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Article: GABAA and GABAC (GABAA0r) receptors affect ocular growth and form-deprivation myopia

TitleGABA<inf>A</inf> and GABA<inf>C</inf> (GABA<inf>A0r</inf>) receptors affect ocular growth and form-deprivation myopia
Authors
KeywordsBicuculline
Ocular development
TPMPA
Chicks
Form-deprivation myopia
γ-Aminobutyric acid
Issue Date2005
Citation
Cutaneous and Ocular Toxicology, 2005, v. 24, n. 3, p. 187-196 How to Cite?
AbstractRoles of γ-aminobutyric acid (GABA) antagonists on the chick model of form-deprivation myopia (FDM) were investigated. Bicuculline (GABA ) or TPMPA (GABA ) was injected intravitreally (1 or 10 mg/mL) into the right eyes of chicks with or without FDM for 13 days. The contralateral eyes served as the control. The eye weight (EW), equatorial diameter (ED), ocular length (OL), axial length (AL), and refraction (RFN) were measured. Histological sections of the retina and sclera were measured, and changes in tissue thickness were compared. The EW, ED, OL, and AL of the FDM eyes went up by 13.1 ± 2.0% (n = 24, p < 0.001), 18.7 ± 2.0% (n = 24, p < 0.001), 7.2 ± 1.9% (n = 24, p < 0.001) and 5.1 ± 1.5% (n = 11, p < 0.05), respectively. Bicuculline and TPMPA significantly reversed these changes (p < 0.05) but not the OL at either concentration used. The RFN measurements confirmed this (n = 2-8, p < 0.01). The drugs have no effect on the retinal thickness but significantly reduced the thickness of cartilaginous scleral layer of chicks with or without FDM (n = 9-120, p < 0.05). Bicuculline and TPMPA reduced form-deprived as well as normal ocular growth. GABAergic-mediated mechanism may directly influence the growth, shape, and refractive state of the developing eye. Copyright © Taylor & Francis Inc. A A0r
Persistent Identifierhttp://hdl.handle.net/10722/298017
ISSN
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorLeung, C. K.S.-
dc.contributor.authorYeung, Chi Kong-
dc.contributor.authorChiang, S. W.Y.-
dc.contributor.authorChan, K. P.-
dc.contributor.authorPang, C. P.-
dc.contributor.authorLam, D. S.C.-
dc.date.accessioned2021-04-08T03:07:29Z-
dc.date.available2021-04-08T03:07:29Z-
dc.date.issued2005-
dc.identifier.citationCutaneous and Ocular Toxicology, 2005, v. 24, n. 3, p. 187-196-
dc.identifier.issn0731-3829-
dc.identifier.urihttp://hdl.handle.net/10722/298017-
dc.description.abstractRoles of γ-aminobutyric acid (GABA) antagonists on the chick model of form-deprivation myopia (FDM) were investigated. Bicuculline (GABA ) or TPMPA (GABA ) was injected intravitreally (1 or 10 mg/mL) into the right eyes of chicks with or without FDM for 13 days. The contralateral eyes served as the control. The eye weight (EW), equatorial diameter (ED), ocular length (OL), axial length (AL), and refraction (RFN) were measured. Histological sections of the retina and sclera were measured, and changes in tissue thickness were compared. The EW, ED, OL, and AL of the FDM eyes went up by 13.1 ± 2.0% (n = 24, p < 0.001), 18.7 ± 2.0% (n = 24, p < 0.001), 7.2 ± 1.9% (n = 24, p < 0.001) and 5.1 ± 1.5% (n = 11, p < 0.05), respectively. Bicuculline and TPMPA significantly reversed these changes (p < 0.05) but not the OL at either concentration used. The RFN measurements confirmed this (n = 2-8, p < 0.01). The drugs have no effect on the retinal thickness but significantly reduced the thickness of cartilaginous scleral layer of chicks with or without FDM (n = 9-120, p < 0.05). Bicuculline and TPMPA reduced form-deprived as well as normal ocular growth. GABAergic-mediated mechanism may directly influence the growth, shape, and refractive state of the developing eye. Copyright © Taylor & Francis Inc. A A0r-
dc.languageeng-
dc.relation.ispartofCutaneous and Ocular Toxicology-
dc.subjectBicuculline-
dc.subjectOcular development-
dc.subjectTPMPA-
dc.subjectChicks-
dc.subjectForm-deprivation myopia-
dc.subjectγ-Aminobutyric acid-
dc.titleGABA<inf>A</inf> and GABA<inf>C</inf> (GABA<inf>A0r</inf>) receptors affect ocular growth and form-deprivation myopia-
dc.typeArticle-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1081/CUS-200068620-
dc.identifier.scopuseid_2-s2.0-26444538977-
dc.identifier.volume24-
dc.identifier.issue3-
dc.identifier.spage187-
dc.identifier.epage196-
dc.identifier.eissn1532-2505-
dc.identifier.isiWOS:000232342900005-
dc.identifier.issnl0731-3829-

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