期刊文献+

模拟斜视矫正术大鼠脑组织c-fos的表达

Expression of c-fos in brain tissues of rats following simulated strabotomy
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摘要 目的:模拟大鼠眼斜视手术脑组织中c-fos的变化,分析c-fos在脑组织不同部位的改变及可能作用机制。方法:实验于2003-07/09在潍坊医学院附属青州医院实验室完成。48只3月龄SD大鼠随机数字表法分为对照组(n=8)和手术组(n=40)。手术组进行右眼模拟眼斜视手术,随机两条动眼肌缩短术,并于术后2h,12h,1d,2d,5d5个时间点采用免疫组织化学染色分别测定各组大鼠脑组织外侧膝状体、嘴侧丘、视区c-fos的变化,c-fos免疫反应阳性神经元的细胞核呈棕黄色,胞浆和核仁均不染色。每只大鼠随机取脑组织切片10张,计数脑组织不同位置c-fos免疫反应阳性细胞数及阳性细胞总和。结果:纳入大鼠48只,均进入结果分析,无脱失。①在损伤眼同侧的外侧膝状体腹侧核、内侧核团和中间核可见c-fos阳性细胞,损伤后2h开始出现(20.58±9.36)个/切片,1d达到高峰(92.36±7.45)个/切片,2d减少(28.19±3.62)个/切片,5d仍有少量c-fos阳性细胞(12.88±3.41)个/切片。与对照组(8.04±3.06)个/切片比较,差异均有显著性意义(P<0.01或P<0.05)。②在损伤眼同侧的嘴侧丘、视区可见c-fos阳性细胞,损伤后2h开始出现(17.28±5.42)和(18.39±4.28)个/切片,1d达到高峰为(83.22±6.75)和(86.17±3.39)个/切片,2d减少为(25.18±4.33)和(29.52±3.27)个/切片,与对照组(9.35±2.98)及(13.72±3.51)个/切片比较,差异均有显著性意义(P<0.01)。5d仍有少量c-fos阳性细胞为(11.47±2.19)和(14.22±3.54)个/切片,与对照组接近,差异无显著性意义。结论:c-fos在脑外侧膝状体、嘴侧丘、视皮质参与损伤作用。脑外侧膝状体c-fos的变化在中枢调节作用中有中介作用,c-fos可能参与引起脑组织改变。 AIM: To simulate the changes of c-fos in brain tissues of rats received strabotomy, and analyze the changes of c-fos in different parts of brain tissues and its possible mechanism. METHODS: The experiment was conducted in the Laboratory of Qingzhou Hospital Affiliated to Weifang Medical College from July to September 2003. Forty-eight SD rats, aged 3 months were randomly divided into control group (n=8) and operation group (n=40). Rats in the operation group received simulated strabotomy on the right eye and shortening of two oculomotor muscles that randomly selected. Changes in pregeniculum, rostral cerebral ganglion and c-fos in visual cortex of brain tissues of rats in all groups were measured with immunohistochemieal stain respectively at 2 hours, 12 hours, 1 day, 2 days and 5 days after the strabotomy. The cellular nucleus of positive neurons in c-fos immune reaction were in buffy, and the endochylema and ehromatospherite were not stained. Ten pieces of brain-tissue sections were randomly selected from each rat, and the number of cofos positive cells in immune reaction of different parts of brain tissues and the total number of positive cells were calculated. RESULTS: A total of 48 enrolled rats were involved in the analysis of results, and no one withdrew from the study.①Expression of c-fos positive cells could be seen'in ventral nucleus, medial nucleus and intermedial nucleus of pregeniculum in the same lateral of injured eye, (20.58±9.36) of which existed on each section at 2 hours after injury, reached the peak (92.36±7.45) per section on the first day, decreased (28.19±3.62) per section on the second day, and there were little c-fos positive cells (12.88±3.41) per section on the fifth day. Compared with the control group (8.04±3.06) per section, the differences were remarkable (P 〈 0.01 or P 〈 0.05). ②The c-fos positive cells could be seen in rostral cerebral ganglion and visual cortex of the same lateral in injured eye. At 2 hours after the injury, (17.28±5.42) and (18.39±4.28) represented in each section, and reached the peak (83.22±6.75) and (86.17±3.39) on the first day, decreased to (25.18±4.33) and (29.52±3.27) on the second day, compared with the control group (9.35±2.98) and (13.72±3.51) per section, the differences were significant (P 〈 0.01). On the fifth day, there were still a small quantity of c-fos positive cells (11.47±2.19) and (14.22±3.54) on each section, which were similar to the control group, and differences were not significant. CONCLUSION: The c-fos in pregeniculum, rostral cerebral ganglion and visual cortex takes part in the injury. The changes of c-fos in pregeniculum play an agent role in the regulation, and c-fos may contribute to the changes of brain tissue.
出处 《中国临床康复》 CSCD 北大核心 2006年第18期107-109,共3页 Chinese Journal of Clinical Rehabilitation
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参考文献10

  • 1赵英.慢性疼痛的生理学基础[J].中国临床康复,2005,9(18):176-176. 被引量:2
  • 2Zhang Y, Qiao JT, Dafny N. et al. c-Fos antisense oligodeoxynucleotide offsets behavioral nociceptive responses and both up-regulations of c-Fos protein and dynorphin a (1-8) in dorsal horn: a study using the formalin test in rats.Int J Neurosci 2005,115(7):935-48
  • 3姚旭,丁新生,吴婷,德伟,袁栎.急性外周神经损伤时大鼠c-fos和c-junmRNA表达的时序性变化[J].中国临床康复,2004,8(31):6905-6907. 被引量:4
  • 4Doya H, Ohtori S, Fujitani M, et al. c-Jun N-terminal kinase activation in dorsal root ganglion contributes to pain hypersensitivity.Biochem Biophys Res Commun 2005,335(1):132-8
  • 5秦晓辉,张宏.病理性疼痛中枢敏感化细胞内的信号转导[J].中国临床康复,2005,9(17):145-147. 被引量:12
  • 6Coggeshall RE. Fos, nociception and the dorsal hom.Prog Neurobiol 2005:77(5):299-352
  • 7Knight YE, Classey JD, Lasalandra MP, et al. Patterns of fos expression in the rostral medulla and caudal pans evoked by noxious craniovascalar stimulation and periaqueductal gray stimulation in the cat.Brain Res 2005,1045(1-2):1-11
  • 8Anseloni VC, Ben K,Dubner B, et al. A brainstem substrate for analgesia elicited by intraoral sucrose.Neuroscience 2005,133(1):231-43
  • 9Chattipakom S, Chattipakom N, Light AR,et al. Comparison of Fos expression within the ferret's spinal trigeminal nuclear complex evoked by electrical or noxious-thermal pulpal stimulation.J Pain 2005,6(9):569-80
  • 10Strassman AM, Vos BP, Mineta Y, et al. Fos-like immunoreactivity in the superficial medullary dorsal horn induced by noxious and innocuous thermal stimulation of facial skin in the rat.J Neurophysiol 1993,70(5):1811-21

二级参考文献28

  • 1Ji RR, Rupp F. Phosphorylation of transcription factor CREB in rat spinal cord after formalin-induced hyperalgesia: relationship to c-fos induction. J Neurosci 1997; 17(5): 1776 -85
  • 2Chan CF, Sun WZ, Lin JK, et al. Activation of transcription factors of nuclear factor kappa B, activator protein-1 and octamer factors in hyperalgesia. Eur J Pharmacol 2000; 402 ( 1 - 2 ): 61 - 8
  • 3Lee KM, Kang BS, Lee HL, et al. Spinal NF-kB activation induces COX-2 upregulation and contributes to inflammatory pain hypersensitivity. Eur J Neurosci 2004; 19(12): 3375 -81
  • 4Laughlin TM, Bethea JR, Yezierski RP, et al. Cytokine involvement in dynorphin-induced allodynia. Pain 2000; 84(2 - 3): 159 - 67
  • 5Brenner GJ, Ji RR, Shaffer S, et al. Peripheral noxious stimulation induces phosphorylation of the NMDA receptor NR1 subunit at the PKC-dependent site, serine-896, in spinal cord dorsal horn neurons. Eur J Neurosci 2004; 20(2): 375 -84
  • 6Wajima Z, Hua XY, Yaksh TL. Inhibition of spinal protein kinase C blocks substance P-mediated hyperalgesia. Brain Res 2000; 877 (2): 314 - 21
  • 7Yajima Y, Narita M, Shimamura M, et al. Differential involvement of spinal protein kinase C and protein kinase A in neuropathic and inflammatory pain in mice. Brain Res 2003;992(2): 288-93
  • 8Malmberg AB, Chen C, Tonegawa S, et al. Preserved acute pain and reduced neuropathic pain in mice lacking PKCgamma. Science 1997; 278 (5336): 279 - 83
  • 9Zou X, Lin Q, Willis WD. Role of protein kinase A in phosphorylation of NMDA receptor 1 subunits in dorsal horn and spinothalamic tract neurons after intradermal injection of capsaicin in rats. Neuroscience 2002; 115(3): 775 - 86
  • 10Aley KO, Levine JD. Role of protein kinase A in the maintenance of inflammatory pain. J Neurosci 1999; 19(6): 2181 -6

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