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Article: Neurovascular unit in diabetic retinopathy: pathophysiological roles and potential therapeutical targets

TitleNeurovascular unit in diabetic retinopathy: pathophysiological roles and potential therapeutical targets
Authors
KeywordsDiabetic retinopathy
Neurovascular unit
Neurodegeneration
Gliosis
Inflammation
Treatment
Issue Date2021
PublisherBioMed Central Ltd. The Journal's web site is located at https://eandv.biomedcentral.com/
Citation
Eye and Vision, 2021, v. 8, article no. 15 How to Cite?
AbstractDiabetic retinopathy (DR), one of the common complications of diabetes, is the leading cause of visual loss in working-age individuals in many industrialized countries. It has been traditionally regarded as a purely microvascular disease in the retina. However, an increasing number of studies have shown that DR is a complex neurovascular disorder that affects not only vascular structure but also neural tissue of the retina. Deterioration of neural retina could precede microvascular abnormalities in the DR, leading to microvascular changes. Furthermore, disruption of interactions among neurons, vascular cells, glia and local immune cells, which collectively form the neurovascular unit, is considered to be associated with the progression of DR early on in the disease. Therefore, it makes sense to develop new therapeutic strategies to prevent or reverse retinal neurodegeneration, neuroinflammation and impaired cell-cell interactions of the neurovascular unit in early stage DR. Here, we present current perspectives on the pathophysiology of DR as a neurovascular disease, especially at the early stage. Potential novel treatments for preventing or reversing neurovascular injuries in DR are discussed as well.
Persistent Identifierhttp://hdl.handle.net/10722/307600
ISSN
PubMed Central ID
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorNian, S-
dc.contributor.authorLo, ACY-
dc.contributor.authorMi, Y-
dc.contributor.authorRen, K-
dc.contributor.authorYang, D-
dc.date.accessioned2021-11-12T13:34:58Z-
dc.date.available2021-11-12T13:34:58Z-
dc.date.issued2021-
dc.identifier.citationEye and Vision, 2021, v. 8, article no. 15-
dc.identifier.issn2326-0246-
dc.identifier.urihttp://hdl.handle.net/10722/307600-
dc.description.abstractDiabetic retinopathy (DR), one of the common complications of diabetes, is the leading cause of visual loss in working-age individuals in many industrialized countries. It has been traditionally regarded as a purely microvascular disease in the retina. However, an increasing number of studies have shown that DR is a complex neurovascular disorder that affects not only vascular structure but also neural tissue of the retina. Deterioration of neural retina could precede microvascular abnormalities in the DR, leading to microvascular changes. Furthermore, disruption of interactions among neurons, vascular cells, glia and local immune cells, which collectively form the neurovascular unit, is considered to be associated with the progression of DR early on in the disease. Therefore, it makes sense to develop new therapeutic strategies to prevent or reverse retinal neurodegeneration, neuroinflammation and impaired cell-cell interactions of the neurovascular unit in early stage DR. Here, we present current perspectives on the pathophysiology of DR as a neurovascular disease, especially at the early stage. Potential novel treatments for preventing or reversing neurovascular injuries in DR are discussed as well.-
dc.languageeng-
dc.publisherBioMed Central Ltd. The Journal's web site is located at https://eandv.biomedcentral.com/-
dc.relation.ispartofEye and Vision-
dc.rightsThis work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.-
dc.subjectDiabetic retinopathy-
dc.subjectNeurovascular unit-
dc.subjectNeurodegeneration-
dc.subjectGliosis-
dc.subjectInflammation-
dc.subjectTreatment-
dc.titleNeurovascular unit in diabetic retinopathy: pathophysiological roles and potential therapeutical targets-
dc.typeArticle-
dc.identifier.emailLo, ACY: amylo@hku.hk-
dc.identifier.authorityLo, ACY=rp00425-
dc.description.naturepublished_or_final_version-
dc.identifier.doi10.1186/s40662-021-00239-1-
dc.identifier.pmid33931128-
dc.identifier.pmcidPMC8088070-
dc.identifier.hkuros329665-
dc.identifier.volume8-
dc.identifier.spagearticle no. 15-
dc.identifier.epagearticle no. 15-
dc.identifier.isiWOS:000645908000002-
dc.publisher.placeUnited Kingdom-

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