Parasympathetic neural activity accounts for the lowering of exercise heart rate at high altitude

Citation
R. Boushel et al., Parasympathetic neural activity accounts for the lowering of exercise heart rate at high altitude, CIRCULATION, 104(15), 2001, pp. 1785-1791
Citations number
31
Categorie Soggetti
Cardiovascular & Respiratory Systems","Cardiovascular & Hematology Research
Journal title
CIRCULATION
ISSN journal
00097322 → ACNP
Volume
104
Issue
15
Year of publication
2001
Pages
1785 - 1791
Database
ISI
SICI code
0009-7322(20011009)104:15<1785:PNAAFT>2.0.ZU;2-D
Abstract
Background-In chronic hypoxia, both heart rate (HR) and cardiac output (Q) are reduced during exercise. The role of parasympathetic neural activity in lowering HR is unresolved, and its influence on Q and oxygen transport at high altitude has never been studied. Methods and Results-HR, Q, oxygen uptake, mean arterial pressure, and leg b lood flow were determined at rest and during cycle exercise with and withou t vagal blockade with glycopyrrolate in 7 healthy lowlanders after 9 weeks' residence at greater than or equal to 5260 m (ALT). At ALT, glycopyrrolate increased resting HR by 80 bpm (73 +/-4 to 153 +/-4 bpm) compared with 53 bpm (61 +/-3 to 114 +/-6 bpm) at sea level (SL). During exercise at ALT, gl ycopyrrolate increased HR by approximate to 40 bpm both at submaximal (127 +/-4 to 170 +/-3 bpm; 118 W) and maximal (141 +/-6 to 180 +/-2 bpm) exercis e, whereas at SL, the increase was only by 16 bpm (137 +/-6 to 153 +/-4 bpm ) at 118 W. with no effect at maximal exercise (181 +/-2 bpm). Despite rest oration of maximal IIR to SL values, glycopyrrolate had no influence on Q, which was reduced at ALT. Breathing FIO2=0.55 at peak exercise restored Q a nd power output to SL values. Conclusions-Enhanced parasympathetic neural activity accounts for the lower ing of HR during exercise at ALT without influencing Q. The abrupt restorat ion of peak exercise Q in chronic hypoxia to maximal SL values when arteria l PO2 and SO2 are similarly increased suggests hypoxia-mediated attenuation of Q.