This study was aimed at comparing the blocking of beta-adrenoceptor activit
y to changes in the resting energy metabolism of 10 cancer patients with pr
ogressive weight loss due to solid malignant tumours. Resting energy expend
iture (REE) as well as whole body carbohydrate and fat oxidation were inves
tigated and related to plasma substrate levels (glucose, glycerol, free fat
ty acids (FFA)) before and after 5 days of oral administration of specific
beta 1 receptor blocker (atenolol, 50 mg/day) and non-specific beta 1.beta
2- adrenoceptor (propranolol. 80 mg/day) blockade. The administration order
of the drugs was random, and a 3-day washout period was used in all indivi
duals between the provision of the first and the second drug in order to mi
nimise the risk of carry-over effects. Resting measurements in the morning
after an overnight fast were performed by indirect calorimetry. Atenolol tr
eatment reduced REE by 77 +/- 14 kcal:day and propranolol by 48 +/- 13 kcal
/day. respectively (P < 0.05 versus pretreatment values). Whole body oxygen
uptake and carbon dioxide production were decreased similarly by both aten
olol and propranolol treatment (P < 0.05). Carbohydrate oxidation was incre
ased by atenolol and decreased by propranolol, whilst fat oxidation was dec
reased by atenolol and unchanged by propranolol. The decrease in REE, accou
nting for the decline in heart rate, was significantly mort pronounced foll
owing treatment with propranolol compared with atenolol (P < 0.05). Atenolo
l and propranolol had no effect on blood glucose, plasma glycerol and FFA.
We conclude that wastage in cancer patients is in part explained by increas
ed beta(1) and beta(2)-adrenoceptor activity, in part secondary to elevated
cardiovascular activity as a result of anaemia, loss of cardiac contractil
e capacity and altered host metabolism. (C) 2000 Elsevier Science Ltd. All
rights reserved.