骨髓增生异常综合症几项实验指标研究进展

本文对MDS染色体、骨髓祖细胞体外培养及免疫功能几项实验指标的研究进展予以介绍。     

对氰基苯代二氢哒嗪酮的设计,合成及抗惊活性的研究

在ＣｏＭＦＡ３Ｄ－ＱＳＡＲ研究的基础上设计并合成了对氰基苯代二氢哒嗪酮。对溴苯甲醛与吗啉、氰化钾反应得α－ｐ－溴苯基－４－吗啉基乙腈，再与丙烯腈反应得３－（ｐ－溴代苯基）丙酸。对溴基被氰基取代后与肼反应得目标化合物。其抗惊活性属中等强度，与ＣｏＭＦＡ方法预计值相差较大。     

颊脂体的外科解剖及其临床意义

对30侧成人颊脂体的形态，位置和血液供应进行了观测。颊脂体血供为多源性，主要血管蒂为上颌动脉的颊动脉和面动脉的颊支。依据上述血管蒂的解剖学走向和分布，颊脂体转位可修复邻近的颌面部和口腔软组织缺损。     

DNA限制性内切酶分析应用于伴放线放线杆菌的鉴定和分型

本文用限制性内切酶分析(REA)作伴放线放线杆菌(Aa)的鉴定和分型研究,提取Aa染色体DNA,井分别用BamHI、HindⅢ,Sal Ⅰ和Xho Ⅰ消化,作琼脂糖凝胶电泳。结果显示,Aa和嗜沫嗜血杆菌的DNA片段图谱明显不同;分属于两种不同血清型的两株Aa菌株,其DNA片段图谱也明显不同。这表明,REA可用于Aa菌的鉴定和分型,在所用的4种酶中,以Sal Ⅰ和Xho Ⅰ消化的DNA片段图谱差异最明显。     

抗蝮蛇毒磷酸二酯酶单克隆抗体的制备及鉴定

从蝮蛇毒中提取磷酸二酯酶,用此酶免疫BALB/c小鼠,取其脾细胞与小鼠骨髓瘤细胞Fo融合,以间接ELISA检测杂交瘤细胞培养上清液和小鼠腹水中的特异性抗体,其效价分别为1∶128和1∶51 200.抗原阻断试验结果表明,此抗体对蛇毒磷酸二酯酶具有特异性.该杂交瘤细胞株定为G_8,该株单抗属鼠IgG_(2a)亚型,经体外持续培养6个月,其分泌抗体性能稳定.     

涎腺恶性肿瘤的回顾性研究

本文对52例涎腺恶性肿瘤进行了回顾性研究。52例中发生于腮腺者27例(51.9％);病理类型以腺样囊性癌和粘液表皮样癌最多见;随访2～8年,死亡19例,病死率最高者为腺癌(5/8)和鳞癌(3/5)。作者对腺样囊性癌的病理分型提出了不同看法。     

Antidepressant-like effects of trazodone on a behavioral screen are mediated by trazodone, not the metabolite m-chlorophenylpiperazine

Trazodone is an atypical antidepressant drug (i.e. blocks neither monoamine uptake nor monoamine oxidase) which tests as an antidepressant drug on the differential-reinforcement-of-low-rate 72-s (DRL 72-s) schedule of reinforcement by increasing the reinforcement rate and decreasing the response rate. m-Chlorophenylpiperazine (m-CPP) is a 5-HT1B and 5-HT1C agonist, weak 5-HT2 antagonist, and trazodone metabolite. It has been suggested that formation of m-CPP is responsible for the antidepressant action of trazodone. Administration of m-CPP (1-10 mg/kg i.p.) 60, 30 or 10 min before the behavioral session did not mimic the reinforcement rate-increasing effects of trazodone (10-20 mg/kg i.p.) on rats performing under the DRL 72-s schedule of water reinforcement. Pretreatment with proadifen (50 mg/kg i.p.), an inhibitor of trazodone metabolism, caused a greater than 30-fold leftward shift in the dose-response curve for both the reinforcement rate and the response rate. These results suggest that the parent compound and not the trazodone metabolite m-CPP, mediates the antidepressant-like effects of trazodone on DRL 72-s behavior.