期刊文献+

发育早期和成年大鼠背侧纹状体内CRF轴突终末的分布和变化 被引量:2

The distribution patterns of CRF axon terminals in the developing and adult rat dorsal striatum
原文传递
导出
摘要 目的:探讨背侧纹状体(dorsalstriatum)内促肾上腺皮质激素释放因子(CRF)阳性轴突终末和CRF表达的分布特征及年龄变化。方法:采用免疫组织化学、原位杂交、免疫印迹和体视学分析方法,观察分析出生后第1~21日龄(P1-21)及成年(P90)大鼠背侧纹状体内的CRF轴突终末及CRF蛋白含量。结果:背内、背外侧纹状体内含大量CRF轴突终末,背外侧纹状体内的CRF轴突终末更为丰富。这些终末集中位于纹状体的尾部区域,与纹状体主要神经元形成典型的环胞体支配。和成年比较,发育早期(P1—14)背侧纹状体内CRF轴突终末的密度较高(p〈0.05),CRF蛋白表达量以P7组相对最高(P〈0.05)。结论:发育早期背侧纹状体内富含CRF轴突终末,提示CRF是影响纹状体神经元生长发育的因子之一。 Objective: To obseve distribution of corticotropin-releasing factor (CRF) in the dorsal striatum. Methods: Immunohistochemistry, in situ hybridization, Western Blotting and stereological analysis were employed to investigate CRF axonal terminals and CRF expression in the dorsal stratum in immature (postnatal day 1 to 21, P1-21 ) and young adult (PgO) rats. Results: Numerous CRF axonal terminals were detected in the dorsal striatum, including the dorsolateral and dorsomedial parts. Particularly, the CRF axonal terminals were distributed in the posterior regions of the dorsal striatum, and they surrounded the cell bodies of spiny striatum neurons to form a typical perlsomatie innervation. CRF axonal termi- nals are abundant during early development (P1-P14) , and CRF expression was on the highest level in P7 as compared with the adult and others ( P 〈 0.05 ). Conclusion: Robust expression and axonal terminals of CRF are observed in the developing dorsal striatum, suggesting that CRF might be one of factors involving in the differentiation.
出处 《神经解剖学杂志》 CAS CSCD 北大核心 2015年第4期497-504,共8页 Chinese Journal of Neuroanatomy
基金 湖北省“楚天学者计划”基金(2012-12)
关键词 纹状体 促肾上腺皮质激素释放因子 发育 大鼠 striatum corticotropin-releasing factor development rat
  • 相关文献

参考文献17

  • 1Faure A, Leblanc-Veyrac P, El Massioui N. Dopamine agonists in- crease perseverative instrumental responses but do not restore habit formation in a rat model of Parkinsonism[J].Neumscience, 2010, 168 : 477 - 486.
  • 2Wang LP, Li F, Wang D, et al. NMDA receptors in dopaminergic neurons are crucial for habit learning l J]. Neuron, 2011, 72: 1055 - 1066.
  • 3Braun S, Hauber W. Acute stressor effects on goal-directed action in rats [J]. Learn Mere, 2013, 20:700 -709.
  • 4Dias-Ferreira E, Sousa JC, Melo I, et al. Chronic stress causes fro- ntostriatal reorganization and affects decision-making [J].Science, 2009, 325 : 621 -625.
  • 5Gourley SL, Swanson AM, Jacobs AM, et al. Action control is me- diated by prefrontal BDNF and glueocortieoid receptor binding [ J]. Proe Natl Acad Sei USA, 2012, 109:20714 -20719.
  • 6Cohen MX, Frank MJ. Neurecomputational models d basal ganglia function in learning, memory and choice [ J ]. Behav Brain Res, 2009, 199:141 - 156.
  • 7Lucassen PJ, Pruessner J, Sousa N, et al. Neumpathology of stress [J]. Acta Neumpathol, 2014; 127:109 - 135.
  • 8Chen Y, Andres AL, Frotscher M, et al. Tuning syuaptic transmis- sion in the hippocampus by stress: the CRH system [ J]. Front Cell Neur~ci, 2012, 6: 13.
  • 9Omzco-Cabal L, PoUandt S, Liu J, et al. Regulation of synaptic transmission by CRF receptors [J]. Rev Neumsci, 2006, 17:279 -307.
  • 10Leuner B, Shots TJ. Stress, anxiety, and dendritic spines: what are the connections.'? [ J ] Neuroscience, 2013, 251 : 108 - 119.

二级参考文献20

  • 1Brunsort KL, Chert Y, Avishai-Elirter S, et al. Stress and the de- veloping hippooampus: a double-edged sword? [ J]. Mol Neurobi- ol, 2003, 27:121 -136.
  • 2Harrison PL The hippooampus in schizophrertia: a review of the neumpathological evidence and its pathophysiological implications [J]. Psychophannacology, 2004; 174:151 -162.
  • 3McEwen BS. Mood disorders and allostatic load[ J ]. Biol Psychia- try, 2003, 54 : 200 - 207.
  • 4Jogls M, Baram TZ. The neum-symphony of stress [ J ]. Nat Rev Neurosci, 2009, 10:459-466.
  • 5Brunson KL, Kramar E, Lin B, et al. Mechanisms of late-onset cognitive decline after early-life stress [ J ]. J Neurosci, 2005, 25 : 9328 - 9338.
  • 6Rice CJ, Sandman CA, Lenjavi MR, et aL A novel mouse model for acute and long-lasting consequences of early life stress[ J]. En- docrinology, 2008, 149 : 4892 - 4900.
  • 7Magarifios AM, Li C J, Gal Toth J, et al. Effect of brain-derived neurotrophie factor haploinsufficiency on stress-induced remodelingof hippocampal neurons. Hippocampus, 2011, 21:253-264.
  • 8Chen Y, Dub6 CM, Rice CJ, et al. Rapid loss of dendritic spines after stress involves derangement of spine dynamics by corticotropin- releasing hormone[J]. J Neumsci, 2008, 28:2903-2911.
  • 9Chen Y, Rex CS, Rice C J, et al. Correlated memory defects and hippocampal dendritic spine loss after acute stress involve cortico- tmpin-releasing hormone signaling[J]. Pmc Nat] Acad Sci USA, 2010, 107 : 13123 - 13128.
  • 10Vale W, Spiess J, Rivier C, et al. Characterization of a 41-residue ovine hypothalamic peptide that stimulates secretion of corticotropin and beta-endorphin[ J]. Science, 1981, 213 : 1394 - 1397.

共引文献3

同被引文献4

引证文献2

二级引证文献4

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部