首页> 外文期刊>European Journal of Pharmacology: An International Journal >The role of voltage-operated and non-voltage-operated calcium channels in endothelin-induced vasoconstriction of rat cerebral arteries
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The role of voltage-operated and non-voltage-operated calcium channels in endothelin-induced vasoconstriction of rat cerebral arteries

机译:电压和非电压操作钙通道在内皮素诱导的大鼠脑动脉血管收缩中的作用

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Endothelin-1 has been identified as a potential mediator in the pathogenesis of ischaemic stroke and cerebral vasospasm. The aim of this study was to analyse the role of voltage-operated calcium channels (VOCC) and non-VOCC in endothelin-1 induced vasoconstriction of rat cerebral arteries. Arterial segments were dissected from different regions of the cerebral circulation and responses assessed using wire myography. Endothelin-1 concentration-contraction curves were constructed in calcium-free medium or in the presence of nifedipine, NNC 55-0396 ((1S,2S)-2-(2-(N-[(3-benzimidazol-2-yl)propyl]-N-methylamino)ethyl)-6-fluoro-1,2,3,4-tetrahydro-1-isopropyl-2-naphtyl cyclopropanecarboxylate dihydrochloride) or SK&F 96365 (1-(2-(3-(4-methoxyphenyl)propoxy)-4-methoxyphenylethyl)-1H-imidazole) to inhibit the L-type VOCC, T-type VOCC and non-VOCC, respectively. Inhibition of the calcium channels or removal of calcium from the medium variably decreased the maximum effects (E-max) of endothelin-1, however its potency (pEC(50)) was unaltered. Endothelin-1 caused a small contraction ( <22%) in calcium-free solution. Pre-treatment with nifedipine (1 mu M) did not affect responses to low concentrations of endothelin-1 but decreased E-max, while NNC 55-0396 (1 mu M) and SK&F 96365 (30-100 mu M) generally attenuated the endothelin-1-induced contraction. Combination of nifedipine with SK&F 96365 further decreased the E-max. The relaxant effect of the calcium channel antagonists was also assessed in pre-contracted arteries. Only nifedipine and SK&F 96365 relaxed the arteries pre-contracted with endothelin-1. In conclusion, VOCC and non-VOCC calcium channels are involved in different phases of the endothelin-1 contraction in rat cerebral vessels. T-type VOCC may be involved in contraction induced by low concentrations of endothelin-1, while L-type VOCC mediate the maintenance phase of contraction. VOCC and non-VOCC may work in concert in mediating contraction induced by endothelin-1. (C) 2014 Elsevier B.V. All rights reserved.
机译:内皮素-1已被鉴定为缺血性卒中和脑血管痉挛发病机制中的潜在介体。本研究的目的是分析内皮素-1诱导的大鼠脑动脉的血管收缩中的电压操作钙通道(VOCC)和非VOCC的作用。从脑循环的不同区域解剖动脉段,并使用丝网评估的反应。内皮素-1浓度 - 收缩曲线在无钙培养基中或在Nifedipine,NNC 55-0396((1S,2S)-2-(2-(N - [(3-苯并咪唑-2-基)的情况下丙基 - 甲基氨基)乙基)-6-氟-1,2,3,4-四氢-1-异丙基-2-萘二氯酰羧酸二盐酸盐)或SK&F 96365(1-(2-(4-甲氧基苯基)丙元素)-4-甲氧基苯基乙基)-1H-咪唑)分别抑制L型VOCC,T型VOCC和非VOCC。抑制钙通道或从培养基中除去钙可变地降低内皮素-1的最大效果(E-MAX),但其效力(PEC(50))未妨碍。内皮素-1在无钙溶液中引起小的收缩(<22%)。用硝苯地平(1μm)预处理不影响对低浓度的内皮素-1而且降低E-MAX的反应,而NNC 55-0396(1μm)和SK&F 96365(30-100μm)通常衰减内皮素-1诱导的收缩。 NifeDipine与SK&F 96365的组合进一步降低了E-Max。在预缩小的动脉中也评估了钙通道拮抗剂的松弛效果。只有NifeDipine和SK&F 96365放松预先用内皮素-1收缩的动脉。总之,VOCC和非VOCC钙通道涉及大鼠脑血管内内皮素-1收缩的不同阶段。 T型VOCC可以参与由低浓度的内皮素-1诱导的收缩,而L型VOCC介导收缩的维持阶段。 Vocc和非Vocc可以在介导的内皮素-1诱导的收缩中协同工作。 (c)2014 Elsevier B.V.保留所有权利。

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