Kather H, Simon B
J Cyclic Nucleotide Res. 1977 Jun;3(3):199-206.
It has been shown that the human fat cell adenylate cyclase is activated by prostaglandins. Of the prostaglandins tested the E-type by causing about a 3-fold increase of enzyme activity, was more effective than the F-prostaglandins. Prostaglandin A2 had no stimulatory effect. Activation by prostaglandin E1 was not influenced by beta-adrenergic blockade in contrast to stimulation by epinephrine. Pretreatment of fat cells with trypsin resulted in an abolishment of PTH-sensitivity, but had no effect on prostaglandin responsiveness. These results suggest that the human fat cell adenylate cyclase is coupled to at least three distinct types of hormone receptors.
业已表明,人脂肪细胞腺苷酸环化酶可被前列腺素激活。在所测试的前列腺素中,E型前列腺素使酶活性增加约3倍,比F型前列腺素更有效。前列腺素A2无刺激作用。与肾上腺素刺激不同,前列腺素E1的激活不受β-肾上腺素能阻断的影响。用胰蛋白酶预处理脂肪细胞会导致甲状旁腺激素敏感性丧失,但对前列腺素反应性无影响。这些结果表明,人脂肪细胞腺苷酸环化酶与至少三种不同类型的激素受体偶联。