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一氧化氮对过氧化氢所致听力损失的保护作用 被引量:8

Protective effect of nitric oxide against hydrogen peroxide-induced hearing loss
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摘要 通过全耳蜗灌流法在体观察一氧化氮(N0)能否通过一氧化氮/环磷酸鸟苷(NO/cGMP)途径对抗过氧化氢这种氧自由基所致的听力损失。实验选用耳廓反射灵敏、无耳毒性药物使用史的健康杂色豚鼠(250-350 g)50只,雌雄不拘,随机分为5组,每组10只动物,分别行全耳蜗灌流人工外淋巴液;过氧化氢(H2O2);L-精氨酸(合成NO的底物);H2O2+L-精氨酸;H2O2+L-精氨酸+L-NNA(一氧化氮合成酶的抑制剂),均灌流2 h。通过圆窗龛电极,每隔30 min记录复合动作电位(compound action potential,CAP:由短声Click诱发)阈值,耳蜗微音器电位(cochlear microphonic,CM;由短纯音Tone Burst诱发)幅度,了解耳蜗功能的变化,并分离取出耳蜗基底膜并制备基底膜硬铺片,通过碘化毗啶(PI)和Hoecbst双染色方法,观察耳蜗组织各类细胞损伤情况。结果显示,灌流H2O2+L-精氨酸组的CAP阈移和CM下降幅度值明显低于单独灌流H2O2组,差异有显著性(氏P<0.05);前者形态学观察未见明显的细胞损伤,后者可见大量坏死红染的细胞。H2O1+L-精氨酸+L-NNA组CAP阈移和CM下降幅度与单独灌流H2O2组比较无统计学差异。实验结果提示NO可能通过NO/cGMP途径部分对抗过氧化氢所致的听力损失。 Previous research showed that reactive oxygen species (ROS) play an important role in ototoxity. The present research was to investigate whether nitric oxide, an important neurotransmitter in the inner ear, could prevent hydrogen peroxide-induced hearing loss through the nitric oxide/cyclic GMP pathway in guinea pig cochlea. Fifty adult pigmented guinea pigs (250-350 g) of either sex with positive prier reflex were randomly divided into five groups. All of the animals underwent whole cochlear perfusion for two hours. The solution that was perfused into the cochlear of different group was artificial perilymph (AP) for group 1200 μmol/L 11202 for group 2100 μmol/L L- Arg for group 3, H2O2+L-Arg for group 4 and H2O2+L- Arg+L-NNA for group 5 respectively. Compound action potential (CAP, evoked by click) and cochlear microphonic (CM, evoked by tone burst) were recorded every thirty minutes to show the effects of different reagents on cochlear function. In order to assess cell viability after perfusion, the fluorescent dyes Hoechst that stains all cell nuclei and propidium iodide (PI) that specifically stains nuclei of dead cells, were used. The CAP threshold shifts and CM amplitude decreased after perfusion with H2O2+L-Arg. They were significantly lower than those of H2O2 group. No obvious cell death was noticed after H2O2+L-Arg perfusion, while only 54% of hair cells were alive after H2O2 perfusion. There were no significant differences between the group of H2O2 and that of H2O2+L-Arg+L-NNA group. Our results suggest that nitric oxide may partly be able to protect guinea pigs from hydrogen peroxide-induced hearing loss.
出处 《生理学报》 CAS CSCD 北大核心 2004年第2期237-242,共6页 Acta Physiologica Sinica
基金 This work was supported by the National Natural Science Foundation of China (No.30070812).
关键词 耳蜗 一氧化氮 环磷酸鸟苷 NO/CGMP 全耳蜗灌流 听力损失 保护作用 过氧化氢 cochlea nitric oxide/cyclic GMP pathway the whole cochlea perfusion
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  • 1[1]Ikeda K, Sunose H, Takasaka T. Effects of free radicals on the introcellular calcium in the isolated outer hair cell of the guinea pig cochlear. Acta Otolaryngol (stockh) 1993; 113: 137-141.
  • 2[2]Meneghini. Iron homeostasis, oxidative stress, and DNA damage. Free Radical Biol Med 1997; 23: 783-792.
  • 3[3]Hyslop PA, Hinshaw DB, Schraufstatter IU, Sklar LA, Spragg RG, Cochrane CG. Intracellular calcium homeostasis during hydrogen peroxide injury to cultured P388D1 cells. J Cell Physiol 1986; 129: 356-366.
  • 4[4]Dehne N, Lautermann J, Ten Cate WJ, Rauen U, De Groot H.In vitro effects of hydrogen peroxide on the cochlear neurosensory epithelium of the guinea pig. Hear Res 2000; 143:162-170.
  • 5[5]Jewell SA, Bellomo G, Thor H, Orrenius S, Smith M. Bleb formation in hepatocytes during drug metabolism is caused by disturbances in thiol and calcium ion homeostasis. Since 1982; 217:1257-1259.
  • 6[6]Thor H, Hartzell P, Orrenius S. Potentiation of oxidative cell injury in hepatocytes which have accumulated Ca2+. J Biol Chem 1984; 259: 6612-6615.
  • 7[7]Orrenius S, Mcconkey DJ, Bellomo G, Nicotera P. Role of Ca2+in toxic cell killing. Trends Pharmacol Sci 1989; 10: 281-285.
  • 8[8]Fessenden JD, Schacht J. The nitric oxide/cyclic GMP pathway:A potential major regulator of cochlear physiology. Hear Res 1998; 118: 168-176.
  • 9[9]Gosepath K, Gath I, Maurer J, Pollock JS, Amedee R,Forstermann U, Mann W. Characterization of nitric oxide synthase isoforms expressed in different structures of the guinea pig cochlea. Brain Res 1997; 747: 26-33.
  • 10[10]Hess A, Bbloch W, Huverstuhl J, Su J, Stennert E, Addicks K. Expression of nitric oxide synthase (iNOS/NOS Ⅱ) in the cochlea of guinea pigs after intra tympanical endotoxintreatment. Brain Res 1999; 830:113-122.

同被引文献74

  • 1杨卫平,胡博华.三种检测耳蜗毛细胞死亡模式方法的比较[J].中华耳科学杂志,2004,2(4):301-304. 被引量:11
  • 2李菊香,汪进益,苏海,饶芳,罗伟,吴清华,程晓曙.氧自由基对血管内皮细胞内源性一氧化氮合酶抑制物的影响及卡托普利的作用[J].中国病理生理杂志,2005,21(3):511-513. 被引量:6
  • 3李兴启,贾学斌,曹效平,于红,张瀛.一氧化氮-环磷酸鸟苷通路对耳蜗灵敏度的调节[J].中华耳鼻咽喉头颈外科杂志,2006,41(7):532-536. 被引量:2
  • 4Hatch M, Tsai M, LaRouere MJ, et al. The effects of Carbogen, carbon dioxide, and oxygen on noise-induced hearing loss. Hear Res, 1999, 56(1-2) : 265-272.
  • 5Fessenden JD, Alstchuler RA, Seasholtz AF, et al. Nitric oxide/ cyclic guanosine monophosphate pathway in the peripheral and central auditory system of the rat. J Comp Neurol, 1999, 404: 52-63.
  • 6Flock A, Flock B, Fridberger A, et al. Supporting cells contribute to control of hearing sensitivity. J Neurosci, 1999, 19: 4498-4507.
  • 7Chung JW, Schacht J. ATP and nitric oxide modulate intracellular calcium in isolated pillar cells of the guinea pig cochlea. J Assoc Res Otolaryngol, 2001, 2: 399-407.
  • 8Zhao HB. Connexin26 is responsible for anionic molecule permeability in the cochlea for intercellular signalling and metabolic communications. Eur J Neurosci, 2005, 21 : 1859-1868.
  • 9Matsunobu T, Schacht J. Nitric oxide/cyclic GMP pathway attenuates ATP-evoked intracellular calcium increase in supporting cells of the guinea pig cochlea. J Comp Neurol, 2000, 423: 452-461.
  • 10Fessenden JD, Schacht J. The nitric oxide/cyclic GMP pathway: a potential major regulator of cochlear physiology. Hear Res, 1998, 118(1-2): 165-176.

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