中国神经再生研究(英文版) ›› 2017, Vol. 12 ›› Issue (7): 1137-1144.doi: 10.4103/1673-5374.211194

• 原著:退行性病与再生 • 上一篇    下一篇

槲皮素联合胡椒碱减轻1-甲基-4-苯基-1,2,3,6-四氢吡啶诱导的神经毒性

  

  • 收稿日期:2017-06-05 出版日期:2017-07-15 发布日期:2017-07-15

Neuroprotective potential of Quercetin in combination with piperine against 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine-induced neurotoxicity

Shamsher Singh1, 2, Sumit Jamwal1, 2, Puneet Kumar1   

  1. 1 Department of Pharmacology, I.S.F College of Pharmacy, Ferozepur Road, Moga, Punjab, India; 2 I.K. Gujral Punjab Technical University, Jalandhar, Punjab, India
  • Received:2017-06-05 Online:2017-07-15 Published:2017-07-15
  • Contact: Puneet Kumar, M. Pharm., P.D.C.R., Ph.D., F.L.S. London, punnubansal79@gmail.com.

摘要:

槲皮素是一种具有抗氧化和抗炎作用的多酚生物类黄酮,其对帕金森神经细胞的保护作用已得到证实,但由于其口服生物利用度低,因而在临床应用过程中受到限制。胡椒碱是一种生物利用度增强剂,可提高抗氧化剂的生物利用度。实验设计发挥槲皮素联合胡椒碱的各自优势对抗1-甲基-4-苯基-1,2,3,6-四氢吡啶诱导神经毒性的作用。做法为实验分别于实验第1,4,7天将MPTP 以100 ??g/??L剂量注射于大鼠双侧黑质,以破坏黑质中产生多巴胺的神经细胞;然后于第8天,单独灌胃25 和 50 mg/kg槲皮素或联合灌胃25 mg/kg槲皮素和2.5 mg/kg胡椒碱,连续14d。实验第1,7,14,21天对大鼠行为学改变进行评估。实验第22天,检测大鼠纹状体氧化应激指标硫巴比妥酸反应物质、亚硝酸盐和还原型谷胱甘肽,神经炎症因子白细胞介素1β, 白细胞介素6和肿瘤坏死因子α和神经递质多巴胺、去甲肾上腺素5-羟色胺、γ-氨基丁酸、谷氨酸、高香草酸、3,4-二羟基苯乙酸、5-羟基吲哚乙酸。发现,槲皮素单独及与胡椒碱联合应用均明显改善MPTP诱导的大鼠行为学和纹状体神经递质的异常改变、减轻纹状体氧化应激状态和炎症反应,且尤以联合应用效果更为明显。说明胡椒碱可提高槲皮素的抗氧化和抗炎作用,两者联合应用对抗1-甲基-4-苯基-1,2,3,6-四氢吡啶诱导的神经毒性的作用显著。

ORCID:0000-0002-7978-1043(Puneet Kumar)

关键词: 神经再生, 1-甲基-4-苯基-1,2,3,6-四氢吡啶, 槲皮素, 胡椒碱, 帕金森病, 兴奋毒性, 氧化应激, 神经炎症, 神经递质

Abstract:

1-Methy-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP) is a neurotoxin that selectively damages dopaminergic neurons in the substantia nigra pars compacta and induces Parkinson’s like symptoms in rodents. Quercetin (QC) is a natural polyphenolic bioflavonoid with potent antioxidant and anti-inflammatory properties but lacks of clinical attraction due to low oral bioavailability. Piperine is a well established bioavailability enhancer used pre-clinically to improve the bioavailability of antioxidants (e.g., Quercetin). Therefore, the present study was designed to evaluate the neuroprotective potential of QC together with piperine against MPTP-induced neurotoxicity in rats. MPTP (100 μg/μL/rat, bilaterally) was injected intranigrally on days 1, 4 and 7 using a digital stereotaxic apparatus. QC (25 and 50 mg/kg, intragastrically) and QC (25 mg/kg, intragastrically) in combination with piperine (2.5 mg/kg, intragastrically) were administered daily for 14 days starting from day 8 after the 3rd injection of MPTP. On day 22, animals were sacrificed and the striatum was isolated for oxidative stress parameter (thiobarbituric acid reactive substances, nitrite and glutathione), neuroinflammatory cytokine (interleukin-1β, interleukin-6, and tumor necrosis factor-α) and neurotransmitter (dopamine, norepinephrine, serotonin, gamma-aminobutyric acid, glutamate, 3,4-dihydroxyphenylacetic acid, homovanillic acid, and 5-hydroxyindoleacetic acid) evaluations. Bilateral infusion of MPTP into substantia nigra pars compacta led to significant motor deficits as evidenced by impairments in locomotor activity and rotarod performance in open field test and grip strength and narrow beam walk performance. Both QC (25 and 50 mg/kg) and QC (25 mg/kg) in combination with piperine (2.5 mg/kg), in particular the combination therapy, significantly improved MPTP-induced behavioral abnormalities in rats, reversed the abnormal alterations of neurotransmitters in the striatum, and alleviated oxidative stress and inflammatory response in the striatum. These findings indicate that piperine can enhance the antioxidant and anti-inflammatory properties of QC, and QC in combination with piperine exhibits strong neuroprotective effects against MPTP-induced neurotoxicity.

Key words: nerve regeneration, 1-methy-4-phenyl-1,2,3,6-tetrahydropyridine, Quercetin, Piperine, Parkinson’s disease, excitotoxicity, oxido-nitrosative stress, neurotransmitters, neural regeneration