Skip to main content
Erschienen in: Translational Stroke Research 2/2017

03.11.2016 | Original Article

Role of Glibenclamide in Brain Injury After Intracerebral Hemorrhage

verfasst von: Bing Jiang, Lin Li, Qianwei Chen, Yihao Tao, Liming Yang, Bo Zhang, John H. Zhang, Hua Feng, Zhi Chen, Jun Tang, Gang Zhu

Erschienen in: Translational Stroke Research | Ausgabe 2/2017

Einloggen, um Zugang zu erhalten

Abstract

Brain edema following intracerebral hemorrhage (ICH) causes severe secondary brain injury, and no efficient pharmacological preventions are available. The present study was designed to demonstrate the neuroprotective effects of glibenclamide on brain edema and key factors of the blood–brain barrier (BBB). The study was divided into two parts. First, we utilized an autoblood-induced rat model to investigate the expression of sulfonylurea receptor 1 (Sur1). Second, rats were randomized into sham, vehicle, and glibenclamide groups. Neurological scores, brain water content, Evans blue extravasation, Morris water maze test, western blots, and immunofluorescence were used to study the effects of glibenclamide. The expression of the Sur1-Trpm4 channel but not the Sur1-KATP channel was increased in the perihematomal tissue following ICH. Glibenclamide administration significantly decreased the brain water content, restored the BBB, and reduced the expression of MMPs. In addition, glibenclamide improved long-term cognitive deficits following ICH. Glibenclamide protected BBB integrity and improved neurological outcomes after ICH by inhibiting the Sur1-Trpm4 channel, which reduces the expression of MMPs and thereby increases BBB tight-junction protein levels. Glibenclamide may have potential to protect the BBB after ICH.
Literatur
6.
7.
8.
Zurück zum Zitat Marble A. Glibenclamide, a new sulphonylurea: whither oral hypoglycaemic agents? Drugs. 1971;1(2):109–15.CrossRefPubMed Marble A. Glibenclamide, a new sulphonylurea: whither oral hypoglycaemic agents? Drugs. 1971;1(2):109–15.CrossRefPubMed
9.
Zurück zum Zitat Chen M, Dong Y, Simard JM. Functional coupling between sulfonylurea receptor type 1 and a nonselective cation channel in reactive astrocytes from adult rat brain. J Neurosci Off J Soc Neurosci. 2003;23(24):8568–77. Chen M, Dong Y, Simard JM. Functional coupling between sulfonylurea receptor type 1 and a nonselective cation channel in reactive astrocytes from adult rat brain. J Neurosci Off J Soc Neurosci. 2003;23(24):8568–77.
11.
Zurück zum Zitat Simard JM, Tsymbalyuk O, Ivanov A, Ivanova S, Bhatta S, Geng Z, et al. Endothelial sulfonylurea receptor 1-regulated NC Ca-ATP channels mediate progressive hemorrhagic necrosis following spinal cord injury. J Clin Invest. 2007;117(8):2105–13. doi:10.1172/JCI32041.CrossRefPubMedPubMedCentral Simard JM, Tsymbalyuk O, Ivanov A, Ivanova S, Bhatta S, Geng Z, et al. Endothelial sulfonylurea receptor 1-regulated NC Ca-ATP channels mediate progressive hemorrhagic necrosis following spinal cord injury. J Clin Invest. 2007;117(8):2105–13. doi:10.​1172/​JCI32041.CrossRefPubMedPubMedCentral
14.
Zurück zum Zitat Simard JM, Geng Z, Woo SK, Ivanova S, Tosun C, Melnichenko L, et al. Glibenclamide reduces inflammation, vasogenic edema, and caspase-3 activation after subarachnoid hemorrhage. Journal of cerebral blood flow and metabolism: official journal of the International Society of Cerebral Blood Flow and Metabolism. 2009;29(2):317–30. doi:10.1038/jcbfm. 2008.120.CrossRef Simard JM, Geng Z, Woo SK, Ivanova S, Tosun C, Melnichenko L, et al. Glibenclamide reduces inflammation, vasogenic edema, and caspase-3 activation after subarachnoid hemorrhage. Journal of cerebral blood flow and metabolism: official journal of the International Society of Cerebral Blood Flow and Metabolism. 2009;29(2):317–30. doi:10.​1038/​jcbfm.​ 2008.​120.CrossRef
17.
Zurück zum Zitat Tan Q, Chen Q, Niu Y, Feng Z, Li L, Tao Y, et al. Urokinase, a promising candidate for fibrinolytic therapy for intracerebral hemorrhage. J Neurosurg. 2016:1–10. doi:10.3171/2016.1.JNS152287. Tan Q, Chen Q, Niu Y, Feng Z, Li L, Tao Y, et al. Urokinase, a promising candidate for fibrinolytic therapy for intracerebral hemorrhage. J Neurosurg. 2016:1–10. doi:10.​3171/​2016.​1.​JNS152287.
20.
Zurück zum Zitat Li L, Tao Y, Tang J, Chen Q, Yang Y, Feng Z, et al. A cannabinoid receptor 2 agonist prevents thrombin-induced blood-brain barrier damage via the inhibition of microglial activation and matrix metalloproteinase expression in rats. Translational stroke research. 2015;6(6):467–77. doi:10.1007/s12975-015-0425-7.CrossRefPubMed Li L, Tao Y, Tang J, Chen Q, Yang Y, Feng Z, et al. A cannabinoid receptor 2 agonist prevents thrombin-induced blood-brain barrier damage via the inhibition of microglial activation and matrix metalloproteinase expression in rats. Translational stroke research. 2015;6(6):467–77. doi:10.​1007/​s12975-015-0425-7.CrossRefPubMed
21.
Zurück zum Zitat Tang J, Chen Q, Guo J, Yang L, Tao Y, Li L, et al. Minocycline attenuates neonatal germinal-matrix-hemorrhage-induced neuroinflammation and brain edema by activating cannabinoid receptor 2. Mol Neurobiol. 2015; doi:10.1007/s12035-015-9154-x. Tang J, Chen Q, Guo J, Yang L, Tao Y, Li L, et al. Minocycline attenuates neonatal germinal-matrix-hemorrhage-induced neuroinflammation and brain edema by activating cannabinoid receptor 2. Mol Neurobiol. 2015; doi:10.​1007/​s12035-015-9154-x.
22.
Zurück zum Zitat Chen Q, Zhang J, Guo J, Tang J, Tao Y, Li L, et al. Chronic hydrocephalus and perihematomal tissue injury developed in a rat model of intracerebral hemorrhage with ventricular extension. Translational stroke research. 2015;6(2):125–32. doi:10.1007/s12975-014-0367-5.CrossRefPubMed Chen Q, Zhang J, Guo J, Tang J, Tao Y, Li L, et al. Chronic hydrocephalus and perihematomal tissue injury developed in a rat model of intracerebral hemorrhage with ventricular extension. Translational stroke research. 2015;6(2):125–32. doi:10.​1007/​s12975-014-0367-5.CrossRefPubMed
23.
Zurück zum Zitat Chen Y, Zhang Y, Tang J, Liu F, Hu Q, Luo C, et al. Norrin protected blood-brain barrier via frizzled-4/beta-catenin pathway after subarachnoid hemorrhage in rats. Stroke; a journal of cerebral circulation. 2015;46(2):529–36. doi:10.1161/STROKEAHA.114.007265.CrossRef Chen Y, Zhang Y, Tang J, Liu F, Hu Q, Luo C, et al. Norrin protected blood-brain barrier via frizzled-4/beta-catenin pathway after subarachnoid hemorrhage in rats. Stroke; a journal of cerebral circulation. 2015;46(2):529–36. doi:10.​1161/​STROKEAHA.​114.​007265.CrossRef
24.
Zurück zum Zitat Tang J, Tao Y, Jiang B, Chen Q, Hua F, Zhang J, et al. Pharmacological preventions of brain injury following experimental germinal matrix hemorrhage: an up-to-date review. Translational stroke research. 2016;7(1):20–32. doi:10.1007/s12975-015-0432-8.CrossRefPubMed Tang J, Tao Y, Jiang B, Chen Q, Hua F, Zhang J, et al. Pharmacological preventions of brain injury following experimental germinal matrix hemorrhage: an up-to-date review. Translational stroke research. 2016;7(1):20–32. doi:10.​1007/​s12975-015-0432-8.CrossRefPubMed
25.
Zurück zum Zitat Zarruk JG, Fernandez-Lopez D, Garcia-Yebenes I, Garcia-Gutierrez MS, Vivancos J, Nombela F, et al. Cannabinoid type 2 receptor activation downregulates stroke-induced classic and alternative brain macrophage/microglial activation concomitant to neuroprotection. Stroke; a journal of cerebral circulation. 2012;43(1):211–9. doi:10.1161/STROKEAHA.111.631044.CrossRef Zarruk JG, Fernandez-Lopez D, Garcia-Yebenes I, Garcia-Gutierrez MS, Vivancos J, Nombela F, et al. Cannabinoid type 2 receptor activation downregulates stroke-induced classic and alternative brain macrophage/microglial activation concomitant to neuroprotection. Stroke; a journal of cerebral circulation. 2012;43(1):211–9. doi:10.​1161/​STROKEAHA.​111.​631044.CrossRef
29.
Zurück zum Zitat Shohami E, Novikov M, Bass R. Long-term effect of HU-211, a novel non-competitive NMDA antagonist, on motor and memory functions after closed head injury in the rat. Brain Res. 1995;674(1):55–62.CrossRefPubMed Shohami E, Novikov M, Bass R. Long-term effect of HU-211, a novel non-competitive NMDA antagonist, on motor and memory functions after closed head injury in the rat. Brain Res. 1995;674(1):55–62.CrossRefPubMed
30.
Zurück zum Zitat Simard JM, Yurovsky V, Tsymbalyuk N, Melnichenko L, Ivanova S, Gerzanich V. Protective effect of delayed treatment with low-dose glibenclamide in three models of ischemic stroke. Stroke; a journal of cerebral circulation. 2009;40(2):604–9. doi:10.1161/STROKEAHA.108.522409.CrossRef Simard JM, Yurovsky V, Tsymbalyuk N, Melnichenko L, Ivanova S, Gerzanich V. Protective effect of delayed treatment with low-dose glibenclamide in three models of ischemic stroke. Stroke; a journal of cerebral circulation. 2009;40(2):604–9. doi:10.​1161/​STROKEAHA.​108.​522409.CrossRef
33.
34.
35.
Zurück zum Zitat Tosun C, Kurland DB, Mehta R, Castellani RJ, deJong JL, Kwon MS, et al. Inhibition of the Sur1-Trpm 4 channel reduces neuroinflammation and cognitive impairment in subarachnoid hemorrhage. Stroke; a journal of cerebral circulation. 2013;44(12):3522–8. doi:10.1161/STROKEAHA.113.002904.CrossRefPubMedCentral Tosun C, Kurland DB, Mehta R, Castellani RJ, deJong JL, Kwon MS, et al. Inhibition of the Sur1-Trpm 4 channel reduces neuroinflammation and cognitive impairment in subarachnoid hemorrhage. Stroke; a journal of cerebral circulation. 2013;44(12):3522–8. doi:10.​1161/​STROKEAHA.​113.​002904.CrossRefPubMedCentral
40.
Zurück zum Zitat Romanic AM, Madri JA. Extracellular matrix-degrading proteinases in the nervous system. Brain Pathol. 1994;4(2):145–56.CrossRefPubMed Romanic AM, Madri JA. Extracellular matrix-degrading proteinases in the nervous system. Brain Pathol. 1994;4(2):145–56.CrossRefPubMed
42.
Zurück zum Zitat Florczak-Rzepka M, Grond-Ginsbach C, Montaner J, Steiner T. Matrix metalloproteinases in human spontaneous intracerebral hemorrhage: an update. Cerebrovasc Dis 2012; 34(4):249–262. doi:10.1159/000341686. Florczak-Rzepka M, Grond-Ginsbach C, Montaner J, Steiner T. Matrix metalloproteinases in human spontaneous intracerebral hemorrhage: an update. Cerebrovasc Dis 2012; 34(4):249–262. doi:10.​1159/​000341686.
44.
Zurück zum Zitat Ortega FJ, Jolkkonen J, Mahy N, Rodriguez MJ. Glibenclamide enhances neurogenesis and improves long-term functional recovery after transient focal cerebral ischemia. Journal of cerebral blood flow and metabolism: official journal of the International Society of Cerebral Blood Flow and Metabolism. 2013;33(3):356–64. doi:10.1038/jcbfm. 2012.166.CrossRef Ortega FJ, Jolkkonen J, Mahy N, Rodriguez MJ. Glibenclamide enhances neurogenesis and improves long-term functional recovery after transient focal cerebral ischemia. Journal of cerebral blood flow and metabolism: official journal of the International Society of Cerebral Blood Flow and Metabolism. 2013;33(3):356–64. doi:10.​1038/​jcbfm.​ 2012.​166.CrossRef
Metadaten
Titel
Role of Glibenclamide in Brain Injury After Intracerebral Hemorrhage
verfasst von
Bing Jiang
Lin Li
Qianwei Chen
Yihao Tao
Liming Yang
Bo Zhang
John H. Zhang
Hua Feng
Zhi Chen
Jun Tang
Gang Zhu
Publikationsdatum
03.11.2016
Verlag
Springer US
Erschienen in
Translational Stroke Research / Ausgabe 2/2017
Print ISSN: 1868-4483
Elektronische ISSN: 1868-601X
DOI
https://doi.org/10.1007/s12975-016-0506-2

Weitere Artikel der Ausgabe 2/2017

Translational Stroke Research 2/2017 Zur Ausgabe

Leitlinien kompakt für die Neurologie

Mit medbee Pocketcards sicher entscheiden.

Seit 2022 gehört die medbee GmbH zum Springer Medizin Verlag

Hirnblutung unter DOAK und VKA ähnlich bedrohlich

17.05.2024 Direkte orale Antikoagulanzien Nachrichten

Kommt es zu einer nichttraumatischen Hirnblutung, spielt es keine große Rolle, ob die Betroffenen zuvor direkt wirksame orale Antikoagulanzien oder Marcumar bekommen haben: Die Prognose ist ähnlich schlecht.

Was nützt die Kraniektomie bei schwerer tiefer Hirnblutung?

17.05.2024 Hirnblutung Nachrichten

Eine Studie zum Nutzen der druckentlastenden Kraniektomie nach schwerer tiefer supratentorieller Hirnblutung deutet einen Nutzen der Operation an. Für überlebende Patienten ist das dennoch nur eine bedingt gute Nachricht.

Thrombektomie auch bei großen Infarkten von Vorteil

16.05.2024 Ischämischer Schlaganfall Nachrichten

Auch ein sehr ausgedehnter ischämischer Schlaganfall scheint an sich kein Grund zu sein, von einer mechanischen Thrombektomie abzusehen. Dafür spricht die LASTE-Studie, an der Patienten und Patientinnen mit einem ASPECTS von maximal 5 beteiligt waren.

Update Neurologie

Bestellen Sie unseren Fach-Newsletter und bleiben Sie gut informiert.