Hereditary retinal degeneration (RD) is a common cause of blindness in canines and humans, making canines an ideal model for studying inherited retinal diseases in humans. As an ophthalmology preclinical research CRO, Ace Therapeutics provides dozens of canine inherited retinal degeneration models to customers around the world. Here, our researchers are able to develop customized protocols to help you ttest novel therapeutic strategies for retinal degenerative diseases.
Hereditary retinal degenerative diseases are a group of genetically and phenotypically heterogeneous disorders that are one of the leading causes of blindness worldwide. Recent advances in molecular genetics and cell biology using large animal models elucidate the pathophysiological mechanisms underlying these diseases are helping to identify new therapeutic approaches, such as gene therapy, stem cell therapy, and optogenetics. Canines are the primary species used, as idiopathic IRD is common in canine pets. Canines represent an increasingly popular animal model for ocular diseases, greatly improving our understanding of their pathogenesis. In addition to this, a significant advantage over rodents is that canine models can be utilized for intraocular drug delivery studies, surgical procedures and in vivo imaging procedures. Which helps test novel therapeutic strategies being developed to treat human patients.
Fig. 1. Histolopathology at the fovea-like area in two canine models of inherited macular degeneration. (Beltran WA, et al., 2014)
Hereditary retinal degeneration (RD) is a common cause of blindness in canines and humans. In the past few years, Ace Therapeutics has been committed to providing a comprehensive ocular disease model and service for global customers through continuous exploration and research. Canines make for an attractive model due to the significant genetic and phenotypic similarities of canine RDs to their human counterparts. This is of significant value for understanding the function of disease-causing genes, deciphering the cellular and molecular mechanisms of disease, and developing effective therapeutic strategies.
In view of this, Ace Therapeutics provides a series of canine hereditary retinal degeneration models to help you understand understand disease mechanisms and develop new treatments. Our canine hereditary retinal degeneration models include, but are not limited to:
Tab.1. Ace Therapeutics' canine models of inherited retinal degeneration.
Canine models | Causative gene |
---|---|
Rod cone dysplasia 1 (RCD1) | PDE6β |
Rod cone dysplasia 3 (RCD1) | PDE6α |
Progressive rod cone degeneration (PRCD) | PRCD |
Leber congenital amaurosis (LCA) | RPE65 |
Canine multifocal retinopathy1 (CMR1) | BEST1 = VMD2 |
Canine multifocal retinopathy1(CMR2) | BEST1 = VMD2 |
Cone degeneration (CD) | CNGB3 |
X-linked progressive retinal atrophy1 (XLPRA1) | RPGR |
X-linked progressive retinal atrophy2 (XLPRA2) | RPGR |
T4R RHO | RHO |
Importantly, our ophthalmic pharmacologists also develop programmed experimental protocols to help you test novel therapeutic strategies for retinal degenerative diseases, and evaluate them with the following tools, including but not limited to:
Ace Therapeutics aims to provide global customers with a powerful experimental tool to explore novel therapies aimed at treating retinal degenerative diseases. If you are interested in our services or need more detailed information, please feel free to contact us. Our experienced scientists are ready to help you!
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