J. Raymond et al., Cardiovascular responses to an orthostatic challenge and electrical-stimulation-induced leg muscle contractions in individuals with paraplegia, EUR J A PHY, 80(3), 1999, pp. 205-212
Citations number
32
Categorie Soggetti
Physiology
Journal title
EUROPEAN JOURNAL OF APPLIED PHYSIOLOGY AND OCCUPATIONAL PHYSIOLOGY
The purpose of this study was to investigate the cardiovascular and haemody
namic responses that occur during moderate orthostatic challenge in people
with paraplegia, and the effect of electrical stimulation (ES)-induced leg
muscle contractions on their responses to orthostatic challenge. Eight male
s with complete spinal lesions between the 5th and 12th thoracic vertebrae
(PARA) and eight able-bodied individuals (AB) volunteered for this study. C
hanges in heart rate (f(c)), stroke volume (SV), cardiac output ((Q)over do
t(c)), mean arterial pressure (MAP), total peripheral resistance (TPR), lim
b volumes and indices of neural modulation of JE, [parasympathetic (PNS) an
d sympathetic (SNS) nervous system indicators] were assessed during: (I) su
pine rest (REST), (2) REST with lower-body negative pressure at -30 torr (L
BNP -30, where 1 torr = 133.32 N/m(2)), and (3) for PARA only, LBNP -30 wit
h ES-induced leg muscle contractions (LBNP + ES). LBNP -30 elicited a decre
ase in SV (by 23% and 22%), (Q)over dot(c) (by 15% and 18%) and the PNS ind
icator, but an increase in f(c) (by 10% and 9%), TPR (by 23% and 17%) and c
alf volume (by 1.51% and 4.04%) in both PARA and AB subjects, respectively.
The SNS indicator was increased in the AB group only. Compared to LBNP -30
, LBNP + ES increased SV (by 20%) and (Q)over dot(c) (by 16%), and decrease
d TPR (by 12%) in the PARA group. MAP was unchanged from REST during all tr
ials, for both groups. The orthostatic challenge induced by LBNP -30 elicit
ed similar cardiovascular adaptations in PARA and AB subjects. ES-induced m
uscle contractions during LBNP -30 augmented the cardiovascular responses e
xhibited by the PARA group, probably via reactivation of the skeletal muscl
e pump and improved venous return.