首页> 外文期刊>Brain research >The kappa-opioid receptor is upregulated in the spinal cord and locus ceruleus but downregulated in the dorsal root ganglia of morphine tolerant rats.
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The kappa-opioid receptor is upregulated in the spinal cord and locus ceruleus but downregulated in the dorsal root ganglia of morphine tolerant rats.

机译:吗啡耐受大鼠的脊髓和蓝斑中的κ阿片受体被上调,而在吗啡背侧神经节的背根神经节中被下调。

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摘要

As a non-selective agonist of opioid receptors, morphine can also act on the kappa-opioid receptor (KOR) when activating the mu-opioid receptor (MOR) and delta-opioid receptor (DOR). Although previous findings indicate that KOR plays an important role in morphine analgesia and antinociceptive tolerance, the reasons for the paradoxical functions of KOR in analgesia and anti-analgesia responses are still unclear. The aim of this study was to explore the role of the KOR in morphine analgesia and antinociceptive tolerance. As such, the changes in KOR expression in different regions of the nervous system in morphine tolerant rats were examined. We were able to attain morphine tolerance in rats via subcutaneous injection of morphine (10 mg/kg) twice daily for 7-consecutive days. Competitive real-time PCR, immunohistochemistry, and Western blot analyses were used to assess KOR expression in related regions of the nervous system, including the thalamus, hypothalamus, hippocampus, locus ceruleus (LC), periaqueductal gray (PAG), lumber-sacral spinal cord, and dorsal root ganglia (DRG). The expression of KOR increased in the locus ceruleus and spinal cord, but was significantly decreased in the DRG of morphine tolerant rats (P<0.05). No other significant changes in KOR expression were observed in the other regions. Consequently, we propose that the locus ceruleus and spinal cord are likely the dominant CNS regions and the DRG is the main peripheral site in which chronic morphine exerts its effect on KOR. Prolonged morphine administration induces inconsistent changes of KOR in the central and peripheral nervous system.
机译:作为阿片受体的非选择性激动剂,吗啡在激活μ阿片受体(MOR)和δ阿片受体(DOR)时也可以作用于阿片受体(KOR)。尽管以前的发现表明,KOR在吗啡镇痛和抗伤害感受性耐受中起着重要作用,但仍不清楚KOR在镇痛和抗镇痛反应中起悖论作用的原因。这项研究的目的是探讨KOR在吗啡镇痛和抗伤害感受性耐受中的作用。这样,研究了吗啡耐受大鼠在神经系统不同区域的KOR表达变化。我们能够通过每天两次皮下注射吗啡(10 mg / kg)连续7天达到大鼠对吗啡的耐受性。使用竞争性实时PCR,免疫组化和Western印迹分析来评估神经系统相关区域(包括丘脑,下丘脑,海马,蓝斑(LC),导水管周围灰质(PAG),腰-部脊柱)的KOR表达索和背根神经节(DRG)。在吗啡耐受大鼠的蓝斑和脊髓中,KOR的表达增加,而在DRG中则显着降低(P <0.05)。在其他区域未观察到KOR表达的其他显着变化。因此,我们认为蓝斑和脊髓可能是中枢神经系统的主要区域,而DRG是慢性吗啡对KOR起作用的主要外周部位。长期服用吗啡会引起中枢和周围神经系统的KOR不一致。

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