Summary
Persistent and transient muscular rigidities were induced by 6-aminonicotinamide (6-AN) and reserpine, respectively, in rats and recorded electromyographically.
Very low doses of lisuride (25 or 50 μg/kg) reduced or abolished the increased electromyographic activity in the gastrocnemius muscle. Similar results were obtained with the combination of L-DOPA (100 mg/kg) plus benserazide (25 mg/kg). Methysergide was inactive. It is suggested that lisuride could be of value in the therapy of Parkinson's disease.
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N-(D-6-methyl-8-isoergolenyl)-N′,N′-diethylcarbamide hydrogen maleate
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Loos, D., Halbhübner, K. & Herken, H. Lisuride, a potent drug in the treatment of muscular rigidity in rats. Naunyn-Schmiedeberg's Arch. Pharmacol. 300, 195–198 (1977). https://doi.org/10.1007/BF00505052
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DOI: https://doi.org/10.1007/BF00505052