The Critical Role of IL-10 in the Anti-neuroinflammatory and Anti-oxidative Effects of Rheum Tanguticum on Activated Microglia
The Critical Role of IL-10 in the Anti-neuroinflammatory and Anti-oxidative Effects of Rheum Tanguticum on Activated Microglia作者机构:Department of Aging Science and PharmacologyFaculty of Dental SciencesKyushu University OBT Research CenterFaculty of Dental SciencesKyushu University Institution of Geriatric Qinghai Provincial Hospital School of Life ScienceBeijing Institute of Technology
出 版 物:《神经药理学报》 (Acta Neuropharmacologica)
年 卷 期:2018年第2期
页 面:26-27页
学科分类:1008[医学-中药学(可授医学、理学学位)] 1006[医学-中西医结合] 100602[医学-中西医结合临床] 10[医学]
主 题:IL The Critical Role of IL-10 in the Anti-neuroinflammatory and Anti-oxidative Effects of Rheum Tanguticum on Activated Microglia NOS TNF
摘 要:Objective:Rheum tanguticum Maxim. ex Balf.(Rt),a traditional Tibetan medicine,is known to exert various bioactivities,including anti-inflammatory and anti-oxidative activities. The present study was conducted to investigate anti-inflammatory and anti-oxidative effects of Rt on activated microglia. Methods:(1)MG6 microglial cell line,primary microglia and mice brain slices culture were stimulated by chromogranin A(CGA),an endogenous microglia activator,to induce proinflammation and oxidation. The anti-inflammatory and anti-oxidative effects of Rt were examined by q-PCR,western blotting and ELISA by checking inflammatory and oxidative molecules,including IL-1β,tumor necrosis factor-α,IL-10 and nitric oxide.(2)Investigation of the involvement of IL-10 in the anti-inflammatory effects of Rt on inflammatory responses of microglia by using neutralizing antibodies against IL-10. Pro-inflammatory molecules expression were checked by q-PCR.(3)Examination of the effects of major components of Rt(aloe-emodin,(+)-cathechin,piceatannol chrisophanol,physcion,β-sitosterol and emodin) on the IL-10 mRNA expression in MG6 cells. Results:(1)The mean mRNA expression levels of TNF-α,IL-1β and i NOS were significantly increased in MG6 cells at 24 h after stimulation with CGA. Rt significantly suppressed the mean mRNA expression levels of TNF-α,IL-1βand i NOS in GGA-stimulated MG6 cells. Furthermore,the production of IL-1β and NO metabolites in the culture medium of MG6 cells were assessed by using ELISA and NO;/NO;assay,respectively. The mean levels of IL-1β and NO;/NO;significantly increased in the culture medium of MG6 cells at 24 h after treatment with CGA. Rt also significantly decreased the mean levels of IL-1β and NO;/NO;in the culture medium of MG6 cells. The mean protein level of IL-1β significantly increased in the organotypic hippocampal slice cultures at 48 h after stimulation with CGA(10 nmol·L;). Rt significantly suppressed the mean protein level of IL-1β in CGA-stimulated o