Restoration of tuber production by exposure to unshaded daylight in Eleocharis kuroguwai Ohwi shaded during the early tuber formation period

The loss of final tuber weight of Eleocharis kuroguwai Ohwi by shading during the early tuber formation period (TFP) is overcome by exposure to unshaded daylight thereafter (late TFP). In the present study, the growth parameters that contribute to the dry matter increase (DMI) per day of tubers in the late TFP were examined. DMI of the tuber during the late TFP was determined by that of the whole plant and the ratio of the DMI of the tuber to that of the whole plant during this period. The ratio of the DMI of the tuber to that of the whole plant during the late TFP was significantly correlated with the DMI of the whole plant during the first 14 days of the late TFP. During the late TFP after the exposure to unshaded daylight, DMI of the whole plant correlated with the surface area of the stem (SAS) and net assimilation ratio (NAR), and the SAS correlated with the stem dry weight (DW) and specific stem-surface area (SSA). SSA negatively influenced NAR, but NAR was increased by unshading. During the late TFP after shading, the effect of the decrease of the stem DW due to shading on the DMI of the whole plant was mitigated by the large SAS and high NAR. These results indicate that the growth parameters that contribute to the DMI of tuber during the late TFP after exposure to unshaded daylight are SAS and NAR just after unshading, and SSA during this period.     

土壤改良对越桔生长的影响

在盆栽条件下,对生长越桔的土壤进行改良。通过土壤pH值的变化、生长量及相关指标的分析对比,获得适合越桔生长的土壤改良类型。试验研究表明,pH值4.0～5.0的苔藓 草炭 原土 S土壤改良类型适合于越桔的生长,植株的高度、粗度、基生枝数等都明显增加。从各指标上观察,原土 2S的土壤改良类型也具有一定优势,说明在土壤有机质充足的基础上,只需调酸,越桔就能正常生长。     

荔枝环剥时期对新梢生长及碳素储备的影响

 枝梢环剥显著抑制了‘怀枝’荔枝新梢的生长，并导致射线细胞和髓部大量积累淀粉。梢芽萌发或伸长前环剥可完全抑制新梢生长，而新梢快速伸长期环剥对其抑制效应最弱。秋季环剥对新梢的抑制和对淀粉积累的促进效应明显高于春季环剥。环剥口以上的老叶面积和环剥位置并不影响环剥对新梢生长的抑制效应和促进淀粉的积累效应，但环剥口以上单位枝梢长度的叶面积与淀粉含量呈显著正相关。     

丝兰属植物提取物降低鸡舍氨气浓度的效果试验

通过在21日龄的肉用仔鸡饲料中添加丝兰属植物提取物(其有效成分为丝兰皂角苷)，研究丝兰属植物提取物对降低鸡舍中氨气浓度和提高肉仔鸡生产性能的效果。试验结果表明，试验组鸡舍内氨气平均浓度为4．75mg／L，对照组鸡舍内氨气平均浓度为13．80mgl／L，试验组比对照组鸡舍内氨气平均浓度降低了9．05mg／L，经t检验，两鸡舍内氨气平均浓度差异显著(P＜0．05)，并且试验组比对照组饲料报酬提高了8.92％。     

不同培养基对杏鲍菇菌丝生长的影响

比较了杏鲍菇一级种和二级种培养基配方 ,试验表明杏鲍菇一级种培养基以配方三最好 ,菌丝干重是配方七 (对照 )的 3 5倍 ,差异极显著 ;杏鲍菇二级种培养基以配方四最好 ,菌丝生长势最强 ,与供试各培养基配方相比较 ,差异均为极显著     

干旱胁迫下保水剂对苗木生长及生理的影响

在盆栽条件下,对不同保水剂处理的土壤吸持水特性以及云南拟单性木兰和绒叶含笑苗的水分生理、生长状况进行试验研究。结果表明,随着保水剂用量的增加,土壤保水能力和供水能力增加,苗木在有限水分条件下生存期延长3-91 d,地径、树高、新增叶片分别增加了16.7％-461.2％,22.7％-368.2％,42.9％-372.7％;随着保水剂用量增加,土壤容重下降了6.2％-35.1％,总孔隙度和毛管孔隙度明显增加了3.6％-20.3％和5.9％-22.6％;在有限水分条件下,通过不同保水剂处理能减少水分的胁迫,净光合速率增长8.9％-461.2％,蒸腾速率增长了22.2％-518.7％,气孔导度增长了4.2％-512.5％。     

Upregulation of neurokinin A levels by nerve growth factor in the experimental asthmatic guinea pig

AIM: To explore the regulatory mechanism of nerve growth factor (NGF) on neurokinin A in the experimental asthmatic guinea pig. METHODS: Radioimmunoassay was used to determine the alteration of neurokinin A levels in the lower respiratory tract and visceral sensory afferent sites while NGF was absent (inhalation of NGF antibody through nasal cavity) in the asthmatic guinea pig. RESULTS: The contents of neurokinin A in the trachea, bronchus, lung, C₇-T₅ spinal ganglia and the correspondent spinal dorsal horn, nodose ganglia and solitary nucleus area in the experimental asthmatic guinea pig with the absent of NGF in the respiratory tract were much lower than those in the asthmatic and control groups (P＜0.01). CONCLUSION: NGF upregulated the contents of neurokinin A in the lower respiratory tract and visceral sensory sites of the experimental asthmatic guinea pig, and both might be involved in the pathogenesis of asthma.     

Inhibition of K562 cell growth by antisense drug targeting with VEGF mRNA in vitro

AIM: To investigate inhibition of K562 cell growth by antisense drug targeted VEGF mRNA. METHODS: X7, 20-mer antisense sequences were selected, synthesized and modified with phosphorothioate. The drug was transfected into K562 cells in the present of lipofection. Cell growth was assayed by trypan blue dye exclusion assay and MTT. The level of VEGF protein in the media was determined by ELISA. The morphology of apoptotic cells were observed by Giemsa staining, and the propotion of apoptotic cells was detected by flow cytometry. RESULTS: The antisense drug inhibited growth of K562 and downregulated expression of VEGF protein significantly, compared with Scrambed control group and showed dose-dependent relation. Signs of apoptosis of K562 cells were not observed. CONCLUSION: Inhibition of K562 cell proliferation, but not cells apoptosis induction is the mechanism of inhibing growth of K562 cells by antisense drug targeted VEGF mRNA. At same time, VEGF has function of promoting K562 cell proliferation, and VEGF mRNA may be a new target attached by drugs.     

Effect of insulin on the secretion of VEGF and its receptor in serum-free cultured bovine thoracic aortic endothelial cells

AIM: This study was designed to investigate the secretion of VEGF and its receptor (flt-1 or flk-1/KDR) protein by cultured bovine thoracic aortic endothelial cells treated with various insulin concentrations. METHODS: Endothelial cells was isolated from bovine thoracic aorta, and cultured in serum-free medium, then incubated with different insulin concentrations (30 mU/L, 300 mU/L, 3 000 mU/L). The level of VEGF and its receptor (flt-1 or flk-1/KDR) protein were detected by immunohistochemical staining. RESULTS: As compared with no insulin group, the expression of VEGF protein in low insulin concentration (30 mU/L and 300 mU/L) groups were significantly increased (P＜0.01). The expression of VEGF protein in high insulin concentration (3 000 mU/L) group was significantly decreased (P＜0.05). Howerer, no difference of the expression of VEGF receptor (flt-1 or flk-1/KDR) protein among all groups (P＞0.05) was observed. CONCLUSION: Low concentration insulin up-regulates the VEGF protein expression while high concentration insulin down-regulates the VEGF protein expression in bovine thoracic aortic endothelial cells, but insulin had no directly effect on the VEGF receptor (flt-1 or flk-1/KDR) protein expression in bovine thoracic aortic endothelial cells.