied on isolated cardiomyocytes from rats. RESULTS: Pue inhibited cardiac I_(Na) in a positive rate-dependent and dose-dependent manner, with an IC_(50) of 349 μmol/L. The kinetics of blockage of cardiac sodium channel by Pue resembled the ClassIa/Ic of antiarrhythmic agents. Pue 300 μmol/L did not alter the shape of the I-V curve of I_(Na), but markedly shifted the steady-state inactivation curve of I_(Na) towards more negative potential by 15.9 mV, and postponed the recovery of I_(Na) inactivation state from (21.9±1.6) ms to (54.4±3.4) ms (P<0.01 ). It demonstrated that the steady state of inactivation was affected by Pue significantly. CONCLUSION: Pue protected ventricular myocytes against cardiac damage and arrhythmias by inhibiting recovery from inactivation of cardiac Na~+ channels.     

Facilitating effect of histamine on spatial memory deficits induced by dizocilpine as evaluated by 8-arm radial maze in SD rats

AIM: To investigate whether or not histamine is involved in spatial memory deficits induced by dizocilpine (MK-801) as evaluated by 8-arm radial maze of rats. METHODS: 8-Arm (4-arm baited) radial maze was used to measure spatial memory in rats. RESULTS: Bilaterally intrahippocampal (ih) injection of MK-801 (0.3 μg/site) impaired working memory and reference memory in rats. Both histamine (50, 100 ng/site, ih) and intraperitoneal (ip) injection of histidine (100, 200 mg/kg) markedly improved the spatial memory deficits induced by MK-801. On the other hand, the ameliorating effect of histidine (100 mg/kg, ip) was completely antagonized by α-fluoromethylhistidine (α-FMH, 5 μg/site, ih), a potent and selective histidine decarboxylase (HDC) inhibitor, and H_1-antagonist pyrilamine (1 μg/site, ih), but not by H_2-antagonist cimetidine, even at a high dose (2.5 μg/site, ih). CONCLUSION: The hippocampal histamine plays an important role in the ameliorating effect on MK-801-induced spatial memory deficits,     

“非典”患者康复出院6个月后免疫功能分析

目的 :检测和分析“非典”患者康复出院半年后的免疫功能。方法 :对 2 8例“非典”康复者出院半年后外周血分别进行免疫功能 :免疫球蛋白、补体、T淋巴细胞亚群检测和分析。结果 :“非典”患者康复出院后 6个月后免疫功能免疫球蛋白、补体、T淋巴细胞亚群检测值和对照组比较差异均无显著性 (P >0 0 5 )。结论 :SARS患者出院 6个月后虽仍存在不同程度的免疫功能异常 ,但与正常对照组比较无显著性差异。其免疫功能异常的原因可能与疾病本身、有基础病及年龄高有关。     

医学论文英文标题及摘要的常见句式

介绍了英文标题及摘要的常见句式。     

结直肠癌组织中Survivin表达与细胞增殖的关系

目的 :探讨结直肠癌组织中Survivin表达的临床病理学意义及其与癌细胞增殖的关系。方法 :免疫组织化学染色方法 (SP法 )检测 10 6例结直肠癌组织中Survivin、Ki 6 7、P5 3的表达 ,分析Survivin表达与Ki 6 7增殖指数、P5 3表达及各临床病理因素的关系。结果 :Survivin阳性表达结直肠癌的Ki 6 7增殖指数 (4 1.31%± 19.83% )明显高于Survivin阴性者 (2 6 .2 1%± 2 0 .36 % ) ,Survivin表达与肿瘤细胞增殖呈正相关 (P <0 .0 5 )。Survivin表达与P5 3表达无显著相关。Survivin在结直肠癌组织中的表达率为 6 4 .2 % (6 8/10 6例 ) ,癌旁形态学正常的结直肠粘膜未见Survivin表达 ;Survivin在中高分化结直肠癌表达阳性率 72 .4 % (6 3/87例 ) ,明显高于低分化结直肠癌 (2 6 .3% ,5 /19例 ) ,P <0 .0 5。此外 ,Survivin表达与患者性别、肿瘤位置、浸润深度、淋巴结转移、远处转移以及Dukes’分期无显著相关 (P >0 .0 5 )。结论 :凋亡抑制蛋白Survivin在结直肠癌组织中阳性表达率为 6 4 .2 % ,与细胞分化程度有关 ,可促进结直肠癌细胞的增殖     

红细胞在抗肿瘤治疗中的作用

红细胞不仅可以运送氧、二氧化碳和清除循环免疫复合物，还能够识别、黏附、提呈肿瘤抗原，此外红细胞能够促进免疫细胞吞噬和杀伤肿瘤细胞的能力，因此红细胞在机体抗肿瘤免疫发挥重要作用。近年来，红细胞也可以开发作为药物载体治疗肿瘤，这与红细胞自身具有生物相容性和半透膜的特性有关。药物可以倍助渗透压梯度的不同、抗生素提高膜通透性，膜受体介导连接，以及交联介导连接等方法载入。已载入红细胞的药物半衰期延长，缓慢释放，受体液中酶等具有生物活性的物质降解，并且可以减轻药物毒副作用。缺点在于其靶向性单一。     

非小细胞肺癌中细胞周期蛋白D1与E的作用及相互关系

目的 :研究细胞周期蛋白D1与E在非小细胞肺癌 (NSCLC)发生、发展中的作用及相互关系。方法 :免疫组化方法检测 87例NSCLC肿瘤组织中细胞周期蛋白D1、E的表达及PCNA估计增殖指数 (PI) ,并将上述结果与临床病理及预后资料进行对比分析。结果 :87例NSCLC中细胞周期蛋白D1、E阳性率分别为 4 4 .8% (39/87)、4 8.3% (42 /87) ,细胞周期蛋白D1阳性组的PI值显著高于阴性组 (P〈0 .0 5 ) ,细胞周期蛋白E阳性组PI值与阴性组无显著差异 (P〉0 .0 5 ) ;细胞周期蛋白D1阳性组肿瘤直径、淋巴结转移率和生存率均与阴性组有显著差异(P〈0 .0 1、〈0 .0 5、〈0 .0 1) ,细胞周期蛋白E阳性组淋巴结转移率、临床分期和生存率均与阴性组有显著差异 (P〈0 .0 5、〈0 .0 5、〈0 .0 1) ;细胞周期蛋白D1阳性组中细胞周期蛋白E的阳性率显著高于其阴性组 (P〈0 .0 5 ) ;细胞周期蛋白D1与细胞周期蛋白E双阳性组的PI值、肿瘤直径、淋巴结转移率显著高于非双阳性组 (P值均〈0 .0 5 ) ,生存率显著低于非双阳性组 (P〈0 .0 1)。结论 :细胞周期蛋白D1、细胞周期蛋白E均参与NSCLC的发生、发展 ,并影响其预后 ,但两者在其中所起作用不同 :细胞周期蛋白D1是调节NSCLC增殖的主要因素 ,细胞周期蛋白E主要与NSCLC进展有关 ;细胞周期蛋白D1可促     

舌诊指导临床辨证论治初探

望舌能够测知体质禀赋强弱；察舌能够准确地进行临床辨证；舌诊可帮助鉴别诊断；望舌能够预测疾病的进退预后；舌诊还能够指导临床定治则、遣方药。如能将舌诊和其他诊法有机地结合起来，将进一步提高临床诊断准确率和治愈好转率。     

抗体夹心酶联免疫吸附法测定重组E.coli L-门冬酰胺酶研究

用重组E.coliL-门冬酰胺酶免疫家兔，DEAE-纤维素柱层析纯化IgG，采用二步戊二醛交联法将辣根过氧化物酶标记抗体，建立抗体夹心酶联免疫吸附法，测定大鼠血浆中重组E.coliL-门冬酰胺酶浓度。本测定方法的线性范围为1～64U/L，灵敏度为0.4U/L。建立的抗体夹心酶联免疫吸附法测定大鼠血浆中重组E.coliL-门冬酰胺酶具有良好的精密度、回收率、灵敏度和特异性。