Molecular neurophysiology – Karima Chergui's research group

Our research aims to identify neuronal alterations in models of Parkinson’s disease, focusing on glutamatergic synapses in the basal ganglia. Another important goal of our research is to increase our understanding of the mechanisms that lead to the rapid and long-lasting antidepressant action of ketamine.


Project 1

NMDA receptors subunits as targets for the treatment of Parkinson’s disease

Parkinson’s disease is characterized by severe motor disturbance which include slowness of movement, rigidity and tremor. Anxiety, depression and anhedonia are also common non-motor symptoms. In Parkinson’s disease, different neuronal populations degenerate progressively, particularly dopamine neurons in the substantia nigra. This neuronal loss leads to a dramatic reduction in the content of dopamine in the striatum, and a resultant imbalance in several neurotransmitter systems in the basal ganglia including glutamatergic neurotransmission. Our research investigates, in models of Parkinson’s disease, if the functions of the NMDA type of glutamate receptors, and their subunit composition, are altered in different neuronal populations of the basal ganglia. An important goal of our research is to determine if the GluN2 subunits of NMDA receptors can be proposed as targets for the treatment of Parkinson’s disease.

Project 2

NMDA and AMPA receptors as targets for the treatment of depression

Low doses of ketamine exert rapid and lasting antidepressant actions in treatment-resistant patients affected by severe depression. Our research aims to better understand how ketamine produces a rapid and lasting antidepressant action and to suggest other therapies for the treatment of depression. We examine the molecular and cellular mechanisms by which ketamine and its metabolites alter glutamatergic transmission and plasticity in brain regions involved in reward-motivated behaviors and in depression. This mesolimbic circuit includes the nucleus accumbens and ventral tegmental area and is involved in reward and motivation, important functions which are impaired in patients with depression. Our studies will allow us to determine if the subunits that compose NMDA receptors and AMPA receptors can be suggested as targets for the development of novel pharmacological tools, with reduced propensity to induce side effects, in the treatment of depression.

Illustration of Karima Chergui's research showing ventral tegmental area (VTA) and the nucleus accumbens (NAc)
From: Yao N, Skiteva O, Zhang X., Svenningsson P and Chergui K. Ketamine and its metabolite (2R,6R)-hydroxynorketamine induce lasting alterations in glutamatergic synaptic plasticity in the mesolimbic circuit. Molecular Psychiatry, 23(10): 2066-2077, 2018.


Selected publications

Staff and contact

Group leader

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Visiting address

Karolinska Institutet, Physiology and Pharmacology, Bioclinicum J5:20 Neuro, Visionsgatan 4, Solna, 171 64, Sweden

Postal address

Karolinska Institutet, Physiology and Pharmacology, Bioclinicum J5:20, Visionsgatan 4, Solna, 171 64, Sweden

Basal Ganglia Neurophysiology Neurosciences Parkinson Disease Receptors, Ionotropic Glutamate
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