Herndon D N, Nguyen T T, Wolfe R R, Maggi S P, Biolo G, Muller M, Barrow R E
Department of Surgery, University of Texas Medical Branch, Galveston.
Arch Surg. 1994 Dec;129(12):1301-4; discussion 1304-5. doi: 10.1001/archsurg.1994.01420360091012.
To determine if the cardiovascular effects of excessive catecholamines could be selectively blocked in severely burned patients without adversely affecting protein or fat kinetics.
Prospective cohort study.
A large tertiary care referral center in Galveston, Tex.
Sixteen patients with greater than 40% body surface area burns.
Patients were randomly selected to receive propranolol hydrochloride, a nonselective beta 1- and beta 2-blocker, or metoprolol tartrate, a selective beta 1-blocker.
Heart rate; rate-pressure product; rate of appearance of urea, glucose, and leucine; and leucine oxidation were measured before and after selective or nonselective beta-adrenergic blockade.
Propranolol and metoprolol caused a significant decrease in heart rate, from a mean (+/- SD) of 143 +/- 15 to 115 +/- 11 and from 147 +/- 17 to 120 +/- 9 beats per minute, respectively, during the 5-day study period. Neither the rate of appearance of urea nor the rate of urea production were significantly altered by propranolol or metoprolol therapy. Only propranolol produced a significant decrease (P < .05) in the rate of appearance of glycerol, from a mean (+/- SD) of 5.54 +/- 0.62 to 3.07 +/- 0.7 mumol/kg per minute. The rate of appearance of leucine, used as an index of total body protein catabolism, was not significantly altered by either beta-blocker.
Selective beta 1-adrenergic blockade did not reduce lipolysis; however, a beta 1- and beta 2-adrenergic blockade significantly reduced lipolysis. Thus, the increased lipolysis, characteristic of severely burned patients, is caused by stimulation of the beta 2-adrenergic receptors for catecholamines.
确定在严重烧伤患者中,过量儿茶酚胺的心血管效应能否被选择性阻断,而又不影响蛋白质或脂肪动力学。
前瞻性队列研究。
得克萨斯州加尔维斯顿的一家大型三级医疗转诊中心。
16例烧伤面积超过40%体表面积的患者。
患者被随机选择接受盐酸普萘洛尔(一种非选择性β1和β2受体阻滞剂)或酒石酸美托洛尔(一种选择性β1受体阻滞剂)治疗。
在选择性或非选择性β肾上腺素能阻断前后,测量心率、心率-血压乘积、尿素、葡萄糖和亮氨酸的生成率以及亮氨酸氧化情况。
在为期5天的研究期间,普萘洛尔和美托洛尔分别使心率显著降低,平均(±标准差)从143±15次/分钟降至115±11次/分钟,从147±17次/分钟降至120±9次/分钟。普萘洛尔或美托洛尔治疗均未显著改变尿素生成率或尿素产生率。只有普萘洛尔使甘油生成率显著降低(P<.05),平均(±标准差)从5.54±0.62降至3.07±0.7μmol/kg每分钟。用作全身蛋白质分解代谢指标的亮氨酸生成率未被任何一种β受体阻滞剂显著改变。
选择性β1肾上腺素能阻断并未减少脂肪分解;然而,β1和β2肾上腺素能阻断显著减少了脂肪分解。因此,严重烧伤患者特有的脂肪分解增加是由儿茶酚胺对β2肾上腺素能受体的刺激引起的。