Ozerkan Dilşad, Ozsoy Nesrin, Cebesoy Suna
Department of Biology, Faculty of Arts and Sciences, Kastamonu University, 37100, Kastamonu, Turkey
Department of Biology, Faculty of Science, Ankara University, 06100, Tandogan/Ankara, Turkey.
Microscopy (Oxf). 2014 Dec;63(6):409-17. doi: 10.1093/jmicro/dfu029. Epub 2014 Aug 21.
Diabetes causes oxidative stress, which in turn generates excessive free radicals resulting in cellular damage. Vitamin C is an antioxidant that protects tissues and organs from oxidative stress. The thymus is one of the most important lymphoid organs, which regulates T-lymphocyte proliferation and maturation. The aim of this study is to investigate the protective effects of vitamin C on the thymus of streptozotocin (STZ)-induced diabetic rats. The mitotic activity and cell integrity of thymic lymphocytes were explored. Wistar Albino rats were divided into three groups: control (Group 1), STZ-diabetes (Group 2) and vitamin C-treated STZ-diabetics (Group 3). Rats received a single intraperitoneal injection of 45 mg/kg STZ to induce diabetes. Vitamin C (20 mg/kg) was administered intragastrically. Semithin and ultrathin sections were examined under a light or an electron microscope, respectively. Considerable numbers of mitotic lymphocytes were observed in the thymus of control rats. In the diabetic rats, however, numbers of mitotic lymphocytes decreased to ∼57% of controls, and cell division abnormalities were observed. Additionally, diabetic rats showed degeneration in the structure of the thymus including trabecular thickening, accumulation of lipid vacuoles, heterochromatic nuclei and loss of mitochondrial cristae. Degradation of medullar and cortical integrity was also detected. In the vitamin C-treated STZ-diabetic group, the structure of the thymus and mitotic activity of the lymphocytes were similar to the control group. These results suggest that vitamin C protects the thymus against injury caused by diabetes and restores thymocyte mitotic activity.
糖尿病会引发氧化应激,进而产生过多自由基,导致细胞损伤。维生素C是一种抗氧化剂,可保护组织和器官免受氧化应激的影响。胸腺是最重要的淋巴器官之一,它调节T淋巴细胞的增殖和成熟。本研究的目的是探讨维生素C对链脲佐菌素(STZ)诱导的糖尿病大鼠胸腺的保护作用。研究了胸腺淋巴细胞的有丝分裂活性和细胞完整性。将Wistar白化大鼠分为三组:对照组(第1组)、STZ糖尿病组(第2组)和维生素C治疗的STZ糖尿病组(第3组)。大鼠腹腔注射45mg/kg STZ以诱导糖尿病。维生素C(20mg/kg)通过胃内给药。分别在光学显微镜或电子显微镜下检查半薄切片和超薄切片。在对照大鼠的胸腺中观察到大量有丝分裂淋巴细胞。然而,在糖尿病大鼠中,有丝分裂淋巴细胞的数量降至对照组的约57%,并观察到细胞分裂异常。此外,糖尿病大鼠的胸腺结构出现退化,包括小梁增厚、脂质空泡积累、异染色质核和线粒体嵴消失。还检测到髓质和皮质完整性的破坏。在维生素C治疗的STZ糖尿病组中,胸腺结构和淋巴细胞的有丝分裂活性与对照组相似。这些结果表明,维生素C可保护胸腺免受糖尿病所致的损伤,并恢复胸腺细胞的有丝分裂活性。