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Retinoprotective Effects of PACAP Eye Drops in Microbead-Induced Glaucoma Model in Rats

Edina Szabó, Evelin Patkó, Alexandra Váczy, Dorottya Molitor, Adrienne Csutak, Gábor K. Tóth, Dóra Reglődi, Tamás Atlasz

2021International Journal of Molecular Sciences22 citationsDOIOpen Access PDF

Abstract

Glaucoma is associated with increased intraocular pressure (IOP), causing the apoptosis of retinal ganglion cells (RGCs) and the loss of their axons leading to blindness. Pituitary adenylate cyclase activating polypeptide (PACAP) is neuroprotective in several neural injuries, including retinopathies. The aim of this study was to investigate the effects of PACAP1-38 eye drops in a model of glaucoma. IOP was elevated bilaterally by injections of microbeads to block the aqueous humor outflow. The control groups received the same volume of saline. Animals were treated with PACAP1-38 (1 µg/drop, 3 × 1 drop/day) or vehicle for 4 weeks starting one day after the injections. Retinal morphology by histology and optical coherence tomography, function by electroretinography, and IOP changes were analyzed. Animals were sacrificed 8 weeks after the injections. Microbeads injections induced a significant increase in the IOP, while PACAP1-38 treatment lowered it to normal levels (~10 mmHg). Significant retinal degeneration and functional impairment were observed in the microbead-injected group without PACAP1-38 treatment. In the microbeads + PACAP1-38 group, the retinal morphology and functionality were close to the normal values. In summary, our results show that PACAP1-38, given in form of eye drops, is neuroprotective in glaucoma, providing the basis for potential future therapeutic administration.

Topics & Concepts

GlaucomaOphthalmologyRetinalMedicineIntraocular pressureElectroretinographySalineNeuroprotectionRetinal degenerationRetinaIntravitreal administrationEndocrinologyInternal medicineBiologyNeuroscienceNeuropeptides and Animal PhysiologyReceptor Mechanisms and SignalingPain Mechanisms and Treatments
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