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首页> 外文期刊>Analytical and bioanalytical chemistry >Study of the acute cardiovascular effects of several antihypertensive agents with the measurement of plasma catecholamines in mice
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Study of the acute cardiovascular effects of several antihypertensive agents with the measurement of plasma catecholamines in mice

机译:通过测定小鼠血浆儿茶酚胺水平来研究几种降压药的急性心血管作用

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摘要

A highly sensitive determination method was established for catecholamines (norepinephrine (NE), epinephrine, and dopamine) with high-performance liquid chromatography-peroxyoxalate chemiluminescence reaction detection. In this study, the method was applied to mouse plasma, and it was determined that only 10 μl of mouse plasma was necessary for the selective and reproducible determination of catecholamines. Studies were then conducted in acute cardiovascular effects of sodium nitroprusside, nicardipine, captopril (angiotensin-converting enzyme (ACE) inhibitor), candesartan, and olmesartan (type 1 angiotensin receptor antagonists (AT_1 antagonists)) by this method. Sodium nitroprusside and nicardipine elevated plasma NE concentrations significantly, whereas the ACE inhibitor and the AT_1 antagonists did not change plasma NE concentrations in anesthetized mice. These results suggested that angiotensin II-induced augmentation may be mainly carried through the central baroreflex pathway.
机译:建立了高效液相色谱-过草酸根化学发光反应检测儿茶酚胺类(去甲肾上腺素(NE),肾上腺素和多巴胺)的高灵敏度测定方法。在这项研究中,该方法应用于小鼠血浆,并确定仅10μl的小鼠血浆对于儿茶酚胺的选择性和可重复测定是必需的。然后通过该方法研究了硝普钠,尼卡地平,卡托普利(血管紧张素转换酶(ACE)抑制剂),坎地沙坦和奥美沙坦(1型血管紧张素受体拮抗剂(AT_1拮抗剂))的急性心血管作用。硝普钠和尼卡地平显着提高了血浆NE的浓度,而ACE抑制剂和AT_1拮抗剂并未改变麻醉小鼠的血浆NE的浓度。这些结果表明血管紧张素II诱导的增强可能主要通过中央压力反射通路进行。

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