Katie A. McDonnell
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The organizations/institutes from the scholar's latest article
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Research Interests
Katie A. McDonnell has a total of 4 co-authors. Here are the top co-authors by number of shared publications:
- Christopher Joseph Martyniuk
Center for Environmental and Human Toxicology, Department of Physiological Sciences, College of Veterinary Medicine, University of Florida, Gainesville, FL 32611, USA
1 shared publication - Cole D. English
Center for Environmental and Human Toxicology, Department of Physiological Sciences, College of Veterinary Medicine, University of Florida, Gainesville, FL 32611, USA
1 shared publication - Emma Ivantsova
Center for Environmental and Human Toxicology, Department of Physiological Sciences, College of Veterinary Medicine, University of Florida, Gainesville, FL 32611, USA
1 shared publication - Lev Avidan
Center for Environmental and Human Toxicology, Department of Physiological Sciences, College of Veterinary Medicine, University of Florida, Gainesville, FL 32611, USA
1 shared publication
Latest Publications
- Open Access
Transcriptome and Behavioral Assessment in Larval Zebrafish (Danio rerio) Following Exposure to Perfluorononanoic Acid (PFNA)
Background/Objectives: Per- and polyfluoroalkyl substances (PFAS) are environmentally persistent chemicals widely detected in aquatic systems and drinking water. Perfluorononanoic acid (PFNA), a long-chain PFAS, has been reported globally in environmental matrices and fish tissues. Although PFNA has been linked to developmental, metabolic, and neurological toxicity, its effects on lipid-related pathways and neurotoxicity remain poorly characterized. Methods: This study evaluated the developmental and neurotoxic effects of PFNA exposure in zebrafish embryos and larvae following a 7-day exposure to environmentally relevant PFNA concentrations. Results: PFNA exposure did not significantly affect survival or deformity rates at the concentrations tested. Apoptosis was significantly increased in larvae exposed to 1 µg/L PFNA compared to controls, whereas reactive oxygen species levels were unaffected. Two concentrations (0.1 µg/L and 10 µg/L) were further examined for transcriptomic responses, and the transcriptome response was largely different for each concentration. Low-dose PFNA exposure primarily affected lipid transport, cholesterol metabolism, sphingolipid signaling, and neurodegeneration-related pathways, whereas high-dose PFNA altered transcripts related to synaptic signaling, axon guidance, and thyroid hormone synthesis. Hypoactivity was observed in the movement of larval zebrafish based on a Visual Motor Response test. Conclusions: Taken together, PFNA exposure induced molecular changes related to neurotoxicity and lipid metabolism in zebrafish, which may contribute to adverse neurodevelopmental outcomes.
Open AccessTranscriptome and Behavioral Assessment in Larval Zebrafish (Danio rerio) Following Exposure to Perfluorononanoic Acid (PFNA)
Background/Objectives: Per- and polyfluoroalkyl substances (PFAS) are environmentally persistent chemicals widely detected in aquatic systems and drinking water. Perfluorononanoic acid (PFNA), a long-chain PFAS, has been reported globally in environmental matrices and fish tissues. Although PFNA has been linked to developmental, metabolic, and neurological toxicity, its effects on lipid-related pathways and neurotoxicity remain poorly characterized. Methods: This study evaluated the developmental and neurotoxic effects of PFNA exposure in zebrafish embryos and larvae following a 7-day exposure to environmentally relevant PFNA concentrations. Results: PFNA exposure did not significantly affect survival or deformity rates at the concentrations tested. Apoptosis was significantly increased in larvae exposed to 1 µg/L PFNA compared to controls, whereas reactive oxygen species levels were unaffected. Two concentrations (0.1 µg/L and 10 µg/L) were further examined for transcriptomic responses, and the transcriptome response was largely different for each concentration. Low-dose PFNA exposure primarily affected lipid transport, cholesterol metabolism, sphingolipid signaling, and neurodegeneration-related pathways, whereas high-dose PFNA altered transcripts related to synaptic signaling, axon guidance, and thyroid hormone synthesis. Hypoactivity was observed in the movement of larval zebrafish based on a Visual Motor Response test. Conclusions: Taken together, PFNA exposure induced molecular changes related to neurotoxicity and lipid metabolism in zebrafish, which may contribute to adverse neurodevelopmental outcomes.