Optic Neuropathies Current and Future Strategies for Optic Nerve Protection and Repair

Optic neuropathies are conditions in which there is damage to the optic nerve (ON) caused by a variety of causes, including glaucoma, inflammation, gene abnormalities, ischemia, trauma, and toxicity. ON damage triggers a process of axon degeneration, inflammatory cytokine upregulation, breakdown of...

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Bibliographic Details
Other Authors: Tsai, Rongkung (Editor), Miller, Neil R. (Editor)
Format: Electronic Book Chapter
Language:English
Published: Basel MDPI - Multidisciplinary Digital Publishing Institute 2023
Subjects:
NMO
BID
MOG
A8
n/a
Online Access:DOAB: download the publication
DOAB: description of the publication
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520 |a Optic neuropathies are conditions in which there is damage to the optic nerve (ON) caused by a variety of causes, including glaucoma, inflammation, gene abnormalities, ischemia, trauma, and toxicity. ON damage triggers a process of axon degeneration, inflammatory cytokine upregulation, breakdown of the blood-optic nerve barrier, and, eventually, the induction of apoptosis of retinal ganglion cells (RGCs), resulting in optic atrophy. To date, there is no effective treatment for most optic neuropathies; however, because the damage initially is axogenic, there may exist a window of therapeutic opportunity before the death of RGCs. Thus, the search for effective treatments for various optic neuropathies before there is permanent damage to prevent or limit visual dysfunction and the development of methods to stimulate axon and/or RGC regeneration to restore vision after damage has occurred is pivotal.This reprint collected 19 articles published in this Special Issue of IJMS which covers the molecular mechanisms to protect RGCs and/or axonal damage, translational research, gene therapy, regenerative medicine, and neuroprotection for glaucoma. 
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653 |a glaucoma 
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653 |a NMO 
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653 |a BID 
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653 |a erythropoietin 
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653 |a optic nerve protection 
653 |a neuromyelitis optica spectrum disease 
653 |a aquaporin-4 
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653 |a ocular coherence tomography 
653 |a complement 
653 |a microcystic macular degeneration 
653 |a Müller cell 
653 |a astrocyte 
653 |a oligodendrocyte 
653 |a microglia 
653 |a optic nerve head 
653 |a lamina cribrosa 
653 |a lamina cribrosa cells 
653 |a scleral fibroblasts 
653 |a glial cells 
653 |a intraocular pressure 
653 |a rat anterior ischemic optic neuropathy model 
653 |a retinal ganglion cell death 
653 |a TBP associated factor 9 
653 |a TP53 regulated inhibitor of apoptosis 1 
653 |a transcriptome 
653 |a optic nerve 
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653 |a MOG 
653 |a MS prevention 
653 |a retina 
653 |a transcription 
653 |a CNS repair 
653 |a oncomodulin 
653 |a myeloid cells 
653 |a glaucomatous optic neuropathy 
653 |a fibrosis 
653 |a miR-29 
653 |a extracellular matrix 
653 |a optic nerve crush 
653 |a azithromycin 
653 |a NAION 
653 |a neural injury 
653 |a neural ischemia 
653 |a neural inflammation 
653 |a Leber's hereditary optic neuropathy 
653 |a LHON 
653 |a whole exome sequencing 
653 |a nuclear modifier genes 
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653 |a mitochondrial disorder 
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653 |a ischemic optic neuropathy 
653 |a pioglitazone 
653 |a HSF1 
653 |a Klf4 
653 |a Oct4 
653 |a Sox2 
653 |a Yamanaka factors 
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653 |a zebrafish 
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653 |a secondary degeneration 
653 |a oxidative stress 
653 |a DNA damage 
653 |a proliferation 
653 |a blood-brain barrier 
653 |a CNS injury 
653 |a optic nerve injury 
653 |a synaptamide 
653 |a A8 
653 |a axonal degeneration 
653 |a neuronal survival 
653 |a visual evoked potential 
653 |a n/a 
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