Spence C D, Campbell D P, Coghlan J P, Denton D A, Mills E H, Nelson M A, Whitworth J A, Scoggins B A
Clin Exp Hypertens A. 1987;9(4):773-95. doi: 10.3109/10641968709161449.
This study investigated the effect of 5 day infusions of 6 alpha and 9 alpha-fluoro and 16 alpha, 17 alpha-acetal analogues of prednisolone on blood pressure in conscious sheep. In vivo mineralocorticoid (MC) and glucocorticoid (GC) activities of these steroids were also measured. Prednisolone (100 mg/d) produced a small increase in mean arterial pressure associated with increased fasting plasma [glucose] and polyuria, but had no MC activity. 9 alpha-fluoro substitution greatly enhanced both the pressor and MC activity of prednisolone. The effect of 9 alpha-fluoro substitution on pressor activity was not affected by beta-methylation at C-16 (betamethasone), but was attenuated by either alpha-hydroxylation or alpha-methylation at C-16 (triamcinolone and dexamethasone, respectively). The effect of 9 alpha-fluoro substitution on MC activity as determined by urinary Na excretion was not altered by a methyl group at C-16 in either alpha or beta configuration but the MC activity was attenuated by an alpha-hydroxyl group at C-16. In contrast, 6 alpha-fluoro substitution had little influence on pressor, MC and GC activities. 16 alpha, 17 alpha-acetonide and 16 alpha, 17 alpha-butylidenedioxy substitution increased the pressor activity of parent compounds, but had no influence on either GC or MC activity. This study demonstrates a dissociation between the pressor effects and the MC and GC activities associated with steroid administration and provides further evidence to support the concept of 'hypertensinogenic' class of steroid activity which can be distinguished from their MC and GC activity.
本研究调查了泼尼松龙的6α和9α-氟以及16α,17α-缩醛类似物连续5天输注对清醒绵羊血压的影响。还测量了这些类固醇在体内的盐皮质激素(MC)和糖皮质激素(GC)活性。泼尼松龙(100mg/d)使平均动脉压略有升高,同时空腹血浆[葡萄糖]升高和出现多尿,但无MC活性。9α-氟取代大大增强了泼尼松龙的升压和MC活性。9α-氟取代对升压活性的影响不受C-16位β-甲基化(倍他米松)的影响,但在C-16位α-羟基化或α-甲基化(分别为曲安西龙和地塞米松)时减弱。9α-氟取代对通过尿钠排泄测定的MC活性的影响,在α或β构型的C-16位有甲基时均未改变,但在C-16位有α-羟基时MC活性减弱。相比之下,6α-氟取代对升压、MC和GC活性影响很小。16α,17α-丙酮缩合物和16α,17α-亚丁基二氧基取代增加了母体化合物的升压活性,但对GC或MC活性均无影响。本研究证明了类固醇给药相关的升压作用与MC和GC活性之间的分离,并提供了进一步的证据支持可与它们的MC和GC活性相区分的“致高血压性”类固醇活性概念。