Kim Gyu Hyun, Paik Sun-Sook, Park Yong Soo, Kim Hyoun Geun, Kim In-Beom
Department of Anatomy, College of Medicine, The Catholic University of Korea, Seoul, South Korea.
Catholic Institute for Applied Anatomy, College of Medicine, The Catholic University of Korea, Seoul, South Korea.
Front Cell Neurosci. 2019 Jul 16;13:319. doi: 10.3389/fncel.2019.00319. eCollection 2019.
Glycyrrhizic acid (GA) is a major component in the root and rhizomes of licorice (), which have been used as an herbal medicine, because of its anti-inflammatory activity. GA is known as an inhibitor of high-mobility group box 1 (HMGB1), which is involved in the pathogenesis of various inflammatory diseases including inner retinal neuropathy. In this study, we examined the effect of GA in a mouse model of retinal degeneration (RD), the leading cause of blindness. RD was induced by exposure to a blue light-emitting diode (LED). In functional assessment, electroretinography showed that the amplitudes of both a- and b-waves were reduced in RD mice, whereas they were significantly increased in GA-treated RD mice ( < 0.05), compared to those in non-treated RD animals. In histological assessment, GA treatment preserved the outer nuclear layer where photoreceptors reside and reduced photoreceptor cell death. GA-treated retinas showed significantly reduced expression of proinflammatory cytokines such as TNF-α, IL-6, IL-1β, CCL2 and 6, iNOS, and COX-2 ( < 0.05), compared to that in non-treated retinas. Immunohistochemistry showed that Iba-1 and GFAP expression was markedly reduced in GA-treated retinas, indicating decreased glial response and inflammation. Interestingly, HMGB1 expression was reduced in non-treated RD retinas whereas GA paradoxically increased its expression. These results demonstrate that GA preserves retinal structure and function by inhibiting inflammation in blue LED-induced RD, suggesting a potential application of GA as a medication for RD. In addition, we propose a potential retinal protective function of HMGB1 in the pathogenesis of RD.
甘草酸(GA)是甘草根及根茎中的主要成分,甘草根及根茎因其抗炎活性而被用作草药。GA是一种已知的高迁移率族蛋白B1(HMGB1)抑制剂,HMGB1参与包括视网膜内层神经病变在内的各种炎症性疾病的发病机制。在本研究中,我们检测了GA对视网膜变性(RD)小鼠模型的影响,RD是失明的主要原因。通过暴露于蓝色发光二极管(LED)诱导RD。在功能评估中,视网膜电图显示RD小鼠的a波和b波振幅均降低,而与未治疗的RD动物相比,GA治疗的RD小鼠的a波和b波振幅显著增加(P<0.05)。在组织学评估中,GA治疗可保留光感受器所在的外核层,并减少光感受器细胞死亡。与未治疗的视网膜相比,GA治疗的视网膜中促炎细胞因子如TNF-α、IL-6、IL-1β、CCL2和6、诱导型一氧化氮合酶(iNOS)和环氧化酶-2(COX-2)的表达显著降低(P<0.05)。免疫组织化学显示,GA治疗的视网膜中Iba-1和胶质纤维酸性蛋白(GFAP)表达明显降低,表明神经胶质反应和炎症减少。有趣的是,未治疗的RD视网膜中HMGB1表达降低,而GA却反常地增加了其表达。这些结果表明,GA通过抑制蓝光LED诱导的RD中的炎症来保留视网膜结构和功能,提示GA作为RD药物的潜在应用。此外,我们提出HMGB1在RD发病机制中具有潜在的视网膜保护功能。