Evidence map›Paper›PMID 25948871›Full record

ArticleJournal of neurophysiology2015

Self-regulation of adult thalamocortical neurons.

Michael R Kasten, Matthew P Anderson

Abstract read
In one paragraph

Article in Journal of neurophysiology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

  1. Article
  2. Article
  3. The role of KActa pharmacologica Sinica · 2018
    Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

2 authors.

Michael R KastenDepartments of Neurology and Pathology, Harvard Medical School and Beth Israel Deaconess Medical Center, Center for Life Science, Boston, Massachusetts;
Matthew P AndersonDepartments of Neurology and Pathology, Harvard Medical School and Beth Israel Deaconess Medical Center, Center for Life Science, Boston, Massachusetts; Program in Neuroscience, Harvard Medical School, Boston, Massachusetts; and Children's Hospital Boston Intellectual and Developmental Disabilities Research Center, Children's Hospital Boston, Boston, Massachusetts mpanders@bidmc.harvard.edu.

Funding

Neurobiological Mechanism of 15q11-13 Duplication Autism Spectrum DisorderR01NS081916 · NINDS · BETH ISRAEL DEACONESS MEDICAL CENTER · PI ANDERSON, MATTHEW P · 2012 to 2016
$1.9M
Role of LGI1 in Autosomal Dominant Lateral Temporal Lobe EpilepsyR01NS057444 · NINDS · BETH ISRAEL DEACONESS MEDICAL CENTER · PI ANDERSON, MATTHEW P · 2008 to 2011
$1.3M
Engineering the Mouse Nervous System To Decipher Network Mechanisms of EpilepsyK02NS054674 · NINDS · BETH ISRAEL DEACONESS MEDICAL CENTER · PI ANDERSON, MATTHEW P · 2006 to 2010
$974k
NINDS NIH HHS K02 NS054674NINDS NIH HHS R01 NS-057444NINDS NIH HHS R01 NS081916
6 · The paper itself

Abstract

The thalamus acts as a conduit for sensory and other information traveling to the cortex. In response to continuous sensory stimulation in vivo, the firing rate of thalamocortical neurons initially increases, but then within a minute firing rate decreases and T-type Ca(2+) channel-dependent action potential burst firing emerges. While neuromodulatory systems could play a role in this inhibitory response, we instead report a novel and cell-autonomous inhibitory mechanism intrinsic to the thalamic relay neuron. Direct intracellular stimulation of thalamocortical neuron firing initially triggered a continuous and high rate of action potential discharge, but within a minute membrane potential (Vm) was hyperpolarized and firing rate to the same stimulus was decreased. This self-inhibition was observed across a wide variety of thalamic nuclei, and in a subset firing mode switched from tonic to bursting. The self-inhibition resisted blockers of intracellular Ca(2+) signaling, Na(+)-K(+)-ATPases, and G protein-regulated inward rectifier (GIRK) channels as implicated in other neuron subtypes, but instead was in part inhibited by an ATP-sensitive K(+) channel blocker. The results identify a new homeostatic mechanism within the thalamus capable of gating excitatory signals at the single-cell level.

Indexed as

Action PotentialsAnimalsCalciumCalcium Channels, T-TypeCerebral CortexG Protein-Coupled Inwardly-Rectifying Potassium ChannelsKATP ChannelsMice, Inbred C57BLMice, KnockoutNeural PathwaysNeuronal PlasticityNeuronsNeurotransmitter AgentsPatch-Clamp TechniquesPotassiumSodiumCacna1g protein, mouseCalciumCalcium Channels, T-TypeG Protein-Coupled Inwardly-Rectifying Potassium ChannelsKATP ChannelsNeurotransmitter AgentsPotassiumSodiumSodium-Potassium-Exchanging ATPaseexcitabilityKATP channelthalamus

Identifiers

PMID25948871
PMCPMC4507976

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.