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From the Division of Neuromuscular Research (Drs. Araki, Higuchi, and Sugita), National Institute of Neuroscience, NCNP, and the Department of Neurology (Dr. Takagi), Toranomon Hospital, Tokyo, Japan.
The neuroleptic malignant syndrome (NMS) is similar to anesthesia-induced malignant hyperthermia (MH) in three major clinical features: hyperthermia, muscular rigidity, and myoglobinuria. In eight cases of NMS, we studied caffeine contracture of single skinned muscle fibers. Sensitivity of the sarcoplasmic reticulum to caffeine was abnormally increased in six of the eight cases. Morphologic studies showed type 2B fiber atrophy in all six cases examined, and there were necrotic fibers in two cases. Since skeletal muscle is affected in NMS, these patients may be susceptible to MH.
Address correspondence and reprint requests to Dr. Araki, Division of Neuromuscular Research, National Institute of Neuroscience, NCNP, Kodaira, Tokyo 187, Japan.
Supported by grant No. 8504 from the National Institute of Neuroscience, NCNP, and a Grant-in-Aid for New Drug Development from the Ministry of Health and Welfare, Japan.
Received October 8, 1986. Accepted for publication in final form April 23, 1987.
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