The DOI matches its Crossref record; 3 of the 3 references it cites were found in a registry or an index.
The Blood–Brain Barrier and Epilepsy
Open accessAbstract
Summary: During the past several years, there has been increasing interest in the role of the blood–brain barrier (BBB) in epilepsy. Advances in neuroradiology have enhanced our ability to image and study the human cerebrovasculature, and further developments in the research of metabolic deficiencies linked to seizure disorders (e.g., GLUT1 deficiency), neuroinflammation, and multiple drug resistance to antiepileptic drugs (AEDs) have amplified the significance of the BBB's relationship to epilepsy. Prior to 1986, BBB research in epilepsy focused on three main areas: ultrastructural studies, brain glucose availability and transport, and clinical uses of AEDs. However, contrast‐based imaging techniques and medical procedures such as BBB disruption provided a framework that demonstrated that the BBB could be reversibly disrupted by pathologic or iatrogenic manipulations, with important implications in terms of CNS drug delivery to “multiple drug resistant” brain. This concept of BBB breakdown for therapeutic purposes has also unveiled a previously unrecognized role for BBB failure as a possible etiologic mechanism in epileptogenesis. Finally, a growing body of evidence has shown that inflammatory mechanisms may participate in the pathological changes observed in epileptic brain, with increasing awareness that blood‐borne cells or signals may participate in epileptogenesis by virtue of a leaky BBB. In this article we will review the relationships between BBB function and epilepsy. In particular, we will illustrate consensus and divergence between clinical reality and animal studies.
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Cites
Osmotic Opening of the Blood–Brain Barrier: Principles, Mechanism, and Therapeutic Applications
Rapoport, S. I. (2000) · Cellular and Molecular Neurobiology · doi:10.1023/a:1007049806660 · Cited by 428
Başkaya, M. K., Muralikrishna Rao, A., Doğan, A., Donaldson, D., & Dempsey, R. J. (1997) · Neuroscience Letters · doi:10.1016/s0304-3940(97)00239-5 · Cited by 332
Recent advances in the molecular biology of nucleoside transporters of mammalian cells
Cass, C. E., Young, J. D., & Baldwin, S. A. (1998) · Biochemistry and Cell Biology · doi:10.1139/o98-095 · Cited by 185
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Shlosberg, D., Benifla, M., Kaufer, D., & Friedman, A. (2010) · Nature Reviews Neurology · doi:10.1038/nrneurol.2010.74 · Cited by 897
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Wong, A. D., Ye, M., Levy, A. F., Rothstein, J. D., Bergles, D. E., & Searson, P. C. (2013) · Frontiers in Neuroengineering · doi:10.3389/fneng.2013.00007 · Cited by 662
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Vezzani, A., Aronica, E., Mazarati, A., & Pittman, Q. J. (2013) · Experimental Neurology · doi:10.1016/j.expneurol.2011.09.033 · Cited by 603
Vezzani, A., Maroso, M., Balosso, S., Sanchez, M.-A., & Bartfai, T. (2011) · Brain, Behavior, and Immunity · doi:10.1016/j.bbi.2011.03.018 · Cited by 362
Inflammation in epilepsy: Clinical observations
Aronica, E., & Crino, P. B. (2011) · Epilepsia · doi:10.1111/j.1528-1167.2011.03033.x · Cited by 306
Losartan prevents acquired epilepsy via TGF‐β signaling suppression
Bar‐Klein, G., Cacheaux, L. P., Kamintsky, L., Prager, O., Weissberg, I., Schoknecht, K., Cheng, P., Kim, S. Y., Wood, L., Heinemann, U., et al. (2014) · Annals of Neurology · doi:10.1002/ana.24147 · Cited by 270
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Maroso, M., Balosso, S., Ravizza, T., Liu, J., Bianchi, M. E., & Vezzani, A. (2011) · Journal of Internal Medicine · doi:10.1111/j.1365-2796.2011.02431.x · Cited by 165
Marchi, N., Granata, T., Freri, E., Ciusani, E., Ragona, F., Puvenna, V., Teng, Q., Alexopolous, A., & Janigro, D. (2011) · PLoS ONE · doi:10.1371/journal.pone.0018200 · Cited by 150
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Cramer, S. P., & Larsson, H. B. (2014) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1038/jcbfm.2014.126 · Cited by 117
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Albumin is taken up by hippocampal NG2 cells and astrocytes and decreases gap junction coupling
Braganza, O., Bedner, P., Hüttmann, K., von Staden, E., Friedman, A., Seifert, G., & Steinhäuser, C. (2012) · Epilepsia · doi:10.1111/j.1528-1167.2012.03665.x · Cited by 64
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Metadata
- Authors
- Oby, E., & Janigro, D.
- Venue
- Epilepsia
- Publisher
- Wiley
- Published
- 2006-10-26
- Volume
- 47
- Issue
- 11
- Pages
- 1761-1774
- ISSN
- 0013-9580 (ISSN-L)
- 1528-1167
- OpenAlex
- W1977291679
- Cited by
- 388
- References
- 3
- FWCI
- 9.70
- Type
- journal article
- Language
- en
- Open access
- bronze
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