Evidence map›Paper›PMID 31614497›Full record

ArticleInternational journal of molecular sciences2019

Species-Specific Glucose-6-Phosphatase Activity in the Small Intestine-Studies in Three Different Mammalian Models.

Viola Varga, Zsófia Murányi, Anita Kurucz, Paola Marcolongo, Angelo Benedetti, Gábor Bánhegyi, Éva Margittai

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.3field-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

6 citing papers in PubMed, 14 citations in OpenAlex.

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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

7 authors at 2 institutions in 2 countries.

Viola VargaInstitute of Translational Medicine, Semmelweis University, 1094 Budapest, Hungary. varga.viola@med.semmelweis-univ.hu.
Zsófia MurányiInstitute of Translational Medicine, Semmelweis University, 1094 Budapest, Hungary. sophie0924@freemail.hu.
Anita KuruczDepartment of Medical Chemistry, Molecular Biology and Pathobiochemistry, Semmelweis University, 1094 Budapest, Hungary. kurucz.anita.andrea@gmail.com.
Paola MarcolongoDepartment of Molecular and Developmental Medicine, University of Siena, 53100 Siena, Italy. paola.marcolongo@unisi.it.ORCID 0000-0001-9330-8570
Angelo BenedettiDepartment of Molecular and Developmental Medicine, University of Siena, 53100 Siena, Italy. benedetti@unisi.it.
Gábor BánhegyiDepartment of Medical Chemistry, Molecular Biology and Pathobiochemistry, Semmelweis University, 1094 Budapest, Hungary. banhegyi@eok.sote.hu.
Éva MargittaiInstitute of Translational Medicine, Semmelweis University, 1094 Budapest, Hungary. margittai.eva@med.semmelweis-univ.hu.
Semmelweis University · HUUniversity of Siena · IT

Funding

Nemzeti Kutatási Fejlesztési és Innovációs Hivatal FK124442Nemzeti Kutatási Fejlesztési és Innovációs Hivatal PD105246
6 · The paper itself

Abstract

Besides the liver, which has always been considered the major source of endogenous glucose production in all post-absorptive situations, kidneys and intestines can also produce glucose in blood, particularly during fasting and under protein feeding. However, observations gained in different experimental animals have given ambiguous results concerning the presence of the glucose-6-phosphatase system in the small intestine. The aim of this study was to better define the species-related differences of this putative gluconeogenic organ in glucose homeostasis. The components of the glucose-6-phosphatase system (i.e., glucose-6-phosphate transporter and glucose-6-phosphatase itself) were analyzed in homogenates or microsomal fractions prepared from the small intestine mucosae and liver of rats, guinea pigs, and humans. Protein and mRNA levels, as well as glucose-6-phosphatase activities, were detected. The results showed that the glucose-6-phosphatase system is poorly represented in the small intestine of rats; on the other hand, significant expressions of glucose-6-phosphate transporter and of the glucose-6-phosphatase were found in the small intestine of guinea pigs and homo sapiens. The activity of the recently described fructose-6-phosphate transporter-intraluminal hexose isomerase pathway was also present in intestinal microsomes from these two species. The results demonstrate that the gluconeogenic role of the small intestine is highly species-specific and presumably dependent on feeding behavior (e.g., fructose consumption) and the actual state of metabolism.

Indexed as

AnimalsFructoseGlucose-6-PhosphataseGuinea PigsHumansIntestine, SmallMicrosomesRatsSpecies SpecificityFructoseGlucose-6-Phosphataseendoplasmic reticulumfructoseglucose-6-phosphataseglucose-6-phosphate transportersmall intestine

Identifiers

PMID31614497
PMCPMC6829527
OpenAlexW2979753741

What OpenQuestion holds

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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.