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Pitfalls of Commonly Used Ischemic and Dementia Models Due to Early Seizure by Carotid Ligation

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Specialties Neurology
Neurosurgery
Date 2021 Apr 1
PMID 33790129
Citations 1
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Abstract

While the bilateral common carotid artery (CCA) ligation model is widely used in cerebrovascular disease and dementia studies, it can frequently cause seizures. We examined the validity of seizure as an experimental model of ischemia. Eight-week-old male Wistar and Sprague-Dawley (SD) rats were implanted with electrocorticography (ECoG) electrodes and bilateral CCA ligation was performed and compared to the sham groups. ECoG monitoring was used to confirm the seizure discharge and count the number of spikes in the interictal phase 2 h after ligation, followed by power spectral analysis. Magnetic resonance imaging (MRI) was performed 6 h after bilateral CCA ligation to assess fractional anisotropy (FA), apparent diffusion coefficient (ADC), and cerebral blood flow (CBF) values. Magnetic resonance spectroscopy (MRS) was also performed and the ischemic parameters and electrophysiological changes were compared. The Wistar rat group had significantly higher mortality, frequency of seizures, incidence of non-convulsive seizures, and number of spikes in the interictal period compared to those in the SD rat group. Power spectral analysis showed increased power in the delta band in both Wistar and SD rat groups. MRI, after CCA ligation, showed significantly lower ADC values, lower glutamine and glutamate levels, and higher lactate values in Wistar rats, although there was no difference in FA values. Metabolic and electrophysiological changes after CCA ligation differed according to the rat strain. Wistar rats were prone to increased lactate and decreased glutamine and glutamate levels and the development of status epilepticus. Seizures can affect the results of ischemic experiments.

Citing Articles

Microbleeds Due to Reperfusion Enhance Early Seizures after Carotid Ligation in a Rat Ischemic Model.

Saito T, Mikami T, Hirano T, Nagahama H, Enatsu R, Komatsu K Neurol Med Chir (Tokyo). 2023; 63(6):228-235.

PMID: 37019650 PMC: 10325778. DOI: 10.2176/jns-nmc.2022-0372.

References
1.
Herman S . Epilepsy after brain insult: targeting epileptogenesis. Neurology. 2002; 59(9 Suppl 5):S21-6. DOI: 10.1212/wnl.59.9_suppl_5.s21. View

2.
Hirano T, Enatsu R, Iihoshi S, Mikami T, Honma T, Ohnishi H . Effects of Hemosiderosis on Epilepsy Following Subarachnoid Hemorrhage. Neurol Med Chir (Tokyo). 2018; 59(1):27-32. PMC: 6350000. DOI: 10.2176/nmc.oa.2018-0125. View

3.
Ueno M, Chiba Y, Matsumoto K, Murakami R, Fujihara R, Kawauchi M . Blood-brain barrier damage in vascular dementia. Neuropathology. 2015; 36(2):115-24. DOI: 10.1111/neup.12262. View

4.
Niu H, Wang J, Wang D, Miao J, Li H, Liu Z . The Orally Active Noncompetitive AMPAR Antagonist Perampanel Attenuates Focal Cerebral Ischemia Injury in Rats. Cell Mol Neurobiol. 2017; 38(2):459-466. PMC: 11481974. DOI: 10.1007/s10571-017-0489-x. View

5.
Farkas E, Luiten P, Bari F . Permanent, bilateral common carotid artery occlusion in the rat: a model for chronic cerebral hypoperfusion-related neurodegenerative diseases. Brain Res Rev. 2007; 54(1):162-80. DOI: 10.1016/j.brainresrev.2007.01.003. View