Neuroprotective Effects of N-acetylcysteine on Experimental Closed Head Trauma in Rats

被引:0
作者
Tufan Hicdonmez
Mehmet Kanter
Mehmet Tiryaki
Turgay Parsak
Sebahattin Cobanoglu
机构
[1] Trakya University,Faculty of Medicine, Department of Neurosurgery
[2] Trakya University,Faculty of Medicine, Department of Histology and Embryology
[3] Trakya University,Faculty of Medicine, Department of Histology and Embryology
来源
Neurochemical Research | 2006年 / 31卷
关键词
Trauma; Brain tissue; MDA; Antioxidant enzyme activity; -acetylcysteine; Caspase-3; Rat;
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学科分类号
摘要
N-acetylcysteine (NAC) is a precursor of glutathione, a potent antioxidant, and a free radical scavenger. The beneficial effect of NAC on nervous system ischemia and ischemia/reperfusion models has been well documented. However, the effect of NAC on nervous system trauma remains less understood. Therefore, we aimed to investigate the therapeutic efficacy of NAC with an experimental closed head trauma model in rats. Thirty-six adult male Sprague–Dawley rats were randomly divided into three groups of 12 rats each: Group I (control), Group II (trauma-alone), and Group III (trauma+NAC treatment). In Groups II and III, a cranial impact was delivered to the skull from a height of 7 cm at a point just in front of the coronal suture and over the right hemisphere. Rats were sacrificed at 2 h (Subgroups I-A, II-A, and III-A) and 12 h (Subgroups I-B, II-B, and III-B) after the onset of injury. Brain tissues were removed for biochemical and histopathological investigation. The closed head trauma significantly increased tissue malondialdehyde (MDA) levels (P<0.05), and significantly decreased tissue superoxide dismutase (SOD) and glutathione peroxidase (GPx) activities (P<0.05), but not tissue catalase (CAT) activity, when compared with controls. The administration of a single dose of NAC (150 mg/kg) 15 min after the trauma has shown protective effect via decreasing significantly the elevated MDA levels (P<0.05) and also significantly (P<0.05) increasing the reduced antioxidant enzyme (SOD and GPx) activities, except CAT activity. In the trauma-alone group, the neurons became extensively dark and degenerated into picnotic nuclei. The morphology of neurons in the NAC treatment group was well protected. The number of neurons in the trauma-alone group was significantly less than that of both the control and trauma+NAC treatment groups. In conclusion, the NAC treatment might be beneficial in preventing trauma-induced oxidative brain tissue damage, thus showing potential for clinical implications.
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页码:473 / 481
页数:8
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共 248 条
  • [31] Ruberg M(2005)The antioxidants alpha-lipoic acid and Neurochem Res 30 737-752
  • [32] Mirabella M(2000)-acetylcysteine reverse memory impairment and brain oxidative stress in aged SAMP8 mice Cardiovasc Res 47 537-548
  • [33] Di Giovanni S(2003)-acetylcysteine prevents endotoxin-induced degeneration of oligodendrocyte progenitors and hypomyelination in developing rat brain Brain Res 971 1-8
  • [34] Silvestri G(2003)Sensory neuroprotection, mitochondrial preservation, and therapeutic potential of Acta Pharmacol Sin 24 1125-1130
  • [35] Tonali P(2004)-acetyl-cysteine after nerve injury J Neurosci Res 76 519-527
  • [36] Servidei S(1988)Protection against cisplatin-induced ototoxicity by Crit Care Med 16 258-265
  • [37] Villa P(1979)-acetylcysteine in a rat model Anal Biochem 95 351-358
  • [38] Kaufmann SH(1951)Effect of antioxidant diets on mitochondrial gene expression in rat brain during aging J Biol Chem 193 265-275
  • [39] Earnshaw WC(1988)Effects of Clin Chem 34 497-500
  • [40] Allen JW(1967)-acetylcysteine in a rat model of ischemia and reperfusion injury J Lab Clin Med 70 158-169