Gastrodin alleviates Tourette syndrome via Nrf-2/HO-1/HMGB1/NF-kB pathway
Gastrodin alleviates Tourette syndrome via Nrf-2/HO-1/HMGB1/NF-kB pathway
复制标题
天麻素通过 Nrf-2/HO-1/HMGB1/NF-kB 通路缓解抽动秽语综合征
DOI:
10.1002/jbt.22389
复制
发表时间:
2019-08-30
影响因子:
3.6
通讯作者:
Huang, Yaruo
中科院分区:
文献类型:
--
作者:
Long, Hongyan;Ruan, Jie;Huang, Yaruo
The aim is to study the effects of gastrodin (GA) on striatal inflammation and oxidative stress in rats with Tourette syndrome (TS). The rat model of TS was induced by 3,3 '-iminodipropionitrile. Behavioral tests were carried out by stereotype experiment. The concentrations of amino acid transmitters glutamic acid (Glu) and gamma-aminobutyric acid (GABA) in striatum were determined by high-performance liquid chromatography. Superoxide dismutase (SOD) and malondialdehyde (MDA) in serum and striatum were detected by commercial kits. Cytokines in serum and striatum were detected by enzyme-linked immunosorbent assay kits. Western blot analysis was used to detect striatum nuclear erythroid factor 2-related factor 2 (Nrf-2)/heme oxygenase-1 (HO-1)/high mobility group box 1 protein (HMGB1)/nuclear factor-kB (NF-kB) pathway-related proteins. The expressions of Nrf-2 and P-NF-kBp65 in striatum were detected by immunohistochemistry. Compared with the control group, the stereotype scores of rats in the model group significantly increased, and the contents of Glu and GABA in striatum obviously increased. GA significantly reduced the stereotype scores and decreased the contents of Glu and GABA. The levels of SOD in serum and striatum were decreased and the content of MDA in serum and striatum were increased compared with the control group, while GA significantly restored the changes. GA significantly adjusted Nrf-2/HO-1/HMGB1/NF-kB pathway-related proteins changes consistent with immunohistochemical changes. GA may protect striatum of rats with TS by regulating Nrf-2/HO-1/HMGB1/NF-kB pathway protein changes in striatum.