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, baseline: 159±5pA, decreased by 56.7%, to 69±3pA, one hour after pairings, Example of tLTD induced by 100 pre-post pairings (?t STDP =-13±0.1ms)
, Example of the lack of plasticity after 100 pre-post pairings (?t STDP =8±0.1ms) with
the mean baseline EPSC amplitude was 119.2±2.62 pA before pairings and a lack of plasticity was observed one hour after pairings: 117.6±2.99 pA). Bottom, time course of Ri (baseline: 213±1M? and 50-60 min after pairings: 209±2M? ,
, Example of the lack of plasticity after 100 pre-post pairings (?t STDP =13±0.1ms) in presence of ANA12 (10µM) (the mean baseline EPSC amplitude was 187.2±3.73 pA before pairings and was not significantly altered one hour after pairings, 184.4±3.32 pA)
, Bottom, time course of Ri (baseline: 114±1M? and 50-60 min after pairings: 116±1M?; change of 1%). (E) Example of the lack of plasticity after 10 post-pre pairings (?t STDP =-12±0.2ms) with K252a (200nM) (the mean baseline EPSC amplitude was 147±5pA before pairings and a tLTD induction was observed one hour after 10 post-pre pairings: 106±3pA). Bottom, time course of Ri (baseline: 64±1 M? and 50-60 min after pairings: 59±1M?; change of 8%). (F) Example of the lack of plasticity after 10 post-pre pairings (?t STDP =-13±0.3ms) in presence of ANA12 (10µM) (the mean baseline EPSC amplitude was 198±4pA before pairings and was not significantly altered one hour after pairings, 186±4pA), Example of tLTP induced by 10 post-pre pairings (?t STDP =-11±0.1ms) (the mean baseline EPSC amplitude was 230±6pA before pairings and was increased by ~67% to 383±5pA one hour after pairings)
, Insets correspond to the average EPSC amplitude during baseline (1, black trace) and the last 10 min of recording after STDP pairings (2, grey trace). Statistics (student t-test
,
, Supplementary Figure 2: Calcium transients in dendritic spines remain unchanged upon ANA12 and DMSO applications
, ANA12 and ANA12 followed by DHF application did not change the time course of Ca2+ elevations triggered by somatic current injections eliciting two bAPs in dendritic spines and shafts. (B) Two consecutive applications of DMSO (DMSO1 and DMSO2, 0.04% final concentration), to mimic successive applications of DHF and DHF+ANA12, did not change the time course of Ca2+ elevations in dendritic spines and shafts, triggered by two bAPs. (C) ANA12 and ANA12 followed by DHF application did not change the time course of Ca 2+ elevations triggered by pre-post paired corticostriatal stimulations in dendritic spines and shafts
, Supplementary Figure 3: Amplitudes of calcium evoked-events in dendritic spines and shafts
, Amplitudes of Ca 2+ evoked-events (normalized to control) were not different upon DHF, ANA12 and DMSO bath-application, in dendritic spines and shafts, triggered by (A) two bAPs (post-stimulation only), or by (B) pre-post pairings, consisting in single evoked corticostriatal EPSP paired with two bAPs with ?t ~+15-20 ms
, Supplementary Figure 4: Long-duration bath-applied DHF did not promote tLTP for 25 post-pre pairings
, Averaged time-courses showing an overall absence of plasticity observed after 25 post-pre pairings with DHF bath-applied during the whole recording (2/5 cells showed tLTP). Error bars represent the SEM. Statistics (student t-test, first vs last 10 min of recording): ns