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从加拿大水藓泥炭中提取的富里酸对RBL-2H3和KU812细胞释放化学介质的抑制作用。

Inhibitory effect of fulvic acid extracted from Canadian sphagnum peat on chemical mediator release by RBL-2H3 and KU812 cells.

作者信息

Yamada Parida, Isoda Hiroko, Han Jun Kyu, Talorete Terence P N, Abe Yukuo

机构信息

Graduate School of Life and Environmental Sciences, University of Tsukuba, Tsukuba, Ibaraki, Japan.

出版信息

Biosci Biotechnol Biochem. 2007 May;71(5):1294-305. doi: 10.1271/bbb.60702. Epub 2007 May 7.

Abstract

Fulvic acid (FA) was extracted and purified from Canadian Sphagnum peat (CP-FA) and characterized by using an element analysis meter, Fourier transform infrared (FT-IR) spectroscopy, electron spin resonance (ESR) spectroscopy, and (13)C-nuclear magnetic resonance ((13)C-NMR) spectroscopy. To investigate the antiallergic effect of CP-FA, we incubated rat basophilic leukemia (RBL-2H3) cells with 0.001-10.0 microg/ml of CP-FA and determined the beta-hexosaminidase release inhibition at different response stages. The intracellular calcium Ca(2+) level was also determined by using Fluo 3-AM, a calcium-specific fluorescent probe, and the cytotoxicity of CP-FA was determined by the 3-(4,5-dimethythiazol-2-yl)-2,5-diphenyl-tetrazolium bromide (MTT) assay. The results revealed that RBL-2H3 cells incubated for 48 h with 0.001-10.0 microg/ml of CP-FA did not show any decreased viability. CP-FA inhibited the beta-hexosaminidase release by IgE-sensitized, antigen-stimulated RBL-2H3 cells at the antigen-antibody binding stage and the antibody-receptor binding stage. CP-FA also inhibited histamine release from A23187 plus PMA- or compound 48/80-stimulated KU812 cells. Furthermore, there was a decrease in the intracellular Ca(2+) level in IgE-sensitized cells incubated with CP-FA and stimulated with antigen. Our results show that CP-FA may be useful for the treatment or prevention of allergic diseases.

摘要

从加拿大泥炭藓(CP-FA)中提取并纯化了富里酸(FA),并使用元素分析仪、傅里叶变换红外(FT-IR)光谱仪、电子自旋共振(ESR)光谱仪和(13)C-核磁共振((13)C-NMR)光谱仪对其进行了表征。为了研究CP-FA的抗过敏作用,我们用0.001-10.0微克/毫升的CP-FA孵育大鼠嗜碱性白血病(RBL-2H3)细胞,并在不同反应阶段测定β-己糖胺酶释放抑制率。还使用钙特异性荧光探针Fluo 3-AM测定细胞内钙[Ca(2+)](i)水平,并通过3-(4,5-二甲基噻唑-2-基)-2,5-二苯基溴化四氮唑(MTT)法测定CP-FA的细胞毒性。结果显示,用0.001-10.0微克/毫升的CP-FA孵育48小时的RBL-2H3细胞活力未出现任何下降。CP-FA在抗原-抗体结合阶段和抗体-受体结合阶段抑制了IgE致敏、抗原刺激的RBL-2H3细胞中β-己糖胺酶的释放。CP-FA还抑制了A23187加PMA或化合物48/80刺激的KU812细胞中组胺的释放。此外,在用CP-FA孵育并用抗原刺激的IgE致敏细胞中,细胞内[Ca(2+)](i)水平有所下降。我们的结果表明,CP-FA可能对过敏性疾病的治疗或预防有用。

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