Conclusions Anti-pain powder by oral administration combined with peripheral opioid receptors could ha.
目的证明口服抗痛粉是否有强镇痛效应。
The research team discovered changes in mu opioid receptors and dopamine transporters of the brain -- areas important to reward pathways.
研究团队发现在的末梢神经及大脑的多巴胺传输中，区域对酬谢路径非常重要。
Naltrexone (NTX) is a general opioid receptor antagonist devoid of intrinsic activity that results in a compensatory elevation in endogenous opioids and opioid receptors.
纳曲酮(ntx)是一个阿片受体的拮抗剂，因为他缺乏内在的活性，所以会导致细胞内的阿片类分子和阿片受体补偿性的增加。
The use of opioid analgesics has a long history in clinical Settings, although the functions of opioid receptors, especially their role in the brain, are not well understood yet.
阿片类镇痛剂的临床应用具有悠久的历史。然而，阿片受体的功能，特别是其在脑内的作用，尚未完全阐明。
After a month, the structure of the brains of these rats ADAPTS to increased dopamine levels, showing fewer of a certain type of dopamine receptor than they used to have and more opioid receptors.
在一个月后，这些大鼠的脑部结构适应了增加的多巴胺浓度，某些类型的多巴胺受体数量较以往更少，而类鸦片受体(opioid receptors)则变多。
While receptor affinity determines the amount of opioid needed to occupy a given percentage of receptors, it is the intrinsic activity of the opioid that determines its analgesic efficacy.
受体亲和力决定了占据一定百分比的受体所需阿片类药物的量，而内在活性决定了阿片类药物的镇痛效果。
While receptor affinity determines the amount of opioid needed to occupy a given percentage of receptors, it is the intrinsic activity of the opioid that determines its analgesic efficacy.
受体亲和力决定了占据一定百分比的受体所需阿片类药物的量，而内在活性决定了阿片类药物的镇痛效果。
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