Adenosine-based cell therapy approaches for pharmacoresistant epilepsies

被引:48
作者
Boison, Detlev
机构
[1] RS Dow Neurol Sci Inst, Portland, OR 97232 USA
[2] Univ Zurich, ETH, NCCR Neural Plast & Repair, Zurich, Switzerland
关键词
adenosine; adenosine kinase; epilepsy; epileptogenesis; kindling; mouse models;
D O I
10.1159/000100356
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Despite recent medical advances pharmacoresistant epilepsy continues to be a major health problem. The knowledge of endogenous protective mechanisms of the brain may lead to the development of rational therapies tailored to a patient's needs. Adenosine has been identified as an endogenous neuromodulator with antiepileptic and neuroprotective properties. However, the therapeutic use of adenosine or its receptor agonists is largely precluded by strong peripheral and central side effects. Thus, local delivery of adenosine to a critical site of the brain may provide a solution for the therapeutic use of adenosine. The following rationale for the local augmentation of the adenosine system as a novel therapeutic principle in the treatment of epilepsy has been established: (1) Deficits in the adenosinergic system are associated with epileptogenesis and these deficits promote seizures. Thus, reconstitution of an inhibitory adenosinergic tone is a rational therapeutic approach. (2) The focal paracrine delivery of adenosine from encapsulated cells suppresses seizures in kindled rats without overt side effects. (3) The anticonvulsant activity of locally released adenosine is maintained in models of epilepsy which are resistant to major antiepileptic drugs. This review summarizes the rationale and recent approaches for adenosine-based cell therapies for pharmacoresistant epilepsies. Copyright (C) 2007 S. Karger AG, Basel.
引用
收藏
页码:28 / 33
页数:6
相关论文
共 35 条
[1]   ACTIVITIES AND SOME PROPERTIES OF 5'-NUCLEOTIDASE, ADENOSINE KINASE AND ADENOSINE-DEAMINASE IN TISSUES FROM VERTEBRATES AND INVERTEBRATES IN RELATION TO CONTROL OF CONCENTRATION AND PHYSIOLOGICAL-ROLE OF ADENOSINE [J].
ARCH, JRS ;
NEWSHOLME, EA .
BIOCHEMICAL JOURNAL, 1978, 174 (03) :965-977
[2]   Embryonic stem cells develop into functional dopaminergic neurons after transplantation in a Parkinson rat model [J].
Björklund, LM ;
Sánchez-Pernaute, R ;
Chung, SM ;
Andersson, T ;
Chen, IYC ;
McNaught, KS ;
Brownell, AL ;
Jenkins, BG ;
Wahlestedt, C ;
Kim, KS ;
Isacson, O .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (04) :2344-2349
[3]   Adenosine and epilepsy: From therapeutic rationale to new therapeutic strategies [J].
Boison, D .
NEUROSCIENTIST, 2005, 11 (01) :25-36
[4]   Seizure suppression in kindled rats by intraventricular grafting of an adenosine releasing synthetic polymer [J].
Boison, D ;
Scheurer, L ;
Tseng, JL ;
Aebischer, P ;
Mohler, H .
EXPERIMENTAL NEUROLOGY, 1999, 160 (01) :164-174
[5]   Embryonic stem cell-derived glial precursors:: A source of myelinating transplants [J].
Brüstle, O ;
Jones, KN ;
Learish, RD ;
Karram, K ;
Choudhary, K ;
Wiestler, OD ;
Duncan, ID ;
McKay, RDG .
SCIENCE, 1999, 285 (5428) :754-756
[6]   Molecular biology and regulation of nucleoside and nucleobase transporter proteins in eukaryotes and prokaryotes [J].
Cabrita, MA ;
Baldwin, SA ;
Young, JD ;
Cass, CE .
BIOCHEMISTRY AND CELL BIOLOGY, 2002, 80 (05) :623-638
[7]   Adenosine and ATP link PCO2 to cortical excitability via pH [J].
Dulla, CG ;
Dobelis, P ;
Pearson, T ;
Frenguelli, BG ;
Staley, KJ ;
Masino, SA .
NEURON, 2005, 48 (06) :1011-1023
[8]   Engineering embryonic stem cell derived glia for adenosine delivery [J].
Fedele, DE ;
Koch, P ;
Scheurer, L ;
Simpson, EM ;
Möhler, H ;
Brüstle, O ;
Boison, D .
NEUROSCIENCE LETTERS, 2004, 370 (2-3) :160-165
[9]   Astrogliosis in epilepsy leads to overexpression of adenosine kinase, resulting in seizure aggravation [J].
Fedele, DE ;
Gouder, N ;
Güttinger, M ;
Gabernet, L ;
Scheurer, L ;
Rülicke, T ;
Crestani, F ;
Boison, D .
BRAIN, 2005, 128 :2383-2395
[10]  
FEDELE DE, 2006, IN PRESS EXP NEUROL