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Neuroprotective effect of hydroxysafflor yellow A on 6-hydroxydopamine-induced Parkinson's disease in rats

机译:羟基红花黄色素A对6-羟基多巴胺诱发的帕金森氏病的神经保护作用

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摘要

Parkinson's disease (PD) is a progressive neurodegenerative disorder affecting predominantly the dopaminergic mesotelencephalic system. Enormous progress has been made in the treatment of PD. Our previous study has shown that hydroxysafflor yellow A (HSYA) could attenuate the neurotoxicity induced by l-methyi-4-phenyl-l,2,3,6-tetrahydropyridine in mice. In the present work, we examined whether HSYA had the neuroprotective effect on dopaminergic neurons of substantia nigra in a rat model of PD. Adult Sprague-Dawley rats were unilaterally injected with 6-hydroxydopamine (6-OHDA) into the medial forebrain bundle. The PD rats were treated with HSYA (2 or 8 mg/kg) via caudal vein injection daily for 4 weeks. Rotational tests showed that HSYA significantly attenuated apomorphine-induced turns in 6-OHDA-induced PD rats. HSYA treatment resulted in a significant protection against the loss of tyrosine hydroxylase-positive cells. Our data showed that HSYA also increased the levels of dopamine and its metabolites, glial cell line-derived neurotrophic factor and brain-derived neurotrophic factor in striatum of PD rats. In conclusion, these results supported a role for HSYA in preserving dopamine neuron integrity and motor function in a rodent model of PD, and implied a potential neuroprotective role for HSYA in this disease.
机译:帕金森氏病(PD)是一种进行性神经退行性疾病,主要影响多巴胺能中脑脑系统。 PD的治疗已取得巨大进展。我们以前的研究表明,羟基红花黄A(HSYA)可以减轻小鼠体内1-甲基-4-苯基-1,2,3,6-四氢吡啶诱导的神经毒性。在目前的工作中,我们检查了HSYA是否对PD大鼠模型的黑质多巴胺能神经元具有神经保护作用。成年Sprague-Dawley大鼠单侧注射6-羟基多巴胺(6-OHDA)到内侧前脑束中。每天通过尾静脉注射用HSYA(2或8 mg / kg)治疗PD大鼠,持续4周。旋转测试表明,HSYA显着减弱了6-OHDA诱导的PD大鼠中由阿扑吗啡引起的转弯。 HSYA处理可有效防止酪氨酸羟化酶阳性细胞的丢失。我们的数据表明,HSYA还增加了PD大鼠纹状体中多巴胺及其代谢物,神经胶质细胞系神经营养因子和脑源性神经营养因子的水平。总之,这些结果支持HSYA在PD啮齿动物模型中在维持多巴胺神经元完整性和运动功能中的作用,并暗示HSYA在该疾病中具有潜在的神经保护作用。

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