UC Davis neuroscientist Lin Tian and her team, Tommaso Patriarchi, Gerard Broussard and Ruqiang Liang, have developed fluorescence sensors that are opening a new era for the optical recording of dopamine activity in the living brain.

The technology precisely captures where and when dopamine activity occurs in the brain within milliseconds and at the cellular level, producing a high-resolution map of dopamine transients associated with behaviors, such as learning.

A broad application of this tool will further understanding of dopamine activity underlying motivation, reward and movement, and pave the way to discover effective and novel therapeutics for depression, addiction and drug abuse.

Their work published May 31 as a First Release in the prestigious journal Science.

What is the current knowledge about the brain and its circuitry, and what don’t we know?

The brain’s “wiring” contains billions of neurons interconnected by trillions of synapses, the space between the end of a nerve cell and another cell that allows the transmission of impulses by chemicals called neurotransmitters. Electrophysiology and imaging studies have provided details on the structure and function of nerve cells and how an action potential at the synapse allows the transmission of signals that govern essential functions, from learning, memory and behavior to movement and sensations. But what we don’t understand as well is what is happening at the molecular level and which factors, conditions and chemical levels drive neurotransmitter release at the synapse.

Why is understanding brain circuitry important?

Altered dynamics of neurotransmitters and neuromodulators are associated with a number of neurological and psychiatric diseases, including Parkinson’s disease, schizophrenia and addiction. Hence, drugs that mimic or block neuromodulators have become important components in the treatment of these disorders. The neurotransmitter dopamine, for example, plays an important role in movement, attention, learning and the brain’s pleasure and reward system. Mental illnesses, such as depression, can occur when this process isn’t working correctly.

Although neuroscientists have discovered more than 100 neurotransmitters and neuromodulators and detailed their structure and function, we don’t know the precise mechanisms by which these molecules regulate the dynamics of healthy and diseased neural circuitry. Linking complex neural phenomena to the structure and function of their composite neural circuits requires a thorough understanding of patterns of neural activity, and the ability to relate this to physiological processes and behavior.

Would you summarize your study published in Science?

We report the development of the first class of fluorescent protein-based optical dopamine (DA) indicators, which we named dLight1, capable of directly reporting spatial and temporal release of DA with high-resolution both in vitro and in vivo. By labeling a specific neuronal population in living animals, we now can track the dynamic change of released dopamine that occurs within milliseconds and at cellular level during specific activities, such as running and reward learning. dLight overcomes major barriers in the field, and dramatically increases the resolution that we can measure dopamine in the brain of behaving mice. This technology is a game-changer. It can record spatioltemporal coding of dopamine in the brain (creating dopamine-transient map) in high resolution that codes motivation, movement, learning and drug abuse.

We can leverage these tools to develop sensors for other neuromodulators, including norepinephrine, serotonin, melatonin and opioid neuropeptides. This toolset offers the ability to gain vital information about release sites and kinetics for these endogenous ligands, thus open a new era for developing effective drugs for neurological disorders and revealing brain functions that underly motivation, movement, learning and drug abuse.

Why is this study important?

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