Ambrosi B, Bochicchio D, Faglia G
Clin Endocrinol (Oxf). 1986 May;24(5):483-9. doi: 10.1111/j.1365-2265.1986.tb03276.x.
The effects of loperamide, an opiate analogue of the piperidine class on pituitary hormone secretion were evaluated in eight patients with Addison's disease. In all patients loperamide administration (16 mg orally) induced a marked fall in plasma ACTH levels (P less than 0.01), without affecting GH, PRL and LH levels. Plasma ACTH concentration fell significantly from 854 +/- 167 pg/ml (mean +/- SEM) to 460 +/- 123 pg/ml at 60 min (P less than 0.01). The inhibition persisted throughout the whole test period, the nadir being reached at 300 min. Low dose naloxone infusion 180 min after loperamide administration caused plasma ACTH to rise from 181 +/- 61 pg/ml to 539 +/- 99 pg/ml (P less than 0.01). The present data suggest that the opiate analogue loperamide is a potent inhibitor of ACTH secretion in patients with Addison's disease, which may be acting on mu receptors, since its effect is blocked by low doses of naloxone.
在8例艾迪生病患者中评估了哌啶类阿片类似物洛哌丁胺对垂体激素分泌的影响。在所有患者中,口服洛哌丁胺(16mg)导致血浆促肾上腺皮质激素(ACTH)水平显著下降(P<0.01),而不影响生长激素(GH)、催乳素(PRL)和促黄体生成素(LH)水平。血浆ACTH浓度在60分钟时从854±167pg/ml(平均值±标准误)显著降至460±123pg/ml(P<0.01)。整个测试期间抑制作用持续存在,在300分钟时达到最低点。洛哌丁胺给药180分钟后输注低剂量纳洛酮导致血浆ACTH从181±61pg/ml升至539±99pg/ml(P<0.01)。目前的数据表明,阿片类似物洛哌丁胺是艾迪生病患者ACTH分泌的有效抑制剂,其可能作用于μ受体,因为低剂量纳洛酮可阻断其作用。