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ApoMorphine pharmacological action

Originally tested in cardiovascular disease, trivastal (x, ET U95) has been proposed as a dopamine receptor stimulant with better oral absorption and longer duration of action than apomorphine. In addition to its direct effect on the receptors the data suggested a weak dopamine and norepinephrine releasing effect. Trivastal blocked caudate EEG spindles as did apomorphine and reduced tremor in monkeys with midbrain lesions . Others have reported its drug dynamics and pharmacological actions . [Pg.22]

See other pages where ApoMorphine pharmacological action is mentioned: [Pg.312]    [Pg.299]    [Pg.339]    [Pg.246]    [Pg.168]    [Pg.583]    [Pg.191]    [Pg.192]    [Pg.240]    [Pg.131]    [Pg.204]    [Pg.67]    [Pg.48]    [Pg.303]    [Pg.183]    [Pg.363]    [Pg.183]    [Pg.221]    [Pg.147]    [Pg.150]    [Pg.21]   
See also in sourсe #XX -- [ Pg.265 ]



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Pharmacological action

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