Blaak E E, Van Baak M A, Kemerink G J, Pakbiers M T, Heidendal G A, Saris W H
Department of Human Biology, University of Limburg, The Netherlands.
Am J Physiol. 1994 Aug;267(2 Pt 1):E316-22. doi: 10.1152/ajpendo.1994.267.2.E316.
In a companion study [Blaak, E.E., M.A. van Baak, G.J. Kemerink, M.T.W. Pakbiers, G.A.K. Heidendal, and W.H.M. Saris. Am. J. Physiol. 267 (Endocrinol. Metab. 30): E306-E315, 1994.], we found that during infusion of the nonselective beta-agonist isoprenaline (Iso), obese males had a lowered Iso-induced rise in arterial glycerol and nonesterified fatty acids (NEFA) and a lowered muscle NEFA oxidation. The present study was intended to investigate whether a period of weight reduction would alter this impaired fat utilization in obese males. Before and after a 5-wk diet intervention (very low calorie diet) whole body energy expenditure was determined during rest and during intravenous infusion of increasing doses of Iso. In addition, forearm muscle metabolism was investigated with Iso infusion with and without simultaneous infusion of the beta 1-blocker atenolol (AT) by measuring skeletal muscle blood flow and arteriovenous concentration differences of various metabolites across muscle. The Iso-induced whole body thermogenesis tended to increase as a result of weight loss when this response was related to the plasma Iso concentration (P = 0.09), whereas both before and after diet there were no changes in the respiratory exchange ratio during Iso infusion. The increases in arterial NEFA and glycerol concentrations as a result of Iso infusion were not significantly different before and after weight reduction. In addition, muscle NEFA uptake did not change as a result of Iso or Iso plus AT infusion both before and after diet, whereas muscle glucose uptake and lactate release tended to be more pronounced after weight reduction.(ABSTRACT TRUNCATED AT 250 WORDS)
在一项相关研究中[布拉克,E.E.,M.A. 范巴克,G.J. 凯梅林克,M.T.W. 帕克比尔斯,G.A.K. 海登达尔,以及W.H.M. 萨里斯。《美国生理学杂志》267卷(内分泌与代谢30期):E306 - E315,1994年],我们发现,在输注非选择性β - 激动剂异丙肾上腺素(Iso)期间,肥胖男性由Iso诱导的动脉甘油和非酯化脂肪酸(NEFA)升高幅度降低,且肌肉NEFA氧化降低。本研究旨在调查一段减肥期是否会改变肥胖男性这种受损的脂肪利用情况。在为期5周的饮食干预(极低热量饮食)前后,分别在静息状态以及静脉输注递增剂量Iso期间测定全身能量消耗。此外,通过测量骨骼肌血流量以及肌肉中各种代谢物的动静脉浓度差,研究了在输注Iso时同时输注或不输注β1阻滞剂阿替洛尔(AT)情况下的前臂肌肉代谢。当将Iso诱导的全身产热与血浆Iso浓度相关联时,减肥后其有升高趋势(P = 0.09),而在饮食前后输注Iso期间呼吸交换率均无变化。减肥前后,Iso输注导致的动脉NEFA和甘油浓度升高并无显著差异。此外,无论饮食前后,输注Iso或Iso加AT均未使肌肉NEFA摄取发生变化,而减肥后肌肉葡萄糖摄取和乳酸释放往往更为明显。(摘要截选至250词)