SINTN Stanford Institute for Neuro-Innovation & Translational Neurosciences

Rob Malenka Laboratory

Research in the Malenka Lab

Long-lasting activity-dependent changes in the efficacy of synaptic transmission play an important role in the development of neural circuits and are thought to mediate many forms of learning and memory. Therefore, elucidating the molecular mechanisms by which these changes occur will have profound implications for understanding many important nervous system functions, including how future behavior is modified by past experience.

Work from my laboratory has demonstrated that there are a variety of related but mechanistically distinct forms of synaptic plasticity. A major goal of my laboratory is to elucidate both the specific molecular events that are responsible for the triggering of these various forms of synaptic plasticity and the exact modifications in synaptic proteins that are responsible for the observed, long-lasting changes in synaptic efficacy.

To accomplish this we primarily use cellular electrophysiological recording techniques to examine synaptic plasticity in a variety of different in vitro preparations including thin slices of various regions of the rodent brain and primary neurons in culture. Viral mediated simultaneous expression of shRNAs and cDNAs are used to manipulate specific synaptic proteins and study their exact roles in synaptic plasticity. Light microscopy is also used to examine the intracellular trafficking of synaptic proteins including neurotransmitter receptors.

A related area of research in my laboratory is the elucidation of the synaptic action of drugs of abuse such as the psychostimulants cocaine and amphetamine. Toward this end, we have developed in-vitro slice preparations of the nucleus accumbens and ventral tegmental area, brain regions that mediate many of the key behavioral effects of drugs of abuse. We are currently using a variety of electrophysiological and molecular techniques, with the goal of determining how acute and chronic exposure to drugs of abuse modify synaptic and circuit function in these brain areas. The knowledge gained from the work on the molecular mechanisms underlying synaptic plasticity will provide important clues to the molecular mechanisms underlying the development of tolerance, dependence and addiction.

Recent Publications

A critical role for PSD-95/AKAP interactions in endocytosis of synaptic AMPA receptors.
Bhattacharyya S, Biou V, Xu W, Schlüter O, Malenka RC.
Nat Neurosci. 2009 12:172-81.

Understanding synapses: past, present, and future.
Südhof TC, Malenka RC.
Neuron. 2008 60:469-76.

Molecular dissociation of the role of PSD-95 in regulating synaptic strength and LTD.
Xu W, Schlüter OM, Steiner P, Czervionke BL, Sabatini B, Malenka RC.
Neuron. 2008 57: 248-62.

Endocannabinoid-mediated rescue of striatal LTD and motor deficits in Parkinson's disease models.
Kreitzer AC, Malenka RC.
Nature. 2007 445: 643-7.

lab members
Other News
NIHM Provides $10 Million to Start a Conte Center for Neuroscience at Stanford

The National Institute of Mental Health has awarded neuroscientists at the Stanford University School of Medicine a $10 million, five-year grant to establish and operate a Silvio O. Conte Center for Neuroscience Research.

The Stanford Conte Center will be devoted to the study of neuroplasticity: how the brain changes during development or when it is exposed to changing conditions.

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