top of page
< Back

Pseudoephedrine

偽麻黃鹼

Mechanism of action:

Pseudoephedrine 是一種間接型與直接型混合的 α₁-腎上腺素受體促效劑(mixed-acting α₁-adrenergic agonist)。Pseudoephedrine 可直接刺激鼻腔與上呼吸道黏膜血管平滑肌上的 α₁-腎上腺素受體,透過 Gq 蛋白偶聯,活化磷脂酶 Cβ(phospholipase Cβ),提升 IP₃/DAG,使細胞質鈣離子上升與活化蛋白激酶 C(protein kinase C),導致血管收縮、減少黏膜血流與組織水腫。Pseudoephedrine 亦可進入交感神經末梢,促使儲存於囊泡中的正腎上腺素(norepinephrine)釋放,進一步增強 α₁-受體介導的血管收縮作用。

​Reference(s):

1. Aviado DM Jr et al. (1958). Cardiovascular effects of sympathomimetic bronchodilators; epinephrine, ephedrine, pseudoephedrine, isoproterenol, methoxyphenamine and isoprophenamine. J Pharmacol Exp Ther. 


2. Chen K et al. (1930). Ephedrine and Related Substances. Medicine. 


3. Volpp M et al. (2019). Determination of plasma protein binding for sympathomimetic drugs by means of ultrafiltration. Eur J Pharm Sci.

bottom of page