WOS: A1991FQ59300005PubMed ID: 2046028After in vivo administration, [H-3]WIN 35,428 accumulated in mouse brain regions containing dopaminergic nerve terminals. The highest accumulation was in the striatum and it peaked between 30 and 60 min. The accumulation was saturable with increasing doses of WIN 35,428, and was blocked by compounds that bind to the dopamine transporter. Paroxetine, a drug that blocks serotonin transporters, had no effect. Moreover, the in vivo potency of cocaine analogs correlated with their in vitro potency. Thus, [H-3]WIN 35,428 is a suitable ligand for labeling cocaine receptors associated with dopamine transporters in vivo.NINDS NIH HHSUnited States Department of Health & Human ServicesNational Institutes of Health...
The development of medications to treat cocaine use disorders has thus far defied success, leaving t...
Several brain imaging agents targeted to the dopamine neurons and associated nerve terminals have be...
Benztropine (BZT) analogs, a family of high-affinity dopamine transporter ligands, are molecules tha...
[3H]WIN 35,065–2 binding to striatal membranes was characterized, primarily by centrifugation assay....
Previous studies showed that the cocaine analog [125I]RTI-55 labels dopamine and serotonergic (5-HT)...
The rate of entry of drugs into brain is thought to be a factor in their abuse liability. In this in...
The dopamine transporter (DAT) is a membrane protein that is responsible for the reuptake of dopamin...
ABSTRACT The novel cocaine analog RTI-121[3~-(4-iodophenyl)tropane-2~-carbox-ylic acid isopropyl est...
Rationale: The discriminative-stimulus effects of cocaine have been reported to be mediated by indir...
Cocaine mediates its powerful reinforcement by binding to recognition sites on the dopamine (DA) tra...
Cocaine binds and inhibits dopamine transporter (DAT), norepinephrine transporter (NET) and serotoni...
In an effort to identify novel binding sites for cocaine and its analogs, we carried out binding stu...
It has been suggested that cocaine and mazindol bind to sep-arate sites on the dopamine transporter....
Cocaine, amphetamines and other psychostimulants inhibit synaptic dopamine uptake by interfering wit...
The dopamine transporter (DAT) is a critical recognition site for cocaine and contributes to its sig...
The development of medications to treat cocaine use disorders has thus far defied success, leaving t...
Several brain imaging agents targeted to the dopamine neurons and associated nerve terminals have be...
Benztropine (BZT) analogs, a family of high-affinity dopamine transporter ligands, are molecules tha...
[3H]WIN 35,065–2 binding to striatal membranes was characterized, primarily by centrifugation assay....
Previous studies showed that the cocaine analog [125I]RTI-55 labels dopamine and serotonergic (5-HT)...
The rate of entry of drugs into brain is thought to be a factor in their abuse liability. In this in...
The dopamine transporter (DAT) is a membrane protein that is responsible for the reuptake of dopamin...
ABSTRACT The novel cocaine analog RTI-121[3~-(4-iodophenyl)tropane-2~-carbox-ylic acid isopropyl est...
Rationale: The discriminative-stimulus effects of cocaine have been reported to be mediated by indir...
Cocaine mediates its powerful reinforcement by binding to recognition sites on the dopamine (DA) tra...
Cocaine binds and inhibits dopamine transporter (DAT), norepinephrine transporter (NET) and serotoni...
In an effort to identify novel binding sites for cocaine and its analogs, we carried out binding stu...
It has been suggested that cocaine and mazindol bind to sep-arate sites on the dopamine transporter....
Cocaine, amphetamines and other psychostimulants inhibit synaptic dopamine uptake by interfering wit...
The dopamine transporter (DAT) is a critical recognition site for cocaine and contributes to its sig...
The development of medications to treat cocaine use disorders has thus far defied success, leaving t...
Several brain imaging agents targeted to the dopamine neurons and associated nerve terminals have be...
Benztropine (BZT) analogs, a family of high-affinity dopamine transporter ligands, are molecules tha...