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99mTc-HMPAO SPECT imaging reveals brain hypoperfusion during status epilepticus
被引:6
|作者:
Bascunana, Pablo
[1
,2
,3
]
Wolf, Bettina J.
[1
,4
]
Jahreis, Ina
[1
,4
]
Brackhan, Mirjam
[1
,2
,3
,4
]
Garcia-Garcia, Luis
[5
,6
]
Ross, Tobias L.
[1
]
Bengel, Frank M.
[1
]
Bankstahl, Marion
[4
,7
]
Bankstahl, Jens P.
[1
]
机构:
[1] Hannover Med Sch, Dept Nucl Med, Carl Neuberg Str 1, D-30625 Hannover, Germany
[2] Univ Oslo, Dept Neuropathol, Oslo, Norway
[3] Oslo Univ Hosp, Oslo, Norway
[4] Univ Vet Med, Dept Pharmacol Toxicol & Pharm, Hannover, Germany
[5] Univ Complutense Madrid, Inst Pluridisciplinar, Unidad Cartografia Cerebral, Paseo Juan XXIII 1, Madrid 28040, Spain
[6] Univ Complutense Madrid, Fac Farm, Dept Farmacol Farmacognosia & Bot, Pl Ramon & Cajal S-N, Madrid 28040, Spain
[7] Hannover Med Sch, Inst Lab Anim Sci, Hannover, Germany
关键词:
Brain perfusion;
Pilocarpine;
Neuroimaging;
Epilepsy;
CEREBRAL-BLOOD-FLOW;
RAT;
SEIZURES;
D O I:
10.1007/s11011-021-00843-z
中图分类号:
R5 [内科学];
学科分类号:
1002 ;
100201 ;
摘要:
Status epilepticus (SE) is a clinical emergency with high mortality. SE can trigger neuronal death or injury and alteration of neuronal networks resulting in long-term cognitive decline or epilepsy. Among the multiple factors contributing to this damage, imbalance between oxygen and glucose requirements and brain perfusion during SE has been proposed. Herein, we aimed to quantify by neuroimaging the spatiotemporal course of brain perfusion during and after lithium-pilocarpine-induced SE in rats. To this purpose, animals underwent Tc-99m-HMPAO SPECT imaging at different time points during and after SE using a small animal SPECT/CT system. Tc-99m-HMPAO regional uptake was normalized to the injected dose. In addition, voxel-based statistical parametric mapping was performed. SPECT imaging showed an increase of cortical perfusion before clinical seizure activity onset followed by regional hypo-perfusion starting with the first convulsive seizure and during SE. Twenty-four hours after SE, brain Tc-99m-HMPAO uptake was widely decreased. Finally, chronic epileptic animals showed regionally decreased perfusion affecting hippocampus and cortical sub-regions. Despite elevated energy and oxygen requirements, brain hypo-perfusion is present during SE. Our results suggest that insufficient compensation of required blood flow might contribute to neuronal damage and neuroinflammation, and ultimately to chronic epilepsy generated by SE.
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页码:2597 / 2602
页数:6
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