Ironslave
Mecca V.I.P.
VIP
- Joined
- Jul 12, 2006
- Messages
- 4,107
- Points
- 38
ABSTRACT: The time-courses of satellite cell (SC) activation and protein
expression of hepatocyte growth factor (HGF), HGF activator (HGFA),
HGFA inhibitor-1 (HAI-1), and HGFA inhibitor-2 (HAI-2) in human skeletal
muscle, as well as serum HGF following a single bout of muscle lengthening
contractions, were determined. Eight recreationally active participants were
recruited for the study. Subjects performed 300 lengthening contractions
involving the quadriceps femoris muscles of a single leg at a fixed velocity of
180°/s. Percutaneous muscle biopsies were taken before (PRE) and at 4 h
(T4), 24 h (T24), 72 h (T72), and 120 h (T120) following the exercise. The protocol resulted in an increase in the number of SCs [neural cell adhesion molecule (NCAM)-labeled cells] expressed relative to total myonuclei, at T24, compared with both PRE and T4 (P 0.05), and peaked at T72 (80% increase vs. PRE, P 0.05). HGF protein increased significantly in serum from baseline (PRE) to T4 (P 0.05). Active HGF protein was detected in skeletal muscle at rest [14.4 1.3 average integrated density value (IDV)/actin average IDV] and tended to increase at early time-points (P 0.12). HGFA protein increased significantly from PRE to T24 (P 0.05). HAI-1 protein increased significantly from PRE to T24 (P 0.05). HAI-2 (32 kDa) increased significantly from baseline (PRE) by T24 (P 0.05), and also by T72 and T120 (P 0.05). We conclude that a single bout of lengthening muscle contractions is sufficient to activate SCs, which may involve both a local and systemic HGF response to contraction-induced injury.
Muscle Nerve 38: 1434–1442, 2008
expression of hepatocyte growth factor (HGF), HGF activator (HGFA),
HGFA inhibitor-1 (HAI-1), and HGFA inhibitor-2 (HAI-2) in human skeletal
muscle, as well as serum HGF following a single bout of muscle lengthening
contractions, were determined. Eight recreationally active participants were
recruited for the study. Subjects performed 300 lengthening contractions
involving the quadriceps femoris muscles of a single leg at a fixed velocity of
180°/s. Percutaneous muscle biopsies were taken before (PRE) and at 4 h
(T4), 24 h (T24), 72 h (T72), and 120 h (T120) following the exercise. The protocol resulted in an increase in the number of SCs [neural cell adhesion molecule (NCAM)-labeled cells] expressed relative to total myonuclei, at T24, compared with both PRE and T4 (P 0.05), and peaked at T72 (80% increase vs. PRE, P 0.05). HGF protein increased significantly in serum from baseline (PRE) to T4 (P 0.05). Active HGF protein was detected in skeletal muscle at rest [14.4 1.3 average integrated density value (IDV)/actin average IDV] and tended to increase at early time-points (P 0.12). HGFA protein increased significantly from PRE to T24 (P 0.05). HAI-1 protein increased significantly from PRE to T24 (P 0.05). HAI-2 (32 kDa) increased significantly from baseline (PRE) by T24 (P 0.05), and also by T72 and T120 (P 0.05). We conclude that a single bout of lengthening muscle contractions is sufficient to activate SCs, which may involve both a local and systemic HGF response to contraction-induced injury.
Muscle Nerve 38: 1434–1442, 2008