甲基毒死蜱对红细胞膜乙酰胆碱酯酶的抑制作用及其与膜脂相互关系

以人红细胞膜为材料,研究了甲基毒死蜱与膜上乙酰胆碱酯酶(AChE)的相互作用及其与膜脂的关系。结果显示,甲基毒死蜱对人红细胞膜AChE有明显的抑制作用,与膜温育30min,其半数抑制浓度约为0.10 mmol/L。动力学分析表明,其抑制作用为非竞争性。0.2％Triton X-100并不改变AChE对甲基毒死蜱的敏感性,亦即AChE上甲基毒死蜱的作用部位与其所处的脂质微环境无关。     

泉州常绿阔叶林的特征与分布

泉州的常绿阔叶林包括南亚热带雨林和南亚热带山地照叶林。通过对这两种植被类型的区分成分、生活型、叶的性质以及群落的结构与分布的分析,说明海拔450m以下具有较明显的以厚壳桂、红楠等为优势种的南亚热带雨林的特征和景观;海拔450～900m主要以米槠等拷类为优势种的群落,但仍有南亚热带雨林的某些特征;海拔900～1400m以甜槠为主要建群种的群落,属于中亚热带照叶林的群落特征。     

两株蓖麻蚕核型多角体病毒DNA同源性的研究

两株不同来源的蓖麻蚕核型多角体病毒(ArscsNPV和ArNPV)经提纯后,使用SDS—苯酚抽提病毒核酸,并使用限制性内切酶EcoRI,BamHI酶解后,用分子杂交方法与缺口平移标记的ArscsNPV-DNA探针杂交,分析了两株蓖麻蚕NPV病毒核酸的同源性。EcoRI酶解的ArNPV-DNA产生8个片段,其中5个片段能与ArscsNPV-DNA探针杂交。BamHI酶解ArNPV-DNA产生7个片段,其中6个片段能与ArscsNPV-DNA探针杂交。结果表明:两株蓖麻蚕NPV之间病毒核酸具有很高的同源性。使用斑点杂交方法分析了ArscsNPV与ArNPV,柞蚕NPV及家蚕NPV之间的核酸同源性,结果表明:ArscsNPV与ArNPV,柞蚕NPV具有同源性。而与家蚕NPV无核酸同源性。     

显脉獐牙菜的单萜环烯醚甙

近年来,肝炎发病率高,青叶胆(Swertia mileensis)因此被大量采挖,野生青叶胆资源逐年减少。为发掘新药源,我们对云南产狭叶獐牙菜(S.angustifolia)和显脉獐牙菜(S.nervasa)的化学成分进行了研究。本文报道从中分离鉴定的4个单萜环烯醚甙Ⅰ—Ⅳ。Ⅰ、Ⅲ、Ⅳ分别为维哥罗甙(vegeloside)、獐牙菜甙(sweroside)和獐牙菜苦甙(swertiamarin),Ⅱ是Ⅰ的同分异构体,命名为显脉獐牙菜甙(nervoside)。显脉獐牙菜甙(Ⅱ)白色无定形粉末,味极苦。UVλ-_(max)~(EtOH):243nm(log ε-3.89)。IR v_(max)~(KBr) cm~(-1):3400、1700和1610,显示单萜环烯醚的特征吸收峰显脉獐牙菜;显脉獐牙菜甙;单萜环烯醚甙     

Investigations of interaction mechanism and conformational variation of serum albumin affected by artemisinin and dihydroartemisinin

In this work, binding interactions of artemisinin (ART) and dihydroartemisinin (DHA) with human serum albumin (HSA) and bovine serum albumin (BSA) were investigated thoroughly to illustrate the conformational variation of serum albumin. Experimental results indicated that ART and DHA bound strongly with the site I of serum albumins via hydrogen bond (H-bond) and van der Waals force and subsequently statically quenched the intrinsic fluorescence of serum albumins through concentration-dependent manner. The quenching abilities of two drugs on the intrinsic fluorescence of HSA were much higher than the quenching abilities of two drugs on the intrinsic fluorescence of BSA. Both ART and DHA, especially DHA, caused the conformational variation of serum albumins and reduced the α-helix structure content of serum albumins. DHA with hydrophilic hydroxyl group bound with HSA more strongly, suggesting the important roles of the chemical polarity and the hydrophilicity during the binding interactions of two drugs with serum albumins. These results reveal the molecular understanding of binding interactions between ART derivatives and serum albumins, providing vital information for the future application of ART derivatives in biological and clinical areas.