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排序方式: 共有137条查询结果,搜索用时 15 毫秒
81.
日本曲霉(Aspergillus japonicus)是土壤和谷物种子表面的一种常见真菌.研究结果表明,日本曲霉所产生的大量黑麦酮酸F(SAF)对玉米(Zea mays)有很强的化感作用,低浓度显著促进玉米幼苗生长,高浓度则抑制.在0.0375mmol·L-1SAF下,玉米幼苗根长增长31.7%,根数量增加13.2%,根活力提高4.73倍,并促进玉米对P、K、Ca、Mg、S等5种营养元素的吸收.高浓度SAF(0.3mmol·L-1)下玉米根活力受抑制(72.1%),根对N、P、K、Ca、Mg、Fe等营养元素的吸收也受抑制.0.6mmol·L-1的SAF下根完全失去活力.电镜观察表明,有SAF的情况下玉米叶绿体片层结构模糊、混乱,双层膜不完整. 相似文献
82.
日本曲霉产生的黑麦酮酸F对玉米的化感作用 总被引:5,自引:0,他引:5
日本曲霉(Aspergillus japonicus)是土壤和谷物种子表面的一种常见真菌。研究结果表明。日本曲霉所产生的大量黑麦酮酸F(SAF)对玉米(Zea mays)有很强的化感作用,低浓度显著促进玉米幼苗生长,高浓度则抑制.在0.0375mmol·L^-1SAF下,玉米幼苗根长增长31.7%,根数量增加13.2%,根活力提高4.73倍,并促进玉米对P、K、Ca、Mg、S等5种营养元素的吸收.高浓度SAF(0.3mmol·L^-1)下玉米根活力受抑制(72.1%),根对N、P、K、Ca、Mg、Fe等营养元素的吸收也受抑制.0.6mmol·L^-1的SAF下根完全失去活力,电镜观察表明,有SAF的情况下玉米叶绿体片层结构模糊、混乱,双层膜不完整。 相似文献
83.
玉米化感物质异羟肟酸的研究进展 总被引:8,自引:1,他引:7
介绍了异羟肟酸在玉米植株中的分布和玉米根系分泌物中异羟肟酸的分析方法.丁布(DIM-BOA)是玉米植株中含量最大的异羟肟酸.不同玉米品种之间异羟肟酸含量的差异很大.种子不含异羟肟酸;但萌发后其含量迅速增加,在萌芽几天后的幼苗植株其含量达最大值,随后逐渐下降;在玉米生长发育的不同时期,幼嫩叶片内异羟肟酸含量始终较高;地上部分异羟肟酸的浓度高于根系.植株异羟肟酸的浓度受生长环境条件影响显著,在紫外辐射、黑暗条件或水分胁迫下其含量明显增加.在各种禾谷类作物中,玉米根系分泌物内含异羟肟酸较高;铁的存在能显著增加玉米根系分泌物中异羟肟酸的含量. 相似文献
84.
Marc Jan Bonder Silva Kasela Mart Kals Riin Tamm Kaie Lokk Isabel Barragan Wim A Buurman Patrick Deelen Jan-Willem Greve Maxim Ivanov Sander S Rensen Jana V van Vliet-Ostaptchouk Marcel G Wolfs Jingyuan Fu Marten H Hofker Cisca Wijmenga Alexandra Zhernakova Magnus Ingelman-Sundberg Lude Franke Lili Milani 《BMC genomics》2014,15(1)
85.
Silvia Bijland Sjoerd A. A. van den Berg Peter J. Voshol Anita M. van den Hoek Hans M. G. Princen Louis M. Havekes Patrick C. N. Rensen Ko Willems van Dijk 《Journal of lipid research》2010,51(1):97-102
The cholesteryl ester transfer protein (CETP) facilitates the bidirectional transfer of cholesteryl esters and triglycerides (TG) between HDL and (V)LDL. By shifting cholesterol in plasma from HDL to (V)LDL in exchange for VLDL-TG, CETP aggravates atherosclerosis in hyperlipidemic APOE*3-Leiden (E3L) mice. The aim of this study was to investigate the role of CETP in TG metabolism and high-fat diet-induced obesity by using E3L mice with and without the expression of the human CETP gene. On chow, plasma lipid levels were comparable between both male and female E3L and E3L.CETP mice. Further mechanistic studies were performed using male mice. CETP expression increased the level of TG in HDL. CETP did not affect the postprandial plasma TG response or the hepatic VLDL-TG and VLDL-apolipoprotein B production rate. Moreover, CETP did not affect the plasma TG clearance rate or organ-specific TG uptake after infusion of VLDL-like emulsion particles. In line with the absence of an effect of CETP on tissue-specific TG uptake, CETP also did not affect weight gain in response to a high-fat diet. In conclusion, the CETP-induced increase of TG in the HDL fraction of E3L mice is not associated with changes in the production of TG or with tissue-specific clearance of TG from the plasma. 相似文献
86.
Ruifang Li-Gao Renée de Mutsert Patrick C. N. Rensen Jan Bert van Klinken Cornelia Prehn Jerzy Adamski Astrid van Hylckama Vlieg Martin den Heijer Saskia le Cessie Frits R. Rosendaal Ko Willems van Dijk Dennis O. Mook-Kanamori 《Metabolomics : Official journal of the Metabolomic Society》2018,14(1):13
Introduction
Fasting metabolite profiles have been shown to distinguish type 2 diabetes (T2D) patients from normal glucose tolerance (NGT) individuals.Objectives
We investigated whether, besides fasting metabolite profiles, postprandial metabolite profiles associated with T2D can stratify individuals with impaired fasting glucose (IFG) by their similarities to T2D.Methods
Three groups of individuals (age 45–65 years) without any history of IFG or T2D were selected from the Netherlands Epidemiology of Obesity study and stratified by baseline fasting glucose concentrations (NGT (n?=?176), IFG (n?=?186), T2D (n?=?171)). 163 metabolites were measured under fasting and postprandial states (150 min after a meal challenge). Metabolite profiles specific for a high risk of T2D were identified by LASSO regression for fasting and postprandial states. The selected profiles were utilised to stratify IFG group into high (T2D probability?≥?0.7) and low (T2D probability?≤?0.5) risk subgroups. The stratification performances were compared with clinically relevant metabolic traits.Results
Two metabolite profiles specific for T2D (nfasting = 12 metabolites, npostprandial = 4 metabolites) were identified, with all four postprandial metabolites also being identified in the fasting state. Stratified by the postprandial profile, the high-risk subgroup of IFG individuals (n?=?72) showed similar glucose concentrations to the low-risk subgroup (n?=?57), yet a higher BMI (difference: 3.3 kg/m2 (95% CI 1.7–5.0)) and postprandial insulin concentrations (21.5 mU/L (95% CI 1.8–41.2)).Conclusion
Postprandial metabolites identified T2D patients as good as fasting metabolites and exhibited enhanced signals for IFG stratification, which offers a proof of concept that metabolomics research should not focus on the fasting state alone.87.
The nucleoporin RanBP2 tethers the cAMP effector Epac1 and inhibits its catalytic activity 总被引:1,自引:0,他引:1
Gloerich M Vliem MJ Prummel E Meijer LA Rensen MG Rehmann H Bos JL 《The Journal of cell biology》2011,193(6):1009-1020
Cyclic adenosine monophosphate (cAMP) is a second messenger that relays a wide range of hormone responses. In this paper, we demonstrate that the nuclear pore component RanBP2 acts as a negative regulator of cAMP signaling through Epac1, a cAMP-regulated guanine nucleotide exchange factor for Rap. We show that Epac1 directly interacts with the zinc fingers (ZNFs) of RanBP2, tethering Epac1 to the nuclear pore complex (NPC). RanBP2 inhibits the catalytic activity of Epac1 in vitro by binding to its catalytic CDC25 homology domain. Accordingly, cellular depletion of RanBP2 releases Epac1 from the NPC and enhances cAMP-induced Rap activation and cell adhesion. Epac1 also is released upon phosphorylation of the ZNFs of RanBP2, demonstrating that the interaction can be regulated by posttranslational modification. These results reveal a novel mechanism of Epac1 regulation and elucidate an unexpected link between the NPC and cAMP signaling. 相似文献
88.
Stienstra R Joosten LA Koenen T van Tits B van Diepen JA van den Berg SA Rensen PC Voshol PJ Fantuzzi G Hijmans A Kersten S Müller M van den Berg WB van Rooijen N Wabitsch M Kullberg BJ van der Meer JW Kanneganti T Tack CJ Netea MG 《Cell metabolism》2010,12(6):593-605
Obesity-induced inflammation originating from expanding adipose tissue interferes with insulin sensitivity. Important metabolic effects have been recently attributed to IL-1β and IL-18, two members of the IL-1 family of cytokines. Processing of IL-1β and IL-18 requires cleavage by caspase-1, a cysteine protease regulated by a protein complex called the inflammasome. We demonstrate that the inflammasome/caspase-1 governs adipocyte differentiation and insulin sensitivity. Caspase-1 is upregulated during adipocyte differentiation and directs adipocytes toward a more insulin-resistant phenotype. Treatment of differentiating adipocytes with recombinant IL-1β and IL-18, or blocking their effects by inhibitors, reveals that the effects of caspase-1 on adipocyte differentiation are largely conveyed by IL-1β. Caspase-1 and IL-1β activity in adipose tissue is increased both in diet-induced and genetically induced obese animal models. Conversely, mice deficient in caspase-1 are more insulin sensitive as compared to wild-type animals. In addition, differentiation of preadipocytes isolated from caspase-1(-/-) or NLRP3(-/-) mice resulted in more metabolically active fat cells. In?vivo, treatment of obese mice with a caspase-1 inhibitor significantly increases their insulin sensitivity. Indirect calorimetry analysis revealed higher fat oxidation rates in caspase-1(-/-) animals. In conclusion, the inflammasome is an important regulator of adipocyte function and insulin sensitivity, and caspase-1 inhibition may represent a novel therapeutic target in clinical conditions associated with obesity and insulin resistance. 相似文献
89.
Gerritsen G van der Hoogt CC Schaap FG Voshol PJ Kypreos KE Maeda N Groen AK Havekes LM Rensen PC van Dijk KW 《Journal of lipid research》2008,49(5):1048-1055
Apolipoprotein E2 (apoE2)-associated hyperlipidemia is characterized by a disturbed clearance of apoE2-enriched VLDL remnants. Because excess apoE2 inhibits LPL-mediated triglyceride (TG) hydrolysis in vitro, we investigated whether direct or indirect stimulation of LPL activity in vivo reduces the apoE2-associated hypertriglyceridemia. Here, we studied the role of LPL and two potent modifiers, the LPL inhibitor apoC-III and the LPL activator apoA-V, in APOE2-knockin (APOE2) mice. Injection of heparin in APOE2 mice reduced plasma TG by 53% and plasma total cholesterol (TC) by 18%. Adenovirus-mediated overexpression of LPL reduced plasma TG by 85% and TC by 40%. Both experiments indicate that the TG in apoE2-enriched particles is a suitable substrate for LPL. Indirect activation of LPL activity via deletion of Apoc3 in APOE2 mice did not affect plasma TG levels, whereas overexpression of Apoa5 in APOE2 mice did reduce plasma TG by 81% and plasma TC by 41%. In conclusion, the hypertriglyceridemia in APOE2 mice can be ameliorated by the direct activation of LPL activity. Indirect activation of LPL via overexpression of apoA-V does, whereas deletion of apoC-III does not, affect the plasma TGs in APOE2 mice. These data indicate that changes in apoA-V levels have a dominant effect over changes in apoC-III levels in the improvement of APOE2-associated hypertriglyceridemia. 相似文献
90.
Abildayeva K Berbée JF Blokland A Jansen PJ Hoek FJ Meijer O Lütjohann D Gautier T Pillot T De Vente J Havekes LM Ramaekers FC Kuipers F Rensen PC Mulder M 《Journal of lipid research》2008,49(4):856-869
The H2 allele of APOC1, giving rise to increased gene expression of apolipoprotein C-I (apoC-I), is in genetic disequilibrium with the APOE4 allele and may provide a major risk factor for Alzheimer's disease (AD). We found that apoC-I protein is present in astrocytes and endothelial cells within hippocampal regions in both human control and AD brains. Interestingly, apoC-I colocalized with beta-amyloid (Abeta) in plaques in AD brains, and in vitro experiments revealed that aggregation of Abeta was delayed in the presence of apoC-I. Moreover, apoC-I was found to exacerbate the soluble Abeta oligomer-induced neuronal death. To establish a potential role for apoC-I in cognitive functions, we used human (h) APOC1(+/0) transgenic mice that express APOC1 mRNA throughout their brains and apoC-I protein in astrocytes and endothelial cells. The hAPOC1(+/0) mice displayed impaired hippocampal-dependent learning and memory functions compared with their wild-type littermates, as judged from their performance in the object recognition task (P = 0.012) and in the Morris water maze task (P = 0.010). ApoC-I may affect learning as a result of its inhibitory properties toward apoE-dependent lipid metabolism. However, no differences in brain mRNA or protein levels of endogenous apoE were detected between transgenic and wild-type mice. In conclusion, human apoC-I expression impairs cognitive functions in mice independent of apoE expression, which supports the potential of a modulatory role for apoC-I during the development of AD. 相似文献