Xie Di, Wang Bingcong, Zhang Yanrong, Gao Yinlu
College of Food Science and Engineering Jilin Agricultural University Changchun China.
College of Chemistry Baicheng Normal University Baicheng China.
Food Sci Nutr. 2025 Sep 3;13(9):e70847. doi: 10.1002/fsn3.70847. eCollection 2025 Sep.
As a dual-purpose medicinal and edible resource, Perilla seeds are rich in bioactive compounds. There are very few studies on the by-product of perilla seed hells. Moreover, there is a lack of systematic research on the chemical composition and biological activity of perilla seed hell polyphenols. We employed ultrasound-assisted extraction (60% ethanol, 410 W power, 30 min, liquid-solid ratio 30:1 mL/g) to obtain polyphenols from PSH, yielding perilla seed hulls polyphenol crude extraction (PSH-C), and further verified the presence of polyphenolic compounds using Fourier transform infrared spectroscopy (FT-IR). Subsequently, PSH-C was further separated and purified using HPD600 macroporous resin to obtain a purified perilla seed hulls polyphenol extract (PSH-P). The polyphenolic composition of PSH-P was characterized by UPLC-MS/MS, and the major polyphenols were quantitatively analyzed using authentic standards. Antioxidant assays demonstrated that PSH-P could effectively scavenge free radicals. PSH-P significantly inhibited nitric oxide (NO) production, suppressed the production of inflammatory factors, and downregulated the transcription of iNOS and COX-2. PSH-P likely exerts anti-inflammatory effects by suppressing LPS-induced nuclear translocation of NF-κB (p65) and inhibiting the expression of P-p65 and P-IκBα, thereby blocking NF-κB signaling pathway activation. PSH-P likely exerts its anti-inflammatory effects by blocking NF-κB pathway activation through suppression of LPS-induced nuclear translocation of p65 and inhibition of P-p65 and P-IκBα expression.
紫苏籽作为一种药食两用资源,富含生物活性化合物。关于紫苏籽壳副产物的研究非常少。此外,对紫苏籽壳多酚的化学成分和生物活性缺乏系统研究。我们采用超声辅助提取法(60%乙醇,功率410W,30分钟,液固比30:1mL/g)从紫苏籽壳中获得多酚,得到紫苏籽壳多酚粗提物(PSH-C),并使用傅里叶变换红外光谱(FT-IR)进一步验证了多酚类化合物的存在。随后,使用HPD600大孔树脂对PSH-C进行进一步分离纯化,得到纯化的紫苏籽壳多酚提取物(PSH-P)。通过超高效液相色谱-串联质谱(UPLC-MS/MS)对PSH-P的多酚成分进行表征,并使用标准品对主要多酚进行定量分析。抗氧化试验表明,PSH-P能有效清除自由基。PSH-P显著抑制一氧化氮(NO)的产生,抑制炎症因子的产生,并下调诱导型一氧化氮合酶(iNOS)和环氧化酶-2(COX-2)的转录。PSH-P可能通过抑制脂多糖(LPS)诱导的核因子κB(NF-κB,p65)核转位以及抑制磷酸化p65(P-p65)和磷酸化IκBα(P-IκBα)的表达,从而阻断NF-κB信号通路激活来发挥抗炎作用。PSH-P可能通过抑制LPS诱导的p65核转位以及抑制P-p65和P-IκBα表达来阻断NF-κB通路激活,从而发挥其抗炎作用。