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豚鼠嗜酸性粒细胞中β2肾上腺素能受体脱敏及β2激动剂引起的对磷酸二酯酶抑制剂的超敏反应

Desensitization of beta2-adrenoceptor and hypersensitization to phosphodiesterase inhibitors elicited by beta2-agonists in guinea pig eosinophils.

作者信息

Mio M, Kirino Y, Kamei C

机构信息

Department of Pharmacology, Faculty of Pharmaceutical Sciences, Okayama University, Okayama, Japan.

出版信息

J Allergy Clin Immunol. 2000 Nov;106(5):896-903. doi: 10.1067/mai.2000.110099.

Abstract

BACKGROUND

Although the existence of functional beta(2)-adrenoceptor on eosinophils has been reported, the effects of desensitization of beta(2)-adrenoceptors on eosinophils have not been well documented.

OBJECTIVE

The effects of desensitization of beta(2)-adrenoceptors on the degranulation of guinea pig eosinophils were investigated.

METHODS

Guinea pig eosinophils were stimulated with the calcium ionophore A23187, and eosinophil peroxidase (EPO) release was determined. Changes in intracellular cyclic adenosine monophosphate (cAMP) levels were also measured.

RESULTS

A23187-induced EPO release from guinea pig eosinophils was inhibited in a concentration-dependent manner by pretreatment for 5 minutes with fenoterol, clenbuterol, and salbutamol. Such effects of beta(2)-agonists were abolished by pretreatment with KT5720, an inhibitor of protein kinase A. Desensitization of the inhibitory effects of beta(2)-agonists was observed when the incubation time was prolonged. Fenoterol (10(-6) mol/L) induced almost complete desensitization after 120 minutes of incubation, whereas clenbuterol did not bring about significant desensitization. The inhibitory effects of fenoterol and clenbuterol on A23187-induced EPO release were correlated with increases in the intracellular cAMP levels evoked by either compound. After incubation of eosinophils with 10(-6) mol/L fenoterol for 120 minutes to induce complete desensitization of beta(2)-adrenoceptors, the inhibitory effects of theophylline and rolipram were increased by about 100-fold in the desensitized cells, although the effects of forskolin and dibutyryl cAMP were not affected by beta(2)-adrenoceptor desensitization.

CONCLUSIONS

Prolonged incubation with beta(2)-agonists induced desensitization of beta(2)-adrenoceptors. Also, we postulated that hypersensitization of phosphodiesterase to its inhibitors occurs in beta(2)-adrenoceptor-desensitized guinea pig eosinophils.

摘要

背景

尽管已有报道称嗜酸性粒细胞上存在功能性β₂肾上腺素能受体,但β₂肾上腺素能受体脱敏对嗜酸性粒细胞的影响尚未得到充分记录。

目的

研究β₂肾上腺素能受体脱敏对豚鼠嗜酸性粒细胞脱颗粒的影响。

方法

用钙离子载体A23187刺激豚鼠嗜酸性粒细胞,并测定嗜酸性粒细胞过氧化物酶(EPO)释放。同时测量细胞内环磷酸腺苷(cAMP)水平的变化。

结果

用非诺特罗、克仑特罗和沙丁胺醇预处理5分钟,可浓度依赖性抑制A23187诱导的豚鼠嗜酸性粒细胞EPO释放。蛋白激酶A抑制剂KT5720预处理可消除β₂激动剂的这种作用。当孵育时间延长时,观察到β₂激动剂的抑制作用出现脱敏。孵育120分钟后,非诺特罗(10⁻⁶ mol/L)几乎诱导完全脱敏,而克仑特罗未引起明显脱敏。非诺特罗和克仑特罗对A23187诱导的EPO释放的抑制作用与两种化合物引起的细胞内cAMP水平升高相关。用10⁻⁶ mol/L非诺特罗孵育嗜酸性粒细胞120分钟以诱导β₂肾上腺素能受体完全脱敏后,茶碱和咯利普兰在脱敏细胞中的抑制作用增加了约100倍,尽管福斯可林和二丁酰cAMP的作用不受β₂肾上腺素能受体脱敏的影响。

结论

用β₂激动剂长时间孵育可诱导β₂肾上腺素能受体脱敏。此外,我们推测在β₂肾上腺素能受体脱敏的豚鼠嗜酸性粒细胞中,磷酸二酯酶对其抑制剂发生了超敏反应。

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