猕猴桃果实水提取物对 Wistar 大鼠口服安全性的评估

Adedoyin T. Agbabiaka, Adejuwon Adewale Adeneye, Joseph A. Olagunju, Ikechukwu I. Okoye
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引用次数: 0

摘要

Annona muricata 果实(即Soursoup 或 custard apple,一种以其可食用果实而闻名的热带植物物种)具有多种药用功效(包括抗菌、消炎、抗原生动物、抗氧化、抗焦虑、抗应激、抗溃疡、伤口愈合、保肝、抗黄疸、保肝、抗癌和抗高血糖活性)以及一些毒理学作用(神经毒性和神经变性)。尽管它在人类健康中有着广泛的应用,但有关其口服安全性的科学信息仍然很少。在本研究中,采用标准急性和 42 天亚慢性口服毒性测试指南,对年轻成年雄性和雌性白化 Wistar 大鼠的人体测量、生化、血液学和组织病理学终点进行了口服 100 毫克/千克/天、200 毫克/千克/天和 400 毫克/千克/天 Annona Muricata(AFAM)果实水提取物的安全性评估。此外,还采用标准程序对 AFAM 进行了初步定性和定量分析。研究结果表明,尽管在测试中出现了短暂但可逆的行为毒性,但经计算,AFAM 急性口服毒性研究的半数致死剂量估计值大于 5 克/千克体重/口服途径。在亚慢性口服毒性测试中,氨基甲酸乙酯处理导致体重大幅增加,血清甘油三酯和极低密度脂蛋白胆固醇以及肝酶下降。同样,长期口服 AFAM 会导致中性粒细胞和血小板计数分别显著下降和上升,而 AFAM 处理的肝脏和肾脏分别出现肝脂肪变性和肾小管塌陷的组织病理学特征,这表明肝内脂质生物合成可能增加,肾毒性也可能增加。AFAM 的初步植物化学分析显示了黄酮类、生物碱、鞣质、苷类、皂苷和还原糖的存在和相对含量,气相色谱-质谱分析则显示了 13 种化合物的相对含量。对提取物进行的综合分析表明,其中含有碳水化合物(64.65%)、蛋白质(2.14%)、水分(8.07%)、灰分(6.73%)、脂质(14.22%)和纤维(4.19%)。总之,研究表明,长期口服 AFAM 可能会因肝内甘油三酯的新生物合成、肾毒性和血液毒性而导致脂肪肝。总之,这项研究的结果表明,长期服用 AFAM 可能会带来严重的健康问题,因此应十分谨慎。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Oral Safety Evaluation of the Aqueous Fruit Extract of Annona Muricata in Wistar Rats
Annona muricata fruit (i.e. Soursoup or custard apple a tropical plant species known for its edible fruit)has been attributed with numerous medicinal benefits (including antimicrobial, anti-inflammatory, anti-protozoan, antioxidant, anxiolytic, anti-stress, anti-ulcerogenic, wound healing, hepato-protective, anti-icteric, hepatoprotective, anticancer and antihyperglycemic activities) as well as some toxicological effects (neurotoxicity and neurodegeneration). Despite its ancestral use and wide applications in human health, scientific information on its oral safety remains scanty. In this study, the oral safety of 100 mg/kd/day, 200 mg/kg/day and 400 mg/kg/day of the aqueous fruit extract of Annona Muricata (AFAM) was evaluated in young adult, male and female white albino Wistar rats using standard acute and 42-days sub-chronic oral toxicity testing guidelines on anthropometric, biochemical, hematological and histo-pathological endpoints. In addition, preliminary qualitative and quantitative analyses of AFAM were undertaken using standard procedures. Results of the study showed that the estimated LD50 value for the acute oral toxicity study of AFAM calculated to be greater than 5 g/kg body weight/oral route although the testing was associated with transient but reversible behavioral toxicities. For its sub-chronic oral toxicity testing, AFAM treatment resulted in profound %weight gain, decreases in the serum triglycerides and very low density lipoprotein cholesterol and liver enzymes. Similarly, prolonged oral AFAM treatments caused significant decrease and increase in the differential neutrophils and platelet counts, respectively while the hist-opathological features of hepatic steatos is and renal tubule collapse in the AFAM-treated livers and kidneys, respectively suggested possible increased intrahepatic lipids biosynthesis and nephrotoxicity. The preliminary phytochemical analyses of AFAM showed the presence and relative amount of flavonoids, alkaloids, tannin, glycosides, saponin, and reducing sugars while the Gas Chromatography-Mass spectroscopy showed the relative abundance of thirteen compounds. Composite analyses conducted on the extract showed the presence of carbohydrate (64.65%), protein (2.14%), moisture content (8.07%), ash value (6.73%), lipid (14.22%) and fiber (4.19%). Overall, the study suggested that the prolonged AFAM oral treatments could predispose to the development of fatty liver disease from de novo intrahepatic biosynthesis of triglycerides, nephrotoxicity and hematotoxicity. In conclusion, the results of this study showed that prolonged consumption of AFAM should be with a great caution as it could pose serious health concerns.
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