Overexpression of serine racemase in retina and overproduction of D-serine in eyes of streptozotocin-induced diabetic retinopathy

Background: recent data indicate that inflammatory mechanisms contribute to diabetic retinopathy (dr). we have determined that serine racemase (sr) expression is increased by inflammatory stimuli including liposaccharide (lps),amyloid β-peptide (a-beta),and secreted amyloid precursor protein (sapp); expression is decreased by the anti-inflammatory drug,dexamethasone. we tested possibility that sr and its product,d-serine,were altered in a rat model of dr.methods: intraperitoneal injection of streptozotocin (stz; 70 mg/kg body weight) to sprague-dawley rats produced type-i diabetic mellitus (fasting blood sugar higher than 300 mg/dl). at 3 and 5 months after stz or saline injection,retinas from some rats were subjected to cryosectioning for immunofluorescent analysis of sr and tunel assay of apoptosis. retinal homogenates were used to detect sr levels and jun n-terminal kinase (jnk) activation by immunoblotting. aqueous humor and retina were also collected to assay for neurotransmitters,including glutamate and d-serine,by reverse-phase hplc.results: compared to saline-injected rats,stz-injected (diabetic) rats showed elevation of sr protein levels in retinal homogenates,attributed to the inner nuclear layer (inl) by immunofluorescence. aqueous humor fluid from stz-injected rats contained significantly higher levels of glutamate and d-serine compared to controls; by contrast,d-serine levels in retinas did not differ. levels of activated jnk were elevated in diabetic retinas compared to controls.conclusions: increased expression of sr in retina and higher levels of glutamate and d-serine in aqueous humor of stz-treated rats may result from activation of the jnk pathway in diabetic sequelae. our data suggest that the inflammatory conditions that prevail during dr result in elevation of d-serine,a neurotransmitter contributing to glutamate toxicity,potentially exacerbating the death of retinal ganglion cells in this condition. © 2011 jiang et al; licensee biomed central ltd.