Eh. Schlenker et Ja. Burbach, THYROXINE AFFECTS VENTILATION, LUNG MORPHOMETRY, AND NECROSIS OF DIAPHRAGM IN DYSTROPHIC HAMSTERS, American journal of physiology. Regulatory, integrative and comparative physiology, 37(3), 1995, pp. 779-785
Male dystrophic hamsters (DH) were treated with pellets containing thy
roxine (T hamsters) or placebo (P hamsters) for 8 wk. O-2 consumption,
ventilation, and ventilation in response to 8% CO2 in O-2 and 10% O-2
in N-2 were evaluated 1 and 8 wk after treatment began. O-2 consumpti
on was elevated in T hamsters at 1 and 8 wk, whereas ventilation was s
imilar in the two groups on the first week. By 8 wk, ventilation and v
entilatory responses to hypoxic and hypercapnic challenges were 100% g
reater in T than in P hamsters (P < 0.05). Morphemetric evaluations at
the end of the treatment period indicated that air space surface dens
ity, tissue volume density, and surface density-to-air space volume ra
tio of the lung parenchyma were greater (P < 0.05) in T than in P hams
ters. In contrast, chord length within the lung parenchyma was shorter
and necrosis in the diaphragm and tongue, but not in the heart, was l
ower (P < 0.05) in T than in P hamsters. Taken together, these results
suggest that T treatment of DH for 8 wk affects O-2 consumption, vent
ilation, lung architecture, and skeletal muscle without increasing tri
iodothyronine levels.