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Oral fingolimod (FTY720) for relapsing multiple sclerosis.口服芬戈莫德(FTY720)用于复发型多发性硬化症。
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2
Fingolimod and sphingosine-1-phosphate--modifiers of lymphocyte migration.芬戈莫德与鞘氨醇-1-磷酸——淋巴细胞迁移的调节剂
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3
FTY720: placebo-controlled study of the effect on cardiac rate and rhythm in healthy subjects.FTY720:在健康受试者中进行的关于其对心率和心律影响的安慰剂对照研究。
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4
Molecular and cellular diversity of neuronal G-protein-gated potassium channels.神经元G蛋白门控钾通道的分子与细胞多样性
J Neurosci. 2005 Dec 7;25(49):11468-78. doi: 10.1523/JNEUROSCI.3484-05.2005.
5
Overview of FTY720 clinical pharmacokinetics and pharmacology.FTY720临床药代动力学与药理学概述。
Ther Drug Monit. 2004 Dec;26(6):585-7. doi: 10.1097/00007691-200412000-00001.
6
Single-dose FTY720 pharmacokinetics, food effect, and pharmacological responses in healthy subjects.单剂量FTY720在健康受试者中的药代动力学、食物影响及药理反应。
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7
Signaling and biological actions of sphingosine 1-phosphate.1-磷酸鞘氨醇的信号传导及生物学作用
Pharmacol Res. 2003 May;47(5):401-7. doi: 10.1016/s1043-6618(03)00046-x.

阿托品预防和逆转芬戈莫德对健康受试者负性变时作用的能力。

The ability of atropine to prevent and reverse the negative chronotropic effect of fingolimod in healthy subjects.

作者信息

Kovarik John M, Slade Alan, Riviere Gilles-Jacques, Neddermann Daniel, Maton Steve, Hunt Thomas L, Schmouder Robert L

机构信息

Novartis Pharmaceuticals, Exploratory Development, Basel, Switzerland.

出版信息

Br J Clin Pharmacol. 2008 Aug;66(2):199-206. doi: 10.1111/j.1365-2125.2008.03199.x. Epub 2008 Apr 11.

DOI:10.1111/j.1365-2125.2008.03199.x
PMID:18507656
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2492924/
Abstract

AIMS

The authors determined whether intravenous atropine can prevent or counteract the negative chronotropic effect of the immunomodulator fingolimod.

METHODS

In this randomized, placebo-controlled, two-period, crossover study, 12 healthy subjects received 5 mg fingolimod orally concurrently with intravenous atropine (titrated to a heart rate of 110-120 beats min(-1)) or intravenous placebo. A second group of 12 subjects received atropine/placebo 4 h after the fingolimod dose. Continuous telemetry measurements were made for 24 h after each fingolimod dose.

RESULTS

Fingolimod administration alone yielded a heart rate nadir of 51 +/- 5 beats min(-1) at a median 4 h postdose with heart rate remaining depressed at 51-64 beats min(-1) over the rest of the day. Concurrent administration of fingolimod and atropine yielded a nadir of 66 +/- 6 beats min(-1) resulting in an atropine: placebo ratio (90% confidence interval) of 1.30 (1.22, 1.36). When atropine was administered at the time of the nadir, it was able to reverse the negative chronotropic effect of fingolimod from a heart rate of 56 +/- 9 beats min(-1) (placebo) to 64 +/- 8 beats min(-1) (atropine) resulting in an atropine: placebo ratio of 1.15 (1.04, 1.26). Atropine had no influence on the pharmacokinetics of fingolimod.

CONCLUSIONS

Atropine administered concurrently with fingolimod prevented the heart rate nadir that typically occurs 4 h postdose. Atropine administered at the time of the heart rate nadir was able to reverse the negative chronotropic effect of fingolimod.

摘要

目的

作者确定静脉注射阿托品是否能预防或对抗免疫调节剂芬戈莫德的负性变时作用。

方法

在这项随机、安慰剂对照、两阶段、交叉研究中,12名健康受试者口服5毫克芬戈莫德,同时静脉注射阿托品(滴定至心率为110 - 120次/分钟)或静脉注射安慰剂。另一组12名受试者在服用芬戈莫德剂量4小时后接受阿托品/安慰剂。每次服用芬戈莫德剂量后进行24小时连续遥测测量。

结果

单独给予芬戈莫德后,在给药后中位数4小时心率最低点为51±5次/分钟,在当天剩余时间内心率保持在51 - 64次/分钟。芬戈莫德与阿托品同时给药时,最低点为66±6次/分钟,导致阿托品与安慰剂的比值(90%置信区间)为1.30(1.22, 1.36)。当在最低点时给予阿托品,它能够将芬戈莫德的负性变时作用从心率56±9次/分钟(安慰剂)逆转至64±8次/分钟(阿托品),导致阿托品与安慰剂的比值为1.15(1.04, 1.26)。阿托品对芬戈莫德的药代动力学没有影响。

结论

与芬戈莫德同时给予阿托品可预防给药后4小时通常出现的心率最低点。在心率最低点时给予阿托品能够逆转芬戈莫德的负性变时作用。