毛茛治疗疟疾感染小鼠CD的变化及其与肝脏胰岛素抵抗指数和甘油三酯36水平的相关性

A. O. Opajobi, U. Uzuegbu, P. Y. Toloyai, E. Ojugbeli, A.C. Ezeh, I. Onyesom
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引用次数: 1

摘要

毛茛是一种用于治疗包括疟疾在内的各种疾病的草药。其抗疟原虫特性和抗氧化能力已被报道,但其对CD36与肝脏胰岛素抵抗和甘油三酯水平的影响知之甚少。因此,本研究旨在评估白桦醇叶提取物分级剂量对伯氏疟原虫感染小鼠肝脏中可溶性CD36浓度的变化及其与肝脏胰岛素抵抗指数和甘油三酯水平的相关性。30只体重在20-30g之间的成年瑞士白化小鼠分为6组(n=5/grp)。分别以150、300和450mg/kg/d的粗乙醇叶提取物为单次日剂量,连续7 d。在研究的第8天,小鼠在禁食一夜后以氯仿麻醉处死。经心脏穿刺取血,离心得到血清,用于血清CD36、葡萄糖和胰岛素的测定,同时取每只小鼠的肝脏,分别取不同剂量(150、300和450mg/kg/d)的毛叶粗乙醇提取物,对感染伯氏疟原虫7 d的实验小鼠进行测定,维持血清可溶性CD36(3.40±0.52pg/ml、3.47±0.46pg/ml和3.37±0.46pg/ml)。肝胰岛素抵抗指数(0.85±0.10,0.77±0.17和0.82±0.13)和肝甘油三酯(134.33±15.95mg/dl, 174.00±11.27mg/dl和163.67±11.02mg/dl)水平的变化趋势与对照组和氯喹处理数据(cd36 = 3.03±0.12pg/ml,肝TAG = 139.33±12.01,HIR指数= 0.64±0.07)比较良好。未经治疗的疟疾感染组CD36与肝脏甘油三酯呈强正相关,与肝脏胰岛素抵抗指数呈强负相关。对照组和氯喹处理组的相关性相似,而提取物处理组的相关性较弱。疟疾感染后小鼠血清可溶性CD36显著升高(p<0.05),影响HIR指数和肝脏TAG。然而,使用文献记载的方法,提取物和氯喹治疗改善了疟疾诱导的血清可溶性CD36和肝甘油三酯水平。结果表明,感染伯氏疟原虫的小鼠肝脏中CD36(5.40±0.70pg/ml)和甘油三酯(259.00±7.21mg/dl)水平显著高于对照组(CD36 = 3.47±0.46pg/ml,肝脏中TAG = 161.00±10.00,HIR指数= 0.68±0.18),在5%概率水平上异常降低(p<0.05)肝脏胰岛素抵抗指数(0.37±0.05)。然而,作为药物起始材料的管理(Sofowora, 1993)。植物为新药研究提供了另一种策略。很可能植物将继续成为新分子的宝贵来源,这些新分子可能在可能的化学操作后提供新的和改进的药物(Shan等人,2006)。其中一种植物是毛莨。大戟属(Phyllanthus amarus)属于大戟科(大戟科),大戟属是其中最大的属。它有大约800种,分布在世界热带和亚热带国家(Mazumder et al., 2005)。在叶提取物中鉴定出的植物化学物质包括生物碱、类黄酮、单宁、皂苷、蒽醌和苷类(Onyesom et al., 2015)。已观察到斑蝶的抗疟活性(Onyesom和Adu, 2015)。疟疾是由疟原虫属真核原生生物引起的一种蚊媒人类传染病。它广泛分布于世界的热带和亚热带地区,包括撒哈拉以南非洲的大部分地区。在尼日利亚,疟疾主要由恶性疟原虫引起。与HIR指数和肝TAG的关联方式与对照趋势相似。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Changes in CD and Correlation with Hepatic Insulin Resistance Index and Triacylglycerol 36 Level in Liver of Malarial Infected Mice Treated with Phyllanthus amarus
Phyllanthus amarus is an herb for the treatment of various ailments including malaria. Its antiplasmodial properties and antioxidant capacity have been reported, but very little is known about its effect on CD36 in relation to hepatic insulin resistance and triacylglycerol level. Hence, this study was undertaken to evaluate the changes in soluble CD36 concentrations and correlation with hepatic insulin resistance index and triacylglycerol levels in liver of Plasmodium berghei malarial parasite infected mice treated with graded doses of Phyllanthus amarus ethanolic leaf extract. Thirty (30) adult Swiss albino mice of both sexes weighing between 20-30g were assigned into six (6) groups (n=5/grp). Crude ethanolic leaf extract of Phyllanthus amarus was administered at 150, 300 and 450mg/kg/d as single daily dose for 7 days. On the 8th day of study, the mice were sacrificed under chloroform anaesthesia after an overnight fast. Blood sample was collected by cardiac puncture and centrifuged to obtain serum which was used for the assay of serum CD36, glucose and insulin, while, liver of each mouse was excised and processed for the assay of varying doses (150, 300 and 450mg/kg/d) of Phyllanthus amarus crude ethanolic leaf extract to experimental mice infected with P. berghei malarial parasite for seven days maintained serum soluble CD36 (3.40±0.52pg/ml, 3.47±0.46pg/ml and 3.37±0.46pg/ml), hepatic insulin resistance index (0.85±0.10, 0.77±0.17 and 0.82±0.13) and liver triacylglycerol (134.33±15.95mg/dl, 174.00±11.27mg/dl and 163.67±11.02mg/dl) levels, respectively, in trends that compared well with the Control and chloroquine – treated data ( C D 3 6 = 3.03±0.12pg/ml, liver TAG = 139.33±12.01, HIR index = 0.64±0.07). Correlation of CD36 with liver triacylglycerol for the malarial infected group without treatment was strongly positive, while, that with hepatic insulin resistance index was strongly negative. The control and chloroquine treated groups produced similar correlation pattern, but those for the extract-treated were weaker. Malarial infection in experimental mice significantly (p<0.05) increased serum soluble CD36 and this impacted HIR index and liver TAG. However, extract and chloroquine treatments ameliorated the malaria-induced level of serum soluble CD36 and hepatic triacylglycerol, using documented methods. Results indicate that infection of mice with Plasmodium berghei malarial parasite yielded significant increase in level of CD36 (5.40±0.70pg/ml) and liver triacylglycerol, TAG (259.00±7.21mg/dl), but abnormal reduced (p<0.05) hepatic insulin resistance, HIR index (0.37±0.05) when compared with the control mice (CD36 = 3.47±0.46pg/ml, liver TAG = 161.00±10.00, HIR index = 0.68±0.18) at the 5% probability level. However, administration of as starting materials for drugs (Sofowora, 1993). Plants have provided an alternative strategy in research for new drugs. It is likely that plants will continue to be a valuable source of new molecules which may after possible chemical manipulations provide new and improved drugs (Shan et al., 2006). One of such plants is Phyllanthus amarus.Phyllanthus amarus belongs to the family Euphorbiaceae (the spurge family) from which the largest genus is the Euphorbia. It has about eight hundred (800) species which are found in tropical and subtropical countries of the world (Mazumder et al., 2005). Phytochemicals identified in the leaf extract include alkaloids, flavonoids, tannins, saponins, anthraquinone and glycosides (Onyesom et al., 2015). The antimalarial activity of P. amarus has been observed (Onyesom and Adu, 2015). Malaria is a mosquito borne infectious disease of humans caused by eukaryotic protists of the genus Plasmodium. It is widespread in tropical and subtropical regions of the world including much of the sub-Saharan Africa. In Nigeria, malaria is mostly caused by Plasmodium falciparum. The association with HIR index and liver TAG in manners that were similar to the control trend.
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