Exposure to paraquat associated with periodontal disease causes motor damage and neurochemical changes in rats.


Journal

Human & experimental toxicology
ISSN: 1477-0903
Titre abrégé: Hum Exp Toxicol
Pays: England
ID NLM: 9004560

Informations de publication

Date de publication:
Jan 2021
Historique:
pubmed: 5 8 2020
medline: 3 9 2021
entrez: 5 8 2020
Statut: ppublish

Résumé

Exposure to paraquat is possibly involved with the development of several conditions, including neurodegenerative diseases, such as Parkinson's disease (PD). This condition is mainly characterized by the loss of dopaminergic neurons in the nigrostriatal pathway and the development of classical motor symptoms. Etiology includes exposure to environmental factors, such as the paraquat exposure, and inflammatory diseases may exacerbate paraquat neurotoxicity. The aim of the study was to investigate whether the exposure to paraquat associated with the presence of periodontal disease is able to induce motor and biochemical changes in rats similar to that observed in PD. Adult male Wistar rats were sent to ligature. After 48 h, they were sent to daily treatment paraquat (1 mg/kg/day; 2 mL/kg; intragastric) or vehicle for 4 weeks. Twenty-four hours after the last administration, the open field test was performed. The rats were euthanized and the left hemimandibles and striatum were dissected for the analysis of dopaminergic and inflammatory markers. Only the combination of periodontal disease model plus paraquat exposure induced motor impairments. Remarkably, the paraquat exposure increased the ligature-induced alveolar bone loss in hemimandibles. Moreover, only the combination of periodontal disease and paraquat exposure induced the loss of dopaminergic neurons and astrocyte activation in the striatum.

Identifiants

pubmed: 32748713
doi: 10.1177/0960327120938851
doi:

Substances chimiques

Herbicides 0
Paraquat PLG39H7695

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

81-89

Auteurs

L C Fernandes (LC)

549253Department of Pharmaceutical Sciences, State University of Ponta Grossa (UEPG), Ponta Grossa, PR, Brazil.

A G Santos (AG)

549253Department of Pharmaceutical Sciences, State University of Ponta Grossa (UEPG), Ponta Grossa, PR, Brazil.

T B Sampaio (TB)

Department of Pharmacology, 28117Federal University of Santa Catarina (UFSC), Florianópolis, SC, Brazil.

Sms Sborgi (S)

549253Department of Pharmaceutical Sciences, State University of Ponta Grossa (UEPG), Ponta Grossa, PR, Brazil.

Rds Prediger (R)

Department of Pharmacology, 28117Federal University of Santa Catarina (UFSC), Florianópolis, SC, Brazil.

M M Ferro (MM)

Department of Biology, 67883State University of Ponta Grossa (UEPG), Ponta Grossa, PR, Brazil.

Gcn Franco (G)

Department of Odontology, 67883State University of Ponta Grossa (UEPG), Ponta Grossa, PR, Brazil.

L Lipinski (L)

Department of Medicine, 67883State University of Ponta Grossa (UEPG), Ponta Grossa, PR, Brazil.

E Miyoshi (E)

549253Department of Pharmaceutical Sciences, State University of Ponta Grossa (UEPG), Ponta Grossa, PR, Brazil.

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Classifications MeSH