Gill Jaskamal Singh, Jamwal Sumit, Kumar Puneet, Deshmukh Rahul
Neuropharmacology Division, Department of Pharmacology, I.S.F College of Pharmacy, Moga, Punjab, India.
Neuropharmacology Division, Department of Pharmacology, I.S.F College of Pharmacy, Moga, Punjab, India; Research Scholar, I. K. Gujral Punjab Technical University, Jalandhar, India.
Pharmacol Rep. 2017 Apr;69(2):306-313. doi: 10.1016/j.pharep.2016.11.008. Epub 2016 Nov 18.
Huntington Disease is autosomal, fatal and progressive neurodegenerative disorder for which clinically available drugs offer only symptomatic relief. Emerging strides have indicated that antidepressants improve motor performance, restore neurotransmitters level, ameliorates striatal atrophy, increases BDNF level and may enhance neurogenesis. Therefore, we investigated sertraline and venlafaxine, clinically available drugs for depression with numerous neuroprotective properties, for their beneficial effects, if any, in quinolinic acid induced Huntington's like symptoms in rats.
Rats were administered quinolinic acid (QA) (200 nmol/2μl saline) intrastriatal bilaterally on 0day. Sertraline and venlafaxine (10 and 20mg/kg, po) each were administered for 21days once a day. Motor performance was assessed using rotarod test, grip strength test, narrow beam walk test on weekly basis. On day 22, animals were sacrificed and rat striatum was isolated for biochemical (LPO, GSH and Nitrite), neuroinflammation (TNF-α, IL-1β and IL-6) and neurochemical analysis (GABA, glutamate, norepinephrine, dopamine, serotonin, DOPAC, HVA and 5-HIAA).
QA treatment significantly altered body weight, motor performance, oxidative defense (increased LPO, nitrite and decreased GSH), pro-inflammatory cytokines levels (TNF-α, IL-6 and IL-1β), neurochemical level (GABA, glutamate, nor-epinephrine, dopamine, serotonin, HVA, DOPAC, 5-HIAA). Sertraline and venlafaxine at selected doses significantly attenuated QA induced alterations in striatum.
The present study suggests that modulation of monoamines level, normalization of GABA and glutamatergic signaling, anti-oxidant and anti-inflammatory properties could underlie the neuroprotective effect of sertraline and venlafaxine in QA induced Huntington's like symptoms.
亨廷顿病是一种常染色体显性、致命且进行性的神经退行性疾病,目前临床上可用的药物仅能缓解症状。新的研究进展表明,抗抑郁药可改善运动表现、恢复神经递质水平、减轻纹状体萎缩、提高脑源性神经营养因子(BDNF)水平,并可能促进神经发生。因此,我们研究了舍曲林和文拉法辛这两种临床上用于治疗抑郁症且具有多种神经保护特性的药物,观察它们对喹啉酸诱导的大鼠亨廷顿样症状是否有有益作用。
在第0天,给大鼠双侧纹状体内注射喹啉酸(QA)(200纳摩尔/2微升生理盐水)。舍曲林和文拉法辛(分别为10毫克/千克和20毫克/千克,口服)每天给药一次,持续21天。每周使用转棒试验、握力试验、窄梁行走试验评估运动表现。在第22天,处死动物并分离大鼠纹状体,进行生化分析(脂质过氧化产物、谷胱甘肽和亚硝酸盐)、神经炎症分析(肿瘤坏死因子-α、白细胞介素-1β和白细胞介素-6)以及神经化学分析(γ-氨基丁酸、谷氨酸、去甲肾上腺素、多巴胺、5-羟色胺、3,4-二羟基苯乙酸、高香草酸和5-羟吲哚乙酸)。
QA治疗显著改变了体重、运动表现、氧化防御(脂质过氧化产物和亚硝酸盐增加,谷胱甘肽减少)、促炎细胞因子水平(肿瘤坏死因子-α、白细胞介素-6和白细胞介素-1β)以及神经化学水平(γ-氨基丁酸、谷氨酸、去甲肾上腺素、多巴胺、5-羟色胺、高香草酸、3,4-二羟基苯乙酸、5-羟吲哚乙酸)。选定剂量的舍曲林和文拉法辛显著减轻了QA诱导的纹状体改变。
本研究表明,单胺水平的调节、γ-氨基丁酸和谷氨酸能信号的正常化、抗氧化和抗炎特性可能是舍曲林和文拉法辛对QA诱导的亨廷顿样症状具有神经保护作用的基础。