Das Mahasweta, Vihlen Christopher S, Legradi Gabor
Department of Pathology and Cell Biology, University of South Florida College of Medicine, Tampa, Florida 33612, USA.
J Comp Neurol. 2007 Feb 1;500(4):761-76. doi: 10.1002/cne.21212.
The hypothalamic paraventricular nucleus (PVN) coordinates major neuroendocrine and behavioral mechanisms, particularly responses to homeostatic challenges. Parvocellular and magnocellular PVN neurons are richly innervated by pituitary adenylate cyclase-activating polypeptide (PACAP) axons. Our recent functional observations have also suggested that PACAP may be an excitatory neuropeptide at the level of the PVN. Nevertheless, the exact localization of PACAP-producing neurons that project to the PVN is not understood. The present study examined the specific contribution of various brain areas sending PACAP innervation to the rat PVN by using iontophoretic microinjections of the retrograde neuroanatomical tracer cholera toxin B subunit (CTb). Retrograde transport was evaluated from hypothalamic and brainstem sections by using multiple labeling immunofluorescence for CTb and PACAP. PACAP-containing cell groups were found to be retrogradely labeled from the PVN in the median preoptic nucleus; preoptic and lateral hypothalamic areas; arcuate, dorsomedial, ventromedial, and supramammillary nuclei; ventrolateral midbrain periaqueductal gray; rostral and midlevel ventrolateral medulla, including the C1 catecholamine cell group; nucleus of the solitary tract; and dorsal motor nucleus of vagus. Minor PACAP projections with scattered double-labeled neurons originated from the parabrachial nucleus, pericoeruleus area, and caudal regions of the nucleus of the solitary tract and ventrolateral medulla. These observations indicate a multisite origin of PACAP innervation to the PVN and provide a strong chemical neuroanatomical foundation for interaction between PACAP and its potential target neurons in the PVN, such as parvocellular CRH neurons, controlling physiologic responses to stressful challenges and other neuroendocrine or preautonomic PVN neurons.
下丘脑室旁核(PVN)协调主要的神经内分泌和行为机制,尤其是对稳态挑战的反应。小细胞和大细胞PVN神经元丰富地接受垂体腺苷酸环化酶激活多肽(PACAP)轴突的支配。我们最近的功能观察还表明,PACAP在PVN水平可能是一种兴奋性神经肽。然而,投射到PVN的PACAP产生神经元的确切定位尚不清楚。本研究通过对逆行神经解剖示踪剂霍乱毒素B亚基(CTb)进行离子电渗微注射,研究了向大鼠PVN发送PACAP神经支配的各个脑区的具体贡献。通过对CTb和PACAP进行多重标记免疫荧光,从下丘脑和脑干切片评估逆行运输。发现含PACAP的细胞群在视前正中核、视前区和下丘脑外侧区、弓状核、背内侧核、腹内侧核和乳头体上核、腹外侧中脑导水管周围灰质、延髓头端和中间腹外侧,包括C1儿茶酚胺细胞群、孤束核和迷走神经背运动核中被PVN逆行标记。来自臂旁核、蓝斑周区以及孤束核和延髓腹外侧尾端区域的PACAP投射较少,有散在的双标记神经元。这些观察结果表明PACAP对PVN的神经支配有多个起源地,并为PACAP与其在PVN中的潜在靶神经元(如小细胞促肾上腺皮质激素释放激素神经元)之间的相互作用提供了强有力的化学神经解剖学基础,这些靶神经元控制着对应激挑战的生理反应以及其他神经内分泌或自主神经前PVN神经元。