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首页> 外文期刊>Neurological Research: An Interdisciplinary Quarterly Journal >Neuroprotective effects of bee venom pharmaceutical acupuncture in acute 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine-induced mouse model of Parkinson's disease.
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Neuroprotective effects of bee venom pharmaceutical acupuncture in acute 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine-induced mouse model of Parkinson's disease.

机译:蜂毒药物针刺对急性1-甲基-4-苯基-1,2,3,6-四氢吡啶诱导的帕金森氏病小鼠模型的神经保护作用。

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摘要

OBJECTIVES: We explored the neuroprotective effects of bee venom acupuncture in acute 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine-induced mouse model of Parkinson's disease. METHODS: Male C57BL/6 mice were divided into three groups: saline-injected control group, 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine-injected group and bee venom acupuncture-pretreated plus 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine-injected group. Mice were injected with 0.02 ml bee venom (1 : 2000 w/v) to GB34 (Yangneungcheon) bilaterally once every 3 days for 2 weeks. After 2 weeks' pre-treatment, the mice were injected with 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (20 mg/kg, i.p.) four times in 2 hour intervals. Tyrosine hydroxylase and phospho-Jun immunoreactivities in the substantia nigra and striatum were observed 3 days after 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine injection. RESULTS: Bee venom acupuncture prevented the 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine-induced loss of tyrosine hydroxylase immunoreactivity in the substantia nigra and striatum. Moreover, bee venom acupuncture attenuated 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine-induced phospho-Jun immunoreactivity in the substantia nigra. DISCUSSION: We found that bee venom acupuncture effectively protected dopaminergic neurons against 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine toxicity, possibly through inhibition of Jun activation. Our results suggest that bee venom acupuncture could be a potential preventive agent for Parkinson's disease.
机译:目的:我们探索了蜂毒针刺对急性1-甲基-4-苯基-1,2,3,6-四氢吡啶诱导的帕金森氏病小鼠模型的神经保护作用。方法:将雄性C57BL / 6小鼠分为三组:注射生理盐水的对照组,注射1-甲基-4-苯基-1,2,3,6-四氢吡啶的组和蜂毒针刺加1-甲基苯丙氨酸预处理的组。注入4-苯基-1,2,3,6-四氢吡啶的基团。每三天一次向小鼠双侧向GB34(良陵川)注射0.02 ml蜂毒(1:2000 w / v),共2周。预处理2周后,每隔2小时向小鼠注射1次甲基4-苯基-1,2,3,6-四氢吡啶(20 mg / kg,腹腔注射)。注射1-甲基-4-苯基-1,2,3,6-四氢吡啶3天后观察到黑质和纹状体中酪氨酸羟化酶和磷酸化Jun免疫反应性。结果:蜂毒针刺预防了黑质和纹状体中1-甲基-4-苯基-1,2,3,6-四氢吡啶引起的酪氨酸羟化酶免疫反应性的丧失。此外,蜂毒针刺减弱了黑质中1-甲基-4-苯基-1,2,3,6-四氢吡啶诱导的磷酸化Jun免疫反应性。讨论:我们发现蜂毒针刺可能通过抑制Jun活化有效保护多巴胺能神经元免受1-甲基-4-苯基-1,2,3,6-四氢吡啶毒性。我们的结果表明,蜂毒针刺可能是帕金森氏病的潜在预防剂。

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