Vissing J, Vissing S F, MacLean D A, Saltin B, Quistorff B, Haller R G
The Copenhagen Muscle Research Center, National University Hospital, Rigshospitalet, DK-2100 Copenhagen, Denmark.
J Clin Invest. 1998 Apr 15;101(8):1654-60. doi: 10.1172/JCI555.
Muscle acidosis has been implicated as a major determinant of reflex sympathetic activation during exercise. To test this hypothesis we studied sympathetic exercise responses in metabolic myopathies in which muscle acidosis is impaired or augmented during exercise. As an index of reflex sympathetic activation to muscle, microneurographic measurements of muscle sympathetic nerve activity (MSNA) were obtained from the peroneal nerve. MSNA was measured during static handgrip exercise at 30% of maximal voluntary contraction force to exhaustion in patients in whom exercise-induced muscle acidosis is absent (seven myophosphorylase deficient patients; MD [McArdle's disease], and one patient with muscle phosphofructokinase deficiency [PFKD]), augmented (one patient with mitochondrial myopathy [MM]), or normal (five healthy controls). Muscle pH was monitored by 31P-magnetic resonance spectroscopy during handgrip exercise in the five control subjects, four MD patients, and the MM and PFKD patients. With handgrip to exhaustion, the increase in MSNA over baseline (bursts per minute [bpm] and total activity [%]) was not impaired in patients with MD (17+/-2 bpm, 124+/-42%) or PFKD (65 bpm, 307%), and was not enhanced in the MM patient (24 bpm, 131%) compared with controls (17+/-4 bpm, 115+/-17%). Post-handgrip ischemia studied in one McArdle patient, caused sustained elevation of MSNA above basal suggesting a chemoreflex activation of MSNA. Handgrip exercise elicited an enhanced drop in muscle pH of 0.51 U in the MM patient compared with the decrease in controls of 0.13+/-0.02 U. In contrast, muscle pH increased with exercise in MD by 0.12+/-0.05 U and in PFKD by 0.01 U. In conclusion, patients with glycogenolytic, glycolytic, and oxidative phosphorylation defects show normal muscle sympathetic nerve responses to static exercise. These findings indicate that muscle acidosis is not a prerequisite for sympathetic activation in exercise.
肌肉酸中毒被认为是运动过程中反射性交感神经激活的主要决定因素。为了验证这一假设,我们研究了代谢性肌病患者的交感神经运动反应,这些患者在运动过程中肌肉酸中毒受损或增强。作为对肌肉反射性交感神经激活的指标,通过微神经电图从腓神经获取肌肉交感神经活动(MSNA)的测量值。在最大自主收缩力的30%进行静态握力运动直至力竭期间,对运动性肌肉酸中毒不存在(7例肌磷酸化酶缺乏患者;MD[麦克尔迪氏病],以及1例肌肉磷酸果糖激酶缺乏患者[PFKD])、增强(1例线粒体肌病患者[MM])或正常(5名健康对照者)的患者测量MSNA。在5名对照受试者、4例MD患者、MM和PFKD患者进行握力运动期间,通过31P磁共振波谱监测肌肉pH值。握力至力竭时,MD患者(17±2次/分钟,124±42%)或PFKD患者(65次/分钟,307%)的MSNA较基线的增加(每分钟爆发次数[bpm]和总活动量[%])未受损,与对照组(17±4次/分钟,115±17%)相比,MM患者(24次/分钟,131%)的MSNA也未增强。在1例麦克尔迪氏病患者中进行的握力后缺血研究显示,MSNA持续高于基础水平,提示MSNA的化学反射激活。与对照组0.13±0.02 U的下降相比,MM患者握力运动引起肌肉pH值下降增强至0.51 U。相比之下,MD患者运动时肌肉pH值增加0.12±0.05 U,PFKD患者增加0.01 U。总之,糖原分解、糖酵解和氧化磷酸化缺陷患者对静态运动表现出正常的肌肉交感神经反应。这些发现表明,肌肉酸中毒不是运动中交感神经激活的先决条件。