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首页> 外文期刊>Autonomic neuroscience: basic & clinical >Central control of atrio-ventricular conduction and left ventricular contractility in the cat heart: Synaptic interactions of vagal preganglionic neurons in the nucleus ambiguus with neuropeptide Y-immunoreactive nerve terminals.
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Central control of atrio-ventricular conduction and left ventricular contractility in the cat heart: Synaptic interactions of vagal preganglionic neurons in the nucleus ambiguus with neuropeptide Y-immunoreactive nerve terminals.

机译:猫心的房室传导和左心室收缩的中央控制:模糊核中迷走神经节前神经元与神经肽Y免疫反应性神经末梢的突触相互作用。

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In the cat, vagal postganglionic controls of heart rate, atrio-ventricular (AV) conduction and left ventricular contractility are mediated by three separate intrinsic cardiac ganglia, the sinoatrial (SA), AV and cranioventricular (CV) ganglia, respectively. The vagal preganglionic neurons (VPNs) that project to these ganglia are located in the ventrolateral nucleus ambiguus (NA-VL). We have previously shown that the VPNs projecting to the SA, AV and CV ganglia are distinct from one another. We have also demonstrated that neuropeptide Y-immunoreactive (NPY-IR) axon terminals synapse upon VPNs projecting to the SA ganglion. In the present study, we test the hypothesis that those VPNs projecting to the AV ganglion (negative dromotropic VPNs) and those projecting to the CV ganglion (negative inotropic VPNs) are innervated by NPY-IR terminals in NA-VL. A retrograde tracer was injected into the AV or CV ganglion of the cat, and the brains subsequently processed for visualization of tracer and the immunocytochemical visualization of NPY by dual labeling electron-microscopic methods. We observed that 11+/-5% of all axodendritic synapses and 8+/-6% of all axosomatic synapses upon negative inotropic VPNs were NPY-IR. Furthermore, 19+/-14% of all axodendritic synapses upon negative dromotropic VPNs were NPY-IR. A few NPY-IR axosomatic synapses upon negative dromotropic neurons were also observed. NPY-IR terminals in NA-VL occasionally formed axosomatic synapses with NPY-IR neurons and axoaxonic synapses with unlabeled terminals. These results suggest that central NPY afferents to the NA-VL modulate the vagal preganglionic control of AV conduction and left ventricular contractility.
机译:在猫中,迷走神经节后心率,房室传导(AV)和左心室收缩的控制是由三个独立的固有心脏神经节介导的,分别是窦房(SA),AV和颅室(CV)神经节。投射到这些神经节的迷走神经节前神经元(VPNs)位于腹侧核(NA-VL)中。先前我们已经证明,投射到SA,AV和CV神经节的VPN彼此不同。我们还证明了神经肽Y免疫反应(NPY-IR)轴突末端突触到投射到SA神经节的VPN上。在本研究中,我们检验了以下假设:NA-VL中的NPY-IR终端支配了投射到AV神经节的VPN(负性变质性VPN)和投射到履带神经节的VPN(负性变质性VPN)。将逆行示踪剂注射到猫的AV或CV神经节中,随后通过双标记电子显微镜方法对大脑进行处理,以进行示踪剂可视化和NPY的免疫细胞化学可视化。我们观察到在负性变力性VPN上,所有轴突突触的11 +/- 5%和所有轴突突触的8 +/- 6%是NPY-IR。此外,在同性阴性VPN上所有轴突突触的19 +/- 14%为NPY-IR。还观察到了在负趋性神经元上的一些NPY-IR无糖突触。 NA-VL中的NPY-IR末端有时会与NPY-IR神经元形成轴突突触,而未标记的末端会形成轴突突触。这些结果表明中央NPY传入NA-VL调节迷走神经节前控制AV传导和左心室收缩。

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