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同时给予低剂量泼尼松龙可预防由规律使用福莫特罗引起的体内β2-肾上腺素能受体敏感性降低。

Concomitant administration of low-dose prednisolone protects against in vivo beta2-adrenoceptor subsensitivity induced by regular formoterol.

作者信息

Tan K S, McFarlane L C, Lipworth B J

机构信息

Department of Clinical Pharmacology, Ninewells Hospital and Medical School, University of Dundee, Scotland.

出版信息

Chest. 1998 Jan;113(1):34-41. doi: 10.1378/chest.113.1.34.

DOI:10.1378/chest.113.1.34
PMID:9440565
Abstract

STUDY OBJECTIVES

To assess whether concomitant administration of low-dose prednisolone (PRED) with regular inhaled formoterol (FM) might prevent the occurrence of beta2-adrenoceptor (beta2-AR) tachyphylaxis.

DESIGN

Eleven healthy male subjects (mean age, 29 years) were randomized to receive 1 week with either inhaled FM, 24 microg bid, and placebo tablets (PL), or inhaled FM, 24 microg bid, and oral PRED, 15 mg daily, in double-blind, crossover fashion, with a 2-week washout between treatments. A dose-response curve (DRC) for systemic beta2-responses to inhaled salbutamol (800 to 3,200 microg) was constructed before and after each treatment period (ie, FM + PL or FM + PRED). Lymphocyte beta2-AR density (Bmax) and maximal cyclic adenosine monophosphate response to isoproterenol (isoprenaline) (Emax) were evaluated ex vivo at each visit; 8 AM serum cortisol level was also evaluated as a marker of systemic glucocorticoid activity. Comparisons for DRC were made as peak responses and area under curve (AUC).

RESULTS

There was significant (p < 0.05) subsensitivity of systemic beta2-AR responses (as AUC) following FM + PL: for heart rate (before vs after), 760 vs 340 beats (95% confidence interval [CI], 160 to 680), for tremor 0.39 vs 0.19 log units/h (95% CI, 0.01 to 0.41), and for potassium, -0.34 vs -0.19 mmol x h/L (95% CI, -0.04 to -0.28). With PRED, there was protection against subsensitivity induced by FM with no significant difference in values before vs after FM: heart rate, 740 vs 640; tremor, 0.35 vs 0.34; and potassium, -0.30 vs -0.25. FM + PL induced significant downregulation of lymphocyte beta2-AR density (log Bmax; fmol/10(6) cells) (before vs after): 0.25 vs 0.11 (95% CI, 0 to 0.22; p < 0.05) and this was not altered by PRED (before vs after): 0.21 vs 0.10 (95% CI, 0.01 to 0.27; p < 0.05). FM + PL also caused desensitization of Emax (pmol/10(6) cells) (before vs after): 6.21 vs 2.29 (95% CI, 1.19 to 6.64; p < 0.05) and this was attenuated by PRED with no significant difference between before and after values: 4.60 vs 3.28.

CONCLUSIONS

Concomitant administration of a low dose of PRED produced protection against FM-induced subsensitivity of systemic beta2-AR, as assessed by the response to inhaled salbutamol. In contrast, prednisolone did not prevent ex vivo beta2-AR downregulation despite causing significant cortisol suppression. This, in turn, suggests that there is a dissociation in the dose of PRED required to protect against beta2-AR downregulation and subsensitivity, following continuous exposure to long-acting beta2-agonist.

摘要

研究目的

评估低剂量泼尼松龙(PRED)与常规吸入福莫特罗(FM)联合使用是否可预防β2肾上腺素能受体(β2-AR)快速减敏的发生。

设计

11名健康男性受试者(平均年龄29岁)被随机分为两组,以双盲、交叉方式接受为期1周的治疗,一组吸入FM,24微克,每日两次,同时服用安慰剂片(PL);另一组吸入FM,24微克,每日两次,同时口服PRED,15毫克,每日一次,两组治疗之间有2周的洗脱期。在每个治疗期(即FM + PL或FM + PRED)前后,构建吸入沙丁胺醇(800至3200微克)后全身β2反应的剂量反应曲线(DRC)。每次访视时,离体评估淋巴细胞β2-AR密度(Bmax)和对异丙肾上腺素的最大环磷酸腺苷反应(Emax);还评估上午8点的血清皮质醇水平,作为全身糖皮质激素活性的标志物。DRC的比较以峰值反应和曲线下面积(AUC)进行。

结果

FM + PL后全身β2-AR反应(以AUC计)出现显著(p < 0.05)的敏感性降低:心率(治疗前与治疗后),760次/分钟对340次/分钟(95%置信区间[CI],160至680),震颤为0.39对0.19对数单位/小时(95%CI,0.01至0.41),血钾为-0.34对-0.19毫摩尔·小时/升(95%CI,-0.04至-0.28)。使用PRED时,可预防FM诱导的敏感性降低,FM前后的值无显著差异:心率,740次/分钟对640次/分钟;震颤,0.35对0.34;血钾,-0.30对-0.25。FM + PL导致淋巴细胞β2-AR密度显著下调(log Bmax;飞摩尔/10⁶细胞)(治疗前与治疗后):0.25对0.11(95%CI,0至0.22;p < 0.05),而PRED未改变此情况(治疗前与治疗后):0.21对0.10(95%CI,0.01至0.27;p < 0.05)。FM + PL还导致Emax(皮摩尔/10⁶细胞)脱敏(治疗前与治疗后):6.21对2.29(95%CI,1.19至6.64;p < 0.05),而PRED可减轻这种情况,前后值无显著差异:4.60对3.28。

结论

如通过对吸入沙丁胺醇的反应评估,低剂量PRED联合使用可预防FM诱导的全身β2-AR敏感性降低。相比之下,泼尼松龙尽管导致显著的皮质醇抑制,但并未预防离体β2-AR下调。这进而表明,在持续暴露于长效β2激动剂后,预防β2-AR下调和敏感性降低所需的PRED剂量存在分离。

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