Estler C J, Mitznegg P
Horm Metab Res. 1976 Mar;8(2):114-7. doi: 10.1055/s-0028-1093664.
Clomiphene (10(-3) - 10(-2) M) in a dose-dependent manner inhibited the lypolytic response of isolated rat epididymal adipose tissue and fat cells to epinephrine, ACTH, and dibutyryl-cyclic AMP. Furthermore, it reduced the non-hormonally stimulated activity of a crude preparation of lipase from epididymal adipose tissue. The accumulation of cyclic AMP produced by epinephrine in fat cells was not prevented by clomiphene at a concentration causing antilipolytic activity. It is concluded from these results that clomiphene unlike most other antilipolytic drugs exerts its antilipolytic effect by an inhibition of the lipase rather than by inhibition of adenylcyclase.
克罗米芬(10⁻³ - 10⁻²M)以剂量依赖方式抑制离体大鼠附睾脂肪组织和脂肪细胞对肾上腺素、促肾上腺皮质激素和二丁酰环磷腺苷的脂解反应。此外,它降低了附睾脂肪组织脂肪酶粗制品的非激素刺激活性。在产生抗脂解活性的浓度下,克罗米芬并不能阻止肾上腺素在脂肪细胞中产生环磷腺苷。从这些结果得出的结论是,与大多数其他抗脂解药物不同,克罗米芬通过抑制脂肪酶而非抑制腺苷酸环化酶发挥其抗脂解作用。