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These results suggested the existence of direct cross-talk between μ opioid receptor and D1 dopamine receptor in striatum.

这些结果表明,纹状体中存在μ阿片受体和D1多巴胺受体直接相互作用。

Endogenous opiate like substances may be involved in the modulation of the acquisition of CTA.

内源性阿片样物质可能参与了CTA形成过程的调制作用。

Naloxone could completedly reverse the stimulation of β-EP, DAGO and morphine on progesterone secretion.

提示β-EP促孕酮分泌是特异地经u-阿片受体介异的。

Demerol / Sedative / 30 Minutes / Demerol is a synthetic opioid analgesic used for the relief of moderate to severe pain.

Demerol /镇静/ 30分钟/ Demerol是一种合成的阿片类镇痛药用于救济的中度到重度疼痛。

Opioids Used for more severe pain, this class of pain relief medication includes morphine, codeine, Demerol and other prescription products.

阿片类药物|用于较严重的疼痛,这一类的止痛药物,包括吗啡,可待因, demerol和其他处方产品。

Our observation indicates that morphine may selectively depolarize most C DRG cells, which might be mediated and enhanced by adenosine.

腺苷可能介导和加强阿片类在脊髓的突触前抑制作用。

D. The expression of aldolase C in some brain regions and DRG of morphine-dependent rats.

推测醛缩酶C表达的调节可能参与了阿片类物质依赖的形成。

However,highly selectiveκagonists produced transient sedation and emesis,although tolerance developed to these effects during chronic treatment.

许多证据表明传统高选择性κ-受体激动剂不仅具有较高的镇痛作用,而且还克服了与μ受体相关的副作用,尤其是能够抑制阿片类物质成瘾。

The anti-cancer effect of these hormones by increasing endorphin second step is to directly activate cells of the opioid receptor.

这些激素的抗癌作用的第二步是通过增加内啡肽直接激活癌细胞的阿片受体。

Sigma and Epsilon receptors are no longer thought to be opioid receptors.

受体和伊普西隆受体不在被认为是阿片受体。

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