食用向日葵产量性状的遗传研究

以食葵不育系17-A26为母本、恢复系17-C19为父本,构建P₁、P₂、F₁、F₂、B₁和B₂ 6个世代群体,研究了产量相关性状盘径、单株总粒数、结实率、百粒重、粒长和粒宽的后代变异及遗传率。结果表明,6个性状均为数量性状,变异幅度排序为单株总粒数>粒长>盘径>结实率>百粒重>粒宽,狭义遗传率排序为百粒重>粒长>单株总粒数>粒宽>盘径>结实率。根据遗传进度结果,百粒重、粒长、单株总粒数和粒宽宜早代根据表型选择,盘径宜晚代选择,结实率宜晚代结合多环境联合选择。     

柚木(Tectona grandis)无性系繁育及造林技术

柚木为马鞭草科柚木属植物,是世界上最珍贵的用材树种之一。文章介绍了柚木的生物学特性、无性繁殖即组培技术要点以及造林技术,论述了柚木在我省的推广前景。     

月季组织培养过程中的影响因素

综述了月季组织培养过程中的影响因素，重点介绍了植物生长调节剂、外植体、培养基和培养条件等对月季试管苗生长的影响。同时分析了月季组培影响因素研究中存在的不足，提出对多因素、复杂因子共同影响行为的研究和探讨是今后月季组培影响因素研究中的重点内容。     

合理调整山西人民食物结构的策略与途径

合理调整我国人民的食物结构是提高全民族身体素质,推进社会文明进步,具有深远的战略意义的一项国策。调整国民食物结构是一个科学性,政策性很强,社会涉及面广,地区人群民食习惯差别大的极为复杂的动态系统工程。作者针对山西省情实际,从追朔我国饮食传统,膳食民习,食物资源及演变趋向探求,提出合理调整山西人民食物结构的策略与途径。     

Expression and modulation of connective tissue growth factor in renal interstitial fibrosis

CTGF, a member of the CCN family of immediate early genes, is a recently discovered profibrotic growth factor, which is involved in many pathophysiologic procedures. CTGF acts as a downstream effector of TGF-β acting on interstitial cells to enhance the progression of fibrotic renal diseases. It has been shown that CTGF gene expression can be induced or blocked by some kinds of cytokine and drugs. It is an interesting candidate target for future intervention strategies of renal interstitial fibrosis.     

贮藏中福桔果皮细胞结构的显微观察及果实理化成分测定

贮藏期间福桔果皮细胞始终具有分裂增殖能力,细胞生长的养分主要通过维管束向果肉吸取,因而促进果肉衰老,形成枯水.枯水果实在贮藏早期就发现果皮细胞层和油腔分泌细胞无丝分裂旺盛,双核细胞多,果皮增厚多.严重枯水时,果皮细胞还具细胞核、线粒体、有色体等超微结构,未枯水果实细胞分裂少见.经预贮后贮藏的果实,由于中断了果皮组织与维管束的联系,果皮细胞生长受抑制,果肉水分、养分消耗少,枯水率最低,     

In vitro expression and inhibition of procoagulant activity produced by bovine alveolar macrophages and peripheral blood cells

Local and systemic activation of coagulation is frequently associated with bacterial sepsis. The coagulopathy is due, at least in part, to expression of tissue factor (TF) by monocytes and macrophages. The purpose of this study was to evaluate the expression of procoagulant activity by bovine alveolar macrophages, leukocytes and platelets, and to determine the relative potency of three chemical inhibitors of TF expression (pentoxifylline, retinoic acid, and cyclosporin A). Bovine alveolar macrophages were stimulated with lipopolysaccharide (LPS) derived from Pasteurella haemolytica or recombinant bovine tumour nervous factor (TNF) and dose- and time-dependent effects on TF expression were studied. LPS and TNF induced TF expression in alveolar macrophages and LPS treatment of whole blood induced TF expression in mononuclear cells. Neutrophils and platelets also expressed procoagulant activity, but this activity was not inhibited by anti-bovine TF monoclonal antibody. Pentoxifylline (40 mol/L), retinoic acid (0.01 mmol/L) and cyclosporin A (0.08 mol/L) inhibited TF expression when added concurrently with LPS or TNF, but not when added 4 h after stimulation. TF mRNA was not detected in unstimulated alveolar macrophages by Northern blot analysis. In contrast, exposure to LPS or TNF for 6 h induced marked expression of TF mRNA, which was inhibited by treatment with pentoxifylline, retinoic acid and cyclosporin A. Expression of TNF by alveolar macrophages stimulated with LPS was also inhibited by these compounds. Our results indicate that procoagulant activity expressed by alveolar macrophages and monocytes is associated with expression of TF, whereas procoagulant activity expressed by neutrophils and platelets is not. The concentrations of pentoxifylline and retinoic acid necessary for inhibition of TF expression in vitro may not be achievable in vivo owing to their toxic effects. However, the in vitro concentration of cyclosporin A that inhibited TF expression did not exceed the plasma concentration observed in humans, and therefore may be useful for inhibition of TF expression in vivo.Abbreviations BAL bronchoalveolar lavage - LPS lipopolysaccharide - cDNA cloned deoxyribonucleic acid - cAMP cyclic adenosine monophosphate - GAPDH glyceraldehyde phosphate dehydrogenase - mRNA messenger ribonucleic acid - TF tissue factor - TNF tumour necrosis factor - DPBS Dulbecco's phosphate-buffered saline     

红千层的离体培养及快速繁殖

 研究了红千层离体快繁的若干影响因素。结果表明: 叶片在MS + 6-BA 115 mg·L ^{- 1}+NAA015 mg·L ^{- 1}中的愈伤组织诱导率43% , 并可直接从愈伤组织表面分化出不定芽, 分化率为69.2%; 腋芽启动培养基为MS + 6-BA 1～1.5 mg·L ^{- 1} + NAA 0.5 mg·L ^{- 1} , 萌动率为77%; 继代和增殖培养基为MS + 6-BA 1 mg·L ^{- 1} +NAA 0.25 mg·L ^{- 1} , 平均增殖系数为16.7; 生根壮苗培养基为1 /2MS +NAA 0.25 mg·L ^{- 1} , 生根率96.1%; 试管苗生根培养30～35 d移栽, 成活率最高可达90%以上。     

木那格葡萄的组培快繁试验

以木那格葡萄的茎尖、单芽茎段为外植体，进行组培快繁试验。蛄果看出，适宜茎尖分化的培养基为B5 BA1．0mg／L IBA 0．1mg／L。适宜单芽茎段一次成苗生长的培养基为B3 BA0．05mg/L IBA0．2mg／L。适宜的生根培齐基为1／2MS IBA 0．2mg／L 蔗糖40g／L。健壮生根的试管苗要待4片叶以上移栽，移栽基质以蛭石较好。时间宜在4—5月份。