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Updated: Feb 10, 2026

In utero Electroporation followed by Primary Neuronal Culture for Studying Gene Function in Subset of Cortical Neurons
Published on: October 8, 2010
Transcriptomic Analysis of Ciguatoxin-Induced Changes in Gene Expression in Primary Cultures of Mice Cortical Neurons
Juan Andrés Rubiolo1,2, Carmen Vale3, Andrea Boente-Juncal4
1Departamento de Farmacología, Farmacia e Tecnoloxía Farmacéutica, Facultade de Veterinaria, Universidade de Santiago de Compostela, 27002 Lugo, Spain. ja.rubiolo@usc.es.
Abstract:
Ciguatoxins are polyether marine toxins that act as sodium channel activators. These toxins cause ciguatera, one of the most widespread nonbacterial forms of food poisoning, which presents several symptoms in humans including long-term neurological alterations. Earlier work has shown that both acute and chronic exposure of primary cortical neurons to synthetic ciguatoxin CTX3C have profound impacts on neuronal function. Thus, the present work aimed to identify relevant neuronal genes and metabolic pathways that could be altered by ciguatoxin exposure. To study the effect of ciguatoxins in primary neurons in culture, we performed a transcriptomic analysis using whole mouse genome microarrays, for primary cortical neurons exposed during 6, 24, or 72 h in culture to CTX3C. Here, we have shown that the effects of the toxin on gene expression differ with the exposure time. The results presented here have identified several relevant genes and pathways related to the effect of ciguatoxins on neurons and may assist in future research or even treatment of ciguatera. Moreover, we demonstrated that the effects of the toxin on gene expression were exclusively consequential of its action as a voltage-gated sodium channel activator, since all the effects of CTX3C were avoided by preincubation of the neurons with the sodium channel blocker tetrodotoxin.
Insights
Ciguatoxins, marine toxins causing food poisoning, alter neuronal gene expression. Tetrodotoxin blocks these effects, confirming ciguatoxin
Area of Science:
- Neuroscience
- Marine Biology
- Toxicology
Background:
- Ciguatoxins are marine polyether toxins that activate sodium channels.
- Ciguatera poisoning, caused by ciguatoxins, is a prevalent foodborne illness with neurological impacts.
- Previous studies indicate ciguatoxin exposure affects neuronal function.
Purpose of the Study:
- To identify neuronal genes and metabolic pathways affected by ciguatoxin exposure.
- To investigate the time-dependent effects of ciguatoxin CTX3C on gene expression in primary neurons.
Main Methods:
- Transcriptomic analysis using whole mouse genome microarrays.
- Primary cortical neurons were exposed to synthetic ciguatoxin CTX3C for 6, 24, and 72 hours.
- Neurons were preincubated with tetrodotoxin (a sodium channel blocker) to assess the mechanism of action.
Main Results:
- Ciguatoxin CTX3C exposure alters gene expression in primary cortical neurons in a time-dependent manner.
- Specific genes and metabolic pathways impacted by ciguatoxin exposure were identified.
- All observed gene expression changes were prevented by tetrodotoxin, confirming the role of sodium channel activation.
Conclusions:
- Ciguatoxin exposure significantly impacts neuronal gene expression.
- The identified genes and pathways provide insights into ciguatera's neurological effects.
- The mechanism involves voltage-gated sodium channel activation.
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