TY - JOUR
T1 - Behavioural and neurochemical effects after repeated administration of N-ethylpentylone (ephylone) in mice
AU - Espinosa-Velasco, María
AU - Reguilón, Marina D.
AU - Bellot, Marina
AU - Nadal-Gratacós, Núria
AU - Berzosa, Xavier
AU - Puigseslloses, Pol
AU - Gómez-Canela, Cristian
AU - Rodríguez-Arias, Marta
AU - Pubill, David
AU - Camarasa, Jordi
AU - Escubedo, Elena
AU - López-Arnau, Raúl
N1 - Funding Information:
This study was supported by Ministerio de Economía y Competitividad (grant number SAF2016‐75347‐R), Ministerio de Ciencia e Innovación (PID2019‐109390RB‐I00) and Plan Nacional sobre Drogas (2020I051). JC, DP, RLA and EE belong to 2017SGR979 from Generalitat de Catalunya.
Funding Information:
This study was supported by Ministerio de Economía y Competitividad (grant number SAF2016-75347-R), Ministerio de Ciencia e Innovación (PID2019-109390RB-I00) and Plan Nacional sobre Drogas (2020I051). JC, DP, RLA and EE belong to 2017SGR979 from Generalitat de Catalunya.
Publisher Copyright:
© 2021 The Authors. Journal of Neurochemistry published by John Wiley & Sons Ltd on behalf of International Society for Neurochemistry
PY - 2022/1
Y1 - 2022/1
N2 - N-ethyl-pentylone (NEP), also known as ‘ephylone’ and N-ethylnorpentylone, has been identified as one of the most recent novel psychostimulants to emerge into the illicit drug market and it has been associated with some intoxications and even fatalities. However, little is known about the consequences of its repeated consumption as well as the role of the monoaminergic system in such consequences. Thus, the aim of our study was to investigate the neurochemical profile and the behavioural effects after both acute and repeated NEP exposure. Male OF1 mice were acutely (1, 3, 10 mg/kg, i.p.) or repeatedly (1, 3, 10 mg/kg, i.p., 5 days, twice/day) exposed to NEP, and anxiety-like behaviour, aggressiveness, social interaction, depressive-like symptoms, body temperature, changes in monoaminergic enzymes and neurotransmitters levels as well as ΔFosB in striatum and prefrontal cortex (PFC) from post-mortem tissue were analysed short after drug-exposure or during drug-withdrawal. Acute administration of NEP induced anxiolytic effects but also an aggressive behaviour and social exploration deficits in mice, which persist during NEP-withdrawal. Moreover, NEP induced hyperthermia as well as depressive-like symptoms after repeated administrations that may be related to the decrease in serotonin and noradrenaline levels observed in striatum and PFC. Finally, the long-term increase in ΔFosB levels in striatum after NEP chronic exposure points to a high risk of dependence. Altogether indicates that NEP consumption induces different neurological and neuropsychiatric disorders accompanied by changes in the monoaminergic system, posing a threat to public health. (Figure presented.).
AB - N-ethyl-pentylone (NEP), also known as ‘ephylone’ and N-ethylnorpentylone, has been identified as one of the most recent novel psychostimulants to emerge into the illicit drug market and it has been associated with some intoxications and even fatalities. However, little is known about the consequences of its repeated consumption as well as the role of the monoaminergic system in such consequences. Thus, the aim of our study was to investigate the neurochemical profile and the behavioural effects after both acute and repeated NEP exposure. Male OF1 mice were acutely (1, 3, 10 mg/kg, i.p.) or repeatedly (1, 3, 10 mg/kg, i.p., 5 days, twice/day) exposed to NEP, and anxiety-like behaviour, aggressiveness, social interaction, depressive-like symptoms, body temperature, changes in monoaminergic enzymes and neurotransmitters levels as well as ΔFosB in striatum and prefrontal cortex (PFC) from post-mortem tissue were analysed short after drug-exposure or during drug-withdrawal. Acute administration of NEP induced anxiolytic effects but also an aggressive behaviour and social exploration deficits in mice, which persist during NEP-withdrawal. Moreover, NEP induced hyperthermia as well as depressive-like symptoms after repeated administrations that may be related to the decrease in serotonin and noradrenaline levels observed in striatum and PFC. Finally, the long-term increase in ΔFosB levels in striatum after NEP chronic exposure points to a high risk of dependence. Altogether indicates that NEP consumption induces different neurological and neuropsychiatric disorders accompanied by changes in the monoaminergic system, posing a threat to public health. (Figure presented.).
UR - http://www.scopus.com/inward/record.url?scp=85120694023&partnerID=8YFLogxK
UR - http://hdl.handle.net/20.500.14342/4438
U2 - 10.1111/jnc.15542
DO - 10.1111/jnc.15542
M3 - Article
C2 - 34816436
AN - SCOPUS:85120694023
SN - 0022-3042
VL - 160
SP - 218
EP - 233
JO - Journal of Neurochemistry
JF - Journal of Neurochemistry
IS - 2
ER -