肾上腺素能的

基本解释 (translations)

adrenergic

与肾上腺素能的相关的网络例句 [注：此内容来源于网络，仅供参考]

However, pretreatment with CP-101,606 (1 mg/kg), a selective antagonist for the NR2B subunit of the N M D A receptor, significantly attenuated catalepsy and the expression of Fos-IR cells in the forebrain after the administration of haloperidol.

受体拮抗剂BD-1407 (3 mg/kg)and α-1肾上腺素能受体拮抗剂哌唑嗪(3 mg/kg)预处理不能影响氟哌啶醇诱导的强直性木僵和Fos-IR细胞表达。

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。

In order to verify nicotine effect to heart of rat , analyzing the electrograph Based on these results , it was demonstrated that nicotine can induce to release acetylcholine locally or act on muscarinic cholinoreceptor controlled by parasympathetic nerve .

为进一步确定烟碱对大鼠心脏的作用，对描记烟碱作用后大鼠心电图进行分析，发现烟碱能引起大鼠心电图显示较长的QT间期，增加了PR间期及T波面积，与肾上腺素或去甲肾上腺素引起的QT间期延长相似，且能被M受体阻断剂阿托品所阻断，说明烟碱能够诱导局部释放乙酰胆碱或者作用于部分副交感神经控制的毒蕈碱受体。

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。

Objective:To observe the distribution of adrenergic fibers in adult cardiac conduction system.

目的：观察成人心脏传导系统中肾上腺素能神经纤维的分布方法：采用荧光显微镜下观察10例成人心脏传导系统中的肾上腺素能神经纤维。

Result The data showed that 30μmol·L 1 7 chlor BTHP increased contractility and ±dT/dtmax,markedly prolonged the functional refractory period of guinea pig left ...

结果 ：7 chlor BTHP能明显延长左心房的功能性不应期，显著抑制肾上腺素诱发的自律性，还能明显增强豚鼠离体左心房的收缩力，±dT/dtmax也同时增加，且能降低右心房的心率。

The actions of δOR on the excitability in spinally projecting LC adrenergic neurons were exanimated using whole-cell current-clamp recordings in the brain slices in vitro.

在离体脑片上，应用全细胞电流钳技术，记录单细胞自发放电活动，研究δ-鸦片能受体对LC-脊髓肾上腺素能神经元兴奋性的影响。

When the effect ofNTP was examined after depletion of monoamines in the spinalcord by intrathecal neurotoxins, the antiallodynic and antihyperalgesiceffects were still observed after serotonergic denervation,but not after noradrenergic denervation.

鞘内给予神经毒素耗竭脊髓单胺递质后检查 NTP 的作用时，去除5羟色胺能神经支配后 NTP 的抗触觉性痛感和抗痛觉过敏作用仍然存在，但是去除去甲肾上腺素能神经支配后则消失。

In the spleen of the adult mouse, GAP-43-like immunoreactive fibers were extensively distributed not only in association with vascular plexuses, but also in the parenchyma of the spleen,.especially in the inner layer of the peripheral arterial Lymph Sheath of the white pulps, where T lymph

在PALS外层、边缘区和红髓，阳性纤维相对较少。6-OHDA化学损毁法证明，脾脏内的GAP-43免疫反应纤维主要是去甲肾上腺素能，也有少数不含去甲肾上腺素的纤维，可能是肽能神经纤维。

Glucose load can significantly lower blood glucose in mice, but also significantly against adrenaline-induced increase in blood glucose response in mice, and it can obviously confrontation Phenformin mice caused by hypoglycemia.

可使葡萄糖负荷的小鼠血糖明显降低，也能明显对抗肾上腺素引起的小鼠血糖升高反应，而且它还能明显对抗苯乙双胍引起的小鼠实验性低血糖。

与肾上腺素能的相关的网络解释 [注：此内容来源于网络，仅供参考]

Noradrenaline Bitartrate：去甲肾上腺素

5.肾上腺素能受体激动剂重点药物:重酒石酸去甲肾上腺素(Noradrenaline Bitartrate)结构、性质、用途;硫酸沙丁胺醇、哌唑嗪、酚苄明的结构、用途和对受体的选择性.

adrenergic：肾上腺素能

长期受到精神压力的困扰,可导致β1-肾上腺素能(adrenergic)受体分子的改变. 慢性肛裂患者的内括约肌显示对β2-催动肌素(agomists)的敏感性增加,故而精神因素可能是诱发肛裂的因素之一. 一氧化氮(NO)代谢失常 正常情况下,

adrenergic：肾上腺素能的

促肾上腺的 adrenalotropic | 肾上腺素能的 adrenergic | 肾上腺素能阻断剂 adrenergic blocking drug

adrenergic：肾上腺能的

adrenergic receptor 肾上腺素受体 | adrenergic 肾上腺能的 | adrenoceptor blocking drug 肾上腺素受体阻断药

adrenergic nerve：肾上腺素能神经

也称为肾上腺素能神经(adrenergic nerve)兴奋时主要释放去甲肾上腺素的神经纤维,包括了绝大部分交感神经节后纤维.

adrenergic drug：肾上腺素药

呈现肾上腺素样的作用,即刺激肾上腺素能神经可引起心脏收缩力增强、心搏数增加、血管收缩、血压上升、胃肠蠕动减少或散瞳者称为拟肾上腺素药(adrenergic drug)或拟交感神经作用药(symp-athomimeticdrug).

adrenergic agent：类肾上腺素能药物

adrenergic 肾上腺素能的 | adrenergic agent 类肾上腺素能药物 | adrenergic receptor 肾上腺素能受体

adrenergic agent：肾上腺素剂

肾上腺初征 adrenarche | 肾上腺素性的;肾上腺素能的 adrenergic | 肾上腺素剂 adrenergic agent

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,

noradrenergic antidepressants：去甲肾上腺素能的抗抑郁剂

5.neutralizing antibodies 中和抗体 | 6.noradrenergic antidepressants 去甲肾上腺素能的抗抑郁剂 | 7.nucleic acids 核酸