Dose-dependent opposite effects of nortriptyline on affective-like behavior in adolescent rats: Comparison with adult rats

Antidepressant drugs elicit different behavioral and neurochemical responses with age. In fact, the use of antidepressants during adolescence is associated with an increased risk of suicidal thinking, being the best pharmacological treatment during this critical period a matter of constant debate in...

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Detalhes bibliográficos
Autores: Bis-Humbert, Cristian, García-Cabrerizo, Rubén, García-Fuster, M Julia
Formato: artículo
Fecha de publicación:2021
País:España
Recursos:Conselleria de Salut i Consum del Govern de les Illes Balears
Repositorio:Docusalut
Idioma:inglés
OAI Identifier:oai:docusalut.com:20.500.13003/19548
Acesso em linha:https://hdl.handle.net/20.500.13003/19548
Access Level:acceso abierto
Palavra-chave:Age Factors
Behavior, Animal
Adult
Hippocampus
Humans
Adolescent
Affective Symptoms
Disease Models, Animal
Neurogenesis
Male
Nortriptyline
Neuronal Plasticity
Rats
Animals
Antidepressive Agents
Brain-Derived Neurotrophic Factor
Rats, Sprague-Dawley
Animales
Antidepresivos
Ratas Sprague-Dawley
Factor Neurotrófico Derivado del Encéfalo
Modelos Animales de Enfermedad
Nortriptilina
Adolescente
Masculino
Plasticidad Neuronal
Síntomas Afectivos
Ratas
Humanos
Conducta Animal
Hipocampo
Factores de Edad
Neurogénesis
Adulto
Antidepressant
Adolescence
BDNF
Descrição
Resumo:Antidepressant drugs elicit different behavioral and neurochemical responses with age. In fact, the use of antidepressants during adolescence is associated with an increased risk of suicidal thinking, being the best pharmacological treatment during this critical period a matter of constant debate in terms of its risk-benefit outcome. In this regard, the present study compared the effects of nortriptyline (3-10 mg/kg, 7 days) on regulating different aspects of affective-like behavior by screening adolescent and adult Sprague-Dawley rats through several consecutive tests (forced-swim, open field, sucrose preference). Brains were later collected to evaluate hippocampal neurogenesis and mBDNF protein content as potential molecular correlates of the observed behavioral responses. The main results in adolescent rats showed that nortriptyline induced dose-dependent opposite effects: while 3 mg/kg decreased immobility and increased mBDNF (indicative of an antidepressant like response), 10 mg/kg decreased exploratory time in the open field and mBDNF (suggestive of an anxiogenic-like response). These effects were not associated with changes in neurogenesis regulation. In adult rats, nortriptyline failed to modulate affective-like behavior or the neuroplasticity markers evaluated at the doses tested. In conclusion, clear behavioral and neurochemical differences were observed between adolescent and adult rats in response to nortriptyline treatment. Interestingly, while nortriptyline displayed an antidepressant like potential at the lowest dose examined in adolescence, a higher dose shifted these results towards a negative outcome, thus reinforcing the need to extreme caution when considering this treatment for our younger population.