Evidence map›Paper›PMID 35556176›Full record

ArticleClinical oral investigations2022

Assessment of redox state and biochemical parameters of salivary glands in rats treated with anti-obesity drug sibutramine hydrochloride.

Damáris Raissa Dos Santos, Gabriela Alice Fiais, Henrique Arnaldo Oliveira, Tayná Buffulin Ribas, Rayne Oliveira Souza, Thaís Verônica Saori Tsosura, Doris Hissako Matsushita, Edilson Ervolino, Rita Cássia Menegati Dornelles, Ana Cláudia de Melo Stevanato Nakamune and 1 more

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In one paragraph

Article in Clinical oral investigations, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.9field-weighted citation impact, top 28% 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

4 citing papers in PubMed, 5 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

11 authors at 1 institution in 1 country.

Damáris Raissa Dos SantosDepartment of Basic Sciences, School of Dentistry of Araçatuba- UNESP - Universidade Estadual Paulista, Rodovia Marechal Rondon, km 527/528, Aracatuba, São Paulo, CEP 16018-805, Brazil.
Gabriela Alice FiaisDepartment of Basic Sciences, School of Dentistry of Araçatuba- UNESP - Universidade Estadual Paulista, Rodovia Marechal Rondon, km 527/528, Aracatuba, São Paulo, CEP 16018-805, Brazil.
Henrique Arnaldo OliveiraDepartment of Basic Sciences, School of Dentistry of Araçatuba- UNESP - Universidade Estadual Paulista, Rodovia Marechal Rondon, km 527/528, Aracatuba, São Paulo, CEP 16018-805, Brazil.
Tayná Buffulin RibasDepartment of Basic Sciences, School of Dentistry of Araçatuba- UNESP - Universidade Estadual Paulista, Rodovia Marechal Rondon, km 527/528, Aracatuba, São Paulo, CEP 16018-805, Brazil.
Rayne Oliveira SouzaDepartment of Basic Sciences, School of Dentistry of Araçatuba- UNESP - Universidade Estadual Paulista, Rodovia Marechal Rondon, km 527/528, Aracatuba, São Paulo, CEP 16018-805, Brazil.
Thaís Verônica Saori TsosuraDepartment of Basic Sciences, School of Dentistry of Araçatuba- UNESP - Universidade Estadual Paulista, Rodovia Marechal Rondon, km 527/528, Aracatuba, São Paulo, CEP 16018-805, Brazil.
Doris Hissako MatsushitaDepartment of Basic Sciences, School of Dentistry of Araçatuba- UNESP - Universidade Estadual Paulista, Rodovia Marechal Rondon, km 527/528, Aracatuba, São Paulo, CEP 16018-805, Brazil.
Edilson ErvolinoDepartment of Basic Sciences, School of Dentistry of Araçatuba- UNESP - Universidade Estadual Paulista, Rodovia Marechal Rondon, km 527/528, Aracatuba, São Paulo, CEP 16018-805, Brazil.
Rita Cássia Menegati DornellesDepartment of Basic Sciences, School of Dentistry of Araçatuba- UNESP - Universidade Estadual Paulista, Rodovia Marechal Rondon, km 527/528, Aracatuba, São Paulo, CEP 16018-805, Brazil.
Ana Cláudia de Melo Stevanato NakamuneDepartment of Basic Sciences, School of Dentistry of Araçatuba- UNESP - Universidade Estadual Paulista, Rodovia Marechal Rondon, km 527/528, Aracatuba, São Paulo, CEP 16018-805, Brazil.
Antonio Hernandes Chaves-NetoDepartment of Basic Sciences, School of Dentistry of Araçatuba- UNESP - Universidade Estadual Paulista, Rodovia Marechal Rondon, km 527/528, Aracatuba, São Paulo, CEP 16018-805, Brazil. antonio.hernandes@unesp.br.
Universidade Estadual Paulista (Unesp) · BR

Funding

Conselho Nacional de Desenvolvimento Científico e Tecnológico Process n° 457912/2014-6
6 · The paper itself

Abstract

objectivesTo investigate the effects of anti-obesity drug sibutramine hydrochloride (SB) on redox state and biochemical parameters in the salivary glands. MATERIALS AND

methodsAdult male Wistar rats were randomly divided into the following groups (n = 8 per group): control rats treated with vehicle (C) and rats treated with SB (10 mg/kg/day) by intragastric gavage for 28 days. The parotid (PG) and submandibular (SMG) glands were processed using histomorphometric analysis, and total protein, amylase, mucin, and oxidative damage to lipids were determined by measuring the formation of thiobarbituric acid reactive substances (TBARS), total antioxidant capacity (TAC), uric acid (UA), total glutathione (tGSH), superoxide dismutase (SOD), catalase (CAT), and glutathione peroxidase (GPx), and AKT phosphorylation.

resultsSB decreased the acinar area, and increased the stromal area in PG, while no effect on the morphometric parameters was observed in SMG. SB also increased oxidative damage to lipids (TBARs). The SB group showed lower total protein, amylase, TAC, UA, tGSH, SOD, CAT, and GPx than the C group in PG, while in SMG, SB decreased total protein, mucin, tGSH, SOD, CAT, and GPx. However, increased AKT phosphorylation observed in both salivary glands suggests that SB exerts low-intensity oxidative stress.

conclusionsSB impaired enzymatic and non-enzymatic antioxidant defenses in the salivary glands of rats. CLINICAL RELEVANCE: Chronic treatment with SB could mitigate salivary gland dysfunction due to disturbance of redox state.

Indexed as

Anti-Obesity AgentsAntioxidantsAmylasesAnimalsCyclobutanesGlutathione PeroxidaseLipidsMaleMucinsOxidation-ReductionOxidative StressProto-Oncogene Proteins c-aktRatsRats, WistarSalivary GlandsSuperoxide DismutaseAmylasesAnti-Obesity AgentsAntioxidantsCyclobutanesGlutathione PeroxidaseLipidsMucinsProto-Oncogene Proteins c-aktsibutramineSuperoxide DismutaseThiobarbituric Acid Reactive SubstancesAnti-obesity agentsOxidative stressParotid glandSibutramine hydrochlorideSubmandibular gland

Identifiers

PMID35556176
OpenAlexW4280541305

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Registered trials

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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.