Corneal angiogenesis based on different protocols of alkaline cauterization in murine models¹

Abstract

Purpose:   To establish and compare protocols of alkaline cauterization for inducing corneal angiogenesis in murine models.

Methods:   Twenty-four adult Wistar rats were distributed into four groups (G1, G2, G3, and G4). The right eye cornea from each rat was cauterized using filter paper (3 mm), soaked in a solution of silver and potassium nitrates (3:1). Cauterization times were 10 (G1 and G4), or 20 seconds (G2 and G3). Cauterized corneas were washed with Ringer’s lactate solution. The filter paper was either removed before washing (G1 and G2), or kept on the corneas (G3 and G4). Corneas were photographed at multiple time points (2, 4, 6, 8, 11, 13, and 15 days after the procedure), and neovascularization parameters were assayed.

Results:   Neovascularization was observed in 66% of G1 corneas, and 100% of G2, G3, and G4 corneas. On day 15, G1 corneas showed smaller vascularized areas (12.63 ± 12.59%) compared to those in the G3 (41.95 ± 17.32%) and G4 (33 ± 11.74%) (P < 0.05) groups.

Conclusions:  The silver and potassium nitrate solution effectively induced corneal angiogenesis. The G2, G3, and G4 protocols showed excellent reproducibility, and induced vascularization in 100% of corneas.

Key words: Corneal Neovascularization; Cautery; Silver; Rats.

Introduction

Angiogenesis represents the formation of new blood vessels from the preexisting vasculature^1-3. In mammals, angiogenesis occurs during embryonic development and continues, in some tissues and organs, during postnatal life. In adult animals, the angiogenic process is related to the cyclical events of the female reproductive cycle (ovulation and pregnancy). Under controlled physiological conditions, angiogenesis contributes to tissue repair and to inflammatory responses^4,5.

The molecular mechanisms that regulate angiogenesis change during the development of many pathological conditions, which are collectively known as angiogenesis-dependent. In ophthalmology, for example, the exacerbation of the angiogenic process is associated with the development of many postoperative conditions or complications, such as corneal neovascularization, neovascular glaucoma, central retinal vein occlusion, corneal graft rejection, retinopathy of prematurity, diabetic retinopathy, age-related macular degeneration, and tumor progression^2,3.

Many studies have focused on the elucidation of the mechanistic basis of angiogenesis, as well as on the development of drugs capable of blocking the progression of angiogenesis-dependent diseases, especially cancer^2,3,6. Therefore, angiogenesis models are being utilized for in vitro applications, and in pre-clinical trials. The cornea has been widely used as a model for preclinical studies involving pro-angiogenic or anti-angiogenic molecules. Due to its transparency and anatomical location, it facilitates the monitorization of vascular responses, and allows their quantification using biomicroscopy. Different protocols have been proposed for the experimental induction of angiogenesis in the cornea^6-9.

Considering the heterogeneity of organic tissues and the complexity of the cellular reactions involved in angiogenesis, the choice of the model should always consider the objectives of the study, and the characteristics (e.g., time of action) of the alleged modulator drug being tested¹⁰.

Protocols involving alkaline cauterization represent a good option for the induction of corneal angiogenesis, given the cost-benefit. However, some authors report unsatisfactory results after using these protocols, as not all corneas develop angiogenesis. The reproducibility of corneal cauterization protocols using alkali remains controversial. While in some studies, alkaline cauterization appears to be very effective in the induction of corneal neovascularization, in others, the lack of reproducibility in the vascular response represented a limiting factor for the validation of the results¹⁰.

We hypothesized that variations in the alkaline cauterization steps, especially in the time of exposure of the cornea to the cauterizing agent, and in the type and size of the instrument used for cauterization, could lead to different vascular responses, thus compromising the reproducibility of the inter-observer results. In the literature, corneal cauterization times with alkali using a combination of 75% silver and 25% potassium nitrate range from 8 to 60 seconds^8,11-16. The cauterizing instrument is usually a stick or filter paper, whose diameter ranges from 1.8 mm to 5 mm^8,11-16.

The aim of this study was to establish and compare the effectiveness of four alkaline cauterization protocols (with silver and potassium nitrate) in the induction of angiogenesis in rat corneas. Several parameters of corneal vascularization were evaluated and compared between the study groups and at different time points after the procedures.

Methods

Animals and procedures for alkaline cauterization

This study adhered to the rules of the Association for Research in Vision and Ophthalmology-ARVO (Statement for the Use of Animals in Ophthalmic and Visual Research). The ethical principles established by the National Institutes of Health Guide for the Care and Use of Laboratory Animals (NIH Publications No. 8023, revised 1978) were followed. The study protocol was approved by the Ethics Committee on Animal Use (protocol number 06174/14) of FCAV/UNESP, Jaboticabal.

Twenty-four male rats (Rattus norvegicus, Wistarlineage), aged between 3 and 4 months, from the vivarium of the General Administration, UNESP, were used in this study. As inclusion criteria, the ocular examination included slit-lamp biomicroscopy (Nidek Co, SL-450, Aichi, Japan) and the fluorescein sodium dye test (Ophthalmos, Sao Paulo, Brazil). All animals were free of signs of eye disease¹⁷. The rats were divided into four groups (n = 6), designated as G1, G2, G3, and G4. The animals were fed a commercial pellet diet (65.82% carbohydrate, 5.36% fiber, 21.0% protein, and 4.96% fat) and they received water ad libitum.

The procedures for the induction of corneal angiogenesis were performed on animals under dissociative anesthesia¹⁸. Antisepsis was performed, and proxymetacaine eye drops (Alcon, Sao Paulo, Brazil) were instilled to promote desensitization of the ocular surface.

For alkaline cauterization, a circular piece of filter paper, with a diameter of 3 mm, embedded in a solution of 75% silver nitrate (Synth, Diadema, Brazil) and 25% potassium nitrate (Dinâmica, Contemporary Chemistry Ltda., Diadema Brazil), was pressed onto the axial region of the cornea, in the right eye of each animal. The contact time of the filter paper with the cornea was 10 seconds for the G1 and G4 groups and 20 seconds for the G2 and G3 groups. After cauterization, the corneas were washed with lactated Ringer’s solution for 1 minute. In the G1 and G2 groups, the filter papers were removed immediately before washing the cornea. In the G3 and G4 groups, the corneas were washed in the presence of the filter paper. Post-cauterization, the animals subcutaneously received tramadol hydrochloride (5 mg/kg) as an analgesic, every 8 hours, for 10 days.

The eyes were examined after 2, 4, 6, 8, 11, 13, and 15 days post-cauterization, to monitor the vascular response^2,22. The examinations were performed after the instillation of anesthetic eye drops. Pupillary dilatation was achieved by instillation of 1% tropicamide (Alcon, Sao Paulo, Brazil). The fluorescein sodium dye test was also used (Ophthalmos, Sao Paulo, Brazil). The presence of edema, corneal ulcer, corneal melting, synechiae, and hypopyon were noted. During the clinical evaluations, the corneas were immediately photographed (laterally and frontally), using digital equipment (TRC-50DX, Topcon, Japan) with a green filter (red free) and without a filter.

Side view images of corneas, photographed at different time points during the postoperative evaluation, were studied by a single examiner, who measured the burn intensity¹⁹. This was scored based on the appearance of blisters and on the extent of their elevation from the corneal surface (0 = no blister; 1 = a small blister that is slightly raised above the surface; 2 = a medium blister that is moderately raised above the surface; 3 = a large blister).

Evaluation of corneal vascularization parameters

Three parameters were evaluated: the development of neovascularization, the neovascularization profile, and the percentage of the corneal area occupied by vessels. Data were collected using frontal profile images of corneas and a green filter (red free). All evaluations were qualitative and quantitative, and were performed by a single examiner.

To assess the development of neovascularization, the extent of new vessel development in the cauterized eyes was graded using the following scores: negative (0), when no new vessels were visible; mild (1), when dense new blood vessels were present at the limbus; moderate (2), when the growth of new blood vessels extended from the limbus towards the periphery of the cauterized site; and severe (3), when new blood vessels reached the cauterized site²⁰.

The neovascularization profile data received scores in the 0-3 range per corneal quadrant, with increments of 0.5, using a grid system based on the centripetal extent of the outgrowth of the neovascular branch from the corneoscleral limbus. The scores for each corneal quadrant were summed for each eye, to obtain the index of corneal neovascularization (range, 0-12)²¹.

The percentages of the corneal areas that were occupied by vessels were calculated using the ImageJ software (http://imagej.nih.gov/ij/; National Institutes of Health, Bethesda, MD, USA)²². A test system containing 110 points was positioned over the photographic images^9,23. The percentage of the area that was occupied by vessels was calculated with the (PV x 100)/PC formula, where PV represents the number of points that touch the vessels, and PC represents the number of points that touch the corneas.

Statistical analysis

Quantitative variables were analyzed using parametric [analysis of variance (ANOVA), single ANOVA, and repeated measures ANOVA, followed by Tukey’s post-hoc test] and non-parametric tests [Kruskal-Wallis (KW), with Dunn’s post-test]. Differences were considered significant when P < 0.05. The evaluations were done using the MedCalc statistical software (MedCalc®, Mariakerke, Belgium).

Results

All eyes presented edema at days 2 and 4, during the evaluations. The occurrence of edema declined in subsequent evaluations. One eye in the G2 (16.6%) and one eye in the G3 groups (16.6%) displayed corneal melting in the evaluations at days 4 and 6, respectively. One animal in the G2 group was euthanized. Synechiae were observed in the G3 group, at day 11 (1 eye, 16.6%) and day 15 (2 eyes, 33.3%) of the evaluation. In all groups, some eyes presented corneal ulcer at the initial stages of the evaluation. Two eyes in the G4 group (33.3%) presented hypopyon, during the evaluation at day 2.

Neovascularization (measured as a cumulative rate) was present in 16.66% of the corneas on day 6, 50% of the corneas on day 8, and 66.66% of the corneas on day 11, in the G1 group. In the G2 group, neovascularization was present in 16.66%, 33.33%, 50%, and 100% of corneas on days 2, 4, 8, and 11, respectively. In the G3 group this occurred in 16.66%, 33.33%, 66.66%, and 100% of the corneas on days 2, 6, 11, and 13, respectively, whereas in the G4 group 16.66%, 83.33%, and 100% of the corneas presented neovascularization on days 4, 8 and 11, respectively.

The burn intensities (Figure 1), at the different evaluation times and in the various groups included in the study, are presented in Table 1. Corneas in the G2, G3, and G4 groups showed an enhanced burn intensity when compared to the corneas in the G1 group (P < 0.05).

Figure 1
Images of corneas with burn intensity due to corneal cauterization induced by alkali (arrows). Grade 0 (A), 1 (B), 2 (C), and 3 (D) (Veterinary Ophthalmology Service, UNESP/FCAV, Jaboticabal, SP, Brazil 2017).

Table 1
Mean values with standard deviation, median, minimum, and maximum values, representing the burn intensity gradation in the G1, G2, G3, and G4 groups, on days 2, 4, 6, 8, 11, 13, and 15. Veterinary Ophthalmology Service, UNESP/FCAV, Jaboticabal, SP, Brazil 2017.

Day	G1				G2				G3				G4
	(n=6)				(n=6)				(n=6)				(n=6)
	Mean ± sd	x	min	max	Mean ± sd	x	min	max	Mean ± sd	x	min	Max	Mean ± sd	x	min	max
2	0.67 ± 0.52	1	0	1	0.67± 0.52*	1	0	1	1.5 ± 0.84*	1	1	3	1.67 ± 0.82	1.5	1	3
4	0.33 ± 0.52	0	0	1	1.5 ± 1.23	1	0	3	1.33 ± 1.03	1	0	3	1.17 ± 0.99	1	0	3
6	0.17 ± 0.41	0	0	1	1.67 ± 1.21	1.5	0	3	1.83 ± 1.33	2	0	3	1.17 ± 0.99	1	0	3
8	0.33 ± 0.82**	0	0	2	1.33 ± 1.37	1	0	3	2.33 ± 0.82**	2.5	1	3	1 ± 1.1	1	0	3
11	0.33 ± 0.52**	0	0	1	1.2 ± 0.84	1	0	2	2 ± 1.1**	2	1	3	1 ± 1.1	1	0	3
13	0.17 ± 0.41**	0	0	1	1.2 ± 0.84	1	0	2	2 ± 0.9**	2	1	3	1 ± 1.1	1	0	3
15	0ꭝ	0	0	0	1.2 ± 0.84ꭝ	1	0	2	1.17 ± 0.41ꭝ	1	1	2	0.83 ± 0.75ꭝ	1	0	2

• *P < 0.05, G2 vs. G3
• **P < 0.05, G1 vs. G3
• P < 0.05, G1 vs.G2, G3, and G4
• Mean ± sd = mean ± standard deviation; x = median; min = minimum value; max = maximum value

In the assessments at days 4, 6, 8, 11, and 13, the development of neovascularization in corneas from all groups was restricted to the limbal region (score 1), or extended from the limbal region to the edges of the cauterized site (score 2) (Table 2).

Table 2
Mean values with standard deviations, representing the development of neovascularization in the G1, G2, G3, and G4 groups, on days 2, 4, 6, 8, 11, 13, and 15 (Veterinary Ophthalmology Service, UNESP/FCAV, Jaboticabal, SP, Brazil 2017).

	G1	G2	G3	G4
Day	(n=6)	(n=6)	(n=6)	(n=6)
2	0*	1*	1*	----
4	0	0.66 ± 0.57	1	1
6	0. 5 ± 1	1.33 ± 0.57	2	1.5 ± 0.57
8	1.33 ± 1.5	2.25 ± 1.5	3	2.4 ± 0.54
11	0.66 ± 1.03	1.4 ± 1.51	1.8 ± 1.6	2.5 ± 1.22
13	0.5 ± 1.22	0.4 ± 0.89	1 ± 1.5	0
15	0	0	0	0

• *P < 0.05, G1 versus G2 and G3
• ---- not assessed

The results of the corneal neovascularization profiles in all groups and at various times during the evaluation are described in Table 3.

Table 3
Mean values with standard deviations, representing the corneal neovascularization profiles in the G1, G2, G3, and G4 groups, on days 2, 4, 6, 8, 11, 13 and 15 (Veterinary Ophthalmology Service, UNESP/FCAV, Jaboticabal, SP, Brazil 2017).

	G1	G2	G3	G4
Day	(n=6)	(n=6)	(n=6)	(n=6)
2	0*	1*	0.25 ± 0.5*	----
4	0	0.55 ± 0.73	0.5 ± 0.57	0.5 ± 0.57
6	0.312 ± 0.7**	0.87 ± 0.68	1 ± 1.15	1.28 ± 0.87**
8	1.21 ± 1.32۵	1.78 ± 1.3	2.6 ± 0.96۵	1.87 ± 0.99
11	1.46 ± 1.4ᵜ	2.27 ± 1.23ᵜ	2.78 ± 0.73ᵜ	2.62 ± 1.01ᵜ
13	1.5 ± 1.5ᵜ	2.27 ± 1.23ᵜ	2.83 ± 0.64ᵜ	2.62 ± 1.01ᵜ
15	1.5 ± 1.5ᵜ	2.22 ± 1.22ᵜ	2.83 ± 0.64ᵜ	2.62 ± 1.01ᵜ

• *P < 0.05, G2 vs. G1 and G3
• **P < 0.05, G1 vs. G4
• ^۵P < 0.05, G1 vs. G3
• ᵜP < 0.05, G1 vs. G2, G3, and G4
• ---- not assessed

Our image analysis using the ImageJ software, showed that corneas in the G3 group showed a larger percentage of vessels in the examined area, when compared with corneas in the G1, G2, and G4 groups (P <0.05) (Figure 2).

Figure 2
A. Images of corneas with vessels, using a green filter (red free) in the G1, G2, G3, and G4 groups, on day 15 of the evaluation. B. Comparison between the percentages of the corneal area containing vessels in the G1, G2, G3, and G4 groups, on day 15 of the evaluation. *P<0.05; G1 vs. G3 and G4 (Veterinary Ophthalmology Service, UNESP/FCAV, Jaboticabal, SP, Brazil 2017).

Discussion

In vivo models for the study of the mechanistic basis of angiogenesis and for investigating the action of alleged anti-angiogenic drugs should be affordable and non-invasive, when monitoring of the growth of new blood vessels. Rats are excellent model organisms for preclinical studies of angiogenesis, since they are small, easy to handle, incur a low cost, and have a mapped genome. The corneas of these animals have dimensions that allow rapid procedures for the induction of angiogenesis^8,24.

To date, there is no consensus on the optimal protocol for the induction of corneal angiogenesis in rats¹⁰. The implantation of pellets containing drugs or pro-angiogenic molecules are emerging in the literature as reliable strategies. However, the vascular response associated with these procedures is very intense and unpredictable²⁵. In addition, the investment required for pellet production is high. Alkaline cauterization remains the most widely used method for the induction of corneal angiogenesis, but its effectiveness may vary according to the protocol that is employed^6,7. The lack of reproducibility represents a common problem, among studies involving models of angiogenesis induced by alkaline cauterization¹⁰.

The aim of this study was to establish a reproducible and inexpensive protocol for the induction of corneal neovascularization using alkali in rats, that is easy to perform, and presents a low risk of undesirable complications, such as the perforation of the eye. The alkaline cauterization produced in corneas in this study leads to a timely inflammatory response^8,11-16, where the release of chemokines recruits leukocytes that produce angiogenic factors, such as the vascular endothelial growth factor, the fibroblast growth factor 2 and the tumor necrosis factor, among others. These growth factors attract endothelial cells, smooth muscle cells, fibroblasts, leukocytes, and platelets, triggering the process of neovascularization²⁶.

In the USA, some biomedical laboratories sell disposable sticks coated with silver nitrate and potassium nitrate, suitable for corneal cauterization^14,16. In Brazil, these sticks are not easily found, and need to be imported. Thus, we opted for preparing an aqueous solution containing 75% silver and 25% potassium nitrate, which was stored in an amber vial (protected from light) to avoid the oxidation of the compounds. For cauterization, filter papers were embedded in this alkaline solution and pressed onto the corneas of rats. The filter paper embedded with alkali used in this study, proved to be as effective, but more economical than commercial sticks.

The vascularization parameters were studied at different times for up to 15 days. In agreement with the literature, vessel growth tends to stabilize by the end of this period of time⁸.

The corneal cauterization observed in this study was similar to that observed in previous reports⁸. Most of the eyes in the current study presented burn intensities of grades 2 and 3. This result is similar to that reported by Hurmeric et al.²⁷ and Habot-Wilner et al.¹³, who used protocols in which the cauterization times were 8 and 10 seconds, respectively. These authors used commercial sticks to induce angiogenesis. We hypothesized that these commercially available coated sticks might be more concentrated. Therefore, this may explain the similarity between the values obtained in these studies and ours, as they used a shorter exposure time.

Groups whose corneas were exposed to alkali for a longer period of time presented higher values for the neovascularization profiles, that were either moderate or intense, as previously described by Yu et al.²⁰. Interestingly, in our study, the vessels developed in a progressive manner until the eighth day post-cauterization in all study groups. In previous studies, vessel development ceased on the third day post-cauterization².

In this study, larger corneal burns (3 mm) were observed compared to those obtained in previous studies using sticks coated with silver and potassium nitrate^8,15. Thus, we expected the corneal fractions containing vessels to be much larger than those reported in previous studies. Interestingly, however, they were smaller. Sella et al.¹⁵ induced 2-mm burns and observed that the vascularized percentage of the corneal area was 42.6 ± 19.59% on the 7^th day after the procedure. Manzano et al.¹² and Hepsen et al.¹¹ induced cauterizations of 1.8 mm and 5 mm, and observed vascularization in 63.5% and 56.9% of the corneal areas, respectively. We hypothesized that if these commercially coated sticks were more concentrated they could induce a greater inflammation, thus obtaining a larger corneal fractions containing vessels.

The time intervals during which the filter papers were in touch with the corneas changed the vascular response. On day 15 of the evaluation, these results differed significantly between the groups. The G3 and G4 groups showed intense neovascularization when compared with the G1 group. This suggested that the exposure time and maintaining the filter paper on the cornea at the time of washing, can modify the result, when corneas are compared at a later time.

Conclusions

We demonstrated the efficacy of an aqueous solution composed of 75% silver and 25% potassium nitrate, for the induction of corneal angiogenesis in rats. Four protocols were studied, and three of these (G2, G3 and G4) provided consistent results, with good reproducibility. As well, we recommend the protocol G3, as a result of these group had the larger corneal neovascularization profiles and corneal fractions containing vessels.

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• Financial sources:
  CNPQ (Proc. 300833/2010-5), and FAPESP (Proc. 2009/51773-4)

• 1
  Research performed at Laboratory of Ophthalmology Service, Department of Clinical and Veterinary Surgery, Faculty of Agrarian and Veterinary Sciences, Universidade Estadual de São Paulo (FCAV-UNESP), Jaboticabal-SP, Brazil. Part of PhD degree thesis, Postgraduate Program in Veterinary Surgery. Tutor: José Luiz Laus.

Publication Dates

• Publication in this collection
  Aug 2017

History

• Received
  19 Apr 2017
• Reviewed
  20 June 2017
• Accepted
  18 July 2017