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. 2015 Mar 3;2015:242517. doi: 10.1155/2015/242517

NaoXinTong Inhibits the Development of Diabetic Retinopathy in db/db Mice

Mengyang Liu 1,2, Quan Pan 1,2, Yuanli Chen 1,3,4, Xiaoxiao Yang 1,2, Buchang Zhao 5, Lifu Jia 5, Yan Zhu 6, Jihong Han 1,2,4, Xiaoju Li 1,*, Yajun Duan 1,2,4,*
PMCID: PMC4363582  PMID: 25821481

Abstract

Buchang NaoXinTong capsule (NXT) is a Chinese Materia Medica standardized product extracted from 16 Chinese traditional medical herbs and widely used for treatment of patients with cerebrovascular and cardiovascular diseases in China. Formation of microaneurysms plays an important role in the development of diabetic retinopathy. In this study, we investigated if  NXT can protect diabetic mice against the development of diabetic retinopathy. The db/db mice (~6 weeks old), a diabetic animal model, were divided into two groups and fed normal chow or plus NXT for 14 weeks. During the treatment, fasting blood glucose levels were monthly determined. After treatment, retinas were collected to determine retinal thickness, accumulation of carbohydrate macromolecules, and caspase-3 (CAS-3) expression. Our results demonstrate that administration of NXT decreased fasting blood glucose levels. Associated with the decreased glucose levels, NXT blocked the diabetes-induced shrink of multiple layers, such as photoreceptor layer and outer nuclear/plexiform layers, in the retina. NXT also inhibited the diabetes-induced expression of CAS-3 protein and mRNA, MMP-2/9 and TNFα mRNA, accumulation of carbohydrate macromolecules, and formation of acellular capillaries in the retina. Taken together, our study shows that NXT can inhibit the development of diabetic retinopathy and suggests a new potential application of NXT in clinic.

1. Introduction

Diabetes is a big public health problem because it can induce multiple complications in different organs. The number of diabetic patients is expected to be 552 million by 2030 globally [1]. Diabetic retinopathy, one of the most common microvascular complications of diabetes, is a leading cause of vision impairment and blindness in adults [2–4]. Nearly all the patients with type 1 diabetes and more than half of the patients with a 20-year history of type 2 diabetes can develop retinopathy [5]. The development of diabetic retinopathy can be regulated by multiple factors, such as hyperglycemia, oxidative stress, proinflammation, and generation of advanced glycation end products (AGEs) [6–9]. These pathological processes can lead to loss of retinal capillary cells, disruption of vascular barrier, formation of microaneurysms, and preretinal neovascularization [2, 10].

Hyperglycemia plays a central role in the initiation of diabetic retinopathy because it substantially induces pathological changes in the retinal vascular. The epidemiological studies on diabetes demonstrate a strong link between the degree of hyperglycemia and the progression of diabetic retinopathy. Accordingly, lowering plasma glucose levels significantly reduces the prevalence of retinopathy in the diabetic patients. Therefore, the timely tight control of blood glucose is an effective way to reduce the development of diabetic retinopathy [11, 12].

Buchang NaoXinTong capsule (NXT) is an approved traditional Chinese medicine and is used to treat patients with stroke and other vascular diseases. NXT contains the following 16 various kinds of traditional Chinese medicines: Astragalus membranaceus, Salvia miltiorrhiza, Ligusticum, Radix Paeoniae Rubra, Szechwan Lovage Rhizome, Semen Persicae, Carthamus tinctorius L., Frankincense, myrrh, Spatholobus suberectus, Achyranthes Root, CassiaTwig, Mulberry Twig, earthworms, scorpions, and Hirudo [13]. Studies with animal models demonstrate that NXT can protect proatherogenic mice against the development of atherosclerosis by ameliorating serum lipid profiles and inhibiting maturation of dendritic cells [14]. NXT also increases the catalytic activity of the drug metabolizing CYP2C19 enzyme. The combined NXT and clopidogrel further increase the antiplatelet effect of clopidogrel in patients with CYP2C19∗2 gene mutation [15]. All the above observations suggest that NXT has protective effects in cardiac and vascular diseases. Formation of diabetic retinopathy is associated with the pathological progress of microvascular system. Therefore, in this study, we determined if NXT can reduce diabetic retinopathy in an animal model.

2. Materials and Methods

2.1. Materials

NXT was kindly provided by Xianyang Buchang Pharmaceutical Co. Ltd. (Shan'xi, China). Rabbit anti-CAS-3 polyclonal antibody was purchased from Santa Cruz Biotechnology (Dallas, Texas). All other chemicals were purchased from Sigma-Aldrich (St. Louis, MO) except as indicated.

2.2. Animals

The protocol for in vivo study with mice was granted by the Committee on the Ethics of Animal Experiments of Nankai University (Tianjin, China) and conforms to the Guide for the Care and Use of Laboratory Animals published by NIH. Both male type 2 diabetic (BKS.C g-m +/+ Leprdb/J, db/db) mice and C57BLKS/J wild type mice at the age of 6 weeks were purchased from the Animal Center of Nanjing University (Nanjing, China). The animals were maintained at the Animal Center of Nankai University with free access to food and drinking water.

Based on the clinical usage, the dose of NXT applied to mice was converted into 624 mg/kg body weight/day (mpk) [14]. The male db/db mice were randomly divided into two groups (10/group) and received following treatment: group 1, mice were fed normal chow; group 2, mice were fed the chow containing NXT (624 mpk). Meanwhile, male C57BLKS/J wild type mice were used as a nondiabetic or normal control. The treatment was continued for ~14 weeks.

2.3. Determination of Fasting Blood Glucose Levels

During the treatment, blood was withdrawn from mouse tail vein after overnight fasting at the different time points. Blood glucose levels were determined with a OneTouch glucometer and test strips (LifeScan, Milpitas, CA) according to the manufacture's instruction.

2.4. Preparation and PAS Staining of Retinal Vasculature and Quantitation of Acellular Capillaries

Retinal vasculature was prepared based on the method as described [16] with minor modifications. Briefly, mouse eyes were fixed in 4% paraformaldehyde freshly made in PBS (PFA/PBS) overnight after enucleation. The retinas were dissected from eyeballs, washed in water overnight with gentle shaking at room temperature (RT), and then digested in 3% trypsin solution (Invitrogen, Grand Island, NY) for 2-3 h at 37°C. The tissue was then transferred into filtered water and the network of vessels was freed from adherent retinal tissue by gentle shaking and manipulation under a dissection microscope. The vessels were then mounted on clean slides, air-dried completely, and stained with periodic acid Schiff (PAS) solution according to the instruction manual of the manufacture. After the tissue was stained and washed in water, it was then dehydrated and mounted (Permount mounting medium, Fisher Scientific, Pittsburgh, PA). The prepared retinal vessels were observed and photographed under a microscope. The density of PAS staining was quantified with the Photoshop software.

Acellular capillaries were randomly counted with 4–6 filed areas around the midretina. Acellular capillaries were defined as capillary sized vessel tubes with no nuclei along their length [17]. Data are presented as number of acellular capillaries per 10 mm2 of retina.

2.5. Preparation of Retina Cross Sections and Evaluation of Retinal Capillary Basement Membrane

To evaluate the retinal capillary basement membrane, mouse eyes were fixed in 4% PFA/PBS at 4°C for 12 h followed by cryoprotection in 30% sucrose/PBS overnight before the quick freezing in OCT compound (Sakura Finetek, Inc., Torrance, CA). The 5 μm frozen cross sections were prepared by a standard procedure. The sections were then stained with hematoxylin and eosin (HE) for evaluation of retinal capillary basement membrane. After being stained, the cross sections were observed and photographed under a microscope.

2.6. Determination of CAS-3 Protein Expression in Mouse Retina

The above cross sections were used to determine expression of caspase-3 (CAS-3) protein by immunofluorescent staining as follows: the cross sections on cover slides were incubated with rabbit anti-CAS-3 polyclonal antibody overnight at 4°C. After removal of the primary antibody by washing with PBS, the slides were stained with rhodamine-conjugated goat anti-rabbit IgG for 2 h at RT. After being washed with PBS, the slides were restained with DAPI solution for nuclei. Images of all the slides were observed and photographed under a fluorescence microscope.

2.7. RNA Isolation and Determination of CAS-3, MMP-9, MMP-2, and TNFα mRNA Expression in Mouse Retina

After treatment, mice retinas were removed and homogenized in Trizol reagent (Invitrogen, Carlsbad, CA) to extract total RNA as described [18]. The cDNA was synthesized with the first-stand cDNA synthesis Kit from Fermentas (Pittsburgh, PA). Expression of CAS-3, matrix metalloprotein 2 (MMP-2), MMP-9, and tumor necrosis factor α (TNFα) mRNA was determined by real time RT-PCR using a SYBR green PCR master mix from Bio-Rad (Los Angeles, CA) and the primers listed in Table 1 and normalized by β-actin mRNA in the corresponding samples.

Table 1.

Sequences of the primers for real time RT-PCR analysis.

Gene Forward Backward
CAS-3 GACTTGCTCCCATGTATGGTC ATCAAAGCGCAGTGTCCTG
MMP-2 TGGCAAGGTGTGGTGTGCGAC TCGGGGCCATCAGAGCTCCAG
MMP-9 GGTGTGCCCTGGAACTCACACG AGGGCACTGCAGGAGGTCGT
TNFα GTTCTATGGCCCAGACCCTCAC GGCACCACTAGTTGGTTGTCTTTG
β-actin ATCTGGCACCACACCTTC AGCCAGGTCCAGACGCA
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2.8. Data Analysis

All experiments were repeated at least three times, and the representative results are presented. Data in Table 2 and Figures 1, 3, and 4 were presented as mean ± standard error and analyzed by Student's t-test (n ≥ 3). The differences were considered significant at P < 0.05.

Table 2.

NXT reduces the fasting blood glucose levels in db/db mice.

Group Time of treatment (days)
0 31 66 96
db/db mice (control) 12.30 ± 1.61 15.29 ± 1.34 26.68 ± 0.84 29.56 ± 1.09
db/db mice (NXT) 12.60 ± 2.00 16.87 ± 1.93 21.06 ± 2.06* 20.48 ± 1.52*
Wild type mice 6.78 ± 0.59 5.96 ± 0.18 5.70 ± 0.16 6.34 ± 0.22
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Male db/db mice (~6 weeks old) were randomly divided into two groups (10/group) and received the following treatment: group 1 (control), mice were fed normal chow; group 2 (NXT), mice were fed the chow containing NXT (624 mpk) for ~14 weeks. Wild type mice on normal chow were used as nondiabetic or normal control. The blood samples were collected at the indicated time points for determination of blood glucose levels as described in Section 2. *Significantly different from control db/db mice at P < 0.05 (n = 10).

Figure 1.

Figure 1

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NXT inhibits the accumulation of carbohydrate macromolecules and the formation of acellular capillaries in retinal vasculature in db/db mice. (a) At the end of the study, mouse eyes were collected and the retinal vascular network was prepared followed by PAS staining and photograph under a microscope as described in Section 2. The representative images from each group were presented. Black arrows indicate acellular capillaries in the retinal vasculature. Bars: 1 mm and 50 μm in the up and middle panels, respectively. (b) The density of PAS staining was quantified by the Photoshop software. (c) Quantitation of acellular capillaries in the retina. ∗ P < 0.05 (n ≥ 3).

Figure 3.

Figure 3

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NXT prevents the reduction of thickness of whole retina and sublayers in retina in db/db mice. After HE staining and photographing, the thickness of whole retina and sublayers in retina was quantified. OPL: the outer plexiform layer; ONL: outer nuclear layer, IS + OS: photoreceptor layer; RPE: retinal pigment epithelium layer. ∗ P < 0.05 (n ≥ 5).

Figure 4.

Figure 4

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NXT inhibits diabetes-induced CAS-3 expression. (a) The frozen sections of mouse eyeballs from each group were prepared and CAS-3 protein expression was determined by immunofluorescent staining as described in Section 2. Bars: 50 μm. (b) CAS-3 mRNA expression in the retinas was determined by real time RT-PCR analysis. (c) TNF-α, MMP-2 and MMP-9 mRNA expression in the retinas was determined by real time RT-PCR analysis. ∗ P < 0.05 (n ≥ 5).

3. Results

3.1. NXT Decreases the Fasting Blood Glucose Levels in db/db Mice

To determine the effect of NXT on fasting blood glucose levels, during the treatment, the blood samples were monthly collected followed by determination of glucose levels. The results in Table 2 show the low and constant blood glucose levels in wild type mice. In contrast, a higher blood glucose level was seen at the beginning of the study in db/db mice than wild type mice. More importantly, the higher blood glucose levels kept increasing in control db/db mice with time. At the end of the study, more than twofold increase (12.3 ± 1.61 versus 29.56 ± 3.43 mM) was determined in control db/db mice. However, although the administration of NXT to db/db mice had little effect on blood glucose levels in the first month of treatment, it substantially reduced blood glucose levels thereafter. At the end of the study (~3 months), the blood glucose levels in db/db mice receiving NXT treatment were reduced to ~60% of control db/db mice suggesting NXT improves blood glucose levels.

3.2. NXT Inhibits the Diabetes-Induced Retinal Vascular Abnormalities

The improvement of blood glucose levels in db/db mice implies that NXT may prevent the animals from the diabetes-induced retinal vascular abnormalities. To determine it, we initially isolated retinal network of vessels and conducted the PAS staining to assess the effect of NXT on retinal vasculature as well as the accumulation of carbohydrate macromolecules. Compared to wild type mice, the results in Figure 1(a) show a denser image in control db/db mice than wild type mice which suggests a severe accumulation of carbohydrate macromolecules in the retinal vasculature (up middle panel). Furthermore, the enlarged image displays formation of numerous acellular capillaries in the retinas of control db/db mice (middle column of Figure 1(a), indicated by the black arrows). However, administration of NXT to db/db mice significantly decreased the density of the vascular vessels after PAS staining that indicates NXT can prevent the accumulation of carbohydrate macromolecules (Figure 1(b)). In addition, the formation of acellular capillaries was substantially inhibited by NXT (right column of Figures 1(a) and 1(c)). Thus, the results in Figure 1 indicate that NXT protects db/db mice against the diabetes-induced retinal vascular abnormalities and prevents the occurrence of diabetic retinopathy.

Diabetic retinopathy causes shrink of whole retina which is contributed by shrink of sublayers in the retina. To further determine the effect of NXT on the development of diabetic retinopathy, we collected mouse eyeballs and determined the retinal thickness and structural alterations. The central retinal thickness is defined as the distance from the ganglion cell layer (GCL) to the retinal pigment epithelium layer (RPE) in the central area of retina. The results in Figure 2 show that the whole central retinal thickness in control db/db mice was significantly reduced when compared to wild type mice. Interestingly, administration of db/db mice with NXT significantly restored the whole retinal thickness to normal suggesting NXT prevents db/db mice from the development of diabetic retinopathy.

Figure 2.

Figure 2

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NXT corrects the retinal abnormalities in db/db mice. Mouse eyeballs were collected at the end of the study and fixed in 4% PFA/PBS. The 5 μm frozen cross sections were prepared and used to conduct HE staining as described in Section 2. The representative images from each group were presented. Bar: 100 μm.

Furthermore, we quantified the thickness of whole retina as well as each sublayer in the retina, such as outer plexiform layer (OPL), outer nuclear layer (ONL), photoreceptor layer (IS + OS), and RPE (Figure 3). Compared to wild type mice, the thickness of OPL, ONL, and the photoreceptor layer (IS + OS) in control db/db mice was significantly reduced mostly in photoreceptor layer. The combined reduction of thickness in these sublayers contributes to the reduction of whole retinal thickness. In contrast, treatment of db/db mice with NXT prevented the reduction of the thickness of whole retina, OPL, ONL, and photoreceptor layers.

3.3. NXT Inhibits Retinal CAS-3, MMP-2, MMP-9, and TNFα Expressions in db/db Mice

The loss of pericytes in the photoreceptor layer is a determinant of diabetic retinopathy at the early stage in humans and animal models [19]. High glucose levels decrease glutathione levels in pericytes that will activate CAS-3 expression and apoptosis of pericytes [19]. To determine if the protection of retinal structure by NXT is related to regulation of CAS-3 expression, we assessed CAS-3 protein levels by immunofluorescent staining. CAS-3 is mainly expressed in the photoreceptor layer. Compared to wild type mice, the results in Figure 4(a) show that CAS-3 expression was increased in the retina of db/db control mice, in particular in the photoreceptor layer. However, the increase was inhibited by NXT. Associated with changes of CAS-3 protein, diabetes substantially increased CAS-3 mRNA expression which was also significantly decreased by NXT treatment (Figure 4(b)).

Diabetes can also induce expression of TNF-α, MMP-2, and MMP-9 in the retina which may enhance apoptosis in the tissue and contribute to the pathogenesis of diabetic retinopathy [20–22]. To determine if NXT can affect TNF-α, MMP-2, and MMP-9 expressions, we assessed mRNA levels of these molecules by real time RT-PCR analysis. Compared to control db/db mice, Figure 4(c) shows that NXT treatment significantly inhibited TNF-α, MMP-2, and MMP-9 mRNA expressions in the retinas of db/db mice. Taken together, the results in Figure 4 indicate that NXT can inhibit the diabetes-induced apoptosis in retina and protect the retinal normal structure and physiological function by reducing production of inflammation as well as apoptosis.

4. Discussion

NXT has been demonstrated to protect patients with cardiac and vascular diseases. The diabetic retinopathy is a prevalent and profound microvascular disease in diabetic patients. The patients with diabetic retinopathy are 25-fold more likely to be blind than normal individuals [5] while the diabetic retinopathy is the leading cause of blindness in working age adults worldwide [3, 23]. In this study, we demonstrate the antidiabetic retinopathy properties of NXT. Our study shows that NXT prevents the formation of acellular capillaries and accumulation of carbohydrate macromolecules and inhibits the shrink of retina and retinal sublayers which is associated with reduction of CAS-3 and some inflammatory molecules expression in the retina. Taken together, NXT well maintains structural integrity of retina in db/db mice and inhibits the development of diabetic retinopathy.

Mounting evidence has supported that hyperglycemia can promote the development of diabetic retinopathy [24–26]. High glucose levels decrease glutathione level in pericytes that can result in mitochondrial overproduction of reactive oxygen species (ROS) in the diabetic microvasculature [27]. In turn, the increased ROS activates diacylglycerol- (DAG-) PKC pathway to induce expression of vascular endothelial growth factor (VEGF) and generation of AGEs. The combination of these effects accelerates the loss of pericytes followed by degeneration of endothelial cells and capillary occlusions [28, 29]. Therefore, lowering plasma glucose levels is believed to be an effective way to reduce the development of diabetic retinopathy. In this study, we determined that NXT reduces fasting blood glucose levels, indicating NXT inhibits diabetic retinopathy which may partially be through the control of glucose levels. Moreover, we observed that the induction of retinal CAS-3, TNF-α, MMP-2, and MMP-9 expressions by diabetes was inhibited by NXT treatment, suggesting an antiapoptotic and anti-inflammatory effects of NXT.

In conclusion, our study indicates that NXT inhibits the development of diabetic retinopathy in db/db mice and implies an important and potential application of NXT for treatment of diabetic retinopathy in clinics.

Acknowledgments

This work was supported by the Ministry of Science and Technology of China Grant no. 2010CB945003 to Jihong Han; the National Science Foundation of China (NSFC) Grants nos. 81272460 and 81473204 to Jihong Han and 31400694 to Yuanli Chen; The Specialized Research Fund for the Doctoral Program of Higher Education Grant no. 20120031110020 to Jihong Han, 111 Project B08011, China Postdoctoral Science Foundation Grant no. 2014M551014 to Yajun Duan; and Tianjin Municipal Science and Technology Commission of China Grants nos. 14JCYBJC25100 and 13JCYBJC24600 to Yajun Duan and Xiaoju Li, respectively.

Conflict of Interests

The authors declare no potential conflict of interests.

References

  • 1.Whiting D. R., Guariguata L., Weil C., Shaw J. IDF diabetes atlas: global estimates of the prevalence of diabetes for 2011 and 2030. Diabetes Research and Clinical Practice. 2011;94(3):311–321. doi: 10.1016/j.diabres.2011.10.029. [DOI] [PubMed] [Google Scholar]
  • 2.Frank R. N. Diabetic retinopathy. The New England Journal of Medicine. 2004;350(1):48–58. doi: 10.1056/nejmra021678. [DOI] [PubMed] [Google Scholar]
  • 3.Klein B. E. K. Overview of epidemiologic studies of diabetic retinopathy. Ophthalmic Epidemiology. 2007;14(4):179–183. doi: 10.1080/09286580701396720. [DOI] [PubMed] [Google Scholar]
  • 4.Cheung N., Mitchell P., Wong T. Y. Diabetic retinopathy. The Lancet. 2010;376(9735):124–136. doi: 10.1016/s0140-6736(09)62124-3. [DOI] [PubMed] [Google Scholar]
  • 5.Fong D. S., Aiello L., Gardner T. W., et al. Retinopathy in diabetes. Diabetes Care. 2004;27(supplement 1):S84–S87. doi: 10.2337/diacare.27.2007.s84. [DOI] [PubMed] [Google Scholar]
  • 6.Klein R., Klein B. E. K., Moss S. E., Cruickshanks K. J. Relationship of hyperglycemia to the long-term incidence and progression of diabetic retinopathy. Archives of Internal Medicine. 1994;154(19):2169–2178. doi: 10.1001/archinte.154.19.2169. [DOI] [PubMed] [Google Scholar]
  • 7.Kowluru R. A., Chan P. S. Oxidative stress and diabetic retinopathy. Experimental Diabetes Research. 2007;2007:12. doi: 10.1155/2007/43603.43603 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 8.Tang J., Kern T. S. Inflammation in diabetic retinopathy. Progress in Retinal and Eye Research. 2011;30(5):343–358. doi: 10.1016/j.preteyeres.2011.05.002. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 9.Yamagishi S.-I., Matsui T. Advanced glycation end products (AGEs), oxidative stress and diabetic retinopathy. Current Pharmaceutical Biotechnology. 2011;12(3):362–368. doi: 10.2174/138920111794480534. [DOI] [PubMed] [Google Scholar]
  • 10.Antonetti D. A., Klein R., Gardner T. W. Diabetic retinopathy. The New England Journal of Medicine. 2012;366(13):1227–1239. doi: 10.1056/nejmra1005073. [DOI] [PubMed] [Google Scholar]
  • 11.Teuscher A., Schnell H., Wilson P. W. F. Incidence of diabetic retinopathy and relationship to baseline plasma glucose and blood pressure. Diabetes Care. 1988;11(3):246–251. doi: 10.2337/diacare.11.3.246. [DOI] [PubMed] [Google Scholar]
  • 12.Diabetes Control and Complications Trial Research Group. Progression of retinopathy with intensive versus conventional treatment in the diabetes control and complications trial. Diabetes control and complications trial research group. Ophthalmology. 1995;102(4):647–661. doi: 10.1016/s0161-6420(95)30973-6. [DOI] [PubMed] [Google Scholar]
  • 13.Zhang F., Huang B., Zhao Y., et al. BNC protects H9c2 cardiomyoblasts from H2O2-induced oxidative injury through ERK1/2 signaling pathway. Evidence-Based Complementary and Alternative Medicine. 2013;2013:12. doi: 10.1155/2013/802784.802784 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 14.Zhao J. J., Zhu H., Wang S. J., et al. Naoxintong protects against atherosclerosis through lipid-lowering and inhibiting maturation of dendritic cells in LDL receptor knockout mice fed a high-fat diet. Current Pharmaceutical Design. 2013;19(33):5891–5896. doi: 10.2174/1381612811319330008. [DOI] [PubMed] [Google Scholar]
  • 15.Chen H., Zhang Y., Wu X., Li C., Wang H. In vitro assessment of cytochrome P450 2C19 potential of naoxintong. Evidence-Based Complementary and Alternative Medicine. 2012;2012:6. doi: 10.1155/2012/430262.430262 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 16.Bell W. R., Green W. R., Goldberg M. F. Histopathologic and trypsin digestion studies of the retina in incontinentia pigmenti. Ophthalmology. 2008;115(5):893–897. doi: 10.1016/j.ophtha.2007.08.027. [DOI] [PubMed] [Google Scholar]
  • 17.Feit-Leichman R. A., Kinouchi R., Takeda M., et al. Vascular damage in a mouse model of diabetic retinopathy: relation to neuronal and glial changes. Investigative Ophthalmology & Visual Science. 2005;46(11):4281–4287. doi: 10.1167/iovs.04-1361. [DOI] [PubMed] [Google Scholar]
  • 18.Chen Y., Liu M., Zhao T., et al. Danhong injection inhibits the development of atherosclerosis in both apoe-/- and Ldlr-/- mice. Journal of Cardiovascular Pharmacology. 2014;63(5):441–452. doi: 10.1097/fjc.0000000000000067. [DOI] [PubMed] [Google Scholar]
  • 19.Miwa K., Nakamura J., Hamada Y., et al. The role of polyol pathway in glucose-induced apoptosis of cultured retinal pericytes. Diabetes Research and Clinical Practice. 2003;60(1):1–9. doi: 10.1016/s0168-8227(02)00248-6. [DOI] [PubMed] [Google Scholar]
  • 20.Behl Y., Krothapalli P., Desta T., DiPiazza A., Roy S., Graves D. T. Diabetes-enhanced tumor necrosis factor-α production promotes apoptosis and the loss of retinal microvascular cells in type 1 and type 2 models of diabetic retinopathy. American Journal of Pathology. 2008;172(5):1411–1418. doi: 10.2353/ajpath.2008.071070. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 21.Mohammad G., Kowluru R. A. Diabetic retinopathy and signaling mechanism for activation of matrix metalloproteinase-9. Journal of Cellular Physiology. 2012;227(3):1052–1061. doi: 10.1002/jcp.22822. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 22.Mohammad G., Kowluru R. A. Novel role of mitochondrial matrix metalloproteinase-2 in the development of diabetic retinopathy. Investigative Ophthalmology and Visual Science. 2011;52(6):3832–3841. doi: 10.1167/iovs.10-6368. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 23.Yau J. W. Y., Rogers S. L., Kawasaki R., et al. Global prevalence and major risk factors of diabetic retinopathy. Diabetes Care. 2012;35(3):556–564. doi: 10.2337/dc11-1909. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 24.Roy R., Das D., Saurabh K., et al. Role of hyperglycemia-mediated erythrocyte redox state alteration in the development of diabetic retinopathy. Retina. 2013;33(7):1480–1481. doi: 10.1097/iae.0b013e318293145e. [DOI] [PubMed] [Google Scholar]
  • 25.Choudhuri S., Dutta D., Chowdhury I. H., et al. Association of hyperglycemia mediated increased advanced glycation and erythrocyte antioxidant enzyme activity in different stages of diabetic retinopathy. Diabetes Research and Clinical Practice. 2013;100(3):376–384. doi: 10.1016/j.diabres.2013.03.031. [DOI] [PubMed] [Google Scholar]
  • 26.King G. L. Hyperglycemia and the pathogenesis of diabetic retinopathy. Journal of General Internal Medicine. 1986;1(2):133–134. doi: 10.1007/BF02599819. [DOI] [PubMed] [Google Scholar]
  • 27.Brownlee M. The pathobiology of diabetic complications: a unifying mechanism. Diabetes. 2005;54(6):1615–1625. doi: 10.2337/diabetes.54.6.1615. [DOI] [PubMed] [Google Scholar]
  • 28.Joussen A. M., Poulaki V., Le M. L., et al. A central role for inflammation in the pathogenesis of diabetic retinopathy. The FASEB Journal. 2004;18(12):1450–1452. doi: 10.1096/fj.03-1476fje. [DOI] [PubMed] [Google Scholar]
  • 29.Kowluru R. A., Tang J., Kern T. S. Abnormalities of retinal metabolism in diabetes and experimental galactosemia. VII. Effect of long-term administration of antioxidants on the development of retinopathy. Diabetes. 2001;50(8):1938–1942. doi: 10.2337/diabetes.50.8.1938. [DOI] [PubMed] [Google Scholar]

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