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            "value": "A vital trace element in the human body, zinc is involved in many physiological functions, including DNA repair, neurotransmission, oxidative stress, and protein synthesis. Intracellular zinc is exported by members of the zinc transporters (ZnTs) family, while extracellular zinc is imported by Zrt-and-Irt-like proteins (ZIPs). The preservation of cellular zinc homeostasis depends on these mechanisms. Neurodegenerative disorders have been associated with imbalances in zinc metabolism. Through processes like ferroptosis, protein phase separation, oxidative stress, neuroinflammation, and cell death control, zinc level disruptions may affect the survival and function of neurons and consequently contribute to the development of neurodegenerative disorders. Our knowledge of the pathophysiology of these illnesses may thus be improved by doing a thorough analysis of the regulatory network of zinc and looking into the connection between neurodegenerative disorders and zinc dysmetabolism. Furthermore, it could provide new perspectives and methods for treating neurodegenerative illnesses.",
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        "kernel_xml": "https://registry.smartscholars.in/resolve.php?doi=10.46243%2Fjst.2023.v8.i02.pp26-63&as=xml"
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}