Mitochondria-targeted antioxidant SKQ1 protects cornea from oxidative damage induced by ultraviolet irradiation and mechanical injury
Cornea protects the eye against natural and anthropogenic ultraviolet (UV) damage and mechanical injury. Corneal incisions produced by UV lasers in ophthalmic surgeries are often complicated by oxidative stress and inflammation, which delay wound healing and result in vision deterioration. This study trialed a novel approach to prevention and treatment of iatrogenic corneal injuries using SkQ1, a mitochondria-targeted antioxidant approved for therapy of polyethiological dry eye disease.
Rabbit models of UV-induced and mechanical corneal damage were employed. The animals were premedicated or treated with conjunctival instillations of 7.5 μM SkQ1. Corneal damage was assessed by fluorescein staining and histological analysis. Oxidative stress in cornea was monitored by measuring malondialdehyde (MDA) using thiobarbituric acid assay. Total antioxidant activity (AOA) was determined using hemoglobin/H2O2/luminol assay. Glutathione peroxidase (GPx) and superoxide dismutase (SOD) activities were measured using colorimetric assays.
In both models corneas exhibited fluorescein-stained lesions, histologically manifesting as basal membrane denudation, apoptosis of keratocytes, and stromal edema, which were accompanied by oxidative stress as indicated by increase in lipid peroxidation and decline in AOA. The UV-induced lesions were more severe and long healing as corneal endothelium was involved and GPx and SOD were downregulated. The treatment inhibited loss of keratocytes and other cells, facilitated re-epithelialization and stromal remodeling, and reduced inflammatory infiltrations and edema thereby accelerating corneal healing approximately 2-fold. Meanwhile the premedication almost completely prevented development of UV-induced lesions. Both therapies reduced oxidative stress, but only premedication inhibited downregulation of the innate antioxidant activity of the cornea.
SkQ1 efficiently prevents UV-induced corneal damage and enhances corneal wound healing after UV and mechanical impacts common to ocular surgery. Its therapeutic action can be attributed to suppression of mitochondrial oxidative stress, which in the first case embraces all corneal cells including epitheliocytes, while in the second case affects residual endothelial cells and stromal keratocytes actively working in wound healing. We suggest SkQ1 premedication to be used in ocular surgery for preventing iatrogenic complications in the cornea.
KeywordsPhotorefractive surgery Iatrogenic ocular damage UV-induced oxidative stress Cornea SkQ1
total antioxidant activity
Laser-assisted in situ keratomileusis
Phosphate buffer saline
Cornea is the quickly regenerating defensive barrier of the eye, protecting intraocular structures from environmental stress. In particular, cornea absorbs ultraviolet (UV) component of sunlight and prevents it from reaching vulnerable parts of the eye, such as the retina . Meanwhile, prolonged UV irradiation of the eye surface is associated with high risk of corneal injury. It is widely regarded that UV-induced damage is mediated by oxidative stress in corneal cells (for review, see ). To endure this exposure, cornea possesses innate antioxidant qualities . While sunlight is the major source of UV rays, in some cases human eyes are exposed to more harmful forms of UV, as, for instance, during medical procedures. Indeed, UV lasers of different wavelengths have wide range of applications in ophthalmology. Far-ultraviolet excimer lasers (150–200 nm) allow evaporating corneal epithelium and stroma and making cuts of precise depth and shape without thermal damage to the adjacent tissue . Thereby, they are utilized in vision correction surgeries, such as laser-assisted in situ keratomileusis (LASIK) and photorefractive keratectomy (PRK) . In both operations excimer laser is employed to remodel the corneal stroma. However, in LASIK, an epithelium flap is temporally created at the site of the operation using either microtome or femtosecond infrared laser and it is put in place after the procedure. In PRK, the epithelium is completely removed mechanically, chemically or with application of excimer laser (transepithelial PRK) . Longer wavelength UV lasers (200–350 nm) are less commonly used to operate on cornea, as they are known to produce irregular cut edges and have varied mutagenic effects on epithelial cells [7, 8, 9, 10].
Even relatively mild irradiations with UV light of different wavelengths can be detrimental to corneal structure and function as they result in elevation of intracellular reactive oxygen species (ROS) [11, 12, 13, 14]. Excessive ROS accumulation leads to oxidative damage to proteins and membranes as well as nuclear and mitochondrial DNA [11, 12]. Mitochondria are mostly sensitive to oxidative stress as they are the major source of the basic ROS levels and depend on redox processes in respect to their functions, biogenesis and turnover . Under intense UV irradiation, the antioxidant mechanisms of the cornea can be overwhelmed, resulting in oxidative damage to mitochondria and other cellular components thereby promoting apoptosis of corneal cells and inducing ocular pathology [11, 12]. Oxidative stress triggers inflammation and deters corneal wound healing, which increases risk of visual complications, as quick restoration of corneal structure after injury is crucial for preservation of its transparency and curvature. Persistent corneal epithelium defects are strongly associated with excessive apoptosis of stromal keratocytes, corneal fibroblasts responsible for remodeling of extracellular matrix and production of growth factors that stimulate proliferation of corneal epithelial cells [15, 16]. Oxidative stress was demonstrated to target both keratocytes and multipotent cells of corneal epithelium, ultimately leading to scarring and opacification of cornea and irreversible deterioration of vision .
In view of this, there is a growing interest in applying antioxidants to prevent and treat iatrogenic complications in cornea associated with UV irradiation. A group of antioxidants capable of bypassing plasma membrane and accumulating in mitochondria emerged in recent decades and they were shown to outperform conventional antioxidants in terms of specificity and activity levels [18, 19, 20, 21]. Among these mitochondria-targeted antioxidants, plastoquinonyl-decyl-triphenylphosphonium bromide (SkQ1) was approved for treating multi-etiological dry eye syndrome (DES) [22, 23]. Recently, using rabbit (Oryctolagus cuniculus) model of anesthesia-induced DES we have demonstrated that SkQ1 at dosage 7.5 μM not only suppresses oxidative stress, but also enhances intrinsic antioxidant defense of the corneal cells thereby exhibiting pronounced cornea-protecting activity .
In this study, using rabbit models involving UV irradiation and corneal scarification, we trialed feasibility of SkQ1 for prevention and treatment of UV-induced and mechanical corneal injury associated with common ophthalmological procedures. The benefits of mitochondria-targeted antioxidant therapy using SkQ1 were assessed by means of clinical and histological analysis as well as biochemical assays. The mechanisms underlying effects of SkQ1 on corneal state and functionality as well as prospective ophthalmological applications of the mitochondria-targeted antioxidant therapy are considered.
SkQ1 (10-(6′-plastoquinonyl)-decyltriphenylphosphonium) was provided by the Institute of Mitoengineering of Moscow State University (Moscow, Russia). Anesthetic preparation containing 50 mg/ml tiletamine and 50 mg/ml zolazepam was bought from Virbac, UK. Fluorescein sodium solution was purchased from Novartis, Switzerland. Superoxide dismutase and malondialdehyde assay kits were from Sigma-Aldrich, USA. Glutathione peroxidase assay kit was from Randox, UK. Reagents and supplies for histology were from Biovitrum, Russia. Other reagents were from Gibco, Sigma-Aldrich, Amresco and Serva and were at least reagent grade. All buffers and other solutions were prepared using ultrapure deionized water.
Experimental animals and ethics statement
The study involved a total of 144 pigmented male rabbits (6 months old, 2.3 to 3 kg). The animals were purchased from a certified farm (Krolinfo, Russia). The rabbits were housed individually in 795x745x1776 mm cages at a 12 h light-dark cycle (8:00–20:00) at a temperature of 22–25 °C and humidity of 55–60% with free access to maintenance rabbit food (BioPro, Russia) and water. The health status of all animals was monitored daily and no adverse events were observed during the course of the study. The treatment of the animals was performed according to the 8th edition “Guide for the Care and Use of Laboratory Animals” of the National Research Council and “Statement for the Use of Animals in Ophthalmic and Visual Research” of The Association for Research in Vision and Ophthalmology (ARVO). The protocol was approved by the Belozersky Institute of Physico-chemical Biology Animal Care and Use Committee (Protocol number 1/2016). For biochemical and histological studies of the cornea, the rabbits were humanely euthanized by introduction into general anesthesia and subsequent intracardiac injection of the 1 ml of 20 mg/ml xylazine hydrochloride. Enucleating of the eyeballs and corneal excision were performed post-mortem.
Experimental models and treatment regimen
The experiments were performed using a single-blind method. The animals were allowed to acclimatize to the research facility for 5–7 days before the start of the experiment. All experimental procedures were carried out in the laboratory. During the UV irradiation and trephination sessions, the animals were placed in a restraining device and anesthetized with intramuscular injection of 1:2 mixture of 50 mg/ml tiletamine/zolazepam and 20 mg/ml xylazine hydrochloride (max. 2.2 mg/kg tiletamine/zolazepam, 1.7 mg/kg xylazine hydrochloride). The UV illuminations of the cornea were performed with halogen lamp (312 nm, 8 W) from the distance of 40 cm for 4 days, 20 min per day. Scarification of the cornea was performed using 7 mm circular trephine knife with incisions depth of 50 μm. After the procedure the animals were returned to the housing. For antioxidant treatment (administration Scheme 1), the animals were medicated by conjunctival instillations of 50 μl of either 7.5 μM SkQ1 in vehicle solution (7 mM phosphate buffer saline (PBS) pH 7.4, 0.0001% benzalkonium chloride) or placebo (vehicle solution) 3 times a day for 1–30 days (1–4 days in case of the scarification model), starting immediately after the final irradiation session/trephination. Antioxidant premedication (administration Scheme 2) was performed 60 min before the irradiation session by conjunctival instillations of 7.5 μM SkQ1 or placebo, 1 instillation each 10 min.
Division of groups
Clinical examination of cornea
The development of corneal injury was monitored by fluorescein staining of the ocular surface as described in . The registered corneal injuries were assigned clinical scores of 0–6 depending on the size of the affected corneal surface: no fluorescein staining (0 points), staining of 0–12.5% of the corneal surface (1 point), 12.5–25% (2 points), 25–50% (3 points), 50–75% (4 points), 75–90% (5 points) and > 90% (6 points). Mean clinical scores were derived by adding the clinical scores for all eyes of the animals in a group and dividing by the number of eyes ± standard error (SE).
The fixation and examination of the cornea was performed as described in . Briefly, the eyeballs were enucleated immediately post-mortem and fixed in 10% neutral buffered formalin in PBS (pH 7.4) for 24 h at room temperature or in Carnoy’s solution (60% ethanol, 30% chloroform, and 10% glacial acetic acid) for 3 h at room temperature. The corneas were trimmed out of fixed eyeballs, dehydrated and embedded in paraffin medium. Eight three-micron-thick nasotemporal cross-sections from anterior to posterior surfaces through peripheral and central areas of each cornea (at 300-μm intervals) were prepared. Corneal sections were stained with hematoxylin and eosin and examined using Axio Scope.A1 microscope (Carl Zeiss, Germany) and Leica DM400 (Leica, Germany) microscopes. Microphotographs were obtained by an AxioCam MRc 5 megapixel color camera (Carl Zeiss) and processed using AxioVision v.3.0 (Carl Zeiss) and Photoshop CS3 software (Adobe systems, USA).
Full-size rabbit corneas were excised, placed into 400 μl of PBS, and frozen at − 70 °C. After thawing, the tissue was sonicated for 10 min on ice. Corneal extracts for biochemical evaluations were obtained by centrifugation of the samples (15,000 g, 10 min) at + 4 °C. The supernatants were aliquoted and stored at − 70 °C, and the pellets were homogenized in MDA lysis buffer (Sigma-Aldrich) and used for MDA measurements as follows.
MDA concentration was measured in corneal homogenates by thiobarbituric acid assay using commercially available kit (Sigma-Aldrich). Intensity of colorimetric reaction at 532 nm was determined using Synergy H4 Hybrid Reader (Biotek, USA). The data were analyzed using SigmaPlot 11 (SYSTAT Software, USA).
Total protein concentration
Protein concentration in corneal extracts was measured by the bicinchoninic acid (BCA) assay using commercially available kit (Thermo Fisher Scientific, USA) in accordance with the manufacturer’s instructions. Intensity of colorimetric reaction at 562 nm was determined using Synergy H4 Hybrid Reader. The data were analyzed using SigmaPlot 11.
Total antioxidant activity
The corneal extracts were analyzed using standardized hemoglobin/H2O2/luminol model system . Standard solutions, containing 1–8 μM Trolox (6-hydroxy-2,5,7,8-tetramethylchroman-2-carboxylic acid) in PBS, were used as reference and total antioxidant activity (AOA) was expressed in Trolox equivalent. Luminol oxidation reaction in the model system was stimulated by the addition of hydrogen peroxide to final concentration of 6 μM, after which chemiluminescence was registered each 1 s for 10 min using Glomax-Multi Detection System luminometer (Promega, USA). The data were analyzed using SigmaPlot 11.
Activity of antioxidant enzymes
The activity of superoxide dismutase (SOD) and glutathione peroxidase (GPx) was evaluated in the corneal extracts, using commercially available kits (Sigma-Aldrich, Randox) in accordance with the manufacturer’s instructions. Intensity of colorimetric reactions was determined using Synergy H4 Hybrid Reader or Ultrospec 1000 (Pharmacia, Sweden). The acquired data were analyzed using SigmaPlot 11. The activity of the enzymes in corneal extracts was normalized to 1 mg of the total protein.
The data were analyzed by the mean standard error (SE) method. Mean, SE, and statistical significance were calculated using SigmaPlot 11. Statistical significance was assessed using unpaired two-tailed t-test for the experiments where SkQ1 and placebo were administered to separate groups, and paired two-tailed t-test for the experiments where every animal received SkQ1 in their left eye and placebo in their right eye. The probability of 0.05 was considered significant.
Clinical characterization of the corneal state after UV irradiation and scarification with or without SkQ1 premedication/treatment
Post-exposure treatment with conjunctival instillations of 7.5 μM SkQ1 significantly improved corneal healing rates in experimental animals. No corneal lesions (score 0–0.5) were detected by fluorescein staining as soon as on day 4 of postoperative period, as opposed to the animals that received placebo (Fig. 2a). Premedication with 7.5 μM SkQ1, in turn, efficiently protected corneas from UV damage (Fig. 2b). The eyes received the antioxidant premedication displayed either none or mild (0–2 points on fluorescein scale) corneal erosion already on the first day after the irradiation, indicative of high level of epitheliocyte survival in contrast to the control eyes, where severe corneal damage (up to 6 points on fluorescein scale) was observed. Thus, according to clinical examination, SkQ1 possesses potent therapeutic action in respect to UV-damaged cornea and effect of the antioxidant is more prominent when it is used as premedication than in the case of its post-exposure administration.
Histological examination of the cornea after UV irradiation and scarification with or without SkQ1 premedication/treatment
The treatment of the UV-irradiated corneas by SkQ1 instillations produced a pronounced therapeutic effect on cornea in agreement with clinical observations. While on the first day there was no observable difference between corneas of treated and control animals (Fig. 4f), by day 3 the treated corneas displayed reduced stromal edema, complete epithelialization and active remodeling of the stroma by collagen-producing keratocytes (Fig. 4g, green arrows). On day 7 in experimental group the advanced stage of stroma remodeling was observed, whereas in control group short coarse collagen fibers were still present (Fig. 4h). Furthermore, the rate of keratocyte death and the level of inflammatory infiltration were significantly lower in the treated samples. By day 30 both control and treated corneas were completely healed (Fig. 4i and e).
Monitoring of oxidative stress in UV and mechanically damaged cornea with or without SkQ1 premedication/treatment
Antioxidant treatment with 7.5 μM SkQ1 notably accelerated normalization of MDA, although its peak levels remained unaffected. Thus, starting from day 3, the treated corneas displayed approximately 2-fold reduction of MDA content as compared to the control. Interestingly, premedication of corneas with SkQ1 much more prominently mitigated elevation of MDA content after the exposure to UV light (Fig. 7b). Thus, MDA only increased 15-fold in SkQ1 pre-treated rabbits in contrast to 70-fold MDA elevation in animals premedicated with placebo. In the aggregate, these data indicate that the revealed therapeutic effects of SkQ1 on the damaged corneas stems from its high efficacy in suppressing UV-induced oxidative stress of the corneal cells.
Alterations in antioxidant defense system of the cornea under conditions of UV and mechanically induced damage with or without SkQ1 premedication/treatment
Collectively, our biochemical data demonstrate that the revealed protective effect of SkQ1 on the cornea in the UV damage model is associated with the suppression of intense oxidative stress and restoration of AOA of this tissue. In the case of mechanical injury model, the oxidative stress in the cornea, although inhibited by SkQ1, is initially less pronounced, and therefore the effect of the antioxidant is likely supported by its additional biochemical activities.
Cornea is the barrier protecting the eye from natural and anthropogenic UV irradiation. Meanwhile, in popular forms of photorefractive surgery, namely LASIK and PRK, cornea is exposed to relatively high doses of UV irradiation coming from excimer lasers, which were reported to induce persistent corneal lesions and mild keratitis [29, 30, 31, 32]. Furthermore, in PRK, the exposure of the cornea to UV irradiation is preceded by mechanical removal of significant part of corneal epithelium (in contrast to LASIK, where epithelium flap is peeled off using precise cuts made by infrared laser and is put in place afterwards), which increases the risk of complications due to longer recovery times. In addition, refractive surgery weakens the protective qualities of the corneal epithelium and makes it more vulnerable to UV irradiation from natural sources. Consistently, the patients are recommended to wear sunglasses and apply anti-inflammatory and antioxidant agents for several months after the operation to avoid complications . In this study we attempted to model all potentially harmful components of excimer laser photorefractive surgery and trial novel mitochondria-targeted antioxidant therapy for prevention of postoperative adverse effects and improvement of corneal wound healing. To this end, we used experimental models of UV and mechanical corneal injury in rabbits. These species are well suited for ophthalmological research due to many similarities in biomechanical properties of rabbit and human eyes . Indeed, in our previous works rabbits were successfully employed for monitoring anesthesia-induced damage and oxidative stress in cornea on clinical, histological and biochemical levels [24, 27, 28].
In our studies, we employed irradiations of the cornea with 312 nm UV light. In general, cornea is highly susceptible to damage induced by a wide range of UV wavelengths. Therefore, the established animal models of UV-induced corneal damage include all three ranges of UV irradiation, namely UVA (315–400), UVB (280–315 nm) and UVC (100–280). Meanwhile, UVB spectrum was shown to have the highest damaging potential: in doses as small as 0.5 J/cm2 it can lead to significant alterations in corneal epithelium and affect the optical properties of the tissue [35, 36, 37]. Furthermore, long wavelength UVB (312 nm) threatens the non-renewable cells of the corneal endothelium and stroma . In early studies, excimer lasers of the UVB range were widely trialed for photorefractive surgery. Yet, these lasers were found to produce harmful side effects on the cornea, and they were outcompeted by lasers of the UVC spectrum (193 nm) [8, 9, 10]. However, the molecular mechanisms of corneal damage induced by UVB and UVC are similar [39, 40, 41]. Since the main objective of our study was to evaluate the effectiveness of antioxidant therapy and premedication in the worst-case scenario, more severe UVB model was considered well suited for these purposes. Another benefit of such model is that it additionally simulates post-operative complications induced by the exposure of the ablated cornea to sunlight. The cumulative dose of UV irradiation received by the animals was 0.36 J/cm2 per day (1.44 J/cm2 total over 4 days). This exposure induced clinically prominent corneal lesions. The damage manifested as complete destruction of corneal epithelium, including its basal layer, which contains dividing cells, crucial for corneal regeneration . Other morphological features included mass apoptosis of keratocytes and corneal endothelium cells, stromal edema and inflammatory cell infiltration. The complete recovery on the clinical level was achieved after 7 days while morphological signs of pathology were only resolved after 30 days. Overall, our model reproduced the key features of long-healing UV-induced injuries described in previous studies , which generally corresponded to epithelial defects observed on corneal surface of some PRK and LASIK patients during the postoperative period [44, 45, 46, 47, 48].
In turn, mechanically induced corneal lesions were simulated by performing experimental corneal scarification. Namely, 50 μm-thick flap of corneal epithelium was removed with circular trephine knife, imitating the procedure involved in PRK. In this model, despite the complete absence of the epithelium in the damaged area, basal membrane and deeper layers of cornea were mostly unaffected; there were many survived and active keratocytes and the endothelium was intact. In general, our model reproduced the mechanical damage to cornea, associated with epithelium displacement, which was shown to contribute to development of persistent corneal defects in patients undergoing similar surgeries [47, 48].
Both models were used for trialing mitochondria-targeted antioxidant therapy for preventing complications and improving corneal healing in postoperative period. Indeed, oxidative stress was recognized as the most severe damaging factor in UV-induced and other types of corneal injury. ROS are known to mediate lipid peroxidation in corneal epithelium exposed to UV light, with generation of MDA . Consistently, in our UV model, concentration of MDA in irradiated corneas increased more than 60-fold. Remarkably, it did not fully normalize until after 30 days following the final UV irradiation session, long after the clinical signs of superficial epithelial damage were resolved. Thus, the oxidative damage might be responsible for delayed recovery of internal epithelium layers and other corneal cells as well as late resolution of corneal edema and inflammation. Oxidative stress was shown to cause keratocyte apoptosis and reduce the natural re-epithelialization rate, which potentially results in irreversible damage to cornea [50, 51, 52]. Indeed, in contrast to the UV model, in corneal scarification model MDA increased only 2.5-fold, which could explain keratocyte survival and preservation of corneal endothelium, as well as faster tissue regeneration.
UV-induced oxidative stress leading to apoptosis of corneal epitheliocytes and other corneal cells is mediated by mitochondrial damage [12, 53, 54]. Indeed, mitochondria are highly sensitive to oxidative stress as they represent intracellular source of ROS and their function depends on redox state of the cell [11, 12]. With this in mind, we applied mitochondria-targeted antioxidant SkQ1 in attempt to prevent or treat the UV-induced oxidative damage. The postoperative therapy with conjunctival instillations of SkQ1 was found to suppress cell death in all corneal layers and accelerate regeneration of the epithelium almost 2-fold. Furthermore, the progress of regeneration strongly correlated with faster resolution of oxidative stress in the treated corneas as indicated by MDA levels. Interestingly, SkQ1 was even more beneficial when administered as premedication. In this case, the development of epithelial lesions on day 1 after the final irradiation session was almost completely prevented both in the center and at the periphery of the cornea, while in the eyes subjected to post-exposure treatment focal epithelial loss still occurred. Furthermore, the histological signs of edema and inflammatory infiltration were also less pronounced in the cornea of the premedicated animals, as compared to the treatment administration scheme. Consistently, the oxidative stress in premedicated animals was weaker as evidenced by lower MDA levels after the UV irradiation sessions. In the case of scarification model, we did not employ SkQ1 premedication because the model involves mechanical removal of a significant portion of antioxidant-loaded tissue right after its administration. Meanwhile, the postoperative therapy with SkQ1, assessed in this case, combines the benefits of both premedication and treatment since it is applied immediately after scarification as distinct from the UV model where SkQ1 is administrated only after 4 days after the initial intervention. Even against moderate oxidative stress observed upon corneal scarification, the effect of SkQ1 was still noticeable, as the treatment resulted in 30% lower MDA level on the 1st day. Overall, SkQ1 is more effective, when used as preventive care, which is consistent with the conclusions of our previous work related to anesthesia-induced corneal abrasions . Taken together, our data clearly demonstrates that SkQ1 can effectively avert and/or heal oxidative damage of the cornea, the main factor inducing postoperative complications after photorefractive surgery.
It is known that SkQ1 specifically targets mitochondria and prevents these organelles from intoxicating the cell with ROS . Thus, the efficacy of SkQ1 action directly depends on amount of the living cells in cornea at the beginning of the antioxidant administration, which explains prominent benefits of the premedication scheme. What are in this case the mechanisms underlying efficacy of post-exposure treatment with SkQ1 in enhancing of corneal wound healing after UV damage? By the time the treatment starts the corneal epitheliocytes are absent due to UV-induced apoptosis. Therefore, antioxidant treatment protects only the cells that survived the initial UV exposure, such as keratocytes and endothelial cells. It is well recognized that UV damage of the cornea includes massive loss of keratocytes that are key participants of corneal regenerative mechanisms and producers of collagen . The hazard of the UVB spectrum also relies on its ability to affect corneal endothelium [17, 41, 56, 57], which is responsible for nutrition of the cornea and maintaining its optical properties [58, 59, 60]. Notably, adult endotheliocytes are unable of division, so that dead and injured cells cannot be replaced . Both keratocytes and endotheliocytes possess high metabolic rates and are thereby highly susceptible to mitochondrial damage associated with excessive ROS production . Thus, the suppression of mitochondrial oxidative stress in survived keratocytes and endothelium by SkQ1 treatment might improve their longevity and functional activity during the energy-consuming process of wound healing.
In attempt to understand biochemical mechanisms underlying survival of corneal cells promoted by SkQ1, we analyzed the dynamics of innate antioxidant activity in the UV and mechanically damaged tissue. Firstly, we addressed total antioxidant activity (AOA), provided by low molecular weight antioxidants of the cornea, mainly glutathione, ascorbate, and α-tocopherol. AOA was prominently reduced by UV irradiation, but was restored early in postoperative period. Interestingly, this profile of the AOA alterations, in general, correlated with the amount of the survived epithelial cells. Indeed, corneal epithelium is the main source of low molecular weight antioxidants in cornea [62, 63]. Consistently, AOA was not affected by the SkQ1 treatment, but it was retained in SkQ1-premedicated corneas, which preserved their epithelium. Thus, we propose that antioxidant action of SkQ1 is reinforced by maintaining the innate antioxidant defense in the cornea provided by the epitheliocyte survival.
Secondly, we monitored activity of two major antioxidant enzymes, superoxide dismutase (SOD) and glutathione peroxidase (GPx). SOD is responsible for superoxide anion disproportionation into hydrogen peroxide and molecular oxygen, whereas GPx acts as a scavenger of intracellular hydrogen peroxide, protecting lipids from oxidation [64, 65, 66]. Both enzymes were reported to undergo UV-induced alterations [51, 67, 68]. Consistently, they were downregulated in our UV model. Interestingly, this downregulation occurred simultaneously with overall elevation of total protein content in corneal samples, despite the complete loss of epithelium, which normally amounts for 80% of the soluble corneal protein . This discrepancy can be explained by pronounced inflammation, observed in our histological studies, and subsequent contamination of the samples with excess of serum proteins. GPx was more susceptible to UV irradiation than SOD. This agrees with previous observations [51, 67, 68] and is commonly speculated to be caused by loss of GPx-producing cells in corneal endothelium . Consistently, the lowest value of GPx activity was observed on day 3 of the post-exposure period, when the most pronounced apoptotic changes in corneal endothelium occurred. In general, neither of the examined enzymes exhibited prominent susceptibility to SkQ1 premedication or therapy. GPx activity was slightly enhanced by SkQ1 treatment, which could be explained by better preservation of endothelial cells. Similar enhancement was observed in another model of corneal damage produced by general anesthesia , although in this case the effect was much more pronounced. Regardless of treatment, GPx and SOD did not recover even when the UV-damage of the epithelium was completely healed, which contrasts with the above described AOA dynamics. We speculate that UV-induced decrease of the antioxidant enzymes activity could be in part a result of the specific regulation of protein expression by UV-dependent signaling pathways known as UV-response [70, 71, 72]. Although SkQ1 does not seem to directly affect these mechanisms, it effectively compensates for the decrease in the antioxidant enzyme activity by suppressing mitochondrial oxidative stress and promoting cell survival in the irradiated cornea.
In this study mitochondria-targeted antioxidant therapy using 7.5 μM SkQ1 was recognized as a promising approach to treating chronic corneal damage, associated with UV irradiation and mechanical injury. Prophylactic administration of SkQ1 efficiently prevented UV-induced damage of all corneal cells including epitheliocytes, whereas the post-exposure treatment with this antioxidant promoted faster restoration of normal corneal metabolism and enhanced corneal wound healing through inhibition of keratocyte apoptosis and endothelial damage. In both administration schemes, SkQ1 possessed cell protector activity via suppressing mitochondrial oxidative stress induced by UV light and mechanical injury. Meanwhile, the most prominent benefit of SkQ1 towards UV-induced damage was observed upon its preemptive application, as in this case effect of the antioxidant is facilitated by innate antioxidant defense of the cornea preserved due to massive survival of epithelial cells. Conveniently, ophthalmic surgeries involving risk of UV-induced and mechanical corneal injury are usually scheduled in advance. Therefore, we propose the SkQ1 premedication in patients undergoing these surgeries to improve corneal regeneration and prevent persistent corneal defects.
The authors acknowledge Ekaterina I. Kabanova from Skryabin Moscow State Academy of Veterinary Medicine and Biotechnology for assistance in animal studies.
This study was supported by the Russian Science Foundation (Project no. 16–15-00255). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Availability of data and materials
The datasets used and/or analyzed during the current study are available from the corresponding author on reasonable request.
EYZ, AAZ, PPP and IIS participated in the design of the study. Literature screening and analysis was performed by EYZ, PPP and AAZ. The animal treatment and clinical studies were performed by VVT and IIS. Histological analysis was performed by OSG. Biochemical studies were carried out by VEB, VVT, IIS and EYZ. The manuscript was prepared by VEB, IIS and EYZ. All authors read and approved the manuscript.
The treatment of the animals was performed according to the 8th edition "Guide for the Care and Use of Laboratory Animals" of the National Research Council and "Statement for the Use of Animals in Ophthalmic and Visual Research" of The Association for Research in Vision and Ophthalmology (ARVO). The protocol was approved by the Belozersky Institute of Physico-chemical Biology Animal Care and Use Committee (Protocol number 1/2016).
Consent for publication
The authors declare that they have no competing interests.
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