Drug Resistance in Epilepsy: Clinical Impact, Potential Mechanisms, and New Innovative Treatment Options

被引:574
作者
Loescher, Wolfgang [1 ,2 ]
Potschka, Heidrun [3 ]
Sisodiya, Sanjay M. [4 ]
Vezzani, Annamaria [5 ]
机构
[1] Univ Vet Med, Dept Pharmacol Toxicol & Pharm, Bunteweg 17, D-30559 Hannover, Germany
[2] Ctr Syst Neurosci, Hannover, Germany
[3] Ludwig Maximilians Univ Munchen, Inst Pharmacol Toxicol & Pharm, Munich, Germany
[4] UCL, Inst Neurol, Dept Clin & Expt Epilepsy, Queen Sq, London, England
[5] Ist Ricovero & Cura Carattere Sci, Mario Negri Inst Pharmacol Res, Dept Neurosci, Milan, Italy
关键词
BLOOD-BRAIN-BARRIER; TEMPORAL-LOBE EPILEPSY; CATION-CHLORIDE COTRANSPORTERS; REFRACTORY STATUS EPILEPTICUS; RECEPTOR SUBUNIT EXPRESSION; GAMMA-AMINOBUTYRIC-ACID; P-GLYCOPROTEIN FUNCTION; INDUCED UP-REGULATION; ANTIEPILEPTIC DRUGS; ANIMAL-MODELS;
D O I
10.1124/pr.120.019539
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Epilepsy is a chronic neurologic disorder that affects over 70 million people worldwide. Despite the availability of over 20 antiseizure drugs (ASDs) for symptomatic treatment of epileptic seizures, about one-third of patients with epilepsy have seizures refractory to pharmacotherapy. Patients with such drug-resistant epilepsy (DRE) have increased risks of premature death, injuries, psychosocial dysfunction, and a reduced quality of life, so development of more effective therapies is an urgent clinical need. However, the various types of epilepsy and seizures and the complex temporal patterns of refractoriness complicate the issue. Furthermore, the underlying mechanisms of DRE are not fully understood, though recent work has begun to shape our understanding more clearly. Experimental models of DRE offer opportunities to discover, characterize, and challenge putative mechanisms of drug resistance. Furthermore, such preclinical models are important in developing therapies that may overcome drug resistance. Here, we will review the current understanding of the molecular, genetic, and structural mechanisms of ASD resistance and discuss how to overcome this problem. Encouragingly, better elucidation of the pathophysiological mechanisms underpinning epilepsies and drug resistance by concerted preclinical and clinical efforts have recently enabled a revised approach to the development of more promising therapies, including numerous potential etiology-specific drugs ("precision medicine") for severe pediatric (monogenetic) epilepsies and novel multitargeted ASDs for acquired partial epilepsies, suggesting that the long hoped-for breakthrough in therapy for as-yet ASD-resistant patients is a feasible goal. Significance Statement-Drug resistance provides a major challenge in epilepsy management. Here, we will review the current understanding of the molecular, genetic, and structural mechanisms of drug resistance in epilepsy and discuss how the problem might be overcome.
引用
收藏
页码:606 / 638
页数:33
相关论文
共 259 条
[1]   Blood-brain barrier structure and function and the challenges for CNS drug delivery [J].
Abbott, N. Joan .
JOURNAL OF INHERITED METABOLIC DISEASE, 2013, 36 (03) :437-449
[2]   Inflammatory mediators and modulation of blood-brain barrier permeability [J].
Abbott, NJ .
CELLULAR AND MOLECULAR NEUROBIOLOGY, 2000, 20 (02) :131-147
[3]   Adjunctive use of verapamil in patients with refractory temporal lobe epilepsy: A pilot study [J].
Asadi-Pooya, Ali A. ;
Razavizadegan, S. Mohammad Ali ;
Abdi-Ardekani, Alireza ;
Sperling, Michael R. .
EPILEPSY & BEHAVIOR, 2013, 29 (01) :150-154
[4]   Dynamic Regulation of P-glycoprotein in Human Brain Capillaries [J].
Avemary, Janine ;
Salvamoser, Josephine D. ;
Peraud, Aurelia ;
Remi, Jan ;
Noachtar, Soheyl ;
Fricker, Gert ;
Potschka, Heidrun .
MOLECULAR PHARMACEUTICS, 2013, 10 (09) :3333-3341
[5]   Pharmacogenomics in epilepsy [J].
Balestrini, Simona ;
Sisodiya, Sanjay M. .
NEUROSCIENCE LETTERS, 2018, 667 :27-39
[6]   A novel non-transcriptional pathway mediates the proconvulsive effects of interleukin-1β [J].
Balosso, Silvia ;
Maroso, Mattia ;
Sanchez-Alavez, Manuel ;
Ravizza, Teresa ;
Frasca, Angelisa ;
Bartfai, Tamas ;
Vezzani, Annamaria .
BRAIN, 2008, 131 :3256-3265
[7]   Pilocarpine-induced epilepsy in mice alters seizure thresholds and the efficacy of antiepileptic drugs in the 6-Hertz psychomotor seizure model [J].
Bankstahl, Marion ;
Bankstahl, Jens P. ;
Loescher, Wolfgang .
EPILEPSY RESEARCH, 2013, 107 (03) :205-216
[8]   Inter-individual variation in the anticonvulsant effect of phenobarbital in the pilocarpine rat model of temporal lobe epilepsy [J].
Bankstahl, Marion ;
Bankstahl, Jens P. ;
Loescher, Wolfgang .
EXPERIMENTAL NEUROLOGY, 2012, 234 (01) :70-84
[9]   Losartan Prevents Acquired Epilepsy via TGF-β Signaling Suppression [J].
Bar-Klein, Guy ;
Cacheaux, Luisa P. ;
Kamintsky, Lyn ;
Prager, Ofer ;
Weissberg, Itai ;
Schoknecht, Karl ;
Cheng, Paul ;
Kim, Soo Young ;
Wood, Lydia ;
Heinemann, Uwe ;
Kaufer, Daniela ;
Friedman, Alon .
ANNALS OF NEUROLOGY, 2014, 75 (06) :864-875
[10]   Imaging blood-brain barrier dysfunction as a biomarker for epileptogenesis [J].
Bar-Klein, Guy ;
Lublinsky, Svetlana ;
Kamintsky, Lyn ;
Noyman, Iris ;
Veksler, Ronel ;
Dalipaj, Hotjensa ;
Senatorov, Vladimir V., Jr. ;
Swissa, Evyatar ;
Rosenbach, Dror ;
Elazary, Netta ;
Milikovsky, Dan Z. ;
Milk, Nadav ;
Kassirer, Michael ;
Rosman, Yossi ;
Serlin, Yonatan ;
Eisenkraft, Arik ;
Chassidim, Yoash ;
Parmet, Yisrael ;
Kaufer, Daniela ;
Friedman, Alon .
BRAIN, 2017, 140 :1692-1705