应用ESR检测方法研究人参总皂甙对缺血再灌注心肌保护作用

本实验应用鼠异位心脏移植模型,将人参总皂甙做为心脏添加剂,研究其对缺血心肌再灌注损伤时产生的氧自由基清除作用。对照组的心停搏液为ST·Thomas液,实验组的心停博液为加入人参总皂甙(80mg/l)的St.Thomas液。Wistar大的鼠40只,雌雄均有,每组

第16届国际理论和应用力学大会

<正> 1.一般情况 国际理论和应用力学联合会(IUTAM)召开的第16届国际理论和应用力学大会(ICTAM),于1984年8月20—25日在丹麦的哥本哈根举行。会议参加者共700余人。会议除开幕大会报告(Alfven:空间研究和宇宙中流体介质力学的新方法)和闭幕大会报告(Keller:力学研究的进展和问题)外,还按分组报告、分组开场报告,一般报告和墙报等多种方式进行,大会重点主题是一个:“海洋与结构的波相互作用”, “多组分介质的微

板壳断裂力学

本书阐明了板壳断裂理论的基础。论证了Reissner型板壳断裂理论的科学性、经典板壳断裂理论的缺陷及在一定范围内仍具有的实用价值；介绍了作者所创意的研究Reissner型板壳断裂纹尖端场的方法等。

目录

Chromosome painting between human and lorisiform prosimians: Evidence for the HSA 7/16 Synteny in the primate ancestral karyotype

Multidirectional chromosome painting with probes derived from flow-sorted chromosomes of humans (Homo sapiens, HSA, 2n = 46) and galagos (Galago moholi, GMO, 2n = 38) allowed us to map evolutionarily conserved chromosomal segments among humans, galagos, a

B2 肾上腺素受体多肽16 位基因型与夜间哮喘表现型的关系

目的　探讨B2 肾上腺素受体(B2AR) 16、27 位基因多态性与夜间哮喘表现型的关系。方法　以最大呼 气流速(PEFR ) 为标准, 将49 例哮喘患者分为夜间哮喘组(25 例) 和非夜间哮喘组(24 例)。用PCR 产物直接测序确 定B2AR 16、27 位基因型分布, 以及分析两个位点各种基因型与两组病例PEFR、第一秒用力呼气量(FEV 1) 以及用药 情况之间的关系。结果　以PEFR 为标准, 夜间哮喘组PEFR 在夜间平均下降33. 6% , 非夜间哮喘组下降7. 0% , 二 者差异显著(P < 0. 001)。夜间哮喘组和非夜间哮喘组(白天) 基础FEV 1 分别为73. 7 % 和85. 8 % , 也具有显著性差 异(P < 0. 001)。Gly16 的等位基因频率在夜间哮喘组56. 0% 明显较非夜间哮喘组22. 9% 高(P < 0. 05) , Gly16 集中 分布于夜间哮喘组。27 位点的多态性在两组间无显著性差异。结论　B2AR Gly16 基因型与夜间哮喘可能有关系。

mtDNA Data Indicate a Single Origin for Dogs South of Yangtze River, Less Than 16,300 Years Ago, from Numerous Wolves

There is no generally accepted picture of where, when, and how the domestic dog originated. Previous studies of mitochondrial DNA (mtDNA) have failed to establish the time and precise place of origin because of lack of phylogenetic resolution in the so fa

Interaction between human interleukin-16 and CD4 receptor of HIV-1

AIM: To study the interaction between human interleukin-16 (IL-16) and the receptor CD4 (T-lymphocyte differentiation antigen) of human immunodeficiency virus type 1 (HIV-1). METHODS: Two structurally con served regions (SCRs) of human IL-16 were built by the SYBYL/Biopolymer module using the corresponding transmembrane (TM) domain of human interleukin-1 (HIL-4) and HIL-2 as the templates. The coordinates for amino-terminal residue sequence, carboxyl-terminal residue sequences, and cytoplasm loops were generated using Biopolymer's LOOP SEARCH algorithm. RESULTS: HIL-16 first formed a homodimer, then contacted with CD4 dimer further forming a dimeric complex. Subsequently, the dimeric complex constructed the tetrameric complex by two disulfide bridges between the cysteines of HIL-16 (Cys31-Cys31). CONCLUSION: The interaction model is useful to propose the action mechanism of HIL-16 and is beneficial for rational designing of novel anti-HIV drugs.