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Differential gene expression in trigeminal ganglia of male and female rats following chronic constriction of the infraorbital nerve

机译:慢性收缩初学神经慢性收缩后雄性雌性大鼠三叉神话中的差异基因表达

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Abstract Background The mechanisms underlying sex‐based differences in pain and analgesia are poorly understood. In this study, we investigated gene expression changes in trigeminal ganglia ( TG ) of male and female rats exposed to infraorbital nerve chronic constriction injury (IoN‐ CCI ). Methods Somatosensory assessments were performed prior to IoN‐ CCI and at selected time points postsurgery. Selected gene expression changes were examined with real‐time quantitative polymerase chain reaction ( RT ‐ PCR ) in ipsilateral TG at 21?days postsurgery. Results Rats exposed to IoN‐ CCI developed significant mechanical allodynia and hyperalgesia on days 19 and 21 postsurgery. During this period, females developed significantly more allodynia but not hyperalgesia compared to males. At 21?days postsurgery, expression levels of 44 of the 84 investigated pain‐related genes in ipsilateral TG were significantly regulated relative to na?ve rats in either sex. Csf1 and Cx3cr1 were up‐regulated in both sexes, but the magnitude of regulation was significantly higher in females ( p ?=?0.02 and p ?=?0.001, respectively). Htr1a and Scn9a were down‐regulated in both sexes, but the down‐regulation was significantly more pronounced in males ( p ?=?0.04 and p ?=?0.02, respectively). Additionally, Cck, Il1a, Pla2g1b and Tnf genes were significantly regulated in females but not in males, and Chrna4 gene was significantly down‐regulated in males but not in females. Conclusions Our findings suggest sex‐dependent gene regulation in response to nerve injury, which may contribute to sex dimorphism of trigeminal neuropathic pain. Further studies are needed to establish gene expression changes over time and correlate these with hormonal and other physiological parameters in male and female. Significance We present novel sex‐specific transcriptional regulation in trigeminal ganglia that may contribute to male‐/female‐based differences in trigeminal neuropathic pain. These findings are expected to open new research horizons, particularly in male versus female targeted therapeutic regimens.
机译:摘要背景痛苦和镇痛症患者潜在的潜在机制很差。在这项研究中,我们研究了暴露于眶腿神经慢性收缩损伤(离子CCI)的雄性和雌性大鼠的三叉甘氨酸(TG)的基因表达变化。方法在离子 - CCI和选定的时间点后进行躯体感觉评估。将所选基因表达在Ipsilidal Tg中的实时定量聚合酶链反应(RT - PCR)在21.Δts后期进行检查。结果暴露于离子的大鼠在第19天和第21天开发了显着的机械异常和痛觉过敏。在此期间,与男性相比,女性显着发展,而不是痛觉过敏。在21岁?天后期,84个研究疼痛相关基因中44中的表达水平相对于任何性别中的Na ve大鼠显着调节。 CSF1和CX3CR1在两性上调,但女性的调节程度明显高(P?= 0.02和P?= 0.001)。 HTR1A和SCN9A在两种性别中受到了下调,但下调在雄性中明显更明显(P?= 0.04和P?= 0.02)。另外,CCK,IL1A,PLA2G1B和TNF基因在雌性中显着调节,但不在男性中,CHRNA4基因在雄性中显着下调,但不是女性。结论我们的研究结果表明,依赖神经损伤的性依赖性基因调节,这可能导致三叉神经性疼痛的性别二态性。需要进一步的研究来建立基因表达随时间的变化,并将这些与血型和女性的荷尔蒙和其他生理参数相关联。意义我们提出了三叉细胞的新型性别转录调节,这可能导致三叉神经病疼痛的男性/女性差异。这些调查结果预计将开辟新的研究视野,特别是在雄性与女性针对治疗方案中。

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  • 来源
    《European journal of pain :》 |2018年第5期|共14页
  • 作者单位

    Department of Diagnostic SciencesRutgersNewark NJ USA;

    The Genomics CenterRutgersNewark NJ USA;

    Eastman Institute for Oral HealthUniversity of Rochester Medical CenterRochester NY USA;

    Eastman Institute for Oral HealthUniversity of Rochester Medical CenterRochester NY USA;

    The Genomics CenterRutgersNewark NJ USA;

    Department of Diagnostic SciencesRutgersNewark NJ USA;

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  • 正文语种 eng
  • 中图分类 诊断学;
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