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Brain derived neurotrophic factor keeps pattern electroretinogram from dropping after superior colliculus lesion in
Bin-Bin Yang1, Xu Yang2, Huai-Yu Ding3
1Department of Ophthalmology, the 2nd Affiliated Hospital of Harbin Medical University, Department of Ophthalmology Key Laboratory, Harbin Medical University, Harbin 150001, Heilongjiang Province, China.
Brain-derived neurotrophic factor (BDNF) protects retinal ganglion cells after superior colliculus lesions. Exogenous BDNF can help maintain retinal function in neurodegenerative diseases.
Area of Science:
- Neuroscience
- Ophthalmology
- Cell Biology
Background:
- Retinal ganglion cells (RGCs) are crucial for vision.
- Damage to the superior colliculus (SC) can impact RGCs.
- Brain-derived neurotrophic factor (BDNF) plays a role in neuronal survival and function.
Purpose of the Study:
- To investigate the protective effects of BDNF on RGCs following SC lesions in mice.
- To assess RGC function and retinal health using electrophysiology and imaging.
Main Methods:
- Seven C57BL/6J mice received BDNF.
- Pattern electroretinogram (PERG) and optical coherence tomography (OCT) were used.
- Measurements were taken before and after SC lesions.
Main Results:
- PERG amplitude decreased slightly but not significantly post-lesion.
- Fast Fourier Transform (FFT) analysis of PERGs indicated stable dominant frequencies.
- OCT revealed no significant changes in retinal thickness.
Conclusions:
- BDNF is vital for normal retinal function.
- External BDNF sources can protect retinas lacking endogenous BDNF.
- BDNF shows therapeutic potential for retinal neurodegenerative diseases like glaucoma.
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