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首页> 外文期刊>Geriatrics & gerontology international. >Effect of rivastigmine on plasma butyrylcholine esterase activity and plasma ghrelin levels in patients with dementia in Alzheimer’s disease
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Effect of rivastigmine on plasma butyrylcholine esterase activity and plasma ghrelin levels in patients with dementia in Alzheimer’s disease

机译:菌毒素对阿尔茨海默病痴呆患者血浆丁酰胆碱酯酶活性和血浆Ghrelin水平的影响

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摘要

Aim Alzheimer’s disease causes loss of appetite, resulting in bodyweight reduction. This, in turn, causes progression of cognitive dysfunction and physical complications that hasten death. Earlier care for loss of appetite is essential in Alzheimer’s disease management. Rivastigmine is a therapeutic agent for Alzheimer’s disease that has dual inhibition effects on acetylcholine esterase and butyrylcholine esterase. Butyrylcholine esterase is known to degrade the gastric hormone, ghrelin, which regulates appetite; therefore, we considered that rivastigmine might have an effect on appetite. The present study aimed to evaluate the hypothesis that rivastigmine improves appetite in Alzheimer’s disease patients. Methods Rivastigmine was given to mild‐to‐moderate Alzheimer’s disease patients for 16?weeks. We evaluated the effects of rivastigmine on food intake, bodyweight, motivation (estimated by the vitality index), cognition function (estimated by the Hasegawa Dementia Scale‐Revised), plasma butyrylcholine esterase activity, active ghrelin and inactive ghrelin. Results Plasma butyrylcholine esterase activity significantly decreased over time (percent change: ?18.9?±?27.0%, P ??0.05 at week?8; percent change: ?33.4?±?45.4%, P ??0.05 at week?16). Negative correlations were detected between percent changes in butyrylcholine esterase activity and active ghrelin ( r s ?=??0.62, P ?=?0.033) or active/inactive ghrelin ratio ( r s ?=??0.73, P ?=?0.007). Furthermore, motivation (including appetite) improved significantly (percent change: 17.9?±?18.6%, P ??0.05 at week?16). Conclusions The present study suggests that rivastigmine might improve appetite in mild‐to‐moderate Alzheimer’s disease patients by suppressing degradation of plasma active ghrelin through the inhibition of plasma butyrylcholine esterase. Geriatr Gerontol Int 2018; 18: 886–891
机译:AIM Alzheimer的疾病导致食欲丧失,导致体重减少。反过来,这导致认知功能障碍和身体并发症的进展,并致死死亡。早些时候在阿尔茨海默病管理中丧失食欲不关会。 RIVASTIGMINE是阿尔茨海默病的治疗剂,其对乙酰胆碱酯酶和丁酰胆碱酯酶具有双重抑制作用。已知丁酰胆碱酯酶降解胃激素Ghrelin,其调节食欲;因此,我们认为Rivastigmine可能对食欲产生影响。本研究旨在评估利凡斯氏菌素在阿尔茨海默病患者患者中提高食欲的假设。方法对患有6〜中度的阿尔茨海默病患者进行牛肝菌患者16?周。我们评估了利凡斯氏菌素对食物摄入,体重,动机(受活力指数估计)的影响,认知功能(由Hasegawa痴呆规模规模估计),血浆丁酰胆碱酯酶活性,活性Ghrelin和无活性Ghrelin。结果血浆丁二醇胆碱酯酶活性随时间显着降低(变化百分比:18.9〜±27.0%,P≤0.Δ0,P≤8.05;百分比变化:?33.4?±45.4%,P?0.05一周?16)。在丁酰胆碱酯酶活性和活性Ghrelin的变化百分比之间检测到阴性相关性(R s?=Δ0.62,p?= 0.033)或活性/无活性ghrelin比(R s?= ?? 0.73,p?= 0.007)。此外,动机(包括食欲)显着改善(变化百分比:17.9?±18.6%,p≤0.05,p≤0.05)。结论本研究表明,通过抑制血浆丁基胆碱酯酶的抑制,利伐地,通过抑制血浆活性Ghrelin的降解,利伐地提高了轻度至中度阿尔茨海默病患者的食欲。 GeriaTr Gerontol int 2018; 18:886-891.

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