首页> 美国卫生研究院文献>Evidence-based Complementary and Alternative Medicine : eCAM >Citrus bergamia Risso Elevates Intracellular Ca2+ in Human Vascular Endothelial Cells due to Release of Ca2+ from Primary Intracellular Stores
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Citrus bergamia Risso Elevates Intracellular Ca2+ in Human Vascular Endothelial Cells due to Release of Ca2+ from Primary Intracellular Stores

机译:佛手柑Risso升高人血管内皮细胞中的细胞内Ca2 +这是由于Ca2 +从主要的细胞内存储中释放

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摘要

The purpose of the present study is to examine the effects of essential oil of Citrus bergamia Risso (bergamot, BEO) on intracellular Ca2+ in human umbilical vein endothelial cells. Fura-2 fluorescence was used to examine changes in intracellular Ca2+ concentration [Ca2+]i . In the presence of extracellular Ca2+, BEO increased [Ca2+]i , which was partially inhibited by a nonselective Ca2+ channel blocker La3+. In Ca2+-free extracellular solutions, BEO increased [Ca2+]i in a concentration-dependent manner, suggesting that BEO mobilizes intracellular Ca2+. BEO-induced [Ca2+]i increase was partially inhibited by a Ca2+-induced Ca2+ release inhibitor dantrolene, a phospholipase C inhibitor , and an inositol 1,4,5-triphosphate (IP3)-gated Ca2+ channel blocker, 2-aminoethoxydiphenyl borane (2-APB). BEO also increased [Ca2+]i in the presence of carbonyl cyanide m-chlorophenylhydrazone, an inhibitor of mitochondrial Ca2+ uptake. In addition, store-operated Ca2+ entry (SOC) was potentiated by BEO. These results suggest that BEO mobilizes Ca2+ from primary intracellular stores via Ca2+-induced and IP3-mediated Ca2+ release and affect promotion of Ca2+ influx, likely via an SOC mechanism.
机译:本研究的目的是研究香柠檬(Beramot Risso)(佛手柑,BEO)精油对人脐静脉内皮细胞内Ca 2 + 的作用。 Fura-2荧光用于检查细胞内Ca 2 + 浓度[Ca 2 + ] i的变化。在细胞外Ca 2 + 的存在下,BEO增加[Ca 2 + ] i,部分受非选择性Ca 2 + 通道的抑制拦截器La 3 + 。在不含Ca 2 + 的细胞外溶液中,BEO以浓度依赖的方式增加[Ca 2 + ] i,这表明BEO可动员细胞内Ca 2+ < / sup>。 BEO诱导的[Ca 2 + ] i的增加被Ca 2 + 诱导的Ca 2 + 释放抑制剂丹特罗(一种磷脂酶)部分抑制C抑制剂和肌醇1,4,5-三磷酸(IP3)门控的Ca 2 + 通道阻滞剂2-氨基乙氧基二苯基硼烷(2-APB)。在线粒体Ca 2 + 吸收抑制剂的羰基氰化物间-氯苯基hydr存在下,BEO也会增加[Ca 2 + ] i。此外,BEO增强了存储操作的Ca 2 + 条目(SOC)。这些结果表明,BEO通过Ca 2 + 诱导和IP3介导的Ca 2 + 释放和影响,从主要细胞内动员Ca 2 + 。 Ca 2 + 流入的促进作用可能是通过SOC机制引起的。

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