Orexin Blockers’ Role in Glucose Homeostasis and Diabetic Retinopathy

Authors

  • Braden Baker Indiana University School of Medicine - Terre Haute; Eugene and Marilyn Glick Eye Institute, Department of Ophthalmology, Indiana University School of Medicine https://orcid.org/0000-0003-3242-0387
  • Rupinder Kaur Sodhi Eugene and Marilyn Glick Eye Institute, Department of Ophthalmology, Indiana University School of Medicine
  • Neha Mahajan Eugene and Marilyn Glick Eye Institute, Department of Ophthalmology, Indiana University School of Medicine
  • Ashay Dilip Bhatwadekar Eugene and Marilyn Glick Eye Institute, Department of Ophthalmology, Indiana University School of Medicine

DOI:

https://doi.org/10.18060/29024

Abstract

Background:  

Diabetic retinopathy (DR) is the most common complication of diabetes and can lead to blindness if untreated. Orexin is a neuropeptide produced by the hypothalamus that regulates the sleep/wake cycle. Orexin-blockers are prescribed for insomnia, which recent studies have shown to decrease blood glucose levels, suggesting a potential therapeutic for DR. This study aims to explore orexin-blockers’ role in glucose homeostasis and diabetic retinopathy through in-vitroin-vivo, and chart-review methods.  

Methods:  

  1. In-vitro: Glucose uptake by human retinal endothelial cells (HRECs) was determined by exposure to varying levels of suvorexant, a commonly prescribed orexin blocker, and orexin-A. Additionally, Orexin expression under high glucose concentrations was examined using fluorescent staining. 
  2. Pre-clinical: Diabetic (db/db) and non-diabetic (db/m) mice were injected with suvorexant daily. Mice weights and blood glucose were regularly compared with the vehicle control.  
  3. Clinical Chart-review: A review that examines individuals retrospectively to determine if orexin-blockers decrease percentages of developing vision-threatening DR or macular edema compared to patients NOT taking orexin-blockers. 

Results: 

  1. In-vitro: HRECs exposed to suvorexant had increased glucose uptake, while those exposed to orexin had a decreased glucose uptake. There were no significant changes in orexin expression in HRECs exposed to high glucose. 
  2. Pre-clinical: Mice treated with suvorexant showed a downward trend in body weight, food intake, and better glucose tolerance than vehicle control diabetic mice. 
  3. Clinical Chart-review: 41 patients treated with orexin blockers were identified. Fewer patients taking suvorexant developed vision-threatening DR than those without treatment. Additionally, there was a trend of decreasing HbA1c while taking suvorexant. 

Conclusion:  

The results of the in-vitro, pre-clinical, and clinical chart review studies indicate suvorexant has blood glucose-lowering properties. Data will continue to be collected for the clinical chart review to further determine the effects of orexin blockers on diabetic retinopathy and HbA1c. 

 

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Published

2025-06-24

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Abstracts