The ventilatory muscles are striated skeletal muscles, and their in si
tu function is governed by the same relationships that determine the c
ontractile force of muscles in vitro. The ventilatory muscles, however
, are functionally distinct from limb skeletal muscles in several aspe
cts, the most notable being that the ventilatory muscles are the only
skeletal muscles upon which life depends. Among the muscles that parti
cipate in ventilation, the diaphragm is closest to its optimal resting
length at functional residual capacity (FRC) and has the greatest cap
acity for shortening and volume displacement, making it the primary mu
scle of inspiration. All inspiratory muscles shorten when the lung is
inflated above FRC, but interactions among the various inspiratory mus
cles make for a wider range of high force output than could be achieve
d by any one muscle group acting in isolation. The velocity of inspira
tory muscle shortening, especially diaphragmatic shortening, causes ma
ximal dynamic inspiratory pressures to be substantially lower than max
imal static pressures. This effect is especially pronounced during max
imal voluntary ventilation, maximal exercise, and maximal inspiratory
flow volume maneuvers over the full vital capacity. During quiet breat
hing, the ventilatory muscles operate well below the limits of their n
eural activation and contractile performance. During intense activity,
however, the diaphragmatic excursion approaches its limits over the e
ntire vital capacity, and respiratory pressures may near their dynamic
maximum. Because the system map operate near its available capacities
during increased ventilatory demands, multiple strategies are availab
le to compensate for deficits. For example, if the diaphragm is acutel
y shortened, it can still generate the required respiratory pressure i
f it receives more neural drive. Alternatively, other muscles can be r
ecruited to take over for an impaired diaphragm. Thus, the whole syste
m is highly versatile.