Publications by authors named "K Wiech"

Article Synopsis
  • Dopamine may play a role in placebo effects related to reward and learning, but its exact function is still not fully understood.
  • The study tested the impact of dopamine modulation through medication (sulpiride and L-dopa) on pain relief expectations and placebo analgesia in 168 healthy participants.
  • Results showed that these medications did not affect the development or maintenance of placebo analgesia, suggesting that dopamine may not directly influence these effects, highlighting the need for further research on the neurochemical mechanisms behind placebo responses.*
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Pain can be conceptualized as a precision signal for reinforcement learning in the brain and alterations in these processes are a hallmark of chronic pain conditions. Investigating individual differences in pain-related learning therefore holds important clinical and translational relevance. Here, we developed and externally validated a novel resting-state brain connectivity-based predictive model of pain-related learning.

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This scientific commentary refers to ‘How side effects can improve treatment efficacy: a randomized trial’ by Schenk . (https://doi.org/10.

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Autofluorescence lifetime imaging microscopy (FLIM) is sensitive to metabolic changes in single cells based on changes in the protein-binding activities of the metabolic co-enzymes NAD(P)H. However, FLIM typically relies on time-correlated single-photon counting (TCSPC) detection electronics on laser-scanning microscopes, which are expensive, low-throughput, and require substantial post-processing time for cell segmentation and analysis. Here, we present a fluorescence lifetime-sensitive flow cytometer that offers the same TCSPC temporal resolution in a flow geometry, with low-cost single-photon excitation sources, a throughput of tens of cells per second, and real-time single-cell analysis.

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Autofluorescence lifetime imaging microscopy (FLIM) is sensitive to metabolic changes in single cells based on changes in the protein-binding activities of the metabolic co-enzymes NAD(P)H. However, FLIM typically relies on time-correlated single-photon counting (TCSPC) detection electronics on laser-scanning microscopes, which are expensive, low-throughput, and require substantial post-processing time for cell segmentation and analysis. Here, we present a fluorescence lifetime-sensitive flow cytometer that offers the same TCSPC temporal resolution in a flow geometry, with low-cost single-photon excitation sources, a throughput of tens of cells per second, and real-time single-cell analysis.

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