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补肾活血方对帕金森病大鼠脑内孤儿受体和酪氨酸羟化酶的影响。

Effect of Bushen Huoxue Decoction on the orphan receptor and tyrosine hydroxylase in the brain of rats with Parkinson's disease.

机构信息

Institute of Traditional Chinese Medicine, General Hospital of PLA, Beijing 100853, China.

出版信息

Chin J Integr Med. 2011 Jan;17(1):43-7. doi: 10.1007/s11655-011-0618-1. Epub 2011 Jan 22.

Abstract

OBJECTIVE

To explore the effect of Bushen Huoxue Decoction (BHD) on the orphan receptor (Nurr1) and tyrosine hydroxylase (TH) in the brain of rats with Parkinson's disease (PD).

METHODS

One hundred and twenty SD rats were divided into 100 in the model group and 20 in the normal control group, fifty-eight SD rats from the model group, established into PD model successfully by injuring their substantia nigra (SSN) with 6-hydroxydopamine, were divided equally into the model group and the test group, and they were treated with saline and BHD, respectively, for eight successive weeks. The change in the rats' behavior before and after treatment was observed by counting the cycles of rotation induced by apomorphine injection; the pathology of neurons, level of Nurr1 mRNA expression, and amount of TH positive cells in SSN were observed after treatment.

RESULTS

The rats' behavior was improved in the tested group significantly, the rotation cycle after treatment being 84.0 ± 20.0 cycles/40 min, which was significantly lower than that in the model group (377.0 ± 62.3 cycles/40 min, P<0.01). Besides, the Nurr1 mRNA expression and TH positive cell in the test group were 0.97 ± 0.15 and 49.40 ± 14.72, respectively, which were significantly higher than those in the model group, 0.22 ± 0.03 and 5.45 ± 2.58, respectively (all P<0.01).

CONCLUSION

BHD could treat PD by enhancing the Nurr1 mRNA expression, increasing the TH content in brain, and promoting the repairing of injured neuron in cerebral SSN.

摘要

目的

探讨补肾活血方对帕金森病(PD)模型大鼠脑内孤儿受体(Nurr1)和酪氨酸羟化酶(TH)的影响。

方法

将 120 只 SD 大鼠分为正常对照组 20 只和模型组 100 只,成功损毁模型组大鼠黑质(SSN)中的 6-羟多巴胺,将其中 58 只大鼠分为模型组和试验组,分别给予生理盐水和补肾活血方,连续 8 周。通过注射阿扑吗啡后计算大鼠旋转的圈数,观察治疗前后大鼠行为的变化;治疗后观察神经元病理、Nurr1mRNA 表达水平和 SSN 中 TH 阳性细胞数量的变化。

结果

试验组大鼠行为明显改善,治疗后旋转周期为 84.0±20.0 圈/40min,明显低于模型组(377.0±62.3 圈/40min,P<0.01)。此外,试验组 Nurr1mRNA 表达和 TH 阳性细胞分别为 0.97±0.15 和 49.40±14.72,明显高于模型组的 0.22±0.03 和 5.45±2.58(均 P<0.01)。

结论

补肾活血方通过增强 Nurr1mRNA 表达,增加脑内 TH 含量,促进 SSN 损伤神经元修复,从而治疗 PD。

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