Oxidative Stress Cluster, Department of Biochemistry, Faculty of Medicine, Chiang Mai University, Chiang Mai, Thailand.
Department of Family Medicine, Faculty of Medicine, Chiang Mai University, Chiang Mai, Thailand.
Biosci Rep. 2021 Jan 29;41(1). doi: 10.1042/BSR20203166.
Perilla frutescens fruit oil (PFO) is rich in α-linolenic acid (ALA) and exhibits biological activities. We aimed to investigate analgesic, anti-inflammatory and anti-ulcer activities of PFO and PFO-supplemented soybean milk (PFO-SM) in animal models. Analgesic activity was assessed in acetic acid-induced writhing in mice, while anti-inflammatory activity was performed in ethyl phenylpropiolate (EPP)-induced ear edema and carrageenan-induced hind paw edema in rats. Anti-ulcer effects were conducted in water immersion stress, HCl/ethanol and indomethacin-induced gastric ulcer in rats. Distinctly, PFO, containing 6.96 mg ALA and 2.61 mg LA equivalence/g, did not induce acute toxicity (LD50 > 10 mL/kg) in mice. PFO (2.5 and 5 mL/kg) and PFO-SM (0.05 mL PFO equivalence/kg) inhibited incidences of writhing (16.8, 18.0 and 32.3%, respectively) in acetic acid-induced mice. In addition, topical applications of PFO (0.1 and 1 mL/ear) significantly inhibited EPP-induced ear edema (59.3 and 65.7%, respectively) in rats, while PFO-SM slightly inhibited ear edema (25.9%). However, PFO and PFO-SM did not inhibit carrageenan-induced hind paw edema in rats. Indeed, PFO (2.5 and 5 mL/kg) significantly inhibited gastric ulcers in rats that induced by water immersion stress (92.4 and 96.6%, respectively), HCl/ethanol (74.8 and 73.3%, respectively) and indomethacin (68.8 and 88.9%, respectively), while PFO-SM did not. PFO displayed potent analgesic, anti-inflammatory and anti-ulcer properties, while PFO-SM exerted only analgesic properties. Thus, Thai PFO and its functional drink offer potential benefits in treatment of analgesic, inflammatory diseases and gastric ulcer.
荏油(PF0)富含α-亚麻酸(ALA),具有生物活性。本研究旨在动物模型中探究 PF0 及其添加到豆浆中的制品(PF0-豆浆)的镇痛、抗炎和抗溃疡活性。在醋酸诱导的小鼠扭体实验中评估镇痛活性,在大鼠的 1-乙基-2-苯基-1-庚烯-3-酮(EPP)诱导的耳肿胀和角叉菜胶诱导的后足肿胀实验中评估抗炎活性,在大鼠水浸应激、盐酸/乙醇和吲哚美辛诱导的胃溃疡实验中评估抗溃疡活性。结果表明,PF0(含 6.96mg ALA 和 2.61mg LA 当量/g)对小鼠无急性毒性(LD50>10mL/kg)。PF0(2.5 和 5mL/kg)和 PF0-豆浆(0.05mL PF0 当量/kg)抑制了醋酸诱导的小鼠扭体反应(分别为 16.8%、18.0%和 32.3%)。此外,PF0(0.1 和 1mL/耳)显著抑制了 EPP 诱导的大鼠耳肿胀(分别为 59.3%和 65.7%),而 PF0-豆浆轻度抑制了耳肿胀(25.9%)。然而,PF0 和 PF0-豆浆对大鼠角叉菜胶诱导的后足肿胀无抑制作用。PF0(2.5 和 5mL/kg)显著抑制了水浸应激诱导的大鼠胃溃疡(分别为 92.4%和 96.6%)、盐酸/乙醇诱导的大鼠胃溃疡(分别为 74.8%和 73.3%)和吲哚美辛诱导的大鼠胃溃疡(分别为 68.8%和 88.9%),而 PF0-豆浆无作用。PF0 表现出较强的镇痛、抗炎和抗溃疡作用,而 PF0-豆浆仅具有镇痛作用。因此,泰国 PF0 及其功能性饮料可能具有治疗镇痛、炎症性疾病和胃溃疡的潜力。