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β-肾上腺素能兴奋剂对人体皮肤组胺反应的抑制作用。II. 关于所用剂量及随时间变化的反应的几种衍生物的研究。

Inhibitory effect of beta-adrenergic stimulants on the histamine reaction of the human skin. II. Studies with several derivatives in regard to the dosage used and reaction depending on time.

作者信息

Jorde W, Schata M

出版信息

Arzneimittelforschung. 1978;28(5):850-2.

PMID:35174
Abstract

In 56 volunteers the inhibitory effects of the beta-adrenergic stimulants fenoterol, salbutamol, isoproterenol, orciprenaline, terbutaline, epinephrine and phenylephrine were studied. There was a difference between the substances in regard to the applied dose and duration of inhibitory effect. The latter parameter particularly depended on the hydrosolubility of the individual substances. Fenoterol and salbutamol had a very low solubility and a very strong and long-lasting effect. The possibly stronger adhesive power of these drugs in the tissue according to their poor solubility and the site of action in the reactive systems of the skin are discussed giving preference to the vascular system over the mast-cells and cAMP.

摘要

在56名志愿者中,研究了β-肾上腺素能兴奋剂非诺特罗、沙丁胺醇、异丙肾上腺素、奥西那林、特布他林、肾上腺素和去氧肾上腺素的抑制作用。这些物质在应用剂量和抑制作用持续时间方面存在差异。后一个参数尤其取决于各物质的水溶性。非诺特罗和沙丁胺醇的溶解度非常低,但作用非常强烈且持久。根据这些药物溶解度低的特点,讨论了它们在组织中可能更强的黏附力以及在皮肤反应系统中的作用部位,认为血管系统比肥大细胞和环磷酸腺苷更受青睐。

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