Key Documents
Robert Malenka
Academic Appointments
Professional Snapshot
Administrative Appointments
- Councilor, Society for Neuroscience (2006 - 2010)
- Scientific Advisory Board, Seaside Therapeutics (2007 - 2009)
- Scientific Advisory Board, Pfizer (2008 - 2009)
Honors and Awards
- Fellow, American Academy of Arts and Sciences (2005)
- Member, Institute of Medicine of the National Academies (2004)
- Associate, Neurosciences Research Program (1999-2006)
- Basic Neuroscience Research Award, Collegium Internationale Neuropsychopharmacologicum-Lilly (2002)
- International Prize in Neuroscience, Dargut and Milena Kemali Foundation (2000)
Postdoctoral Advisees
Mohiuddin Ahmad , Samarjit Bhattacharyya , Gabor Brasnjo , Amihai Citri , Gul Dolen , Marc Fuccillo , Debanjan Goswami , Brad Grueter , Sandra Jurado , Stephan Lammel , Byungkook Lim , Jai Polepalli , Gilberto Soler-Llavina
Industry Relationships
Stanford is committed to ethical and transparent interactions with our industry partners. It is our policy to disclose payments of $5,000 or more, equity valued at $5,000 or more in a publicly traded company, or any equity in a privately held company, to physicians and scientists employed by Stanford University from companies or other commercial entities with which they interact as part of their professional activities. View Full Information
| Consulting: | Pfizer Inc , Seaside Therapeutics |
| Equity: | Seaside Therapeutics |
Scientific Focus
Research Interests
Long-lasting activity-dependent changes in the efficacy of synaptic transmission play an important role in the development of neural circuits and may mediate many forms of learning and memory. Work from my laboratory over the last 10 years 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 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. We also use cell biological and molecular techniques to examine the activity-dependent modulation of neurotransmitter receptors and to express dominant negative forms of various synaptic proteins so that their exact functions can be determined. An additional complementary approach has involved examining synaptic physiology and synaptic plasticity in various mutant mouse lines lacking specific synaptic proteins.
A related but independent 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 which are thought to mediate several of the behavioral effects of drugs of abuse. We have characterized a novel form of synaptic plasticity in the nucleus accumbens and have done an extensive pharmacological characterization of the synaptic effects of dopamine, cocaine, and amphetamine. Currently we are examining in more detail the underlying mechanisms of dopamine's actions...
Publications
- Molecular dissociation of the role of PSD-95 in regulating synaptic strength and LTD. Neuron. 2008; (2): 248-62
- Understanding synapses: past, present, and future. Neuron. 2008; (3): 469-76
- Endocannabinoid-mediated rescue of striatal LTD and motor deficits in Parkinson's disease models. Nature. 2007; (7128): 643-7
- Synaptic scaling mediated by glial TNF-alpha. Nature. 2006; (7087): 1054-9
- Spike timing-dependent long-term potentiation in ventral tegmental area dopamine cells requires PKC. J Neurophysiol. 2008; (1): 533-8

