Lead (Pb2+) neurotoxicity: ion-mimicry with calcium (Ca2+) impairs synaptic transmission. a review with animated illustrations of the pre- and post-synaptic effects of lead
Abstract
Lead (Pb 2+ ) is ubiquitously distributed in the environment and shows significant health effects in humans, especially in the nervous system. In this review we illustrate how (Pb 2+ ) neurotoxicity is associated with its ability to partially mimic the function of Ca 2+ and modifies synaptic transmission pre- and post-synaptically. As Pb 2+ binds to calcium-binding sites it alters their functionality, ranging from reduced currents through voltage and receptor gated channels, to modulation of ion-transporters and alterations of calcium-dependent signaling pathways. Overall Pb 2+ exposure not only reduces pre-synaptically the transmitter release, but also post-synaptically the likelihood to generate a new action potential. This review will highlight the major-interactions with the different targets in schemes and short animated sequences to allow a general understanding of lead neurotoxicity to a wider audience; therefore, not all possible mechanisms will be mentioned or discussed.
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Lead acts as a calcium mimetic, interfering with Ca2+-dependent signaling, compromising synaptic transmission fidelity, and disrupting early neurodevelopment.
“Lead poses a particular risk because it can act as a calcium mimetic, thereby interfering with Ca2+-dependent signaling pathways, compromising the fidelity of synaptic transmission, and severely disrupting early neurodevelopment (Florea et al., 2013; Sharma et al., 2015).”
From Environmental endocrine disruptors at the synapse: mechanisms linking chemical exposure to cognitive and behavioral dysfunction (2026) · cites this paper as Florea et al., 2013
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Jocsak, G., Kiss, D. S., Alymbaeva, D., Diebald, A., Zsarnovszky, A., Heinzlmann, A., & Bartha, T. (2026) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2026.1821381 · Cited by 1 · see citing works
“Lead poses a particular risk because it can act as a calcium mimetic, thereby interfering with Ca 2+ -dependent signaling pathways, compromising the fidelity of synaptic transmission, and severely disrupting early neuro-development (Florea et al., 2013; Sharma et al., 2015).”
- Authors
- Florea, A.-M., Taban, J., Varghese, E., Alost, B. T., Moreno, S., & Büsselberg, D.
- Venue
- Journal of Local and Global Health Science
- Published
- 2013-08-01
- Volume
- 2013
- Issue
- 1
- ISSN
- 2223-0440 (ISSN-L)
- OpenAlex
- W2091896545
- Cited by
- 50
- References
- 0
- Citations by year
- 2026: 13 · 2025: 8 · 2024: 4 · 2023: 2 · 2022: 2 · 2021: 7 · 2020: 1 · 2019: 4 · 2018: 2 · 2017: 2 · 2016: 2 · 2015: 3
- FWCI
- 1.22
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Journal of Local and Global Health Science (publishedVersion)
- Funders
- Centers for Disease Control and Prevention
- Topics
- Physical Sciences › Environmental Science › Health, Toxicology and Mutagenesis › Heavy Metal Exposure and Toxicity
- Life Sciences › Agricultural and Biological Sciences › Plant Science › Aluminum toxicity and tolerance in plants and animals
- Health Sciences › Nursing › Nutrition and Dietetics › Trace Elements in Health
- Keywords
- lead neurotoxicity, synaptic transmission, calcium binding sites, voltage-gated calcium channels, ion transporters, calcium-dependent signaling, presynaptic neurotransmitter release, lead exposure
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