Antioxidant Effects of DPP-4 Inhibitors in Early Stages of Experimental Diabetic Retinopathy

Hyperglycemia-induced oxidative stress plays a key role in the impairment of the retinal neurovascular unit, an early event in the pathogenesis of DR. The aim of this study was to assess the antioxidant properties of topical administration (eye drops) of sitagliptin in the diabetic retina. For this...

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Main Authors: Hugo Ramos (Author), Patricia Bogdanov (Author), Jordi Huerta (Author), Anna Deàs-Just (Author), Cristina Hernández (Author), Rafael Simó (Author)
Format: Book
Published: MDPI AG, 2022-07-01T00:00:00Z.
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001 doaj_a935c9fdc8524c748c9bf0d15d0d71c5
042 |a dc 
100 1 0 |a Hugo Ramos  |e author 
700 1 0 |a Patricia Bogdanov  |e author 
700 1 0 |a Jordi Huerta  |e author 
700 1 0 |a Anna Deàs-Just  |e author 
700 1 0 |a Cristina Hernández  |e author 
700 1 0 |a Rafael Simó  |e author 
245 0 0 |a Antioxidant Effects of DPP-4 Inhibitors in Early Stages of Experimental Diabetic Retinopathy 
260 |b MDPI AG,   |c 2022-07-01T00:00:00Z. 
500 |a 10.3390/antiox11071418 
500 |a 2076-3921 
520 |a Hyperglycemia-induced oxidative stress plays a key role in the impairment of the retinal neurovascular unit, an early event in the pathogenesis of DR. The aim of this study was to assess the antioxidant properties of topical administration (eye drops) of sitagliptin in the diabetic retina. For this purpose, db/db mice received sitagliptin or vehicle eye drops twice per day for two weeks. Age-matched db/+ mice were used as the control group. We evaluated retinal mRNA (RT-PCR) and protein levels (Western blotting and immunohistochemistry) of different components from both the antioxidant system (NRF2, CAT, GPX, GR, CuZnSOD, and MnSOD) and the prooxidant machinery (PKC and TXNIP). We also studied superoxide levels (dihydroethidium staining) and oxidative damage to DNA/RNA (8-hydroxyguanosine immunostaining) and proteins (nitrotyrosine immunostaining). Finally, NF-кB translocation and IL-1β production were assessed through Western blotting and/or immunohistochemistry. We found that sitagliptin protected against diabetes-induced oxidative stress by reducing superoxide, TXNIP, PKC, and DNA/RNA/protein oxidative damage, and it prevented the downregulation of NRF2 and antioxidant enzymes, with the exception of catalase. Sitagliptin also exerted anti-inflammatory effects, avoiding both NF-кB translocation and IL-1β production. Sitagliptin prevents the diabetes-induced imbalance between ROS production and antioxidant defenses that occurs in diabetic retinas. 
546 |a EN 
690 |a diabetes 
690 |a diabetic retinopathy 
690 |a sitagliptin 
690 |a dipeptidyl peptidase-4 
690 |a DPP-4 inhibitors 
690 |a oxidative stress 
690 |a Therapeutics. Pharmacology 
690 |a RM1-950 
655 7 |a article  |2 local 
786 0 |n Antioxidants, Vol 11, Iss 7, p 1418 (2022) 
787 0 |n https://www.mdpi.com/2076-3921/11/7/1418 
787 0 |n https://doaj.org/toc/2076-3921 
856 4 1 |u https://doaj.org/article/a935c9fdc8524c748c9bf0d15d0d71c5  |z Connect to this object online.