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红花黄色素对帕金森病大鼠的改善效果及机制研究OACHSSCD

Improvement Effects and Mechanisms of Safflower Yellow Pigment on Parkinson's Disease Rats

中文摘要英文摘要

目的:基于蛋白激酶B(AKT)/糖原合成酶激酶3β(GSK3β)信号通路探究红花黄色素对帕金森病大鼠的干预效果并分析其机制.方法:以脑纹状体注射6-羟基多巴胺的方法构建帕金森病大鼠模型,将64只帕金森病模型大鼠按随机数表法分为:模型组、红花黄色素低、高剂量组、美多芭组.另设假手术组.连续干预4周后,旷场实验和旋转实验检测大鼠运动能力和运动障碍;苏木精-伊红染色观察脑黑质病理学;酶联免疫吸附试验测定血清炎症[白细胞介素-6(IL-6)、IL-18]和脑黑质氧化应激[超氧化物歧化酶(SOD)、丙二醛(MDA)]指标;荧光定量聚合酶链式反应和蛋白印迹法检测脑黑质AKT、GSK3β信使RNA(mRNA)和蛋白水平.结果:与假手术组比较,模型组脑黑质病理损伤严重,爬过的方格数量、脑黑质SOD、AKT、GSK3β mRNA和蛋白水平显著降低,转圈次数、血清IL-6、IL-18、脑黑质MDA水平显著升高(P<0.05);与模型组比较,红花黄色素低、高剂量组脑黑质病理损伤逐渐减轻,爬过的方格数量、脑黑质SOD、AKT、GSK3β mRNA和蛋白水平呈剂量依赖性升高,转圈次数、血清IL-6、IL-18、脑黑质MDA水平呈剂量依赖性降低(P<0.05).结论:红花黄色素能改善帕金森病大鼠运动能力、运动障碍以及脑黑质病理损伤,降低血清炎症和脑黑质氧化应激,激活AKT/GSK3β信号通路可能是其作用机制.

Objective:To investigate the intervention effects of safflower yellow pigment on Parkinson's disease(PD)rats via the protein kinase B(AKT)/glycogen synthase kinase 3β(GSK3β)signaling pathway and to analyze its underlying mechanisms.Methods:A PD rat model was established by injecting 6-hydroxydopamine into the striatum.Sixty-four PD model rats were random-ly assigned using a random number table to a model group,low-and high-dose safflower yellow pigment groups,and a Madopar group,with a separate sham operation group as control.After 4 weeks of continuous intervention,motor ability and motor disorders were assessed by open field and rotation tests.Pathological changes in the substantia nigra were observed using hematoxylin-eosin staining.Serum inflammatory markers[interleukin-6(IL-6),IL-18]and substantia nigra oxidative stress markers[superoxide dis-mutase(SOD),malondialdehyde(MDA)]were measured by enzyme-linked immunosorbent assay.The mRNA and protein levels of AKT and GSK3β in the substantia nigra were detected using quantitative polymerase chain reaction and Western blot.Results:Compared with the sham operation group,the model group showed severe pathological damage in the substantia nigra,significantly decreased number of squares crossed,SOD levels,and AKT and GSK3β mRNA and protein levels,and significantly increased rota-tion counts,serum IL-6,IL-18,and substantia nigra MDA levels(P<0.05).Compared with the model group,safflower yellow pig-ment treatment dose-dependently reduced pathological damage,increased the number of squares crossed,SOD levels,and AKT and GSK3β mRNA and protein levels,and decreased rotation counts,serum IL-6,IL-18,and MDA levels in a dose-dependent manner(P<0.05).Conclusion:Safflower yellow pigment improves motor ability,motor disorders,and substantia nigra pathology in PD rats,reduces serum inflammation and oxidative stress,and its mechanism may involve activation of the AKT/GSK3 β signaling path-way.

娄展;彭涛;刘星亮;靳彦芬;邢存晶;李英敏

河北北方学院附属第一医院神经内科,张家口,075061河北北方学院附属第一医院内镜中心,张家口,075061河北北方学院附属第一医院神经内科,张家口,075061河北北方学院附属第一医院急诊科,张家口,075061河北北方学院附属第一医院神经内科,张家口,075061河北医科大学基础医学院,石家庄,050013

医药卫生

红花黄色素帕金森病大鼠蛋白激酶B糖原合成酶激酶3β病理损伤炎症反应氧化应激

Safflower yellow pigmentParkinson's diseaseRatsProtein kinase BGlycogen synthase kinase 3βPathologyIn-flammationOxidative stress

《世界中医药》 2026 (3)

392-397,6

国家自然科学基金面上项目(81971787)河北省医学科学研究课题计划项目(20230129)张家口市科技计划项目(2421045D).

10.3969/j.issn.1673-7202.2026.03.004

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