Plonk J, Feldman J
J Clin Endocrinol Metab. 1976 Feb;42(2):291-5. doi: 10.1210/jcem-42-2-291.
The effect of the serotonin antagonist, cyproheptadine (Cypro), on metyrapone-induced stimulation of the pituitary-adrenal axis was evaluated in nine normal subjects. The subjects underwent standard oral metyrapone tests (750 mg every four h, for six doses) while taking no medications and while receiving oral Cypro (4 mg every six h). Cypro administration caused a significant reduction in: 1) baseline 17-hydroxycorticosteroid (17-OH) excretion (-31 +/- 7.2%), 2) the increase above baseline in 24 h 17-OH excretion on the day after metyrapone (-32 +/- 4.9%), 3) serum 11-deoxycortisol concentrations 8 h (-45 +/- 5.5%) and 24 h (-18 +/- 3.6%) after the first dose of metyrapone, and 4) plasma ACTH concentration 8 h (-32 +/- 8.2%) and 24 h (-22 +/- 8.0%) after the first dose of metyrapone. When compared with the control test, Cypro administration did not alter: 1) baseline 17-ketosteroid secretion, 2) the fall in serum cortisol concentration while taking metyrapone, 3) the serum free metyrapone concentration, 4) cortisol metabolism, 5) the adrenal response to ACTH, and 6) assay methods for measurement of serum and urinary corticosteroids. Our data suggest that Cypro can reduce pituitary-adrenal responsiveness by reducing plasma ACTH concentrations. If Cypro acts as a serotonin antagonist, our data lends support to the idea that serotoninergic mechanisms are important in the control of pituitary ACTH secretion in normal human subjects.
在9名正常受试者中评估了血清素拮抗剂赛庚啶(Cypro)对甲吡酮诱导的垂体 - 肾上腺轴刺激的影响。受试者在未服用药物以及口服Cypro(每6小时4mg)的情况下接受标准口服甲吡酮试验(每4小时750mg,共6剂)。给予Cypro后导致以下各项显著降低:1)基线17 - 羟皮质类固醇(17 - OH)排泄量(-31±7.2%),2)甲吡酮给药后第2天24小时17 - OH排泄量相对于基线的增加量(-32±4.9%),3)首次服用甲吡酮后8小时(-45±5.5%)和24小时(-18±3.6%)的血清11 - 脱氧皮质醇浓度,以及4)首次服用甲吡酮后8小时(-32±8.2%)和24小时(-22±8.0%)的血浆促肾上腺皮质激素(ACTH)浓度。与对照试验相比,给予Cypro未改变:1)基线17 - 酮类固醇分泌,2)服用甲吡酮时血清皮质醇浓度的下降,3)血清游离甲吡酮浓度,4)皮质醇代谢,5)肾上腺对ACTH的反应,以及6)血清和尿皮质类固醇测量的测定方法。我们的数据表明,Cypro可通过降低血浆ACTH浓度来降低垂体 - 肾上腺反应性。如果Cypro作为血清素拮抗剂起作用,我们的数据支持血清素能机制在正常人类受试者垂体ACTH分泌控制中起重要作用这一观点。