Institute of Anatomy, Faculty of Medicine, Lithuanian University of Health Sciences, Kaunas, Lithuania.
Auton Neurosci. 2013 Jun;176(1-2):32-47. doi: 10.1016/j.autneu.2013.01.006. Epub 2013 Feb 9.
The mouse heart is a popular model to study the function and autonomic control of the specialized cardiac conduction system (CCS). However, the precise identity and anatomical distribution of the intrinsic cardiac nerves that modulate the function of the mouse CCS have not been adequately studied. We aimed at determining the organization and distribution of the intrinsic cardiac nerves that supply the CCS of the mouse. In whole mouse heart preparations, intrinsic neural structures were revealed by histochemical staining for acetylcholinesterase (AChE). Adrenergic, cholinergic and peptidergic neural components were identified, respectively, by immunohistochemical labeling for tyrosine hydroxylase (TH), choline acetyltransferase (ChAT), calcitonin gene related peptide (CGRP), substance P (SP), and protein gene product 9.5 (PGP 9.5). Myocytes of the CCS were identified by immunolabeling of hyperpolarization activated cyclic nucleotide-gated potassium channel 4 (HCN4). In addition, the presence of CCS myocytes in atypical locations was verified using fluorescent immunohistochemistry performed on routine paraffin sections. The results demonstrate that four microscopic epicardial nerves orientated toward the sinuatrial nodal (SAN) region derive from both the dorsal right atrial and right ventral nerve subplexuses. The atrioventricular nodal (AVN) region is typically supplied by a single intrinsic nerve derived from the left dorsal nerve subplexus at the posterior interatrial groove. SAN myocytes positive for HCN4 were widely distributed both on the medial, anterior, lateral and even posterior sides of the root of the right cranial (superior caval) vein. The distribution of HCN4-positive myocytes in the AVN region was also wider than previously considered. HCN4-positive cells and thin slivers of the AVN extended to the roots of the ascending aorta, posteriorly to the orifice of the coronary sinus, and even along both atrioventricular rings. Notwithstanding the fact that cholinergic nerve fibers and axons clearly predominate in the mouse CCS, adrenergic nerve fibers and axons are abundant therein as well. Altogether, these results provide new insight into the anatomical basis of the neural control of the mouse CCS.
鼠心是研究心脏特殊传导系统(CCS)功能和自主控制的常用模型。然而,调节鼠 CCS 功能的内在心脏神经的确切性质和解剖分布尚未得到充分研究。我们旨在确定供应鼠 CCS 的内在心脏神经的组织和分布。在整个鼠心标本中,通过乙酰胆碱酯酶(AChE)组织化学染色显示内在神经结构。通过免疫组织化学标记酪氨酸羟化酶(TH)、胆碱乙酰转移酶(ChAT)、降钙素基因相关肽(CGRP)、P 物质(SP)和蛋白基因产物 9.5(PGP 9.5),分别鉴定出肾上腺素能、胆碱能和肽能神经成分。通过免疫标记超极化激活环核苷酸门控钾通道 4(HCN4)鉴定 CCS 心肌细胞。此外,还通过在常规石蜡切片上进行荧光免疫组织化学证实了非典型位置的 CCS 心肌细胞的存在。结果表明,四个朝向窦房结(SAN)区域的微小心外膜神经源自右心房背侧和右腹侧神经亚丛。房室结(AVN)区域通常由发自左心房背侧神经亚丛的单个内在神经供应,位于房间隔后沟的后内侧。HCN4 阳性的 SAN 心肌细胞广泛分布于右头臂静脉(superior caval)根部的内侧、前侧、外侧甚至后侧。HCN4 阳性心肌细胞在 AVN 区域的分布也比以前认为的更广泛。HCN4 阳性细胞和 AVN 的薄层延伸到升主动脉根部,向后延伸到冠状窦口,甚至沿着房室环的两侧。尽管胆碱能神经纤维和轴突在鼠 CCS 中明显占主导地位,但肾上腺素能神经纤维和轴突也很丰富。总的来说,这些结果为鼠 CCS 的神经控制的解剖基础提供了新的见解。