| Literature DB >> 35386624 |
Ana Maria Dascalu1,2, Anca Anghelache2, Daniela Stana2, Andreea Cristina Costea3, Vanessa Andrada Nicolae1,2, Denisa Tanasescu4, Daniel Ovidiu Costea5,6, Laura Carina Tribus7,8, Anca Zgura9,10, Dragos Serban11,12, Lucian Duta12, Miruna Tudosie13, Simona Andrea Balasescu12, Ciprian Tanasescu14,15, Mihail Silviu Tudosie16,17.
Abstract
Diabetic retinopathy (DR) is a microvascular disorder occurring due to the long-term effects of diabetes, leading to vision-threatening damage to the retina. The human body has an elaborate system for managing and regulating the number of key trace metals circulating in the blood and stored cells. Inadequate zinc (Zn) and concurrent excess of copper (Cu) levels are associated with an increased level of oxidative stress, which may aggravate the microvascular lesions in diabetes mellitus. Several studies have revealed a significantly lower serum Zn concentration and increased Cu levels in DR when compared with diabetic patients without retinopathy and normal controls. These abnormalities are correlated with the duration of diabetes and higher levels of HbA1C. Multiple pathological mechanisms are proposed to explain these changes including hyperzincuria associated with polyuria, glycosuria, and proteinuria in diabetic patients, as well as impaired absorption of Zn at the gastrointestinal level. Increased levels of free Cu ions may be attributed to glycation and the release of Cu ions from the Cu-binding sites of proteins. Zn supplements and selective Cu chelators may be useful to alleviate oxidative stress and prevent DR progression.Entities:
Keywords: copper; diabetic retinopathy; inflammation; microcirculation; oxidative stress; trace elements; zinc
Year: 2022 PMID: 35386624 PMCID: PMC8972839 DOI: 10.3892/etm.2022.11253
Source DB: PubMed Journal: Exp Ther Med ISSN: 1792-0981 Impact factor: 2.447