健康猪心腔不同代谢物谱的蓝图

Retu Haikonen , Topi Meuronen , Ville Koistinen , Olli Kärkkäinen , Tomi Tuomainen , Gloria I Solano-Aguilar , Joseph F. Urban Jr. , Marko Lehtonen , Pasi Tavi , Kati Hanhineva
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引用次数: 0

摘要

心脏是研究最多的器官之一,有生理过程和疾病研究。虽然心室之间存在显著的结构和功能差异是公认的,但大多数研究只关注单个心脏腔,主要是左心室。本研究旨在全面表征所有四个心脏腔室的代谢特征,在接近人类代谢的健康动物模型中,猪。我们采用液相色谱-质谱代谢组学分析了30头健康猪(N = 30)的心脏室代谢物谱,这些猪饲喂自由饮食,饲养在标准的非应激生理条件下。我们的研究结果揭示了左心室更高的能量需求,正如电子传递链相关代谢物如NAD+和FAD水平升高所证明的那样。此外,己糖磷酸和几种酰基肉碱的丰度表现出室依赖性变化。心室,尤其是左心室,表现出不同的氧化还原状态,谷胱甘肽和抗坏血酸水平不同,表明不同心室的氧化应激存在差异。此外,氨基酸具有室特异性丰度模式,心室对蛋白质合成的需求增加,这可能与活性氧(ROS)诱导的细胞损伤后的修复机制有关。我们的研究揭示了健康猪心脏中四个心脏腔的代谢谱存在显著差异,强调了心脏组织的代谢异质性。这些发现强调了研究室特异性代谢途径以更好地了解心脏功能的必要性。这些见解可以为更精确的治疗策略的发展提供信息,这些治疗策略可以根据心脏腔内的代谢需求和功能角色量身定制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Blueprint of the distinct metabolite profiles of healthy pig heart chambers
The heart is one of the most studied organs, with physiological processes and disease research. While it is well-established that significant structural and functional differences exist between the chambers, most studies focus on only a single heart chamber, predominantly the left ventricle. This study aims to comprehensively characterise the chamber-specific metabolic profiles of all four heart chambers in a healthy animal model close to human metabolism, pigs. We employed liquid chromatography-mass spectrometry metabolomics to analyse the metabolite profiles of heart chambers in healthy pigs (N = 30) maintained on an ad libitum diet and housed under standard, non-stressed physiological conditions. Our findings reveal a higher energy demand in the left ventricle, as evidenced by elevated levels of electron transport chain-related metabolites such as NAD+ and FAD. Additionally, hexose-phosphates and several acylcarnitines exhibited chamber-dependent variations in abundance. The ventricles, particularly the left, demonstrated distinct redox states, with differential levels of glutathione and ascorbic acid, suggesting variations in oxidative stress across chambers. Furthermore, amino acids had chamber-specific abundance patterns, and ventricles showed an increased requirement for protein synthesis, likely associated with repair mechanisms following reactive oxygen species (ROS)-induced cellular damage. Our study reveals significant differences in the metabolic profiles across four heart chambers in healthy pig hearts, underscoring the metabolic heterogeneity of cardiac tissue. These findings highlight the necessity of investigating chamber-specific metabolic pathways to better understand heart functionality. Such insights could inform the development of more precise therapeutic strategies tailored to metabolic demands and functional roles in heart chambers.
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来源期刊
Journal of molecular and cellular cardiology plus
Journal of molecular and cellular cardiology plus Cardiology and Cardiovascular Medicine
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