College of Pharmacy, Sunchon National University, 255 Jungangno, Suncheon 540-950, Korea.
Singapore Bioimaging Consortium, Agency for Science, Technology and Research, 11 Biopolis Way, No. 02-02 Helios, Singapore 138667, Singapore.
Molecules. 2017 Nov 21;22(11):2019. doi: 10.3390/molecules22112019.
Although astaxanthin has a variety of biological activities such as anti-oxidant effects, inhibitory effects on skin deterioration and anti-inflammatory effects, its effect on asthma has not been studied. In this paper, the inhibitory effect of astaxanthin on airway inflammation in a mouse model of ovalbumin (OVA)-induced asthma was investigated. We evaluated the number of total cells, Th1/2 mediated inflammatory cytokines in bronchoalveolar lavage fluid (BALF) and airway hyperresponsiveness as well as histological structure. The level of total IgE, IgG1, IgG2a, OVA-specific IgG1, and OVA-specific IgG2a were also examined. The oral administration of 50 mg/mL astaxanthin inhibited the respiratory system resistance, elastance, newtonian resistance, tissue damping, and tissue elastance. Also, astaxanthin suppressed the total cell number, IL-4, and IL-5, and increased the IFN-γ in the BALF. In the sera, total IgE, IgG1, and OVA-specific IgG1 were reduced by astaxanthin exposure and IgG2a and OVA-specific IgG2a were enhanced via oral administration of astaxanthin. Infiltration of inflammatory cells in the lung, production of mucus, lung fibrosis, and expression of caspase-1 or caspase-3 were suppressed in OVA-induced asthmatic animal treated with astaxanthin. These results suggest that astaxanthin may have therapeutic potential for treating asthma via inhibiting Th2-mediated cytokine and enhancing Th1-mediated cytokine.
尽管虾青素具有抗氧化、抑制皮肤恶化和抗炎等多种生物活性,但它对哮喘的作用尚未得到研究。本文研究了虾青素对卵清蛋白(OVA)诱导的哮喘小鼠模型气道炎症的抑制作用。我们评估了支气管肺泡灌洗液(BALF)中总细胞数、Th1/2 介导的炎症细胞因子、气道高反应性以及组织学结构。还检查了总 IgE、IgG1、IgG2a、OVA 特异性 IgG1 和 OVA 特异性 IgG2a 的水平。口服 50mg/mL 虾青素可抑制呼吸系统阻力、弹性、牛顿阻力、组织阻尼和组织弹性。此外,虾青素还抑制 BALF 中的总细胞数、IL-4 和 IL-5,并增加 IFN-γ。在血清中,总 IgE、IgG1 和 OVA 特异性 IgG1 被虾青素暴露降低,而 IgG2a 和 OVA 特异性 IgG2a 通过口服虾青素增强。虾青素处理的 OVA 诱导的哮喘动物的肺部炎症细胞浸润、黏液产生、肺纤维化和半胱氨酸蛋白酶-1 或半胱氨酸蛋白酶-3 的表达均受到抑制。这些结果表明,虾青素通过抑制 Th2 介导的细胞因子和增强 Th1 介导的细胞因子,可能具有治疗哮喘的潜力。