Evidence map›Paper›PMID 26038839›Full record

ArticleScientific reports2015

CD38-mediated Ca(2+) signaling contributes to glucagon-induced hepatic gluconeogenesis.

So-Young Rah, Uh-Hyun Kim

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
2.2field-weighted citation impact, top 14% 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

18 citing papers in PubMed, 38 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. CD38/ADP-ribose/TRPM2-mediated nuclear CaExperimental & molecular medicine · 2023
    Article
  7. Review
  8. Article
  9. Article
  10. Review
  11. Article
  12. Article
  13. Age-related NADExperimental gerontology · 2020
    Review
  14. Article
  15. Fratricide of NK Cells in Daratumumab Therapy for Multiple Myeloma Overcome byClinical cancer research : an official journal of the American Association for Cancer Research · 2018
    Article
  16. NAADP-mediated CaFASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2017
    Article
  17. Article
  18. Article
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 at 1 institution in 1 country.

So-Young RahDepartment of Biochemistry and National Creative Research Laboratory for Ca2+ signaling Network.
Uh-Hyun Kim1] Department of Biochemistry and National Creative Research Laboratory for Ca2+ signaling Network [2] The Institute of Cardiovascular Research, Chonbuk National University Medical School, Jeonju, 561-182.
Creative Research · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

CD38 is a multifunctional enzyme for the synthesis of Ca(2+) second messengers. Glucagon promotes hepatic glucose production through Ca(2+) signaling in the fasting condition. In this study, we investigated the role of CD38 in the glucagon signaling of hepatocytes. Here, we show that glucagon induces cyclic ADP-ribose (cADPR) production and sustained Ca(2+) increases via CD38 in hepatocytes. 8-Br-cADPR, an antagonistic cADPR analog, completely blocked glucagon-induced Ca(2+) increases and phosphorylation of cAMP response element-binding protein (CREB). Moreover, glucagon-induced sustained Ca(2+) signals and translocation of CREB-regulated transcription coactivator 2 to the nucleus were absent and glucagon-induced glucose production and expression of glucose-6-phosphatase (G6Pase) and phosphoenolpyruvate carboxykinase (Pck1) are remarkably reduced in hepatocytes from CD38(-/-) mice. Furthermore, in the fasting condition, CD38(-/-) mice have decreased blood glucose and hepatic expression of G6Pase and Pck1 compared to wild type mice. Our data suggest that CD38/cADPR-mediated Ca(2+) signals play a key role in glucagon-induced gluconeogenesis in hepatocytes, and that the signal pathway has significant clinical implications in metabolic diseases, including type 2 diabetes.

Indexed as

Calcium SignalingGluconeogenesisADP-ribosyl Cyclase 1AnimalsBlood GlucoseCell NucleusCyclic ADP-RiboseCyclic AMP Response Element-Binding ProteinGene Expression RegulationGlucagonGlucoseGlucose-6-PhosphataseHepatocytesLiverMaleMiceADP-ribosyl Cyclase 1Blood GlucoseCrtc2 protein, mouseCyclic ADP-RiboseCyclic AMP Response Element-Binding ProteinGlucagonGlucoseGlucose-6-Phosphatasep21-Activated KinasesPak1 protein, mouseTranscription Factors

Identifiers

PMID26038839
PMCPMC4454144
OpenAlexW2257937472

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LicenceCC BY
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Registered trials

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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.