Fallo F, Boscaro M, Sonino N, Mantero F
Institute of Semeiotica Medica, University of Padova, Italy.
Am J Hypertens. 1988 Jul;1(3 Pt 1):280-2. doi: 10.1093/ajh/1.3.280.
Endogenous opioids have been suggested to play a pathogenetic role in idiopathic hyperaldosteronism (IHA). To investigate this issue, the opiate antagonist naloxone was administered to 8 normals and 14 patients with primary aldosteronism, 6 with an aldosterone-producing adenoma (APA) and 8 with IHA. In normals, APA, and IHA, naloxone caused a significant increase in plasma cortisol and no change in ACTH, renin activity (PRA), and aldosterone levels. All subjects were retested after dexamethasone 2 mg. ACTH and cortisol were reduced and PRA was unchanged without modifications after naloxone. Baseline aldosterone was unaltered in all. While normals and APA failed to show any aldosterone response to naloxone under dexamethasone, IHA patients demonstrated a significant decrease. beta-Endorphin concentrations were in the normal range before and after dexamethasone. In normals as well as in APA and IHA, naloxone may act directly on the adrenal cortex increasing zona fasciculata responsiveness to physiological levels of ACTH. The decrease of aldosterone induced by naloxone in IHA under dexamethasone may be due to an intra-adrenal opioid control of zona glomerulosa in this disorder.
内源性阿片类物质被认为在特发性醛固酮增多症(IHA)的发病机制中起作用。为了研究这个问题,对8名正常人以及14名原发性醛固酮增多症患者(6例醛固酮瘤(APA)患者和8例IHA患者)给予阿片拮抗剂纳洛酮。在正常人、APA患者和IHA患者中,纳洛酮导致血浆皮质醇显著升高,而促肾上腺皮质激素(ACTH)、肾素活性(PRA)和醛固酮水平无变化。所有受试者在给予2mg地塞米松后再次接受检测。ACTH和皮质醇降低,PRA不变,纳洛酮给药后无改变。所有患者的基础醛固酮均未改变。虽然正常人及APA患者在地塞米松作用下对纳洛酮未表现出任何醛固酮反应,但IHA患者醛固酮显著降低。地塞米松前后β-内啡肽浓度均在正常范围内。在正常人以及APA患者和IHA患者中,纳洛酮可能直接作用于肾上腺皮质,增加束状带对生理水平ACTH的反应性。地塞米松作用下纳洛酮诱导IHA患者醛固酮降低可能是由于该疾病中肾上腺内阿片类物质对球状带的控制作用。