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松果菊苷对帕金森病亚急性模型小鼠的神经保护作用。

Neuroprotective Effect of Echinacoside in Subacute Mouse Model of Parkinson's Disease.

机构信息

Nanjing University of Chinese Medicine, Nanjing, Jiangsu, China.

Department of Neurology, The Third Affiliated Hospital of Nanjing University of Chinese Medicine, Nanjing, Jiangsu, China.

出版信息

Biomed Res Int. 2019 Jan 30;2019:4379639. doi: 10.1155/2019/4379639. eCollection 2019.

Abstract

OBJECTIVE

To study the protective effect of Echinacoside for 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP) induced dopaminergic (DA) neurons injury in the subacute mouse model of Parkinson's disease (PD) and to explore its mechanism of action.

METHODS

We chose 10 weeks of healthy wild type C57BL/6 male mice, hypodermic MPTP 30 mg/kg/day, five days, to prepare PD subacute mouse model. Behavior indexes of open field test and pole test were applied to examine the function of ECH to PD subacute mice model of PD sample action. The effects of ECH on dopaminergic neurons and astrocyte were examined using Immunohistochemistry including tyrosine hydroxylase (TH) and glial fibrillary acidic protein (GFAP) expression. The total numbers of TH-positive neurons and GFAP-positive cells in the substantia nigra pars compacts (SNpc) and ventral tegmental area (VTA) were obtained stereologically using the optical fractionator method. Enzyme-linked immunosorbent assay (ELISA) method was used to detect the inflammatory cytokines in the serum, including TNF- (Ttumor necrosis factor alpha) and IFN- (interferon gamma). Protein expressions of ionized calcium binding adaptor molecule 1 (IBA-1), TNF-, Cleaved caspase-3, glial derived neurotrophic factor (GDNF), and phosphorylated and total extracellular signal-regulated kinase (p-ERK and ERK) in the anatomical region of substantia nigra (SN) were tested by protein immunoblot method (i.e., Western blotting).

RESULTS

ECH reversed the reduction of total distance in open field test in MPTP-induced PD model mice (P < 0.01), shortened the return time and total time of PD subacute model mice in pole test (P < 0.01, P < 0.05), significantly reversed the reduction of TH positive neurons induced by MPTP (P < 0.05), and reduced the activation of astrocytes (P < 0.05). Meanwhile, ECH significantly inhibited the expression of IBA-1, Cleaved caspase-3, and TNF- in midbrain of MPTP model mice (P < 0.05, P < 0.05, and P < 0.05) and upregulated the expression of GDNF (P < 0.05). And ECH lowered the level of TNF- and IFN- in serum (P < 0.05, P < 0.05).

CONCLUSION

ECH has protective effects on the MPTP subacute model mice, its mechanism may be through inhibiting activation of microglia and astrocytes, reducing inflammatory reaction and promoting the secretion of neurotrophic factors, and eventually resulting in the reduction of the DA neurons apoptosis.

摘要

目的

研究松果菊苷对 1-甲基-4-苯基-1,2,3,6-四氢吡啶(MPTP)诱导的帕金森病(PD)亚急性小鼠模型中多巴胺能(DA)神经元损伤的保护作用,并探讨其作用机制。

方法

选择 10 周龄健康野生型 C57BL/6 雄性小鼠,皮下注射 MPTP 30mg/kg/天,连续 5 天,制备 PD 亚急性小鼠模型。采用旷场试验和棒试验检测行为学指标,观察 ECH 对 PD 亚急性模型小鼠的作用。采用免疫组织化学法检测酪氨酸羟化酶(TH)和胶质纤维酸性蛋白(GFAP)表达,观察 ECH 对多巴胺能神经元和星形胶质细胞的影响。采用光学分割器方法立体学测量黑质致密部(SNpc)和腹侧被盖区(VTA)中 TH 阳性神经元和 GFAP 阳性细胞的总数。采用酶联免疫吸附试验(ELISA)法检测血清中炎症细胞因子肿瘤坏死因子-α(TNF-α)和干扰素-γ(IFN-γ)的含量。采用蛋白质免疫印迹法(Western blotting)检测黑质(SN)解剖区域中离子钙结合衔接蛋白 1(IBA-1)、TNF-α、Cleaved caspase-3、胶质细胞源性神经营养因子(GDNF)和磷酸化及总细胞外信号调节激酶(p-ERK 和 ERK)的蛋白表达。

结果

ECH 逆转了 MPTP 诱导的 PD 模型小鼠旷场试验中总距离的减少(P<0.01),缩短了 PD 亚急性模型小鼠棒试验的返回时间和总时间(P<0.01,P<0.05),显著逆转了 MPTP 诱导的 TH 阳性神经元减少(P<0.05),并减少了星形胶质细胞的激活(P<0.05)。同时,ECH 显著抑制了 MPTP 模型小鼠中脑 IBA-1、Cleaved caspase-3 和 TNF-α的表达(P<0.05、P<0.05 和 P<0.05),并上调了 GDNF 的表达(P<0.05)。ECH 降低了血清中 TNF-α和 IFN-γ的水平(P<0.05、P<0.05)。

结论

ECH 对 MPTP 亚急性模型小鼠具有保护作用,其机制可能是通过抑制小胶质细胞和星形胶质细胞的激活,减少炎症反应,促进神经营养因子的分泌,最终减少 DA 神经元的凋亡。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d853/6374833/edb9bdcbb2f3/BMRI2019-4379639.001.jpg

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