中草药水果饮料对雌性Wistar大鼠的体内外营养及安全性评价

Siti Noorwanie Abdul Hamid, N. Zakaria, F. A. Abdul Majid, A. F. I. Awang, S. N. Zainol, Ain Nabihah Zainudin, Siti Nur Hidayah Muhamad
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引用次数: 0

摘要

简介:本研究旨在评估ALLURATM与女性健康和皮肤美容相关的安全性和营养保健特性。材料与方法:采用比色法测定总酚(TPC)和类黄酮(TFC)含量,采用高效液相色谱法测定没食子酸的含量。采用2,2 -二苯基-2-吡啶肼(DPPH)和2,2 ' -氮基-双(3-乙基苯并噻唑-6-磺酸(ABTS)自由基法测定其抗氧化活性,采用酶联免疫吸附法(ELISA)测定其抗炎活性。分别用猪弹性酶和蘑菇酪氨酸酶活性测定其抗衰老和美白效果。用体外划痕法评价皮肤细胞的生长促进和年轻化。采用HSF1184和3T3 BALB/c细胞株进行细胞毒性试验。对照组和治疗组各6只Wistar大鼠进行急性毒性试验。根据近似分析对其营养特性进行了评价。结果:ALLURATM dph - ic50值为180.40µg/mL, ABTS-IC50值为174.40µg/mL。TPC为67.31 mg GAE/g提取物,TFC为43.21 mg CE/g提取物,没食子酸为10.98 mg/g。ALLURATM降低促炎因子TNF-α和IL-6,具有抗衰老作用(IC50 ~ 162.40µg/mL)和美白作用(IC50 ~ 167.70µg/mL)。ALLURA™还增加了HSF1184的增殖(≤1000µg/ mL),产生显著的表皮生长因子(EGF)分泌,并显示无细胞毒性。最高剂量2000 mg/kg b.w.t.未见大鼠死亡,也未见行为学和形态学改变。近似分析的结果是水分含量高,热量低。结论:这些发现首次提供了ALLURA™抗炎、抗氧化和营养保健功能的初步报告。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
In vitro and In vivo Assessments on Nutraceutical and Safety of Herb-Fruit Based Drink on Female Wistar Rats
INTRODUCTION: The study aimed to assess the safety and nutraceutical properties of ALLURATM related to women’s health and skin beautification. MATERIALS AND METHODS: Determinations of total phenolic (TPC) and flavonoid contents (TFC) were done using the colorimetric method, followed by the identification of gallic acid via highperformance liquid chromatography (HPLC). Antioxidant activity was analyzed using 2,2 -diphenyl-2-picrylhydrazyl (DPPH) and 2,2’-azino-bis(3-ethylbenzthiazoline-6-sulphonic acid (ABTS) radicals while its anti-inflammatory activity was measured using enzymelinked immunosorbent assay (ELISA). Anti-aging and whitening effects were determined by porcine elastase and mushroom tyrosinase activities, respectively. Skin cell growth promotion and rejuvenation were evaluated using in vitro scratch assay. Cytotoxicity assay was done using HSF1184 and 3T3 BALB/c cell lines. While, acute toxicity test was done on two groups (control and treatment) of six Wistar rats each. The nutraceutical properties were evaluated based on proximate analysis. RESULTS: ALLURATM exhibited DPPH-IC50 values of 180.40 µg/mL and ABTS-IC50 value of 174.40 µg/mL. TPC and TFC were 67.31 mg GAE/g extract and 43.21 mg CE/g extract, respectively while 10.98 mg/g of gallic acid were quantified. ALLURATM reduced pro-inflammatory cytokines of TNF-α and IL-6 and showed anti-aging (IC50-162.40 µg/mL) and whitening effects (IC50- 167.70 µg/mL). ALLURA™ also increased the proliferation of HSF1184 (≤ 1000 µg/ mL), producing significant secretion of epidermal growth factor (EGF) and shown to be non-cytotoxic. No mortality was observed at the highest dose of 2000 mg/kg b.w.t. nor the behavioral and morphological changes in rats. The proximate analysis resulted in high content of moisture and low calories. CONCLUSION: These findings provided preliminary reports for the first time on the functionality of ALLURA™ for its anti-inflammatory, antioxidant, and nutraceutical properties.
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