Evidence map›Paper›PMID 16691292›Full record

ArticleThe Journal of clinical investigation2006

Neuronal calcium sensor-1 enhancement of InsP3 receptor activity is inhibited by therapeutic levels of lithium.

Christina Schlecker, Wolfgang Boehmerle, Andreas Jeromin, Brenda DeGray, Anurag Varshney, Yogendra Sharma, Klara Szigeti-Buck, Barbara E Ehrlich

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of clinical investigation, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 83 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
83citing papers in PubMed, 1 pooled it
2.6field-weighted citation impact, top 11% of its field
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

83 citing papers in PubMed, 1 synthesis or guideline pooled it, 155 citations in OpenAlex.

  1. Calcium and arrhythmogenesis.Physiological reviews · 2007
    Pooled it
  2. Trial
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Intranasal Delivery of Lithium Salt Suppresses Inflammatory Pyroptosis in the Brain and Ameliorates Memory Loss and Depression-like Behavior in 5XFAD Mice.Journal of neuroimmune pharmacology : the official journal of the Society on NeuroImmune Pharmacology · 2025
    Article
  9. Article
  10. Review
  11. Review
  12. Review
  13. Article
  14. The Janus-faced functions of Apolipoproteins L in membrane dynamics.Cellular and molecular life sciences : CMLS · 2024
    Article
  15. Review
  16. Article
  17. Response to Kochan et al., 2023.Supportive care in cancer : official journal of the Multinational Association of Supportive Care in Cancer · 2023
    Article
  18. Article
  19. Article
  20. Review

23 more citing papers are in PubMed but not listed here.

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

8 authors at 4 institutions in 3 countries.

Christina SchleckerDepartment of Pharmacology, Yale University, New Haven, Connecticut 06520-8066, USA.
Wolfgang Boehmerle
Andreas Jeromin
Brenda DeGray
Anurag Varshney
Yogendra Sharma
Klara Szigeti-Buck
Barbara E Ehrlich
Yale University · USCentre for Cellular and Molecular Biology · INCharité - Universitätsmedizin Berlin · DEThe University of Texas at Austin · US

Funding

Dynamic Interactions of IP3 Receptor LigandsR01GM063496 · NIGMS · YALE UNIVERSITY · PI EHRLICH, BARBARA E. · 2001 to 2004
$1.1M
NIGMS NIH HHS GM63496NIGMS NIH HHS R01 GM063496
6 · The paper itself

Abstract

Regulation and dysregulation of intracellular calcium (Ca2+) signaling via the inositol 1,4,5-trisphosphate receptor (InsP3R) has been linked to many cellular processes and pathological conditions. In the present study, addition of neuronal calcium sensor-1 (NCS-1), a high-affinity, low-capacity, calcium-binding protein, to purified InsP3R type 1 (InsP3R1) increased the channel activity in both a calcium-dependent and -independent manner. In intact cells, enhanced expression of NCS-1 resulted in increased intracellular calcium release upon stimulation of the phosphoinositide signaling pathway. To determine whether InsP3R1/NCS-1 interaction could be functionally relevant in bipolar disorders, conditions in which NCS-1 is highly expressed, we tested the effect of lithium, a salt widely used for treatment of bipolar disorders. Lithium inhibited the enhancing effect of NCS-1 on InsP3R1 function, suggesting that InsP3R1/NCS-1 interaction is an essential component of the pathomechanism of bipolar disorder.

Indexed as

Bipolar DisorderLithiumAnimalsCalciumCalcium-Binding ProteinsCalcium ChannelsCalcium SignalingElectrophysiologyHumansInositol 1,4,5-Trisphosphate ReceptorsIn Vitro TechniquesMiceNeuronal Calcium-Sensor ProteinsNeuronsNeuropeptidesPC12 CellsCalciumCalcium-Binding ProteinsCalcium Channelsfrequenin calcium sensor proteinsInositol 1,4,5-Trisphosphate ReceptorsITPR1 protein, humanLithiumNeuronal Calcium-Sensor ProteinsNeuropeptidesReceptors, Cytoplasmic and NuclearRyanodine Receptor Calcium Release Channel

Identifiers

PMID16691292
PMCPMC1459068
OpenAlexW2096403396

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.