Synergistic protective effects of escin and low‑dose glucocorticoids on blood‑retinal barrier breakdown in a rat model of retinal ischemia

Introduction

Numerous diseases cause breakdown of the blood-retinal barrier (BRB) and macular edema. Hypoxia, altered blood flow and retinal ischemia are closely correlated with the development and progression of macular edema (1,2).

Currently, glucocorticoids (GCs) are the most commonly used medicine for ocular applications. Recent studies have demonstrated the efficacy and complications associated with intravitreal GC injection for diabetic macular edema (3,4). GCs may act by suppressing inflammation and directly affecting endothelial cells, through regulation of the phosphorylation, organization and content of tight junction proteins. GCs have also been demonstrated to reduce the breakdown of the BRB (5). It has been identified that GCs upregulate the tight junction transmembrane proteins, occludin and claudin 5, in primary retinal endothelial cells through transactivation of the promoters for these genes (6).

Although GCs have been demonstrated to ameliorate macular edema, the side-effects accompanying treatment with GCs cause their frequent use to be problematic. One of the major side-effects of intravitreal injection of triamcinolone acetonide (TA), a synthetic corticosteroid, is steroid-induced increases in intraocular pressure (IOP). One study demonstrated that a rise in IOP to values >21 mmHg may be expected to occur in ~50% of treated eyes (7). The frequency of cataract surgery following intravitreal injection of high-dose TA in elderly patients is increasing (8).

Escin is a natural mixture of triterpene saponins, mainly consisting of A-, B-, C- and D-escin (Fig. 1). Accumulating experimental evidence suggests that escin exerts anti-inflammatory and anti-edematous effects. Escin inhibits acetic acid-induced increases in capillary permeability and adhesion formation in animal models. It also attenuates cognitive deficits and hippocampal injury following transient global cerebral ischemia in mice, by regulating certain inflammatory genes (9,10). Furthermore, escin has been demonstrated to be a safe and potent anti-inflammatory drug with long-term, effective anti-inflammatory action without immunosuppression (11,12). Escin also exerts synergistic anti-inflammatory effects with low doses of GCs in vivo and in vitro(13). In China, escin is widely used (clinically) for the treatment of retinal vein occlusion and central serous chorioretinopathy (14–16).

Figure 1 Structure of escin.

In the present study, we investigated whether the combination of escin and GCs was able to produce synergistic protective effects on BRB breakdown in a rat model of acute retinal ischemia.

Materials and methods

Subjects and drugs

Male Sprague-Dawley rats (weight, 180±20 g) were obtained from the Experimental Animal Center of Luye Pharma Group (Yantai, China). Rats were kept in an air-conditioned room (temperature, 23±2°C) with a 12-h light-dark cycle, with free access to food and water. Animal experimental procedures were conducted in strict accordance with the National Institutes of Health regulations on the use and care of animals for scientific purposes (NIH Publication No. 0-23, revised 1996). Surgical procedures and the sacrifice of animals (at the end of the observation period) were performed under general anesthesia induced by an intraperitoneal (i.p.) injection of chloral hydrate (350 mg/kg).

Sodium salt of escin (sodium escinate), consisting of A-, B-, C- and D-escin, was obtained from Shandong Luye Pharmaceutical Co., Ltd. (batch no. 1206043; Yantai, China) and TA injections were provided by Kunming Jida Pharmaceutical Co., Ltd. (batch no. 120105; Kunming, China). Evans blue dye (Sinopharm Chemical Reagent Co., Ltd, Shanghai, China) was prepared by dissolving the dye in normal saline (45 mg/ml).

Retinal ischemia-reperfusion study protocol

Rats were anesthetized intraperitoneally with chloral hydrate (350 mg/kg) and chlorpromazine (3 mg/kg). Five minutes following administration of the anesthetics, the anterior chamber of the left eye was cannulated with a 30-gauge needle connected by silicone elastomer tubing to a reservoir of balanced oxyglutathione solution. The IOP was raised to 120 mmHg by increasing the height of reservoir. The eye was examined with an ophthalmoscope to confirm that the retinal vessels had collapsed and the retina appeared gray, indicating that the retina was ischemic. After 50 min of retinal ischemia, the IOP had returned to normal and ophthalmoscopy was used to confirm that the circulation had also returned to normal. The body temperature of the rats was maintained at 37°C with a heating pad during ischemia, until the rats had recovered from anesthesia.

Following surgery, the rats were divided randomly into four groups: the ischemia-reperfusion (IR); TA (2 and 5 μl) treatment; escin (0.9 and 1.8 mg/kg) treatment; and combined escin (0.9 mg/kg) and TA (2 μl) treatment groups. Following the induction of general anesthesia, pupils were dilated with 0.5% tropicamide. The rats were treated with escin through the caudal vein and with TA through the vitreous body. A group of rats underwent surgery without increased IOP, in order to serve as a sham group. Twenty-four hours after surgery, the BRB permeability was assayed.

Evaluation of BRB permeability

Following the induction of general anesthesia with chloral hydrate (350 mg/kg), Evans blue was injected into the blood through the caudal vein at a dosage of 45 mg/kg. When the dye had circulated for 120 min, the chest cavity was opened and the rats were perfused via the left ventricle with citrate buffer (0.05 M, pH 3.5) for 2 min at 37°C. Immediately after perfusion, both eyes were enucleated and bisected at the equator. The retinas were then carefully dissected away. Following measurement of the retinal weight, Evans blue was extracted by incubating each retina in 180 μl formamide for 18 h at 70°C. The extract was ultracentrifuged for 60 min at 12,000 × g and 25°C. In total, 60 μl supernatant was used for spectrophotometry. The background-subtracted absorbance was determined by measuring the absorbance of each sample at 620 nm (the absorbance maximum for Evans blue in formamide) and at 740 nm (the absorbance minimum). BRB breakdown was calculated as follows: Evans blue weight (ng) × retinal weight (mg)-1.

Morphological analysis

Retinal thickness was evaluated in hematoxylin and eosin-stained sections using the Metamorph/BX51 Microscopic image analysis software (Molecular Devices, USA). The eyes were cut vertically through the center of the cornea and optic nerve, and the two halves were embedded face down. Care was taken to maintain a consistent cutting angle for all the eyes measured for retinal thickness. Images of retinal sections were captured and retinal thickness was measured under the same conditions.

Immunohistochemistry

Twenty-four hours after renal ischemia, rats were deeply anesthetized and transcardially perfused with saline solution, followed by 4% paraformaldehyde in 0.1 M phosphate-buffered saline (PBS) for 2 min. The eyes were enucleated and post-fixed in 4% paraformaldehyde for 24 h. Coronal sections (10 μm) were obtained using a Leica CM1950S cryostat (Leica Microsystems, Wetzlar, Germany). Sections were blocked with 3% normal goat serum (diluted in PBS containing 0.3% Triton X-100) for 1 h and incubated with primary antibodies (anti-occludin; 1:200; Abcam, Cambridge, MA, USA) overnight at 4°C. Following rinsing with PBS, sections were incubated with horseradish peroxidase-conjugated goat anti-rabbit IgG secondary antibody (1:200; Beyotime Institute of Biotechnology, Haimen, China) for 2 h at room temperature. The images from five fields of each ischemic region, from six rats in each group, were examined using the same brightness and exposure settings.

Western blot analysis

Twenty-four hours after retinal ischemia, fresh retinal tissues were homogenized on ice in cold lysis buffer (Beyotime Institute of Biotechnology) with a 1:100 volume of phenylmethyl sulfonylfluoride (PMSF). The homogenates were centrifuged at 14,000 × g for 5 min at 4°C. The supernatants were aliquoted and stored at −80°C following the removal of a small aliquot for protein estimation. Protein concentrations were determined using a bicinchoninic acid (BCA) protein assay kit (Beyotime Institute of Biotechnology). The samples were thawed on ice and mixed with 4X sample buffer (Invitrogen Life Technologies, Carlsbad, CA, USA), before heating at 100°C for 5 min. Equivalent quantities of proteins (50 μg) were loaded on 12% Tris-glycine sodium dodecyl sulfate (SDS)-polyacrylamide gels for fractionation at 160 V. Predetermined molecular weight standards (Beyotime Institute of Biotechnology) were used as markers. Protein on the gel was blotted onto nitrocellulose membranes at 106 V for 70 min at 4°C. Following transfer, the membranes were incubated with blocking buffer (5% skim milk in wash buffer) for 2 h at room temperature and washed three times (5 min/wash) with 0.1% Tris-buffered saline with Tween 20 (TBST). Incubation with occludin antibody in diluent buffer (5% bovine serum albumin and 0.1% TBST) was performed overnight at 4°C (1:1,000 dilution). The membranes were then washed three times (5 min each) with TBST. The primary antibody was probed with horseradish peroxidase-conjugated IgG goat anti-rabbit secondary antibody (1:2,000) for 2 h, washed three times in TBST and processed with enhanced chemiluminescence (ECL) detection reagents (Beyotime Institute of Biotechnology). The processed membranes were then exposed to photographic films for visualization of the signals. β-actin western blot analysis was performed for each membrane as an internal control of protein loading.

Evaluation of drug interactions

The interaction between escin and TA was analyzed using Berenbaum’s method, to determine whether the combination was synergistic. The method is performed based on the following equation: E(da,db) > E(da) + E(db), where E is the observed effect and da and db are the doses of agents a and b, respectively. Synergism is indicated when the total effect of a combination is greater than expected from the sum of its effects (17).

Statistical analysis

Quantitative data from the experiments were expressed as the mean ± standard deviation and significance was determined by one-way analysis of variance (ANOVA) followed by Tukey’s test. In all cases, P<0.05 was considered to indicate a statistically significant difference.

Results

Effects of escin and TA on BRB permeability

The IR rats demonstrated a greater level of retinal Evans blue leakage than the sham rats (P<0.01). High doses (H) of escin (1.8 mg/kg) and TA (5 μl) significantly inhibited retinal Evans blue leakage compared with the IR group (P<0.05 and P<0.01, respectively; Fig. 2). Low doses (L) of escin (0.9 mg/kg) and TA (2 μl) did not significantly affect retinal Evans blue leakage compared with the IR group; however, administered together, they significantly inhibited retinal Evans blue leakage (Table I).

Figure 2 Effects of escin and triamcinolone acetonide (TA) on blood-retinal barrier (BRB) permeability. Escin and TA dose-dependently inhibited retinal Evans blue leakage. IR, ischemia-reperfusion; TA, triamcinolone acetonide; L, low-dose; H, high-dose. Data are expressed as the mean ± standard deviation; n=6 per group. *P<0.05 and **P<0.01 vs. the IR group; ΔΔP<0.01 vs. the sham group.

Table I Effects of the combination of escin and TA on blood-retinal barrier permeability.

Table I

Effects of the combination of escin and TA on blood-retinal barrier permeability.

Group	Evans blue (ng/mg)	Inhibition rate (%)
Sham	14.1±10.2	-
IR	47.0±17.2a	-
TA (L)	34.6±8.3	26.4
Escin (L)	37.9±16.3	19.3
TA (L) and escin (L)	24.9±8.5b	47.1c

a P<0.01 vs. the sham group;

b P<0.05 vs. the IR group;

c E(da,db) > E(da) + E(db).

{ label (or @symbol) needed for fn[@id='tfn4-mmr-07-05-1511'] } IR, ischemia-reperfusion; TA, triamcinolone acetonide; L, low-dose. Data are expressed as the mean ± standard deviation; n=6 per group.

Effects of escin and TA on retinal thickness

The retinal thickness in the IR group was significantly increased compared with that of the sham group (P<0.05). Escin (H) and TA (H) significantly reduced retinal thickness compared with the IR group (P<0.05). There were no significant differences in retinal thickness between the TA (L), escin (L) and IR retinas (Fig. 3).

Figure 3 Retinal thickness was measured on hematoxylin and eosin (H&E)-stained sections at the same location in each sample. (A) Micrograph showing representative retina samples from the different groups. The white arrow in the photograph of the control (sham) group demonstrates one measurement of retinal thickness. (B) Retinal thickness in the different groups. IR, ischemia-reperfusion; TA, triamcinolone acetonide; L, low-dose; H, high-dose. Data are expressed as the mean ± standard deviation; n=5 per group. *P<0.05 vs. the IR group and ΔΔP<0.01 vs. the sham group. Scale bar, 40 μm.

Effects of escin and TA on occludin expression following retinal ischemia

Escin (L) and TA (L) did not enhance occludin expression compared with IR alone. However, when escin and TA were administered together, occludin expression in the ganglion cell layer increased significantly, as demonstrated by the immunohistochemistry results (Fig. 4A and B). Western blot analysis produced consistent results (Fig. 4C).

Figure 4 Effects of escin and triamcinolone acetonide (TA) on occludin expression in the retina following ischemia. Immunohistochemistry results: (A) Positive signals for occludin were localized in the retinal ganglion cell layer; and (B) low doses of escin and TA did not increase occludin expression compared with the IR group; however, when escin and TA were administered together, the occludin expression in the ganglion cell layer significantly increased. Western blot analysis results: (C) When escin and TA were administered together, the occludin expression increased significantly compared with when they were administered alone. Data are expressed as the mean ± standard deviation; n=3 per group. *P<0.05 vs. the IR group and ΔΔP<0.01 vs. the sham group. aE(da,db) > E(da) + E(db). Scale bar, 40 μm. IR, ischemia-reperfusion; TA, triamcinolone acetonide; L, low-dose; E, observed effect; da, dose of agent a; db, dose of agent b.

Discussion

The retina is a highly specialized neural tissue that requires a unique vascular structure and tight control of permeability to allow correct visual function. Regulation of the flux of blood-borne metabolites into the retina is controlled by the BRB. Hypoxia, altered blood flow and retinal ischemia may lead to BRB breakdown and the development of macular edema. Numerous experimental studies have demonstrated that ischemia is capable of inducing retinal damage (18). The retina is highly vulnerable to ischemic injury and its ischemic tolerance is ≤60 min (19).

In the present study, a retinal ischemia model was established in rats, in which ischemia was induced by increasing the IOP. The results revealed that BRB permeability and retinal thickness significantly increased following retinal ischemia. Treatment with escin (L) or TA (L) alone did not inhibit BRB permeability; however, when administered together, they significantly reduced BRB permeability following ischemia. This indicates that escin and TA have synergistic effects on reducing BRB permeability.

The BRB is composed of tight and adherent junction complexes. Retinal vascular endothelium and pigment epithelium have well-developed tight junctions that confer a high degree of control on solute and fluid permeability, thus maintaining the neural environment of the retina. Occludin is an important transmembrane protein in tight junctions that is responsible for forming the permeability barrier (20). In rats, the tight junction protein content is reduced following retinal ischemia (21). There is an inverse correlation between the tight junction protein content and endothelial permeability. Therefore, in vivo reduction of the tight junction protein content correlates with increased vascular permeability. The immunohistochemistry and western blot analysis results of the present study demonstrated that escin and glucocorticoids have synergistic protective effects on occludin.

In conclusion, escin and GCs were demonstrated to have synergistic protective effects on BRB breakdown; the molecular mechanism of which is correlated with the upregulation of occludin. Administration of escin may allow a reduction in the dose of GCs for the treatment of macular edema. The combination of escin with GCs is a potentially beneficial method of treatment for BRB breakdown and requires further study.

References