丹daniela茎皮和叶乙醇提取物GC-MS谱及对Fenton反应大鼠脑钠泵和体外器官硫醇状态影响的比较研究

E. M. Ale, Steve Osagie Asuelimen, V. I. Ayo, O. Akinseye, David Chinonso Anih, Bilyaminu Habibu, Siman Rambo Samaila
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引用次数: 0

摘要

Daniellia oliveri是尼日利亚和一些西非国家最广泛使用的药用植物之一,用于治疗各种疾病。在本研究中,研究了Daniellia oliveri茎皮和叶的乙醇提取物对H2O2和Fe2+ (fenton反应)攻击大脑和肝脏组织匀浆中脂质过氧化、Na+/K+- atp酶活性和硫醇含量的影响。茎皮和叶用无水乙醇提取72小时,在旋转蒸发器中浓缩。对Wistar大鼠实施安乐死,取其脑和肝脏,匀浆,离心,上清液在促氧化剂(1mM H2O2或10μM Fe2+或H2O2和Fe2+)存在下进行脂质过氧化,Na+/K+- atp酶活性和硫醇测定。结果表明,叶和茎皮乙醇提取物均能抑制H2O2、Fe2+及H2O2与Fe2+联合诱导的脂质过氧化,并能明显减少大鼠肝脏和脑匀浆中脂质过氧化加合物的形成,其中茎皮的作用更明显。此外,Na+/K+-ATPase和硫醇检测结果显示,H2O2和Fe2+抑制了脑组织Na+/K+-ATPase的活性,而H2O2/Fe2+显著降低了组织匀浆中蛋白质和非蛋白硫醇的水平。然而,Daniellia oliveri乙醇提取物通过增加大鼠肝脏和脑组织中Na+/K+- atp酶的活性以及硫醇水平来消除这种异常。最后,对Daniellia oliveri茎皮和叶的乙醇提取物进行气相色谱-质谱分析,结果发现茎皮中含有1,2-苯并异噻唑-3-胺、1h -吲哚-2-羧酸、2-乙基吖啶、2-(2-氯乙酰氨基)-3,3,3-三氟-2-(3-氟苯胺)丙酸乙酯和反式1-丁基-2-甲基环丙烷等21种化合物,甲基硫乙腈、2-甲基- z、z -3,13-十八烯二烯醇、在Daniellia oliveri的叶子中含有脱硫素和4h -1,2,4-三唑-3,5-二胺,证明了Daniellia oliveri的生物活性,而茎皮的高效力可能归因于其中存在更多的生物活性成分。因此,本研究证明了Daniellia oliveri的叶子和茎皮的药用价值,并建议在与氧化应激相关的病因变性疾病的治疗和管理中考虑Daniellia oliveri。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A Comparative Study on GC-MS Profiles and Effect of Ethanolic Extracts of Stem-Bark and Leaves of Daniellia oliveri on Cerebral Sodium Pump and Thiols Status in Fenton Reaction Treated Rat Organs In-vitro
Daniellia oliveri is one of the most extensively utilized medicinal plants in Nigeria and some West African countries for the treatment of various ailments. In the present study, the GC-MS profiles and effect of ethanolic extracts of stem bark and leaves of Daniellia oliveri on lipid peroxidation, Na+/K+-ATPase activity and thiols status in H2O2 and Fe2+ (fenton reaction) assaulted cerebral and hepatic tissue homogenates was investigated. The stem bark and leaves were extracted with absolute ethanol for 72hrs and concentrated in a rotary evaporator. Wistar rats were euthanized and the brains and livers were removed, homogenized, centrifuged and the supernatants were used for lipid peroxidation, Na+/K+-ATPase activity, and thiol assays in the presence of prooxidants (1mM H2O2 or 10μM Fe2+ or H2O2 and Fe2+).The results revealed that ethanol extract of both the leaf and stem-bark inhibited lipid peroxidation induced by H2O2, Fe2+ and combination of H2O2 and Fe2+ and this was evident in the reduction of lipid peroxidation adducts formation in rat liver and brain homogenates with the stem-bark possessing more efficacy. Furthermore, the results of  Na+/K+-ATPase and thiol assays revealed that H2O2 and Fe2+ inhibited the activity of cerebral Na+/K+-ATPase, while  H2O2/Fe2+ caused a marked reduction in the levels of both protein and non-protein thiols in the tissues homogenates. However, the ethanolic extract of Daniellia oliveri extirpated this anomaly by increasing the activity of cerebral Na+/K+-ATPase as well as the thiol level in the rat hepatic and cerebral tissues. Finally, GC-MS analysis was carried out on the ethanolic extracts of the stem bark and leaves of Daniellia oliveri and results revealed the presence of 21 compounds including 1,2-Benzisothiazol-3-amine, 1H-Indole-2-carboxylic acid, 2-Ethylacridine, Ethyl 2-(2-chloroacetamido)-3,3,3-trifluoro-2-(3-fluoroanilino) propionate and trans-1-Butyl-2-methylcyclopropane in the stem bark and 10 compounds including Methylthio-acetonitrile, 2-Methyl-Z,Z-3,13-octadecadienol, Desulphosinigrin and 4H-1,2,4-triazole-3,5-diamine in the leaves, justifying the observed biological activities of Daniellia oliveri and the higher potency of the stem bark may be attributed to the presence of more bioactive constituents found in it. This study therefore justifies the medicinal usage of leaves and stem-bark of Daniellia oliveri and suggests its consideration in the treatment and management of degeneration diseases with etiology associated with oxidative stress.
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