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作用于肾上腺素能和腺苷受体的药物对眼压、睫状体中腺苷酸环化酶活性及其对百日咳毒素敏感性的影响。

Effects of drugs acting on adrenergic and adenosine receptors on the intraocular pressure and the activity of adenylyl cyclase in ciliary processes and their sensitivity to pertussis toxin.

作者信息

Cepelík J, Caicedo M, Dedina M, Hynie S

机构信息

Institute of Pharmacology, First Faculty of Medicine, Charles University, Prague, Czech Republic.

出版信息

Physiol Res. 1997;46(3):203-8.

PMID:9728508
Abstract

The effects of the selective alpha2-adrenergic agonist p-aminoclonidine, the nonselective adrenergic agonist epinephrine, the selective beta2-adrenergic agonist fenoterol and the adenosine A1 agonist R-PIA on intraocular pressure were studied in control and pertussis toxin-pretreated rabbits. Pretreatment of rabbits with pertussis toxin decreased the ocular hypotensive effects of p-aminoclonidine and epinephrine, did not influence the same effects of fenoterol or R-PIA and markedly potentiated the initial ocular hypertensive effects of epinephrine and R-PIA. As far as the action on adenylyl cyclase in ciliary processes is concerned, isoproterenol stimulated its activity in control rabbits and epinephrine exerted dual, i.e. stimulatory and inhibitory effects on the activity of this enzyme. The data obtained with epinephrine and p-aminoclonidine confirm the view that their ocular hypotensive effects are associated with their inhibitory action on adenylyl cyclase and contradict the opinion that the hypotensive action of adrenergic drugs depends on adenylyl cyclase activation.

摘要

在对照兔和百日咳毒素预处理的兔中,研究了选择性α2-肾上腺素能激动剂对氨基可乐定、非选择性肾上腺素能激动剂肾上腺素、选择性β2-肾上腺素能激动剂非诺特罗和腺苷A1激动剂R-PIA对眼压的影响。用百日咳毒素预处理兔可降低对氨基可乐定和肾上腺素的眼降压作用,不影响非诺特罗或R-PIA的相同作用,并显著增强肾上腺素和R-PIA最初的眼升压作用。就对睫状体中腺苷酸环化酶的作用而言,异丙肾上腺素刺激对照兔中其活性,而肾上腺素对该酶的活性产生双重作用,即刺激和抑制作用。用肾上腺素和对氨基可乐定获得的数据证实了它们的眼降压作用与其对腺苷酸环化酶的抑制作用相关的观点,并且与肾上腺素能药物的降压作用取决于腺苷酸环化酶激活的观点相矛盾。

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