Methods currently available to study the electrophysiological and cont
ractile properties of single human motor units (MUs) preclude the same
MU from being studied on repeated occasions. We have developed a meth
od which allows single thenar MUs to be studied longitudinally. Sites
were located along the median nerve where, using percutaneous stimulat
ion, it was possible to selectively activate a single thenar motor axo
n as determined by: (a) the presence of an ''all-ornothing'' surface-d
etected motor unit action potential (S-MUAP); (b) the occasional prese
nce of F-responses identical in size and shape to the direct S-MUAP; (
c) excitation thresholds widely separated from the next highest thresh
old motor axon so as to allow high frequency stimulation. To ensure th
at the same motor axon had been located and stimulated in successive s
tudies, additional criteria included: (a) the motor axon was found at
approximately the same site along the nerve; (b) the threshold for exc
itation remained widely separate from the next highest threshold motor
axon; (c) the shape of the S-MUAP was al most identical on repeated s
tudies; (d) S-MUAP and F-response latencies were similar. This method
provides, for the first time, the ability to track longitudinally the
electrical and contractile properties of single MUs in health and duri
ng the course and treatment of disease. (C) 1994 John Wiley & Sons, In
c.