Department of Cardiology, RWTH Aachen University, Pauwelsstr 30, D-52074 Aachen, Germany.
Circ Res. 2011 May 13;108(10):1209-19. doi: 10.1161/CIRCRESAHA.110.234518. Epub 2011 Mar 24.
Recently, we provided a technique of chronic high-frequency electric stimulation (HFES) of the right inferior ganglionated plexus for ventricular rate control during atrial fibrillation in dogs and humans. In these experiments, we observed a decrease of the intrinsic ventricular rate during the first 4 to 5 months when HFES was intermittently shut off.
We thus hypothesized that HFES might elicit trophic effects on cardiac neurons, which in turn increase baseline parasympathetic tone of the atrioventricular node.
In mongrel dogs atrial fibrillation was induced by rapid atrial pacing. Endocardial HFES of the right inferior ganglionated plexus, which contains abundant fibers to the atrioventricular node, was performed for 2 years. Sham-operated nonstimulated dogs served as control. In chronic neurostimulated dogs, we found an increased neuronal cell size accompanied by an increase of choline acetyltransferase and unchanged tyrosine hydroxylase protein expression as compared with unstimulated dogs. Moreover, β-nerve growth factor (NGF) and neurotrophin (NT)-3 were upregulated in chronically neurostimulated dogs. In vitro, HFES of cultured neurons of interatrial ganglionated plexus from adult rats increased neuronal growth accompanied by upregulation of NGF, NT-3, glial-derived neurotrophic factor (GDNF), ciliary neurotrophic factor (CNTF) and brain-derived neurotrophic factor (BDNF) expression. NGF was identified as the main growth-inducing factor, whereas NT-3 did not affect HFES-induced growth. However, NT-3 could be identified as an important acetylcholine-upregulating factor.
HFES of cardiac neurons in vivo and in vitro causes neuronal cellular hypertrophy, which is mediated by NGF and boosters cellular function by NT-3-mediated acetylcholine upregulation. This knowledge may contribute to develop HFES techniques to augment cardiac parasympathetic tone.
最近,我们提供了一种慢性高频电刺激(HFES)右下神经节丛的技术,用于控制犬和人类心房颤动时的心室率。在这些实验中,当 HFES 间歇性关闭时,我们观察到最初 4 到 5 个月内在固有心室率降低。
因此,我们假设 HFES 可能对心脏神经元产生营养作用,进而增加房室结的基础副交感神经张力。
在杂种犬中,通过快速心房起搏诱导心房颤动。进行右下心神经节丛的心内膜 HFES,该神经节丛含有丰富的纤维到房室结。进行了 2 年的 HFES。作为对照的 Sham 手术非刺激犬。在慢性神经刺激犬中,我们发现神经元细胞大小增加,同时胆碱乙酰转移酶增加,酪氨酸羟化酶蛋白表达不变。此外,β-神经生长因子(NGF)和神经营养素(NT)-3 在慢性神经刺激犬中上调。在体外,HFES 对成年大鼠心房神经节丛培养神经元的刺激伴随着神经元生长的增加,同时伴有 NGF、NT-3、胶质源性神经营养因子(GDNF)、睫状神经营养因子(CNTF)和脑源性神经营养因子(BDNF)表达的上调。NGF 被确定为主要的生长诱导因子,而 NT-3 不影响 HFES 诱导的生长。然而,NT-3 可以被认为是一种重要的乙酰胆碱上调因子。
体内和体外 HFES 对心脏神经元的刺激导致神经元细胞肥大,这是由 NGF 介导的,而 NT-3 介导的乙酰胆碱上调增强了细胞功能。这些知识可能有助于开发 HFES 技术来增强心脏副交感神经张力。