变量筛选方法对郁闭度遥感估测模型的影响比较

比较基于偏最小二乘回归的Bootstrap方法与传统的平均残差平方和(RMSq)准则所选变量建立模型的精度差别.结果表明:Bootstrap方法是一种更优秀的变量筛选方法,比RMSq方法精度提高约5%;而且它不受变量多带来的运算困难的限制,更便于实际应用.     

应用PCR诊断隐孢子虫病

应用聚合酶链反应（ Ｐ Ｃ Ｒ）建立了一种诊断人及牛等哺乳动物隐孢子虫病的方法。试验采用甘油漂浮 Ｇ３ 耐酸漏斗过滤法纯化隐孢子虫卵囊，以液氮冻融法制备模板 Ｄ Ｎ Ａ，根据隐孢子虫 １８ Ｓｒ Ｒ Ｎ Ａ 序列设计 Ｐ Ｃ Ｒ 引物建立其诊断方法。该方法特异性强，可检出鼠隐孢子虫（ Ｃｒｙｐｔｏｓｐ ｏｒｉｄｉｕｍ ｍ ｕｒｉｓ）和小球隐孢子虫（ Ｃ．ｐａｒｖｕｍ ）卵囊；敏感性高，每克粪便可检出 ４００ 个卵囊。初步应用结果表明，所建立的 Ｐ Ｃ Ｒ 方法适合于人、牛等哺乳动物隐孢子虫病的临床诊断和流行病学调查。     

对乙酰氨基酚对大鼠原代肝细胞的损伤机制

胶原酶两步灌流法获取SD大鼠的原代肝细胞,并用不同剂量的对乙酰氨基酚处理.MTT法测定肝细胞的存活率,分光光度法测定培养上清液中乳酸脱氢酶(LDH)的含量.Western blotting法测定大鼠肝细胞中细胞色素P450酶2E1(CYP2E1)的表达水平.结果表明,对乙酰氨基酚可导致肝细胞存活率降低,LDH含量显著升高,CYP2E1表达增加.说明达到一定的剂量时.对乙酰氨基酚可引起肝细胞的损伤.     

贮藏期间板栗呼吸特性研究

对板栗贮藏期间呼吸速率及影响因素的研究发现：０－５℃贮藏能显著抑制板栗呼吸，能使板栗缓慢呼吸的稳定期延长至次年 ３月，但随贮期延长板栗组织愈加不耐受低 Ｏ２高 ＣＯ２环境；降低起始Ｏ２或提高起始 ＣＯ２浓度不能降低板栗的呼吸速率。     

气候变化对中国东北地区生态与环境的影响

【研究目的】综述了气候变化对东北地区的影响,以期在区域发展中能利用气候变化的有利方面,降低其不利的影响;【方法】根据近年来发表的相关论文,文章综述了东北地区已经发生的气候变化影响及未来可能受到的影响;【结果】结果表明,过去100年东北地区的温度升高明显且降水普遍减少,干旱化趋势严峻。温度的升高改善了东北的热量资源,部分农业生产从中受益。但由于气候变化,目前特殊的生态系统如湿地,冻土退化或消失。未来的气候变化,会改变农业生产布局,降低主要作物的产量,生态系统结构发生改变,农牧带沙漠化的风险增加;【结论】东北地区必须客观认识气候变化的利弊影响,采取相应的适应和应对措施,促进区域发展。     

猪脓肿引发大网膜脐疝的手术治疗

2006年5月,贵州省余庆县白泥镇子营社区草坪三组张某饲养的1头60 kg重架子猪脐部脓肿,请人用针穿刺两次,均有血脓流出,未见好转,求诊,笔者决定手术摘除,现报告如下。1临床检查脓肿直径约10 cm,触摸硬实,表面红肿、发烫,反复触摸无疝轮,穿刺流脓。2手术处理(1)保定:右侧卧保定。     

Role of p38 MAPK in cyclic mechanical stretch induced HMGB1 expression in alveolar macrophages

AIM: To investigate the role of p38 mitogen-activated protein kinase (MAPK) in cyclic mechanical stretch induced the expression of high mobility group box 1 protein (HMGB1) in alveolar macrophages (AMs). METHODS: AMs were cultured and seeded at 1×108 cells/L in 6-well Bioflex cell culture plates. Subsequently, the cells were exposed to cyclic mechanical stretch at 20% (group B) elongation using Flexercell 4000T cell stretching unit. In group C, cells were pre-treated with SB203580 (40 μmol/L) for 2 h before mechanical stretch. Group A served as control. The expression of HMGB1 mRNA in alveolar macrophages was detected by RT-PCR. p38 MAPK activity and the expression of HMGB1 protein were measured by Western blotting analysis. RESULTS: The expression of HMGB1 mRNA and protein, and the activity of p38 MAPK in AMs were significantly increased in group B than those in group A (P<0.05). SB203580, an inhibitor of p38 MAPK, significantly inhibited the inducing effect of mechanical stretch (P<0.05). CONCLUSION: Mechanical stretch regulates the expression of HMGB1 mRNA and protein in alveolar macrophages by activating p38 MAPK signal pathway.     

Chemical Synthesis and Structure-Activity Relationship Study Yield Desotamide a Analogues with Improved Antibacterial Activity

Desotamides A, a cyclohexapeptide produced by the deep-sea-derived Streptomyces scopuliridis SCSIO ZJ46, displays notable antibacterial activities against strains of Streptococcus pnuemoniae, Staphylococcus aureus, and methicillin-resistant Staphylococcus epidermidis (MRSE). In this study, to further explore its antibacterial potential and reveal the antibacterial structure-activity relationship of desotamides, 13 cyclopeptides including 10 new synthetic desotamide A analogues and wollamides B/B1/B2 were synthesized and evaluated for their antibacterial activities against a panel of Gram-positive and -negative pathogens. The bioactivity data reveal that residues at position II and VI greatly impact antibacterial activity. The most potent antibacterial analogues are desotamide A4 (13) and A6 (15) where l-allo-Ile at position II was substituted with l-Ile and Gly at position VI was simultaneously replaced by d-Lys or d-Arg; desotamides A4 (13) and A6 (15) showed a 2–4-fold increase of antibacterial activities against a series of Gram-positive pathogens including the prevalent clinical drug-resistant pathogen methicillin-resistant Staphylococcus aureus (MRSA) with MIC values of 8–32 μg/mL compared to the original desotamide A. The enhanced antibacterial activity, broad antibacterial spectrum of desotamides A4 and A6 highlighted their potential as new antibiotic leads for further development.     

miRNA在哺乳动物配子发生中的作用研究进展

哺乳动物配子发生的基因表达调控包括编码基因的阶段特异性表达调控及非编码基因的转录和转录后水平调控。微小RNA(microRNA, miRNA)作为一类小的非编码RNA, 通过识别靶基因非翻译区的结合位点, 导致mRNA降解或者蛋白质翻译抑制, 从而在转录后水平发挥调控作用。近年来, miRNA在哺乳动物生殖活动中的作用逐渐被揭示, 越来越多的研究表明, miRNA在哺乳动物精子发生、精子成熟、卵母细胞成熟、卵泡发育及早期胚胎发育等过程中都发挥着重要的调节作用, 其可通过调节支持细胞的增殖和凋亡或精原细胞、精母细胞及精细胞的细胞周期进程, 在精子发生的不同阶段发挥间接或直接调控作用, 也可通过调节卵母细胞、卵丘细胞以及颗粒细胞的增殖、凋亡、激素合成和细胞间作用, 对卵母细胞的发育和成熟过程进行调控。作者主要介绍了在哺乳动物配子发生过程中, miRNA的细胞和阶段特异性表达及其对靶基因的调节作用, 以期为深入研究哺乳动物配子发生的调控机制提供参考。     

猪流行性腹泻病毒SYBR Green I荧光定量RT-PCR检测方法的建立与应用

为快速、准确、灵敏检测猪流行性腹泻病毒（porcine epidemic diarrhea virus,PEDV）,以PEDV N基因为靶标设计引物,建立了一种PEDV SYBR Green I荧光定量RT-PCR检测方法。该方法最低可以检测到10个拷贝的病毒核酸,与猪传染性胃肠炎病毒、猪δ冠状病毒和猪轮状病毒等胃肠道病毒均无交叉反应,批内、批间重复试验的变异系数均在2%以内,表明该方法具有较好的敏感性、特异性和重复性。运用该方法对2018—2019年采集自山东省不同地区猪场的161份临床样品进行检测,检测结果与RT-PCR方法完全一致。以上结果说明,本试验所建立的SYBR Green I实时荧光定量RT-PCR检测方法为PEDV的快速检测提供了良好工具和技术支持。