Manganese(II) Chloride Alters Nucleotide and Nucleoside Catabolism in Zebrafish (Danio Rerio) Adult Brain

Overview

Journal Mol Neurobiol

Specialties Molecular Biology
Neurology

Date 2017 May 27

PMID 28547528

Citations 5

Authors

Stefani Altenhofen

Debora Dreher Nabinger

Talita Carneiro Brandao Pereira

Carlos Eduardo Leite

Mauricio Reis Bogo

Carla Denise Bonan

Affiliations

Soon will be listed here.

Abstract

ATP and adenosine, the main signaling molecules of purinergic system, are involved in toxicological effects induced by metals. The manganese (Mn) exposure induces several cellular changes, which could interfere with signaling pathways, such as the purinergic system. In this study, we evaluated the effects of exposure to manganese(II) chloride (MnCl) during 96 h on nucleoside triphosphate diphosphohydrolase (NTPDase), ecto-5'-nucleotidase, and adenosine deaminase (ADA) activities, followed by analyzing the gene expression patterns of NTPDases (entpd1, entpd2a.1, entpd2a.2, entpd2-like, entpd3) and ADA (ADA , ADA , ADA , ADAasi, ADAL) families in zebrafish brain. In addition, the brain metabolism of nucleotides and nucleosides was evaluated after MnCl exposure. The results showed that MnCl exposure during 96 h inhibited the NTPDase (1.0 and 1.5 mM) and ecto-ADA (0.5, 1.0, and 1.5 mM) activities, further decreasing ADA2.1 expression at all MnCl concentrations analyzed. Purine metabolism was also altered by the action of MnCl. An increased amount of ADP appeared at all MnCl concentrations analyzed; however, AMP and adenosine levels are decreased at the concentrations of 1.0 and 1.5 mM MnCl, whereas decreased inosine (INO) levels were observed at all concentrations tested. The findings of this study demonstrated that MnCl may inhibit NTPDase and ecto-ADA activities, consequently modulating nucleotide and nucleoside levels, which may contribute for the toxicological effects induced by this metal.

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