分子生物学
IVD分子诊断
细胞培养与分析
蛋白研究
细胞因子
重组蛋白
抗体
高通量测序建库
病原检测UCF系列
生物医药
工具酶
抑制剂激活剂与常用试剂
仪器
耗材

A proteoglycan isolated from Ganoderma lucidum attenuates diabetic kidney disease by inhibiting oxidative stress-induced renal fibrosis both in vitro and in vivo

Yanna Pan, Ying Zhang, Jiaqi Li, Zeng Zhang, Yanming He, Qingjie Zhao, Hongjie Yang, Ping Zhou

Journal:JOURNAL OF ETHNOPHARMACOLOGY

IF:5.4

DOI:10.1016/j.jep.2023.116405

PMID:36966849

Published:2023-03-24

research field:分子生物学药理学细胞生物学结构生物学糖尿病民族药理学肾病学生物化学

Abstract

Ethnopharmacological relevance Ganoderma lucidum ( G. lucidum ) was regarded as “miraculous herb” by the Chinese and recorded detailly in the “Shen Nong Ben Cao Jing” as a tonic to improve health and prolong life. A proteoglycan (namely, FYGL ) was extracted from Ganoderma lucidum , which was a water-soluble hyperbranched proteoglycan, and was found to be able to protect pancreatic tissue against oxidative stress damage. Aim of the study Diabetic kidney disease (DKD) is a complication of diabetes, but the effective treatment is still lack. Chronic hyperglycemia in diabetic patients induce the accumulation of ROS , which injure the renal tissue and lead to the renal dysfunction. In this work, the efficacy and target mechanics of FYGL on diabetic renal function were investigated. Materials and methods In the present study, the mechanism of the reno-protection of FYGL was analyzed on diabetic db/db mice and rat glomerular mesangial cells (HBZY-1) induced by high glucose (HG) with palmitate (PA) (HG/PA). In vitro , the levels of reactive oxygen species (ROS), malondialdehyde (MDA) and superoxide dismutase (SOD) were evaluated by commercial kits. the expressions of NOX1 and NOX4, phosphorylation of MAPK and NF-κB, and pro-fibrotic proteins were measured by Western blot . In vivo , diabetic db/db mice were gavaged with FYGL for 8 weeks, body weight and fasting blood glucose (FBG) were tested weekly. On 8th week, the serum, urine and renal tissue were collected for glucose tolerance test (OGTT), redox indicator (SOD, CAT , GSH and MDA), lipid metabolism (TC, TG , LDL and HDL), blood urea nitrogen (BUN), serum creatinine (Scr), uric acid (UA), 8-oxo-deoxyguanosine (8-OHdG), and the changes of histopathology and expression of collagen IV and AGEs . Results The results in vitro showed that FYGL significantly inhibited the HG/PA-induced HBZY-1  cells proliferation , ROS generation, MDA production, promoted SOD activity, and suppressed

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