Department of Chemistry, Biochemistry Division, Istanbul University-Cerrahpasa, Avcilar, 34320, Istanbul, Turkey.
Faculty of Science, Department of Biology, Istanbul University, Vezneciler, 34134, Istanbul, Turkey.
Biol Trace Elem Res. 2021 Apr;199(4):1515-1523. doi: 10.1007/s12011-020-02269-7. Epub 2020 Jul 9.
Vanadium compounds are being investigated as potential therapeutic agents in the treatment of many health problems, primarily diabetes. We aimed to provide the effect of N(1)-4-hydroxysalicylidene-N(4)-salicylidene-S-methyl-isothiosemicarbazidato-oxovanadium(IV) (VOL) on small intestinal injury in experimental male diabetic rats. Four groups were created of 3.0-3.5-month-old rats. The rats were made diabetic by a single dose of streptozotocin (STZ) at 65 mg/kg and grouped as follows: control animals, VOL-given control animals, STZ-induced diabetic animals and STZ-induced diabetic animals given VOL. A daily dose of 0.2 mM/kg vanadium complex was administered orally for 12 days after the inducement of diabetes. On the 12th day, small intestine tissue samples were taken. According to the data obtained from the biochemical analysis, reduced glutathione (GSH) level, catalase (CAT), glutathione peroxidase (GPx), glutathione-S-transferase (GST), superoxide dismutase (SOD), Na/K-ATPase and paraoxanase (PON) activities were increased, whereas sialic acid (SA), xanthine oxidase (XO) and disaccharidases (maltase and saccharidase) activities were decreased in the small intestine tissue of VOL-treated diabetic rats. Microscopic examinations revealed a remarkable decrease in the mucosal necrotic areas, discontinuity in the brush border, deterioration of the villi integrity and oedema inside the villi, but with a mild decrease in the inflammatory cells, deterioration and loss of integrity of the gland in the small intestine of VOL-treated diabetic rats. Moreover, VOL treatment markedly decreased the proliferation of villus cells and especially inflammatory cells in the small intestine of diabetic rats. According to the obtained data, the administration of VOL is a potentially convenient strategy to reducing small intestine injury in diabetic rats.
钒化合物正被作为治疗多种健康问题(主要是糖尿病)的潜在治疗剂进行研究。我们旨在研究 N(1)-4- 羟基水杨醛缩 N(4)- 水杨醛缩 S- 甲基异硫代氰酸根合氧钒(IV)(VOL)对实验性雄性糖尿病大鼠小肠损伤的影响。将 3.0-3.5 个月大的大鼠分为 4 组。大鼠一次性给予 65mg/kg 的链脲佐菌素(STZ)诱导糖尿病,并分为以下几组:对照组动物、给予 VOL 的对照组动物、STZ 诱导的糖尿病动物和给予 VOL 的 STZ 诱导的糖尿病动物。糖尿病诱导后,每天口服给予 0.2mM/kg 的钒复合物 12 天。第 12 天,取小肠组织样本。根据生化分析数据,还原型谷胱甘肽(GSH)水平、过氧化氢酶(CAT)、谷胱甘肽过氧化物酶(GPx)、谷胱甘肽-S-转移酶(GST)、超氧化物歧化酶(SOD)、Na/K-ATP 酶和对氧磷酶(PON)活性增加,而小肠组织中唾液酸(SA)、黄嘌呤氧化酶(XO)和二糖酶(麦芽糖酶和蔗糖酶)活性降低。显微镜检查显示,VOL 治疗的糖尿病大鼠的黏膜坏死区域显著减少,刷状缘不连续,绒毛完整性恶化,绒毛内水肿,但炎症细胞减少,小肠腺体的恶化和完整性丧失减轻。此外,VOL 治疗显著降低了糖尿病大鼠小肠绒毛细胞和特别是炎症细胞的增殖。根据获得的数据,VOL 的给药是减少糖尿病大鼠小肠损伤的一种潜在便捷策略。