肾上腺素

基本解释 (translations)

adrenaline  ·  adrenin  ·  adrenine  ·  epinephrine  ·  suprarenalin  ·  adrenalin

与肾上腺素相关的网络例句 [注：此内容来源于网络，仅供参考]

Or probably you are one of the adrenalin lovers that usually go for adrenalin activities?

或者可能是你的肾上腺素一个情人，通常去肾上腺素的活动？

A bioselective membrane electrode sensistive to adrenine has been prepared and made in flow type by means of banana tissue covering an oxygen electrode.

将香蕉组织偶合氧电极研制成肾上腺素生物组织电极，并装制成流通型式。文中对此电极的响应特性进行了研究，探讨了各种实验条件及有关参量的影响。并将电极用于肾上腺素原粉的含量测定，结果与标准方法基本一致

Baxter, working on cats under experimental conditions comparable to ours, however, reported that intravenous injection of adrenalin either had no marked effect or a slightly augmentative effect on the histamine-induced secretion, and that stimulation of the splanchnic nerve yielded similar results.

若用较长的间隔如每10—30分钟收集一次胃分泌，则此双相效应就会被掩盖，因而得出肾上腺素对猫胃分泌无明显效应或有增加分泌的效应的结论，如Baxter等人所得到的一样。在急性实验中，刺激大内脏神经对组织胺引起的猫胃分泌有显著的抑制效应。与肾上腺素的效应不同，刺激大内脏神经的效应通常是单相的。

The concrete usage of noradrenalin: mix 4mg noradrenalin or 8 mg noradrenaline bitartrate (The potency of 2mg noradrenaline bitartrate equals to that of 1mg noradrenalin) with 250ml equilibrium liquid with or without salt. They will form 16ug/ml noradrenalin solution or 32ug/ml noradrenaline bitartrate solution.

去甲肾上腺素的具体用法：将去甲肾上腺素4mg或重酒石酸去甲肾上腺素8mg(2mg重酒石酸去甲肾上腺素效价与1mg去甲肾上腺素相同)加入250ml含盐或不含盐的平衡液中，产生16ug/mL去甲肾上腺素液或32ug/mL重酒石酸去甲肾上腺素液。

RESULTS: Basilar artery, thoracic aorta and ventricular papillary muscle Resting tension of basilar artery was increased by DL but decreased by niof basilar artery and thoracic aorta induced by noradrenaline bitartrate and KCl can be relaxed by DL in a dose dependant manner, and the half-effective concentration was (6.69±3.12)×10-4,(3.41±1.52)×10-3mmol/L for basilar artery, and (1.49±0.59)×10-3,(2.91±0.99)×10-3 mmol/L for thoracic aorta, displaying stronger inhibition on the constriction of basilar artery induced by noradrenaline bitartrate than on the contraction induced by KCl.

重酒石酸去甲肾上腺素、KCl所致基底动脉及胸主动脉收缩，二氢石蒜碱使之呈剂量依赖性松弛，其半数有效浓度值：对基底动脉分别为(6.69±3.12)×10-，(3.41±1.52)×10-3 mmol/L；对胸主动脉分别为(1.49±0.59)×10-3，(2.91±0.99)×10-3 mmol/L。拮抗重酒石酸去甲肾上腺素所致基底动脉收缩作用明显强于KCl。尼莫地平对KCl所致收缩的抑制显著强于对重酒石酸去甲肾上腺素。

Consider to discover, OSAHS patient appears because of relapsing in nightly Morpheus disease of blood of low oxygen, tall carbonic acid, consensual as disorder as parasympathetic nerve function, already made coronary heart disease (the cardiovascular disease such as CHD) sparks importantly element, can cause all sorts of rhythm of the heart wrong, aggravating cardiac muscle is short of blood, produce sudden death of heart source sex even. 1 O SAH S and hypertensive disease consider to discover, OSAHS patient's nightly small arousal can bring about sympathetic stimulant increase, adrenalin can nerve medium if adrenalin, go adrenalin secretes armour grow in quantity, heighten of material of phenolic amine of catechu of nightly make water.

探究发现，OSAHS患者夜间睡眠中因反复出现低氧、高碳酸血症、交感和副交感神经功能紊乱，已成为冠心病等心血管疾病重要的触发因素，可诱发各种心律失常、加重心肌缺血，甚至发生心源性猝死。1 O SAH S和高血压病探究发现，OSAHS患者夜间的微觉醒可导致交感神经兴奋性增强，肾上腺素能神经介质如肾上腺素、去甲肾上腺素分泌增多，夜间尿儿茶酚胺类物质增高。

Intravoneous injection of 0.5mg/kgBW jingsongling cause the 60 minutesrelaxation of goat gastric motor.The effects of jingsongling on the gastric motor ofgoat is major of effects of α2 -adrenoceptor agonist,as well as that of α1 -adrenoceptor agonist,the effects of α1 -adrenoceptor agonist concentrate at thecardic and pylorus;the function of α2 -adrenoceptor exit widely at cardic,pylorus,rumen,reticulum,omasum and abomasum,the function at different part is not the same.The lowestdose of jingsonglinginhibiting the amplitude and frequency of the gastricmyoelectric is 0.01mg/kgBW;the influence of jingsonglingto the gastricmotility of goat is dose-dependent,and the amplitude regain after the frequency ofgastric myoelectriv wave.When the goat revived,the gastric motor function is notreach the level of the normal;the major reason ofjingsongling cause the goat gastricrelaxation is the amplitude renew slowly.The intravoneous injection ofjingsonglingfirst,after 5 minutes,intravoneous injection the antagonist,the effect of prazosin and idazoxan mixed is best,which can fast reversal of theinhibition of jingsongling on the gastric motor of goat,the effects of idazoxan isgood,and the prazosin block the effection of jingsongling is better than that ofxylazine,especially at cardia and pylorus.When intravoneous injection of0.5mg/kgBW idazoxan and/or prazosin only,the amplitude of gastric myoelectric ingoat increases at a certain degree,but the frequency is not changed.

静脉注射0.5mk/kgBW的静松灵引起山羊胃蠕动弛缓长达60分钟；静脉注射0.5mg/kgBW的静松灵对山羊胃蠕动机能的影响是以α2肾上腺素受体作用为主的，兼有α1肾上腺素受体的作用，而且静松灵的α1肾上腺素受体的作用主要集中在幽门和贲门；α2肾上腺素受体的作用广泛存在于贲门、瘤胃、网胃、瓣胃、皱胃和幽门中，不同部位间有功能上的差异；静注0.01mg/kgBW的静松灵是对山羊的贲门、瘤胃、网胃、瓣胃、皱胃和幽门的肌电波频率和振幅均产生影响的最低剂量；静注一定剂量的静松灵对山羊胃蠕动的抑制作用与剂量呈相关性；而且山羊胃肌电波振幅的恢复比肌电波频率的恢复慢；苏醒时山羊的胃蠕动机能尚未恢复到正常状态；静松灵引起山羊胃弛缓的主要原因是由于胃肌电波的振幅恢复慢；静注0.5mg/kgBW的静松灵，5分钟后静注0.5mg/kgBW的拮抗剂时，咪唑克生+哌唑嗪的作用最好，能迅速地逆转静松灵对山羊胃蠕动的抑制作用，咪唑克生也有很强的拮抗作用，而哌唑嗪对静松灵的拮抗效果好于对隆朋的拮抗；单独静注0.5mg/kgBW的咪唑克生和/或哌唑嗪时，山羊的瘤胃、网胃、瓣胃、皱胃、贲门和幽门的肌电波振幅有一定程度的增强，而肌电波频率未见变化。

Although epinephrine is the vasopressor of choice for cardiopulmonary resuscitation, the prognosis of patients with cardiac arrest who require epinephrine remains extremely poor, regardless of the cumulative epinephrine dose given.

尽管肾上腺素是作为心肺复苏中的血管加压药物而选用的，但那些接受肾上腺素治疗甚至接受累计多次剂量的肾上腺素治疗的心搏骤停病人的预后依然很差。

Adrenaline and its oxidative product adrenochrome are widely used in medicine. It is very important to study the electrochemistry properties of them for their applies in medicine, and electroanalytical.

肾上腺素和其氧化产物肾上腺素红在医药上都有十分广泛的用途，研究其电化学反应性能，对于深入探讨肾上腺素及肾上腺素红在医药上和电分析方面的应用均具有重要的意义。

ADRENOCHROME / Recreational / 30 Minutes / Adrenochrome is an oxidation product of adrenaline.

肾上腺素/休闲/ 30分钟/肾上腺素是一种氧化产物肾上腺素（ ephinephrine ，去甲肾上腺素）。

与肾上腺素相关的网络解释 [注：此内容来源于网络，仅供参考]

adrenaline tartrate：酒石酸肾上腺素

肾上腺素 Adrenaline | 酒石酸肾上腺素 Adrenaline tartrate | 肾上腺素杂质 Adrenaline impurity mixture

adrenin：肾上腺素

adrenergic nerve 肾上腺素激导性神经 | adrenin 肾上腺素 | adrenochrome 肾上腺素红

adrenergic agonist：肾上腺素促效剂

肾上腺素剂 adrenergic agent | 肾上腺素促效剂 adrenergic agonist | 肾上腺素拮抗剂 adrenergic antagonist

adrenergic agonist：腎上腺素能激動藥 肾上腺素激动药

adrenergic 腎上腺素能藥 拟肾上腺素药 | adrenergic agonist 腎上腺素能激動藥 肾上腺素激动药 | adrenergic;adrenomimetics 擬腎上腺素劑 拟肾上腺素药

adrenaline,epinephrine：肾上腺素

"adrenaline oxidase","肾上腺素氧化酶" | "adrenaline; epinephrine","肾上腺素" | "adrenergic blocking agent","肾上腺素堵剂;肾上腺素阻断剂"

adrenergic receptor：肾上腺素受体

肾上腺素受体(Adrenergic Receptor),是G蛋白耦联受体超家族中最具代表性的成员之一. 作为交感神经递质的去甲肾上腺素(Noradrenaline)及内分泌激素的肾上腺素(Adrenaline),正是通过与靶器官上的肾上腺素受体结合,激发一系列的细胞内信号传递与物质合成,

hyperadrenalemia：高肾上腺素血 高肾上腺素血症

hyperadiposity 肥胖过度 | hyperadrenalemia 高肾上腺素血 高肾上腺素血症 | hyperadrenalinemia 血肾上腺素过多

adrenoceptor agonists：肾上腺素受体激动药

肾上腺素受体激动药(adrenoceptor agonists)是一类能与肾上腺素受体结合并激动该受体,产生与肾上腺素能递质(去甲肾上腺素)作用相似的药物. 肾上腺素受体激动药的基本化学结构为β-苯乙胺,其中肾上腺素、去甲肾上腺素、异丙肾上腺素、多巴胺和多巴酚丁胺的化学结构含有儿茶酚,

noradrenalin：去甲基肾上腺素

noradio 无线电讯号消失 | noradrenalin 去甲基肾上腺素 | noradrenaline 去甲基肾上腺素 去甲肾上腺素 降肾上腺素

noradrenaline：去甲肾上腺素

儿茶酚胺类激素(catecholamine hormones)包括肾上腺素(adrenaline)、去甲肾上腺素(noradrenaline)以及多巴胺(dopamine). 肾上腺髓质主要分泌肾上腺素,交感神经末梢主要分泌去甲肾上腺素,多巴胺则主要存在于脑内神经束中.