23 DOI: https://doi.org/10.1016/j.jgeb.2026.100663 English eng Ashour, Ahmed M. Contributor <div id="as005" style="margin: 0px; padding: 0px; color: rgb(31, 31, 31); font-family: ElsevierGulliver, Georgia, "Times New Roman", Times, STIXGeneral, "Cambria Math", "Lucida Sans Unicode", "Microsoft Sans Serif", "Segoe UI Symbol", "Arial Unicode MS", serif, sans-serif; font-size: 16px;"><h3 class="u-h4 u-margin-m-top u-margin-xs-bottom" id="st010" style="margin-right: 0px; margin-left: 0px; padding: 0px; margin-top: 24px !important; margin-bottom: 8px !important; font-size: 20px !important; line-height: 30px !important;">Background</h3><div class="u-margin-s-bottom" id="sp0005" style="margin-top: 0px; margin-right: 0px; margin-left: 0px; padding: 0px; margin-bottom: 16px !important;">Diabetes is a serious and rapidly growing global health issue that can affect many organs, including the brain. It is often linked to complications such as cardiovascular disease and cerebral ischemia. Propolis, a natural resin produced by honey bees, is rich in phenols and flavonoids known for their antioxidant, anti-inflammatory, and immune-modulating properties.</div></div><div id="as010" style="margin: 0px; padding: 0px; color: rgb(31, 31, 31); font-family: ElsevierGulliver, Georgia, "Times New Roman", Times, STIXGeneral, "Cambria Math", "Lucida Sans Unicode", "Microsoft Sans Serif", "Segoe UI Symbol", "Arial Unicode MS", serif, sans-serif; font-size: 16px;"><h3 class="u-h4 u-margin-m-top u-margin-xs-bottom" id="st015" style="margin-right: 0px; margin-left: 0px; padding: 0px; margin-top: 24px !important; margin-bottom: 8px !important; font-size: 20px !important; line-height: 30px !important;">Objective</h3><div class="u-margin-s-bottom" id="sp0010" style="margin-top: 0px; margin-right: 0px; margin-left: 0px; padding: 0px; margin-bottom: 16px !important;">This primary aim in this research was to evaluate the neuroprotective effects of propolis on brain tissue in rats that have diabetes which is introduced through nicotinamide (NA) and streptozotocin (STZ).</div></div><div id="as015" style="margin: 0px; padding: 0px; color: rgb(31, 31, 31); font-family: ElsevierGulliver, Georgia, "Times New Roman", Times, STIXGeneral, "Cambria Math", "Lucida Sans Unicode", "Microsoft Sans Serif", "Segoe UI Symbol", "Arial Unicode MS", serif, sans-serif; font-size: 16px;"><h3 class="u-h4 u-margin-m-top u-margin-xs-bottom" id="st020" style="margin-right: 0px; margin-left: 0px; padding: 0px; margin-top: 24px !important; margin-bottom: 8px !important; font-size: 20px !important; line-height: 30px !important;">Methods</h3><div class="u-margin-s-bottom" id="sp0015" style="margin-top: 0px; margin-right: 0px; margin-left: 0px; padding: 0px; margin-bottom: 16px !important;">Male Wistar rats were separated into categories. Except for the control category, all were fed a diet that had high fat levels. Diabetes was induced using intraperitoneal injections of NA and STZ. After induction, diabetic rats received oral propolis at doses of 50 or 100 mg/kg daily for eight weeks. Throughout the study, lipid profiles, fasting blood glucose, insulin levels, and oxidative stress markers were assessed by taking measurements. At the end of the experiment, brain tissues were analyzed for cytokine levels, antioxidant activity, and DNA damage using the COMET assay, in addition to histopathological and immunohistochemical examinations.</div></div><div id="as020" style="margin: 0px; padding: 0px; color: rgb(31, 31, 31); font-family: ElsevierGulliver, Georgia, "Times New Roman", Times, STIXGeneral, "Cambria Math", "Lucida Sans Unicode", "Microsoft Sans Serif", "Segoe UI Symbol", "Arial Unicode MS", serif, sans-serif; font-size: 16px;"><h3 class="u-h4 u-margin-m-top u-margin-xs-bottom" id="st025" style="margin-right: 0px; margin-left: 0px; padding: 0px; margin-top: 24px !important; margin-bottom: 8px !important; font-size: 20px !important; line-height: 30px !important;">Results</h3><div class="u-margin-s-bottom" id="sp0020" style="margin-top: 0px; margin-right: 0px; margin-left: 0px; padding: 0px; margin-bottom: 16px !important;">Treatment with propolis significantly reduced fasting blood glucose and insulin levels, improved profiles of lipid, and decreased oxidative stress and inflammatory mediators. Histological analysis showed that rats treated with propolis had noticeably less brain tissue damage compared to untreated diabetic rats.</div></div><div id="as025" style="margin: 0px; padding: 0px; color: rgb(31, 31, 31); font-family: ElsevierGulliver, Georgia, "Times New Roman", Times, STIXGeneral, "Cambria Math", "Lucida Sans Unicode", "Microsoft Sans Serif", "Segoe UI Symbol", "Arial Unicode MS", serif, sans-serif; font-size: 16px;"><h3 class="u-h4 u-margin-m-top u-margin-xs-bottom" id="st030" style="margin-right: 0px; margin-left: 0px; padding: 0px; margin-top: 24px !important; margin-bottom: 8px !important; font-size: 20px !important; line-height: 30px !important;">Conclusion</h3><div class="u-margin-s-bottom" id="sp0025" style="margin-top: 0px; margin-right: 0px; margin-left: 0px; padding: 0px; margin-bottom: 16px !important;">Propolis demonstrated clear neuroprotective effects in diabetic rats, likely through its antioxidant and anti-inflammatory mechanisms. These findings suggest that propolis may present a considerably potential solution as a natural therapeutic agent for reducing diabetes-induced brain damage.</div></div> Elsevier March 2026 pdf Journal of Genetic Engineering and Biotechnology Propolis alleviates brain tissue damage and oxidative abnormalities in streptozotocin (STZ)-induced diabetes mixed material Elsevier