Department of Biochemistry, School of Medicine, Hamadan University of Medical Sciences, Hamadan, Iran.
Department of Pathology, School of Medicine, Hamadan University of Medical Sciences, Hamadan, Iran.
Biomed Pharmacother. 2018 Jan;97:729-735. doi: 10.1016/j.biopha.2017.10.097. Epub 2017 Nov 6.
The aim of this study was to explore the efficacy of insulin-loaded trimethylchitosan nanoparticles on certain destructive effects of diabetes type one.
Twenty-five male Wistar rats were randomly divided into three control groups (n=5) and two treatment groups (n=5). The control groups included normal diabetic rats without treatment and diabetic rats treated with the nanoparticles. The treatment groups included diabetic rats treated with the insulin-loaded trimethylchitosan nanoparticles and the diabetic rats treated with trade insulin. The experiment period was eight weeks and the rats were treated for the last two weeks.
The livers of the rats receiving both forms of insulin showed less severe microvascular steatosis and fatty degeneration, and ameliorated blood glucose, serum biomarkers, and oxidant/antioxidant parameters with no significant differences. The gene expression of pyruvate kinase could be compensated by both the treatment protocols and the new coated form of insulin could not significantly influence the gene expression of glucokinase (p<0.05). The result of the present study showed the potency of the nanoparticle form of insulin to attenuate hyperglycemia, oxidative stress, and inflammation in diabetes, which indicate the bioavailability of insulin-encapsulated trimethylchitosan nanoparticles.
本研究旨在探讨载胰岛素三甲基壳聚糖纳米粒对 1 型糖尿病某些破坏作用的疗效。
将 25 只雄性 Wistar 大鼠随机分为三组(每组 n=5):未治疗的正常糖尿病大鼠组、未治疗的糖尿病大鼠组、载胰岛素三甲基壳聚糖纳米粒治疗组。治疗组包括载胰岛素三甲基壳聚糖纳米粒治疗组和普通胰岛素治疗组。实验周期为 8 周,最后两周对大鼠进行治疗。
两种胰岛素治疗组大鼠的肝脏显示出较轻的微血管脂肪变性和脂肪变性,血糖、血清标志物和氧化/抗氧化参数均得到改善,差异无统计学意义。两种治疗方案均可补偿丙酮酸激酶的基因表达,而新的包被胰岛素形式不能显著影响葡糖激酶的基因表达(p<0.05)。本研究结果表明,胰岛素纳米粒形式具有减轻糖尿病高血糖、氧化应激和炎症的作用,提示胰岛素包封三甲基壳聚糖纳米粒具有生物利用度。