Oxidative damage following cerebral ischemia depends on reperfusion - a biochemical study in rat

D A Nita; V Nita; S Spulber; M Moldovan; D P Popa; A M Zagrean; L Zagrean

Oxidative damage following cerebral ischemia depends on reperfusion - a biochemical study in rat

D A Nita, V Nita, S Spulber, M Moldovan, D P Popa, A M Zagrean, L Zagrean

Motor Control

Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › peer review

139 Citationer (Scopus)

Abstract

Udgivelsesdato: null-null

Originalsprog	Engelsk
Tidsskrift	Journal of Cellular and Molecular Medicine
Vol/bind	5
Udgave nummer	2
Sider (fra-til)	163-70
Antal sider	7
ISSN	1582-1838
Status	Udgivet - 2002

Bibliografisk note

Keywords: Animals; Antioxidants; Brain; Brain Ischemia; Catalase; Electroencephalography; Electrophysiology; Free Radicals; Glutathione Peroxidase; Ischemia; Male; Oxidative Stress; Rats; Rats, Wistar; Reperfusion Injury; Superoxide Dismutase

Citationsformater

@article{ca3bdbd0b45311df825b000ea68e967b,

title = "Oxidative damage following cerebral ischemia depends on reperfusion - a biochemical study in rat",

abstract = "The extent of brain injury during reperfusion appears to depend on the experimental pattern of ischemia/reperfusion. The goals of this study were: first, to identify the rate of free radicals generation and the antioxidant activity during ischemia and reperfusion by means of biochemical measurement of lipid peroxidation (LPO) and both enzymatic (superoxide dismutase - SOD, catalase - CAT, glutathione peroxidase - GPx) and non-enzymatic antioxidants activity (glutathione - GSH); and second, to try to find out how the pattern of reperfusion may influence the balance between free radical production and clearance. Wistar male rats were subject of four-vessel occlusion model (Pulsinelly & Brierley) cerebral blood flow being controlled by means of two atraumatic arterial microclamps placed on carotid arteries. The level of free radicals and the antioxidant activity were measured in ischemic rat brain tissue homogenate using spectrophotometrical techniques. All groups subjected to ischemia shown an increase of LPO and a reduction of the activity of enzymatic antioxidative systems (CAT, GPx, SOD) and non-enzymatic systems (GSH). For both groups subjected to ischemia and reperfusion, results shown an important increase of LPO but less significant than the levels found in the group with ischemia only. Statistically relevant differences (p<0.01) between continuous reperfusion and fragmented reperfusion were observed concerning the LPO, CAT, SOD and GSH levels, oxidative aggression during fragmented reperfusion being more important.",

author = "Nita, {D A} and V Nita and S Spulber and M Moldovan and Popa, {D P} and Zagrean, {A M} and L Zagrean",

note = "Keywords: Animals; Antioxidants; Brain; Brain Ischemia; Catalase; Electroencephalography; Electrophysiology; Free Radicals; Glutathione Peroxidase; Ischemia; Male; Oxidative Stress; Rats; Rats, Wistar; Reperfusion Injury; Superoxide Dismutase",

year = "2002",

language = "English",

volume = "5",

pages = "163--70",

journal = "Journal of Cellular and Molecular Medicine",

issn = "1582-1838",

publisher = "Wiley-Blackwell",

number = "2",

}

TY - JOUR

T1 - Oxidative damage following cerebral ischemia depends on reperfusion - a biochemical study in rat

AU - Nita, D A

AU - Nita, V

AU - Spulber, S

AU - Moldovan, M

AU - Popa, D P

AU - Zagrean, A M

AU - Zagrean, L

N1 - Keywords: Animals; Antioxidants; Brain; Brain Ischemia; Catalase; Electroencephalography; Electrophysiology; Free Radicals; Glutathione Peroxidase; Ischemia; Male; Oxidative Stress; Rats; Rats, Wistar; Reperfusion Injury; Superoxide Dismutase

PY - 2002

Y1 - 2002

N2 - The extent of brain injury during reperfusion appears to depend on the experimental pattern of ischemia/reperfusion. The goals of this study were: first, to identify the rate of free radicals generation and the antioxidant activity during ischemia and reperfusion by means of biochemical measurement of lipid peroxidation (LPO) and both enzymatic (superoxide dismutase - SOD, catalase - CAT, glutathione peroxidase - GPx) and non-enzymatic antioxidants activity (glutathione - GSH); and second, to try to find out how the pattern of reperfusion may influence the balance between free radical production and clearance. Wistar male rats were subject of four-vessel occlusion model (Pulsinelly & Brierley) cerebral blood flow being controlled by means of two atraumatic arterial microclamps placed on carotid arteries. The level of free radicals and the antioxidant activity were measured in ischemic rat brain tissue homogenate using spectrophotometrical techniques. All groups subjected to ischemia shown an increase of LPO and a reduction of the activity of enzymatic antioxidative systems (CAT, GPx, SOD) and non-enzymatic systems (GSH). For both groups subjected to ischemia and reperfusion, results shown an important increase of LPO but less significant than the levels found in the group with ischemia only. Statistically relevant differences (p<0.01) between continuous reperfusion and fragmented reperfusion were observed concerning the LPO, CAT, SOD and GSH levels, oxidative aggression during fragmented reperfusion being more important.

AB - The extent of brain injury during reperfusion appears to depend on the experimental pattern of ischemia/reperfusion. The goals of this study were: first, to identify the rate of free radicals generation and the antioxidant activity during ischemia and reperfusion by means of biochemical measurement of lipid peroxidation (LPO) and both enzymatic (superoxide dismutase - SOD, catalase - CAT, glutathione peroxidase - GPx) and non-enzymatic antioxidants activity (glutathione - GSH); and second, to try to find out how the pattern of reperfusion may influence the balance between free radical production and clearance. Wistar male rats were subject of four-vessel occlusion model (Pulsinelly & Brierley) cerebral blood flow being controlled by means of two atraumatic arterial microclamps placed on carotid arteries. The level of free radicals and the antioxidant activity were measured in ischemic rat brain tissue homogenate using spectrophotometrical techniques. All groups subjected to ischemia shown an increase of LPO and a reduction of the activity of enzymatic antioxidative systems (CAT, GPx, SOD) and non-enzymatic systems (GSH). For both groups subjected to ischemia and reperfusion, results shown an important increase of LPO but less significant than the levels found in the group with ischemia only. Statistically relevant differences (p<0.01) between continuous reperfusion and fragmented reperfusion were observed concerning the LPO, CAT, SOD and GSH levels, oxidative aggression during fragmented reperfusion being more important.

M3 - Journal article

C2 - 12067499

VL - 5

SP - 163

EP - 170

JO - Journal of Cellular and Molecular Medicine

JF - Journal of Cellular and Molecular Medicine

SN - 1582-1838

IS - 2

ER -