Masuyama Kiyoshi, Lee Jong-Kook, Yokoyama Teruki, Li Jun, Yasutake Hideki, Kuramoto Yuki, Hidaka Kyoko, Sakata Yasushi
Departments of Cardiovascular Medicine, Graduate School of Medicine, The University of Osaka, 2-2 Yamadaoka, Suita, 565-0871, Japan.
Departments of Cardiovascular Regenerative Medicine and Drug Discovery, Graduate School of Medicine, The University of Osaka, 2-2 Yamadaoka, Suita, 565-0871, Japan.
Sci Rep. 2025 Mar 26;15(1):10479. doi: 10.1038/s41598-025-94349-8.
Takotsubo syndrome (TTS) is an acute cardiac syndrome characterized by transient left ventricular dysfunction. Although the wall motion abnormality resolves completely, the prognosis is poor. Defect of I-metaiodobenzylguanidine uptake, interpreted as sympathetic impairment, persisted in TTS patients, but the mechanism is not fully understood. We aimed to elucidate morphological sympathetic nerve change in a TTS model mouse using three-dimensional imaging techniques, with a particular focus on the role of factors in these alterations. The TTS model was induced by a single intraperitoneal injection of 2.0 mg/kg adrenaline to C57BL/6 mice, resulting in transient akinesis localized to the inferior apical region of the heart. Three-dimensional morphological assessment revealed that sympathetic nerve length within the inferior apical area of TTS mice reduced during the chronic phase compared with the sham mice. Notably, the study observed a pattern of denervation during the acute phase, followed by re-innervation and subsequent denervation in the chronic phase. The neurotrophic factors expressions changed in a time-dependent manner, corresponding to the phase-specific damage both to cardiomyocytes and sympathetic neurons. The bimodal change in sympathetic nerves and altered neurotrophic factors in TTS mice provide novel insights into the pathophysiological mechanism of TTS to establish therapeutic strategies for TTS.
应激性心肌病(TTS)是一种以短暂性左心室功能障碍为特征的急性心脏综合征。尽管室壁运动异常可完全恢复,但预后较差。TTS患者存在间碘苄胍摄取缺陷,被认为是交感神经功能受损,但具体机制尚不完全清楚。我们旨在利用三维成像技术阐明TTS模型小鼠的形态学交感神经变化,特别关注这些改变中各种因素的作用。通过向C57BL/6小鼠腹腔内单次注射2.0 mg/kg肾上腺素诱导TTS模型,导致心脏心尖下区域出现短暂性运动不能。三维形态学评估显示,与假手术小鼠相比,TTS小鼠慢性期心尖下区域的交感神经长度缩短。值得注意的是,该研究观察到急性期出现去神经支配模式,随后在慢性期重新神经支配并再次去神经支配。神经营养因子表达呈时间依赖性变化,与心肌细胞和交感神经元的阶段特异性损伤相对应。TTS小鼠交感神经的双峰变化和神经营养因子的改变为TTS的病理生理机制提供了新的见解,有助于制定TTS的治疗策略。