Time course of AMPA receptors after blocking exocytosis/endocytosis.

Slides:



Advertisements
Similar presentations
Free Phone $25 a month 100 minutes then 35c per min Free Phone $25 a month 100 minutes then 35c per min Free Phone $20 a month 75 minutes then 25c per.
Advertisements

The Chemistry of Perpetual Memory From Mechanisms of Memory by J. David Sweatt, Ph.D.
Average for the DV ratio (DVR) images for [11C]raclopride for the controls (n = 20) and the alcoholics (n = 20) at the level of striatum after placebo.
The effect of rotation from a primary LAO or RAO angle on PSD for female patients: (A) primary 30° LAO projection; (B) primary 30° RAO projection and (C)
Detection rate for EGFR mutations in cfDNA.
Shigeyoshi Fuziwara, Kaori Inoue, Mitsuhiro Denda 
Active avoidance is impaired in aged mice in both multimodal and visual versions of the task. Active avoidance is impaired in aged mice in both multimodal.
A–E, Active avoidance (A–D) and optokinetic testing (E) in an independent cohort. A–E, Active avoidance (A–D) and optokinetic testing (E) in an independent.
Glutamate Receptor Dynamics in Dendritic Microdomains
Example of sequential spectral analysis during the tilt test.
Effects of E2 on levels of phospho-CREB in the DH of OVX females, sham males, and GDX males. Effects of E2 on levels of phospho-CREB in the DH of OVX females,
Peptide abundances are uniformly distributed across the capsid protein in the recoded T7 strain. Peptide abundances are uniformly distributed across the.
The regression lines between the asynchrony index (AI) and the double true index (DTI) shown for overall data, and for mask and helmet separately. The.
Diagram of a double-gap concentric cylinder measurement geometry.
A Dynamic Corral Model of Receptor Trafficking at a Synapse
Cellular iron metabolism
Loss of αsyn does not affect mitochondrial-derived ATP levels at the nerve terminal. Loss of αsyn does not affect mitochondrial-derived ATP levels at the.
Whisker deprivation increases PPR
Top, Mean tracking accuracy of high and low improvers during early and late compatible and incompatible blocks. Top, Mean tracking accuracy of high and.
Proposed encoding of VLS MSNs
Conversion of proBDNF to mature BDNF occurs after the first pairing session of conditioning as shown by Western blot analysis. Conversion of proBDNF to.
Depolarization-induced postsynaptic NT secretion depends on Ca2+ influx. Depolarization-induced postsynaptic NT secretion depends on Ca2+ influx. Hippocampal.
Interaction between lighting condition and circadian phase in GABAAR protein-IR in whole SCN and the dorsal and ventral subdivisions of the SCN. Lighting.
Caspase activation occurs after AIF translocation and nuclear condensation. Caspase activation occurs after AIF translocation and nuclear condensation.
Increased proIGF-II and decreased IGF-IIR in BTBR compared with B6 mice. Increased proIGF-II and decreased IGF-IIR in BTBR compared with B6 mice. Western.
Increased phosphorylation of Akt, Girdin S1416, and NR2B of NMDA receptor in the hippocampus of mouse after fear conditioning. Increased phosphorylation.
Impairments of NMDA receptor-dependent hippocampal synaptic plasticity in DGCs in GirdinSA/SA and Girdin+/− mice. Impairments of NMDA receptor-dependent.
Experimental paradigm.
RT-PCR analysis of different rat brain regions.
HFOs resulting from noisy input to pyramidal cell population.
Synaptic density is significantly impaired in male FBN-ARO-KO mice.
Synapse composition is unaltered in SynDIG1-deficient synapses.
SiRNA directed at Ngn1 inhibited differentiation of inner ear stem cells to β-III tubulin-positive cells. a, Inner ear stem cells treated with siRNA to.
Spike timing-dependent plasticity
The effect of benzolamide on NH4+-induced pHi transients in cultured mouse hippocampal neurons. The effect of benzolamide on NH4+-induced pHi transients.
PC and DC loss in Prox1DTA mice is progressive and followed by outer HC loss. PC and DC loss in Prox1DTA mice is progressive and followed by outer HC loss.
Interaction between reboxetine and ADRA2B genotype influences post-treatment symptoms of irritability, anxiety, and dizziness. Interaction between reboxetine.
The results of the analysis for rates of symptomatic IDH, asymptomatic IDH, and symptoms alone remained consistent with the primary analysis. The results.
Pyknosis in the RGC layer.
A loading dose decreases the time to achieve the target concentration.
Activation of LHAGal neurons reduces compulsive burying.
Brain and plasma cholesterol levels in Abca1−B/−B mice.
Effects of pain-stress on striatal dopamine release as a function of HTR2C genotype. Effects of pain-stress on striatal dopamine release as a function.
Effects of an AMPA receptor antagonist on numbers of pCofilin-positive spines. Effects of an AMPA receptor antagonist on numbers of pCofilin-positive spines.
Glycogen content of rat optic nerves after glucose deprivation and pharmacological manipulation. Glycogen content of rat optic nerves after glucose deprivation.
Responses measured by BOLD fMRI in areas V1, V2, V3, and MT+ as two subjects (S2, gray; S3, black) switched between the speed and the contrast discrimination.
A, Elevation in the amount of solution consumed (without sucrose or salt) during the depletion test following sodium depletion compared with the baseline.
Schematic diagram illustrating the distribution of postsynaptic receptors on an SPn for monosynaptic inputs arising from the thalamus (Thal.) and the CP,
A, B, Startle magnitude and PPI after treatment with CNO
Motivational effects of withdrawal in opiate-dependent animals after blocking BDNF function in the VTA. a, Knocking down TrkB in the VTA with LV-siRNAs.
Comparison of the posterior–anterior location of perceptual and mnemonic peaks in both hemispheres. Comparison of the posterior–anterior location of perceptual.
Reduction of surface receptor and increased intracellular retention with elevated temperature in mutant γ2(K289M) subunit-containing α1β2γ2 receptors was.
Inhibition of forskolin-induced cAMP accumulation in microglia by group III mGlu receptor agonists and receptor coupling to pertussis toxin-sensitive G-proteins.
A proposed scheme for GSK-3-involved suppression of synaptic transmission. A proposed scheme for GSK-3-involved suppression of synaptic transmission. According.
The dopamine (DA) response to cocaine infusion in the NAc in constitutive p11 KO mice is restored by nicotinic or muscarinic receptor stimulation in the.
Cue-evoked dopamine release dynamics in the NAc shell and core.
Exogenous NR2B-expressing cells are more dynamic than control or exogenous NR2A-expressing cells. Exogenous NR2B-expressing cells are more dynamic than.
Lecture Order 1) Receptor Trafficking Scaffolding Proteins at the PSD
OGD treatment increased tonic current through an oxidative reaction.
Effects of receptor antagonists, Ca2+ channel blocker, Ca2+depletion, and protein kinase inhibitors on CREB phosphorylation in cultured hippocampal neurons.
Rate of current rundown through VDCC and NMDA receptor channels is reduced in gelsolin-deficient hippocampal neurons. Rate of current rundown through VDCC.
Basal and NMDA receptor-dependent changes in reporter gene activity for Bdnf promoter deletions. Basal and NMDA receptor-dependent changes in reporter.
Effects of CNO on spontaneous locomotion and amphetamine-induced hyperlocomotion. Effects of CNO on spontaneous locomotion and amphetamine-induced hyperlocomotion.
Target-specific DSI at TRN synapses.
Cold temperature-dependent percentage BOLD signal changes in different cortical areas. a, Group mean time courses of BOLD signals to nociceptive cold (4°C.
Synaptic depression in principal neurons of the rat MNTB
Depression of NMDA receptor-mediated EPSCs
Nomadic AMPA Receptors and LTP
Exogenous expression and knockdown of NR2A and NR2B decrease AMPAR-mediated synaptic transmission. Exogenous expression and knockdown of NR2A and NR2B.
The effect of roscovitine on Ca2+-dependent glutamate release from synaptosomes prepared from rat brains in response to membrane depolarization with 1.
Presentation transcript:

Time course of AMPA receptors after blocking exocytosis/endocytosis. Time course of AMPA receptors after blocking exocytosis/endocytosis. A, Blocking exocytosis. With receptors at basal steady state at time t < 0, exocytosis is blocked by setting σj = 0 (j = 1,2) at t = 0. The number of AMPA receptors in the PSD almost halves in <10 min (because of the loss of free receptors) and decreases to ∼1 over ∼10 d (data not shown). B, Blocking endocytosis. Endocytosis is blocked by setting kj = 0 (j = 1,2) at t = 0. The number of AMPA receptors in the PSD nearly doubles within 1 h (because of the addition of free receptors) and reaches a new steady-state value of ∼84. These results are consistent with those of Luscher et al. (1999). Berton A. Earnshaw, and Paul C. Bressloff J. Neurosci. 2006;26:12362-12373 ©2006 by Society for Neuroscience