Department of Pathophysiology, Iuliu Haţieganu University of Medicine and Pharmacy Cluj-Napoca, Victor Babeş Str., No. 4-6, 400012 Cluj-Napoca, Romania.
Department of Medical Informatics and Biostatistics, Iuliu Haţieganu University of Medicine and Pharmacy Cluj-Napoca, Louis Pasteur Str., No. 6, 400349 Cluj-Napoca, Romania.
Biomed Res Int. 2017;2017:4754701. doi: 10.1155/2017/4754701. Epub 2017 Oct 24.
Our study aimed to investigate the analgesic and antioxidative stress effects of Curcumin (CC) in experimental migraine induced by Nitroglycerin (NTG) on rats, compared with Indomethacin (ID) and Propranolol (PP) treatments.
Five groups of 10 rats treated i.p. were investigated: control group (healthy rats) injected with saline solution (0.9%), NTG-control group injected with NTG (1 mg/100 gbw, bw = body weight), and three groups with pretreatment applied 30 min previous to the formalin test (NTG + CC group: Curcumin (10 mg/100 gbw), NTG + PP group: Propranolol (100 g/100 gbw), and NTG + ID group: Indomethacin (0.5 mg/100 gbw)). Formalin test was performed and number of flinches and shakes were counted. Several oxidative stress parameters were also assessed.
The smallest values of malondialdehyde (MDA), nitric oxide (NOx), and total oxidative status (TOS) were observed on NTG + CC with significant differences as compared with the control group ( < 0.0001). The group pretreated with Curcumin proved significantly smaller number of flinches and shakes compared with both NTG + PP and NTG + ID.
Our study demonstrates a superior activity of Curcumin not only versus control, but also versus Propranolol and Indomethacin.
本研究旨在探讨姜黄素(CC)对硝酸甘油(NTG)诱导的实验性偏头痛大鼠的镇痛和抗氧化应激作用,并与吲哚美辛(ID)和普萘洛尔(PP)进行比较。
对 5 组 10 只大鼠进行腹腔注射治疗:对照组(健康大鼠)注射生理盐水(0.9%),NTG 对照组注射 NTG(1mg/100gbw,bw=体重),另外 3 组在正式测试前 30 分钟进行预处理(NTG+CC 组:姜黄素(10mg/100gbw)、NTG+PP 组:普萘洛尔(100g/100gbw)和 NTG+ID 组:吲哚美辛(0.5mg/100gbw))。进行福尔马林测试并计数抽搐和颤抖次数。还评估了几种氧化应激参数。
在与对照组(<0.0001)相比,NTG+CC 组的丙二醛(MDA)、一氧化氮(NOx)和总氧化状态(TOS)的数值最小。与 NTG+PP 和 NTG+ID 相比,用姜黄素预处理的组显示出明显较少的抽搐和颤抖次数。
我们的研究表明,姜黄素的活性不仅优于对照组,而且优于普萘洛尔和吲哚美辛。