Mersmann H J
Comp Biochem Physiol C Comp Pharmacol Toxicol. 1984;77(1):39-42. doi: 10.1016/0742-8413(84)90127-0.
Fenoterol (beta 2-agonist) and several analogs stimulated swine adipose tissue lipolysis in addition to epinephrine, norepinephrine and isoproterenol. Lipolytic activity was inhibited by propranolol (beta 1 + beta 2) greater than metoprolol (beta 1) greater than ICI 118,551 (beta 2) greater than practolol (beta 1) much greater than butoxamine (beta 2) regardless of the agonist used in the test system. The swine adipose adrenoceptor is not readily classified into a beta 1 or beta 2 subtype. It may be unique or the classification systems devised in laboratory animals may not be applicable across species.
非诺特罗(β2 激动剂)及其几种类似物除了能刺激猪脂肪组织的脂解作用外,还能与肾上腺素、去甲肾上腺素和异丙肾上腺素产生同样效果。脂解活性受到普萘洛尔(β1 + β2)的抑制作用大于美托洛尔(β1)大于 ICI 118,551(β2)大于普拉洛尔(β1),且远大于布托沙明(β2),无论在测试系统中使用何种激动剂。猪脂肪组织肾上腺素能受体不易被归类为β1 或β2 亚型。它可能是独特的,或者在实验动物中设计的分类系统可能不适用于所有物种。