首页> 美国卫生研究院文献>International Journal of Molecular Sciences >UV-B Filter Octylmethoxycinnamate Induces Vasorelaxation by Ca2+ Channel Inhibition and Guanylyl Cyclase Activation in Human Umbilical Arteries
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UV-B Filter Octylmethoxycinnamate Induces Vasorelaxation by Ca2+ Channel Inhibition and Guanylyl Cyclase Activation in Human Umbilical Arteries

机译:UV-B滤光剂辛基甲氧基肉桂酸酯通过人脐动脉中的Ca2 +通道抑制和胍基环化酶激活诱导血管舒张。

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摘要

Ultraviolet (UV) filters are chemicals widely used in personal care products (PCPs). Due to their effect as endocrine disruptor compounds (EDCs), the toxicity of UV filters is a current concern for human health. EDC exposure may be correlated to cardiovascular diseases (CVD), but to our knowledge, no studies assessed the UV filters effects as human EDCs at the vascular level. Octylmethoxycinnamate (OMC) is the world’s most widely used UV-B filter, present in more than 90% of PCPs. Due to its demonstrated multiple hormonal activities in animal models, this substance is also suspected to be a human EDC. The purpose of this study was to assess the rapid/short-term effects of OMC on arterial tonus and analyse its mode of action (MOA). Using human umbilical arteries, the endocrine effects of OMC were evaluated in in vitro (cellular and organ) experiments by planar cell surface area (PCSA) and organ bath, respectively. Our data show that OMC induces a rapid/short-term smooth muscle relaxation acting through an endothelium-independent MOA, which seems to be shared with oestrogens, involving an activation of soluble guanylyl cyclase (sGC) that increases the cyclic guanosine monophosphate (cGMP) intracellular levels and an inhibition of L-type voltage-operated Ca2+ channels (L-Type VOCC).
机译:紫外线(UV)过滤器是广泛用于个人护理产品(PCP)中的化学物质。由于其作为内分泌干扰物(EDC)的作用,紫外线过滤剂的毒性已成为人类健康的当前关注点。 EDC暴露可能与心血管疾病(CVD)相关,但据我们所知,尚无研究评估紫外线过滤剂在血管水平上作为人类EDC的作用。甲氧基肉桂酸辛酯(OMC)是世界上使用最广泛的UV-B过滤器,存在于90%以上的PCP中。由于在动物模型中显示出多种荷尔蒙活性,因此该物质也被怀疑是人类EDC。这项研究的目的是评估OMC对动脉瓣的快速/短期影响,并分析其作用方式(MOA)。使用人脐动脉,分别通过平面细胞表面积(PCSA)和器官浴在体外(细胞和器官)实验中评估了OMC的内分泌作用。我们的数据显示,OMC通过内皮依赖性MOA诱导快速/短期平滑肌松弛,这似乎与雌激素共有,涉及激活可溶性鸟苷基环化酶(sGC)并增加环状鸟苷单磷酸(cGMP)细胞内水平和抑制L型电压操纵的Ca 2 + 通道(L型VOCC)。

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