番荔枝醇提物对不同促氧化剂诱导的大鼠脑和肝脏脂质过氧化的抗氧化活性

E. M. Ale, Adesola Oluwaseun Adeleye, O. Akinseye, Ebenezer Kayode Toluwalase
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摘要

背景和目的:多年来,大量的研究已经证明了番荔枝的抗氧化能力,以及它对无数疾病的药物作用。然而,关于其对多种类型的氧化剂的抗氧化能力,目前还没有明确的信息。本研究通过体外模型研究了木楝乙醇提取物对大鼠脑和肝组织中不同促氧化剂的抗氧化能力。方法:将鲜木香叶洗净、风干、粉碎、乙醇提取。对大鼠实施安乐死,取脑组织和肝脏,用50mM Tris-HCl (pH 7.4)匀浆。匀浆在4000rpm下离心10min,获得低速上清,在提取物和五种不同的促氧化剂存在下用于TBARS测定;硫酸铁,过氧化氢,3-硝基丙酸,硝普钠和喹啉酸。结果:结果表明,无论使用何种促氧化剂,木香提取物均能抑制硫代巴比妥酸活性物质的产生,从而对脑和肝组织匀浆中的脂质过氧化有较强的抑制作用。这种多酚性抗氧化能力可能与其高多酚含量有关,这使其具有很强的氧化还原性和供氢能力。因此,本研究为进一步研究村田草对脂质过氧化介导的疾病的治疗作用铺平了道路。
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Antioxidant activities of ethanolic extract of Annona muricata against different pro-oxidant induced lipid peroxidation in rat brain and liver
Background and objective: Over the years, numerous works have documented the antioxidant potency of Annona muricata as well as it medicinal actions against myriad of ailments. However, there is still vague information as regard its antioxidant ability against diverse types of prooxidants. This work is carried out to deduce the antioxidant capacity of ethanol extract of A. muricata against different pro-oxidants in the cerebral and hepatic tissues of rats in in vitro models. Methods: Fresh leaves of A. muricata were washed, air-dried, pulverized and extracted with ethanol. Rats were euthanized and the tissues (brain and liver) were removed and homogenized in 50mM Tris-HCl, pH 7.4. The homogenates were centrifuged for 10min at 4000rpm to obtain a low-speed supernatant that was used for TBARS assay in the presence of extract and five different pro-oxidants; Iron (II) sulphate, hydrogen peroxide, 3-Nitropropionic acid, Sodium nitroprusside and quinolinic acid. Results: The results reveal that A. muricata extract displayed strong potency against lipid peroxidation in both the brain and liver tissue homogenates by inhibiting the production of thiobarbituric acid reactive substances irrespective of the prooxidant used. This polytropic antioxidant ability of A. muricata extract could be linked to its high polyphenolic content which confers on it, a strong redox property as well as a hydrogen donating power. This research therefore paves way for further investigation on the therapeutic actions of A. muricata in lipid peroxidation mediated ailments and diseases.
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