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Using Chicken Embryo as a Powerful Tool in Assessment of Developmental Cardiotoxicities
Published on: March 21, 2021
Mercuric Chloride-Mediated Neurotoxicity in Chicken Embryos: Disruption of the Blood-Brain Barrier Integrity and Iron
Hong-Yu Fu1,2, Yi-Tong Fu1,2, Jie Yang1,2
1College of Veterinary Medicine, Shandong Agricultural University, Tai'an, Shandong, China.
Mercuric chloride (HgCl2) is an environmental pollutant with neurotoxicity. The blood-brain barrier (BBB) serves as a critical protective interface, shielding the brain from exposure to heavy metals and maintaining neurological homeostasis. Ferroptosis, a programmed cell death initiated by iron-dependent lipid peroxidation, was recently reported to be associated with various neurological disorders. Nevertheless, the relationship between HgCl2-induced neurotoxicity, BBB dysfunction, and ferroptosis remains unclear. This study investigated the effects of embryonic exposure to HgCl2 (35, 50, and 65 μg/kg) on brain tissue and the underlying mechanisms. These results demonstrated that HgCl2 exposure induced brain injury by compromising BBB integrity. Intriguingly, we identified ferroptosis as a central mechanism contributing to this damage, supported by the observation of mitochondrial abnormalities. Moreover, HgCl2 exposure induced oxidative stress, characterized by a decrease in antioxidant capacity and an increase in lipid peroxidation. Further studies revealed increased total iron level and dysregulation of iron metabolism-related proteins. It can be concluded that HgCl2 exposure disrupted BBB integrity, promoted iron overload-mediated oxidative stress, initiated ferroptosis, and ultimately exacerbated brain injury in embryos. These findings highlight the critical role of ferroptosis in HgCl2-induced neurotoxicity and offer novel mechanistic insights that may inform future strategies for preventing or treating heavy metal-related neurological disorders.
Mercuric chloride (HgCl2) is an environmental pollutant with neurotoxicity. The blood-brain barrier (BBB) serves as a critical protective interface, shielding the brain from exposure to heavy metals and maintaining neurological homeostasis. Ferroptosis, a programmed cell death initiated by iron-dependent lipid peroxidation, was recently reported to be associated with various neurological disorders. Nevertheless, the relationship between HgCl2-induced neurotoxicity, BBB dysfunction, and ferroptosis remains unclear. This study investigated the effects of embryonic exposure to HgCl2 (35, 50, and 65 μg/kg) on brain tissue and the underlying mechanisms. These results demonstrated that HgCl2 exposure induced brain injury by compromising BBB integrity. Intriguingly, we identified ferroptosis as a central mechanism contributing to this damage, supported by the observation of mitochondrial abnormalities. Moreover, HgCl2 exposure induced oxidative stress, characterized by a decrease in antioxidant capacity and an increase in lipid peroxidation. Further studies revealed increased total iron level and dysregulation of iron metabolism-related proteins. It can be concluded that HgCl2 exposure disrupted BBB integrity, promoted iron overload-mediated oxidative stress, initiated ferroptosis, and ultimately exacerbated brain injury in embryos. These findings highlight the critical role of ferroptosis in HgCl2-induced neurotoxicity and offer novel mechanistic insights that may inform future strategies for preventing or treating heavy metal-related neurological disorders.
