For the measurements of diaphragm contractile force, we adapted a previously described protocol [55 (link)]. We dissected ~4 mm midcostal diaphragm strips and placed these in the organ bath of the 3-in-1 animal system (Aurora Scientific Inc., Aurora, ON, Canada) filled with mammalian Ringer solution containing 120.5 mM NaCl, 20.4 mM NaHCO3, 10 mM dextrose, 4.8 mM KCl, 1.6 mM CaCl2, 1.2 mM MgSO4, 1.2 mM NaH2PO4, and 1.0 mM pyruvate. Upon dissection and force measurement, the solution was perfused continuously with 95% O2–5% CO2 and maintained at 25 °C. Diaphragm strips were then set to optimal length, maximum force (F0) was meassured by stimulating for 1000 ms at 120 Hz. Specific force (sFo) was calculated by normalizing maximum force with the division of the diaphragm strip mass (mg) by the product of diaphragm strip length (mm) and 1.06 mg/mm3 as the density of skeletal muscle. The force frequency was determined by stimulating the diaphragm strip with 1000 ms trains of 0.5 ms stimuli at 10, 25, 50, 75, 100, 125, 140, and 150 Hz.
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