Rabbits fed cholesterol-enriched diets exhibit pathological features of inclusion body myositis

被引:16
作者
Chen, Xuesong [1 ]
Ghribi, Othman [1 ]
Geiger, Jonathan D. [1 ]
机构
[1] Univ N Dakota, Sch Med & Hlth Sci, Dept Pharmacol Physiol & Therapeut, Grand Forks, ND 58203 USA
关键词
amyloid precursor protein; amyloid beta; Alzheimer's disease; skeletal muscle;
D O I
10.1152/ajpregu.00639.2007
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Sporadic inclusion body myositis (IBM) is the most common age-related muscle disease in humans; however, its etiology is unknown, there are few animal models for this disease, and effective treatments have not been identified. Similarities between pathological findings in Alzheimer's disease brain and IBM skeletal muscle include increased levels of amyloid precursor protein (APP) and amyloid beta-protein (A beta). Moreover, there have been suggestions that elevated levels of free cholesterol might participate in the pathogenesis of Alzheimer's disease and IBM due, in part, to its role in A beta generation. Here, we tested the hypothesis that rabbits fed cholesterol-enriched diets might faithfully exhibit human-like IBM pathological features. In skeletal muscle of one-third of the female rabbits fed cholesterol-enriched diet but not control diet, we found features of IBM, including vacuolated muscle fibers, increased numbers of mononuclear inflammatory cells, increased intramuscular deposition of A beta, hyperphosphorylated tau, and increased numbers of muscle fibers immunopositive for ubiquitin. The cholesterol-enriched diet increased mRNA and protein levels of APP, increased the protein levels of beta APP cleaving enzyme, and shifted APP processing in favor of A beta production. Our study has demonstrated that increased ingestion of high levels of dietary cholesterol can result in pathological features that resemble IBM closely and thus may serve as an important new model with which to study this debilitating disorder.
引用
收藏
页码:R829 / R835
页数:7
相关论文
共 28 条
[11]   Sporadic inclusion body myositis - diagnosis, pathogenesis and therapeutic strategies [J].
Dalakas, Marinos C. .
NATURE CLINICAL PRACTICE NEUROLOGY, 2006, 2 (08) :437-447
[12]   RAPID EXAMINATION OF MUSCLE TISSUE - AN IMPROVED TRICHROME METHOD FOR FRESH-FROZEN BIOPSY SECTIONS [J].
ENGEL, WK ;
CUNNINGHAM, GG .
NEUROLOGY, 1963, 13 (11) :919-&
[13]  
Ghribi O., 2006, J NEUROCHEM, V99, P438
[14]   High cholesterol content in neurons increases BACE, β-amyloid, and phosphorylated tau levels in rabbit hippocampus [J].
Ghribi, Othman ;
Larsen, Brian ;
Schrag, Matthew ;
Herman, Mary M. .
EXPERIMENTAL NEUROLOGY, 2006, 200 (02) :460-467
[15]   Cardiac systolic and diastolic dysfunction after a cholesterol-rich diet [J].
Huang, Y ;
Walker, KE ;
Hanley, F ;
Narula, J ;
Houser, SR ;
Tulenko, TN .
CIRCULATION, 2004, 109 (01) :97-102
[16]   Three lipoprotein receptors and cholesterol in inclusion-body myositis muscle [J].
Jaworska-Wilczynska, M ;
Wilczynski, GM ;
Engel, WK ;
Strickland, DK ;
Weisgraber, KH ;
Askanas, V .
NEUROLOGY, 2002, 58 (03) :438-445
[17]   AMYLOID FILAMENTS IN INCLUSION BODY MYOSITIS - NOVEL FINDINGS PROVIDE INSIGHT INTO NATURE OF FILAMENTS [J].
MENDELL, JR ;
SAHENK, Z ;
GALES, T ;
PAUL, L .
ARCHIVES OF NEUROLOGY, 1991, 48 (12) :1229-1234
[18]   Transgenic expression of β-APP in fast-twitch skeletal muscle leads to calcium dyshomeostasis and IBM-like pathology [J].
Moussa, Charbel E-H. ;
Fu, Qinghao ;
Kumar, Pravir ;
Shtifman, Alexander ;
Lopez, Jose R. ;
Allen, Paul D. ;
LaFerla, Frank ;
Weinberg, David ;
Magrane, Jordi ;
Aprahamian, Tamar ;
Walsh, Kenneth ;
Rosen, Kenneth M. ;
Querfurth, Henry W. .
FASEB JOURNAL, 2006, 20 (12) :2165-+
[19]   Inclusion-body myositis and Alzheimer disease - Two sides of the same coin, or different currencies altogether? [J].
Murphy, MP ;
Golde, TE .
NEUROLOGY, 2006, 66 :S65-S68
[20]  
Phillips BA, 2000, MUSCLE NERVE, V23, P970, DOI 10.1002/(SICI)1097-4598(200006)23:6<970::AID-MUS20>3.3.CO