Molecular Toxicology Laboratory, Department of Biotechnology, Bharathiar University, Coimbatore, Tamilnadu, 641 046, India.
Biofactors. 2015 Mar-Apr;41(2):90-100. doi: 10.1002/biof.1203. Epub 2015 Apr 2.
Fluoride induced hepatotoxicity has been extensively studied in both humans and animals. However, the mechanism underlying in the hepatotoxicity of experimental fluorosis remains obscure. The severity of fluoride toxicity was reduced by oral administration of certain plant derived antioxidants. Caffeic acid (CA) a polyphenolic compound has diverse range of pharmacological activity in the biological system. Therefore, the present study was aimed to investigate the protective mechanism of CA, against fluoride induced hepatotoxicity in rats. The rats were treated with 300 ppm of NaF via drinking water ad libitum alone and in combination with CA at a dose of 50 mg/kg daily for 30 days by oral intubation. CA treatment significantly prevented fluoride induced hepatic damage as evident from the histopathological studies and declined levels of serum fluoride and liver marker enzymes. A significant decrease in the levels of enzymatic (SOD2, CAT, GPx, and GSTpi class) and nonenzymatic (GSH and Vitamin C) antioxidants along with increased ROS, lipid peroxidation, protein carbonyl content, and nitrate levels by fluoride were also prevented in these groups. In addition, CA inhibits fluoride induced apoptosis by altering the Bax and caspase-3p20 expressions. Further, fluoride induced upregulation of Nox4, p38α MAPK, Hsp60, and downregulation of Hsp27 are the indicators for the detection of oxidative damage, apoptosis, and mitochondrial stress was also modulated by CA. These findings reveal that CA supplementation has a protective effect against fluoride induced hepatotoxicity in rats.
氟诱导的肝毒性已在人类和动物中得到广泛研究。然而,实验性氟中毒导致肝毒性的机制仍不清楚。某些植物来源的抗氧化剂的口服给药可降低氟化物毒性的严重程度。咖啡酸(CA)是一种多酚化合物,在生物系统中具有多种药理活性。因此,本研究旨在探讨 CA 对大鼠氟诱导肝毒性的保护机制。大鼠通过口服灌胃每天给予 50mg/kg 的 CA,同时自由饮用 300ppm 的 NaF 水 30 天。CA 处理显著预防了氟化物诱导的肝损伤,这从组织病理学研究和血清氟化物和肝标志物酶水平的降低中可以看出。CA 还可防止氟化物引起的酶(SOD2、CAT、GPx 和 GSTpi 类)和非酶(GSH 和维生素 C)抗氧化剂水平显著降低,同时还可防止 ROS、脂质过氧化、蛋白质羰基含量和硝酸盐水平增加。此外,CA 通过改变 Bax 和 caspase-3p20 的表达来抑制氟化物诱导的细胞凋亡。此外,氟化物诱导的 Nox4、p38αMAPK、Hsp60 上调和 Hsp27 下调是检测氧化损伤、细胞凋亡和线粒体应激的指标,CA 也可调节这些指标。这些发现表明,CA 补充剂对大鼠氟诱导的肝毒性具有保护作用。