Mannelli M, Maggi M, De Feo M L, Cuomo S, Delitala G, Giusti G, Serio M
Acta Endocrinol (Copenh). 1984 Jul;106(3):357-61. doi: 10.1530/acta.0.1060357.
To evaluate a possible role for endogenous opiates in modulating sympathetic-adrenal function in humans, we measured plasma epinephrine and norepinephrine (radioenzymatic method), blood pressure and heart rate in 8 normal men (aged 24-33 years) before and after placebo or different doses (0.4, 4.8, 10 mg) of naloxone. In 6 subjects plasma insulin and glucagon levels were also measured by radioimmunoassay after placebo and 10 mg naloxone. Naloxone had no significant effect upon blood pressure, heart rate, plasma insulin, glucagon or norepinephrine. Placebo, 0.4 and 4.8 mg naloxone caused no significant change in peripheral levels of epinephrine while 10 mg produced an increase in epinephrine concentrations 15 min after iv injection (186 +/- 23 vs 99 +/- 9 pmol/l, P less than 0.01). Since naloxone did not modify plasma levels of insulin and glucagon, an indirect effect of naloxone on adrenal medullary secretion seems to be excluded. These results are in agreement with in vitro experimental data obtained in animals and suggest that endogenous opiates also have a role in modulating adrenal medullary secretion in man.
为评估内源性阿片类物质在调节人类交感-肾上腺功能中可能发挥的作用,我们采用放射酶法测量了8名正常男性(年龄24 - 33岁)在服用安慰剂或不同剂量(0.4、4.8、10毫克)纳洛酮前后的血浆肾上腺素和去甲肾上腺素水平、血压及心率。在6名受试者中,还通过放射免疫分析法测量了服用安慰剂和10毫克纳洛酮后的血浆胰岛素和胰高血糖素水平。纳洛酮对血压、心率、血浆胰岛素、胰高血糖素或去甲肾上腺素均无显著影响。安慰剂、0.4毫克和4.8毫克纳洛酮对肾上腺素外周水平无显著改变,而10毫克纳洛酮静脉注射15分钟后可使肾上腺素浓度升高(186±23对99±9皮摩尔/升,P<0.01)。由于纳洛酮未改变血浆胰岛素和胰高血糖素水平,似乎可排除纳洛酮对肾上腺髓质分泌的间接作用。这些结果与在动物身上获得的体外实验数据一致,表明内源性阿片类物质在调节人类肾上腺髓质分泌中也发挥作用。