Topical administration of somatostatin prevents retinal neurodegeneration in experimental diabetes

  1. Rafael Simó1,2
  1. 1Diabetes and Metabolism Research Unit. Vall d’Hebron Research Institute. Universitat Autònoma de Barcelona, Spain
  2. 2Centro de Investigación Biomédica en Red de Diabetes y Enfermedades Metabólicas Asociadas (CIBERDEM), ISCIII, Spain
  3. 3BCN Peptides, Barcelona, Spain
  4. 4Instituto de Investigaciones Biomédicas Alberto Sols (CSIC/UAM), Madrid, Spain
  1. Corresponding author: Cristina Hernández, cristina.hernandez{at}vhir.org

Abstract

Retinal neurodegeneration is an early event in the pathogenesis of diabetic retinopathy (DR). Somatostatin (SST) is an endogenous neuroprotective peptide which is downregulated in the diabetic eye. The aim of the study was to test the usefulness of topical administration of SST in preventing retinal neurodegeneration. For this purpose, streptozotocin-induced diabetic rats (STZ-DM) were treated with either SST eye-drops or vehicle for 15 days. Non-diabetic rats treated with vehicle served as control group. Functional abnormalities were assessed by electroretinography (ERG) and neurodegeneration was assessed by measuring glial activation and the apoptotic rate. In addition, proapoptotic (FasL, Bid, and activation of caspase-8 and caspase-3) and survival signalling pathways (Bclxl) were examined. Intraretinal concentrations of glutamate and its main transporter GLAST (glutamate/aspartate transporter) were also determined. Treatment with SST eye drops prevented ERG abnormalities, glial activation, apoptosis and the misbalance between proapoptotic and survival signalling detected in STZ-DM rats. In addition, SST eye drops inhibited glutamate accumulation in the retina and GLAST downregulation induced by diabetes. We conclude that topical administration of SST has a potent effect in preventing retinal neurodegeneration induced by diabetes. In addition, our findings open up a new preventive pharmacological strategy targeted to early stages of DR.

  • Received July 12, 2012.
  • Accepted March 1, 2013.

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