Grill V, Rosenqvist U
Acta Med Scand. 1975 Apr;197(4):283-7. doi: 10.1111/j.0954-6820.1975.tb04918.x.
In short-term incubations of fat cells isolated from human adipose tissue, noradrenaline (0.2-2x10--5 M), a mixed alpha and beta-adrenergic agonist, stimulated only slightly cyclic AMP accumulation. In the presence of the alpha-adrenergic blocking agent phentolamine (0.05-5mug/ml), noradrenaline markedly augmented the amount of labelled cyclic nucleotide. The stiumlatory effect of noradrenaline and noradrenaline plus phentolamine was abolished by propranolol (0.1-10 mug/ml). Theophylline (10--4-10--3 M) slightly increased the (3-H) cyclic AMP levels per se and magnified the stiumulatory action of other agents, but did not mimic the potentiating effect of phentolamine on noradrenaline action.
在对从人脂肪组织分离出的脂肪细胞进行短期培养时,去甲肾上腺素(0.2 - 2×10⁻⁵M),一种α和β肾上腺素能混合激动剂,仅轻微刺激环磷酸腺苷(cAMP)的积累。在存在α肾上腺素能阻断剂酚妥拉明(0.05 - 5μg/ml)的情况下,去甲肾上腺素显著增加了标记环核苷酸的量。去甲肾上腺素以及去甲肾上腺素加酚妥拉明的刺激作用被普萘洛尔(0.1 - 10μg/ml)消除。茶碱(10⁻⁴ - 10⁻³M)本身略微增加了(³H)环磷酸腺苷水平,并放大了其他试剂的刺激作用,但并未模拟酚妥拉明对去甲肾上腺素作用的增强效果。