Combination of Neuroprotective and Regenerative Agents for AGE-Induced Retinal Degeneration: In Vitro Study

To determine the most effective combination of neuroprotective and regenerative agents for cultured retinal neurons from advanced glycation end products- (AGEs-) induced degeneration, retinal explants of 7 adult Sprague-Dawley rats were three-dimensionally cultured in collagen gel and incubated in s...

Full description

Bibliographic Details
Main Authors: Guzel Bikbova, Toshiyuki Oshitari, Takayuki Baba, Shuichi Yamamoto
Format: Article
Language:English
Published: Hindawi Limited 2017-01-01
Series:BioMed Research International
Online Access:http://dx.doi.org/10.1155/2017/8604723
id doaj-d532d30b3cfa497aaa46d4f3470ac836
record_format Article
spelling doaj-d532d30b3cfa497aaa46d4f3470ac8362020-11-25T00:15:32ZengHindawi LimitedBioMed Research International2314-61332314-61412017-01-01201710.1155/2017/86047238604723Combination of Neuroprotective and Regenerative Agents for AGE-Induced Retinal Degeneration: In Vitro StudyGuzel Bikbova0Toshiyuki Oshitari1Takayuki Baba2Shuichi Yamamoto3Department of Ophthalmology and Visual Science, Chiba University Graduate School of Medicine, Inohana 1-8-1, Chuo-ku, Chiba, Chiba Prefecture 260-8670, JapanDepartment of Ophthalmology and Visual Science, Chiba University Graduate School of Medicine, Inohana 1-8-1, Chuo-ku, Chiba, Chiba Prefecture 260-8670, JapanDepartment of Ophthalmology and Visual Science, Chiba University Graduate School of Medicine, Inohana 1-8-1, Chuo-ku, Chiba, Chiba Prefecture 260-8670, JapanDepartment of Ophthalmology and Visual Science, Chiba University Graduate School of Medicine, Inohana 1-8-1, Chuo-ku, Chiba, Chiba Prefecture 260-8670, JapanTo determine the most effective combination of neuroprotective and regenerative agents for cultured retinal neurons from advanced glycation end products- (AGEs-) induced degeneration, retinal explants of 7 adult Sprague-Dawley rats were three-dimensionally cultured in collagen gel and incubated in serum-free media and in 7 media; namely, AGEs, AGEs + 100 μM citicoline, AGEs + 10 ng/mL NT-4, AGEs + 100 μM TUDCA, AGEs + 100 μM citicoline + TUDCA (doublet), and AGEs + 100 μM citicoline + TUDCA + 10 ng/mL NT-4 (triplet) were examined. The number of regenerating neurites was counted after 7 days of culture, followed by performing TUNEL and DAPI staining. The ratio of TUNEL-positive cells to the number of DAPI-stained nuclei was calculated. Immunohistochemical examinations for the active form of caspase-9 and JNK were performed. All of the neuroprotectants increased the number of neurites and decreased the number of TUNEL-positive cells. However, the number of neurites was significantly higher, and the number of TUNEL-positive cells and caspase-9- and JNK-immunopositive cells was fewer in the retinas incubated with the combined three agents. Combination solutions containing citicoline, TUDCA, and NT-4 should be considered for neuroprotective and regenerative therapy for AGE-related retinal degeneration.http://dx.doi.org/10.1155/2017/8604723
collection DOAJ
language English
format Article
sources DOAJ
author Guzel Bikbova
Toshiyuki Oshitari
Takayuki Baba
Shuichi Yamamoto
spellingShingle Guzel Bikbova
Toshiyuki Oshitari
Takayuki Baba
Shuichi Yamamoto
Combination of Neuroprotective and Regenerative Agents for AGE-Induced Retinal Degeneration: In Vitro Study
BioMed Research International
author_facet Guzel Bikbova
Toshiyuki Oshitari
Takayuki Baba
Shuichi Yamamoto
author_sort Guzel Bikbova
title Combination of Neuroprotective and Regenerative Agents for AGE-Induced Retinal Degeneration: In Vitro Study
title_short Combination of Neuroprotective and Regenerative Agents for AGE-Induced Retinal Degeneration: In Vitro Study
title_full Combination of Neuroprotective and Regenerative Agents for AGE-Induced Retinal Degeneration: In Vitro Study
title_fullStr Combination of Neuroprotective and Regenerative Agents for AGE-Induced Retinal Degeneration: In Vitro Study
title_full_unstemmed Combination of Neuroprotective and Regenerative Agents for AGE-Induced Retinal Degeneration: In Vitro Study
title_sort combination of neuroprotective and regenerative agents for age-induced retinal degeneration: in vitro study
publisher Hindawi Limited
series BioMed Research International
issn 2314-6133
2314-6141
publishDate 2017-01-01
description To determine the most effective combination of neuroprotective and regenerative agents for cultured retinal neurons from advanced glycation end products- (AGEs-) induced degeneration, retinal explants of 7 adult Sprague-Dawley rats were three-dimensionally cultured in collagen gel and incubated in serum-free media and in 7 media; namely, AGEs, AGEs + 100 μM citicoline, AGEs + 10 ng/mL NT-4, AGEs + 100 μM TUDCA, AGEs + 100 μM citicoline + TUDCA (doublet), and AGEs + 100 μM citicoline + TUDCA + 10 ng/mL NT-4 (triplet) were examined. The number of regenerating neurites was counted after 7 days of culture, followed by performing TUNEL and DAPI staining. The ratio of TUNEL-positive cells to the number of DAPI-stained nuclei was calculated. Immunohistochemical examinations for the active form of caspase-9 and JNK were performed. All of the neuroprotectants increased the number of neurites and decreased the number of TUNEL-positive cells. However, the number of neurites was significantly higher, and the number of TUNEL-positive cells and caspase-9- and JNK-immunopositive cells was fewer in the retinas incubated with the combined three agents. Combination solutions containing citicoline, TUDCA, and NT-4 should be considered for neuroprotective and regenerative therapy for AGE-related retinal degeneration.
url http://dx.doi.org/10.1155/2017/8604723
work_keys_str_mv AT guzelbikbova combinationofneuroprotectiveandregenerativeagentsforageinducedretinaldegenerationinvitrostudy
AT toshiyukioshitari combinationofneuroprotectiveandregenerativeagentsforageinducedretinaldegenerationinvitrostudy
AT takayukibaba combinationofneuroprotectiveandregenerativeagentsforageinducedretinaldegenerationinvitrostudy
AT shuichiyamamoto combinationofneuroprotectiveandregenerativeagentsforageinducedretinaldegenerationinvitrostudy
_version_ 1725386355353059328