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Experimental hypoxia in human eyes: implications for ischaemic disease
Beatrix Feigl1, Ian Stewart, Brian Brown
1Institute of Health and Biomedical Innovation, Queensland University of Technology, Australia. b.feigl@qut.edu.au
Objective:
This study investigated neuroretinal activity under normoxic and hypoxic conditions with the multifocal electroretinogram (mfERG).
Methods:
We used two mfERG paradigms, the fast flicker and slow flash stimulation modes, to measure neuroretinal activity in five healthy participants who breathed room air and a reduced oxygen mixture (14% oxygen, balance nitrogen). We analysed concentric ring N1P1 and P1N2 response density amplitudes, the P1 implicit times as well as the local scalar product (SP) response densities.
Results:
During hypoxia there was a significant reduction of the scalar product response density for the fast flicker (p<0.001) and for the slow flash mfERG (p<0.001). The N1P1 and P1N2 response densities were lower especially for the central three rings; although these reductions were not significant between the two oxygen conditions, they indicated an overall distortion of the mfERG waveform.
Conclusions:
It is demonstrated that a post-receptoral, primarily ON and OFF bipolar cell deficit is evident in the central retina of healthy young people during short term hypoxia.
Significance:
Our findings suggest that persons with pre-existing ischaemic eye disease may be at risk when exposed to hypoxic conditions.
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