Wu Cheng-Rong, Lee Shih-Yu, Chen Chien-Hung, Lin Sheng-Dun
Department of Food Science and Technology, Hungkuang University, Taichung 433304, Taiwan.
College of Nursing, Hungkuang University, Taichung 433304, Taiwan.
Foods. 2023 Feb 2;12(3):636. doi: 10.3390/foods12030636.
Extractions of the underground parts of valerian were prepared with water and ethanol (25-95%) at 25-75 °C. Extraction yields, bioactive compounds, and the 1,1-Diphenyl-2-picrylhydrazyl (DPPH) radical scavenging ability of lyophilized extracts were determined. The inhibitory effects of the extracts, valerenic acid derivatives and phenolic acids, on metabolic syndrome (MS)-related enzymes activities were further examined. Both roots and rhizomes extracted with 95% ethanol at 75 °C had the highest levels of bioactive compounds. The antioxidant capacity and inhibition of MS-related enzymes of the roots extract were better than those of the rhizomes. The roots extract more strongly inhibited pancreatic lipase (inhibition of 50% of enzyme activity (IC), 17.59 mg/mL), angiotensin-converting enzyme (ACE, IC, 3.75 mg/mL), α-amylase (IC, 12.53 mg/mL), and α-glucosidase (IC, 15.40 mg/mL). These four phenolic acids inhibited the activity of MS-related enzymes. Valerenic acid demonstrated more of an inhibitory ability for ACE (IC, 0.225 mg/mL, except for caffeic acid) and α-glucosidase (IC, 0.617 mg/mL) than phenolic acids. Valerian extract inhibited key enzyme activities that were associated with obesity (lipase), hypertension (ACE), and type 2 diabetes (α-amylase and α-glucosidase), suggesting that it is a potential candidate for the development of functional supplements.
缬草地下部分的提取物分别用水和乙醇(25%-95%)在25-75℃下制备。测定了冻干提取物的提取产率、生物活性化合物以及1,1-二苯基-2-苦基肼(DPPH)自由基清除能力。进一步研究了提取物、缬草烯酸衍生物和酚酸对代谢综合征(MS)相关酶活性的抑制作用。75℃下用95%乙醇提取的根和根茎中生物活性化合物含量最高。根提取物的抗氧化能力和对MS相关酶的抑制作用优于根茎提取物。根提取物对胰脂肪酶(酶活性抑制50%(IC)时浓度为17.59mg/mL)、血管紧张素转换酶(ACE,IC为3.75mg/mL)、α-淀粉酶(IC为12.53mg/mL)和α-葡萄糖苷酶(IC为15.40mg/mL)的抑制作用更强。这四种酚酸抑制了MS相关酶的活性。缬草烯酸对ACE(IC为0.225mg/mL,咖啡酸除外)和α-葡萄糖苷酶(IC为0.617mg/mL)的抑制能力比酚酸更强。缬草提取物抑制了与肥胖(脂肪酶)、高血压(ACE)和2型糖尿病(α-淀粉酶和α-葡萄糖苷酶)相关的关键酶活性,表明它是开发功能性补充剂的潜在候选物。