Bladder dysfunction in mice with experimental autoimmune encephalomyelitis

被引:26
作者
Altuntas, Cengiz Z. [1 ]
Daneshgari, Firouz [2 ,3 ]
Liu, Guiming [2 ]
Fabiyi, Adebola [2 ,3 ]
Kavran, Michael [2 ,3 ]
Johnson, Justin M. [1 ]
Gulen, A. Fatih [1 ]
Jaini, Ritika [1 ]
Li, Xiaoxia [1 ]
Frenkl, Tara L. [2 ,3 ]
Tuohy, Vincent K. [1 ]
机构
[1] Cleveland Clin, Lerner Res Inst, Dept Immunol, Cleveland, OH 44195 USA
[2] Cleveland Clin, Lerner Res Inst, Dept Biomed Engn, Cleveland, OH 44195 USA
[3] Cleveland Clin, Glickman Urol & Kidney Inst, Cleveland, OH 44195 USA
基金
美国国家卫生研究院;
关键词
EAE/MS; Autoimmune; Micturition; Neurogenic bladder;
D O I
10.1016/j.jneuroim.2008.06.038
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The vast majority of patients with multiple sclerosis (MS) develop bladder control problems including urgency to urinate, urinary incontinence, frequency of urination, and retention of urine. Over 60% of MS patients show detrusor-sphincter dyssynergia, an abnormality characterized by obstruction of urinary outflow as a result of discoordinated contraction of the urethral sphincter muscle and the bladder detrusor muscle. In the current study we examined bladder function in female SWXJ mice with different defined levels of neurological impairment following induction of experimental autoimmune encephalomyelitis (EAE), an animal model of central nervous system inflammation widely used in MS research. We found that EAE mice develop profound bladder dysfunction characterized by significantly increased micturition frequencies and significantly decreased urine output per micturition. Moreover, we found that the severity of bladder abnormalities in EAE mice was directly related to the severity of clinical EAE and neurologic disability. Our study is the first to show and characterize micturition abnormalities in EAE mice thereby providing a most useful model system for understanding and treating neurogenic bladder. (C) 2008 Elsevier B.V. All rights reserved.
引用
收藏
页码:58 / 63
页数:6
相关论文
共 31 条
[1]   The standardisation of terminology in lower urinary tract function: Report from the standardisation sub-committee of the International Continence Society (Reprinted from Neurourology and Urodynamics, vol 21, pg 167-178, 2002) [J].
Abrams, P ;
Cardozo, L ;
Fall, M ;
Griffiths, D ;
Rosier, P ;
Ulmsten, U ;
Van Kerrebroeck, P ;
Victor, A ;
Wein, A .
UROLOGY, 2003, 61 (01) :37-49
[2]   Management of detrusor-external sphincter dyssynergia [J].
Ahmed, Hashim U. ;
Shergill, Iqbal S. ;
Arya, Manit ;
Shah, P. Julian R. .
NATURE CLINICAL PRACTICE UROLOGY, 2006, 3 (07) :368-380
[3]   The basis for drug treatment of the overactive bladder [J].
Andersson, KE ;
Chapple, C ;
Wein, A .
WORLD JOURNAL OF UROLOGY, 2001, 19 (05) :294-298
[4]   Brain responses to changes in bladder volume and urge to void in healthy men [J].
Athwal, BS ;
Berkley, KJ ;
Hussain, I ;
Brennan, A ;
Craggs, M ;
Sakakibara, R ;
Frackowiak, RSJ ;
Fowler, CJ .
BRAIN, 2001, 124 :369-377
[5]  
BIRDER LA, 1998, AM J PHYSIOL, V275, P226
[6]   DETRUSOR-EXTERNAL SPHINCTER DYSSYNERGIA IN MEN WITH MULTIPLE-SCLEROSIS - AN OMINOUS UROLOGIC CONDITION [J].
BLAIVAS, JG ;
BARBALIAS, GA .
JOURNAL OF UROLOGY, 1984, 131 (01) :91-94
[7]   Central pathways controlling micturition and urinary continence [J].
Blok, BFM .
UROLOGY, 2002, 59 (5A) :13-17
[8]   Brain activation during micturition in women [J].
Blok, BFM ;
Sturms, LM ;
Holstege, G .
BRAIN, 1998, 121 :2033-2042
[9]   A PET study on brain control of micturition in humans [J].
Blok, BFM ;
Willemsen, ATM ;
Holstege, G .
BRAIN, 1997, 120 :111-121
[10]   Mechanisms and current treatments of urogenital dysfunction in multiple sclerosis [J].
Fernández, O .
JOURNAL OF NEUROLOGY, 2002, 249 (01) :1-8