Skip to main content
Neuroscience Bulletin logoLink to Neuroscience Bulletin
. 2008 Dec 5;24(6):351–358. doi: 10.1007/s12264-008-0711-4

Correlation of free radical level and apoptosis after intracerebral hemorrhage in rats

大鼠脑出血模型中神经细胞凋亡与自由基水平的相关性

Ning Han 1,2, Su-Ju Ding 1,, Tao Wu 1, You-Li Zhu 2
PMCID: PMC5552598  PMID: 19037320

Abstract

Objective

To investigate the correlation of perihematomal free radical level and neuronal apoptosis following the intracerebral hemorrhage (ICH).

Methods

Animals were randomly divided into 4 groups: sham operation group, model group, 1 mg/kg edaravone group, and 3 mg/kg edaravone group. Each group was then divided into seven subgroups, in which the rats were correspondingly killed at 6 h, 12 h, 24 h, 48 h, 72 h, 7 d or 14 d (n = 1 in each subgroup of the sham group, and n = 6 in each subgroup of the other 3 groups). By Horseley-Clarke technique, autoblood (80 μL) were administered into the left caudate putamen of SD rats in a double administration-withdrawal way. Rats in the sham group were needled in but not administered with autoblood. The ICH model was then evaluated by Bederson’s scale. Around the hematoma, the levels of malonaldehyde (MDA) and hydroxyl radical were tested by spectrophotometer, and the process of apoptosis was tested by terminal deoxynucleotidyltransferase-mediated dUTP-biotin nick end labeling (TUNEL) method.

Results

(1) ICH significantly increased the levels of MDA and hydroxyl radicals. Significant differences in MDA and hydroxyl radical contents were observed among the four groups. (2) In the sham group, a small number of TUNEL-positive cells were found. In the other three groups, the TUNEL-positive cells were observed at 6 h, increased significantly at 24 h, and reached peak level at 3 d, then fell profoundly at 7 d, but remained detectable at 14 d. (3) The positive correlation existed between apoptosis and free radical level (r = 0.2003), and existed between apoptosis and MDA content (r = 0.6563) in the brain.

Conclusion

Post-hemorrhagic apoptosis was related to the production of free radicals, indicating that the elevated free radicals following the ICH could induce neuron and glial cell apoptosis.

Keywords: intracerebral hemorrhage, free radical, apoptosis, TUNEL, edaravone

References

  • [1].Qureshi A.I., Suri M.F., Ostrow P.T., Kim S.H., Ali Z., Shatla A.A., et al. Apoptosis as a form of cell death in intracerebral hemorrhage. Neurosurgery. 2003;52:1041–1048. doi: 10.1227/01.NEU.0000057694.96978.BC. [DOI] [PubMed] [Google Scholar]
  • [2].Xue M., Del Bigio M.R. Intracerebral injection of autologous whole blood in rats: time course of inflammation and cell death. Neurosci Lett. 2000;283:230–232. doi: 10.1016/S0304-3940(00)00971-X. [DOI] [PubMed] [Google Scholar]
  • [3].Viña J., Lloret A., Vallés S.L., Borrás C., Badía M.C., Pallardó F.V., et al. Mitochondrial oxidant signalling in Alzheimer’s disease. J Alzheimers Dis. 2007;11:175–181. doi: 10.3233/jad-2007-11205. [DOI] [PubMed] [Google Scholar]
  • [4].Saeed S.A., Shad K.F., Saleem T., Javed F., Khan M.U. Some new prospects in the understanding of the molecular basis of the pathogenesis of stroke. Exp Brain Res. 2007;182:1–10. doi: 10.1007/s00221-007-1050-9. [DOI] [PubMed] [Google Scholar]
  • [5].Han J., Goldstein L.A., Gastman B.R., Rabinovitz A., Wang G.Q., Fang B., et al. Differential involvement of Bax and Bak in TRAIL-mediated apoptosis of leukemic T cells. Leukemia. 2004;18:1671–1680. doi: 10.1038/sj.leu.2403496. [DOI] [PubMed] [Google Scholar]
  • [6].Nutt L.K., Gogvadze V., Uthaisang W., Mirnikjoo B., McConkey D.J., Orrenius S. Indirect effects of Bax and Bak initiate the mitochondrial alterations that lead to cytochrome c release during arsenic trioxide-induced apoptosis. Cancer Biol Ther. 2005;4:459–467. doi: 10.4161/cbt.4.4.1652. [DOI] [PubMed] [Google Scholar]
  • [7].Cox A.G., Pullar J.M., Hughes G., Ledgerwood E.C., Hampton M.B. Oxidation of mitochondrial peroxiredoxin 3 during the initiation of receptor-mediated apoptosis. Free Radic Biol Med. 2008;44:1001–1009. doi: 10.1016/j.freeradbiomed.2007.11.017. [DOI] [PubMed] [Google Scholar]
  • [8].Kandasamy K., Srinivasula S.M., Alnemri E.S., Thompson C.B., Korsmeyer S.J., Bryant J.L., et al. Involvement of proapoptotic molecules Bax and Bak in tumor necrosis factor-related apoptosisinducing ligand (TRAIL)-induced mitochondrial disruption and apoptosis: differential regulation of cytochrome c and Smac/DIABLO release. Cancer Res. 2003;63:1712–1721. [PubMed] [Google Scholar]
  • [9].Deinsberger W., Vogel J., Kuschinsky W., Auer L.M., Böker D.K. Experimental intracerebral hemorrhage: description of a double injection model in rats. Neurol Res. 1996;18:475–477. doi: 10.1080/01616412.1996.11740456. [DOI] [PubMed] [Google Scholar]
  • [10].Zhou Z.H., Qu F., He X., Wang Y.S. An improved rat autoblood cerebral hemorrhage model: twice blood injection/needle withdrawal method. Chin J Clin Neurosci. 2004;12:406–408. [Google Scholar]
  • [11].Bao X.M., Shu S.Z. Rat Brain Stereotaxic Atlas. Beijing: People’s Health Publishing Company; 1991. pp. 39–40. [Google Scholar]
  • [12].Wang Y.F., Li C.C., Cai J.X. Aniracetam attenuates H2O2-induced deficiency of neuron viability, mitochondria potential and hippocampal long-term potentiation of mice in vitro. Neurosci Bull. 2006;22:274–280. [PubMed] [Google Scholar]
  • [13].Folbergrová J., He Q.P., Li P.A., Smith M.L., Siesjö B.K. The effect of α-phenyl-N-tert-butyl nitrone on bioenergetic state in substantia nigra following flurothyl-induced status epilepticus in rats. Neurosci Lett. 1999;266:121–124. doi: 10.1016/S0304-3940(99)00279-7. [DOI] [PubMed] [Google Scholar]
  • [14].Gupta R.C., Milatovic D., Dettbarn W.D. Depletion of energy metabolites following acetylcholinesterase inhibitor-induced status epilepticus: protection by antioxidants. Neurotoxicology. 2001;22:271–282. doi: 10.1016/S0161-813X(01)00013-4. [DOI] [PubMed] [Google Scholar]
  • [15].Kovács R., Schuchmann S., Gabriel S., Kann O., Kardos J., Heinemann U. Free radical-mediated cell damage after experimental status epilepticus in hippocampal slice cultures. J Neurophysiol. 2002;88:2909–2918. doi: 10.1152/jn.00149.2002. [DOI] [PubMed] [Google Scholar]
  • [16].Yuan H., Zheng J.C., Liu P., Zhang S.F., Xu J.Y., Bai L.M. Pathogenesis of Parkinson’s disease: oxidative stress, environmental impact factors and inflammatory processes. Neurosci Bull. 2007;23:125–130. doi: 10.1007/s12264-007-0018-x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • [17].Matz P.G., Fujimura M., Lewen A., Morita-Fujimura Y., Chan P.H. Increased cytochrome c-mediated DNA fragmentation and cell death in manganese-superoxide ismutase-deficient mice after exposure to subarachnoid hemolysate. Stroke. 2001;32:506–515. doi: 10.1161/01.str.32.2.506. [DOI] [PubMed] [Google Scholar]
  • [18].Garrido C., Galluzzi L., Brunet M., Puig P.E., Didelot C., Kroemer G. Mechanisms of cytochrome c release from mitochondria. Cell Death Differ. 2006;13:1423–1433. doi: 10.1038/sj.cdd.4401950. [DOI] [PubMed] [Google Scholar]
  • [19].Tejima E., Zhao B.Q., Tsuji K., Rosell A., van Leyen K., Gonzalez R.G., et al. Astrocytic induction of matrix metalloproteinase-9 and edema in brain hemorrhage. J Cereb Blood Flow Metab. 2007;27:460–468. doi: 10.1038/sj.jcbfm.9600354. [DOI] [PubMed] [Google Scholar]
  • [20].Wang X., Mori T., Sumii T., Lo E.H. Hemoglobin-induced cytotoxicity in rat cerebral cortical neurons: caspase activation and oxidative stress. Stroke. 2002;33:1882–1888. doi: 10.1161/01.STR.0000020121.41527.5D. [DOI] [PubMed] [Google Scholar]
  • [21].Yamamoto S., Teng W., Nishizawa S., Kakiuchi T., Tsukada H. Improvement in cerebral blood flow and metabolism following subarachnoid hemorrhage in response to prophylactic administration of the hydroxyl radical scavenger, AVS, (+/−)-N,N′-propylenedinicotinamide: a positron emission tomography study in rats. J Neurosurg. 2000;92:1009–1015. doi: 10.3171/jns.2000.92.6.1009. [DOI] [PubMed] [Google Scholar]
  • [22].Imperatore C., Germanò A., d’Avella D., Tomasello F., Costa G. Effects of the radical scavenger AVS on behavioral and BBB changes after experimental subarachnoid hemorrhage. Life Sci. 2000;66:779–790. doi: 10.1016/S0024-3205(99)00651-7. [DOI] [PubMed] [Google Scholar]

Articles from Neuroscience Bulletin are provided here courtesy of Springer

RESOURCES