Editorial (Thematic issue: Possible Therapeutic Targets for the Treatment of Diabetic Retinopathy: Evidences from Experimental Models)

2013 ◽  
Vol 8 (4) ◽  
pp. 265-265
Author(s):  
Jacqueline Lopes de Faria ◽  
Diego Duarte
2020 ◽  
Vol 19 (10) ◽  
pp. 102636
Author(s):  
Samuel Deshayes ◽  
Hubert de Boysson ◽  
Anaël Dumont ◽  
Denis Vivien ◽  
Alain Manrique ◽  
...  

2019 ◽  
Vol 28 (153) ◽  
pp. 190096 ◽  
Author(s):  
Ridhima Wadhwa ◽  
Kamal Dua ◽  
Ian M. Adcock ◽  
Jay C. Horvat ◽  
Richard Y. Kim ◽  
...  

Severe steroid-resistant asthma is clinically important, as patients with this form of the disease do not respond to mainstay corticosteroid therapies. The heterogeneity of this form of asthma and poor understanding of the pathological mechanisms involved hinder the identification of therapeutic targets and the development of more effective therapies. A major limiting factor in the understanding of severe steroid-resistant asthma is the existence of multiple endotypes represented by different immunological and inflammatory phenotypes, particularly in adults. Several clinical and experimental studies have revealed associations between specific respiratory infections and steroid-resistant asthma in adults. Here, we discuss recent findings from other authors as well as our own studies that have developed novel experimental models for interrogating the association between respiratory infections and severe steroid-resistant asthma. These models have enabled the identification of new therapies using macrolides, as well as several novel disease mechanisms, including the microRNA-21/phosphoinositide 3-kinase/histone deacetylase 2 axis and NLRP3 inflammasomes, and highlight the potential of these mechanisms as therapeutic targets.


2014 ◽  
Vol 2014 ◽  
pp. 1-18 ◽  
Author(s):  
Sher Zaman Safi ◽  
Rajes Qvist ◽  
Selva Kumar ◽  
Kalaivani Batumalaie ◽  
Ikram Shah Bin Ismail

The growing number of people with diabetes worldwide suggests that diabetic retinopathy (DR) and diabetic macular edema (DME) will continue to be sight threatening factors. The pathogenesis of diabetic retinopathy is a widespread cause of visual impairment in the world and a range of hyperglycemia-linked pathways have been implicated in the initiation and progression of this condition. Despite understanding the polyol pathway flux, activation of protein kinase C (KPC) isoforms, increased hexosamine pathway flux, and increased advanced glycation end-product (AGE) formation, pathogenic mechanisms underlying diabetes induced vision loss are not fully understood. The purpose of this paper is to review molecular mechanisms that regulate cell survival and apoptosis of retinal cells and discuss new and exciting therapeutic targets with comparison to the old and inefficient preventive strategies. This review highlights the recent advancements in understanding hyperglycemia-induced biochemical and molecular alterations, systemic metabolic factors, and aberrant activation of signaling cascades that ultimately lead to activation of a number of transcription factors causing functional and structural damage to retinal cells. It also reviews the established interventions and emerging molecular targets to avert diabetic retinopathy and its associated risk factors.


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