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首页> 外文期刊>Pharmacology, Biochemistry and Behavior >Pharmacological inhibition of inducible nitric oxide synthase (iNOS) and nicotinamide adenine dinucleotide phosphate (NADPH) oxidase, convalesce behavior and biochemistry of hypertension induced vascular dementia in rats
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Pharmacological inhibition of inducible nitric oxide synthase (iNOS) and nicotinamide adenine dinucleotide phosphate (NADPH) oxidase, convalesce behavior and biochemistry of hypertension induced vascular dementia in rats

机译:诱导型一氧化氮合酶(InOS)和烟酰胺腺嘌呤二核苷酸(NADPH)氧化酶的药理抑制,促进性行为和高血压诱导大鼠血管痴呆的生物化学

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摘要

Cognitive disorders are likely to increase over the coming years (5-10). Vascular dementia (VaD) has heterogeneous pathology and is a challenge for clinicians. Current Alzheimer's disease drugs have had limited clinical efficacy in treating VaD and none have been approved by major regulatory authorities specifically for this disease. Role of iNOS and NADPH-oxidase has been reported in various pathological conditions but there role in hypertension (Hypt) induced VaD is still unclear. This research work investigates the salutiferous effect of aminoguanidine (AG), an iNOS inhibitor and 4??-hydroxy-3??- methoxyacetophenone (HMAP), a NADPH oxidase inhibitor in Hypt induced VaD in rats. Deoxycorticosterone acetate-salt (DOCA-S) hypertension has been used for development of VaD in rats. Morris water-maze was used for testing learning and memory. Vascular system assessment was done by testing endothelial function. Mean arterial blood pressure (MABP), oxidative stress [aortic superoxide anion, serum and brain thiobarbituric acid reactive species (TBARS) and brain glutathione (GSH)], nitric oxide levels (serum nitrite/nitrate) and cholinergic activity (brain acetyl cholinesterase activity-AChE) were also measured. DOCA-S treated rats have shown increased MABP with impairment of endothelial function, learning and memory, reduction in serum nitrite/nitrate & brain GSH levels along with increase in serum & brain TBARS, and brain AChE activity. AG as well as HMAP significantly convalesce Hypt induced impairment of learning, memory, endothelial function, and alterations in various biochemical parameters. It may be concluded that AG, an iNOS inhibitor and HMAP, a NADPH-oxidase inhibitor may be considered as potential agents for the management of Hypt induced VaD. ? 2012 Elsevier Inc.
机译:认知障碍可能会增加未来几年(5-10)。血管痴呆(VAD)具有异质病理学,对临床医生挑战。目前的阿尔茨海默病药物在治疗Vad临床疗效有限,没有专门针对这种疾病的主要监管机构批准。在各种病理条件下报道了InOS和NADPH-氧化酶的作用,但在高血压(HYPT)诱导的VAD中存在作用尚不清楚。该研究工作研究了氨基胍(Ag),InOS抑制剂和4· - 羟基-3? - 甲氧基乙酮(HMAP),在大鼠中诱导VAD中的NADPH氧化酶抑制剂的良碱基效果。醋酸盐(DOCA-S)高血压已被用于大鼠VAD的发育。莫里斯水迷宫被用于测试学习和记忆。通过测试内皮功能来完成血管系统评估。平均动脉血压(MABP),氧化应激[主动脉超氧化物阴离子,血清和脑硫氨基碱酸反应性物种(TBARS)和脑谷胱甘肽(GSH)],一氧化氮水平(亚硝酸盐/硝酸盐)和胆碱能活性(脑乙酰胆碱酯酶活性-ache)也被衡量。 Doca-S处理的大鼠表现出增加的MABP,具有内皮函数,学习和记忆,血清亚硝酸盐/硝酸盐和脑GSH水平的损害以及血清和脑TBAR和脑疼痛活动的增加。 AG以及HMAP显着康复诱导各种生化参数中的学习,记忆,内皮功能和改变的损害。可以得出结论,Ag,InOS抑制剂和HMAP,NADPH-氧化酶抑制剂可以被认为是用于管理Hypt诱导的VAD的潜在剂。还2012年elsevier公司

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