Journal of Diabetes Research

Journal of Diabetes Research / 2013 / Article
Special Issue

Chronic Vascular Complications in Diabetes

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Review Article | Open Access

Volume 2013 |Article ID 425854 |

Xiao Miao, Weixia Sun, Lining Miao, Yaowen Fu, Yonggang Wang, Guanfang Su, Quan Liu, "Zinc and Diabetic Retinopathy", Journal of Diabetes Research, vol. 2013, Article ID 425854, 8 pages, 2013.

Zinc and Diabetic Retinopathy

Academic Editor: Weiping Jia
Received11 Jan 2013
Accepted08 Feb 2013
Published17 Mar 2013


Zinc (Zn) is an important nutrient that is involved in various physiological metabolisms. Zn dyshomeostasis is often associated with various pathogeneses of chronic diseases, such as metabolic syndrome, diabetes, and related complications. Zn is present in ocular tissue in high concentrations, particularly in the retina and choroid. Zn deficiencies have been shown to affect ocular development, cataracts, age-related macular degeneration, and even diabetic retinopathy. However, the mechanism by which Zn deficiency increases the prevalence of diabetic retinopathy remains unclear. In addition, due to the negative effect of Zn deficiency on the eye, Zn supplementation should prevent diabetic retinopathy; however, limited available data do not always support this notion. Therefore, the goal of this paper was to summarize these pieces of available information regarding Zn prevention of diabetic retinopathy. Current theories and possible mechanisms underlying the role of Zn in the eye-related diseases are discussed. The possible factors that affect the preventive effect of Zn supplementation on diabetic retinopathy were also discussed.

1. Introduction

Zinc (Zn) is the second most abundant trace element in the human body and is an important nutrient and cofactor of numerous enzymes and transcription factors [13]. There are more than 300 catalytically active Zn metalloproteinase and more than 2000 Zn-dependent transcription factors. Zn is involved in homeostasis, immune responses, oxidative stress, apoptosis, and aging. Zn homeostasis results from the coordinated regulation by metallothioneins (MTs) and proteins in the Zrt/Irt-like protein (ZIP) and Zn transporter (ZnT) families [47]. These proteins are involved in the uptake, excretion, and intracellular storage/trafficking of Zn. Abnormalities in Zn homeostasis, such as its deficiency, may be associated with various pathogeneses of chronic diseases.

Metallothionein (MT) play a key role in scavenging of free radicals and is the main regulator of the intracellular transport and mobilization, storage, and transferring of Zn [8]. It is a cysteine-rich protein that binds metals such as Zn and copper and acts as an antioxidant that is very efficient in scavenging various free radicals or reactive oxygen species (ROS) [9, 10].

Diabetes mellitus affects 200 million people worldwide [11], including 20 million people in the United States alone [12]. Diabetic retinopathy (DR), a specific microvascular complication of diabetes, is the leading cause of blindness in working-aged persons in the United States [12]. The prevalence of DR increases with duration of diabetes [13], and nearly all persons with type 1 diabetes and more than 60% of those with type 2 have some retinopathy after 20 years.

Clinically, DR can be classified as nonproliferative DR (NPDR) and proliferative DR (PDR) [14]. NPDR is characterized ophthalmoscopically by the presence of microaneurysms and dot and blot hemorrhages. Severe NPDR (also called preproliferative DR) shows increased retinal microvascular damage as evidenced by cotton wool spots, venous beading, venous loops, and intraretinal microvascular abnormalities. If left untreated, PDR (characterized by abnormal retinal neovascularization) can develop. Clinically important outcomes of PDR are retinal and vitreous hemorrhage and tractional retinal detachment [14], which ultimately result in blindness. Previous studies have shown that Zn supplementation attenuates oxidative changes at the early stage of diabetic rats, potentially preventing the early stages of DR, and delay its progression.

Several complications of diabetes may be related to increased intracellular oxidants and free radicals associated to decreases in intracellular Zn and Zn-dependent antioxidant enzymes [15]. Zinc effectively ameliorates diabetes-related complications in various animal models [16]. It is also an effective inducer of gene and protein expressions of MT, a potent antioxidant [17]. Therefore, the goal of the present paper was to summarize the information from the literature regarding (1) the role of Zn in diabetes, (2) the effect of Zn on the eye, and (3) the evidence that Zn prevents DR, as well as the possible mechanisms underlying this role. Finally, the future of Zn therapy for DR is briefly discussed.

2. Zinc and Oxidative Stress

It is well accepted that oxidative stress is elevated in various tissues that are associated with microvascular and macrovascular complications of diabetes [18, 19]. Increased oxidative stress contributes to the development of DR [20, 21], as an increase in reactive oxygen species (ROS) is considered a causal link between elevated glucose and other metabolic abnormalities that are important in its development [22]. Various antioxidants and nutrients have provided encouraging results in experimental models of DR [20, 21], although the results from clinical trials have been less conclusive [2325]. In diabetic mice, overexpression of manganese superoxide dismutase (MnSOD), the enzyme responsible for scavenging mitochondrial superoxide, prevents early retinal lesions of retinopathy [26].

Zn has antioxidant properties and protects tissue from oxidative stress by two main mechanisms: (i) protection of protein sulfhydryl groups from free radical attack and (ii) reduction of free radical formation through the antagonism of redox-active transition metals, such as iron and copper (Cu) [27]. Each of these mechanisms results in decreased reactivity of sulfhydryl groups. The protection of protein sulfhydryls is thought to involve reduction of sulfhydryl reactivity through one of three mechanisms: (i) direct binding of Zn to sulfhydryl groups, (ii) steric hindrance as a result of Zn binding to another protein site in close proximity to the sulphydryl group, and (iii) a conformational change that results from Zn binding to another site on the protein. Some examples of proteins that Zn protects are dihydroorotase, DNA Zn-binding proteins (Zn fingers), and protein farnesyltransferase (Figure 1) [28].

As an antioxidant, Zn reduces the formation of free radicals by acting as an inhibitor of NADPH oxidase, which is an inducer of MTs (free radical scavengers) and an integral metal of Cu/Zn-SOD. ROS are known to activate NF-κB, which in turn, activates growth factors, antiapoptotic molecules resulting in cell proliferation (cancer), inflammatory cytokines, and adhesion molecules [29]. Zn also reduces inflammatory cytokine production by upregulating a Zn-finger protein, A20, which inhibits NF-κB activation via the TRAF pathway [30]. Thus, Zn not only functions as an antioxidant, but also as an anti-inflammatory agent (Figure 1). In contrast to plasma Cu, plasma Zn concentrations and the Zn/Cu ratio were lower in diabetic subjects [31]. Meanwhile, it has been suggested that Zn supplementation protects against oxidative changes in the early stages of diabetes [32]. Zn supplementation also appears to have beneficial antioxidant effects in people with type 2 diabetes [33] (Figure 1).

3. Zinc and the Eye

Zn is indispensable to the growth and development of microorganisms, plants, and animals. It is found in all body tissues and secretions in relatively high concentrations, with 85% of whole body Zn found within the muscle and bones, 11% found in the skin and the liver, and the remaining found in all other tissues, with the highest concentrations in the prostate and parts of the eye [34], such as retina [35]. Zn appears to play an integral role in maintaining normal ocular function and is present in high concentrations in the ocular tissue, particularly in the retina and the choroid. Zn deficiency has been shown in a number of species to result in a variety of gross, ultrastructural, and electrophysiologic ocular manifestations.

Zn deficiency in rats dramatically affects ocular development. Severe Zn deficiency, when imposed upon rats during gestation, results in optic cup invagination failure, colobomata, retinal dysplasia, and occasionally anophthalmia in pups [36]. Acrodermatitis enteropathica is a rare early childhood disease, with multiple systemic manifestations caused by abnormalities in Zn metabolism. The ocular abnormalities include blepharitis, photophobia, conjunctivitis, corneal opacities, and cataracts [37]. Superficial punctate opacities, nebulous subepithelial opacities, and linear corneal erosions have also been reported in cases of acrodermatitis enteropathica [37]. Recently, differential display was used to investigate gene expression in acrodermatitis enteropathica, and the results showed an insertional mutation that affects the mRNA of a Zn transport protein, resulting in decreased Zn absorption [38]. Recalcitrant corneal ulcers have been reported in conjunction with low serum Zn [39]. In addition, Zn has been indirectly linked with corneal ulcers because it may be required for the functional activity of collagenases [40].

Zn deficiency in humans results in poor dark adaptation and night blindness [41, 42], which in most cases can be reversed by Zn supplementation [43]. These alterations appear to be the consequence of defects in retinol processing in retinal pigment epithelial (RPE) cells during the visual cycle. The Zn metalloenzyme, retinol dehydrogenase, catalyzes the oxidation of retinol to retinal, and animal experiments and in vitro studies have demonstrated that the activity of retinol dehydrogenase can be impaired by Zn deficiency [44]. The above-mentioned changes in the localization of histochemically reactive Zn within the dark- and light-adapted states of the photoreceptor suggest that Zn possesses a unique role in the phototransduction process and/or the photoreceptor-RPE interaction, as occurs for vitamin A [45]. The presence of reactive Zn (Zn2+) within photoreceptor terminals, and the evidence that exogenous Zn affects the electrophysiological activity of the distal retina, has led to the presumption that its corelease with glutamate may play an essential role in the modulation of information at the first synapse in the visual pathway. Although Zn release can be visualized in the outer synaptic layer of a retinal slice preparation, it cannot be ascertained with certainty that the release sites are at the presynaptic terminal and not from the mitochondria-rich inner segment or within the distal processes of photoreceptors and Müller cells. Synaptically released Zn may significantly influence neural processing in the vertebrate retina by modulating the activity of excitatory and/or inhibitory receptors as well as intracellular signaling proteins [46]. Therefore, the possibility exists that abnormal dark adaptation in Zn-deficient states is the result of an impaired Zn-dependent reaction in the visual cycle within the photoreceptors.

Cataracts are a common disease in older adults worldwide. Although some epidemiological studies have shown Zn involvement in the development of cataracts, the lowest concentration of Zn in crystalline lenses has been detected in patients with mature senile cataracts, while the highest concentrations have been detected in patients with traumatic cataracts [47]. However, the results from the largest randomized trial done in the United States showed no beneficial effect of supplement Zn with cupric oxide on the development or progression of cataracts [48].

Zn has a strong effect on the acceleration of MT synthesis [49]. Some studies have reported that MT-III plays a pivotal role as an endogenous neuroprotectant against light-induced retinal damage [50]. The mRNAs of MT isoforms (I–III) were upregulated in the murine retina by light exposure, and light-induced retinal damage is exacerbated in MT-III-deficient mice [50]. Furthermore, it has also been demonstrated that MT isoforms I and II do not have pivotal roles in protecting against light-induced retinal photoreceptor cell loss, whereas MT-III has neuroprotective effects, possibly due to its strong interaction with ROS.

Age-related macular degeneration is a leading cause of visual loss in older adults and is characterized by accumulation of membranous debris on both sides of the RPE basement membrane. This condition is thought to result from oxidative stress, and Zn deficiency is involved in its pathogenesis. It has been demonstrated that Zn [51, 52] and MT [53] levels are reduced in the RPE of the human eye in aged-related macular degeneration. In accordance with this, a study using a monkey model of early-onset aged-related macular degeneration [54] showed a four-fold decrease in retinal Zn content, decreased synthesis of MT, and increased oxidative stress in affected retinas compared to unaffected controls. In addition, it has been suggested that Zn supplementation prevents the appearance of age-related macular degeneration [55] and decreases the progression of the dry form of the disease [56]. These findings support the view that Zn deficiency is involved in the pathogenesis of age-related macular degeneration. Moreover, a clinical study showed a significant reduction in the Zn/Cu ratio in serum involved in the development of DR, thus demonstrating the importance of Zn in disease progression [57].

4. Zn Plays an Important Role in DR

Zn is a key element for maintenance of the structural and functional integrity of eukaryotic cells and tissues [58]. Many studies have addressed the importance of Zn as an antioxidant and therapeutic agent in several free radical initiation systems [5961]. Some studies have reported the beneficial effects of antioxidants and Zn supplementation in preventing progression to advanced age-related macular degeneration, and people supplemented with antioxidants and Zn are less likely to lose visual acuity [62]. Moreover, Zn has been shown to protect the retina from diabetes-induced increased lipid peroxidation and decreased glutathione levels in rats either by stabilizing the membrane structure or by inducing MT synthesis [32]. Zn is essential for Cu-Zn SOD and inhibits diabetes-induced increases in plasma malondialdehyde and decreases in erythrocyte antioxidant defense enzymes [63]. Cu oxide functions as the active center of many cuproenzymes, including Cu-Zn SOD [64], and Cu deficiencies result in oxidative damage to lipids, DNA, and proteins [65]. The precise mechanism by which Zn and Cu exert their protective effects against retinal damage remains unclear, but there is a strong possibility that these nutrients help decrease oxidative damage.

It is apparent that DR can best be managed by tight glycemic control [21]. Moreover, antioxidant therapy may be a suitable approach for inhibiting intrinsic changes within the retinal capillary bed that leads to the development of DR. A previous study showed that alloxan causes a reduction in GSH levels and an increase in the levels of lipid peroxidation products (TBA reactants) in the retinas of diabetic rats, supporting the role of oxidative stress in the development of DR [32]. Many studies have addressed the importance of antioxidants in the control of abnormalities in diabetic retinas [6668]; however, many of these studies have indicated the inability of these antioxidants to lower blood hexose levels [20, 67, 69, 70]. Other studies have indicated the inability of some antioxidants to inhibit lipid peroxidation in diabetic eyes [71]. Above all, these studies reveal the ability of Zn to both minimize perturbations in plasma glucose levels in alloxan-diabetic rats and ameliorate deteriorative changes in the levels of TBA reactants and GSH in the retina [32].

The previous study indicates increased lipid peroxidation in the retinas of alloxan-treated rats that was associated with increased plasma glucose levels. On the other hand, the study reported elevated rates of liver lipid peroxidation accompanied by deterioration in glucose tolerance in GSH-depleted rats [72]. It has been suggested that in free radicals initiation systems, deterioration in glucose tolerance is attributed to impaired insulin action [73]. One study showed that impaired insulin-stimulated glucose transport across the cell membrane is a major mechanism underlying age-associated glucose intolerance in aged rats [74]. Free radicals are hypothesized to be one of the underlying causes of aging [75]. Initiating lipid peroxidation by free radicals in the lipid moiety of the cell membrane is presumed to result in distortion of the structural and functional integrity of the cell membrane or internal cellular components. This would interfere with the ability of insulin to initiate and propagate its normal sequence of actions [74], which may account, at least in part, for alloxan-induced hyperglycemia. Previous studies have shown that the treatment of alloxan-diabetic rats with Zn chloride resulted in the reduction of both plasma glucose levels and lipid peroxidation in the retinas of these rats [32]. The protective effects of Zn against increases in lipid peroxidation may be due to its ability to bind and stabilize cellular membranes against lipid peroxidation and disintegration [76]. An alternative protective mechanism of Zn may be its ability to induce MT synthesis. The high sulfhydryl content enables MT to efficiently scavenge oxyradicals [77, 78]. Another possible protective mechanism of MT is its ability to release Zn to bind to sites on membrane surfaces, thereby displacing adventitious iron and inhibiting lipid peroxidation [76]. Moreover, the suggested effect of Zn in inducing SH-rich MT synthesis may preserve the SH residue in many functional proteins. Therefore, Zn may preserve the structural and functional integrity of SH-dependent enzymes, including those that regulate glucose metabolism. More recently, it was hypothesized that MT, which is cysteine-rich, plays a role in nitric oxide signaling events via sequestration or release of Zn2+ by the unique thiolate clusters of the protein [79].

The protective effect of Zn against lipid peroxidation that is observed in the retinas of alloxan-diabetic rats could be of considerable importance for halting the progression of diabetes-related retinal degeneration, since a strong positive correlation has been found between lipid peroxidation products and vascular endothelial growth factor (VEGF) concentrations in the vitreous of patients with proliferative DR [68]. Moreover, one type of SOD, a major antioxidant enzyme, is Zn-dependent (Cu/Zn-SOD). Cu/Zn-SOD is a potent antioxidant enzyme that has recently been proposed to have a tumor-suppression effect [80]; therefore, its role in the protection against the development of DR should not be excluded. Thus, the importance of Zn as a protective antioxidant against DR may lie in its ability to initially exert good glycemic control, thus inhibiting the development of the deleterious consequences of hyperglycemia. In addition, Zn may be an important factor in inhibiting the progression of the intrinsic changes in diabetic retinas that eventually lead to the development of DR.

5. Possible Mechanisms of Zn Prevention of DR

As discussed above, Zn acts as a potent antioxidant. Therefore, the antioxidant action of Zn could be considered as the first possible mechanism. It is well known that hyperglycemia accelerates the formation of advanced glycation end products (AGEs), which have been implicated in the pathogenesis of DR [81]. They can stimulate ROS production in retinal pericytes, largely via activation of NADPH oxidase, which results in retinal pericyte apoptosis [82]. Other studies have suggested that the critical role of oxidative stress in pericyte apoptosis, as treatment of diabetic rats with a mixture of different antioxidants [20] or with trolox [66], was able to prevent pericyte loss in retina. As discussed above, Zn can prevent cells from oxidative damage, and NADPH oxidase is inhibited by zinc and SOD, which is both a zinc and copper-containing enzyme [29]. It is suggested that Zn might prevent retinal pericyte apoptosis via inhibition of NADPH oxidase in DR.

Ocular neovascularization, which is most potently caused by hypoxia and ischemia, is also a key component in DR [83, 84]. It has been convincingly demonstrated that hypoxia inducible factor-1 (HIF-1) and VEGF are involved in the initiation and progression of neovascularization in DR [85]. This has led to the finding of many new agents targeting VEGF [86]. Ischemia and hypoxia are similar conditions in cancer. Zn reduces inflammatory cytokine production by upregulating the Zn-finger protein, A20, which inhibits NF-κB activation via the TRAF pathway [30]. Some studies have shown that Zn supplementation can reduce VEGF expression by inhibiting NF-κB in prostate cancer [87]. It has been suggested that Zn might prevent neovascularization by inhibiting VEGF expression in DR (Figure 2). In addition, recent finding suggests that ZnT8 expression was reduced by ischemic insults and to restore the ZnT8 to its basal homeostatic levels can prevent retinas from ischemia induced injury [88]. Ischemia is also a key component in DR. Therefore, Zn supplement might rescue retina from DR (Figure 2).

Vascular leakage is also an important part of DR. p38 MAPK and NF-κB signaling pathways contribute to the regulation of claudin-5 expression, and these factors induce endothelial permeability [89]. It has been reported that Zn associates with p38 MAPK activation in the diabetic testis [90]. Moreover, recent studies have shown VEGF-induced vascular leakage in DR [91]. As discussed above, Zn might reduce VEGF by inhibiting NF-κB under conditions of hypoxia and ischemia; thus Zn might prevent vascular leakage in DR (Figure 2).

6. Conclusions

Increased oxidative stress plays an important role in many human diseases, such as diabetes and its complication. Zn supplementation seems beneficial for the patients with diabetes to control glucose levels. Zn as an antioxidant or via induction of MT attenuates ROS effect. Zn might protect retina from ROS induced pericytes apoptosis, capillary leakage, and neovascularization (Figure 2), thereby might have protective on DR. However whether this means that Zn supplementation can immediately be used to treat or prevent DR remains to be determined. A promising future for Zn supplementation will warrant further studies.




  1. J. E. Coleman, “Zinc Proteins: enzymes, storage proteins, transcription factors, and replication proteins,” Annual Review of Biochemistry, vol. 61, pp. 897–946, 1992. View at: Google Scholar
  2. B. L. Vallee and K. H. Falchuk, “The biochemical basis of zinc physiology,” Physiological Reviews, vol. 73, no. 1, pp. 79–118, 1993. View at: Google Scholar
  3. L. Cai, X. K. Li, Y. Song, and M. G. Cherian, “Essentiality, toxicology and chelation therapy of zinc and copper,” Current Medicinal Chemistry, vol. 12, no. 23, pp. 2753–2763, 2005. View at: Publisher Site | Google Scholar
  4. R. D. Palmiter and S. D. Findley, “Cloning and functional characterization of a mammalian zinc transporter that confers resistance to zinc,” EMBO Journal, vol. 14, no. 4, pp. 639–649, 1995. View at: Google Scholar
  5. L. A. Gaither and D. J. Eide, “The human zip1 transporter mediates zinc uptake in human k562 erythroleukemia cells,” Journal of Biological Chemistry, vol. 276, no. 25, pp. 22258–22264, 2001. View at: Publisher Site | Google Scholar
  6. T. Kambe, Y. Yamaguchi-Iwai, R. Sasaki, and M. Nagao, “Overview of mammalian zinc transporters,” Cellular and Molecular Life Sciences, vol. 61, no. 1, pp. 49–68, 2004. View at: Publisher Site | Google Scholar
  7. R. D. Palmiter, “Protection against zinc toxicity by metallothionein and zinc transporter 1,” Proceedings of the National Academy of Sciences of the United States of America, vol. 101, no. 14, pp. 4918–4923, 2004. View at: Publisher Site | Google Scholar
  8. J. P. Liuzzi and R. J. Cousins, “Mammalian zinc transporters,” Annual Review of Nutrition, vol. 24, pp. 151–172, 2004. View at: Publisher Site | Google Scholar
  9. Z. Zhou, X. Sun, and Y. James Kang, “Metallothionein protection against alcoholic liver injury through inhibition of oxidative stress,” Experimental Biology and Medicine, vol. 227, no. 3, pp. 214–222, 2002. View at: Google Scholar
  10. L. Cai, “Metallothionein as an adaptive protein prevents diabetes and its toxicity,” Nonlinearity in Biology, Toxicology and Medicine, vol. 2, pp. 89–103, 2004. View at: Google Scholar
  11. P. Lefèbvre, “Diabetes yesterday, today and tomorrow. The action of the Internation Diabetes Federation,” Revue Medicale de Liege, vol. 60, no. 5-6, pp. 273–277, 2005. View at: Google Scholar
  12. National Estimates and General Information on Diabetes and Prediabetes in the United States, Centers for Disease Control and Prevention, Atlanta, Ga, USA, 2011.
  13. R. Klein, B. E. K. Klein, S. E. Moss, and K. J. Cruickshanks, “The wisconsin epidemiologic study of diabetic retinopathy: XVII. The 14- year incidence and progression of diabetic retinopathy and associated risk factors in type 1 diabetes,” Ophthalmology, vol. 105, no. 10, pp. 1801–1815, 1998. View at: Publisher Site | Google Scholar
  14. N. Cheung, P. Mitchell, and T. Y. Wong, “Diabetic retinopathy,” The Lancet, vol. 376, no. 9735, pp. 124–136, 2010. View at: Publisher Site | Google Scholar
  15. S. R. Powell, “The antioxidant properties of zinc,” Journal of Nutrition, vol. 130, pp. 1447S–1454S, 2000. View at: Google Scholar
  16. Y. Adachi, J. Yoshida, Y. Kodera et al., “Oral administration of a zinc complex improves type 2 diabetes and metabolic syndromes,” Biochemical and Biophysical Research Communications, vol. 351, no. 1, pp. 165–170, 2006. View at: Publisher Site | Google Scholar
  17. D. M. Alscher, N. Braun, D. Biegger et al., “Induction of metallothionein in proximal tubular cells by zinc and its potential as an endogenous antioxidant,” Kidney and Blood Pressure Research, vol. 28, no. 3, pp. 127–133, 2005. View at: Publisher Site | Google Scholar
  18. J. W. Baynes and S. R. Thorpe, “Role of oxidative stress in diabetic complications: a new perspective on an old paradigm,” Diabetes, vol. 48, no. 1, pp. 1–9, 1999. View at: Publisher Site | Google Scholar
  19. L. Piconi, L. Quagliaro, and A. Ceriello, “Oxidative stress in diabetes,” Clinical Chemistry and Laboratory Medicine, vol. 41, no. 9, pp. 1144–1149, 2003. View at: Publisher Site | Google Scholar
  20. R. A. Kowluru, J. Tang, and T. S. Kern, “Abnormalities of retinal metabolism in diabetes and experimental galactosemia. Vii. Effect of long-term administration of antioxidants on the development of retinopathy,” Diabetes, vol. 50, no. 8, pp. 1938–1942, 2001. View at: Google Scholar
  21. R. A. Kowluru and A. Kennedy, “Therapeutic potential of anti-oxidants and diabetic retinopathy,” Expert Opinion on Investigational Drugs, vol. 10, no. 9, pp. 1665–1676, 2001. View at: Publisher Site | Google Scholar
  22. M. Brownlee, “The pathobiology of diabetic complications: a unifying mechanism,” Diabetes, vol. 54, no. 6, pp. 1615–1625, 2005. View at: Publisher Site | Google Scholar
  23. S. E. Bursell, A. C. Clermont, L. P. Aiello et al., “High-dose vitamin E supplementation normalizes retinal blood flow and creatinine clearance in patients with type 1 diabetes,” Diabetes Care, vol. 22, no. 8, pp. 1245–1251, 1999. View at: Publisher Site | Google Scholar
  24. M. Nebbioso, M. Federici, D. Rusciano, M. Evangelista, and N. Pescosolido, “Oxidative stress in preretinopathic diabetes subjects and antioxidants,” Diabetes Technology and Therapeutics, vol. 14, no. 3, pp. 257–263, 2012. View at: Publisher Site | Google Scholar
  25. A. E. Millen, M. Gruber, R. Klein, B. E. K. Klein, M. Palta, and J. A. Mares, “Relations of serum ascorbic acid and α-tocopherol to diabetic retinopathy in the Third National Health and Nutrition Examination Survey,” American Journal of Epidemiology, vol. 158, no. 3, pp. 225–233, 2003. View at: Publisher Site | Google Scholar
  26. M. Kanwar, P. S. Chan, T. S. Kern, and R. A. Kowluru, “Oxidative damage in the retinal mitochondria of diabetic mice: possible protection by superoxide dismutase,” Investigative Ophthalmology and Visual Science, vol. 48, no. 8, pp. 3805–3811, 2007. View at: Publisher Site | Google Scholar
  27. T. M. Bray and W. J. Bettger, “The physiological role of zinc as an antioxidant,” Free Radical Biology and Medicine, vol. 8, no. 3, pp. 281–291, 1990. View at: Publisher Site | Google Scholar
  28. K. Jomova and M. Valko, “Advances in metal-induced oxidative stress and human disease,” Toxicology, vol. 283, no. 2-3, pp. 65–87, 2011. View at: Publisher Site | Google Scholar
  29. A. S. Prasad, “Zinc: role in immunity, oxidative stress and chronic inflammation,” Current Opinion in Clinical Nutrition and Metabolic Care, vol. 12, no. 6, pp. 646–652, 2009. View at: Publisher Site | Google Scholar
  30. A. S. Prasad, “Clinical, immunological, anti-inflammatory and antioxidant roles of zinc,” Experimental Gerontology, vol. 43, no. 5, pp. 370–377, 2008. View at: Publisher Site | Google Scholar
  31. R. M. Walter, J. Y. Uriu-Hare, K. L. Olin et al., “Copper, zinc, manganese, and magnesium status and complications of diabetes mellitus,” Diabetes Care, vol. 14, no. 11, pp. 1050–1056, 1991. View at: Google Scholar
  32. S. A. Moustafa, “Zinc might protect oxidative changes in the retina and pancreas at the early stage of diabetic rats,” Toxicology and Applied Pharmacology, vol. 201, no. 2, pp. 149–155, 2004. View at: Publisher Site | Google Scholar
  33. A. M. Roussel, A. Kerkeni, N. Zouari, S. Mahjoub, J. M. Matheau, and R. A. Anderson, “Antioxidant effects of zinc supplementation in Tunisians with type 2 diabetes mellitus,” Journal of the American College of Nutrition, vol. 22, no. 4, pp. 316–321, 2003. View at: Google Scholar
  34. B. D. A. Calesnick, “Zinc deficiency and zinc toxicity,” American Family Physician, vol. 37, pp. 267–270, 1988. View at: Google Scholar
  35. M. Ugarte, G. W. Grime, G. Lord et al., “Concentration of various trace elements in the rat retina and their distribution in different structures,” Metallomics, vol. 4, pp. 1245–1254, 2012. View at: Google Scholar
  36. J. M. Rogers and L. S. Hurley, “Effects of zinc deficiency on morphogenesis of the fetal rat eye,” Development, vol. 99, no. 2, pp. 231–238, 1987. View at: Google Scholar
  37. B. H. Grahn, P. G. Paterson, K. T. Gottschall-Pass, and Z. Zhang, “Zinc and the eye,” Journal of the American College of Nutrition, vol. 20, no. 2, pp. 106–118, 2001. View at: Google Scholar
  38. S. J. Muga and A. Grider, “Partial characterization of a human zinc-deficiency syndrome by differential display,” Biological Trace Element Research, vol. 68, no. 1, pp. 1–12, 1999. View at: Google Scholar
  39. S. K. Pati and R. Mukherji, “Serum zinc in corneal ulcer—a preliminary report,” Indian Journal of Ophthalmology, vol. 39, no. 3, pp. 134–135, 1991. View at: Google Scholar
  40. M. B. Berman and R. Manabe, “Corneal collagenases: evidence for zinc metalloenzymes,” Annals of Ophthalmology, vol. 5, no. 11, pp. 1193–1209, 1973. View at: Google Scholar
  41. S. A. Morrison, R. M. Russell, E. A. Carney, and E. V. Oaks, “Zinc deficiency: a cause of abnormal dark adaptation in cirrhotics,” American Journal of Clinical Nutrition, vol. 31, no. 2, pp. 276–281, 1978. View at: Google Scholar
  42. H. I. Afridi, T. G. Kazi, N. Kazi et al., “Evaluation of status of zinc, copper, and iron levels in biological samples of normal children and children with night blindness with age groups of 3–7 and 8–12 years,” Biological Trace Element Research, vol. 142, pp. 323–334, 2011. View at: Google Scholar
  43. K. Mochizuki, H. Murase, M. Imose, H. Kawakami, and A. Sawada, “Improvement of scotopic electroretinograms and night blindness with recovery of serum zinc levels,” Japanese Journal of Ophthalmology, vol. 50, no. 6, pp. 532–536, 2006. View at: Publisher Site | Google Scholar
  44. A. M. Huber and S. N. Gershoff, “Effects of zinc deficiency on the oxidation of retinol and ethanol in rats,” Journal of Nutrition, vol. 105, no. 11, pp. 1486–1490, 1975. View at: Google Scholar
  45. D. Bok, “Retinal photoreceptor-pigment epithelium interactions,” Investigative Ophthalmology and Visual Science, vol. 26, no. 12, pp. 1659–1694, 1985. View at: Google Scholar
  46. S. Redenti, H. Ripps, and R. L. Chappell, “Zinc release at the synaptic terminals of rod photoreceptors,” Experimental Eye Research, vol. 85, no. 4, pp. 580–584, 2007. View at: Publisher Site | Google Scholar
  47. I. Jeru, “The role of zinc in the appearance of cataract,” Oftalmologia, vol. 41, no. 4, pp. 329–332, 1997. View at: Google Scholar
  48. A. Kassoff, J. Kassoff, J. Buehler et al., “A randomized, placebo-controlled, clinical trial of high-dose supplementation with vitamins c and e and beta carotene for age-related cataract and vision loss: AREDS report no. 9,” Archives of Ophthalmology, vol. 119, no. 10, pp. 1439–1452, 2001. View at: Google Scholar
  49. M. Sato and I. Bremner, “Oxygen free radicals and metallothionein,” Free Radical Biology and Medicine, vol. 14, no. 3, pp. 325–337, 1993. View at: Publisher Site | Google Scholar
  50. K. Tsuruma, H. Shimazaki, Y. Ohno et al., “Metallothionein-iii deficiency exacerbates light-induced retinal degeneration,” Investigative Ophthalmology & Visual Science, vol. 53, pp. 7896–7903, 2012. View at: Google Scholar
  51. J. C. Erie, J. A. Good, J. A. Butz, and J. S. Pulido, “Reduced zinc and copper in the retinal pigment epithelium and choroid in age-related macular degeneration,” American Journal of Ophthalmology, vol. 147, no. 2, pp. 276–282, 2009. View at: Publisher Site | Google Scholar
  52. D. Organisciak, P. Wong, C. Rapp, A. Ziesel, R. Rangarajan, and J. Lang, “Light-induced retinal degeneration is prevented by zinc, a component in the age-related eye disease study formulation,” Photochemistry and Photobiology, vol. 88, no. 6, pp. 1396–1407, 2012. View at: Publisher Site | Google Scholar
  53. D. J. Tate, D. A. Newsome, and P. D. Oliver, “Metallothionein shows an age-related decrease in human macular retinal pigment epithelium,” Investigative Ophthalmology and Visual Science, vol. 34, no. 7, pp. 2348–2351, 1993. View at: Google Scholar
  54. M. G. Nicolas, K. Fujiki, K. Murayama et al., “Studies on the mechanism of early onset macular degeneration in cynomolgus monkeys. II. Suppression of metallothionein synthesis in the retina in oxidative stress,” Experimental Eye Research, vol. 62, no. 4, pp. 399–408, 1996. View at: Publisher Site | Google Scholar
  55. M. Sasaki, H. Shinoda, T. Koto, A. Uchida, K. Tsubota, and Y. Ozawa, “Use of micronutrient supplement for preventing advanced age-related macular degeneration in Japan,” Archives of Ophthalmology, vol. 130, no. 2, pp. 254–255, 2012. View at: Publisher Site | Google Scholar
  56. J. H. Olson, J. C. Erie, and S. J. Bakri, “Nutritional supplementation and age-related macular degeneration,” Seminars in Ophthalmology, vol. 26, no. 3, pp. 131–136, 2011. View at: Publisher Site | Google Scholar
  57. N. A. Hasan, “Effects of trace elements on albumin and lipoprotein glycation in diabetic retinopathy,” Saudi Medical Journal, vol. 30, no. 10, pp. 1263–1271, 2009. View at: Google Scholar
  58. E. Rudolf, J. Peychl, J. Radocha, and M. Cervinka, “Zinc and its role in the regulation of cell death,” Ceskoslovenska Fysiologie, vol. 50, no. 4, pp. 201–210, 2001. View at: Google Scholar
  59. P. M. Hanna, M. B. Kadiiska, S. J. Jordan, and R. P. Mason, “Role of metallothionein in zinc(II) and chromium(III) mediated tolerance to carbon tetrachloride hepatotoxicity: evidence against a trichloromethyl radical-scavenging mechanism,” Chemical Research in Toxicology, vol. 6, no. 5, pp. 711–717, 1993. View at: Google Scholar
  60. S. A. Moustafa, “Effect of glutathione (GSH) depletion on the serum levels of triiodothyronine (T3), thyroxine (T4), and T3/T4 ratio in allyl alcohol-treated male rats and possible protection with zinc,” International Journal of Toxicology, vol. 20, no. 1, pp. 15–20, 2001. View at: Publisher Site | Google Scholar
  61. M. Provinciali, A. Donnini, K. Argentati, G. Di Stasio, B. Bartozzi, and G. Bernardini, “Reactive oxygen species modulate Zn2+-induced apoptosis in cancer cells,” Free Radical Biology and Medicine, vol. 32, no. 5, pp. 431–445, 2002. View at: Publisher Site | Google Scholar
  62. J. R. Evans, “Antioxidant vitamin and mineral supplements for age-related macular degeneration.,” Cochrane Database of Systematic Reviews, no. 1, Article ID CD000254, 2002. View at: Google Scholar
  63. V. Duzguner and S. Kaya, “Effect of zinc on the lipid peroxidation and the antioxidant defense systems of the alloxan-induced diabetic rabbits,” Free Radical Biology and Medicine, vol. 42, no. 10, pp. 1481–1486, 2007. View at: Publisher Site | Google Scholar
  64. S. Puig and D. J. Thiele, “Molecular mechanisms of copper uptake and distribution,” Current Opinion in Chemical Biology, vol. 6, no. 2, pp. 171–180, 2002. View at: Publisher Site | Google Scholar
  65. J. Y. Uriu-Adams and C. L. Keen, “Copper, oxidative stress, and human health,” Molecular Aspects of Medicine, vol. 26, no. 4-5, pp. 268–298, 2005. View at: Publisher Site | Google Scholar
  66. N. H. Ansari, W. Zhang, E. Fulep, and A. Mansour, “Prevention of pericyte loss by trolox in diabetic rat retina,” Journal of Toxicology and Environmental Health A, vol. 54, no. 6, pp. 467–475, 1998. View at: Google Scholar
  67. R. A. Kowluru, R. L. Engerman, G. L. Case, and T. S. Kern, “Retinal glutamate in diabetes and effect of antioxidants,” Neurochemistry International, vol. 38, no. 5, pp. 385–390, 2001. View at: Publisher Site | Google Scholar
  68. I. G. Obrosova, A. G. Minchenko, V. Marinescu et al., “Antioxidants attenuate early up regulation of retinal vascular endothelial growth factor in streptozotocin-diabetic rats,” Diabetologia, vol. 44, no. 9, pp. 1102–1110, 2001. View at: Publisher Site | Google Scholar
  69. C. D. Agardh, E. Agardh, B. Hultberg, Y. Qian, and C. G. Östenson, “The glutathione levels are reduced in Goto-Kakizaki rat retina, but are not influenced by aminoguanidine treatment,” Current Eye Research, vol. 17, no. 3, pp. 251–256, 1998. View at: Publisher Site | Google Scholar
  70. R. A. Kowluru, R. L. Engerman, and T. S. Kern, “Abnormalities of retinal metabolism in diabetes or experimental galactosemia VIII. Prevention by aminoguanidine,” Current Eye Research, vol. 21, no. 4, pp. 814–819, 2000. View at: Publisher Site | Google Scholar
  71. A. C. S. Woollard, Z. A. Bascal, G. R. Armstrong, and S. P. Wolff, “Abnormal redox status without increased lipid peroxidation in sugar cataract,” Diabetes, vol. 39, no. 11, pp. 1347–1352, 1990. View at: Google Scholar
  72. S. A. Moustafa, “Effect of glutathione depletion on carbohydrate metabolism in the rat,” Research Communications in Pharmacology and Toxicology, vol. 3, no. 1-2, pp. 55–64, 1998. View at: Google Scholar
  73. R. I. Fink, T. Huecksteadt, and Z. Karaoghlanian, “The effects of aging on glucose metabolism in adipocytes from Fischer rats,” Endocrinology, vol. 118, no. 3, pp. 1139–1147, 1986. View at: Google Scholar
  74. S. A. Moustafa, J. E. Webster, and F. E. Mattar, “Effects of aging and antioxidants on glucose transport in rat adipocytes,” Gerontology, vol. 41, no. 6, pp. 301–307, 1995. View at: Google Scholar
  75. A. Kowald and T. B. L. Kirkwood, “Towards a new theory of aging and the protein error theory,” Journal of Theoretical Biology, vol. 168, pp. 75–94, 1994. View at: Google Scholar
  76. J. P. Thomas, G. J. Bachowski, and A. W. Girotti, “Inhibition of cell membrane lipid peroxidation by cadmium- and zinc-metallothioneins,” Biochimica et Biophysica Acta, vol. 884, no. 3, pp. 448–461, 1986. View at: Google Scholar
  77. Z. E. Suntres and E. M. K. Lui, “Biochemical mechanism of metallothionein-carbon tetrachloride interaction in vitro,” Biochemical Pharmacology, vol. 39, no. 5, pp. 833–840, 1990. View at: Publisher Site | Google Scholar
  78. P. J. Thornalley and M. Vasak, “Possible role for metallothionein in protection against radiation-induced oxidative stress. Kinetics and mechanism of its reaction with superoxide and hydroxyl radicals,” Biochimica et Biophysica Acta, vol. 827, no. 1, pp. 36–44, 1985. View at: Publisher Site | Google Scholar
  79. C. M. St Croix, K. J. Wasserloos, K. E. Dineley, I. J. Reynolds, E. S. Levitan, and B. R. Pitt, “Nitric oxide-induced changes in intracellular zinc homeostasis are mediated by metallothionein/thionein,” American Journal of Physiology, vol. 282, no. 2, pp. L185–L192, 2002. View at: Google Scholar
  80. Y. Zhang, W. Zhao, H. J. Zhang, F. E. Domann, and L. W. Oberley, “Overexpression of copper zinc superoxide dismutase suppresses human glioma cell growth,” Cancer Research, vol. 62, no. 4, pp. 1205–1212, 2002. View at: Google Scholar
  81. S. I. Yamagishi, S. Amano, Y. Inagaki et al., “Advanced glycation end products-induced apoptosis and overexpression of vascular endothelial growth factor in bovine retinal pericytes,” Biochemical and Biophysical Research Communications, vol. 290, no. 3, pp. 973–978, 2002. View at: Publisher Site | Google Scholar
  82. J. Kim, K. M. Kim, C.-S. Kim et al., “Puerarin inhibits the retinal pericyte apoptosis induced by advanced glycation end products in vitro and in vivo by inhibiting NADPH oxidase-related oxidative stress,” Free Radical Biology and Medicine, vol. 53, no. 2, pp. 357–365, 2012. View at: Publisher Site | Google Scholar
  83. A. C. Clermont, L. P. Aiello, F. Mori, L. M. Aiello, and S. E. Bursell, “Vascular endothelial growth factor and severity of nonproliferative diabetic retinopathy mediate retinal hemodynamics in vivo: a potential role for vascular endothelial growth factor in the progression of nonproliferative diabetic retinopathy,” American Journal of Ophthalmology, vol. 124, no. 4, pp. 433–446, 1997. View at: Google Scholar
  84. X. Wang, G. Wang, and Y. Wang, “Intravitreous vascular endothelial growth factor and hypoxia-inducible factor 1a in patients with proliferative diabetic retinopathy,” American Journal of Ophthalmology, vol. 148, no. 6, pp. 883–889, 2009. View at: Publisher Site | Google Scholar
  85. A. P. Adamis, J. W. Miller, M. T. Bernal et al., “Increased vascular endothelial growth factor levels in the vitreous of eyes with proliferative diabetic retinopathy,” American Journal of Ophthalmology, vol. 118, no. 4, pp. 445–450, 1994. View at: Google Scholar
  86. C. M. Andreoli and J. W. Miller, “Anti-vascular endothelial growth factor therapy for ocular neovascular disease,” Current Opinion in Ophthalmology, vol. 18, no. 6, pp. 502–508, 2007. View at: Publisher Site | Google Scholar
  87. R. G. Uzzo, P. L. Crispen, K. Golovine, P. Makhov, E. M. Horwitz, and V. M. Kolenko, “Diverse effects of zinc on NF-κB and AP-1 transcription factors: implications for prostate cancer progression,” Carcinogenesis, vol. 27, no. 10, pp. 1980–1990, 2006. View at: Publisher Site | Google Scholar
  88. M. DeNiro and F. A. Al-Mohanna, “Zinc transporter 8 (znt8) expression is reduced by ischemic insults: a potential therapeutic target to prevent ischemic retinopathy,” PLoS ONE, vol. 7, no. 11, Article ID e50360, 2012. View at: Publisher Site | Google Scholar
  89. T. Adachi, M. Teramachi, H. Yasuda, T. Kamiya, and H. Hara, “Contribution of p38 MAPK, NF-κB and glucocorticoid signaling pathways to ER stress-induced increase in retinal endothelial permeability,” Archives of Biochemistry and Biophysics, vol. 520, no. 1, pp. 30–35, 2012. View at: Publisher Site | Google Scholar
  90. Y. Zhao, Y. Tan, J. Dai et al., “Exacerbation of diabetes-induced testicular apoptosis by zinc deficiency is most likely associated with oxidative stress, p38 MAPK activation, and p53 activation in mice,” Toxicology Letters, vol. 200, no. 1-2, pp. 100–106, 2011. View at: Publisher Site | Google Scholar
  91. L. Scheppke, E. Aguilar, R. F. Gariano et al., “Retinal vascular permeability suppression by topical application of a novel VEGFR2/Src kinase inhibitor in mice and rabbits,” Journal of Clinical Investigation, vol. 118, no. 6, pp. 2337–2346, 2008. View at: Publisher Site | Google Scholar

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