Liu Jiang-Yue, Zheng Chen-Zhao, Hao Xin-Ping, Zhang Dai-Juan, Mao An-Wei, Yuan Ping
Department of Pathophysiology, Weifang Medical University Weifang, Shandong, China.
Department of Thoracic Surgery, Weifang Traditional Chinese Hospital Weifang, Shandong, China.
Am J Transl Res. 2016 Oct 15;8(10):4278-4288. eCollection 2016.
Catalpol, isolated from the roots of , Chinese foxglove, is an iridoid glycoside with antioxidant, anti-inflammatory and anti-hyperglycemic agent. The present study was to investigate the effects of catalpol on diabetic atherosclerosis in alloxan-induced diabetic rabbits. Diabetes was induced in rabbits by a hyperlipidemic diet and intravenous injection of alloxan (100 mg/kg). Rabbits were treated for 12 weeks. The fasting blood glucose, insulin, homeostasis model of insulin resistance, total cholesterol and triglyceride were measured. The thoracic aorta was excised for histology. The plasma and vascular changes including some markers of oxidative stress, inflammatory cytokines and fibrosis factors were examined. Plasma levels of fasting blood glucose, insulin and homeostasis model of insulin resistance were significantly decreased in catalpol group. Catalpol treatment ameliorated diabetic atherosclerosis in diabetic rabbits as demonstrated by significantly inhibited neointimal hyperplasia and macrophages recruitment. Catalpol treatment also enhanced the activities of superoxide dismutase, glutathione peroxidase, and increased the plasma levels of total antioxidant status, meanwhile reduced the levels of malondialdehyde, protein carbonyl groups and advanced glycation end product. Furthermore, catalpol also reduced circulating levels of tumor necrosis factor-α, monocyte chemotactic protein-1 and vascular cell adhesion molecule-1. Catalpol also decreased transforming growth factor-β1 and collagen IV mRNA and protein expressions in the vessels. Catalpol exerts an ameliorative effect on atherosclerotic lesion in alloxan-induced diabetic rabbits. The possible mechanisms may be related to inhibition of oxidative stress inflammatory response and anti-fibrosis and reduced aggregation of extracellular matrix.
梓醇是从地黄根中分离出的一种环烯醚萜苷,具有抗氧化、抗炎和抗高血糖作用。本研究旨在探讨梓醇对四氧嘧啶诱导的糖尿病兔动脉粥样硬化的影响。通过高脂饮食和静脉注射四氧嘧啶(100mg/kg)诱导兔糖尿病。对兔进行12周治疗。测定空腹血糖、胰岛素、胰岛素抵抗稳态模型、总胆固醇和甘油三酯。切除胸主动脉进行组织学检查。检测血浆和血管变化,包括氧化应激、炎性细胞因子和纤维化因子的一些标志物。梓醇组空腹血糖、胰岛素和胰岛素抵抗稳态模型的血浆水平显著降低。梓醇治疗改善了糖尿病兔的动脉粥样硬化,表现为显著抑制内膜增生和巨噬细胞募集。梓醇治疗还增强了超氧化物歧化酶、谷胱甘肽过氧化物酶的活性,提高了血浆总抗氧化状态水平,同时降低了丙二醛、蛋白质羰基和晚期糖基化终产物的水平。此外,梓醇还降低了肿瘤坏死因子-α、单核细胞趋化蛋白-1和血管细胞黏附分子-1的循环水平。梓醇还降低了血管中转化生长因子-β1和IV型胶原mRNA及蛋白表达。梓醇对四氧嘧啶诱导的糖尿病兔动脉粥样硬化病变具有改善作用。其可能机制可能与抑制氧化应激炎症反应、抗纤维化及减少细胞外基质聚集有关。