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诃子(Terminalia chebula(Retz.))的还原能力和铁螯合特性可缓解铁诱导的小鼠肝毒性。

Reducing power and iron chelating property of Terminalia chebula (Retz.) alleviates iron induced liver toxicity in mice.

机构信息

Division of Molecular Medicine, Bose Institute, P-1/12 CIT Scheme VIIM, Kolkata 700054, India.

出版信息

BMC Complement Altern Med. 2012 Aug 31;12:144. doi: 10.1186/1472-6882-12-144.

Abstract

BACKGROUND

The 70% methanol extract of Terminalia chebula Retz. fruit (TCME) was investigated for its in vitro iron chelating property and in vivo ameliorating effect on hepatic injury of iron overloaded mice.

METHODS

The effect of fruit extract on Fe2+-ferrozine complex formation and Fe2+ mediated pUC-18 DNA breakdown was studied in order to find the in vitro iron chelating activity. Thirty-six Swiss Albino mice were divided into six groups of: blank, patient control and treated with 50, 100, 200 mg/kg b.w. of TCME and desirox (standard iron chelator drug with Deferasirox as parent compound). Evaluations were made for serum markers of hepatic damage, antioxidant enzyme, lipid per oxidation and liver fibrosis levels. The reductive release of ferritin iron by the extract was further studied.

RESULTS

In vitro results showed considerable iron chelation with IC50 of 27.19 ± 2.80 μg/ml, and a significant DNA protection with [P]50 of 1.07 ± 0.03 μg/ml along with about 86% retention of supercoiled DNA. Iron-dextran injection (i.p.) caused significant increase in the levels of the serum enzymes, viz., alanine aminotransferase (ALAT), aspartate aminotransferase (ASAT), alkaline phosphatase (ALP) and Bilirubin, which were subsequently lowered by oral administration of 200 mg/kg b.w. dose of the fruit extract by 81.5%, 105.88%, 188.08% and 128.31%, respectively. Similarly, treatment with the same dose of the extract was shown to alleviate the reduced levels of liver antioxidant enzyme superoxide dismutase, catalase, glutathione S-transferase and non-enzymatic reduced glutathione, by 49.8%, 53.5%, 35.4% and 11% respectively, in comparison to the iron overloaded mice. At the same time, the fruit extract effectively lowered the iron-overload induced raised levels of lipid per oxidation, protein carbonyl, hydroxyproline and liver iron by 49%, 67%, 67% and 26%, respectively, with oral treatment of 200 mg/kg b.w. dose of TCME. The fruit extract also showed potential activity for reductive release of ferritin iron.

CONCLUSIONS

These findings suggest that Terminalia chebula extract may contain active substances capable of lessening iron overload induced toxicity, and hence possibly be useful as iron chelating drug for iron overload diseases.

摘要

背景

研究了诃子(Terminalia chebula Retz.)果实 70%甲醇提取物(TCME)的体外铁螯合特性及其对铁过载小鼠肝损伤的体内改善作用。

方法

为了寻找体外铁螯合活性,研究了果实提取物对 Fe2+-ferrozine 络合物形成和 Fe2+介导的 pUC-18 DNA 断裂的影响。将 36 只瑞士白化病小鼠分为六组:空白组、患者对照组和 50、100、200mg/kg b.w.的 TCME 和去铁酮(以地拉罗司为母体化合物的标准铁螯合剂药物)治疗组。评估血清肝损伤标志物、抗氧化酶、脂质过氧化和肝纤维化水平。进一步研究了提取物对铁蛋白铁的还原释放作用。

结果

体外结果表明,该提取物具有相当强的铁螯合能力,IC50 为 27.19±2.80μg/ml,[P]50 为 1.07±0.03μg/ml,同时超螺旋 DNA 的保留率约为 86%。铁右旋糖酐(i.p.)注射导致血清酶丙氨酸氨基转移酶(ALAT)、天冬氨酸氨基转移酶(ASAT)、碱性磷酸酶(ALP)和胆红素水平显著升高,随后经口服 200mg/kg b.w.剂量的果实提取物治疗后,这些酶的水平分别降低了 81.5%、105.88%、188.08%和 128.31%。同样,与铁过载小鼠相比,用相同剂量的提取物处理可分别使肝脏抗氧化酶超氧化物歧化酶、过氧化氢酶、谷胱甘肽 S-转移酶和非酶还原型谷胱甘肽的降低水平提高 49.8%、53.5%、35.4%和 11%。同时,果实提取物还能有效降低铁过载诱导的脂质过氧化、蛋白质羰基、羟脯氨酸和肝铁水平升高,口服 200mg/kg b.w.剂量的 TCME 治疗后,这些水平分别降低了 49%、67%、67%和 26%。果实提取物对铁蛋白铁的还原释放也表现出潜在的活性。

结论

这些发现表明,诃子提取物可能含有能够减轻铁过载诱导的毒性的活性物质,因此可能可作为铁过载疾病的铁螯合剂药物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6c5a/3489879/cc2cdbf4fee1/1472-6882-12-144-1.jpg

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