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沙丁胺醇的β2肾上腺素能受体部分激动剂/拮抗剂活性在低肾上腺素能张力和高肾上腺素能张力状态下的表现。

Expression of the beta 2 adrenoceptor partial agonist/antagonist activity of salbutamol in states of low and high adrenergic tone.

作者信息

Grove A, McFarlane L C, Lipworth B J

机构信息

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

出版信息

Thorax. 1995 Feb;50(2):134-8. doi: 10.1136/thx.50.2.134.

Abstract

BACKGROUND

Salbutamol exhibits partial agonist/antagonist activity at airway beta 2 receptors in vitro in that it attenuates the bronchorelaxant effect of the full agonist isoprenaline. The aim of the present study was to characterise the partial beta 2 agonist/antagonist activity of salbutamol in vivo during supine rest and exercise, in states of low and high adrenergic tone.

METHODS

Eight normal subjects were randomised to receive single oral doses of salbutamol 2 mg, 4 mg, 8 mg (S2, S4, S8), placebo (PL), or propranolol 80 mg (PR). The beta 2 adrenoceptor responses were evaluated after supine rest and subsequently in response to maximal exercise.

RESULTS

Salbutamol demonstrated a dose-related increase in resting heart rate and tremor and a fall in serum potassium level consistent with beta 2 agonism. On exercise, the hyperkalaemic response was augmented by propranolol compared with placebo consistent with beta 2 blockade: mean difference for delta response (95% CI) PR v PL was 0.60 (0.02 to 1.27) mmol/l. This effect also occurred with salbutamol in a dose-related fashion: S8 v PL 0.33 (0.01 to 0.71) mmol/l, S8 v S2 0.31 (-0.02 to 0.61) mmol/l. Whilst propranolol blunted exercise heart rate in keeping with beta 1 blockade, salbutamol had no effect. Exercise produced an increase in lymphocyte beta 2 receptor binding density (Bmax) which was not affected by salbutamol. Plasma levels of adrenaline and noradrenaline at peak exercise were also unaltered by salbutamol in comparison with placebo.

CONCLUSIONS

In a state of low adrenergic tone at rest salbutamol produces effects consistent with beta 2 agonism. In contrast, in a state of increased adrenergic tone during exercise salbutamol produced beta 2 selective antagonism as evidenced by its effects on exercise-induced hyperkalaemia (beta 2) but not on exercise-induced tachycardia (beta 1). The effects of salbutamol on beta 2 receptor density do not explain its effects on exercise-induced hyperkalaemia since upregulation rather than downregulation was observed. This in vivo phenomenon of partial beta 2 agonist/antagonist activity of salbutamol may be of relevance in the setting of acute asthma if adrenergic tone is increased.

摘要

背景

沙丁胺醇在体外对气道β2受体表现出部分激动剂/拮抗剂活性,因为它会减弱完全激动剂异丙肾上腺素的支气管舒张作用。本研究的目的是在仰卧休息和运动期间,在低肾上腺素能状态和高肾上腺素能状态下,表征沙丁胺醇在体内的部分β2激动剂/拮抗剂活性。

方法

八名正常受试者被随机分配接受单次口服剂量的2毫克、4毫克、8毫克沙丁胺醇(S2、S4、S8)、安慰剂(PL)或80毫克普萘洛尔(PR)。在仰卧休息后以及随后对最大运动的反应中评估β2肾上腺素能受体反应。

结果

沙丁胺醇显示出静息心率和震颤与剂量相关的增加以及血清钾水平下降,这与β2激动作用一致。在运动时,与安慰剂相比,普萘洛尔增强了高钾血症反应,这与β2阻断一致:PR与PL的δ反应平均差异(95%CI)为0.60(0.02至1.27)毫摩尔/升。沙丁胺醇也以剂量相关的方式出现这种效应:S8与PL为0.33(0.01至0.71)毫摩尔/升,S8与S2为0.31(-0.02至0.61)毫摩尔/升。虽然普萘洛尔如预期的β1阻断一样使运动心率减弱,但沙丁胺醇没有影响。运动使淋巴细胞β2受体结合密度(Bmax)增加,这不受沙丁胺醇影响。与安慰剂相比,运动峰值时血浆肾上腺素和去甲肾上腺素水平也未被沙丁胺醇改变。

结论

在静息时低肾上腺素能状态下,沙丁胺醇产生与β2激动作用一致的效应。相反,在运动期间肾上腺素能状态增加时,沙丁胺醇产生β2选择性拮抗作用,这通过其对运动诱导的高钾血症(β2)的影响而非对运动诱导的心动过速(β1)的影响得到证明。沙丁胺醇对β2受体密度的影响并不能解释其对运动诱导的高钾血症的影响,因为观察到的是上调而非下调。如果肾上腺素能状态增加,沙丁胺醇在体内的这种部分β2激动剂/拮抗剂活性现象可能与急性哮喘的情况相关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/243c/473898/9eda59909698/thorax00307-0038-a.jpg

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