Torii N
Nihon Naibunpi Gakkai Zasshi. 1985 Sep 20;61(9):859-71. doi: 10.1507/endocrine1927.61.9_859.
Ca ions and cAMP are known to be involved in the action of hormones. In this study, the actions of Ca ions and cAMP in ACTH lipolysis were investigated by comparing ACTH1-24, ACTH1-10 and ACTH11-24 with regard to: lipolytic activity, binding affinity to the fat cell membrane, changes in Ca ion binding to the fat cell membrane and cAMP formation. Rat adipocytes were used. Lipolytic activity was measured in terms of the amount of FFA released from fat cells into the medium after incubation with the ACTH analogs at 37 degrees C for 30 minutes. Binding affinity to the fat cell membrane was expressed as competitive binding affinity, determined by simultaneously incubating fat cell ghosts with 125I-ACTH1-24 and unlabelled ACTH analogs at 4 degrees for 40 minutes. Changes in Ca ion binding to the fat cell membrane was expressed as Ca binding capacity, measured by simultaneously incubating fat cell ghosts with 45Ca and ACTH analogs at 24 degrees C for 20 minutes. CAMP formation was measured by RIA as the amount of cAMP formed in fat cells incubated with 10(-6)M ACTH analogs at 37 degrees C for 0, 3, 5 and 10 minutes. FFA release after incubation with each of the ACTH analogs at 10(-6) M was 1.17 mEq/L/tube for ACTH1-24, 0.26 mEq/L/tube for ACTH1-10 and 0.25 mEq/L/tube for ACTH11-24, showing a high value only for ACTH1-24. The binding affinity to the fat cell membrane (high affinity constant) was 4.4 X 10(-8) M for ACTH1-24, 4.6 X 10(-8) M for ACTH1-10 and 4.6 X 10(-8) M for ACTH11-24. There were no significant differences among the binding affinities of these ACTH analogs. The binding capacity of 45Ca++ to the fat cell membrane (high affinity constant) was 3.64 X 10(-6) M for ACTH1-24, 4.49 X 10(-6) M for ACTH1-10 and 5.46 X 10(-6) M for ACTH11-24. There were no significant differences among these ACTH analogs. The increase in cAMP formation during the first 3 minutes of incubation was 35.5 fmol/mg dry weight of fat cells for ACTH1-24, 2.2 fmol/mg for ACTH1-10 and 1.8 fmol/mg for ACTH11-24. An increase was only observed for ACTH1-24. The fact that FFA release and cAMP formation were high only with ACTH1-24 among the ACTH analogs tested indicates that cAMP formation plays an important role in the lipolytic activity of ACTH in fat cells and that the three-dimensional structure of ACTH is important for cAMP formation.
已知钙离子和环磷酸腺苷(cAMP)参与激素的作用。在本研究中,通过比较促肾上腺皮质激素(ACTH)1 - 24、ACTH1 - 10和ACTH11 - 24在以下方面来研究钙离子和cAMP在促肾上腺皮质激素脂解作用中的影响:脂解活性、与脂肪细胞膜的结合亲和力、钙离子与脂肪细胞膜结合的变化以及cAMP的形成。使用大鼠脂肪细胞。脂解活性通过在37℃下将脂肪细胞与促肾上腺皮质激素类似物孵育30分钟后,从脂肪细胞释放到培养基中的游离脂肪酸(FFA)量来测量。与脂肪细胞膜的结合亲和力以竞争结合亲和力表示,通过在4℃下将脂肪细胞膜微粒与125I - ACTH1 - 24和未标记的促肾上腺皮质激素类似物同时孵育40分钟来测定。钙离子与脂肪细胞膜结合的变化以钙结合能力表示,通过在24℃下将脂肪细胞膜微粒与45Ca和促肾上腺皮质激素类似物同时孵育20分钟来测量。cAMP的形成通过放射免疫分析(RIA)测定,即脂肪细胞在37℃下与10(-6)M促肾上腺皮质激素类似物孵育0、3、5和10分钟后形成的cAMP量。在10(-6)M浓度下,与每种促肾上腺皮质激素类似物孵育后,ACTH1 - 24的FFA释放量为1.17 mEq/L/管,ACTH1 - 10为0.26 mEq/L/管,ACTH11 - 24为0.25 mEq/L/管,仅ACTH1 - 24显示出高值。ACTH1 - 24与脂肪细胞膜的结合亲和力(高亲和力常数)为4.4×10(-8)M,ACTH1 - 10为4.6×10(-8)M,ACTH11 - 24为4.6×10(-8)M。这些促肾上腺皮质激素类似物的结合亲和力之间无显著差异。45Ca++与脂肪细胞膜的结合能力(高亲和力常数),ACTH1 - 24为3.64×10(-6)M,ACTH1 - 10为4.49×10(-6)M,ACTH11 - 24为5.46×10(-6)M。这些促肾上腺皮质激素类似物之间无显著差异。孵育的前3分钟内,ACTH1 - 24使脂肪细胞中cAMP形成增加35.5 fmol/mg干重,ACTH1 - 10为2.2 fmol/mg,ACTH11 - 24为1.8 fmol/mg。仅ACTH1 - 24观察到增加。在所测试的促肾上腺皮质激素类似物中,仅ACTH1 - 24的FFA释放和cAMP形成较高,这一事实表明cAMP的形成在脂肪细胞中促肾上腺皮质激素的脂解活性中起重要作用,并且促肾上腺皮质激素的三维结构对cAMP的形成很重要。