Keyword search (4,163 papers available)

"Brake WG" Authored Publications:

Title Authors PubMed ID
1 Combined effects of the contraceptive hormones, ethinyl estradiol and levonorgestrel, on the use of place and response memory in gonadally-intact female rats Lacasse JM; Boulos V; Fisher C; Hamilton S; Heron M; Mac Cionnaith CE; Peronace V; Tito N; Brake WG; 36403510
PSYCHOLOGY
2 Modeling hormonal contraception in female rats: a framework for studies in behavioral neurobiology Lacasse JM; Gomez-Perales E; Brake WG; 35952797
PSYCHOLOGY
3 Estrogen receptors observed at extranuclear neuronal sites and in glia in the nucleus accumbens core and shell of the female rat: Evidence for localization to catecholaminergic and GABAergic neurons Almey A; Milner TA; Brake WG; 35397175
CSBN
4 Progesterone rapidly alters the use of place and response memory during spatial navigation in female rats Lacasse JM; Patel S; Bailey A; Peronace V; Brake WG; 35158200
PSYCHOLOGY
5 Depression, Estrogens, and Neuroinflammation: A Preclinical Review of Ketamine Treatment for Mood Disorders in Women Gagne C; Piot A; Brake WG; 35115970
CSBN
6 The priming effect of food persists following blockade of dopamine receptors. Evangelista C, Hantson A, Shams WM, Almey A, Pileggi M, Voisard JR, Boulos V, Al-Qadri Y, Gonzalez Cautela BV, Zhou FX, Duchemin J, Habrich A, Tito N, Koumrouyan RA, Patel S, Lorenc V, Gagne C, El Oufi K, Shizgal P, Brake WG 31350860
CSBN
7 Estrogen receptor α and G-protein coupled estrogen receptor 1 are localized to GABAergic neurons in the dorsal striatum. Almey A, Milner TA, Brake WG 27080432
PSYCHOLOGY
8 High estrogen and chronic haloperidol lead to greater amphetamine-induced BOLD activation in awake, amphetamine-sensitized female rats. Madularu D, Kulkarni P, Yee JR, Kenkel WM, Shams WM, Ferris CF, Brake WG 27154458
CSBN
9 Modulation of spatial and response strategies by phase of the menstrual cycle in women tested in a virtual navigation task. Hussain D, Hanafi S, Konishi K, Brake WG, Bohbot VD 27213559
PSYCHOLOGY
10 17β-Estradiol infusions into the dorsal striatum rapidly increase dorsal striatal dopamine release in vivo. Shams WM, Sanio C, Quinlan MG, Brake WG 27256507
PSYCHOLOGY
11 Interactions between estradiol and haloperidol on perseveration and reversal learning in amphetamine-sensitized female rats. Almey A, Arena L, Oliel J, Shams WM, Hafez N, Mancinelli C, Henning L, Tsanev A, Brake WG 28062232
PSYCHOLOGY
12 17β-estradiol locally increases phasic dopamine release in the dorsal striatum. Shams WM, Cossette MP, Shizgal P, Brake WG 29175028
CSBN
13 Modulatory effect of 17-β estradiol on performance of ovariectomized rats on the Shock-Probe test. Gervais NJ, Jacob S, Brake WG, Mumby DG 24768650
PSYCHOLOGY
14 Changes in brain volume in response to estradiol levels, amphetamine sensitization and haloperidol treatment in awake female rats. Madularu D, Kulkarni P, Ferris CF, Brake WG 26032742
CSBN
15 Attenuation of dendritic spine density in the perirhinal cortex following 17β-Estradiol replacement in the rat. Gervais NJ, Mumby DG, Brake WG 26104963
CSBN
16 Ovarian steroids alter dopamine receptor populations in the medial preoptic area of female rats: implications for sexual motivation, desire, and behaviour. Graham MD, Gardner Gregory J, Hussain D, Brake WG, Pfaus JG 26536143
PSYCHOLOGY
17 High Oestradiol Replacement Reverses Response Memory Bias in Ovariectomised Female Rats Regardless of Dopamine Levels in the Dorsal Striatum. Hussain D, Cossette MP, Brake WG 26929121
PSYCHOLOGY
18 Intra-perirhinal cortex administration of estradiol, but not an ERβ agonist, modulates object-recognition memory in ovariectomized rats. Gervais NJ, Hamel LM, Brake WG, Mumby DG 27321161
PSYCHOLOGY
19 Varying the rate of intravenous cocaine infusion influences the temporal dynamics of both drug and dopamine concentrations in the striatum Minogianis EA; Shams WM; Mabrouk OS; Wong JT; Brake WG; Kennedy RT; du Souich P; Samaha AN; 29757478
MASSSPEC

 

Title:Varying the rate of intravenous cocaine infusion influences the temporal dynamics of both drug and dopamine concentrations in the striatum
Authors:Minogianis EAShams WMMabrouk OSWong JTBrake WGKennedy RTdu Souich PSamaha AN
Link:https://pubmed.ncbi.nlm.nih.gov/29757478/
DOI:10.1111/ejn.13941
Publication:The European journal of neuroscience
Keywords:
PMID:29757478 Category:Eur J Neurosci Date Added:2019-05-31
Dept Affiliation: MASSSPEC
1 Department of Pharmacology and Physiology, Faculty of Medicine, Université de Montréal, C.P. 6128, Succursale Centre-ville, Montreal, QC, H3C 3J7, Canada.
2 Department of Psychology, Center for Studies in Behavioral Neurobiology (CSBN), Concordia University, Montreal, QC, Canada.
3 Department of Pharmacology, University of Michigan, Ann Arbor, MI, USA.
4 Department of Chemistry, University of Michigan, Ann Arbor, MI, USA.
5 Groupe de recherche sur le système nerveux central, Faculty of Medicine, Université de Montréal, Montreal, QC, Canada.

Description:

The faster drugs of abuse reach the brain, the greater is the risk of addiction. Even small differences in the rate of drug delivery can influence outcome. Infusing cocaine intravenously over 5 vs. 90-100 s promotes sensitization to the psychomotor and incentive motivational effects of the drug and preferentially recruits mesocorticolimbic regions. It remains unclear whether these effects are due to differences in how fast and/or how much drug reaches the brain. Here, we predicted that varying the rate of intravenous cocaine infusion between 5 and 90 s produces different rates of rise of brain drug concentrations, while producing similar peak concentrations. Freely moving male Wistar rats received acute intravenous cocaine infusions (2.0 mg/kg/infusion) over 5, 45 and 90 s. We measured cocaine concentrations in the dorsal striatum using rapid-sampling microdialysis (1 sample/min) and high-performance liquid chromatography-tandem mass spectrometry. We also measured extracellular concentrations of dopamine and other neurochemicals. Regardless of infusion rate, acute cocaine did not change concentrations of non-dopaminergic neurochemicals. Infusion rate did not significantly influence peak concentrations of cocaine or dopamine, but concentrations increased faster following 5-s infusions. We also assessed psychomotor activity as a function of cocaine infusion rate. Infusion rate did not significantly influence total locomotion, but locomotion increased earlier following 5-s infusions. Thus, small differences in the rate of cocaine delivery influence both the rate of rise of drug and dopamine concentrations, and psychomotor activity. A faster rate of rise of drug and dopamine concentrations might be an important issue in making rapidly delivered cocaine more addictive.





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