FeTPPS protects against global cerebral ischemic-reperfusion injury in gerbils.

Abstract:

:Neuronal damage following cerebral ischemia is mediated by various mechanisms, among which nitrosative stress plays an important role. Peroxynitrite, a powerful oxidant, contributes heavily to the neuronal damage in cerebral ischemic-reperfusion (IR) injury. In the present study, we have investigated the neuroprotective effects of a peroxynitrite decomposition catalyst, 5,10,15,20-tetrakis(4-sulfonatophenyl) porphyrinato iron(III) [FeTPPS] in global cerebral IR injury in gerbils. Neurological damage was significantly attenuated by FeTPPS treatment (1 and 3mgkg(-1), i.p.) as evident from reduction in neurological symptoms, hyperlocomotion, memory impairment and CA1 hippocampal neuronal damage in IR challenged gerbils. FeTPPS treatment also attenuated the increased malondialdehyde (MDA) levels and terminal deoxynucleotidyl transferase-mediated dUTP nick end labeling (TUNEL) positive cells after cerebral IR injury. Results of this study demonstrates the neuroprotective activity of FeTPPS in global cerebral IR injury and its neuroprotective effects may be attributed to reduction in oxidative stress and DNA fragmentation.

journal_name

Pharmacol Res

journal_title

Pharmacological research

authors

Sharma SS,Dhar A,Kaundal RK

doi

10.1016/j.phrs.2007.01.002

subject

Has Abstract

pub_date

2007-04-01 00:00:00

pages

335-42

issue

4

eissn

1043-6618

issn

1096-1186

pii

S1043-6618(07)00016-3

journal_volume

55

pub_type

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