| Autor: |
Ejdrup AL; Department of Circuit Biology, H. Lundbeck A/S, Valby 2500, Denmark.; Department of Neuroscience, Faculty of Health and Medical Sciences, Maersk Tower 7.5, University of Copenhagen, Copenhagen 2200, Denmark., Wellbourne-Wood J; Department of Circuit Biology, H. Lundbeck A/S, Valby 2500, Denmark., Dreyer JK; Department of Bioinformatics, H. Lundbeck A/S, Valby 2500, Denmark., Guldhammer N; Department of Circuit Biology, H. Lundbeck A/S, Valby 2500, Denmark., Lycas MD; Department of Neuroscience, Faculty of Health and Medical Sciences, Maersk Tower 7.5, University of Copenhagen, Copenhagen 2200, Denmark., Gether U; Department of Neuroscience, Faculty of Health and Medical Sciences, Maersk Tower 7.5, University of Copenhagen, Copenhagen 2200, Denmark., Hall BJ; Department of Circuit Biology, H. Lundbeck A/S, Valby 2500, Denmark., Sørensen G; Department of Circuit Biology, H. Lundbeck A/S, Valby 2500, Denmark. |
| Abstrakt: |
A fundamental concept in neuroscience is the transmission of information between neurons via neurotransmitters, -modulators, and -peptides. For the past decades, the gold standard for measuring neurochemicals in awake animals has been microdialysis (MD). The emergence of genetically encoded fluorescence-based biosensors, as well as in vivo optical techniques such as fiber photometry (FP), has introduced technologically distinct means of measuring neurotransmission. To directly compare MD and FP, we performed concurrent within-animal recordings of extracellular dopamine (DA) in the dorsal striatum (DS) before and after administration of amphetamine in awake, freely behaving mice expressing the dopamine sensor dLight1.3b. We show that despite temporal differences, MD- and FP-based readouts of DA correlate well within mice. Down-sampling of FP data showed temporal correlation to MD data, with less variance observed using FP. We also present evidence that DA fluctuations periodically reach low levels, and naïve animals have rapid, predrug DA dynamics measured with FP that correlate to the subsequent pharmacodynamics of amphetamine as measured with MD and FP. |
