2011
DOI: 10.1007/7657_2011_7
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Intracellular Whole-Cell Patch-Clamp Recordings of Cortical Neurons in Awake Head-Restrained Mice

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Cited by 8 publications
(6 citation statements)
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“…Over 4 days of habituation, the duration of head‐fixation was gradually increased to 1 h. On the fifth day, the animal was anaesthetised with 3% of isoflurane circulation through the face mask and the Kwik‐Kast was removed. The skull was drilled circularly (Crochet, ) over the location of the C2 intrinsic signal, which was marked with a shallow drill hole during the first surgery. The centre of drilling (∼300 μm) was thinned to the level of the dura mater, avoiding the blood vessels.…”
Section: Methodsmentioning
confidence: 99%
“…Over 4 days of habituation, the duration of head‐fixation was gradually increased to 1 h. On the fifth day, the animal was anaesthetised with 3% of isoflurane circulation through the face mask and the Kwik‐Kast was removed. The skull was drilled circularly (Crochet, ) over the location of the C2 intrinsic signal, which was marked with a shallow drill hole during the first surgery. The centre of drilling (∼300 μm) was thinned to the level of the dura mater, avoiding the blood vessels.…”
Section: Methodsmentioning
confidence: 99%
“…Two silver wires were inserted on both sides of the cerebellum for reference and grounding. A light-weight metal head-post was also cemented to the skull allowing painless head-fixation during recording sessions (Crochet 2012). At the end of the recording sessions, the animals were deeply anesthetized with pentobarbital (60 mg/kg; intraperitoneally).…”
Section: Animal Preparationmentioning
confidence: 99%
“…In the last decade, these intracellular recording techniques have been expanded to nonanesthetized animals during the natural sleep-wake cycle or quiet wakefulness using either sharp microelectrodes (Steriade et al, 2001;Mahon et al, 2006;Okun et al, 2010) or the whole-cell patch-clamp technique (Margrie et al, 2002;Petersen et al, 2003;Okun et al, 2010). Because whole-cell patch-clamp recordings are less sensitive to mechanical movements of brain tissue than sharp microelectrode recordings (see Crochet, 2012 for a detailed comparison of the two techniques), it has recently become a key approach to study membrane potential dynamics in awake behaving animals (Crochet and Petersen, 2006;Poulet and Petersen, 2008;Harvey et al, 2009;Haider et al, 2013). Combining patch-clamp recordings with twophoton microscopy furthermore allows targeted whole-cell recordings of specific neuronal populations in anesthetized (Margrie et al, 2003) and awake (Gentet et al, 2010(Gentet et al, , 2012 mice.…”
Section: Optical Imagingmentioning
confidence: 99%