Certain discrepancies between the electrical and mechanical activity of skeletal muscle in patients with myasthenia gravis have been pointed out previously ( 1 ). However, simultaneously recorded action potentials and tension have been reported only once in patients with this disorder (2) and no quantitative analysis has been made of the relationship between electrical and mechanical activity of skeletal muscle of patients with myasthenia gravis. The results of the present study of simultaneously recorded electrical and mechanical activity of intact muscle in six patients with myasthenia gravis indicate that changes in tension reflect more accurately the degree of muscle weakness than do changes in electrical activity and changes in contractile ability of the muscle can occur, both before and after neostigmine, without similar changes detectable in neuromuscular transmission.
APPARATUS AND METHODSThe method and apparatus have been described in detail elsewhere (3). In brief, we recorded simultaneously action potentials from and isometric tension developed by the adductor pollicis muscle, which was induced to contract by supramaximal, percutaneous stimulation of the ulnar nerve at the elbow. We are cognizant of the fact that movements of the thumb are complex and therefore we might not be recording mechanical and electrical activity from the same group of muscles. However, an electrode on the belly of the adductor pollicis was certainly picking up electrical activity of muscles which are innervated by the ulnar nerve. When supramaximal stimuli were used potentials of duplicate single twitches, successive twitches with 3/sec. and successive responses with 30/sec. did not vary more than 10 per cent in 48 normal subjects. The same was true of tension. When the ulnar nerve is stimulated at the elbow, the hypothenar,