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利拉鲁肽和 ghrelin 的双重治疗促进亨廷顿病 R6/2 小鼠模型的脑和外周能量代谢。

Dual Therapy with Liraglutide and Ghrelin Promotes Brain and Peripheral Energy Metabolism in the R6/2 Mouse Model of Huntington's Disease.

机构信息

CNC - Center for Neuroscience and Cell Biology, University of Coimbra, Coimbra, Portugal.

Institute for Interdisciplinary Research (IIIUC), University of Coimbra, Coimbra, Portugal.

出版信息

Sci Rep. 2018 Jun 12;8(1):8961. doi: 10.1038/s41598-018-27121-w.

DOI:10.1038/s41598-018-27121-w
PMID:29895889
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5997749/
Abstract

Neuronal loss alongside altered energy metabolism, are key features of Huntington's disease (HD) pathology. The orexigenic gut-peptide hormone ghrelin is known to stimulate appetite and affect whole body energy metabolism. Liraglutide is an efficient anti-type 2 diabetes incretin drug, with neuroprotective effects alongside anorectic properties. Combining liraglutide with the orexigenic peptide ghrelin may potentially promote brain/cognitive function in HD. The R6/2 mouse model of HD exhibits progressive central pathology, weight loss, deranged glucose metabolism, skeletal muscle atrophy and altered body composition. In this study, we targeted energy metabolism in R6/2 mice using a co-administration of liraglutide and ghrelin. We investigated their effect on brain cortical hormone-mediated intracellular signalling pathways, metabolic and apoptotic markers, and the impact on motor function in HD. We here demonstrate that liraglutide, alone or together with ghrelin (subcutaneous daily injections of 150 µg/kg (ghrelin) and 0.2 mg/kg (liraglutide), for 2 weeks), normalized glucose homeostatic features in the R6/2 mouse, without substantially affecting body weight or body composition. Liraglutide alone decreased brain cortical active GLP-1 and IGF-1 levels in R6/2 mice, alongside higher ADP levels. Liraglutide plus ghrelin decreased brain insulin, lactate, AMP and cholesterol levels in R6/2 mice. Taken together, our findings encourage further studies targeting energy metabolism in HD.

摘要

神经元丢失和能量代谢改变是亨廷顿病(HD)病理学的关键特征。食欲肽激素胃饥饿素已知可刺激食欲并影响全身能量代谢。利拉鲁肽是一种有效的 2 型糖尿病肠促胰岛素药物,具有神经保护作用和厌食特性。将利拉鲁肽与食欲肽 ghrelin 结合使用可能会促进 HD 患者的大脑/认知功能。R6/2 HD 小鼠模型表现出进行性中枢病理学、体重减轻、葡萄糖代谢紊乱、骨骼肌萎缩和身体成分改变。在这项研究中,我们使用利拉鲁肽和 ghrelin 的联合给药来靶向 R6/2 小鼠的能量代谢。我们研究了它们对大脑皮质激素介导的细胞内信号通路、代谢和凋亡标志物的影响,以及对 HD 运动功能的影响。我们在此证明,利拉鲁肽单独或与 ghrelin 一起(皮下每日注射 150μg/kg(ghrelin)和 0.2mg/kg(利拉鲁肽),持续 2 周)可使 R6/2 小鼠的葡萄糖稳态特征正常化,而不会显著影响体重或身体成分。利拉鲁肽单独降低了 R6/2 小鼠大脑皮质中活性 GLP-1 和 IGF-1 水平,同时 ADP 水平升高。利拉鲁肽加 ghrelin 降低了 R6/2 小鼠大脑中的胰岛素、乳酸、AMP 和胆固醇水平。总之,我们的研究结果鼓励进一步研究针对 HD 能量代谢的治疗方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0fdd/5997749/10f08f7de536/41598_2018_27121_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0fdd/5997749/eba3dc5c120d/41598_2018_27121_Fig1_HTML.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0fdd/5997749/e63eaa9c375e/41598_2018_27121_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0fdd/5997749/10f08f7de536/41598_2018_27121_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0fdd/5997749/eba3dc5c120d/41598_2018_27121_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0fdd/5997749/eb99366d6af7/41598_2018_27121_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0fdd/5997749/c5b301237f7a/41598_2018_27121_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0fdd/5997749/e63eaa9c375e/41598_2018_27121_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0fdd/5997749/10f08f7de536/41598_2018_27121_Fig5_HTML.jpg

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Body weight is a robust predictor of clinical progression in Huntington disease.
韩国亨廷顿舞蹈症患者诊断检查及特殊注意事项实用指南。
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