Tokaç Mehmet, Bacanli Merve, Dumlu Ersin Gürkan, Aydin Sevtap, Engin Merve, Bozkurt Birkan, Yalçin Abdüssamed, Erel Özcan, Kiliç Mehmet, Başaran Nurşen
Yeni Yüzyıl University, Faculty of Medicine, Gaziosmanpaşa Hospital, Clinic of General Surgery, İstanbul, Turkey.
Hacettepe University, Faculty of Pharmacy, Department of Pharmaceutical Toxicology, Ankara, Turkey.
Turk J Pharm Sci. 2017 Dec;14(3):257-263. doi: 10.4274/tjps.49369. Epub 2017 Nov 20.
Pycnogenol (PYC), a standardized extract from the bark of , consists of different phenolic compounds. PYC has shown to have protective effects on chronic diseases such as diabetes, asthma, cancer, and immune disorders. The aim of this study was to determine the effects of PYC against the DNA damage and biochemical changes in blood, liver, and lung tissues of ischemia-reperfusion (IR)-induced Wistar albino rats.
A sham group, IR injury-induced group, and IR+PYC group were formed. Ischemia was induced and sustained for 45 min, then the ischemic liver was reperfused, which was sustained for a further 120 min at the end of this period. After anesthesia and before the IR inducement, 100 mg/kg PYC was given to the IR+PYC group through intraperitoneal injections. The total oxidant (TOS) and total antioxidant status (TAS), total thiol levels (TTL), advanced oxidation protein products (AOPP), and biochemical parameters [myeloperoxidase (MPO), aspartate aminotransferase (AST), alanine aminotransferase (ALT) and lactate dehydrogenase (LDH)] in the rats were analyzed using spectrophotometric methods and DNA damage was assessed using single-cell gel electrophoresis.
The levels of TOS, TTL, MPO, AOPP, ALT, AST, and LDH were significantly decreased in the IR+PYC group compared with the IR group (p<0.05). The levels of TAS were significantly increased in the IR+PYC group compared with the IR group (p<0.05). PYC reduced the DNA damage when compared with the IR group (p<0.05).
The present results suggest that PYC treatment might have a role in the prevention of IR-induced oxidative damage by decreasing DNA damage and increasing antioxidant status.
碧萝芷(PYC)是从法国沿海松树树皮中提取的标准化提取物,由多种酚类化合物组成。PYC已显示出对糖尿病、哮喘、癌症和免疫紊乱等慢性疾病具有保护作用。本研究的目的是确定PYC对缺血再灌注(IR)诱导的Wistar白化大鼠血液、肝脏和肺组织中DNA损伤和生化变化的影响。
组建假手术组、IR损伤诱导组和IR+PYC组。诱导缺血并持续45分钟,然后对缺血肝脏进行再灌注,在此阶段结束时再持续120分钟。在麻醉后且IR诱导前,通过腹腔注射给予IR+PYC组100mg/kg的PYC。使用分光光度法分析大鼠体内的总氧化剂(TOS)和总抗氧化状态(TAS)、总巯基水平(TTL)、晚期氧化蛋白产物(AOPP)以及生化参数[髓过氧化物酶(MPO)、天冬氨酸转氨酶(AST)、丙氨酸转氨酶(ALT)和乳酸脱氢酶(LDH)],并使用单细胞凝胶电泳评估DNA损伤。
与IR组相比,IR+PYC组的TOS、TTL、MPO、AOPP、ALT、AST和LDH水平显著降低(p<0.05)。与IR组相比,IR+PYC组的TAS水平显著升高(p<0.05)。与IR组相比,PYC减少了DNA损伤(p<0.05)。
目前的结果表明,PYC治疗可能通过减少DNA损伤和提高抗氧化状态,在预防IR诱导的氧化损伤中发挥作用。