2) Opiate receptor
阿片受体
1.
Effect of methionine-enkephalin on proliferation and mechanism involved by opiate receptor of peripheral blood lymphocyte from patients with systemic lupus erythematosus;
甲硫氨酸脑啡肽对系统性红斑狼疮患者外周血淋巴细胞增殖反应的影响及阿片受体介导机制的研究
3) opioid receptor
阿片受体
1.
The function of C-terminal tail of opioid receptors and the proteins interaction with C-terminal tail of opioid receptors;
阿片受体C-末端的功能及与其相互作用蛋白的研究进展
2.
Role of opioid receptors in cerebral ischemic tolerance induced by electroacupuncture preconditioning in rats;
阿片受体在电针预处理诱导大鼠脑缺血耐受效应中的作用
3.
Role of opioid receptor in nucleus submedius in mediating electroacupuncture analgesia in rats;
丘脑中央下核内的阿片受体在介导大鼠电针镇痛中的作用
4) Opioid receptors
阿片受体
1.
The new development of the research on cloning of the opioid receptors;
阿片受体克隆研究新进展
2.
Aim: To investigate the effect on myocardial apoptosis and Bcl-2/Bax induced by remote preconditioning(RP) and to discuss the hypothesis from opioid receptors in pigs.
目的:确定骨骼肌缺血预适应对猪心肌凋亡及其调控基因Bcl-2/Bax的影响,并探讨阿片受体在此机制中可能的作用。
3.
It binds to μ-、δ-and κ-opioid receptors with a high affinity,and this binding is naloxone-displaceable.
BAM22神经肽能够与μ、-δ-和κ-阿片受体特异性地结合,具有阿片样生物活性。
5) human opioid receptor-like 1
阿片受体样受体
1.
Stable expression of human opioid receptor-like 1 in Chinese hamster ovary cells
人重组阿片受体样受体在CHO细胞稳定表达系统的建立
6) μ opioid receptor
μ阿片受体
1.
Dependent potency of endomorphin-1 and its regulation of μ opioid receptor;
内吗啡肽1的依赖潜力及其对μ阿片受体的调节
2.
Objective:To investigate the effects of agmatine by activation I1 imidazoline receptor on DAMGO-induced down-regulation and internalization of μ opioid receptor(MOR).
目的:观察胍丁胺通过激活I1咪唑啉受体(I1R)对阿片预处理引起的μ阿片受体(MOR)下调的影响及可能的分子基础。
3.
Objective To investigate the synaptic connections between endomorphin-immunoreactive(ir) terminals and μ opioid receptor-ir neurons in the superficial layers(laminae Ⅰ and Ⅱ) of the rat spinal dorsal horn.
目的观察大鼠脊髓背角内吗啡肽阳性终末与μ阿片受体阳性神经元的突触联系。
补充资料：阿片受体
分子式：
CAS号：
性质：为介导阿片类镇痛药及内源性阿片肽作用的受体。药理学实验已证明至少存在着μ、K、δ三种阿片受体，属于G蛋白偶联受体；并认为每种阿片受体仍具有多个亚型。目前已知μ、K、δ受体均可介导镇痛。
CAS号：
性质：为介导阿片类镇痛药及内源性阿片肽作用的受体。药理学实验已证明至少存在着μ、K、δ三种阿片受体，属于G蛋白偶联受体；并认为每种阿片受体仍具有多个亚型。目前已知μ、K、δ受体均可介导镇痛。
说明：补充资料仅用于学习参考，请勿用于其它任何用途。
参考词条