The impact of anorexigenic peptides in experimental models of Alzheimer's disease pathology

被引:18
|
作者
Maletinska, Lenka [1 ]
Popelova, Andrea [1 ]
Zelezna, Blanka [1 ]
Bencze, Michal [1 ,2 ]
Kunes, Jaroslav [1 ,2 ]
机构
[1] AS CR, Inst Organ Chem & Biochem, Prague, Czech Republic
[2] AS CR, Inst Physiol, Prague, Czech Republic
关键词
Alzheimer's disease pathology; experimental rodent models; leptin; anorexigenic neuropeptides; PROLACTIN-RELEASING PEPTIDE; AMYLOID-BETA-PROTEIN; HIPPOCAMPAL SYNAPTIC PLASTICITY; TRANSGENIC MOUSE MODEL; LONG-TERM POTENTIATION; MODULATING TAU HYPERPHOSPHORYLATION; GLYCOGEN-SYNTHASE KINASE-3-BETA; LIRAGLUTIDE IMPROVES MEMORY; GLP-1 RECEPTOR AGONIST; INSULIN-RESISTANCE;
D O I
10.1530/JOE-18-0532
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Alzheimer's disease (AD) is the most prevalent neurodegenerative disorder in the elderly population. Numerous epidemiological and experimental studies have demonstrated that patients who suffer from obesity or type 2 diabetes mellitu s have a higher risk of cognitive dysfunction and AD. Several recent studies demonstrat ed that food intakelowering (anorexigenic) peptides have the potential to improve metabolic disorders and that they may also potentially be useful in the treatment of neurodegenerative diseases. In this review, the neuroprotective effects of anorexigenic pept ides of both peripheral and central origins are discussed. Moreover, the role of leptin as a key modulator of energy homeostasis is discussed in relation to its interaction with anorexigenic peptides and their analogs in AD-like pathology. Although there is no pe rfect experimental model of human AD pathology, animal studies have already proven that anorexigenic peptides exhibit neuroprotective properties. This phenomenon is extremely important for the potential development of new drugs in view of the aging of the human population and of the significantly increasing incidence of AD.
引用
收藏
页码:R47 / R72
页数:26
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