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1.
Chemosphere ; 239: 124608, 2020 Jan.
Article in English | MEDLINE | ID: mdl-31499312

ABSTRACT

Freshwater systems are faced with a myriad of stressors including geomorphological alterations, nutrient overloading and pollution. Previous studies in marine fish showed polyaromatic hydrocarbons (PAHs) to be cardiotoxic. However, the cardiotoxicity of anthropogenic pollutants in freshwater fishes is unclear and has not been examined across multiple levels of cardiac organization. Here we investigated the effect of phenanthrene (Phe), a pervasive anthropogenic pollutant on a sentinel freshwater species, the brown trout (Salmo trutta). We first examined the electrical activity of the whole heart and found prolongation (∼8.6%) of the QT interval (time between ventricular depolarization and repolarization) of the electrocardiogram (ECG) and prolongation (∼13.2%) of the monophasic action potential duration (MAPD) following ascending doses of Phe. At the tissue level, Phe significantly reduced trabecular force generation by ∼24% at concentration 15 µM and above, suggesting Phe reduces cellular calcium cycling. This finding was supported by florescent microscopy showing a reduction (∼39%) in the intracellular calcium transient amplitude following Phe exposure in isolated brown trout ventricular myocytes. Single-cell electrophysiology was used to reveal the mechanism underlying contractile and electrical dysfunction following Phe exposure. A Phe-dependent reduction (∼38%) in the L-type Ca2+ current accounts, at least in part, for the lowered Ca2+ transient and force production. Prolongation of the MAPD and QT interval was explained by a reduction (∼70%) in the repolarising delayed rectifier K+ current following Phe exposure. Taken together, our study shows a direct impact of Phe across multiple levels of cardiac organization in a key freshwater salmonid.


Subject(s)
Myocytes, Cardiac/drug effects , Myocytes, Cardiac/pathology , Phenanthrenes/toxicity , Trout/physiology , Water Pollutants, Chemical/toxicity , Animals , Cardiotoxicity , Electrocardiography , Fresh Water/chemistry
2.
J Biol Chem ; 286(25): 22546-57, 2011 Jun 24.
Article in English | MEDLINE | ID: mdl-21504902

ABSTRACT

Predatory marine cone snails (genus Conus) utilize complex venoms mainly composed of small peptide toxins that target voltage- and ligand-gated ion channels in their prey. Although the venoms of a number of cone snail species have been intensively profiled and functionally characterized, nothing is known about the initiation of venom expression at an early developmental stage. Here, we report on the expression of venom mRNA in embryos of Conus victoriae and the identification of novel α- and O-conotoxin sequences. Embryonic toxin mRNA expression is initiated well before differentiation of the venom gland, the organ of venom biosynthesis. Structural and functional studies revealed that the embryonic α-conotoxins exhibit the same basic three-dimensional structure as the most abundant adult toxin but significantly differ in their neurological targets. Based on these findings, we postulate that the venom repertoire of cone snails undergoes ontogenetic changes most likely reflecting differences in the biotic interactions of these animals with their prey, predators, or competitors. To our knowledge, this is the first study to show toxin mRNA transcripts in embryos, a finding that extends our understanding of the early onset of venom expression in animals and may suggest alternative functions of peptide toxins during development.


Subject(s)
Conotoxins/genetics , Conotoxins/metabolism , Conus Snail/embryology , Conus Snail/metabolism , Embryo, Nonmammalian/metabolism , Gene Expression Regulation , Amino Acid Sequence , Animals , Conotoxins/chemistry , Conus Snail/anatomy & histology , Conus Snail/genetics , Mass Spectrometry , Models, Molecular , Molecular Sequence Data , Neurons/metabolism , Peptide Fragments/chemistry , Peptide Fragments/metabolism , Protein Conformation , RNA, Messenger/genetics , RNA, Messenger/metabolism , Sequence Alignment
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