Toxicology and Diseases Group, The Institute of Pharmaceutical Sciences (TIPS), Tehran University of Medical Sciences, Tehran, Iran.
Medicinal Plants Research Center, Institute of Medicinal Plants, ACECR, Karaj, Iran.
J Cell Biochem. 2019 Apr;120(4):4766-4782. doi: 10.1002/jcb.27807. Epub 2018 Oct 26.
We aimed to review and meta-analyze the inflammatory and oxidative factors following alpha lipoic acid (ALA) and its derivative "andrographolid-lipoic acid-1" (AL-1) in ulcerative colitis (UC). ALA plays an important role in scavenging intracellular radicals and inflammatory elements. AL-1 is found in herbal medicines with potent anti-inflammatory properties. Data were collected from the Google Scholar, PubMed, Scopus, Evidence-based medicine/clinical trials, and Cochrane library database until 2017, which finally resulted in 22 animal studies (70 rats and 162 mice). The beneficial effects of ALA or AL-1 on the most important parameters of UC were reviewed; also, studies were considered separately in mice and rats. Administration of ALA and AL-1 significantly reduced the tumor necrosis factor-α level compared with the controls, while data were not noteworthy in the meta-analysis (mean differences = -18.57 [95% CI = -42.65 to 5.51], P = 0.13). In spite of insignificant decrease in meta-analysis outcomes (differences = 6.92 [95% CI = -39.33 to 53.16], P = 0.77), a significant reduction in myeloperoxidase activity was shown following ALA or AL-1 treatment compared with the controls. Despite significant differences in each study, we had to exclude some studies to homogenize data for meta-analyzing as they showed insignificant results. Interleukin 6, cyclooxygenase-2, glutathione, malondialdehyde, superoxide dismutase, histopathological score, macroscopic and microscopic scores, disease activity index, body weight change, and colon length were also reviewed. Most studies have emphasized on significant positive effects of ALA and AL-1. Comprehensive clinical trials are obligatory to determine the precious position of ALA or AL-1 in the management of UC.
我们旨在综述并荟萃分析α-硫辛酸(ALA)及其衍生物“安德拉格列醇-硫辛酸-1”(AL-1)在溃疡性结肠炎(UC)中的炎症和氧化因子。ALA 在清除细胞内自由基和炎症因子方面发挥着重要作用。AL-1 存在于具有强大抗炎特性的草药中。数据从 Google Scholar、PubMed、Scopus、循证医学/临床试验和 Cochrane 图书馆数据库中收集,时间截至 2017 年,最终纳入了 22 项动物研究(70 只大鼠和 162 只小鼠)。综述了 ALA 或 AL-1 对 UC 最重要参数的有益影响;同时,分别在小鼠和大鼠中考虑了研究。与对照组相比,ALA 和 AL-1 的给药显著降低了肿瘤坏死因子-α水平,而荟萃分析中数据无显著意义(平均差异=-18.57 [95%CI=-42.65 至 5.51],P=0.13)。尽管荟萃分析结果无显著下降(差异=6.92 [95%CI=-39.33 至 53.16],P=0.77),但与对照组相比,ALA 或 AL-1 治疗后髓过氧化物酶活性显著降低。尽管每项研究均有显著差异,但我们不得不排除一些研究以进行数据同质化分析,因为它们显示出无显著结果。白细胞介素 6、环氧化酶-2、谷胱甘肽、丙二醛、超氧化物歧化酶、组织病理学评分、宏观和微观评分、疾病活动指数、体重变化和结肠长度也进行了综述。大多数研究都强调了 ALA 和 AL-1 的显著积极作用。必须进行综合临床试验以确定 ALA 或 AL-1 在 UC 管理中的宝贵地位。