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In DRG11 knock-out mice, trigeminal cell death is extensive and does not account for failed brainstem patterning.在DRG11基因敲除小鼠中,三叉神经细胞死亡广泛,且并非脑干模式形成失败的原因。
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大鼠脑桥间极亚核中的结构 - 功能关系。X. 出生时眶下神经损伤后 spared 触须投射扩大的潜在机制。

Structure-function relationships in rat brainstem subnucleus interpolaris. X. Mechanisms underlying enlarged spared whisker projections after infraorbital nerve injury at birth.

作者信息

Jacquin M F, Zahm D S, Henderson T A, Golden J P, Johnson E M, Renehan W E, Klein B G

机构信息

Department of Anatomy and Neurobiology, St. Louis University School of Medicine, Missouri 63104.

出版信息

J Neurosci. 1993 Jul;13(7):2946-64. doi: 10.1523/JNEUROSCI.13-07-02946.1993.

DOI:10.1523/JNEUROSCI.13-07-02946.1993
PMID:7687282
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6576669/
Abstract

Prior studies indicate that the central projections of noninfraorbital vibrissae occupy greater than normal transverse areas in the rat trigeminal brainstem complex after infraorbital nerve section at birth. Here, we assessed the development of this phenomenon and possible underlying mechanisms. Cytochrome oxidase patches representing spared supraorbital (SO) or posteroorbital (PO) whiskers in the trigeminal subnucleus interpolaris (SpVi) were not reliably larger than those on the control side 24 hr after the infraorbital lesion. By 72 hr, SO and PO patches were 91% and 28% larger than those on the control side. Reliable increases were also observed on postnatal day 5 (PND5), PND7, and PND10 for the SO (59%, 65%, 66%) and PO (23%, 44%, 51%) patches. To test the hypothesis that central reorganization reflects the maintenance of peripheral supernumerary axons, myelinated and unmyelinated axons in SO vibrissa follicles were counted at PND0, PND7, PND17, and PND60. A corollary hypothesis, that peripheral regeneration errors result in both SO and surviving infraorbital axons, contributing to central SO patches, was tested with retrograde double-labeling methods. Both hypotheses were rejected. Thus, enlargement of SO patches is not due to either the maintenance of an immature peripheral innervation pattern, or regeneration of infraorbital axons into SO follicles. To determine if the enlargement of SO and PO patches produced by infraorbital nerve section is due to an activity-dependent competitive disadvantage imposed upon infraorbital afferents, TTX or bupivicaine was applied to the intact infraorbital nerve over the first 5-9 postnatal days. Brainstem maps developed normally and SO and PO patch areas were unaffected. Thus, impulse activity-based mechanisms do not appear to contribute to injury-induced patch enlargement. To test the hypothesis that patch enlargement is due to central collateral reorganization, intra-axonal recording and staining methods were applied to control and spared-whisker primary afferents in adult rats. Total bouton or collateral numbers did not differ in SpVi; however, arbor areas were reliably larger in experimental (14,879 +/- 350 microns 2) versus control (5527 +/- 1811 microns 2) fibers.(ABSTRACT TRUNCATED AT 400 WORDS)

摘要

先前的研究表明,出生时切断眶下神经后,大鼠三叉神经脑干复合体中非眶下触须的中枢投射占据的横向面积大于正常水平。在此,我们评估了这一现象的发展过程及其可能的潜在机制。在眶下损伤24小时后,三叉神经脑桥核间亚核(SpVi)中代表保留的眶上(SO)或眶后(PO)触须的细胞色素氧化酶斑并不比对照侧可靠地更大。到72小时时,SO和PO斑分别比对照侧大91%和28%。在出生后第5天(PND5)、PND7和PND10时,SO(分别为59%、65%、66%)和PO(分别为23%、44%、51%)斑也出现了可靠的增大。为了验证中枢重组反映外周多余轴突的维持这一假说,在PND0、PND7、PND17和PND60时对SO触须毛囊中的有髓和无髓轴突进行了计数。用逆行双标记法检验了另一个推论假说,即外周再生错误导致SO和存活的眶下轴突都出现,从而形成中枢SO斑。两个假说均被否定。因此,SO斑的增大既不是由于未成熟外周神经支配模式的维持,也不是由于眶下轴突向SO毛囊的再生。为了确定眶下神经切断导致的SO和PO斑增大是否是由于对眶下传入神经施加了基于活动的竞争劣势,在出生后的前5至9天,将TTX或布比卡因应用于完整的眶下神经。脑干图谱正常发育,SO和PO斑面积未受影响。因此,基于冲动活动的机制似乎并未导致损伤诱导的斑增大。为了验证斑增大是由于中枢侧支重组这一假说,对成年大鼠的对照和保留触须的初级传入神经应用了轴突内记录和染色方法。SpVi中的总终扣或侧支数量没有差异;然而,实验性纤维(14,879±350平方微米)的树突面积比对照纤维(5527±1811平方微米)可靠地更大。(摘要截于400字)