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Karima Chergui

Researcher at Karolinska Institutet

Publications -  57
Citations -  4443

Karima Chergui is an academic researcher from Karolinska Institutet. The author has contributed to research in topics: Dopamine & Nucleus accumbens. The author has an hindex of 30, co-authored 52 publications receiving 4221 citations. Previous affiliations of Karima Chergui include University of Birmingham & Centre national de la recherche scientifique.

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Alterations in 5-HT1B Receptor Function by p11 in Depression-Like States

TL;DR: Overexpression of p11 increases 5-HT1B receptor function in cells and recapitulates certain behaviors seen after antidepressant treatment in mice, which contributes to depression-like phenotype and reduced behavioral reactions to an antidepressant.
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Dopamine and cAMP-Regulated Phosphoprotein 32 kDa Controls Both Striatal Long-Term Depression and Long-Term Potentiation, Opposing Forms of Synaptic Plasticity

TL;DR: Evidence is provided that the D1-like receptor-dependent activation of DA and cyclic adenosine 3′,5′ monophosphate-regulated phosphoprotein 32 kDa is a crucial step for the induction of both long-term depression (LTD) and long- term potentiation (LTP), two opposing forms of synaptic plasticity.
Journal Article

Neurochemical Characteristics of Amisulpride, an Atypical Dopamine D2/D3 Receptor Antagonist with Both Presynaptic and Limbic Selectivity

TL;DR: Amisulpride is characterized as a specific dopamine receptor antagonist with high and similar affinity for the dopamine D2 and D3 receptor with a degree of limbic selectivity and a preferential effect, at low doses, on dopamine D 2/D3 autoreceptors.
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Tonic Activation of NMDA Receptors Causes Spontaneous Burst Discharge of Rat Midbrain Dopamine Neurons In Vivo

TL;DR: The data suggest that burst‐firing of midbrain dopamine neurons in vivo results from the tonic activation of NMDA receptors by endogenous excitatory amino acids, a major physiological substrate in the control of the dopamine level in target areas.
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Relationship between dopamine release in the rat nucleus accumbens and the discharge activity of dopaminergic neurons during local in vivo application of amino acids in the ventral tegmental area

TL;DR: Dopaminergic terminals convert physiological impulse flow into dopamine release as a high pass filter which favors bursts of action potentials and N-methyl-D-aspartate was twice as potent as quisqualate.