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Changes in Primate Social Behavior After Treatment with Alpha-Methyl-Para-Tyrosine

Bibliographic Data

ID19301221
AuthorsEugene Redmond (corresponding author), Eugene D Redmond, James W Maas (corresponding author), Arthur Kling (University of Illinois Chicago), Haroutune Dekirmenjian
Year1971
Volume33
Issue2
Pages97-113
Publication date1971-03-01
Open AccessNo
TypeARTICLE
VenuePsychosomatic Medicine (JOURNAL)
Journal identifiersISSN: 0033-3174 • E-ISSN: 1534-7796
PublisherOvid Technologies (Wolters Kluwer Health) (PUBLISHER)
DOI10.1097/00006842-197103000-00001
PMID4994347
OpenAlexW2314336649
LanguageEN

The catecholamine hypothesis of the affective disorders relates the depressive syndromes in man to a deficiency of dopamine and norepinephrine. Two subjects within a social group of nonhuman primates were treated with alpha-methyl-paratyrosine, an inhibitor of the synthesis of these catecholamines. Quantifiable social interactions and appearance changed with drug treatment. Both treated animals initiated fewer total social interactions, including grooming, threats and attacks. Total social responses and social-sexual presentations remained stable. The animals showed retarded motor activity and assumed withdrawn postures, huddled with arms crossed and heads hung low. Their social-affective responses and facial expressions suggested a lack of concern with the environment. These behaviors, similar in some ways to the depressive state as seen in man, were reversible, and were accompanied by a decreased excretion of two metabolites of norepinephrine. An attempt to reverse the syndrome in 1 animal using L-DOPA was unsuccessful. This model may provide some insight into the neurochemical mechanisms of the human depressive syndromes. Further efforts to reverse the syndrome may have therapeutic relevance as well

Alpha (finance) · Catecholamine · Developmental psychology · Dopamine · Neurochemical · Norepinephrine · Social behavior · Tyrosine hydroxylase · Endocrinology · Internal Medicine · Medicine · Neuroscience · Neuroscience and Neuropharmacology Research · Physiology · Psychology · Stress Responses and Cortisol · Tryptophan and brain disorders

Highly citedNo

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