Differential vulnerability of neurochemically identified subpopulations of retinal neurons in a monkey model of glaucoma
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2021, Experimental Eye ResearchWho's lost first? Susceptibility of retinal ganglion cell types in experimental glaucoma
2017, Experimental Eye ResearchQuantitative measurement of retinal ganglion cell populations via histology-based random forest classification
2016, Experimental Eye ResearchCitation Excerpt :The question of whether or not specific RGC sub-types are preferentially susceptible to glaucomatous damage is of intense interest, but also controversial. Early work involving quantitative studies of Nissl-stained RGCs in a non-human primate model of glaucoma revealed that the larger cells that give rise to the magnocellular pathway are particularly vulnerable to apoptosis (Glovinsky et al., 1991; Vickers et al., 1995). Similar observations were subsequently made in some, but not all, follow-up studies with primate (Quigley, 1999; Morgan et al., 2000; Morgan, 2002) and human tissue (Quigley et al., 1989; Chaturvedi et al., 1993; Quigley, 1999).
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2013, NeuroscienceCitation Excerpt :However, reduction in IOP is frequently insufficient to prevent progression of visual field loss (Baltmr et al., 2010). Rather, glutamate-induced excitotoxicity has been suggested to play an important role in glaucoma by some investigators (Vickers et al., 1995; Brooks et al., 1997; Dkhissi et al., 1999; Nucci et al., 2005), while others have pointed out that the role of glutamate excitotoxicity in glaucoma remains elusive (Lotery, 2005). Glutamate is the major excitatory neurotransmitter released from bipolar cells onto ganglion cells in the vertebrate retina (Massey and Redburn, 1987; Copenhagen, 1991).