Thirty-two Cases of Acne Treated with Blood-letting Puncture,. Cupping and Chinese-Drug Facemask

To observe the therapeutic effect on acne treated with blood-letting puncture,cupping and Chinese-drugfacemask.Thirty-two patients with acne were treated with above-mentioned therapeutic method.Cure,improvement and ineffectiveness were respectively found in 24,7 and 1 case,with a curative rate of 75.0%and a total effective rate of 96.8%.The combination of blood-letting puncture,cupping and externalapplication of Chinese-drug facemask is effective in treating acne.     

TNF-α和低氧对胰腺癌细胞表达VEGF-A、C的调节

目的:探讨细胞活素肿瘤坏死因子-α(TNF-α)、SNAP(S-Nitroso-Nacetyl-penicillamine)对胰腺癌细胞产生血管内皮生长因子A、C(VEGF-A、C)的调节.方法:用Northern杂交和Western杂交法分析6种人胰腺癌细胞株中VEGF-A、C基因和蛋白的表达;以TNF-α或SNAP刺激其中两个细胞株后用逆转录-聚合酶链式反应技术(RT-PCR)分析其VEGF-A、C基因的表达.结果:Northern杂交法显示这6种胰腺癌细胞株均有4.1kb VEGF-A基因和2.4kb VEGF-C基因的表达;Western杂交法显示它们均有分子量为43kD的VEGF-A蛋白质和分子量为55kD的VEGF-C蛋白质的表达.RT-PCR分析法显示:TNF-α使细胞株COLO-357产生VEGF-A、VEGF-C mRNA分别减少约1～2.5倍、1～2倍,使细胞株CAPAN-1产生VEGF-A、VEGF-C mRNA分别减少约1倍、1.6～2.5倍;而SNAP刺激细胞株COLO-357产生VEGF-A mRNA增加约5倍,刺激细胞株CAPAN-1产生VEGF-A mRNA增加约4倍,但对这两种细胞株产生VEGF-C mRNA均无明显刺激作用.结论:细胞活素TNF-α和低氧通过调节血管内皮生长因子A、C的表达而影响胰腺癌细胞的生物学特性,抑制癌细胞的增殖,促进其凋亡、死亡或进展、恶化.     

Production and characterization of monoclonal antibody against colon cancer associated antigen in Chinese]

Although many monoclonal antibodies have been made in human colon cancer, none of them are from the Chinese species. Recently, a colon cancer cell line CC-M2 established from a Chinese patient has been completely characterized and used as immunogen to produce monoclonal antibodies. Monoclonal antibodies were produced by standard hybridoma technique. The fusion rate was 95.8%. An isotype IgG1 of high proliferation named as Sam-2 was used in this study. The titers were measured around 10(4). Further studies on MoAb Sam-2 through indirect immunofluorescent and immunoperoxidase tests revealed its good specificity and sensitivity in colorectal cancer tissue. In CEA study, the result indicated that Sam-2 may react on a non-CEA related antigen. For further clinical application, the antigen was identified as a glycoprotein by chemical resistant test. In preliminary studies using sodium dodecyl sulfate-polyacrylamide gel electrophoresis and immunoblotting techniques, Sam-2 could recognize two closed antigens or a dimer antigen with molecular weight 25.2 and 27 Kd respectively.     

Brain natriuretic peptide enhances the endothelium-independent cAMP and vasorelaxant responses of calcitonin gene-related peptide in rat aorta

Calcitonin gene-related peptide (CGRP) causes vasorelaxation in rat aorta involving endothelium/nitric oxide (NO)-dependent elevations of both cAMP and cGMP levels. When endothelium is removed, preincubation with exogenous NO uncovers and potentiates direct (endothelium-independent) cAMP elevations and vasorelaxations caused by CGRP. This enhancing effect of NO potentially involves elevation of cGMP and inhibition of Type III (cGMPinhibitable) phosphodiesterase, causing accumulation of cAMP. However, NO may have other actions. The aim of the present study was to determine if brain natriuretic peptide (BNP), which elevates cGMP levels independent of NO, could enhance cAMP accumulations and vasorelaxations induced by CGRP in rat aortic rings denuded of endothelium. When added separately, neither CGRP (100 nM) nor BNP (10 nM) altered cAMP levels. When added in combination, CGRP (100 nM) and BNP (10 nM) significantly elevated cAMP levels (from control of 0.95 ± 0.08 to 1.53 ± 0.09 pmol/mg protein) at 2 min. BNP (10 nM) elevated cGMP levels 10-fold at 2 min and this response was not altered by co-administration of CGRP (100 nM).Pretreatment with BNP at concentrations as low as 1 nM in endothelium-denuded aortic rings greatly enhanced the direct vasorelaxant effects of CGRP (100 nM) (from control of 0% to 57.6 ± 6.8% relaxation of phenylephrineprecontractions). Our findings indicate that BNP enhances direct (endothelium-independent) cAMP elevations and vasorelaxations caused by CGRP in rat aorta, thus supporting the concept that cGMP inhibits cAMP metabolism and enhances CGRP-induced responses in aortic smooth muscle cells.     

蚓激酶生物活性检测方法的研究

本文采用组织纤溶酶原激活剂（ＴＰＡ）─纤维蛋白平板法测定蚓激酶的生物活性。该法操作简便，易于观察，重现性好。     

多发性肌炎的动物模型及雷公藤多甙对其疗效的研究

目的　寻找一种多发性肌炎的良好动物模型及其有效的治疗药物。　　方法　给动物注射同种大鼠的肌匀浆 ,观察其活动状态 ;通过肌肉组织染色及ELISA法 ,研究肌肉的病理学变化 ,同时给动物喂服雷公藤多甙观察药物疗效。　　结果　部分动物表现肌无力和肌萎缩 ,大多数肌肉组织学检查示肌纤维炎性变 ;免疫组化检查可见肌膜、肌内膜和肌束膜中有IgG沉积。动物服雷公藤多甙后肌肉病变明显减轻 ,其疗效与强的松相似。　　结论　用同种大鼠肌匀浆免疫动物可诱导出多发性肌炎的动物模型 ;雷公藤多甙能有效地治疗多发性肌炎。     

竹荪深层发酵菌丝体对小鼠免疫功能的影响及其抗肿瘤作用

过对食药用真菌──竹荪深层发酵菌丝体提取液对小鼠免疫功能及S－180肿瘤细胞的作用观察，表明其发酵菌丝体可明显提高小鼠腹腔巨噬细胞的吞噬功能（P＜0．01），并显著增加免疫器官的重量（P＜0．05）；对小鼠S－180肿瘤的抑瘤率为40．63％。     

蓖麻油引产餐对妊娠大鼠分娩的影响

目的蓖麻油引产餐用于妊娠晚期引产效果明显，但其作用机制不清楚。本研究通过引产餐灌服妊娠大鼠建立动物引产模型，以期了解引产餐对妊娠大鼠分娩启动和产程的影响，并初步探讨蓖麻油引产餐活性成份。方法于大鼠妊娠第１８～２０天灌服引产餐，观察大鼠分娩启动和分娩产程变化。利用高压液相分析蓖麻油和蓖麻油引产餐中脂肪酸成份。结果引产餐可提前妊娠大鼠分娩启动时间，缩短分娩产程。蓖麻油引产餐和蓖麻油两者脂肪酸对比结果显示，成份相同，蓖麻酸均占９０％，未见花生四烯酸成份。结论引产餐对妊娠晚期大鼠具有引产、催产作用，可以利用引产餐灌服妊娠大鼠建立动物引产模型。推测蓖麻酸是引产餐启动分娩和缩短产程的活性物质。     

双氯芬酸钠滴眼液稳定性研究

采用高效液相色谱法测定双氯芬酸钠滴眼液的含量，方法简便，准确，能将药与杂质峰完全分离。应用化学动力学原理以恒温加试验预测双氯芬酸钠滴眼液稳定性及有效期，室温下有效期ｔ＾２５℃０．９约为２．５７年，与留样观察结果相符。     

动脉灌注灭活再植治疗骨肉瘤的体会

本组１２例骨肉瘤均采用动脉区域灌注灭活再植及术后化疗方法，术后２年存活率平均为７５％，１例因经验不足致局部复发，仅占８．３％，表明在化疗保障下，采用此种方法即能保肢，又能获得与截肢治疗相同的手术效果，优于单纯行灭活再植术后中方法。