Chang Wei-Chih, Hung Chang-Tsen, Chen Yuh-Shuen, Hsueh Chih-Chi, Hou Chien-Wei, Lay Horng-Liang
Graduate Institute of Bioresources, National Pingtung University of Science and Technology, Pingtung, Taiwan.
Department of Health and Leisure Management, Yuanpei University of Medical Technology, Hsinchu, Taiwan.
Iran J Basic Med Sci. 2018 Mar;21(3):230-235. doi: 10.22038/ijbms.2018.21545.5554.
(AC) is found with anti-inflammatory and immunomodulatory biological activities. In this study, we investigated the anti-hepatitis effect of the emulsified AC extract from RO water or supercritical fluid CO with ethanol co-solvent extract methods of AC preparations.
Five groups of eight to ten weeks male rats with a count of ten for each group were studied to evaluate the protection of two kinds of AC extract from hepatic injury. Acute liver injury of rats was induced by injecting 40% carbon tetrachloride (CCl) 1 mg/kg intraperitoneally. Positive and negative control groups rats were perfused with CCl or isotonic saline, respectively. Experimental groups received oral administration once/day of AC preparations before CCl treatment: water AC extract (WAE group), or emulsified AC extract from supercritical fluid extraction (EAE group) for 5 days, and sacrificed on the 6 day and the blood and liver samples were collected under chloral hydrate anesthesia. The anti-inflammatory, antioxidant markers, and relevant signaling pathways were measured (AST, ALT, ROS, IL-1, IL-6, NO, and COX-2, MAPKs, and caspase-3).
EAE at 50 mg/kg significantly decreased the serum AST, ALT, IL-1, IL-6, NO, and ROS levels. Both extracts reduced the activation of p-ERK in the liver samples, but EAE inhibited COX-2 and caspase-3 protein expression better than WAE. The EAE ameliorated CCl-induced hepatic injury significantly; as compared with WAE and the positive control.
The hepatoprotection of EAE could be attributed to the antioxidant and anti-inflammatory effects of .
已发现(AC)具有抗炎和免疫调节生物活性。在本研究中,我们采用RO水乳化AC提取物或超临界流体CO与乙醇共溶剂萃取法制备AC制剂,研究其抗肝炎作用。
研究五组8至10周龄雄性大鼠,每组10只,以评估两种AC提取物对肝损伤的保护作用。通过腹腔注射1mg/kg 40%四氯化碳(CCl)诱导大鼠急性肝损伤。阳性和阴性对照组大鼠分别灌注CCl或等渗盐水。实验组在CCl处理前每天口服一次AC制剂:水AC提取物(WAE组)或超临界流体萃取乳化AC提取物(EAE组),持续5天,并在第6天处死,在水合氯醛麻醉下采集血液和肝脏样本。检测抗炎、抗氧化标志物及相关信号通路(AST、ALT、ROS、IL-1、IL-6、NO、COX-2、MAPKs和caspase-3)。
50mg/kg的EAE显著降低了血清AST、ALT、IL-1、IL-6、NO和ROS水平。两种提取物均降低了肝脏样本中p-ERK的激活,但EAE比WAE更好地抑制了COX-2和caspase-3蛋白表达。与WAE和阳性对照相比,EAE显著改善了CCl诱导的肝损伤。
EAE的肝保护作用可能归因于其抗氧化和抗炎作用。