MECHANISM OF CARDIORESPIRATORY RHYTHM IN NEONATES
MECHANISM OF CARDIORESPIRATORY RHYTHM IN NEONATES
批准号:
6197625
负责人:
David Mendelowitz
金额:
$13.96万
依托单位国家:
美国
项目类别:
财政年份:
1998
资助国家:
美国
项目状态:
已结题
起止时间:
1998-04-01 至 2002-03-31
关键词:
NMDA receptors biological clocks brain regulatory center electrophysiology fluorescent dye /probe heart rate heart rhythm laboratory rat laryngeal nerves medulla oblongata motor neurons neural facilitation neural inhibition neural transmission neuronal transport neurophysiology newborn animals respiration regulatory center synapses voltage /patch clamp
中文摘要
心血管和呼吸系统的神经控制是
高度相互关联的。例如,在每个呼吸周期中,心脏
在灵感方面跳动得更快,在灵感后和
呼气(通常称为呼吸性窦性心律失常)。作为另一个人
例如,刺激感觉喉感受器会唤起一段时间的
呼吸暂停,并保持心率急剧下降。这喉头
反射在新生儿中可能被如此夸大,可能导致新生儿死亡
动物,并被认为可能是突然出生的婴儿的原因
死亡综合征(SIDS)。这种心肺相互作用发生在
并在很大程度上(如果不是完全的话)通过
心脏的迷走神经支配。然而,令人惊讶的是,尽管
心脏迷走神经活动的生理和临床重要性
已知其在中枢神经系统内的启动和控制
在新生儿或成人中,没有从已识别的呼吸道到
延髓内的心脏迷走神经细胞尚未被发现。
这个项目将直接检验喉上段的假设
运动神经元通过直接刺激迷走神经兴奋心脏抑制神经元
单突触通路,此外,在突触前作用于增强
其他突触撞击心脏迷走神经。喉上段
神经元可能是心肺相互作用的媒介,因为
这些神经元在吸气后活跃,与心脏共存。
迷走神经,在疑核内有许多轴突侧支。
为了验证这一假设,该领域相当新的技术,如
心脏迷走神经和上心的AS荧光逆行识别
喉运动神经元与双膜片钳电生理
将使用各种技术。这项工作不仅将解决问题和
了解心肺疾病基础的基本机制
新生儿延髓的节律,但也会提示哪些受体和
心脏呼吸系统疾病的过程可能会改变。
例如小岛屿发展中国家。
英文摘要
The neural control of the cardiovascular and respiratory systems are
highly interrelated. For example, in each respiratory cycle the heart
beats more rapidly in inspiration and slows during post-inspiration and
expiration (often referred to as respiratory sinus arrhythmia). As another
example, stimulation of sensory laryngeal receptors evokes a period of
apnea and maintained a dramatic decrease in heart rate. This laryngeal
reflex can be so exaggerated in newborns in can lead to death in neonatal
animals, and has been suggested as a possible cause for sudden infant
death syndrome (SIDS). This cardio-respiratory interactions occur within
the central nervous system and are mediated largely, if not entirely, via
the vagal innervation of the heart. Surprisingly, however, despite the
physiological and clinical importance of cardiac vagal activity, little is
known about its initiation and control within the central nervous system
in neonates or adults, and no pathway from identified respiratory to
cardiac vagal neurons within the medulla has yet been identified.
This project will directly test the hypothesis that superior laryngeal
motor-neurons excite vagal cardioinhibitory neurons via a direct
monosynaptic pathway, and, in addition, act presynaptically to enhance
other synapses impinging on cardiac vagal neurons. Superior laryngeal
neurons are likely mediators of cardio-respiratory interaction because
these neurons are active in post-inspiration, co-localized with cardiac
vagal neurons, and have many axon collaterals within the nucleus ambiguus.
To test this hypothesis, techniques that are quite new to this field, such
as fluorescent retrograde identification of cardiac vagal and superior
laryngeal motor-neurons, and dual patch clamp electrophysiological
techniques will be used. This work will not only address issues and
mechanisms fundamental to understanding the basis of cardio-respiratory
rhythms in the neonatal medulla, but will also suggest which receptors and
processes could be altered in diseases of the cardio-respiratory system
such as SIDS.
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