Department of Biochemistry, Shri B. M. Patil Medical College, Hospital and Research Centre, BLDE (Deemed to be University), Vijayapura, Karnataka, 586103, India.
Laboratory of Vascular Physiology and Medicine, Department of Physiology, Shri B. M. Patil Medical College, Hospital and Research Centre, BLDE (Deemed to be University), Vijayapura, Karnataka, 586103, India.
Biol Trace Elem Res. 2020 May;195(1):178-186. doi: 10.1007/s12011-019-01829-w. Epub 2019 Jul 23.
Nickel, a widely used heavy metal is suspected as a cardiotoxic element. The aim of the present study was to assess the possible protective role of l-ascorbic acid on nickel-induced alterations of cardiovascular pathophysiology in male albino rats. Twenty-four albino rats (b.wt. 170-250 g) were randomized into four groups: control; l-ascorbic acid (50 mg/100 g b.wt., orally); NiSO (2.0 mg/100 g b.wt., i.p.); NiSO with l-ascorbic acid. Cardiovascular electrophysiology, serum and cardiac tissue malondialdehyde (MDA), nitric oxide (NO), ascorbic acid, serum α-tocopherol and serum vascular endothelial growth factor (VEGF) were evaluated. Histopathology of cardiac and aortic tissues was also assessed. NiSO-treated rats showed a significant increase in heart rate, LF/HF ratio and blood pressure (SBP, DBP and MAP). A significant increase of serum MDA, NO and VEGF in NiSO treatment with a concomitant decrease of serum ascorbic acid and α-tocopherol as compared to their respective controls were also observed. Simultaneous supplementation of l-ascorbic acid with NiSO significantly decreased LF/HF ratio, BP and oxidative stress parameters, whereas ascorbic acid and α-tocopherol concentration was found to be increased. Histopathology of cardiac and aortic tissues showed nickel-induced focal myocardial hypertrophy and degeneration in cardiac tissue with focal aneurism in aortic tissues. Supplementation with l-ascorbic showed a protective action in both cardiac and aortic tissues. Results indicated the possible beneficial effect of l-ascorbic acid on nickel-induced alteration of the cardiovascular pathophysiology in experimental rats.
镍是一种广泛使用的重金属,被怀疑是一种心脏毒性元素。本研究旨在评估 L-抗坏血酸对雄性白化大鼠镍诱导的心血管病理生理学改变的可能保护作用。24 只白化大鼠(体重 170-250g)随机分为四组:对照组;L-抗坏血酸(50mg/100g 体重,口服);NiSO(2.0mg/100g 体重,腹腔注射);NiSO 加 L-抗坏血酸。评估心血管电生理学、血清和心肌组织丙二醛(MDA)、一氧化氮(NO)、抗坏血酸、血清α-生育酚和血清血管内皮生长因子(VEGF)。还评估了心脏和主动脉组织的组织病理学。NiSO 处理的大鼠心率、LF/HF 比值和血压(SBP、DBP 和 MAP)显著增加。与各自的对照组相比,NiSO 处理后血清 MDA、NO 和 VEGF 显著增加,而血清抗坏血酸和α-生育酚含量降低。与 NiSO 同时补充 L-抗坏血酸可显著降低 LF/HF 比值、BP 和氧化应激参数,同时发现抗坏血酸和α-生育酚浓度增加。心脏和主动脉组织的组织病理学显示镍诱导的心肌局灶性肥大和心脏组织变性,以及主动脉组织局灶性动脉瘤。补充 L-抗坏血酸对心脏和主动脉组织均具有保护作用。结果表明,L-抗坏血酸对实验大鼠镍诱导的心血管病理生理学改变可能具有有益作用。