Influence of triamcinolone intravitreal injection on retinochoroidal healing processes
To analyze the effects of triamcinolone intravitreal injection on the wound healing processes after argon laser retinal photocoagulation, wild type C57BL/6J mice, 8–12 weeks old underwent a standard argon laser photocoagulation protocol. After pentobarbital anesthesia and pupil dilatation, argon las...
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Published in | Experimental eye research Vol. 84; no. 6; pp. 1081 - 1089 |
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Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
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England
Elsevier Ltd
01.06.2007
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Abstract | To analyze the effects of triamcinolone intravitreal injection on the wound healing processes after argon laser retinal photocoagulation, wild type C57BL/6J mice, 8–12
weeks old underwent a standard argon laser photocoagulation protocol. After pentobarbital anesthesia and pupil dilatation, argon laser lesions were induced (50
μm, 400
mW, 0.05
s). Two photocoagulation impacts created two disc diameters from the optic nerve in both eyes. The photocoagulated mice were divided into four groups: Group I (
n
=
12), photocoagulation controls, did not receive any intravitreous injection. Group II (
n
=
12), received an intravitreous injection of 1
μl of balanced salt solution (BSS). Group III (
n
=
12), received an intravitreous injection of 1
μl containing 15
μg of triamcinolone acetonide (TAAC) in BSS. Two mice from each of these three groups were sacrificed at 1, 3, 7, 14
days and 2 and 4
months after photocoagulation. Group IV (
n
=
10) received 1.5, 3, 7.5, 15, or 30
μg of TAAC and were all sacrificed on day 14. The enucleated eyes were subjected to systematic analysis of the cellular remodeling processes taking place within the laser lesion and its vicinity. To this purpose, specific antibodies against GFAP, von Willebrand factor, F4/80 and KI67 were used for the detection of astrocytes, activated Müller cells, vascular endothelial cells, infiltrating inflammatory cells and actively proliferating cells. TUNEL reaction was also carried out along with nuclear DAPI staining. Temporal and spatial observations of the created photocoagulation lesions demonstrate that 24
h following the argon laser beam, a localized and well-delineated affection of the RPE cells and choroid is observed in mice in Groups I and II. The inner retinal layers in these mice eyes are preserved while TUNEL positive (apoptotic) cells are observed at the retinal outer nuclear layer level. At this stage, intense staining with GFAP is associated with activated retinal astrocytes and Müller cells throughout the laser path. From day 3 after photocoagulation, dilated new choroidal capillaries are detected on the edges of the laser lesion. These processes are accompanied by infiltration of inflammatory cells and the presence of proliferating cells within the lesion site. Mice in Group III treated with 15
μg/μl of triamcinolone showed a decreased number of infiltrating inflammatory cells and proliferating cells, which was not statistically significant compared to uninjected laser treated controls. The development of new choroidal capillaries on the edges of the laser lesion was also inhibited during the first 2
months after photocoagulation. However, on month 4 the growth of new vessels was observed in these mice treated with TAAC. Mice of Group IV did not show any development of new capillaries even with small doses. After argon laser photocoagulation of the mouse eye, intravitreal injection of triamcinolone markedly influenced the retina and choroid remodeling and healing processes. Triamcinolone is a powerful inhibitor of the formation of neovessels in this model. However, this inhibition is transient. These observations should provide a practical insight for the mode of TAAC use in patients with wet AMD. |
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AbstractList | To analyze the effects of triamcinolone intravitreal injection on the wound healing processes after argon laser retinal photocoagulation, wild type C57BL/6J mice, 8–12
weeks old underwent a standard argon laser photocoagulation protocol. After pentobarbital anesthesia and pupil dilatation, argon laser lesions were induced (50
μm, 400
mW, 0.05
s). Two photocoagulation impacts created two disc diameters from the optic nerve in both eyes. The photocoagulated mice were divided into four groups: Group I (
n
=
12), photocoagulation controls, did not receive any intravitreous injection. Group II (
n
=
12), received an intravitreous injection of 1
μl of balanced salt solution (BSS). Group III (
n
=
12), received an intravitreous injection of 1
μl containing 15
μg of triamcinolone acetonide (TAAC) in BSS. Two mice from each of these three groups were sacrificed at 1, 3, 7, 14
days and 2 and 4
months after photocoagulation. Group IV (
n
=
10) received 1.5, 3, 7.5, 15, or 30
μg of TAAC and were all sacrificed on day 14. The enucleated eyes were subjected to systematic analysis of the cellular remodeling processes taking place within the laser lesion and its vicinity. To this purpose, specific antibodies against GFAP, von Willebrand factor, F4/80 and KI67 were used for the detection of astrocytes, activated Müller cells, vascular endothelial cells, infiltrating inflammatory cells and actively proliferating cells. TUNEL reaction was also carried out along with nuclear DAPI staining. Temporal and spatial observations of the created photocoagulation lesions demonstrate that 24
h following the argon laser beam, a localized and well-delineated affection of the RPE cells and choroid is observed in mice in Groups I and II. The inner retinal layers in these mice eyes are preserved while TUNEL positive (apoptotic) cells are observed at the retinal outer nuclear layer level. At this stage, intense staining with GFAP is associated with activated retinal astrocytes and Müller cells throughout the laser path. From day 3 after photocoagulation, dilated new choroidal capillaries are detected on the edges of the laser lesion. These processes are accompanied by infiltration of inflammatory cells and the presence of proliferating cells within the lesion site. Mice in Group III treated with 15
μg/μl of triamcinolone showed a decreased number of infiltrating inflammatory cells and proliferating cells, which was not statistically significant compared to uninjected laser treated controls. The development of new choroidal capillaries on the edges of the laser lesion was also inhibited during the first 2
months after photocoagulation. However, on month 4 the growth of new vessels was observed in these mice treated with TAAC. Mice of Group IV did not show any development of new capillaries even with small doses. After argon laser photocoagulation of the mouse eye, intravitreal injection of triamcinolone markedly influenced the retina and choroid remodeling and healing processes. Triamcinolone is a powerful inhibitor of the formation of neovessels in this model. However, this inhibition is transient. These observations should provide a practical insight for the mode of TAAC use in patients with wet AMD. To analyze the effects of triamcinolone intravitreal injection on the wound healing processes after argon laser retinal photocoagulation, wild type C57BL/6J mice, 8-12 weeks old underwent a standard argon laser photocoagulation protocol. After pentobarbital anesthesia and pupil dilatation, argon laser lesions were induced (50microm, 400mW, 0.05s). Two photocoagulation impacts created two disc diameters from the optic nerve in both eyes. The photocoagulated mice were divided into four groups: Group I (n=12), photocoagulation controls, did not receive any intravitreous injection. Group II (n=12), received an intravitreous injection of 1microl of balanced salt solution (BSS). Group III (n=12), received an intravitreous injection of 1microl containing 15microg of triamcinolone acetonide (TAAC) in BSS. Two mice from each of these three groups were sacrificed at 1, 3, 7, 14 days and 2 and 4 months after photocoagulation. Group IV (n=10) received 1.5, 3, 7.5, 15, or 30microg of TAAC and were all sacrificed on day 14. The enucleated eyes were subjected to systematic analysis of the cellular remodeling processes taking place within the laser lesion and its vicinity. To this purpose, specific antibodies against GFAP, von Willebrand factor, F4/80 and KI67 were used for the detection of astrocytes, activated Müller cells, vascular endothelial cells, infiltrating inflammatory cells and actively proliferating cells. TUNEL reaction was also carried out along with nuclear DAPI staining. Temporal and spatial observations of the created photocoagulation lesions demonstrate that 24h following the argon laser beam, a localized and well-delineated affection of the RPE cells and choroid is observed in mice in Groups I and II. The inner retinal layers in these mice eyes are preserved while TUNEL positive (apoptotic) cells are observed at the retinal outer nuclear layer level. At this stage, intense staining with GFAP is associated with activated retinal astrocytes and Müller cells throughout the laser path. From day 3 after photocoagulation, dilated new choroidal capillaries are detected on the edges of the laser lesion. These processes are accompanied by infiltration of inflammatory cells and the presence of proliferating cells within the lesion site. Mice in Group III treated with 15microg/mul of triamcinolone showed a decreased number of infiltrating inflammatory cells and proliferating cells, which was not statistically significant compared to uninjected laser treated controls. The development of new choroidal capillaries on the edges of the laser lesion was also inhibited during the first 2 months after photocoagulation. However, on month 4 the growth of new vessels was observed in these mice treated with TAAC. Mice of Group IV did not show any development of new capillaries even with small doses. After argon laser photocoagulation of the mouse eye, intravitreal injection of triamcinolone markedly influenced the retina and choroid remodeling and healing processes. Triamcinolone is a powerful inhibitor of the formation of neovessels in this model. However, this inhibition is transient. These observations should provide a practical insight for the mode of TAAC use in patients with wet AMD. |
Author | Dot, C. May, F. Doat, M. Behar-Cohen, F. Jonet, L. BenEzra, D. Jeanny, J.C. |
Author_xml | – sequence: 1 givenname: C. surname: Dot fullname: Dot, C. organization: U598 INSERM, Physiopathologie des Maladies Oculaires: Innovations Thérapeutiques, Institut Biomédical des Cordeliers, 15 Rue de l'Ecole de Médecine, 75270 Paris Cedex 06, France – sequence: 2 givenname: F. surname: Behar-Cohen fullname: Behar-Cohen, F. organization: U598 INSERM, Physiopathologie des Maladies Oculaires: Innovations Thérapeutiques, Institut Biomédical des Cordeliers, 15 Rue de l'Ecole de Médecine, 75270 Paris Cedex 06, France – sequence: 3 givenname: D. surname: BenEzra fullname: BenEzra, D. organization: U598 INSERM, Physiopathologie des Maladies Oculaires: Innovations Thérapeutiques, Institut Biomédical des Cordeliers, 15 Rue de l'Ecole de Médecine, 75270 Paris Cedex 06, France – sequence: 4 givenname: M. surname: Doat fullname: Doat, M. organization: U598 INSERM, Physiopathologie des Maladies Oculaires: Innovations Thérapeutiques, Institut Biomédical des Cordeliers, 15 Rue de l'Ecole de Médecine, 75270 Paris Cedex 06, France – sequence: 5 givenname: L. surname: Jonet fullname: Jonet, L. organization: U598 INSERM, Physiopathologie des Maladies Oculaires: Innovations Thérapeutiques, Institut Biomédical des Cordeliers, 15 Rue de l'Ecole de Médecine, 75270 Paris Cedex 06, France – sequence: 6 givenname: F. surname: May fullname: May, F. organization: Service d'Ophtalmologie, Hôpital d'Instruction des Armées Legouest, Metz, France – sequence: 7 givenname: J.C. surname: Jeanny fullname: Jeanny, J.C. email: jcjeanny@infobiogen.fr organization: U598 INSERM, Physiopathologie des Maladies Oculaires: Innovations Thérapeutiques, Institut Biomédical des Cordeliers, 15 Rue de l'Ecole de Médecine, 75270 Paris Cedex 06, France |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/17408616$$D View this record in MEDLINE/PubMed |
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Keywords | retinal remodeling wound healing laser photocoagulation corticosteroids choroidal neovascularization triamcinolone |
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SubjectTerms | Animals Anti-Inflammatory Agents - pharmacology Anti-Inflammatory Agents - therapeutic use Apoptosis - drug effects Cell Proliferation - drug effects choroidal neovascularization Choroidal Neovascularization - etiology Choroidal Neovascularization - prevention & control corticosteroids Disease Models, Animal Dose-Response Relationship, Drug Drug Evaluation, Preclinical Female Glucocorticoids - pharmacology Glucocorticoids - therapeutic use In Situ Nick-End Labeling Laser Coagulation laser photocoagulation Mice Mice, Inbred C57BL retinal remodeling triamcinolone Triamcinolone Acetonide - pharmacology Triamcinolone Acetonide - therapeutic use wound healing Wound Healing - drug effects |
Title | Influence of triamcinolone intravitreal injection on retinochoroidal healing processes |
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