Whitley G S, Bell J B, Chu F W, Tait J F, Tait S A
Proc R Soc Lond B Biol Sci. 1984 Sep 22;222(1228):273-94. doi: 10.1098/rspb.1984.0064.
The effects of various concentrations of serotonin, ACTH, K+, angiotensin II (AII), angiotensin III (AIII) and [Sar1]angiotensin II (SAII) on steroidogenesis and the incorporation of 32P (after preincubation to near equilibrium with the ATP pool) into phosphatidylinositol (PI), phosphatidic acid (PA) and phosphatidylcholine (PC) in a preparation of capsular cells from rat adrenals, consisting of 95% zona glomerulosa (z.g.) and 5% zona fasciculata plus reticularis (z.f.r.) cells, were investigated. Serotonin and ACTH stimulated steroidogenesis in the usual manner but had little or no effect on 32P incorporation into any of the three phospholipids. However, AII, AIII and SAII stimulated steroidogenesis and also 32P incorporation into PA and PI (maximally to about 280% of control values) but not into PC. These results taken together with other data on effects on the cAMP output and Ca2+ fluxes of z.g. cells suggest that stimulation by ACTH and serotonin is mediated by cAMP as second messenger. However, the angiotensins probably act through Ca2+, with associated changes in phospholipid metabolism. The 32P incorporation into PA as a function of lg concentration of AII was linear and showed a reasonable index of precision (0.36 +/- 0.03, eight experiments, 0.23 +/- 0.02 for a further eight experiments) and correlation with steroidogenesis. The corresponding incorporation into PI showed a maximum effect and a much poorer index of precision (1.02 +/- 0.30 (4.69 +/- 3.7] over the same full range of AII concentration used. The effects of AIII and SAII showed similar characteristics for 32P incorporation into both PA and PI, but, as for stimulation of steroidogenesis, at higher concentrations for AIII than for AII. The effects of different doses of AII, AIII and ACTH on the corticosterone output and 32P incorporation into PA, PI and PC of a preparation of cells, consisting of more than 98% z.f.r. cells, from rat decapsulated adrenals were also studied. ACTH, at low doses, which nevertheless markedly stimulated corticosterone output, had a small (maximally to about 125% of control values) but significant effect on 32P incorporation into PA, PI and PC. The maximum effect was usually at about 10(-10) M ACTH and was not significant at 10(-8) M.
研究了不同浓度的5-羟色胺、促肾上腺皮质激素(ACTH)、钾离子(K⁺)、血管紧张素II(AII)、血管紧张素III(AIII)和[Sar¹]血管紧张素II(SAII)对大鼠肾上腺被膜细胞制备物中类固醇生成以及³²P(预孵育至与ATP池接近平衡后)掺入磷脂酰肌醇(PI)、磷脂酸(PA)和磷脂酰胆碱(PC)的影响。该被膜细胞制备物由95%的球状带(z.g.)细胞和5%的束状带加网状带(z.f.r.)细胞组成。5-羟色胺和ACTH以通常方式刺激类固醇生成,但对³²P掺入三种磷脂中的任何一种几乎没有影响或无影响。然而,AII、AIII和SAII刺激类固醇生成,也刺激³²P掺入PA和PI(最大达到对照值的约280%),但不掺入PC。这些结果与关于对z.g.细胞的环磷酸腺苷(cAMP)输出和钙离子通量影响的其他数据一起表明,ACTH和5-羟色胺的刺激是由cAMP作为第二信使介导的。然而,血管紧张素可能通过钙离子起作用,并伴有磷脂代谢的相关变化。³²P掺入PA作为AII浓度对数的函数呈线性,并且显示出合理的精密度指标(0.36±0.03,八项实验,另外八项实验为0.23±0.02)以及与类固醇生成的相关性。在相同的AII浓度全范围内,³²P掺入PI显示出最大效应且精密度指标差得多(1.02±0.30(4.69±3.7))。AIII和SAII对³²P掺入PA和PI的影响显示出相似特征,但对于类固醇生成的刺激,AIII的浓度高于AII。还研究了不同剂量的AII、AIII和ACTH对大鼠去被膜肾上腺细胞制备物(由超过98%的z.f.r.细胞组成)中皮质酮输出以及³²P掺入PA、PI和PC的影响。低剂量的ACTH尽管显著刺激皮质酮输出,但对³²P掺入PA、PI和PC有小的(最大达到对照值的约125%)但显著的影响。最大效应通常在约10⁻¹⁰ M的ACTH时出现,在10⁻⁸ M时不显著。