Welle S, Schwartz R G, Statt M
Department of Medicine (Endocrine and Cardiology Units), University of Rochester School of Medicine and Dentistry, NY.
Metabolism. 1991 Jun;40(6):619-22. doi: 10.1016/0026-0495(91)90053-y.
We previously reported that 1 week of propranolol treatment (160 to 240 mg/d, orally) reduced resting metabolic rate (RMR) an average of 9% in healthy men. To determine whether this response was caused by the 25% reduction in serum triidothyronine (T3), rather than beta-adrenergic blockade, we examined the effect of nadolol on RMR in five healthy men. Nadolol is a nonselective beta-adrenergic antagonist that does not affect T3 production. After 6 to 10 days of nadolol treatment (240 mg/d), mean postabsorptive RMR declined 7% (P less than .01), with no significant change in serum T3 or thyroxine (T4) concentrations. This effect is significantly different from that of a hospitalized control group that received no drug and had no change in mean RMR, and was not different from the response to propranolol (previously published data). Nadolol slightly reduced the mean thermic response to a meal (12%), but this effect was not statistically significant. Mean postprandial RMR was 8% lower after nadolol treatment (P less than .01), mainly because of the reduced postabsorptive RMR, rather than a change in the response to the meal. These data suggest that beta-adrenergic activity makes a small but significant contribution to resting energy expenditure in man.
我们之前报道过,在健康男性中,为期1周的普萘洛尔治疗(160至240毫克/天,口服)可使静息代谢率(RMR)平均降低9%。为了确定这种反应是由血清三碘甲状腺原氨酸(T3)降低25%引起的,还是由β-肾上腺素能阻断引起的,我们研究了纳多洛尔对5名健康男性RMR的影响。纳多洛尔是一种非选择性β-肾上腺素能拮抗剂,不影响T3的产生。在接受纳多洛尔治疗(240毫克/天)6至10天后,平均吸收后RMR下降了7%(P<0.01),血清T3或甲状腺素(T4)浓度无显著变化。这种效应与未用药且平均RMR无变化的住院对照组有显著差异,与对普萘洛尔的反应(先前发表的数据)无差异。纳多洛尔略微降低了对一顿饭的平均热反应(12%),但这种效应无统计学意义。纳多洛尔治疗后餐后平均RMR降低了8%(P<0.01),主要是因为吸收后RMR降低,而不是对餐食反应的改变。这些数据表明,β-肾上腺素能活性对人类静息能量消耗有微小但显著的贡献。