Neutel Cédric H G, van der Laan Koen W F, Wesley Callan D, Krüger Dustin N, Pencheva Margarita G, Schalkwijk Casper G, De Meyer Guido R Y, Martinet Wim, Delhaas Tammo, Reesink Koen D, Giudici Alessandro, Guns Pieter-Jan, Spronck Bart
Laboratory of Physiopharmacology, University of Antwerp, Campus Drie Eiken, Antwerp, Belgium.
Department of Biomedical Engineering, Cardiovascular Research Institute Maastricht (CARIM), Maastricht University, Maastricht, The Netherlands.
Pulse (Basel). 2024 Nov 25;13(1):1-10. doi: 10.1159/000542694. eCollection 2025 Jan-Dec.
Arterial stiffening is a hallmark of vascular ageing, and unravelling its underlying mechanisms has become a central theme in the field of cardiovascular disease. While various techniques and experimental setups are accessible for investigating biomechanics of blood vessels both in vivo and ex vivo, comparing findings across diverse methodologies is challenging.
Arterial stiffness in the aorta of adult (5 months) and aged (24 months) wild-type C57Bl/6J mice was measured in vivo, after which ex vivo biomechanical evaluation was performed using the Rodent Oscillatory Tension Setup to study Arterial Compliance (ROTSAC; University of Antwerp, Belgium) and the DynamX setup (Maastricht University, The Netherlands). Stiffness of aortic tissue was measured in both absence and presence of activated smooth muscle cells (i.e., contraction). Measurements in both setups were conducted in parallel with matched protocols and identical buffers and chemicals.
Overall, both methods revealed age-related increased aortic stiffness, although parameters of aortic mechanics showed different numerical values, suggesting that results are not directly interchangeable between methods. Surprisingly, smooth muscle cell contraction had opposing effects between the setups. Indeed, smooth muscle cell contraction increased arterial stiffness in the ROTSAC but decreased stiffness in the DynamX. These opposing effects could be attributed to how the two setups differentially load the collagen fibres in the arterial wall, ex vivo.
Overall, this study provided critical insights into how different experimental setups can influence the interpretation of aortic biomechanics, emphasizing the need for careful consideration and contextualization of results based on the methodology used.
动脉僵硬度是血管老化的一个标志,揭示其潜在机制已成为心血管疾病领域的一个核心主题。虽然有各种技术和实验装置可用于在体内和体外研究血管生物力学,但比较不同方法的研究结果具有挑战性。
在成年(5个月)和老年(24个月)野生型C57Bl/6J小鼠的主动脉中测量体内动脉僵硬度,之后使用啮齿动物振荡张力装置(ROTSAC;比利时安特卫普大学)和DynamX装置(荷兰马斯特里赫特大学)进行体外生物力学评估,以研究动脉顺应性。在存在和不存在激活的平滑肌细胞(即收缩)的情况下测量主动脉组织的僵硬度。两种装置中的测量均按照匹配的方案并使用相同的缓冲液和化学物质平行进行。
总体而言,两种方法均显示与年龄相关的主动脉僵硬度增加,尽管主动脉力学参数显示出不同的数值,这表明不同方法的结果不能直接互换。令人惊讶的是,平滑肌细胞收缩在两种装置中的作用相反。实际上,平滑肌细胞收缩在ROTSAC中增加了动脉僵硬度,但在DynamX中降低了僵硬度。这些相反的作用可归因于两种装置在体外对动脉壁中胶原纤维的加载方式不同。
总体而言,本研究为不同实验装置如何影响主动脉生物力学的解释提供了重要见解,强调了根据所用方法仔细考虑和结合结果背景的必要性。