Department of Anesthesia, Critical Care, and Pain Medicine, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts, USA.
Antioxid Redox Signal. 2011 Jul 15;15(2):343-52. doi: 10.1089/ars.2010.3671. Epub 2011 Apr 5.
Parkinson's disease is one of the major neurodegenerative disorders. Neurotoxin 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP) can cause Parkinson's disease-like symptoms and biochemical changes in humans and animals. Hydrogen sulfide (H(2)S) has been shown to protect neurons. The goal of this study was to examine the effects of inhaled H(2)S in a mouse model of Parkinson's disease induced by MPTP. Male C57BL/6J mice received MPTP at 80 mg/kg and breathed air with or without 40 ppm H(2)S for 8 h/day for 7 days. Administration of MPTP induced movement disorder and decreased tyrosine hydroxylase (TH)-containing neurons in the substantia nigra and striatum in mice that breathed air. Inhalation of H(2)S prevented the MPTP-induced movement disorder and the degeneration of TH-containing neurons. Inhaled H(2)S also prevented apoptosis of the TH-containing neurons and gliosis in nigrostriatal region after administration of MPTP. The neuroprotective effect of inhaled H(2)S after MPTP administration was associated with upregulation of genes encoding antioxidant proteins, including heme oxygenase-1 and glutamate-cysteine ligase. These observations suggest that inhaled H(2)S prevents neurodegeneration in a mouse model of Parkinson's disease induced by MPTP, potentially via upregulation of antioxidant defense mechanisms and inhibition of inflammation and apoptosis in the brain.
帕金森病是主要的神经退行性疾病之一。神经毒素 1-甲基-4-苯基-1,2,3,6-四氢吡啶(MPTP)可引起人类和动物帕金森病样症状和生化变化。硫化氢(H₂S)已被证明可保护神经元。本研究的目的是在 MPTP 诱导的帕金森病小鼠模型中研究吸入 H₂S 的作用。雄性 C57BL/6J 小鼠接受 80mg/kg 的 MPTP,并在 7 天内每天呼吸空气或 40ppm 的 H₂S 8 小时。MPTP 给药诱导运动障碍,并减少了呼吸空气的小鼠黑质和纹状体中含酪氨酸羟化酶(TH)的神经元。吸入 H₂S 可预防 MPTP 诱导的运动障碍和含 TH 的神经元变性。吸入 H₂S 还可预防 MPTP 给药后黑质纹状体区域中 TH 神经元的凋亡和神经胶质增生。MPTP 给药后吸入 H₂S 的神经保护作用与抗氧化蛋白(包括血红素加氧酶-1 和谷胱甘肽半胱氨酸连接酶)编码基因的上调有关。这些观察结果表明,吸入 H₂S 可预防 MPTP 诱导的帕金森病小鼠模型中的神经退行性变,可能通过上调抗氧化防御机制以及抑制大脑中的炎症和细胞凋亡来实现。