- 更多网络例句与受体部位相关的网络例句 [注：此内容来源于网络，仅供参考]
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The effects, of protection and treatment with, combined Ch, NaF and a trophie were significantly better than that with atropine alone. In isolated phrenic nerve-diaphragm preparation of rat, isolated jejuneal preparation of, guinea pig, and the metabolic experiment of rat liver, the results of the, assay on the rat blood ChE activity indicated that antidotal effect of NaF may be due to the antidese...
大鼠离体膈神经膈肌、豚鼠离体空肠和大鼠肝脏代谢实验及对大鼠全血胆碱酯酶活力测定的结果表明，NaF的抗毒作用可能是由于其对神经肌肉接头和/或神经节中的N受体的抗脱敏作用；而Ch则可能通过其对ChE的保护和/或加速被抑制ChE的复能，阻碍Ach到达M受体部位而发挥作用。
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Mu opioid receptor was not observed in the wrist, funnel, abdomen of mantle, mouth, craw, stomach theca, intestine, rectum, sialoid gland, liver. Weak positive mu opioid receptor immunoreaction was found in inner epidermis, ectoblast, connective tissue of the esophagus and the keratolytic of the stomach and positive immunoreaction in epidermis of back of mantle and membrane of wrist.
结果表明，短蛸腕、漏斗、外套膜腹面、口球、嗉囊、胃盲囊、肠、直肠、前唾液腺、后唾液腺、肝胰脏均呈μ受体阴性，但食道内上皮、外膜、结缔组织和胃角质层有μ受体分布，外套膜背面、腕间膜的上皮或近上皮部位呈μ受体阳性。
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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。
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This suggested that the mechanism of alleviating asthma was that when drugs were combined with the active part ofβ2 receptor ,the conformation of receptor was changed and receptor was activated,spasm of bronchial smooth muscle was alleviated,of which relieved edema of air passage、restrained inflammatory cell and so on,these would contribute to pursiness.
这表明，麻杏石甘汤的平喘机制应该是通过和β2受体活性部位结合，改变了受体的构象，受体被激活，使得支气管平滑肌松弛，减轻了气道水肿，抑制了炎症细胞等，有利于缓解和消除喘息。
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Puzzlingly, such effect is transient and depression is usually reinstated after the first episode of recovery sleep, or even after short naps .
睡眠剥夺可能通过改变5-羟色胺(serotonin 5-HT)系统起作用，5-HT_(1A)受体作为突触前的自身受体在调节中缝核5-HT神经元的活性中发挥着关键作用，并且作为突触后受体介导5-HT对边缘系统、皮层、下丘脑及其它一些脑区部位的作用，使得5-HT_(1A)受体的调节对于精神疾病非常重要。
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The calculation can take up to 45 minutes, but needs to be done only once for each receptor site.
计算需要占用45分钟，但对每个受体部位只需要做一次。
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A noncompetitive antagonist prevents the agonist from producing any effect at a given receptor site.
非竞争性拮抗剂可阻止激动剂在特定受体部位产生任何效应。
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According to the prediction results of secondary structure of receptor β chain, the general theory about relationship between cytokine and its receptor at binding site and blocking results of polyclonal antiserum against D1 (9～114 residure of β chain), the new three peptides, which comprised residures of 45～75, 56～75 and 66～75, were designed and synthesized.
依据对受体β链二级结构的预测、受体与细胞因子结合部位的结构理论以及抗受体β链D1(9～114)片段多克隆抗血清有阻断GM-CSF促进DMSO诱导HL60细胞增殖活性的结果，设计和固相合成了受体β链第45～75，56～75和66～75三个人工合成多肽片段。
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The potency of morphine and the competitivity of the blockingeffect points to a specific mechanism at a receptor site ratherthan an unspecific membrane effect.
吗啡的效能竞争性制作用说明了吗啡作用于某一受体部位的机制，而非对细胞膜的非特异性作用。
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Immunohistochemical study showed that ER and PR were mainly localized in karyon of epithelial and stroma cell, and also in smooth muscle cell in all specimen. Marked difference of intense staining was observed between implantation site and non-implantation site in the same patient, and the latter is stronger for both ER and PR . There are significant difference between implantation site and non-implantation site for ER expression or PR expression (t=- 3.895, p=0.001; t=- 3.574, p=0.001, respectively).
第一部分输卵管妊娠种植部位、非种植部位和慢性输卵管炎中雌孕激素受体的表达方法：采用免疫组化方法对30例输卵管妊娠患者的种植部位和非种植部位，12例分泌中期慢性炎症输卵管壶腹部ER、PR的定位及半定量研究，并以17例分泌中期正常壶腹部输卵管为对照。
- 更多网络解释与受体部位相关的网络解释 [注：此内容来源于网络，仅供参考]
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accessary; accessory：附加物,附件,零件
"受体部位","acceptor site" | "附加物,附件,零件","accessary,accessory" | "辅助因素","accessory factor"
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putamen：豆状核
抗体接合(antibodiesantibodies)利用有相对之激子与受体接合)利用有相对之激子与受体接合由静脉注射18F-FDOPA后,其会分布於相关基底核(basal ganglia)部位,尤其是尾状核(caudate nucleus),豆状核(putamen)等(上图)自体产物
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receptor site：受点
多年以来,有人就曾提出,药物所以能够发生作用,是由于它与机体效应器的某一部位相结合,这一部位当时被称为"接受物质",以后又被称为"受体"(receptor)或"受点"(receptor site).
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receptor site：受体部位
receptor 感受器;受体 | receptor site 受体部位 | recessive 隐性
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receptor binding site：受体结合部位
receptor-associated molecule 受体相关分子 | receptor binding site 受体结合部位 | receptor clustering 受体群集,受体聚集,受体成簇
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Scopolamine：东茛菪碱
胃肠道,骨骼肌,眼的作用;为季胺盐,口服不被吸收,阿托品(Atropine)体内过程,对M胆碱受体的竞争性阻断作用.不同部位M受体的敏感性差山茛菪碱(Anisodamine)及东茛菪碱(Scopolamine):抗M样作用及中枢作用特点,
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topography：分子构图
2.乙酰胆碱与受体的结合方式:胆碱能受体的分子构图(topography)与AchE有相似之处,但又不完全相同. 如M受体有两个活性中心(负性部位、亲酯部位)和疏水区. 当Ach与受体接近时发生①Ach的季铵氮与受体分子的负性部位以静电引力和范德华引力相互结合;
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nicotinic receptor：烟碱受体
烟碱受体( nicotinic receptor )是人们最早知道的 离子通道型神经递质受体. 法国神经科学家 Jean-Pierre Changeux 在烟碱受体的鉴定方面做出了决定性的工作,并阐明了其功能结构的主要特性,尤其是调节部位(与递质或药物的结合部位)和活化部位(离子通道)的特性以及它的活化机制,
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septal nuclei：隔核
从海马、杏仁体、隔核(septal nuclei)和前额叶皮质注射兴奋性谷氨酸均能传导到伏隔核的神经元. 阿片类以强大的镇痛作用、情绪效应和成瘾性成为一类极惹人注目的药物. 用放射性标记行受体结合分析法证明脑内有阿片受体结合部位.
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cholinoceptor agonists：胆碱受体激动药
胆碱受体激动药(cholinoceptor agonists)可激动胆碱受体. 产生与乙酰胆碱类似的作用. 乙酰胆碱是中枢和外周神经系统的内源性神经递质,其主要释放部位在神经突触和神经效应器接头部位,主要作用为激动毒蕈碱型胆碱受体(M胆碱受体)和烟碱型胆碱受体(N胆碱受体). 前者医'学教育网搜集整理主要分布于副交感神经 ...