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Unravelling the developmental toxicity of heavy metals using zebrafish as a model: a narrative review
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This review summarizes research on how heavy metals, including cadmium, lead, mercury, and arsenic, harm developing zebrafish embryos, which share about 80% of their genes with humans. These metals cause oxidative stress, disrupt brain development, and trigger cell death at environmentally relevant levels. The findings are relevant to microplastics research because microplastics can carry and concentrate these same heavy metals, potentially worsening their toxic effects on human development.
Developmental toxicity is the disruption of an organism's normal development which may occur in either the parent before conception or in the growing creature itself. Zebrafish (Danio rerio) are being employed as effective vertebrate models to evaluate the safety and toxicity of chemicals because they can breed multiple times in a year so we can observe the toxic effects in the next generation and their development mental stages can be observed and define clearly because their 1 cell stage to prime stage is transparent so we can observe the development of every organ also they have nearly about 80% genetic similarity with humans and shares the similar neuromodulatory structure along with multiple neurotransmitter. The recent research endeavours to examine the harmful outcome of various heavy metals such as cadmium, chromium, nickel, arsenic, lead, mercury, bismuth, iron, manganese, and thallium along with microplastics on zebrafish embryos when subjected to environmentally acceptable levels of every single metal in addition to co-exposure at various points in time. These heavy metals can alter the mRNA expression levels, increase the reactive oxygen species (ROS) generation, decrease antioxidant expression, damage neuronal function, alter neurotransmitter release, alter the expression of several apoptotic proteins, interfere with the different signalling pathways, decrease heat rates, increase malformations like - pericardial oedema, heart oedema, reduce in length tail bending abnormal formation in fins. Thereafter we concluded that due to its involvement in the food chain, it also causes severe effects on human beings.
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Exploring developmental toxicity of microplastics and nanoplastics (MNPS): Insights from investigations using zebrafish embryos
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This review summarizes research on how micro- and nanoplastics harm embryo development using zebrafish as a model organism that shares genetic similarities with humans. Studies show these tiny plastic particles cause damage to the brain, heart, gut, and immune system of developing embryos, largely through oxidative stress and cell death pathways.
Transcriptomic Insights into Micro- and Nanoplastic Toxicity in Zebrafish: A Narrative Review
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This review pulls together existing research on how tiny plastic particles (micro- and nanoplastics) affect zebrafish, a small fish whose genes are surprisingly similar to ours and is commonly used to study health effects. The studies show these plastic particles can damage the brain, liver, gut, and reproductive organs by triggering harmful changes in gene activity, cell stress, and inflammation. Since zebrafish are often used as an early warning system for human health risks, this research suggests plastic pollution exposure — something we all experience through food, water, and air — deserves serious attention as a potential health concern.
Effects of microplastics on the accumulation and neurotoxicity of methylmercury in zebrafish larvae
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Researchers found that microplastics can adsorb methylmercury and act as carriers, increasing its accumulation in zebrafish larvae and worsening neurotoxicity by disrupting locomotor activity and triggering oxidative stress.
Research progress of model animal zebrafish in toxicity evaluation of microplastics
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This review examines the use of zebrafish as a model organism for evaluating the toxicity of microplastics, synthesizing research on how microplastic exposure affects development, reproduction, and physiological function in this well-established vertebrate model. The authors highlight zebrafish as a particularly valuable system for mechanistic toxicology studies given its genetic tractability and the breadth of endpoints assessable across life stages.
Microplastics- and copper-induced changes in neurogenesis and DNA methyltransferases in the early life stages of zebrafish
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Researchers found that exposure to microplastics and copper, alone or combined, disrupted neurogenesis and DNA methylation in zebrafish embryos, downregulating genes involved in neuronal development and suggesting epigenetic mechanisms underlying neurotoxicity.
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