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不同分区溶剂对华西箬竹叶片提取物化学成分和生物利用度的影响。

Impact of different partitioned solvents on chemical composition and bioavailability of Sasa quelpaertensis Nakai leaf extract.

机构信息

College of Agriculture & Life Sciences, SARI, Jeju National University, Jeju 63243, Republic of Korea.

Department of Veterinary Medicine and Veterinary Medical Research Institute, Jeju National University, Jeju 63243, Republic of Korea.

出版信息

J Food Drug Anal. 2017 Apr;25(2):316-326. doi: 10.1016/j.jfda.2016.08.006. Epub 2016 Nov 2.

Abstract

The leaves of Sasa quelpaertensis Nakai were extracted with 80% ethanol and further partitioned with n-hexane, chloroform, ethyl acetate, n-butanol, and aqueous fractions to evaluate the biological activity through assessment via various in vitro assays, including total phenol content; 1,1-diphenyl-1-picrylhydrazyl (DPPH) and 2,2-azino-bis-(3-ethylbenzothiazothiazoline-6-sulfornic acid (ABTS) radical scavenging; reducing power; α-glucosidase and tyrosinase inhibitory; and alcohol dehydrogenase (ADH) and aldehyde dehydrogenase (ALDH) activity assays. The highest activity was found in the ethyl acetate fraction for all assays and showed stronger DPPH radical scavenging, reducing power, and tyrosinase inhibitory activity than the positive controls (butylated hydroxytoluene, α-tocopherol, and arbutin, respectively). When compared to the ethyl acetate fraction, the n-butanol fraction had lower rates, but it still demonstrated relatively high activity. The activity of the n-hexane fraction was high for DPPH and ABTS radical scavenging activity and contained significant amounts of phenol content, whereas the chloroform fraction possessed the highest reducing power, tyrosinase inhibitory, and ADH and ALDH activity, despite having the lowest phenol content when compared to the other fractions. These findings clearly indicate that S. quelpaertensis Nakai leaves can be a good natural source of antioxidants and tyrosinase inhibitors, as well as ADH and ALDH activity inducers, suggesting that may have potential for treating various diseases and improving human health.

摘要

对刚毛柊叶的叶片用 80%乙醇提取,然后用正己烷、氯仿、乙酸乙酯、正丁醇和水进一步萃取,通过各种体外测定评估生物活性,包括总酚含量;1,1-二苯基-1-苦基肼基(DPPH)和 2,2-连氮-双-(3-乙基苯并噻唑啉-6-磺酸)(ABTS)自由基清除;还原能力;α-葡萄糖苷酶和酪氨酸酶抑制;以及醇脱氢酶(ADH)和醛脱氢酶(ALDH)活性测定。所有测定中,乙酸乙酯部分的活性最高,并且 DPPH 自由基清除、还原能力和酪氨酸酶抑制活性均强于阳性对照物(丁基羟基甲苯、α-生育酚和熊果苷)。与乙酸乙酯部分相比,正丁醇部分的活性较低,但仍表现出相对较高的活性。正己烷部分对 DPPH 和 ABTS 自由基清除活性的活性较高,并且含有大量的酚含量,而氯仿部分具有最高的还原能力、酪氨酸酶抑制以及 ADH 和 ALDH 活性,尽管与其他部分相比,其酚含量最低。这些发现清楚地表明,刚毛柊叶可以作为抗氧化剂和酪氨酸酶抑制剂以及 ADH 和 ALDH 活性诱导剂的良好天然来源,这表明它可能具有治疗各种疾病和改善人类健康的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0eb6/9332518/42d540dcdadb/jfda-25-02-316f1.jpg

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