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吗啡是否会增强大鼠脊髓中5-羟色胺的释放?一项体内差分脉冲伏安法研究。

Does morphine enhance the release of 5-hydroxytryptamine in the rat spinal cord? An in vivo differential pulse voltammetry study.

作者信息

Chiang C Y, Xiang X K

出版信息

Brain Res. 1987 May 19;411(2):259-66. doi: 10.1016/0006-8993(87)91077-8.

Abstract

Differential pulse voltammetry used in combination with an electrochemically treated carbon fiber electrode allowed the detection of 5-hydroxyindoles (5-HI) in the dorsal horn of the urethane-anesthetized rat. Voltammograms were recorded every 3 min for up to 4 h. One component of the signal, peak 3, corresponding to 5-HI and uric acid was first identified separately in vitro as well as in vivo, and then further examined by means of systemic L- and D-trytophan administration and by local application of uricase, respectively. It was found that the height of peak 3 was unaffected by systemic morphine. Even following pretreatment with probenecid, the height of peak 3 was increased only 8.6-13.7% over that with saline, by morphine given either intraperitoneally or intracerebrally into the nucleus raphe magnus. However, these increments of peak 3 were not statistically significant. These findings suggest that the serotonin descending system is unlikely to play an important role in morphine analgesia.

摘要

差分脉冲伏安法与经电化学处理的碳纤维电极联合使用,可检测经乌拉坦麻醉的大鼠背角中的5-羟吲哚(5-HI)。每3分钟记录一次伏安图,持续4小时。信号的一个成分,即对应于5-HI和尿酸的峰3,首先在体外和体内分别被鉴定出来,然后分别通过全身给予L-色氨酸和D-色氨酸以及局部应用尿酸酶进行进一步研究。结果发现,峰3的高度不受全身吗啡的影响。即使在用丙磺舒预处理后,腹腔内或脑室内向中缝大核注射吗啡,峰3的高度也仅比生理盐水组增加8.6%-13.7%。然而,峰3的这些增加在统计学上并不显著。这些发现表明,5-羟色胺下行系统在吗啡镇痛中不太可能起重要作用。

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