Evidence map›Paper›PMID 22038824›Full record

ArticleAmerican journal of physiology. Gastrointestinal and liver physiology2012

SIRT1 inhibits the mouse intestinal motility and epithelial proliferation.

Yi Wang, Xuemei Shi, Jian Qi, Xiaojie Li, Karen Uray, Xinfu Guan

Open access · greenAbstract read
In one paragraph

Article in American journal of physiology. Gastrointestinal and liver physiology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.2field-weighted citation impact, top 20% 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

14 citing papers in PubMed, 27 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Review
  6. Article
  7. Article
  8. Review
  9. Regulation and function of SIRT1 in rheumatoid arthritis synovial fibroblasts.Journal of molecular medicine (Berlin, Germany) · 2016
    Article
  10. Article
  11. Article
  12. Article
  13. GLP-2 receptor in POMC neurons suppresses feeding behavior and gastric motility.American journal of physiology. Endocrinology and metabolism · 2012
    Article
  14. 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

6 authors at 2 institutions in 2 countries.

Yi WangUSDA/ARS Children's Nutrition Research Center, Department of Pediatrics, Baylor College of Medicine, Houston TX 77030, USA.
Xuemei Shi
Jian Qi
Xiaojie Li
Karen Uray
Xinfu Guan
Arkansas Children's Nutrition Center · USThe University of Texas at Austin · US

Funding

Physiological role of GLP-2 receptor in the mouse intestinal growth and functionK01DK075489 · NIDDK · BAYLOR COLLEGE OF MEDICINE · PI GUAN, XINFU · 2006 to 2009
$562k
Physiological Role of CNS GLP-2 Receptor in Energy HomeostasisR03DK084125 · NIDDK · BAYLOR COLLEGE OF MEDICINE · PI GUAN, XINFU · 2009 to 2010
$136k
NIDDK NIH HHS DK075489NIDDK NIH HHS DK084125NIDDK NIH HHS K01 DK075489NIDDK NIH HHS R03 DK084125
6 · The paper itself

Abstract

Sirtuin 1 (SIRT1), a NAD(+)-dependent histone deacetylase, is involved in a wide array of cellular processes including glucose homeostasis, energy metabolism, proliferation and apoptosis, and immune response. However, it is unknown whether SIRT1 plays any physiological role in the regulation of intestinal homeostasis and motility. Thus the aim was to define SIRT1 expression and function in the gastrointestinal (GI) tract under physiological conditions. Forty 12-14-wk-old SIRT1 knockout (KO) and wild-type (WT) mice were fasted 21 h and/or refed 3 h. Fasted mice were injected intraperitoneally with bromodeoxyuridine (120 mg/kg body wt) 2 h before euthanasia. SIRT1 protein was localized to gastric and intestinal epithelial nuclei and was responsive to the nutritional status. SIRT1 was required for intestinal epithelial homeostasis. The SIRT1 KO mice showed enhanced crypt proliferation and suppressed villous apoptosis, resulting in increased intestinal villous height. In the SIRT1 KO intestine, the abundance of Forkhead box protein O1 and p53 protein decreased, whereas the subcellular localization of β-catenin protein accumulated mainly in the crypts. The SIRT1 KO mice showed accelerated gastric emptying rate with increased abundance of ghrelin mRNA and protein in the stomach. Moreover, the SIRT1 KO mouse intestine showed enhanced ex vivo spontaneous contraction. We concluded that, SIRT1 plays a critical role in the control of intestinal homeostasis (by promoting apoptosis and inhibiting proliferation) and gastrointestinal motility (by reducing gastric emptying and intestinal contractile activity), implicating a novel role for SIRT1.

Indexed as

AnimalsApoptosisbeta CateninCell ProliferationEatingFastingGastric EmptyingGastric MucosaGhrelinIntestinal MucosaMiceMice, KnockoutMuscle ContractionSirtuin 1Tumor Suppressor Protein p53beta CateninGhrelinSirt1 protein, mouseSirtuin 1Tumor Suppressor Protein p53

Identifiers

PMID22038824
PMCPMC3341113
OpenAlexW2167862888

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.