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首页> 外文期刊>Evidence-based complementary and alternative medicine: eCAM >Citrus bergamia Risso Elevates Intracellular Ca~(2+) in Human Vascular Endothelial Cells due to Release of Ca~(2+) from Primary Intracellular Stores
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Citrus bergamia Risso Elevates Intracellular Ca~(2+) in Human Vascular Endothelial Cells due to Release of Ca~(2+) from Primary Intracellular Stores

机译:由于从原始细胞内存储中释放Ca〜(2+),柑桔柑橘Risso升高了人类血管内皮细胞的细胞内Ca〜(2+)。

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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 Ca~(2+) in human umbilical vein endothelial cells. Fura-2 fluorescence was used to examine changes in intracellular Ca~(2+) concentration [Ca~(2+)]_i . In the presence of extracellular Ca~(2+), BEO increased [Ca~(2+)]_i , which was partially inhibited by a nonselective Ca~(2+) channel blocker La~(3+). In Ca~(2+)-free extracellular solutions, BEO increased [Ca~(2+)]_i in a concentration-dependent manner, suggesting that BEO mobilizes intracellular Ca~(2+). BEO-induced [Ca~(2+)]_i increase was partially inhibited by a Ca~(2+)-induced Ca~(2+) release inhibitor dantrolene, a phospholipase C inhibitor U73122, and an inositol 1,4,5-triphosphate (IP_3)-gated Ca~(2+) channel blocker, 2-aminoethoxydiphenyl borane (2-APB). BEO also increased [Ca~(2+)]_i in the presence of carbonyl cyanide m-chlorophenylhydrazone, an inhibitor of mitochondrial Ca~(2+) uptake. In addition, store-operated Ca~(2+) entry (SOC) was potentiated by BEO. These results suggest that BEO mobilizes Ca~(2+) from primary intracellular stores via Ca~(2+)-induced and IP3-mediated Ca~(2+) release and affect promotion of Ca~(2+) influx, likely via an SOC mechanism.
机译:本研究的目的是检验香柠檬(Beramot Risso)(佛手柑,BEO)精油对人脐静脉内皮细胞内Ca〜(2+)的影响。使用Fura-2荧光检查细胞内Ca〜(2+)浓度[Ca〜(2 +)] _ i的变化。在细胞外Ca〜(2+)存在下,BEO增加[Ca〜(2 +)] _ i,部分受非选择性Ca〜(2+)通道阻滞剂La〜(3+)抑制。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+)。 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,磷脂酶C抑制剂U73122和肌醇1,4,5部分抑制-三磷酸(IP_3)门控的Ca〜(2+)通道阻滞剂,2-氨基乙氧基二苯基硼烷(2-APB)。在羰基氰化物间氯苯hydr存在下,BEO也会增加[Ca〜(2 +)] _ i,后者是线粒体Ca〜(2+)吸收的抑制剂。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+)释放从主要的细胞内存储中动员Ca〜(2+),并可能通过以下方式影响Ca〜(2+)流入的促进。 SOC机制。

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