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Neuroprotection from delayed postischemic administration of a metalloporphyrin catalytic antioxidant.

Publication ,  Journal Article
Mackensen, GB; Patel, M; Sheng, H; Calvi, CL; Batinic-Haberle, I; Day, BJ; Liang, LP; Fridovich, I; Crapo, JD; Pearlstein, RD; Warner, DS
Published in: J Neurosci
July 1, 2001

Reactive oxygen species contribute to ischemic brain injury. This study examined whether the porphyrin catalytic antioxidant manganese (III) meso-tetrakis (N-ethylpyridinium-2-yl)porphyrin (MnTE-2-PyP(5+)) reduces oxidative stress and improves outcome from experimental cerebral ischemia. Rats that were subjected to 90 min focal ischemia and 7 d recovery were given MnTE-2-PyP(5+) (or vehicle) intracerebroventricularly 60 min before ischemia, or 5 or 90 min or 6 or 12 hr after reperfusion. Biomarkers of brain oxidative stress were measured at 4 hr after postischemic treatment (5 min or 6 hr). MnTE-2-PyP(5+), given 60 min before ischemia, improved neurologic scores and reduced total infarct size by 70%. MnTE-2-PyP(5+), given 5 or 90 min after reperfusion, reduced infarct size by 70-77% and had no effect on temperature. MnTE-2-PyP(5+) treatment 6 hr after ischemia reduced total infarct volume by 54% (vehicle, 131 +/- 60 mm(3); MnTE-2-PyP(5+), 300 ng, 60 +/- 68 mm(3)). Protection was observed in both cortex and caudoputamen, and neurologic scores were improved. No MnTE-2-PyP(5+) effect was observed if it was given 12 hr after ischemia. MnTE-2-PyP(5+) prevented mitochondrial aconitase inactivation and reduced 8-hydroxy-2'-deoxyguanosine formation when it was given 5 min or 6 hr after ischemia. In mice, MnTE-2-PyP(5+) reduced infarct size and improved neurologic scores when it was given intravenously 5 min after ischemia. There was no effect of 150 or 300 ng of MnTE-2-PyP(5+) pretreatment on selective neuronal necrosis resulting from 10 min forebrain ischemia and 5 d recovery in rats. Administration of a metalloporphyrin catalytic antioxidant had marked neuroprotective effects against focal ischemic insults when it was given up to 6 hr after ischemia. This was associated with decreased postischemic superoxide-mediated oxidative stress.

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Published In

J Neurosci

DOI

EISSN

1529-2401

Publication Date

July 1, 2001

Volume

21

Issue

13

Start / End Page

4582 / 4592

Location

United States

Related Subject Headings

  • Treatment Outcome
  • Rats, Wistar
  • Rats
  • Oxidative Stress
  • Neuroprotective Agents
  • Neurology & Neurosurgery
  • Necrosis
  • Mitochondria
  • Mice, Inbred C57BL
  • Mice
 

Citation

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MLA
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Mackensen, G. B., Patel, M., Sheng, H., Calvi, C. L., Batinic-Haberle, I., Day, B. J., … Warner, D. S. (2001). Neuroprotection from delayed postischemic administration of a metalloporphyrin catalytic antioxidant. J Neurosci, 21(13), 4582–4592. https://doi.org/10.1523/JNEUROSCI.21-13-04582.2001
Mackensen, G. B., M. Patel, H. Sheng, C. L. Calvi, I. Batinic-Haberle, B. J. Day, L. P. Liang, et al. “Neuroprotection from delayed postischemic administration of a metalloporphyrin catalytic antioxidant.J Neurosci 21, no. 13 (July 1, 2001): 4582–92. https://doi.org/10.1523/JNEUROSCI.21-13-04582.2001.
Mackensen GB, Patel M, Sheng H, Calvi CL, Batinic-Haberle I, Day BJ, et al. Neuroprotection from delayed postischemic administration of a metalloporphyrin catalytic antioxidant. J Neurosci. 2001 Jul 1;21(13):4582–92.
Mackensen, G. B., et al. “Neuroprotection from delayed postischemic administration of a metalloporphyrin catalytic antioxidant.J Neurosci, vol. 21, no. 13, July 2001, pp. 4582–92. Pubmed, doi:10.1523/JNEUROSCI.21-13-04582.2001.
Mackensen GB, Patel M, Sheng H, Calvi CL, Batinic-Haberle I, Day BJ, Liang LP, Fridovich I, Crapo JD, Pearlstein RD, Warner DS. Neuroprotection from delayed postischemic administration of a metalloporphyrin catalytic antioxidant. J Neurosci. 2001 Jul 1;21(13):4582–4592.

Published In

J Neurosci

DOI

EISSN

1529-2401

Publication Date

July 1, 2001

Volume

21

Issue

13

Start / End Page

4582 / 4592

Location

United States

Related Subject Headings

  • Treatment Outcome
  • Rats, Wistar
  • Rats
  • Oxidative Stress
  • Neuroprotective Agents
  • Neurology & Neurosurgery
  • Necrosis
  • Mitochondria
  • Mice, Inbred C57BL
  • Mice