PURPOSE: To investigate the involvement of glial cells in the autoregulation of optic nerve head (ONH) blood flow in response to elevated intraocular pressure (IOP). METHODS: Rabbit eyes were treated with an intravitreal injection of l-2-aminoadipic acid (LAA), a gliotoxic compound. Twenty-four hours after the injection IOP was artificially elevated from a baseline of 20 to 50 or 70 mm Hg and maintained at each IOP level for 30 minutes. ONH blood flow was measured by laser speckle flowgraphy every 10 minutes. Ocular perfusion pressure (OPP) was calculated to investigate the relationship between ONH blood flow and OPP. To evaluate the effects of LAA on the function and morphology of retinal neurons and glial cells, electroretinogram (ERG) was monitored after injections of LAA (2.0 and 6.0 mM) or saline as a control. Histologic and immunohistochemical examinations were then performed. RESULTS: In the LAA-treated eyes, histologic changes selectively occurred in the retinal Müller cells and ONH astrocytes. There was not any significant reduction of amplitude or elongation of implicit time of each parameter in the ERG after LAA injection compared with control. ONH blood flow in LAA-treated eyes was significantly decreased with a reduction of OPP during IOP elevation to 50 and 70 mm Hg, whereas blood flow was maintained in control eyes during IOP elevation to 50 mm Hg. CONCLUSIONS: These results indicate the involvement of glial ells in the autoregulation of ONH blood flow during IOP elevation.
PURPOSE: To investigate the involvement of glial cells in the autoregulation of optic nerve head (ONH) blood flow in response to elevated intraocular pressure (IOP). METHODS:Rabbit eyes were treated with an intravitreal injection of l-2-aminoadipic acid (LAA), a gliotoxic compound. Twenty-four hours after the injection IOP was artificially elevated from a baseline of 20 to 50 or 70 mm Hg and maintained at each IOP level for 30 minutes. ONH blood flow was measured by laser speckle flowgraphy every 10 minutes. Ocular perfusion pressure (OPP) was calculated to investigate the relationship between ONH blood flow and OPP. To evaluate the effects of LAA on the function and morphology of retinal neurons and glial cells, electroretinogram (ERG) was monitored after injections of LAA (2.0 and 6.0 mM) or saline as a control. Histologic and immunohistochemical examinations were then performed. RESULTS: In the LAA-treated eyes, histologic changes selectively occurred in the retinal Müller cells and ONH astrocytes. There was not any significant reduction of amplitude or elongation of implicit time of each parameter in the ERG after LAA injection compared with control. ONH blood flow in LAA-treated eyes was significantly decreased with a reduction of OPP during IOP elevation to 50 and 70 mm Hg, whereas blood flow was maintained in control eyes during IOP elevation to 50 mm Hg. CONCLUSIONS: These results indicate the involvement of glial ells in the autoregulation of ONH blood flow during IOP elevation.
Authors: Guodong Liu; Hui Li; Grant Cull; Laura Wilsey; Hongli Yang; Jesica Reemmer; Hai-Ying Shen; Fang Wang; Brad Fortune; Bang V Bui; Lin Wang Journal: Invest Ophthalmol Vis Sci Date: 2021-01-04 Impact factor: 4.799
Authors: Agnes Boltz; Reinhard Told; Katarzyna J Napora; Stefan Palkovits; René M Werkmeister; Doreen Schmidl; Alina Popa-Cherecheanu; Gerhard Garhöfer; Leopold Schmetterer Journal: PLoS One Date: 2013-12-06 Impact factor: 3.240
Authors: Katarzyna J Witkowska; Ahmed M Bata; Giacomo Calzetti; Nikolaus Luft; Klemens Fondi; Piotr A Wozniak; Doreen Schmidl; Matthias Bolz; Alina Popa-Cherecheanu; René M Werkmeister; Gerhard Garhöfer; Leopold Schmetterer Journal: PLoS One Date: 2017-09-12 Impact factor: 3.240