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托烷司琼对纤维肌痛患者血清P物质水平的影响。

Influence of tropisetron on the serum substance P levels in fibromyalgia patients.

作者信息

Stratz T, Fiebich B, Haus U, Müller W

机构信息

Hochrhein Institute of Rehabilitation Research, Department of Clinical Research, Bad Säckingen, Germany.

出版信息

Scand J Rheumatol Suppl. 2004;119:41-3. doi: 10.1080/03009740410007023.

DOI:10.1080/03009740410007023
PMID:15515412
Abstract

BACKGROUND

Substance P is found at an elevated level in the cerebrospinal fluid of fibromyalgia (FM) patients. Treatment with tropisetron leads in a subgroup of FM patients to pain reduction. The question arises of whether the substance P level in the serum can be changed by tropisetron treatment.

METHOD

Twenty patients with FM diagnosed according to the ACR criteria were treated for 5 days with a 5 mg tropisetron intravenous (i.v.) bolus injection daily. Before the first injection, 3 h later, and before and 3 h after the last injection, the serum levels of substance P were determined. The determination of this substance was carried out by means of an immunoassay from Assay Design Biotrend, Cologne. To evaluate the success of the tropisetron treatment, patients made a global assessment as 'clearly better', 'better', 'unchanged', or 'poor'. Patients who answered 'clearly better' and 'better' were regarded as responders.

RESULTS

Of the 20 patients, ten reported a good or very good influence on their pain (responders). In these responders, the means of the serum substance P levels were elevated in comparison with the non-responders, though the difference was not significant. In responders, the 5-HT3 receptor antagonist tropisetron produced a significant decrease in the serum substance P levels, while this did not occur in the non-responders.

CONCLUSION

It is possible that the responders to tropisetron represent a subgroup of FM patients for whom substance P and 5-HT3 receptors play key roles in the development of the pain symptoms.

摘要

背景

在纤维肌痛(FM)患者的脑脊液中发现P物质水平升高。曲吡那敏治疗可使一部分FM患者的疼痛减轻。问题在于曲吡那敏治疗是否能改变血清中P物质的水平。

方法

20例根据美国风湿病学会(ACR)标准诊断为FM的患者,每天静脉推注5mg曲吡那敏,治疗5天。在首次注射前、3小时后、最后一次注射前及3小时后,测定血清中P物质的水平。采用科隆市Assay Design Biotrend公司的免疫分析法测定该物质。为评估曲吡那敏治疗的效果,患者进行总体评价,分为“明显好转”“好转”“无变化”或“差”。回答“明显好转”和“好转”的患者被视为有反应者。

结果

20例患者中,10例报告疼痛有良好或非常好的改善(有反应者)。与无反应者相比,这些有反应者血清P物质水平的均值有所升高,尽管差异不显著。在有反应者中,5-羟色胺3(5-HT3)受体拮抗剂曲吡那敏使血清P物质水平显著降低,而无反应者则未出现这种情况。

结论

对曲吡那敏有反应者可能代表FM患者中的一个亚组,对于他们而言,P物质和5-HT3受体在疼痛症状的发生中起关键作用。

相似文献

1
Influence of tropisetron on the serum substance P levels in fibromyalgia patients.托烷司琼对纤维肌痛患者血清P物质水平的影响。
Scand J Rheumatol Suppl. 2004;119:41-3. doi: 10.1080/03009740410007023.
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Intravenous treatment of fibromyalgia with the 5-HT3 receptor antagonist tropisetron in a rheumatological practice.在风湿病科实践中,使用5-羟色胺3(5-HT3)受体拮抗剂托烷司琼对纤维肌痛进行静脉治疗。
Scand J Rheumatol Suppl. 2004;119:72-5. doi: 10.1080/03009740410007104.
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Short-term treatment of primary fibromyalgia with the 5-HT3-receptor antagonist tropisetron. Results of a randomized, double-blind, placebo-controlled multicenter trial in 418 patients.5-羟色胺3受体拮抗剂托烷司琼对原发性纤维肌痛的短期治疗。418例患者的随机、双盲、安慰剂对照多中心试验结果。
Int J Clin Pharmacol Res. 2001;21(1):1-13.
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Efficacy and tolerability of tropisetron in primary fibromyalgia--a highly selective and competitive 5-HT3 receptor antagonist. German Fibromyalgia Study Group.托烷司琼在原发性纤维肌痛中的疗效和耐受性——一种高选择性竞争性5-羟色胺3受体拮抗剂。德国纤维肌痛研究组
Scand J Rheumatol Suppl. 2000;113:49-54. doi: 10.1080/030097400446643.
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Oral treatment of fibromyalgia with tropisetron given over 28 days: influence on functional and vegetative symptoms, psychometric parameters and pain.用托烷司琼对纤维肌痛进行为期28天的口服治疗:对功能和自主神经症状、心理测量参数及疼痛的影响
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