A Study on Antioxidant and Anti-inflammatory of Salvia microphylla Ethanol Extract

Guen Won Choi, Hyeon Mi Jo, In Ho Choi
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Abstract

Purpose: This study was aimed at investigating the anti-inflammatory and antioxidant properties of Salvia microphylla (SM) extract (SME).Methods: Powdered SM was treated with ethanol and decocted to acquire SME. The antioxidant activities of SME were assessed by evaluating its total polyphenolic, and flavonoid , contents and performing 2,2-diphenyl-1-picryl-hydrazyl-hydrate (DPPH) and 2,2′-azino-bis(3-ethylbenzothiazoline-6-sulfonic acid) (ABTS) radical scavenging assays. The anti-inflammatory activities of SME were verified by examining the inhibition of nitric oxide (NO) production, and inducible nitric oxide synthase (iNOS) expression in lipopolysaccharide (LPS) activated RAW 264.7 macrophages.Results: The total polyphenol and flavonoid contents in SME were 102.26±0.39 mg GAE/g and 377.42±0.77 mg QUE/g, respectively. The DPPH and ABTS assays revealed the antioxidant activities of SME by exhibiting their ability to scavenge radicals in a concentration-dependent manner (50-1000 μg/mL). The cell viability of SME exceeded 99% at 50-1000 μg/mL. The concentration-dependent reduction in the expression of the inflammation mediator iNOS and subsequent NO production indicated an approximately 100% inhibition efficacy at 600 μg/mL (0.00±1.34%). These results confirmed the potential of SME as a component of cosmeceuticals.Conclusion: Based on the findings of this study, SME is explicitly acknowledged for its applicability as a natural preservative possessing antioxidant and anti-inflammatory activities as well as a raw material for cosmeceuticals intended to alleviate skin irritation.
小叶鼠尾草乙醇提取物抗氧化和抗炎作用的研究
目的:研究小叶鼠尾草(Salvia microphylla, SM)提取物(SME)的抗炎抗氧化作用。方法:用乙醇对SM粉末进行煎煮,获得SME。通过测定其总多酚和类黄酮含量,以及2,2-二苯基-1-吡啶-水合肼(DPPH)和2,2 ' -氮基-双(3-乙基苯并噻唑-6-磺酸)(ABTS)自由基清除试验来评估其抗氧化活性。通过对脂多糖(LPS)激活的RAW 264.7巨噬细胞中一氧化氮(NO)生成和诱导型一氧化氮合酶(iNOS)表达的抑制,验证了SME的抗炎活性。结果:丹参总多酚含量为102.26±0.39 mg GAE/g,总黄酮含量为377.42±0.77 mg QUE/g。DPPH和ABTS实验显示,SME具有浓度依赖性的自由基清除能力(50 ~ 1000 μg/mL),显示了其抗氧化活性。在50 ~ 1000 μg/mL浓度下,SME细胞存活率超过99%。在600 μg/mL(0.00±1.34%)浓度下,炎症介质iNOS表达和随后NO生成的浓度依赖性降低表明其抑制效果约为100%。这些结果证实了SME作为药妆成分的潜力。结论:根据本研究结果,明确承认SME作为具有抗氧化和抗炎活性的天然防腐剂,以及用于减轻皮肤刺激的药妆原料的适用性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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