Romero Steven A, McCord Jennifer L, Ely Matthew R, Sieck Dylan C, Buck Tahisha M, Luttrell Meredith J, MacLean David A, Halliwill John R
Department of Human Physiology, University of Oregon, Eugene, Oregon; and.
Division of Medical Sciences, Northern Ontario School of Medicine, Sudbury, Ontario, Canada.
J Appl Physiol (1985). 2017 Mar 1;122(3):603-610. doi: 10.1152/japplphysiol.00633.2016. Epub 2016 Aug 25.
In humans, acute aerobic exercise elicits a sustained postexercise vasodilation within previously active skeletal muscle. This response is dependent on activation of histamine H and H receptors, but the source of intramuscular histamine remains unclear. We tested the hypothesis that interstitial histamine in skeletal muscle would be increased with exercise and would be dependent on de novo formation via the inducible enzyme histidine decarboxylase and/or mast cell degranulation. Subjects performed 1 h of unilateral dynamic knee-extension exercise or sham (seated rest). We measured the interstitial histamine concentration and local blood flow (ethanol washout) via skeletal muscle microdialysis of the vastus lateralis. In some probes, we infused either α-fluoromethylhistidine hydrochloride (α-FMH), a potent inhibitor of histidine decarboxylase, or histamine H/H-receptor blockers. We also measured interstitial tryptase concentrations, a biomarker of mast cell degranulation. Compared with preexercise, histamine was increased after exercise by a change (Δ) of 4.2 ± 1.8 ng/ml ( < 0.05), but not when α-FMH was administered (Δ-0.3 ± 1.3 ng/ml, = 0.9). Likewise, local blood flow after exercise was reduced to preexercise levels by both α-FMH and H/H blockade. In addition, tryptase was elevated during exercise by Δ6.8 ± 1.1 ng/ml ( < 0.05). Taken together, these data suggest that interstitial histamine in skeletal muscle increases with exercise and results from both de novo formation and mast cell degranulation. This suggests that exercise produces an anaphylactoid signal, which affects recovery, and may influence skeletal muscle blood flow during exercise. Blood flow to previously active skeletal muscle remains elevated following an acute bout of aerobic exercise and is dependent on activation of histamine H and H receptors. The intramuscular source of histamine that drives this response to exercise has not been identified. Using intramuscular microdialysis in exercising humans, we show both mast cell degranulation and formation of histamine by histidine decarboxylase contributes to the histamine-mediated vasodilation that occurs following a bout of aerobic exercise.
在人类中,急性有氧运动可引起先前活动的骨骼肌内持续的运动后血管舒张。这种反应依赖于组胺H1和H2受体的激活,但肌肉内组胺的来源仍不清楚。我们检验了这样一个假设,即骨骼肌中的间质组胺会随着运动而增加,并且依赖于通过诱导酶组氨酸脱羧酶的从头合成和/或肥大细胞脱颗粒。受试者进行了1小时的单侧动态伸膝运动或假运动(坐姿休息)。我们通过对股外侧肌进行骨骼肌微透析来测量间质组胺浓度和局部血流(乙醇洗脱)。在一些探针中,我们注入了组氨酸脱羧酶的强效抑制剂盐酸α-氟甲基组胺(α-FMH)或组胺H1/H2受体阻滞剂。我们还测量了间质类胰蛋白酶浓度,这是肥大细胞脱颗粒的生物标志物。与运动前相比,运动后组胺增加了4.2±1.8 ng/ml(P<0.05),但给予α-FMH时组胺没有增加(Δ-0.3±1.3 ng/ml,P = 0.9)。同样,α-FMH和H1/H2受体阻断均使运动后的局部血流降至运动前水平。此外,运动期间类胰蛋白酶升高了6.8±1.1 ng/ml(P<0.05)。综上所述,这些数据表明骨骼肌中的间质组胺随着运动而增加,并且是从头合成和肥大细胞脱颗粒共同作用的结果。这表明运动产生了一种类过敏信号,该信号影响恢复,并且可能在运动期间影响骨骼肌血流。一次急性有氧运动后,先前活动的骨骼肌的血流仍保持升高,并且依赖于组胺H1和H2受体的激活。驱动这种运动反应的肌肉内组胺来源尚未确定。通过对运动中的人类进行肌肉内微透析,我们发现肥大细胞脱颗粒和组氨酸脱羧酶形成组胺均有助于有氧运动后发生的组胺介导的血管舒张。