Evidence map›Paper›PMID 31689911›Full record

ArticleNutrients2019

Metabolic Effects of the Sweet Protein MNEI as a Sweetener in Drinking Water. A Pilot Study of a High Fat Dietary Regimen in a Rodent Model.

Rosa Cancelliere, Serena Leone, Cristina Gatto, Arianna Mazzoli, Carmine Ercole, Susanna Iossa, Giovanna Liverini, Delia Picone, Raffaella Crescenzo

Open access · goldAbstract read
In one paragraph

Article in Nutrients, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed, 1 pooled it
0.3field-weighted citation impact, top 40% 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

5 citing papers in PubMed, 1 synthesis or guideline pooled it, 7 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Review
  5. 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

9 authors at 1 institution in 1 country.

Rosa CancelliereDepartment of Biology, Federico II University, Via Cintia, 80126 Naples, Italy. cancelliererosa@gmail.com.
Serena LeoneDepartment of Chemical Sciences, Federico II University, Via Cintia, 80126 Naples, Italy. serena.leone@unina.it.ORCID 0000-0003-4787-0882
Cristina GattoDepartment of Biology, Federico II University, Via Cintia, 80126 Naples, Italy. cristina.gatto@unina.it.
Arianna MazzoliDepartment of Biology, Federico II University, Via Cintia, 80126 Naples, Italy. arianna.mazzoli@unina.it.
Carmine ErcoleDepartment of Chemical Sciences, Federico II University, Via Cintia, 80126 Naples, Italy. ercoleca@hotmail.com.
Susanna IossaDepartment of Biology, Federico II University, Via Cintia, 80126 Naples, Italy. susanna.iossa@unina.it.ORCID 0000-0001-6103-718X
Giovanna LiveriniDepartment of Biology, Federico II University, Via Cintia, 80126 Naples, Italy. liverini@unina.it.
Delia PiconeDepartment of Chemical Sciences, Federico II University, Via Cintia, 80126 Naples, Italy. delia.picone@unina.it.ORCID 0000-0002-7582-2581
Raffaella CrescenzoDepartment of Biology, Federico II University, Via Cintia, 80126 Naples, Italy. rcrescen@unina.it.ORCID 0000-0001-6138-6961
Federico II University Hospital · IT

Funding

Fondazione CON IL SUD 2011-PDR-19
6 · The paper itself

Abstract

Sweeteners have become integrating components of the typical western diet, in response to the spreading of sugar-related pathologies (diabetes, obesity and metabolic syndrome) that have stemmed from the adoption of unbalanced dietary habits. Sweet proteins are a relatively unstudied class of sweet compounds that could serve as innovative sweeteners, but their introduction on the food market has been delayed by some factors, among which is the lack of thorough metabolic and toxicological studies. We have tried to shed light on the potential of a sweet protein, MNEI, as a fructose substitute in beverages in a typical western diet, by studying the metabolic consequences of its consumption on a Wistar rat model of high fat diet-induced obesity. In particular, we investigated the lipid profile, insulin sensitivity and other indicators of metabolic syndrome. We also evaluated systemic inflammation and potential colon damage. MNEI consumption rescued the metabolic derangement elicited by the intake of fructose, namely insulin resistance, altered plasma lipid profile, colon inflammation and translocation of lipopolysaccharides from the gut lumen into the circulatory system. We concluded that MNEI could represent a valid alternative to fructose, particularly when concomitant metabolic disorders such as diabetes and/or glucose intolerance are present.

Indexed as

Diet, High-FatDrinking WaterAnimalsBiomarkersBody CompositionColonEnergy MetabolismGlucose Tolerance TestInflammationLipidsMaleMuscle, SkeletalObesityPilot ProjectsProteinsRatsBiomarkersDrinking WaterLipidsProteinsSweetening Agentsfructosehigh fat dietMNEIsweet protein

Identifiers

PMID31689911
PMCPMC6893535
OpenAlexW2982963139

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.