Nedvídková J, Felt V
Arch Int Pharmacodyn Ther. 1976 Jun;221(2):208-11.
The effect of Trimepranol on the binding of 3H norepinephrine to myocardial particles from dogs (to fractions 1,000 g and 78,000 g resp.) has been studied and compared with the effect of propranolol, isoprenaline, phentolamine and ephedrine. Displacement of 3H norepinephrine by propranolol and isoprenaline was found in both fractions. Trimepranol, in low concentrations, inhibited the binding of 3H norepinephrine; in higher concentrations the binding of 3H norepinephrine was stimulated. Phentolamine and ephedrine were without effect in both fractions. The problem of specificity of adrenergic binding sites is discussed.
研究了曲美托嗪对狗心肌颗粒(分别为1000g和78000g组分)中3H去甲肾上腺素结合的影响,并与普萘洛尔、异丙肾上腺素、酚妥拉明和麻黄碱的作用进行了比较。在两个组分中均发现普萘洛尔和异丙肾上腺素能取代3H去甲肾上腺素。低浓度的曲美托嗪抑制3H去甲肾上腺素的结合;高浓度时则刺激3H去甲肾上腺素的结合。酚妥拉明和麻黄碱在两个组分中均无作用。文中讨论了肾上腺素能结合位点的特异性问题。