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Clonidine and scopolamine: Differences and similarities in how they change human information processing

Callaway, Enoch ; Halliday, Roy ; Naylor, Hilary ; Brandeis, Daniel

Progress in neuro-psychopharmacology & biological psychiatry, 1991, Vol.15 (4), p.497-502 [Periódico revisado por pares]

Amsterdam: Elsevier Inc

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Título:
Clonidine and scopolamine: Differences and similarities in how they change human information processing
Autor: Callaway, Enoch ; Halliday, Roy ; Naylor, Hilary ; Brandeis, Daniel
Assuntos: Adult ; averaged event related potentials ; Biological and medical sciences ; clonidine ; Clonidine - pharmacology ; Cognition - drug effects ; Double-Blind Method ; Drug toxicity and drugs side effects treatment ; Evoked Potentials - drug effects ; Humans ; information processing ; Male ; Medical sciences ; Mental Processes - drug effects ; Miscellaneous (drug allergy, mutagens, teratogens...) ; Pharmacology. Drug treatments ; reaction time ; Reaction Time - drug effects ; scopolamine ; Scopolamine - pharmacology
É parte de: Progress in neuro-psychopharmacology & biological psychiatry, 1991, Vol.15 (4), p.497-502
Notas: ObjectType-Article-2
SourceType-Scholarly Journals-1
ObjectType-Feature-1
content type line 23
Descrição: 1. Humans have been tested on a choice reaction time task designed to disclose interactions between stimulus complexity and drug effect. 2. Tests were carried out using oral scopolamine (1.2 mg) and clonidine (0.2 mg). 3. Reaction times and event related potentials were measured. 4. Both drugs slowed reaction time and the N1 component of the ERP. 5. SCOP slows RTs to easy-to-discriminate stimuli more than RTs to harder stimuli. Its effect on P3 is the same for both types of stimuli. 6. CLON tends to slow P3 latencies to easy stimuli more than P3 latencies to harder stimuli, while the RT slowing is almost identical for both types of stimuli.
Editor: Amsterdam: Elsevier Inc
Idioma: Inglês

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Clonidine and scopolamine: Differences and similarities in how they change human information processing

Callaway, Enoch ; Halliday, Roy ; Naylor, Hilary ; Brandeis, Daniel

Amsterdam: Elsevier Inc

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