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甲肾上腺素

网络NE; noradrenaline; isoproterenol

甲肾上腺素

甲肾上腺素

甲肾上腺素

NE

而甲肾上腺素(NE)再摄取被抑制的话,不会导致发胖的.感谢| 向我提问感谢| 向我提问

noradrenaline

　　1、甲肾上腺素(noradrenaline)：因其以兴奋α受体为主兼有轻度兴奋β受体的血管收缩药，临床上主要用它升高血压，静脉滴注 …

isoproterenol

5.5.异丙墓去甲肾上腺素异丙基去甲肾上腺素(isoproterenol)〔7655一59一幻 (15)，C，，H，，NO3，分子量211.24。1一(3，…

Noradrenalin

去 甲肾上腺素(Noradrenalin)从浙江大学医学院附属二院药房购置. 2.2 系统构成及实验仪器光学多普勒层析成像系统由本实验 …

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If the person feels anxious and angry all day , his cerebrum will produce toxic hormones called "noradrenalin and adrenalin " .

若人整天焦躁不安、怒气攻心，大脑就会产生 “去甲肾上腺素和肾上腺素 ”的 “毒性 ”荷尔蒙。

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The chemicals responsible for "that lovin' feeling " (adrenaline , dopamine, norepinephrine, phenylethylamine, etc. ) dwindle .

那些负责 “爱情情感 ”的化学物质（肾上腺素，多巴胺，去甲肾上腺素，苯基乙胺等）也逐渐减少。

6

Among them, the final target of norepinephrine organizations , including the heart .

其中，去甲肾上腺素的最后靶组织包括心脏。

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Dopamine, norepinephrine bound to generate a large number of reactive oxygen species .

多巴胺、去甲肾上腺素必定大量产生活性氧。

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To master the physiological functions of adrenal medulla hormones (Epinephrine and norepinephrine). Understand their secretion regulations .

掌握肾上腺髓质激素 —肾上腺素与去甲肾上腺素的生物学作用，了解其分泌调节。

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The Sympathomimetic Actions of l-Ephedrine and d-Pseudoephedrine: Direct Receptor Activation or Norepinephrine Release ?

l-肾上腺素和 d-假肾上腺素的拟交感样作用：直接受体激活或去甲肾上腺素释放？

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Thirty minutes after subcutaneous injection of norepinephrine, the same phenomena mentioned above also happened .

皮下注射去甲肾上腺素后也有上述现象发生。

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The values of electrodermal parameters were the lowest in the group with noradrenergic antidepressant .

价值观念的皮肤电参数最低的抗抑郁药组，去甲肾上腺素。

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Activates adrenal medulla to release adrenaline and noradrenaline .

激活肾上腺髓质释放肾上腺素和去甲肾上腺素

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For instance , their heart rate shoots up more dramatically when stimulated by noradrenaline .

例如，在去甲肾上腺素的刺激下，他们的心率加速得更快。

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We are only now just studying how the combination of the other Yohimbine compounds in Meltdown work in concert to increase NE even further .

我们现在才刚刚研究如何结合其他育亨宾化合物消融协同工作，以进一步提高去甲肾上腺素。

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The effects of dihyromyricetin were noted on the contraction of rabbit aortic strips caused by noradrenaline (NA) and high K+solution.

用兔胸主动脉条实验，观察其对去甲肾上腺素（NA ）和高 K+所致主动脉条收缩的影响。

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A sympathomimetic that acts mainly by causing release of norepinephrine but also has direct agonist activity at some adrenergic receptors .

一种拟交感神经药物，主要以引发去甲肾上腺素释放起作用，对交感神经受体也有直接的促进作用。

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