大鼠不同脑区突触体钙水平的年龄差异

本实验使用荧光指示剂Ｆｕｒａ－２与Ｔｂ~（３＋）,检测了不同年龄组大鼠的不同脑区（海马、皮层、间脑、小脑）突触体内游离钙与膜结合钙水平。结果显示,与青年对照组相比,老年大鼠大部分脑区（海马、皮层、间脑）突触体内游离钙水平显著增高,尤其是海马突触体内游离钙增高极为显著;其突触体膜结合钙水平表现为：海马、小脑两脑区明显升高,而皮层、间脑两脑区明显下降,呈现一种全脑范围内的钙水平失衡。提示动物的衰老与其脑内钙自体平衡失调有关。     

Mechanisms of the actions of aromatase inhibitors 4-hydroxyandrostenedione, fadrozole, and aminoglutethimide on aromatase in JEG-3 cell culture

Selective inhibition of estrogen production with aromatase inhibitors has been found to be an effective strategy for breast cancer treatment. Most studies have focused on inhibitor screening and in vitro kinetic analysis of aromatase inhibition using placental microsomes. In order to determine the effects of different inhibitors on aromatase in the whole cell, we have utilized the human choriocarcinoma cell line, JEG-3 in culture to compare and study three classes of aromatase inhibitors, 4-hydroxyandrostenedione, fadrozole (CGS 16949A), and aminoglutethimide. Fadrozole is the most potent competitive inhibitor and aminoglutethimide is the least potent among the three. However, stimulation of aromatase activity was found to occur when JEG-3 cells were preincubated with aminoglutethimide. In contrast, 4-OHA and fadrozole caused sustained inhibition of aromatase activity in both JEG-3 cells and placental microsomes, which was not reversed even after the removal of the inhibitors. 4-OHA bound irreversibly to the active site of aromatase and caused inactivation of the enzyme which followed pseudo-first order kinetics. However, 4-OHA appears to be metabolized rapidly in JEG-3 cells. Sustained inhibition of aromatase induced by fadrozole occurs by a different mechanism. Although fadrozole bound tightly to aromatase at a site distinct from the steroid binding site, the inhibition of aromatase activity by fadrozole does not involve a reactive process. None of the inhibitors stimulated aromatase mRNA synthesis in JEG-3 cells during 8 h treatment. The stimulation of aromatase activity by AG appeared to be due to stabilization of aromatase protein. According to these results, 4-OHA and fadrozole would be expected to be more beneficial in the treatment of breast cancer patients than AG. The increase in aromatase activity by AG may counteract its therapeutic effect and might be partially responsible for relapse of breast cancer patients from this treatment.     

棘口属吸虫一新种(复殖目:棘口科)

本文记述采自寄生在我国陕西省洋县山区的濒危鸟朱Nipponianipponn（鹳形目Ciconiitormes）体内的棘口吸虫一新种,洋县棘口吸虫Echinostomayangxianensissp.nov.,对新种的形态特征作详细的描述并与近似种进行了比较。     

大针茅草原蝗虫的群落结构和能流研究

大针茅草原蝗虫的常见种类有１１种,其中７种属蝗亚科。毛足棒角蝗短星翅蝗和鼓翅皱膝蝗狭翅雏蝗分别构成蝗虫早、中、晚期的优势种类蝗虫九落的物 丰富度及多样性指数在蝗虫的性中期较高。蝗虫的次级生产力为５．１８ｋＪ／ｍ＾２．ａ,是地上净初级生产国物０．１８％。通过整个蝗虫群落的能流为１６．８４ｋＪ／ｍ＾２．ａ不同的蝗虫各 在生态秕有流中具有不同的贡献;其中毛尼中棒角蝗天整个蝗虫 能流中直着十分重要的作用,     

大兴安岭北部地区原始林火干扰历史的研究

在大兴安岭阿龙山林业局的一个集水区,通过样地法（９６个样地）,调查了大量的火疤木,研究了景观水平上的火状况。结果表明,由１８２５至１９９３年间样区共发生１４次火灾,火烧种类主要是地表火,但也有少量树冠火;火烧强度主要为弱度火;火场面积通常很大;火烧平均间隔期为３７ａ,火烧轮回期的约３０ａ。这些指标对大于大兴安岭北部林区有一定的代表意义。大兴安岭北部林区的火状况主要决定于兴安落叶松的抗火特性和森林群     

西藏南迦巴瓦峰地区孟加拉虎的初步研究

１９９４年５～６月、９～１０月及１９９５年６～１２月,作者对西藏东南部南迦巴瓦峰和邻近地区的孟加拉虎的分布及生态进行了野外调查,初步弄清了该地区虎的现状。通过在墨脱县格当乡的抽样调查及跟踪观察虎的移动和觅食,查明了金珠藏布江流域内近两年有关虎捕食大型牲畜的报告属实。１９９３年１０月至１９９５年７月,该河谷内因虎捕食共损失牛、马和骡３０２头,估计活体总重量约５９８８１ｋｇ,平均月损失２７２２ｋｇ,相当于自然状态下１１头虎的月进食量。全乡１２个村的牲畜均受到不同程度的影响,受损的户数占该乡总户数的６２％,户牲畜损失率为７．７％～１００％不等。对其它动物的调查表明,虎大量捕食牲畜与低海拔河谷的开发和环境中虎的自然食物缺乏有关     

豫西黄土高原农作区鼠类群落动态：时空尺度格局的初步分析

本文分析了豫西农业生态系统中鼠类群落局部空间尺度的短期动态格局。在区域尺度上,该群落为棕色田鼠＋大仓鼠型,群落多样性与丰富度和均匀度都有显著的正相关,丰富度的作用大于均匀度的作用。由于资源分布的斑块性,群落优势种和次优势种对环境变异的季节性反应不同,故群落的时空格局具有明显的变化。在农田中,群落在秋季分化为棕色田鼠＋大仓鼠亚群落型和大仓鼠＋棕色田鼠型,后者的生境斑块为单一的玉米田和油葵田;在作物轮作的格局下,群落多样性与丰富度和均匀度都有显著的正相关。在果园中,无论果树树龄和季节的变化,棕色田鼠的多度总是大于大仓鼠,即群落格局是不变的,而群落多样性与丰富度和多度之间均无显著的相关性。然而,灌溉可使大仓鼠与棕色田鼠的数量关系发生逆转,因此灌溉不仅影响果园中鼠类群落格局的分化,而且也将影响到农田中的这种分化。在一年弃耕地中,群落格局从夏季开始由棕色田鼠＋大仓鼠亚群落型转化为大仓鼠＋棕色田鼠亚群落型;在第３年末演替结束时,多年生植物取代一年生植物成为优势种,大仓鼠＋棕色田鼠群落格局则趋于稳定。在此过程中,群落多样性和丰富度与均匀度均无显著的相关性。本研究结果还表明,异质性可导致农作区鼠类群落的多样性     

利用固定化酵母细胞转化反式肉桂酸生产L—苯丙氨酸

研究了深红酵母（Ｒｈｏｄｏｔｏｒｕｌａｒｕｂｒａ）的培养基成分,培养固定化及转化条件,实验表明最佳基成分（％）葡萄糖０．５,胰蛋白胨０．５,酵母膏０．５,磷酸二氢钾０．０５,Ｌ－Ｐｈｅ０．０５,ｐＨ７．０,３０℃２０Ｌ发酵罐中培养１５～１７ｈ,最佳固定化条件为：用２．５％卡拉胶包埋１８％的湿菌体,最佳转化条件为：１．０％反式肉桂酸,４ｍｏｌ／Ｌ铵离子,ｐＨ０．５,３０℃,用卡拉胶固定化深红酵母（Ｒ     

The Mammalian Protein (rbet1) Homologous to Yeast Bet1p Is Primarily Associated with the Pre-Golgi Intermediate Compartment and Is Involved in Vesicular Transport from the Endoplasmic Reticulum to the Golgi Apparatus

Yeast Bet1p participates in vesicular transport from the endoplasmic reticulum to the Golgi apparatus and functions as a soluble N-ethylmaleimide–sensitive factor attachment protein receptor (SNARE) associated with ER-derived vesicles. A mammalian protein (rbet1) homologous to Bet1p was recently identified, and it was concluded that rbet1 is associated with the Golgi apparatus based on the subcellular localization of transiently expressed epitope-tagged rbet1. In the present study using rabbit antibodies raised against the cytoplasmic domain of rbet1, we found that the majority of rbet1 is not associated with the Golgi apparatus as marked by the Golgi mannosidase II in normal rat kidney cells. Rather, rbet1 is predominantly associated with vesicular spotty structures that concentrate in the peri-Golgi region but are also present throughout the cytoplasm. These structures colocalize with the KDEL receptor and ERGIC-53, which are known to be enriched in the intermediate compartment. When the Golgi apparatus is fragmented by nocodazole treatment, a significant portion of rbet1 is not colocalized with structures marked by Golgi mannosidase II or the KDEL receptor. Association of rbet1 in cytoplasmic spotty structures is apparently not altered by preincubation of cells at 15°C. However, upon warming up from 15 to 37°C, rbet1 concentrates into the peri-Golgi region. Furthermore, rbet1 colocalizes with vesicular stomatitis virus G-protein en route from the ER to the Golgi. Antibodies against rbet1 inhibit in vitro transport of G-protein from the ER to the Golgi apparatus in a dose-dependent manner. This inhibition can be neutralized by preincubation of antibodies with recombinant rbet1. EGTA is known to inhibit ER-Golgi transport at a stage after vesicle docking but before the actual fusion event. Antibodies against rbet1 inhibit ER-Golgi transport only when they are added before the EGTA-sensitive stage. These results suggest that rbet1 may be involved in the docking process of ER- derived vesicles with the cis-Golgi membrane.     

Principles of protein folding--a perspective from simple exact models.

General principles of protein structure, stability, and folding kinetics have recently been explored in computer simulations of simple exact lattice models. These models represent protein chains at a rudimentary level, but they involve few parameters, approximations, or implicit biases, and they allow complete explorations of conformational and sequence spaces. Such simulations have resulted in testable predictions that are sometimes unanticipated: The folding code is mainly binary and delocalized throughout the amino acid sequence. The secondary and tertiary structures of a protein are specified mainly by the sequence of polar and nonpolar monomers. More specific interactions may refine the structure, rather than dominate the folding code. Simple exact models can account for the properties that characterize protein folding: two-state cooperativity, secondary and tertiary structures, and multistage folding kinetics--fast hydrophobic collapse followed by slower annealing. These studies suggest the possibility of creating "foldable" chain molecules other than proteins. The encoding of a unique compact chain conformation may not require amino acids; it may require only the ability to synthesize specific monomer sequences in which at least one monomer type is solvent-averse.