Tornello S, Orti E, Weisenberg L, De Nicola A F
Metabolism. 1984 Mar;33(3):224-9. doi: 10.1016/0026-0495(84)90041-6.
The effect of adrenal cortical hormones on basal and prostaglandin-E2 (PGE2)-stimulated levels of cAMP was studied in incubated rat anterior pituitaries. It was found that oral administration of dexamethasone (DEX) at the concentration of 10 micrograms/mL of drinking saline to adrenalectomized (ADX) rats for four days decreases basal and PGE2-stimulated cAMP levels in the pituitary but not in the hypothalamus. Furthermore, a time-course study demonstrated that acute intraperitoneally (IP) DEX treatment had no effect; whereas, after one day of oral DEX, PGE2-stimulated levels, but not basal, were already reduced. The effect of DEX was also obtained with two natural rat adrenal hormones like corticosterone and deoxycorticosterone, whereas, progesterone and testosterone, which share with the corticoids a ring A-unsaturated-three-ketone structure but are devoid of corticoid activity, did not modify at physiological doses the levels of cAMP. More physiological validation of these results was given by experimental procedures that modified endogenous adrenal secretion. Thus, reduction of plasma corticoids by ADX significantly increased basal and PGE2-stimulated cAMP levels in the pituitary, whereas, increments of plasma corticosterone produced by ACTH had the reverse effect in intact rats. It is suggested that adrenal gland regulation of cAMP may reflect involvement of the nucleotide in the mechanism of action of corticoids at the pituitary level.
在孵育的大鼠垂体前叶中研究了肾上腺皮质激素对基础和前列腺素 - E2(PGE2)刺激的环磷酸腺苷(cAMP)水平的影响。发现以10微克/毫升的地塞米松(DEX)浓度加入饮水中,对肾上腺切除(ADX)的大鼠口服给药四天,可降低垂体中基础和PGE2刺激的cAMP水平,但对下丘脑无此作用。此外,一项时间进程研究表明,急性腹腔内(IP)给予DEX没有效果;然而,口服DEX一天后,PGE2刺激的水平(而非基础水平)已经降低。用两种天然大鼠肾上腺激素如皮质酮和脱氧皮质酮也得到了DEX的效果,而孕酮和睾酮虽然与皮质激素具有相同的A环不饱和三酮结构但缺乏皮质激素活性,在生理剂量下不会改变cAMP水平。通过改变内源性肾上腺分泌的实验程序对这些结果进行了更多生理学验证。因此,ADX使血浆皮质激素减少,显著增加了垂体中基础和PGE2刺激的cAMP水平,而促肾上腺皮质激素(ACTH)使血浆皮质酮增加,在完整大鼠中则产生相反的效果。有人提出,肾上腺对cAMP的调节可能反映了该核苷酸在垂体水平上参与皮质激素的作用机制。