Evidence map›Paper›PMID 19407215›Full record

ArticleAmerican journal of physiology. Gastrointestinal and liver physiology2009

Role of lysophosphatidylcholine in brush-border intestinal alkaline phosphatase release and restoration.

Takanari Nakano, Ikuo Inoue, David H Alpers, Yasutada Akiba, Shigehiro Katayama, Rina Shinozaki, Jonathan D Kaunitz, Susumu Ohshima, Masumi Akita, Seiichiro Takahashi and 3 more

Abstract read
In one paragraph

Article in American journal of physiology. Gastrointestinal and liver physiology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
2.8field-weighted citation impact, top 9% 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

17 citing papers in PubMed, 52 citations in OpenAlex.

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  9. Duodenal chemosensing.Current opinion in gastroenterology · 2018
    Review
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  14. Review
  15. Article
  16. Article
  17. 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

13 authors at 1 institution in 1 country.

Takanari NakanoDepartment of Biochemistry, Biomedical Research Center, Saitama Medical University, Saitama, Japan. nk.takanari@gmail.com
Ikuo Inoue
David H Alpers
Yasutada Akiba
Shigehiro Katayama
Rina Shinozaki
Jonathan D Kaunitz
Susumu Ohshima
Masumi Akita
Seiichiro Takahashi
Iwao Koyama
Makoto Matsushita
Tsugikazu Komoda
Saitama Medical University · JP

Funding

Washington University Nutrition Obesity Research CenterP30DK056341 · NIDDK · WASHINGTON UNIVERSITY · PI Brian N Finck · 1999 to 2026
$30.2M
Duodenal Muscosal Defense MechanismsR01DK054221 · NIDDK · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI KAUNITZ, JONATHAN D. · 1999 to 2016
$4.4M
NIDDK NIH HHS DK56341NIDDK NIH HHS P30 DK056341NIDDK NIH HHS R01 DK54221
6 · The paper itself

Abstract

Intestinal alkaline phosphatase (IAP) is a brush-border membrane ectoenzyme (BBM-IAP) that is released into the lumen (L-IAP) after a high-fat diet. We examined the effects of oil feeding and the addition of mixed-lipid micelles on the formation of L-IAP in oil-fed rat intestine, Caco-2 cell monolayers, and mouse intestinal loops. We localized IAP in the duodenum of rats fed corn oil using fluorescence microscopy with enzyme-labeled fluorescence-97 as substrate. Four hours after oil feeding, L-IAP increased approximately 10-fold accompanied by the loss of BBM-IAP, consistent with BBM-IAP release. Rat IAP isozyme mRNAs progressively increased 4-6 h after oil feeding, followed by the increase of IAP activity in the subapical location at 6 h, consistent with the restoration of IAP protein. Postprandial lipid-micelle components, sodium taurocholate with or without oleic acid, mono-oleylglycerol, cholesterol, or lysophosphatidylcholine (lysoPC) were applied singly or as mixed-lipid micelles to the apical surface of polarized Caco-2 cell monolayers. LysoPC increased L-IAP >10-fold over basal release. LysoPC released IAP into the apical medium more than other intestinal brush-border enzymes, 5'-nucleotidase, sucrase, aminopeptidase N, and lactase, without comparable lactate dehydrogenase release or cell injury. LysoPC increased human IAP mRNA levels by 1.5-fold in Caco-2 cells. Luminally applied lysoPC also increased release of IAP preferentially in mouse intestinal loops. These data show that lysoPC accelerates the formation of L-IAP from BBM-IAP, followed by enhanced IAP synthesis, suggesting the role that lysoPC might play in the turnover of brush-border proteins.

Indexed as

Alkaline PhosphataseAnimalsAntigens, NeoplasmCaco-2 CellsCorn OilDuodenumEpithelial CellsGPI-Linked ProteinsHumansIntestinesIsoenzymesLysophosphatidylcholinesMaleMiceMice, Inbred C57BLMicellesAlkaline PhosphataseALPI protein, humanAntigens, NeoplasmCorn OilGPI-Linked ProteinsIsoenzymesLysophosphatidylcholinesMicellesRNA, Messenger

Identifiers

PMID19407215
PMCPMC3817256
OpenAlexW2165545940

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.