Abstract:The process of wound healing of the avascular outer layers of the retina is studied on a series of Laser lcsions of the monkey, Ccrc.oliitl/fr.ilt;~~~~.~ uelhio/).s. T h e extent of the retinal lesions is limited to thc pigment epithelium and photoreceptor cells, whereas Bruch's membrane anti the vascular inner layers of the retina remain intact. The retinal lesions arc not seen to be invaded by cells from the chortiid. nor from the retinal vessels. During the first three days after irradiation the pigment epi… Show more
“…Clinical and histological works have elucidated the changes following experimental induced damage to the pigment epithelium in vivo (Noell 1973;Nilsson et al 1977;Zinn & Marmor 1979;Ts'o et al 1977;Friedman & Kuwabara 1968;Bulow 1978;Armstrong et al 1978).…”
Explants from the retinal pigment epithelium and the underlying choroid and sclera were dissected from human eyes and transferred to culture wells. The mechanical trauma caused by the dissection and removal of the explants, and the changes in biological milieu caused by transfer of the tissue to an in vitro system causes injury, necrosis and detachment of cells from Bruch's membrane. In the retinal pigment epithelium, cells adjacent to damaged, spherical and detaching cells and smaller cell free zones from rosettes. At the periphery of big defects, the cells spread out to cover the denuded areas of Bruch's membrane. The present work has shown that cell injury in the human retinal pigment epithelium is followed by reactive cellular changes in vitro. The result of these reactive changes are increased variation in cellular form and magnitude and in pigment concentration per unit area.
“…Clinical and histological works have elucidated the changes following experimental induced damage to the pigment epithelium in vivo (Noell 1973;Nilsson et al 1977;Zinn & Marmor 1979;Ts'o et al 1977;Friedman & Kuwabara 1968;Bulow 1978;Armstrong et al 1978).…”
Explants from the retinal pigment epithelium and the underlying choroid and sclera were dissected from human eyes and transferred to culture wells. The mechanical trauma caused by the dissection and removal of the explants, and the changes in biological milieu caused by transfer of the tissue to an in vitro system causes injury, necrosis and detachment of cells from Bruch's membrane. In the retinal pigment epithelium, cells adjacent to damaged, spherical and detaching cells and smaller cell free zones from rosettes. At the periphery of big defects, the cells spread out to cover the denuded areas of Bruch's membrane. The present work has shown that cell injury in the human retinal pigment epithelium is followed by reactive cellular changes in vitro. The result of these reactive changes are increased variation in cellular form and magnitude and in pigment concentration per unit area.
“…The reduction in EOG after photocoagulation of diabetic retinopathy appears to remain at an unchanged low level, being also found 6-8 weeks after the treatment, at a time when the healing processes after photocoagulation have usually been completed as demonstrated in animal experiments by Bulow (1978). The EOG itself is due predominantly to a difference in potential over the pigment epithelium and a change in this potential during adaptation from dark to light.…”
Ten patients with bilateral, proliferative diabetic retinopathy and normal visual acuity in both eyes received photocoagulation in one eye by argon-laser. Electrooculography (EOG) was performed on the day before, the day after, and 6-8 weeks after the photocoagulation. The pre-treatment Arden coefficient was reduced in all patients. After the photocoagulation an immediate reduction in the Arden coefficient occurred remaining unchanged for 6-8 weeks after treatment. The untreated eye showed an unchanged Arden coefficient during the observation period, not differing from the EOG in the treated eye before the photocoagulation.The object of this study was to demonstrate a possible effect, temporary or permanent, of panretinal photocoagulation upon the EOG. It is known that the EOG mainly reflects changes in the potential over the pigment epithlium (Noel1 1952; Brown & Wiesel 1958). Since the light energy applied in photocoagulation is absorbed to a marked extent as heat in the pigment epithelium, leaving histological changes ( Tso et al. 1977; Biilow 1978), we investigated possible alterations in potential over the pigment epithelium at photocoagulation as reflected indirectly by the EOG. This problem has previously been studied by Francois et al. (1978) who found a fall in the EOG after photocoagulation. In their material, however, the EOG was normal in only 7 out of 50 cases prior to photocoagulation, and the EOG was not related to the value in the untreated eye. In our opinion this should be done in a group of patients who seem to develop a spontaneous drop in the EOG.
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