Ghate Nikhil Baban, Chaudhuri Dipankar, Panja Sourav, Mandal Nripendranath
Division of Molecular Medicine, Bose Institute , Kolkata, West Bengal , India.
Pharm Biol. 2015 Jul;53(7):1066-74. doi: 10.3109/13880209.2014.959612. Epub 2015 Jan 22.
Nerium indicum Mill. (Apocynaceae) was reported for its efficient in vitro antioxidant and iron-chelating properties.
This study demonstrates the effect of 70% methanol extract of N. indicum leaf (NIME) towards in vitro DNA protection and ameliorating iron-overload-induced liver damage in mice.
Phytochemical and HPLC analyses were carried out to standardize the extract and the effect of Fe(2+)-mediated pUC18 DNA cessation was studied. Thirty-six Swiss Albino mice were divided into six groups of blank, negative control (iron overload only), and iron-overloaded mice receiving 50, 100, and 200 mg/kg b.w. doses of NIME and desirox (20 mg/kg b.w.). The biochemical markers of hepatic damage, various liver and serum parameters, and reductive release of ferritin iron were studied.
The presence of different phytocomponents was revealed from phytochemical and HPLC analyses. A substantial supercoiled DNA protection, with [P]50 of 70.33 ± 0.32 µg, was observed. NIME (200 mg/kg b.w.) significantly normalized the levels of alanine aminotransferase, aspartate aminotransferase, alkaline phosphatase, and bilirubin by 126.27, 125.25, 188.48, and 45.47%, respectively. NIME (200 mg/kg b.w.) was shown to alleviate the reduced levels of superoxide dismutase, catalase, glutathione-S-transferase, and non-enzymatic-reduced glutathione, by 48.95, 35.9, 35.42, and 13.22%, respectively. NIME also lowered raised levels of lipid peroxidation, protein carbonyl, hydroxyproline, and liver iron by 32.28, 64.58, 136.81, and 83.55%, respectively.
These findings suggest that the active substances present in NIME may be capable of lessening iron overload-induced toxicity, and possibly be a useful drug for iron-overloaded diseases.
夹竹桃(夹竹桃科)因其高效的体外抗氧化和铁螯合特性而被报道。
本研究证明夹竹桃叶70%甲醇提取物(NIME)对体外DNA保护以及改善小鼠铁过载诱导的肝损伤的作用。
进行了植物化学和高效液相色谱分析以标准化提取物,并研究了Fe(2+)介导的pUC18 DNA断裂的影响。将36只瑞士白化小鼠分为六组,分别为空白组、阴性对照组(仅铁过载)以及接受50、100和200 mg/kg体重剂量NIME和去铁胺(20 mg/kg体重)的铁过载小鼠组。研究了肝损伤的生化标志物、各种肝脏和血清参数以及铁蛋白铁的还原释放。
植物化学和高效液相色谱分析揭示了不同植物成分的存在。观察到显著的超螺旋DNA保护,[P]50为70.33±0.32μg。NIME(200 mg/kg体重)分别使丙氨酸氨基转移酶、天冬氨酸氨基转移酶、碱性磷酸酶和胆红素水平显著正常化126.27%、125.25%、188.48%和45.47%。NIME(200 mg/kg体重)分别使超氧化物歧化酶、过氧化氢酶、谷胱甘肽-S-转移酶和非酶还原型谷胱甘肽降低的水平分别提高了48.95%、35.9%、35.42%和13.22%。NIME还分别使脂质过氧化、蛋白质羰基、羟脯氨酸和肝脏铁升高的水平降低了32.28%、64.58%、136.81%和83.55%。
这些发现表明NIME中存在的活性物质可能能够减轻铁过载诱导的毒性,并且可能是治疗铁过载疾病的有用药物。