Oxidative stress and diabetic retinopathy: development and treatment

Abstract

Diabetic retinopathy (DR) is the most common microvascular complication in diabetic patients and one of the main causes of acquired blindness in the world. From the 90s until date, the incidence of this complication has increased. Reactive oxygen species (ROS) is a free radical with impaired electron that usually participates in the redox mechanisms of some body molecules such as enzymes, proteins, and so on. In normal biological conditions, ROS is maintained in equilibrium, however its overproduction can lead to biological process called oxidative stress and this is considered the main pathogenesis of DR. The retina is susceptible to ROS because of high-energy demands and exposure to light. When the balance is broken, ROS produces retinal cell injury by interacting with the cellular components. This article describes the possible role of oxidative stress in the development of DR and proposes some treatment options based on its stages. The review of the topic shows that blindness caused by DR can be avoided by early detection and timely treatment.

Diabetic retinopathy

According to WHO, diabetes mellitus is a chronic degenerative disease that occurs when the pancreas does not produce enough insulin or when the body does not effectively use the insulin produced by the pancreas. The high mortality and morbidity caused by diabetes is as a result of its vascular complications. Approximately 400 million people worldwide have type 2 diabetes, and more than 45% of them have diabetic retinopathy (DR). The progress of diabetes to retinopathy happens over time thus, DR is a time-dependent disease that develops in stages. The incidence increases to 50% at 10 years after the diagnosis of diabetes, and goes up to 90% at 25 years. These figures put this complication as the most common microvascular complication in diabetic patients and one of the major causes of acquired blindness in the world. This increase in prevalence may be attributed to prolonged survival of diabetic patients. In the United States, it is the leading cause of blindness among adults aged 20–74 years.¹ The more advanced form of DR is diabetic macular edema (DME), which significantly increases the risk of blindness. Diabetic maculopathy is the result of multifactorial and complex alterations of the retinal capillaries in association with diabetes mellitus and it is divided into two forms, ischemic maculopathy and DME.² The high mortality and morbidity caused by diabetes is as a result of its vascular complications.

Two of the complications of DR that threaten the vision of the patients are DME and proliferative DR.³ Patients with DM2 usually begin to develop retinopathy 7 years after diagnosis of the disease.⁴

Naruse et al⁵ suggests that DR cause reactive oxygen species (ROS) to increase the level of reactive oxygen metabolites. Catabolites of biomolecules such as nitric oxide (NO), catalase, glutathione peroxide, and lipoperoxide increase with the progression of DR in DM2 patients.⁶ High glucose level and diabetically induced activation of retinal vascularization is linked with elevation in the enzymatic activity of arginase as well as in the reduction of bioavailability of NO.⁷ The over activity of arginase plays an important role in the development of DR through its reducing effect on NO and increase of oxidative stress. One of the pathways for the generation of NO is through the activity of inducible nitric oxide synthase, an isoform of NOS. This enzyme acts on 1-arginine and converts it to 1-citrulline.⁸ NO produced from S-nitrosoglutathione (GSNO) plays a second messenger role and regulates the activity and expression of some proteins by A-nitrosylation and hence plays vital role in many cellular processes. It is involved in physiological functions such as vasodilation, neurotransmission, and host defense.

Diabetic retinopathy mechanism

In the biosynthetic pathway of hexosamine, there is an increase in the activity of dumping of post-translational modifications of Ser/Thr residues through O-linked β-N-acetylglucosamine (O-GlcNAc). This increased influx of residues is dumped on the proteins and thus, reduce their capacity to capture the blood glucose and in this way leads to diabetes. It is known that as in protein phosphorylation, O-GlcN acylation plays a regulatory role in many nuclear and cytoplasmic proteins.⁹ The development of different vascular complications (macro and micro) is one of the key risks of suffering from diabetes and in the ocular regions, and these complications usually culminate in DR.¹⁰

DR is the principal cause of blindness in working adults. The mechanism underlying this is the inflammation of the retinal blood vessel caused by deposit of arteriosclerotic plates produced by excess blood glucose and thus making them susceptible to microrupture leading to the leakage of fluids into the retina. If unchecked, there is a growth of new vessels that distorts the microvasculature of the retina and this eventually provokes retinal detachment.^{11, 12}

The crucial point in the pathogenesis of the disease is inflammation in addition with oxidative stress.¹³ Its progress is characterized by loss of neuronal and pericytic cells that gives rise to growth of acellular-occluded capillaries. Such occlusion leads to the formation of microaneurysms and hence increased leucostasis resulting to the thickening of basal vascular membrane. The loss of pericyte cells begins with the stimulation of PKC-δ signaling by high level of blood glucose. This signaling cascade enhances the expression of protein kinase C-δ (PKC-δ, encoded by Prkcd) and p38 mitogen-activated protein kinase, and dephosphorylates PDGF receptors and diminishes its downstream signaling and thus brings about apoptotic death of the pericytic cells.¹⁴ The pericytic cell death gradually changes the architecture of the microvessels of the retina, a situation that provokes the collapse of blood–retinal barrier and hence extensive bleeding, microaneurysms exudates, and neovascularization that appear on the retinal surface.¹⁵

There is evidence indicating that local inflammation and oxidative stress are involved in the pathogenesis of DR and that they constitute crucial factors for the development of the disorder.¹⁶ In vascular inflammation, the involvement of biomolecules as lipoprotein-PLA2, pro-inflammatory cytokines (TNF-alpha and IL-1), and secretory phospholipase A2 IIA has been pinpointed.¹⁷

Since the underlying problem in this pathology is the high levels of blood glucose, the progressive damage can be retarded or completely abated by intensive insulin therapy. In addition, to reduce pericytic cell death, it has been found that thioredoxin, a novel gene and drug, is a potent therapeutic agent to prevent pericytic cell death and DR progression.¹⁸ Moreover, a comprehensive knowledge of cytokine-induced changes in lipid metabolism will promote the development of novel concepts and steer bench-to-bedside therapeutic developments.¹⁸

Screening and gene expression

DR prevention lies on its timely diagnosis achieved by a well-established medical care delivery plan based on a well-implemented screening program for the detection of its onset and its prompt medical treatment to reduce the incidence of radical management (vitrectomy) and blindness.¹⁹ British Diabetic Association established a standard value for DR screening program with a sensitivity of 80 and specificity of 95%, and has created a world record in DR screening with a coverage of 85.7%.

Chromosome 21 has a protective effect against DR as seen in Down’s syndrome patients with three copies of the chromosome and high level of endostatin, an anti-angiogenic protein from collagen XVIII whose gene is located in the chromosome 21.²⁰ Patients with deleterious polymorphisms in the uncoupling protein 1 (UCP1) have a high risk of developing DR. In type I diabetic patients, the expression of this protein occurs in the retina and impacts downwardly in the production of ROS by the mitochondria. This was confirmed in a study carried out by Brondani et al,²¹ where it was reported that 3826A/G polymorphism affects UCP1 expression and decreases mitochondrial production of ROS. There is high energy consumption in the molecular pathways that contribute to retinal signal transduction with its consequences on the structure and function of this organ.²² Such elevated metabolic rates in the retina together with the vascularization play a part in the oxidative stress and influence age-related processes. In this way, high-energy demand increases the oxidative load and enhances, in chronic manner, the increase of oxidative stress and ROS to impressive levels. The frequent exposure of the eye to ambient oxygen, environmental chemicals, and sunlight makes the ocular tissues susceptible to damage by ROS. In addition, the free radical (FR) catalyzes peroxidation of long-chain polyunsaturated acids (LCPUFAs) as docosahexaenoic acid and arachidonic acid and brings about the generation of LCPUFA metabolites as well as neuroprostanes and isoprostanes, which exercise extra pharmacological and toxicological actions in the ocular tissues.²³

Reactive radical species

Actually, it is known that a set of processes such as inflammation, the polyol pathway accumulation of advanced glycation end products, the flux of hexosamine pathway, and PKC activation are involved in the formation of FRs. These mechanisms appear to be associated with mitochondrial overproduction of ROS.²⁴ In obesity and dyslipidemia, DR appears to be also associated with oxidation of fatty acids, resulting in the increased production of ROS by nicotinamide adenine dinucleotide phosphate oxidase.

The generation of FR occurs in varieties of pathways. However, an addition of an electron to a stable molecule is the most common. In the organism, majority of the molecules contain non-radicals, ie, there is only an even number of electrons in their atomic orbits. The FRs generated attain a stable state by interaction with other molecules through redox reactions involving electron transfer among the participating chemical species. In such electron transfer, a molecule is oxidized by losing free electrons (oxidation process), which is captured or gained by the other molecule (reduction process). The term oxidizing or oxidant agent refers to the molecule that loses electron, while reducing agent is the molecule that gains the electron. In a nutshell, the oxidation of one chemical species implies the reduction of another. In a reaction between a FR and a non-radical molecule, there are three possible results: (1) the FR molecule can gain an electron or (2) it can lose electron, or (3) bond with the non-radical molecule. The end result of such reaction is the conversation of the non-radical agent to FR, a situation which results in an unstoppable or chain reaction that is only detained when two FRs meet.²⁵

FRs are classified depending on their functional groups.²⁶ The oxygen FR has oxygen as the functional group, the thiol radical has sulfur (S), nitrogen radical contain nitrogen (N), and carbon radical has carbon (C) while phosphorous radical contains phosphorous (P). The influence of exogenous factors can exacerbate normal metabolic process of the production of FRs.²⁷ The first and most common such exogenous influence is through normal metabolic processes and the second is from organic compounds such as alcoxyl, peroxyl, hydrogen peroxide, and singlet oxygen.²⁸

The term ROS as hydrogen peroxide, hydroperoxides, hypochlorous acid, and epoxide metabolites, refers to chemical species that function like oxidizing agents but are not FRs (Table 1).²⁹ Superoxide is mainly produced in the mitochondrial respiratory chain; however, the exact location and the precise mechanism underlying the production of physiologically relevant ROS remain to be known. Since the pathogenesis of many clinical disorders is linked to oxidative stress, it is very essential to have a good knowledge of the mechanism leading to the generation of ROS.³⁰ mtDNA transcription is enhanced by mitochondrial transcription factor A. It has been found that this factor can undergo ubiquitinylation, ie, modified by covalent attachment of ubiquitin and this usually hampers its transport to the mitochondria. The end result is lower mtDNA transcription and mitochondrial dysfunction, a situation which can favor the development or progression of diabetes and hence DR. Therefore, the inhibition of ubiquitinylation restores mitochondrial homeostasis, and inhibits the development/progression of DR.³¹ Lipid peroxidation plays a notable role in the progression of DR.²³ FRs such as hydroxyl and hydroperoxyl species with oxygen as functional group oxidize lipids and phospholipids, and at cellular level bring about membrane lipid peroxidation and in this way can trigger DR.

Table 1. Main reactive oxygen species.

Name	Formula	Formation
Superoxide	02−	Intermediate in 02 reduction to H2O
Hydroxyl	HO	Powerful oxidant in biological systems
Peroxyl	ROO	Low oxidant ability, but high diffusibility
Alkoxyl	RO	Medium oxidant ability with lipids
Hydrogen peroxide	H202	Originated from 02
Hypochlorous acid	HClO	Formed through mieloperoxidase action
Single oxygen	lO2	Molecularly excited oxygen through sunlight and radiation

On the basis of the report by Olguín and Guzman.²⁹

Prevention and treatment of diabetic retinopathy

Presently, new avenues of treatment of DR are being explored to cut down the incidence and progression of the disease. The need for adequate screening program for retinal surveillance for timely determination of retinal condition and perhaps level of damage has been reiterated. Moreover, new salvation treatment modalities have arisen and these have served as a source of hope even to patients with advanced DR, where it is calculated that 95% of them could continue with their vision when treated before the retina is severely damaged. These salvation treatment modalities are vitrectomy, corticosteroids, or Anti-VEGF injection into the eye and laser surgery. Though, all these treatment modalities are not DR curative, they can salvage the patient’s vision.

DR treatment depends on its stage or type. It should be remembered that this complication can be classified as nonproliferative and proliferative or macula edema. For the mild to moderate nonproliferative DR, the recommendation is a screening program well-implemented for the control of blood sugar and constant ophthalmological revision. Controlling diabetes and maintaining HbA1c level in the range of 6–7% are the goals in the optimal management of diabetes and DR. According to Diabetes Control and Complications Trial,³² if the levels of blood glucose are maintained, then the progression of DR will be substantially reduced. In the case of proliferative type or macular edema, the key treatment modality is surgery as photocoagulation where retinal tissues are burned using thermal energy. The principle underlying this is the injection of energy from a strong light source, which is absorbed by the retinal pigment epithelium that converts it into thermal energy that provokes necrotic coagulation with denaturation of cellular proteins as the temperature rises above 65°C.³³ Actually, laser retinal photocoagulation is a therapeutic option in many retinal and eye conditions. The Early Treatment for Diabetic Retinopathy Study has found that laser surgery for macular edema reduces the incidence of moderate visual loss (doubling of visual angle or roughly a two-line visual loss) from 30 to 15% over a 3-year period.³⁴ A 2-year result of The Diabetic Retinopathy Clinical Research network (DRCR.net) Randomized Trial Evaluating Ranibizumab Plus Prompt or Deferred Laser or Triamcinolone Plus Prompt Laser for Diabetic Macular Edema, known as the Laser-Ranibizumab-Triamcinolone for DME Study, demonstrated that ranibizumab with prompt or deferred focal/grid laser achieved superior visual acuity and optical coherence tomography outcomes compared with focal/grid laser treatment alone. In the ranibizumab groups, ~50% of the eyes had substantial improvement (10 or more letters) and 30% gained 15 or more letters. Intravitreal triamcinolone combined with focal/grid laser did not result in superior visual acuity outcomes compared with laser alone, but appear to have a visual acuity benefit similar to ranibizumab in pseudophakic eyes³⁵ (Table 2).

Table 2. Indications for retinal photocoagulation.

Indications	Specific treatment
Neovascular proliferative diseases for example: proliferative diabetic retinopathy, sickle cell retinopathy, and venous occlusive diseases	Panretinal photocoagulation (PRP)
Macular edema form diabetes or branch vein occlusion	Focal or grid photocoagulation
Macular edema form diabetes or branch vein occlusion	Closure of retinal microvascular
Extrafoveal choroidal neovascular membrane	Focal ablation
Pigment abnormalities	Focal treatment

On the basis of the report by Elman et al.³⁵

Corticosteroids in diabetic retinopathy

Corticosteroids have shown to be useful in the treatment of DME. This complication of diabetes is actually treated using focal laser photocoagulation, vascular endothelial growth factor (VEGF) inhibitors, and intravitreal corticosteroid injections and implants. Anti-VEGF antibodies have revolutionized the treatment of DR but a significant subset of patients fail to respond to treatment and accumulating evidence indicates that inflammatory cytokines and chemokines other than VEGF may contribute to the disease process.³⁶

Corticosteroids, dexamethasone, triamcinolone, and fluocinolone acetonide are an attractive treatment option because these drugs down regulate VEGF, and an array of cytokines, and in spite of increasing intraocular pressure, dexamethasone implant has demonstrated its benefit in the treatment of this disease.³⁷ Level of intravitreal triamcinolone acetonide exposure is related to the development of elevated intraocular pressure and cataract; this does not seem to be the case for dexamethasone, where two different doses showed similar mean intraocular pressure and incidence of cataract surgery. With fluocinolone acetonide, rates of intraocular pressure elevations requiring surgery seem to be dose related, and available corticosteroids for DME exhibit different pharmacokinetic profiles that impact on efficacy and adverse events, and should be taken into account.³⁸ In eyes with DME, intravitreal dexamethasone implant showed morphological and functional improvement as early as 1 month of its use and 4 months after the treatment,³⁹ and switching to intravitreal corticosteroids may be of particular benefit to pseudophakic patients. Anti-VEGF combined with corticosteroid implant of sustained release is a promising option for refractory DME.⁴⁰ Indeed, corticosteroids are of therapeutic benefit because of their anti-inflammatory, anti-angiogenic, and blood–retinal barrier stabilizing properties.

In spite of all these treatment options, laser photocoagulation, according to the guidelines of the Early Treatment of Diabetic Retinopathy Study (ETDRS), continues to be the primary standard care treatment in most communities.⁴¹

Anti-VEGF injection therapy

Anti-VEGF drugs are injected into the vitreous gel to block VEGF protein, which can stimulate the growth of abnormal blood vessels and leakage of fluid. VEGF is an endothelial cell-specific angiogenic factor, which plays a major role in the pathological condition as opposed to physiological and in ocular neovascularization leading to PDR. VEGF is also a vasopermeable factor, which increases vascular permeability by relaxing endothelial cell junctions and this mechanism is known to contribute to the development of DME. Inhibition of VEGF blocks these effects to some extent in DR, as demonstrated in several recent clinical trials and case series involving the anti-VEGF molecules. Currently, the anti-VEGF molecules being studied in the management of DR are: pegaptanib (Macugen), ranibizumab (Lucentis), bevacizumab (Avastin), and VEGF Trap-eye. Of the available VEGF antagonists, bevacizumab is the most frequently used outside a formal clinical trial because it is less expensive.⁴² Anti-VEGF therapy is currently indicated for DME associated with vision loss, whereas laser photocoagulation prevents severe vision loss in eyes with proliferative DR.⁴³ Corticosteroids, either injected or implanted into the eye, may be used alone or in combination with other drugs or laser surgery to treat DME.

Vitrectomy

Vitrectomy is an important resource for the treatment of long-standing vitreous hemorrhage, tractional retinal detachment, and combined tractional and rhegmatogenous retinal detachment. However, its use in the treatment of epiretinal membrane formation and macular dragging is still uncommon. The Diabetic Retinopathy Vitrectomy Study has recommended the use of this procedure for the treatment of eyes with vitreous hemorrhage that fails to resolve spontaneously within 6 months. Early vitrectomy (<6 months, mean 4 months) results in the greater recovery of vision in patients with type 1 diabetes. Laser photocoagulation through indirect delivery systems or through the EndoProbe (Toronto, ON, Canada) can be performed as an adjunctive procedure during vitrectomy to initiate or continue laser treatment. In fact, ultrasound monitoring of the posterior segment of the eyes in search of signs of macular detachment is necessary in all cases of late type 1 diabetes.

Recent studies have focused on the introduction of NrF2 as a new treatment of DR. NrF2 is a transcription factor that masterminds cellular detoxification and redox (oxidation) response status, and so provides a protective action against various forms of oxidative stress and damage regulator. It also acts as cytoprotector and it is found in different natural compounds as polyphenols.^{44, 45}

A deep understanding of the pathophysiology of DR and the underlying molecular mechanisms are essential for the development of new screening modalities that would improve and increase its timely detection and hence its timely prevention or treatment. Table 3 summarizes the treatment options for clinical management of DR complications.^{46, 47, 48, 49, 50, 51, 52, 53, 54, 55, 56, 57, 58, 59, 60, 61, 62, 63, 64} Table 4 also depicts the data of a study in an animal model where some pertinent particles believed to improve oxidative stress as well as prevent or delay DR development.^{65, 66, 67, 68, 69, 70, 71, 72, 73, 74, 75} It is a proven fact that oxidative stress enhances the progression of DR hence, decreasing the degree of such stress has been observed in clinical situations to contra arrest DR pathological problems. Guarantying the integrity of the neurons of the retina is a primordial factor in DR management. Damage of the retinal vessel can be protected if the retinal neurons are integrally and functionally maintained and the progression of DR can be abated. This highlights the importance of regular eye screening and aggressive control of glucose and blood pressure to prevent ocular damage,⁷⁶ especially when we take into consideration that more than a half of young onset of diabetic patients manifest some degree of retinopathy within 10–12 years of diagnosis.

Table 3. Clinical disorders and biomarkers related to diabetic retinopathy.

Disorders	Tissue	Effect or biomarkers	Ref.
Diabetic retinopathy	Retina	Two single-nucleotide polymorphisms (SNPs) (rs1073203 and rs4838605) were found to be significantly associated with DR	McAuley et al46
Diabetic retinopathy	Retinal capillary cell	Retinal capillary cell apoptosis and the number of degenerative capillaries were increased by three- to four-fold. Gene expression of mtDNA-encoded proteins was decreased, and VEGF, interleukin- 1β, and NF-kB levels were elevated	Kowluru et al47
Diabetic retinopathy	Retinal pigment epithelium (RPE)	Glycogen storage is increased in the RPE of diabetic patients and demonstrates the role of glycogen deposits in the pathogenesis of DR	Hernández et al48
Retinal inflammation	Neural retina	Cells derived from the stromal fraction of adipose tissue are able to rescue the neural retina from hyperglycemia-induced degeneration	Rajashekhar et al49
Retinal inflammation	Retina	Upregulation of oxidative/nitrosative stress, A2AAR, ENT1, Iba1, TNF-α, ICAM1, retinal cell death, and downregulation of AK	Elsherbiny et al50
Diabetic retina	Retina	Brain-derived neurotrophic factor (BDNF) is reduced by high-mobility group box-1 (HMGB1), thiobarbituric acid reactive substances (TBARS) ↑	Abu El-Asrar et al51
Retinopathy induced by hiperoxia (80% O2)	Retinal microglia	Activation of microglia and induction of microvascular injury through the release of Sema3A from adjacent neurons	Rivera et al52
Experimental diabetic retinopathy	Retina	SS31, a mitochondria-targeted antioxidant peptide in the retina of diabetic patients, could be a potential new treatment for diabetic retinopathy.	Huang et al53
Diabetic retinopathy	Retina	Adiponectin on the retinal vasculature may help improve potential therapies for retinal vascular disorders.	Omae et al54
Diabetic retinopathy	Retina	Increased binding of Nrf2 to Keap1; its translocation to the nucleus is compromised, contributing to decreased GSH levels; regulation of Nrf2-Keap1 by pharmacological or molecular means could serve as a potential adjunct therapy to combat oxidative stress and inhibit the development of DR	Zhong et al55
Diabetic retina	Cultured retina	The expression patterns of HO-1, Nox2, Nox4 in db/db mouse retinas, and the suppressive effects of NADPH oxidase inhibitors on the expression of HO-1, which is at least partially mediated by NADPH oxidase	He et al56
Retinopathy animal model	Retina	Lack of glutathione peroxidase-1 was associated with increased oxidative stress, an increase in the retinal avascular area, and upregulation of retinal vascular endothelial growth factor (VEGF).	Tan et al57
Diabetic retina	Retina	Sigma receptor 1 (σR1) is a non-opioid transmembrane protein that plays a key role in modulating retinal stress. It may be an important target in retinal disease.	Ha et al58
Diabetic retinopathy	Plasma	Decreased plasma purpose Dickkopf-1 (DKK-1) levels, which may contribute to Wnt/β-catenin pathway activation, are associated with the presence and progression of DR	Qiu et al59
Diabetic retinopathy	Retina	Strategies targeting T-cell lymphoma invasion and metastasis—Ras-related C3 botulinum toxin substrate 1 (TIAM1-RAC1) signaling could have the potential to halt the progression of diabetic retinopathy in the early stages of the disease.	Kowluru et al60
Diabetic retinopathy	Retina	Hypoxia might be involved in DR development through the stimulation of two key events of RD, such as neo-angiogenesis and apoptosis	Cervellati et al61
Diabetic retina	Retina	Levels of circulating oxidized LDL immune complexes (ox-LDL-IC) predict the development of diabetic retinopathy	Fu et al62
Diabetic retinopathy	Retina	Therapies targeting the retinal dopaminergic system may be beneficial in early-stage DR	Aung et al63

Up (↑), Down (↓).

On the basis of the report by Calderon et al.⁶⁴

Table 4. Substances with antioxidant activity used in diabetic retinopathy.

Substance	Effects	Ref.
Alpha-lipoic acid	ALA treatment has been shown to suppress expression of vascular endothelial growth factor, angiopoietin 2, and erythropoietin via blockade of superoxide formation	Nebbioso et al65
Telmisartan	Brain-derived neurotrophic factor and glutathione are increased in the sera and retina of a diabetic retinopathy animal model, decreasing signs of apoptosis	Ola et al66
Phlorizin	Significantly reduced fasting blood glucose and levels of advanced glycation end products, and remarkably inhibited retina cell apoptosis and the expression of glial fibrillary acidic protein in the retinas	Zhang et al67
Photobio-modulation	Daily 670 nm PBM treatment (6 J/cm2) resulted in the significant reduction in diabetes-induced death of retinal ganglion cells	Tang et al68
Astaxanthin	Reduced apoptosis of retinal ganglion cells and improved levels of superoxide anion, malondialdehyde (a marker of lipid peroxidation), 8-hydroxy-2-deoxyguanosine (8-OHdG, indicator of oxidative DNA damage), and manganese superoxide dismutase activity in the retinal tissue	Dong et al69
Hydrogen sulfide	Abated oxidative stress, alleviated mitochondrial dysfunction, suppressed NF-κB activation, and attenuated inflammation in DR animal models	Si et al70
Resveratrol	Alleviated hyperglycemia, induced weight loss, enhanced lipid peroxidation index, and oxidization to reduce the glutathione ratio and superoxide dismutase activity in retina	Soufi et al71
Hesperetin (flavonoids)	Showed inhibitory effects on caspase-3, which could be effective for the prevention of DR	Kumar et al72
Green tea, rich source of epigallocatech ingallate	Protects the retina in DR, due to an increase in the expression of glial fibrillary acidic protein (GFAP), oxidative retinal markers, and glutamine synthetase levels	Silva et al73
Methylene blue or apocynin	Pharmaceuticals targeting photoreceptor oxidative stress could offer a unique therapy for diabetic retinopathy	Du et al74
Tauroursodeoxycholic acid	Decreased protein carbonyl groups and reactive oxygen species production	Gaspar et al75

On the basis of the report by Calderon Guzman et al.⁶⁴

Conclusions

Obesity, poor glycemic control, and oxidative stress have been shown to contribute to the development of eye complications as DR. Diabetes is a complicated metabolic disorder with both short- and long-term undesirable events. Hence, diabetic patients should be educated on eye complications that may arise from their condition. Regular eye screening with fundus camera should be part of the routine management of diabetic patients. Oxidative stress reduction and restoration of retinal antioxidant system using exogenous antioxidants or anti-inflammatory drugs or food, which may improve postprandial hyperglycemia and adipose tissue metabolism, as well as dyslipidemia and insulin resistance to modulate carbohydrate and lipid metabolism should be the key modalities to fight against this disorder. We believe that all the events previously mentioned may be a promising issue for further research. The treatment depends on the stage of DR. The use of anti-VEGF in DME associated with vision loss has been recommended and laser photocoagulation can prevent severe vision loss in eyes with proliferative DR. According to the findings in the present paper, oxidative stress plays an important role in the pathophysiology of DR. Many studies have shown that different natural compounds, such as polyphenols, can suppress oxidative stress and inflammation through Nrf2 orientation and hence the activation of gene cytoprotectors related antioxidant response factor. Currently, the application of Nrf2 in the treatment of DR as cytoprotective mechanism in response to ischemic-reperfusion injury has been studied. The understanding of the mechanisms of oxidative stress is crucial in the development of new therapeutic strategies.