The use of spreading depression waves for acute and long-term monitoring of the penumbra zone of focal ischemic damage in rats
Jazyk angličtina Země Spojené státy americké Médium print
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
8623001
PubMed Central
PMC39677
DOI
10.1073/pnas.93.8.3710
Knihovny.cz E-zdroje
- MeSH
- arteriae cerebrales MeSH
- časové faktory MeSH
- elektrofyziologie MeSH
- evokované potenciály MeSH
- ischemie mozku etiologie patologie patofyziologie MeSH
- krysa rodu Rattus MeSH
- modely nemocí na zvířatech MeSH
- mozková kůra patofyziologie MeSH
- neurotransmiterové látky metabolismus MeSH
- zvířata MeSH
- Check Tag
- krysa rodu Rattus MeSH
- mužské pohlaví MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- neurotransmiterové látky MeSH
Slow potential recording was used for long-term monitoring of the penumbra zone surrounding an ischemic region produced by middle cerebral artery (MCA) occlusion in adult hooded rats (n = 32). Four capillary electrodes (El-E4) were chronically implanted at 2-mm intervals from AP -3, L 2 (El) to AP 0, L 5 (E4). Spontaneous or evoked slow potential waves of spreading depression (SD) were recorded during and 4 h after a 1-h MCA occlusion and at 2- to 3-day intervals afterward for 3 weeks. Duration of the initial focal ischemic depolarization was maximal at E4 and decreased with distance from the focus. SD waves in the penumbra zone were high at El and E2, low and prolonged at E3, and almost absent at E4. Amplitude of elicited SD waves was further reduced 3 days later and slowly increased in the following week. Cortical areas displaying marked reduction of SD waves in the first days after MCA occlusion either remained low or showed substantial (60%) recovery, the probability of which decreased with the duration of the initial focal ischemic depolarization and increased with the distance from the focus. It is concluded that the outcome of ischemia monitored by long-term SD recovery in the perifocal region can be partly predicted from the acute signs of MCA occlusion.
Zobrazit více v PubMed
Electroencephalogr Clin Neurophysiol. 1987 Apr;66(4):440-7 PubMed
An Acad Bras Cienc. 1984 Dec;56(4):495-504 PubMed
Pflugers Arch Gesamte Physiol Menschen Tiere. 1957;264(4):325-34 PubMed
Brain Res. 1972 Apr 14;39(1):255-9 PubMed
Brain Res. 1987 Dec 29;437(2):360-4 PubMed
J Cereb Blood Flow Metab. 1994 Jan;14(1):12-9 PubMed
Physiol Rev. 1985 Jan;65(1):101-48 PubMed
Brain Res. 1988 Aug 9;457(2):226-40 PubMed
J Cereb Blood Flow Metab. 1986 Oct;6(5):607-15 PubMed
J Cereb Blood Flow Metab. 1992 Sep;12(5):727-33 PubMed
Am J Physiol. 1953 Apr;173(1):171-5 PubMed
Neurochem Pathol. 1988 Jul-Dec;9:195-209 PubMed
J Neurosci. 1991 Apr;11(4):1049-56 PubMed
Acta Neurol Scand. 1988 Feb;77(2):81-101 PubMed
Naunyn Schmiedebergs Arch Exp Pathol Pharmakol. 1957;231(6):550-61 PubMed
Brain Res. 1990 Jun 11;519(1-2):351-4 PubMed
J Cereb Blood Flow Metab. 1992 Mar;12(2):223-9 PubMed
Brain Res. 1993 Mar 26;606(2):251-8 PubMed
J Cereb Blood Flow Metab. 1989 Apr;9(2):127-40 PubMed
J Cereb Blood Flow Metab. 1991 Jan;11(1):88-98 PubMed
Am J Physiol. 1964 Oct;207:921-4 PubMed
J Cereb Blood Flow Metab. 1994 Mar;14(2):301-11 PubMed
J Cereb Blood Flow Metab. 1988 Oct;8(5):757-62 PubMed
J Cereb Blood Flow Metab. 1992 May;12(3):371-9 PubMed
J Cereb Blood Flow Metab. 1994 Jan;14(1):20-8 PubMed