TY - JOUR
T1 - Neurochemical and behavioral effects elicited by bupropion and diethylpropion in rats
AU - Santamaría, Abel
AU - Arias, Hugo R.
N1 - Funding Information:
This work was supported by CONACyT-México Grant 48370-Q (to A.S.) and by grants from the Science Foundation Arizona and Stardust Foundation and from the Office of Research and Sponsored Programs, Midwestern University (to H.R.A.). The authors gratefully acknowledge the excellent technical assistance of Angélica Gómez during the microdialysis experiments.
PY - 2010/7/1
Y1 - 2010/7/1
N2 - This study is an attempt to demonstrate whether bupropion (BP) and diethylpropion (DEP) exert their pharmacological actions by similar neurochemical mechanisms in the dorsal striatum. In this regard, the release of dopamine (DA), glutamate (Glu), and GABA, was determined in the rat dorsal striatum after acute (5. min) and chronic (15 consecutive days) treatments, and subsequently correlated with the locomotor activities produced by these drugs. The results from the acute experiments indicate that BP and DEP (40. mg/kg) increase locomotor activity, whereas chronic DEP treatment decreases locomotor activity by unspecific mechanisms. Acute BP treatment produces significant DA and Glu, but not GABA, releases. A lesser extent of DA release and tissue content of DA and its metabolites, and consequently less locomotor activity, was observed after chronic BP treatment. Acute DEP (5. mg/kg) was only able to slightly increase DA release and to decrease the tissue levels of DA, but no other markers, with practically nil locomotor activity, whereas chronic DEP produced even less neurotransmitter release. The observed difference between BP and DEP might be based on that although both drugs inhibit the DA and norepinephrine transporters, the BP-induced nicotinic receptor inhibition has yet to be demonstrated for DEP.
AB - This study is an attempt to demonstrate whether bupropion (BP) and diethylpropion (DEP) exert their pharmacological actions by similar neurochemical mechanisms in the dorsal striatum. In this regard, the release of dopamine (DA), glutamate (Glu), and GABA, was determined in the rat dorsal striatum after acute (5. min) and chronic (15 consecutive days) treatments, and subsequently correlated with the locomotor activities produced by these drugs. The results from the acute experiments indicate that BP and DEP (40. mg/kg) increase locomotor activity, whereas chronic DEP treatment decreases locomotor activity by unspecific mechanisms. Acute BP treatment produces significant DA and Glu, but not GABA, releases. A lesser extent of DA release and tissue content of DA and its metabolites, and consequently less locomotor activity, was observed after chronic BP treatment. Acute DEP (5. mg/kg) was only able to slightly increase DA release and to decrease the tissue levels of DA, but no other markers, with practically nil locomotor activity, whereas chronic DEP produced even less neurotransmitter release. The observed difference between BP and DEP might be based on that although both drugs inhibit the DA and norepinephrine transporters, the BP-induced nicotinic receptor inhibition has yet to be demonstrated for DEP.
KW - Antidepressant
KW - Bupropion
KW - Diethylpropion
KW - Dopamine release
KW - GABA release
KW - Glutamate release
KW - Locomotor activity
KW - Microdialysis
UR - http://www.scopus.com/inward/record.url?scp=77952319621&partnerID=8YFLogxK
U2 - 10.1016/j.bbr.2010.03.023
DO - 10.1016/j.bbr.2010.03.023
M3 - Article
C2 - 20307582
AN - SCOPUS:77952319621
SN - 0166-4328
VL - 211
SP - 132
EP - 139
JO - Behavioural Brain Research
JF - Behavioural Brain Research
IS - 1
ER -