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5-HT2A 受体在大鼠脑内 5-HT 过度释放引起的 5-HT 综合征中的作用。

Involvement of 5-HT2A receptors in the serotonin (5-HT) syndrome caused by excessive 5-HT efflux in rat brain.

机构信息

Charles E. Schmidt College of Biomedical Science, Florida Atlantic University, Boca Raton, FL, USA.

出版信息

Basic Clin Pharmacol Toxicol. 2010 Oct;107(4):830-41. doi: 10.1111/j.1742-7843.2010.00586.x.

DOI:10.1111/j.1742-7843.2010.00586.x
PMID:20456331
Abstract

Previous studies have demonstrated that serotonin (5-HT) syndromes, particularly for the malignant cases, can be alleviated by ice water mists, cooling blankets and many other external cooling measures. In this study, we tested the hypothesis that external cooling measures reduce the responsivity of 5-HT(2A) receptors to excessive 5-HT efflux, which may be a possible mechanism underlying the treatment of serotonin syndrome. To test this, rat experiments were carried out in the standard and cool ambient temperature (T(amb) ) by administration of the 5-HT precursor 5-hydroxy-L-tryptophan combined with the monoamine oxidase inhibitor clorgyline. The first set of experiments was to assess severity of the syndromes by measuring body temperature responses. Consistent with the hypothesis, we found that the syndrome was malignant at the standard T(amb) of 22°C but alleviated at 12 or 6°C, these results being similar to those in rats pre-treated with the 5-HT(2A) receptor antagonist ketanserin. The second set of experiments was to utilize microdialysis to determine the relationship between the syndrome severity and 5-HT levels at the above-mentioned T(amb) . We found that excessive 5-HT efflux consisted of primary and secondary components through two distinct mechanisms. Furthermore, the secondary component efflux, which can be ascribed to 5-HT(2A) receptor activation, was proportionally reduced at the cool T(amb) of 12 and 6°C. In conclusion, results of this study support the hypothesis that cooling T(amb) reduces the functional activity of 5-HT(2A) receptors, thus alleviating the malignant syndrome.

摘要

先前的研究表明,对于恶性病例,通过冰水喷雾、冷却毯和许多其他外部冷却措施可以缓解血清素(5-HT)综合征。在这项研究中,我们检验了这样一个假设,即外部冷却措施降低了 5-HT(2A)受体对过度 5-HT 外排的反应性,这可能是治疗血清素综合征的一种可能机制。为了验证这一点,我们在标准环境温度(T(amb))和凉爽环境温度(T(amb))下进行了大鼠实验,方法是给予 5-HT 前体 5-羟色氨酸-L-色氨酸和单胺氧化酶抑制剂氯丙嗪。第一组实验通过测量体温反应来评估综合征的严重程度。与假设一致,我们发现,在标准环境温度 22°C 下,该综合征为恶性,但在 12°C 或 6°C 下得到缓解,这些结果与预先用 5-HT(2A)受体拮抗剂酮色林处理的大鼠的结果相似。第二组实验利用微透析来确定在上述 T(amb)下,综合征严重程度与 5-HT 水平之间的关系。我们发现,过度的 5-HT 外排包括通过两种不同机制的原发性和继发性成分。此外,继发性成分外排可以归因于 5-HT(2A)受体的激活,在 12°C 和 6°C 的凉爽 T(amb)下,该成分外排按比例减少。总之,这项研究的结果支持这样一个假设,即冷却 T(amb)降低了 5-HT(2A)受体的功能活性,从而缓解了恶性综合征。

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