MECHANISMS OF TRIGEMINAL PRIMARY AFFERENT ARBOR FORMATION
三叉神经初级传入轴的形成机制
基本信息
- 批准号:3753688
- 负责人:
- 金额:--
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:
- 资助国家:美国
- 起止时间:至
- 项目状态:未结题
- 来源:
- 关键词:
项目摘要
This application is designed to a) examine the sprouting response of
undamaged and damaged trigeminal primary afferent neurons following
neonatal peripheral nerve lesions and b) to study some of the mechanisms
which may be important in the generation of lesion-induced central terminal
arbor abnormalities. To accomplish these goals we propose the following
three experiments: 1) The potential of undamaged trigeminal primary
afferents to alter their central projections via sprouting, arbor expansion
or arbor displacement will be examined by cauterizing all vibrissa
follicles of the mystical pad with the exception of those in row C or D.
Using intraaxonal and intracellular labeling techniques, we will determine
the response of primary afferents with undisturbed peripheral terminations
to partial denervation of their central target. 2) We will utilize
quantitative electron microscopic techniques to investigate the impact of
neonatal infraorbital (IO) nerve transection on the central terminal
populations of two subsets of small diameter primary afferent neurons
(substance P-like immunoreactive and fluoride resistant acid phosphatase-
positive). By examining animals at sequenced intervals after the nerve
injury we will determine if the number of terminals per unit area of the
substantia gelatinosa and magnocellular region of subnucleus caudalis is
maintained, decrease or increased (indicative of sprouting). 3) To
determine the importance of patterned primary afferent activity in the
development and maintenance of trigeminal primary afferent central terminal
arbors, we will expose the IO nerve to tetrodotoxin beginning on the day of
birth. This will inhibit primary afferent activity without transecting the
nerve, thus causing no apparent disruption in the transport of any trophic
substances important to information regarding the response of damaged and
undamaged neurons to lesion-induced deafferentation of a portion of the
trigeminal system. This knowledge has important clinical benefits in
addition to its value as a contribution to our understanding of
somatosensory development.
此应用程序用于a)检查发芽响应
未损伤和受损的三叉神经初级传入神经元
新生儿周围神经损害及b)部分机制的研究
这在病变诱导的中央终末的产生中可能是重要的
乔木异常。为了实现这些目标,我们提出了以下建议
三个实验:1)未损伤的三叉神经初级神经的潜能
传入神经通过萌发、乔木扩张改变其中枢投射
或通过烧灼所有触觉来检查刀杆移位
神秘垫上的卵泡,C或D排的除外。
使用轴突内和细胞内标记技术,我们将确定
未受干扰的外周终末的初级传入反应
导致他们的中心目标部分丧失神经。2)我们将利用
定量电子显微镜技术研究影响
新生儿眶下神经中央终末横断术
两个小直径初级传入神经元亚集的种群
(P物质样免疫反应和抗氟酸性磷酸酶-
阳性)。通过在神经后按顺序间隔检查动物
我们将确定单位面积的航站楼数量是否
尾侧亚核的胶状质和大细胞区
保持、减少或增加(表示发芽)。3)至
确定有模式的初级传入活动在
三叉神经初级传入中枢终末的发育与维持
乔木,我们将从年月日开始将IO神经暴露于河豚毒素
出生。这将抑制初级传入活动,而不会切断
神经,因此没有造成任何营养物质运输的明显中断
对关于受损和有害物质反应的信息重要的物质
未受损伤的神经元对损伤引起的部分脑区去传入的影响
三叉神经系统。这一知识在临床上有重要的好处
除了它的价值之外,还有助于我们理解
体感发育。
项目成果
期刊论文数量(0)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
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WILLIAM E RENEHAN其他文献
WILLIAM E RENEHAN的其他文献
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{{ truncateString('WILLIAM E RENEHAN', 18)}}的其他基金
STRUCTURE/FUNCTION RELATIONSHIP OF BRAINSTEM TASTE CELLS
脑干味觉细胞的结构/功能关系
- 批准号:
2126227 - 财政年份:1992
- 资助金额:
-- - 项目类别:
STRUCTURE FUNCTION RELATIONSHIPS IN BRAINSTEM TASTE CELL
脑干味觉细胞的结构功能关系
- 批准号:
6379292 - 财政年份:1992
- 资助金额:
-- - 项目类别:
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