首页> 外文期刊>The Journal of Physiology >Adrenaline but not noradrenaline is a determinant of exercise-induced lipid mobilization in human subcutaneous adipose tissue.
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Adrenaline but not noradrenaline is a determinant of exercise-induced lipid mobilization in human subcutaneous adipose tissue.

机译:肾上腺素而非去甲肾上腺素不是人皮下脂肪组织中运动诱导的脂质动员的决定因素。

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The relative contribution of noradrenaline (norepinephrine) and adrenaline (epinephrine) in the control of lipid mobilization in subcutaneous adipose tissue (SCAT) during exercise was evaluated in men treated with a somatostatin analogue, octreotide. Eight lean and eight obese young men matched for age and physical fitness performed 60 min exercise bouts at 50% of their maximal oxygen consumption on two occasions: (1) during i.v. infusion of octreotide, and (2) during placebo infusion. Lipolysis and local blood flow changes in SCAT were evaluated using in situ microdialysis. Infusion of octreotide suppressed plasma insulin and growth hormone levels at rest and during exercise. It blocked the exercise-induced increase in plasma adrenaline while that of noradrenaline was unchanged. Plasma natriuretic peptides (NPs) level was higher at rest and during exercise under octreotide infusion in lean men. Under placebo, no difference was found in the exercise-induced increase in glycerol between the probe perfused with Ringer solution alone and that with phentolamine (an alpha-adrenergic receptor antagonist) in lean subjects while a greater increase in glycerol was observed in the obese subjects. Under placebo, propranolol infusion in the probe containing phentolamine reduced by about 45% exercise-induced glycerol release; this effect was fully suppressed under octreotide infusion while noradrenaline was still elevated and exercise-induced lipid mobilization maintained in both lean and obese individuals. In conclusion, blockade of beta-adrenergic receptors during exercise performed during infusion of octreotide (blocking the exercise-induced rise in adrenaline but not that of noradrenaline) does not alter the exercise-induced lipolysis. This suggests that adrenaline is the main adrenergic agent contributing to exercise-induced lipolysis in SCAT. Moreover, it is the combined action of insulin suppression and NPs release which explains the lipolytic response which remains under octreotide after full local blockade of fat cell adrenergic receptors. For the moment, it is unknown if results apply specifically to SCAT and exercise only or if conclusions could be extended to all forms of lipolysis in humans.
机译:在用生长抑素类似物奥曲肽治疗的男性中,评估了去甲肾上腺素(去甲肾上腺素)和肾上腺素(肾上腺素)在控制运动过程中皮下脂肪组织(SCAT)脂质动员方面的相对贡献。根据年龄和身体健康状况相匹配的八名瘦小肥胖男性和八名肥胖年轻男性进行了60分钟的运动训练,两次运动均消耗了其最大耗氧量的50%:( 1)输注奥曲肽,以及(2)安慰剂输注期间。使用原位微透析评估了SCAT中的脂解和局部血流变化。在休息和运动期间输注奥曲肽可抑制血浆胰岛素和生长激素水平。它阻止了运动引起的血浆肾上腺素增加,而去甲肾上腺素没有改变。瘦男人在休息和运动过程中奥曲肽输注时血浆利钠肽(NPs)水平较高。在安慰剂下,在瘦受试者中,单独使用林格溶液灌注的探针与酚妥拉明(α-肾上腺素能受体拮抗剂)灌注的探针之间,运动引起的甘油增加没有差异,而在肥胖受试者中,甘油的增加更大。在安慰剂下,将普萘洛尔输注到含有酚妥拉明的探针中,可使运动诱导的甘油释放减少约45%;在奥曲肽输注过程中,这种作用被完全抑制,而去甲肾上腺素仍然升高,并且在肥胖和肥胖个体中都保持了运动诱导的脂质动员。总之,在输注奥曲肽期间进行的运动期间对β-肾上腺素受体的阻断(阻断了运动诱导的肾上腺素升高,但没有去甲肾上腺素的升高)不会改变运动诱导的脂解作用。这表明肾上腺素是导致运动引起的SCAT脂解的主要肾上腺素能药物。此外,胰岛素抑制和NPs释放的共同作用解释了在脂肪细胞肾上腺素受体被完全局部阻断后在奥曲肽下仍然存在的脂解反应。目前,尚不清楚结果是否仅适用于SCAT并仅运动,还是可以将结论扩展到人类的所有形式的脂解。

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