Evidence map›Paper›PMID 32966299›Full record

ArticlePloS one2020

Gene expression of the immunoinflammatory and immunological status of obese dogs before and after weight loss.

Thiago Henrique Annibale Vendramini, Henrique Tobaro Macedo, Andressa Rodrigues Amaral, Mariana Fragoso Rentas, Matheus Vinícius Macegoza, Rafael Vessecchi Amorim Zafalon, Vivian Pedrinelli, Lígia Garcia Mesquita, Júlio César de Carvalho Balieiro, Karina Pfrimer and 5 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.7field-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

9 citing papers in PubMed, 16 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

15 authors at 2 institutions in 1 country.

Thiago Henrique Annibale VendraminiPet Nutrology Research Center, Nutrition and Production Department, School of Veterinary Medicine and Animal Science, University of Sao Paulo-USP, Pirassununga, São Paulo, Brazil.
Henrique Tobaro MacedoPet Nutrology Research Center, Nutrition and Production Department, School of Veterinary Medicine and Animal Science, University of Sao Paulo-USP, Pirassununga, São Paulo, Brazil.
Andressa Rodrigues AmaralVeterinary Nutrology Service, Teaching Veterinary Hospital, School of Veterinary Medicine and Animal Science, University of Sao Paulo-USP, São Paulo, São Paulo, Brazil.ORCID 0000-0002-3852-0525
Mariana Fragoso RentasPet Nutrology Research Center, Nutrition and Production Department, School of Veterinary Medicine and Animal Science, University of Sao Paulo-USP, Pirassununga, São Paulo, Brazil.
Matheus Vinícius MacegozaPet Nutrology Research Center, Nutrition and Production Department, School of Veterinary Medicine and Animal Science, University of Sao Paulo-USP, Pirassununga, São Paulo, Brazil.
Rafael Vessecchi Amorim ZafalonPet Nutrology Research Center, Nutrition and Production Department, School of Veterinary Medicine and Animal Science, University of Sao Paulo-USP, Pirassununga, São Paulo, Brazil.
Vivian PedrinelliVeterinary Nutrology Service, Teaching Veterinary Hospital, School of Veterinary Medicine and Animal Science, University of Sao Paulo-USP, São Paulo, São Paulo, Brazil.
Lígia Garcia MesquitaPet Nutrology Research Center, Nutrition and Production Department, School of Veterinary Medicine and Animal Science, University of Sao Paulo-USP, Pirassununga, São Paulo, Brazil.
Júlio César de Carvalho BalieiroPet Nutrology Research Center, Nutrition and Production Department, School of Veterinary Medicine and Animal Science, University of Sao Paulo-USP, Pirassununga, São Paulo, Brazil.
Karina PfrimerMedical School of Ribeirão Preto, University of São Paulo-USP, Ribeirão Preto, São Paulo, Brazil.
Raquel Silveira PedreiraGrandfood Indústria e Comércio, Dourado, São Paulo, Brazil.
Victor NowoshDepartment of Pathology, School of Veterinary Medicine and Animal Science, University of São Paulo-USP, São Paulo, São Paulo, Brazil.
Cristiana Fonseca Ferreira PontieriGrandfood Indústria e Comércio, Dourado, São Paulo, Brazil.ORCID 0000-0002-8029-5499
Cristina de Oliveira MassocoDepartment of Pathology, School of Veterinary Medicine and Animal Science, University of São Paulo-USP, São Paulo, São Paulo, Brazil.
Marcio Antonio BrunettoPet Nutrology Research Center, Nutrition and Production Department, School of Veterinary Medicine and Animal Science, University of Sao Paulo-USP, Pirassununga, São Paulo, Brazil.ORCID 0000-0003-3240-0343
Universidade de São Paulo · BRUniversidade de Ribeirão Preto · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Obesity is characterized by a low degree of chronic inflammation state that, along with metabolic modifications, promotes important changes in the animal's organism. Adipose tissue actively participates in inflammation and immunity, and several defense cells of the organism may, therefore, be involved in the diversity found between obese and ideal weight individuals. Studies regarding this subject have shown immune cell changes in humans and rats, however, the literature is scarce in relation to dogs. Thus, the present study aimed to evaluate the gene expression profile of immunoinflammatory response and the lymphoproliferation of obese dogs before and after weight loss. Eight female dogs, neutered, of different breeds, aged between 1 and 8 years (4.74±3.19), obese, with body condition score (BCS) of 9 out of a 9-point scale and body composition determined by the deuterium isotope dilution method were included. The obese dogs were enrolled in a weight loss program and after losing 20% of their initial weight became a second experimental group. A third experimental group consisted of eight female dogs, neutered, aged between 1 and 8 years (3.11±0.78) and with ideal BCS (5 out of a 9-point scale). Gene expression of immunoinflammatory cytokines (resistin, leptin, adiponectin, TNF-α, IL-6, IL-8, and IL-10) was assessed by qRT-PCR and immunity was assessed by lymphoproliferative response using the flow cytometry technique. The data that presented normal distribution was evaluated by analysis of variance by the PROC MIXED of the SAS and when differences were detected, these were compared by the Tukey test. Regarding the gene expression data, the procedure PROC GLIMMIX was adopted and the methodology of generalized linear model was used, in which the Gama distribution proved to be adequate. Values of p<0.05 were considered significant. The mean weight loss period of the animals included in the study was 194.25 ± 28.31 days and the mean weekly weight loss rate was 1.02 ± 0.82%. The average fat mass, both in percentage (P<0.001) and in kilograms (P = 0.012), was higher in the obese group (40.88%; 8.91kg), returning to normal and without difference between the control group (19.16%; 3.01kg) and after weight loss (22.10%; 4.11kg). The weight loss program resulted in an increase in percentage of lean body mass (P = 0.001), 55.50% in obese animals vs 77.90% in obese dogs after weight loss, the latter with no difference when compared to the control group (80.84%). The obese group presented increased gene expression of resistin and IL-8 in relation to the weight loss group (P = 0.002). In adiponectin, the obese group presented increased mRNA gene expression when compared to the weight loss group (P = 0.003). The evaluation of lymphocyte proliferation showed differences between the group of obese animals before and after weight loss (P = 0.004). Weight loss resulted in an increase in the lymphoproliferation rate (18.48%) compared to obese dogs at the beginning of the study (10.71%). These results indicate that weight loss modulates the immunoinflammatory response of obese dogs and may present important benefits to health and longevity of dogs.

Indexed as

Gene Expression RegulationAdipokinesAnimalsDogsFemaleInflammationLymphocytesObesityRNA, MessengerWeight LossAdipokinesRNA, Messenger

Identifiers

PMID32966299
PMCPMC7510989
OpenAlexW3087981513

What OpenQuestion holds

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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.