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J.Q. Wang

Researcher at East Carolina University

Publications -  4
Citations -  387

J.Q. Wang is an academic researcher from East Carolina University. The author has contributed to research in topics: Striatum & Nucleus accumbens. The author has an hindex of 4, co-authored 4 publications receiving 384 citations.

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A single injection of amphetamine or methamphetamine induces dynamic alterations in c-fos,zif/268 and preprodynorphin messenger RNA expression in rat forebrain

TL;DR: A detailed dynamic description of the differential modulation of c-fos, zif/268 and preprodynorphin messenger RNA expression in the cerebral cortex and striatum by amphetamines over time is provided.
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Repeated amphetamine administration induces a prolonged augmentation of phosphorylated cyclase response element-binding protein and Fos-related antigen immunoreactivity in rat striatum

TL;DR: It is demonstrated that repeated amphetamine administration results in a prolonged induction of phosphorylated cyclase response element-binding protein and Fos-related antigen immunoreactivity in the dorsal striatum, indicating that alterations in striatal gene expression associated with the development of behavioral sensitization may be mediated, in part, by these transcription factors.
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Muscarinic receptors regulate striatal neuropeptide gene expression in normal and amphetamine-treated rats.

TL;DR: The concept that cholinergic transmission, via interaction with muscarinic receptors, inhibits basal and D1 receptor-stimulated striatonigral dynorphin/substance P gene expression and facilitates striatopallidal enkephalin gene expression is supported.
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Scopolamine augments C-fos and zif/268 messenger rna expression induced by the full D1 dopamine receptor agonist SKF-82958 in the intact rat striatum

TL;DR: Ability of SKF-82958 to induce immediate early gene messenger RNA expression in normosensitive dorsal and ventral striatum of the rat is demonstrated and intrinsic muscarinic receptor-mediated cholinergic transmission in the striatum may provide an activity-dependent inhibitory control on striatal D(1) receptor stimulation.