Distinct sub-second dopamine signaling in dorsolateral striatum measured by a genetically-encoded fluorescent sensor

Armando G. Salinas*, Jeong Oen Lee, Shana M. Augustin, Shiliang Zhang, Tommaso Patriarchi, Lin Tian, Marisela Morales, Yolanda Mateo, David M. Lovinger*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

20 Scopus citations

Abstract

The development of genetically encoded dopamine sensors such as dLight has provided a new approach to measuring slow and fast dopamine dynamics both in brain slices and in vivo, possibly enabling dopamine measurements in areas like the dorsolateral striatum (DLS) where previously such recordings with fast-scan cyclic voltammetry (FSCV) were difficult. To test this, we first evaluated dLight photometry in mouse brain slices with simultaneous FSCV and found that both techniques yielded comparable results, but notable differences in responses to dopamine transporter inhibitors, including cocaine. We then used in vivo fiber photometry with dLight in mice to examine responses to cocaine in DLS. We also compared dopamine responses during Pavlovian conditioning across the striatum. We show that dopamine increases were readily detectable in DLS and describe transient dopamine kinetics, as well as slowly developing signals during conditioning. Overall, our findings indicate that dLight photometry is well suited to measuring dopamine dynamics in DLS.

Original languageEnglish (US)
Article number5915
JournalNature communications
Volume14
Issue number1
DOIs
StatePublished - Dec 2023

Funding

We would like to thank Dr. Huaibin Cai for the Casp3 virus, Dr. Joseph Cheer for his comments on the data and manuscript, Dr. Gabriel Loewinger for advice on data analysis/statistics, and Jacob Nadel and Lucas Voyvodic for their expert technical assistance with stereotaxic virus infusions. We also thank Rong Ye and Kevin Yu of the Confocal and Electron Microscopy Core, NIDA IRP, for collecting confocal and immune-electron microscopic images used in this study. This work was supported by research grants from the National Institute on Alcohol Abuse and Alcoholism (K99R00 AA025991 to A.G.S., K99R00 AA027740 to S.M.A., and ZIA AA000407 & ZIA000416 to D.M.L.), the Intramural Research Program of the National Institute on Drug Abuse, the BRAIN Initiative (U01NS090604 and U01NS013522 to L.T.), the National Institutes of Health (DP2MH107056 to L.T.), the European Union’s Horizon 2020 (Grant agreement: 891959 to T.P.), and the Swiss National Science Foundation (Grant agreement: 310030_196455 to T.P.).

ASJC Scopus subject areas

  • General Chemistry
  • General Biochemistry, Genetics and Molecular Biology
  • General Physics and Astronomy

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