2010
DOI: 10.1016/j.jphysparis.2009.11.009
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Voltage-sensitive dye imaging: Technique review and models

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Cited by 149 publications
(121 citation statements)
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“…8), in which our knowledge of activity patterns is limited (Seelke and Blumberg, 2010). Notable weaknesses of VSD imaging include a limited contribution to the signal from deep layers of cortex (Berger, 2007;Chemla and Chavane, 2010;Mohajerani et al, 2010), particularly relevant because synaptic inputs to superficial layers 2/3 are weak during early life (Stern, 2001;Bureau, 2004). This weakness contributes to the more complex EEG signal compared with the VSD signal (Fig.…”
Section: Use Of Vsd To Study Developmental Activitymentioning
confidence: 99%
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“…8), in which our knowledge of activity patterns is limited (Seelke and Blumberg, 2010). Notable weaknesses of VSD imaging include a limited contribution to the signal from deep layers of cortex (Berger, 2007;Chemla and Chavane, 2010;Mohajerani et al, 2010), particularly relevant because synaptic inputs to superficial layers 2/3 are weak during early life (Stern, 2001;Bureau, 2004). This weakness contributes to the more complex EEG signal compared with the VSD signal (Fig.…”
Section: Use Of Vsd To Study Developmental Activitymentioning
confidence: 99%
“…1C) (Devonshire, 2010). It is also worth noting that VSD signals can reflect subthreshold, dendritic depolarization (Grinvald and Hildesheim, 2004;Chemla and Chavane, 2010) making direct comparisons to patterns of calcium waves attributable to spiking (Schwartz, 1998;Garaschuk et al, 2000;Adelsberger et al, 2005) difficult (Berger, 2007). Nevertheless, it has been suggested recently that the diverse patterns of developmental activity previously reported are in fact all manifestations of spindle bursts under different experimental conditions (Khazipov and Buzaki, 2010), and in vivo VSD imaging may provide important clues to resolve this issue.…”
Section: Use Of Vsd To Study Developmental Activitymentioning
confidence: 99%
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“…While glia may contribute to the formation of IS initiation sites, the glial signals are relatively slow (Chemla and Chavane 2009) and unlikely to play a role in the short time frames where STDP occurs. In our experiments, glial membranes are also stained and are likely to contribute to the VSD signals.…”
Section: Discussionmentioning
confidence: 99%
“…Simulating those experiments is constrained to the presence of detailed and multi-scale volumetric models of the brain that are capable of addressing light interaction with the tissue including absorption and scattering. There are also other in silico experiments, such as voltage sensitive dye imaging [CC10] and calcium imaging [SGHK03], that require more complicated models to simulate fluorescence. These volumetric models must be annotated with the actual spectral characteristics of the fluorescent structures embedded in the tissue to reflect an accurate response upon excitation at specific input wavelength.…”
Section: Challenges and Related Studiesmentioning
confidence: 99%