Molecular Vision 2021; 27:365-369
Received 12 March 2021 | Accepted 19 May 2021 | Published 21 May 2021
Li Liu, Youde Jiang, Jena J. Steinle
Department of Ophthalmology, Visual, and Anatomical Sciences, Wayne State University School of Medicine, Detroit, MI
Correspondence to: Jena J Steinle, Professor, Department of Ophthalmology, Visual, and Anatomical Sciences, Wayne State University School of Medicine, Detroit, MI, Phone: (313) 577-9731, email: email@example.com
Purpose: To determine whether forskolin, a protein kinase A (PKA) agonist, eye drops could reduce neuronal and vascular damage after exposure to ischemia/reperfusion (I/R).
Methods: C57BL/6J mice were exposed to the I/R protocol. A group of mice were given forskolin eye drops (10 μM) daily. Two days after I/R, neuronal measurements were performed, while vascular measurements were performed at 10 days post-I/R. Western blotting was conducted to investigate whether forskolin could increase PKA levels and reduce the levels of inflammatory mediators.
Results: Forskolin statistically significantly increased PKA levels, but not exchange protein activated by cAMP 1 (Epac1). The forskolin eye drops also reduced neuronal and vascular damage compared to I/R alone. Tumor necrosis factor alpha (TNF-α) and interleukin-1-β (IL-1β) levels were statistically significantly reduced after administration of forskolin eye drops compared to I/R alone.
Conclusions: Forskolin eye drops were protective against I/R. The findings offer a new therapeutic for local delivery.
Increased understanding of upstream modulators of diabetic retinal damage is key to development of novel therapeutics. A new treatment should be able to reduce neuronal and vascular damage associated with diabetes. To more rapidly screen potential therapeutics, some researchers found that an ischemia/reperfusion (I/R) model recapitulated some of the retinal damage commonly observed in the diabetic retina, but the I/R model took much less time [1,2]. We previously used this model to show that an eye drop of Compound 49b, a novel β-adrenergic receptor agonist, was protective against neuronal (2 days) and vascular (10 days) retina damage after exposure to I/R . We found similar results using endothelial cell–specific knockout mice for exchange protein activated by cAMP 1 (Epac1) to show that Epac1 is protective against I/R .
In addition to Epac1, Compound 49b could signal through protein kinase A (PKA). Literature suggests that PKA and Epac1 pathways may become activated after stimulation of the β-adrenergic receptor, leading to initiation of distinct signaling cascades . Some studies have shown that PKA and Epac1 modulate microvascular endothelial actions differently , while others showed that PKA and Epac1 work cooperatively to activate downstream pathways [7,8]. The role of PKA in I/R models is less clear. Additionally, it is not clear whether an eye drop of a PKA agonist is protective against retinal damage. As a β-adrenergic receptor agonist could signal through either Epac1 or PKA, these experiments were designed to investigate whether PKA could protect the retina against I/R damage through the use of an eye drop of forskolin, a PKA agonist.
C57BL/6J mice (30 mice) were purchased from Jackson Laboratories (Bar Harbor, ME). The mice were split into two groups. One group received I/R only, and one group was treated with forskolin eye drops during I/R exposure and then daily for the remainder of the experimental time. Forskolin eye drops were given at 10 µM (about 5 µl to each eye) one time/day at the same time of the day about 10 a.m. Mouse samples were collected at 2 days for neuronal measurements and at 10 days post-I/R for vascular and protein assessments. All studies were approved by the Wayne State University IACUC protocol #20-07-2490. These studies adhere to the ARVO statement for Use of Animals in Research.
Animals were anesthetized with an injection of ketamine and xylazine (60 mg/kg and 30mg/kg subcutaneous). After anesthesia, a 32-gauge needle attached to an infusion line of sterile saline was used to cannulate the anterior chamber of the eye. Hydrostatic pressure of 80–90 mmHg (TonoPen, Medtronic, Jacksonville, FL) was maintained for 90 min to induce retinal ischemia, noted by blanching of the iris and loss of red reflex [3,9]. After 90 min, the needle was withdrawn, and intraocular pressure normalized. The contralateral eye was used as an intra-animal control.
Two days after exposure to I/R, 5 mice in each group were euthanized (CO2 inhalation) to measure the neuronal thickness, as we have done previously . Ten-micrometer sections were taken from throughout the retina. Multiple sections from each animal were assessed for retinal thickness and cell numbers in the ganglion cell layer (GCL) [10,11]. The measurements were not performed in a blinded fashion.
Ten days after I/R exposure, 10 mice in each group were euthanized (CO2 inhalation) to measure degenerate capillaries, as we have done previously [3,12]. The analyses were not conducted in a blinded manner.
Retinal lysates were collected into lysis buffer with protease and phosphatase inhibitors. Equal amounts of protein were separated using precast Tris-Glycine gels (Invitrogen, Carlsbad, CA) and blotted onto nitrocellulose membranes. After blocking in TBST (10 mM Tris-HCl buffer, pH 8.0, 150 mM NaCl, 0.1% Tween-20) and 5% (w/v) bovine serum albumin (BSA), membranes were treated with an Epac1, PKA, TNF-α, IL-1β (Abcam, Cambridge, MA), and β-actin (Santa Cruz Biotechnology, Santa Cruz, CA) primary antibodies followed by incubation with secondary antibodies tagged with horseradish peroxidase. Antigen-antibody complexes were visualized with an Azure C500 machine (Azure Biosystems, Dublin, CA) after application of a chemiluminescence reagent kit (Thermo Scientific, Pittsburgh, PA). Western blot band densities were measured using Image Studio Lite software (Li-Cor Biosciences, Lincoln, NE).
Statistics were calculated using Prism 7.0 (GraphPad, San Diego, CA). A one-way ANOVA with Tukey’s post-hoc test was used for the data analyses. A p value of less than 0.05 was considered statistically significant.
Before we initiated the analyses of the neurons and the vasculature, we ensured that the dosage of choice (10 µM as eye drops) could increase PKA levels. Figure 1 shows that I/R reduced PKA (Figure 1A) and Epac1 levels. Forskolin eye drops increased the PKA levels (Figure 1A), but not the Epac1 levels (Figure 1B). These data confirm the specificity of forskolin for PKA versus Epac1.
As forskolin increased PKA levels in the whole retina, we measured changes in neurons 2 days after I/R. Figure 2 confirmed previous findings of reduced retinal thickness and cell numbers in the GCL after I/R. Forskolin had no effect on the control eyes but statistically significantly increased the retinal thickness (Figure 2C) and cell numbers (Figure 2B) following exposure to I/R. These data suggest that forskolin eye drops can protect the retina against neuronal damage after retinal stressors.
Ten days following exposure to I/R, globes were removed for measurement of degenerate capillaries. Exposure to I/R statistically significantly increased formation of degenerate capillaries (Figure 3). Forskolin eye drops statistically significantly reduced the number of degenerate capillaries after exposure to I/R (Figure 3).
Because we previously reported that PKA has anti-inflammatory properties , we also wanted to test this in the I/R model. Figure 4A,B show that I/R statistically significantly increased IL-1β and TNF-α levels, which were statistically significantly reduced by forskolin eye drops, suggesting that the eye drops were effective in reducing inflammatory pathways.
We have previously reported that the β-adrenergic receptor agonist, Compound 49b, was able to protect the diabetic retina . Because β-adrenergic receptor agonists could activate Epac1 or PKA, we investigated whether Epac1 knockout mice (endothelial cell specific) had more damage in the retina in response to I/R when compared to mice with intact Epac1 . However, application of a drug agonist offers new avenues for therapeutic development versus genetic models.
To address this issue, we tested the ability of forskolin eye drops (PKA agonist) to reduce damage to the retina after exposure to I/R. Based on our previous experience with Compound 49b, we first tested whether 10 μM forskolin could increase retinal levels of PKA. We found that forskolin was specific for PKA, because forskolin increased PKA levels after I/R, while no changes in Epac1 were observed. We also evaluated changes in the neurons and vasculature after the administration of forskolin eye drops. We replicated previous findings showing that I/R reduced retinal thickness and decreased cell numbers in the GCL, while increasing formation of degenerate capillaries. When forskolin eye drops were used for 2 and 10 days, respectively, we found a statistically significant decrease in damage in the neurons and vasculature. To support these histological findings, we also measured protein levels of TNF-α and IL-1β, two inflammatory pathways we have shown to be increased in diabetic models using Compound 49b, the β-adrenergic receptor agonist, or in Epac1 knockout mice [11,14]. In this study, we showed that forskolin eye drops were able to reduce the levels of both inflammatory proteins in whole retinal lysates, suggesting that forskolin eye drops have anti-inflammatory actions.
These findings suggest that forskolin eye drops may offer a new therapeutic opportunity for reducing retinal damage after ischemia. Additional work on permeability, safety, corneal penetration, and cell-specific targeting studies are all required before this treatment can move forward for development into a treatment modality. However, this study offers a good first step showing successful use of a PKA agonist for protection against a retinal stressor.
This study was supported by R01EY030284 (JJS), P30EY04068 (Hazlett), and an Unrestricted Grant to the Department of Ophthalmology from Research to Prevent Blindness (Kresge Eye Institute). The funders did not influence the design or execution of these studies.