B. Loehrke et al., EFFECTS OF STRESS-RELATED SIGNAL MOLECULES ON CELLS ASSOCIATED WITH MUSCLE-TISSUE, Analytical and quantitative cytology and histology, 18(5), 1996, pp. 383-388
OBJECTIVE: To elucidate the physiologic background that makes muscle h
ypertrophy, especially that due to strenuous exercise, often parallel
to stress sensitivity and signs of acute phase immune response. STUDY
DESIGN: We used an animal model: lines of mice with hypertrophied (H)
and normally developed (N) hind leg muscles, six in each case. Functio
nal and receptor tests on cells from digested muscle tissue were made
and analyzed by microplate cytofluorimetry and flow cytometry. RESULTS
: Higher percentages of cells with a phagocyte marker (> 2-fold) and w
ith opioid (about 1.3-fold) receptors were found, whereas the portion
of glucocorticoid receptor-bearing cells tended to differ only among H
and N. Naloxone, an opioid receptor antagonist, failed only in H to e
xert a suppressive effect on dihydrorhodamine 123 oxidation. CONCLUSIO
N: These results and differences in responses of lipid trafficking and
proteolytic activities to cortisol, naloxone and adrenergic receptor
agonists suggest that not only the cell population associated with mus
cle tissue but also receptor-mediated responses that are known to be r
elated to stress coping are different between H and N.