A novel set‐up for the ex vivo analysis of mechanical properties of mouse aortic segments stretched at physiological pressure and frequency. (2nd August 2016)

• Record Type: Journal Article
• Authors: Leloup, Arthur J. A.; Van Hove, Cor E.; Kurdi, Ammar; De Moudt, Sofie; Martinet, Wim; De Meyer, Guido R. Y.; Schrijvers, Dorien M.; De Keulenaer, Gilles W.; Fransen, Paul
• Is Part Of: Journal of physiology. Volume 594:Number 21(2016:Nov.)
• Page Start: 6105
• Page End: 6115
• Publication Date: 2016-08-02
• Subjects: arterial stiffness -- basal nitric oxide -- cyclic stretch -- VSMC tone; Physiology -- Periodicals; 612.005
• DOI: 10.1113/JP272623
• Languages: English
• ISSNs: 0022-3751

Abstract

Abstract : Key points: Cyclic stretch is known to alter intracellular pathways involved in vessel tone regulation. We developed a novel set‐up that allows straightforward characterization of the biomechanical properties of the mouse aorta while stretched at a physiological heart rate (600 beats min –1 ). Active vessel tone was shown to have surprisingly large effects on isobaric stiffness. The effect of structural vessel wall alterations was confirmed using a genetic mouse model. This set‐up will contribute to a better understanding of how active vessel wall components and mechanical stimuli such as stretch frequency and amplitude regulate aortic mechanics. Abstract: Cyclic stretch is a major contributor to vascular function. However, isolated mouse aortas are frequently studied at low stretch frequency or even in isometric conditions. Pacing experiments in rodents and humans show that arterial compliance is stretch frequency dependent. The Rodent Oscillatory Tension Set‐up to study Arterial Compliance is an in‐house developed organ bath set‐up that clamps aortic segments to imposed preloads at physiological rates up to 600 beats min –1 . The technique enables us to derive pressure–diameter loops and assess biomechanical properties of the segment. To validate the applicability of this set‐up we aimed to confirm the effects of distension pressure and vascular smooth muscle tone on arterial stiffness. At physiological stretch frequency (10 Hz), the Peterson modulus ( E P ; 293 (10) mmHg) for wild‐type mouse aorta increased 22% upon a rise in pressure from 80–120 mmHg to 100–140 mmHg, while, at normal pressure, E P increased 80% upon maximal contraction of the vascular smooth muscle cells. We further validated the method using a mouse model with a mutation in the fibrillin‐1 gene and an endothelial nitric oxide synthase knock‐out model. Both models are known to have increased arterial stiffness, and this was confirmed using the set‐up. To our knowledge, this is the first set‐up that facilitates the study of biomechanical properties of mouse aortic segments at physiological stretch frequency and pressure. We believe that this set‐up can contribute to a better understanding of how cyclic stretch frequency, amplitude and active vessel wall components influence arterial stiffening. Key points: Cyclic stretch is known to alter intracellular pathways involved in vessel tone regulation. We developed a novel set‐up that allows straightforward characterization of the biomechanical properties of the mouse aorta while stretched at a physiological heart rate (600 beats min –1 ). Active vessel tone was shown to have surprisingly large effects on isobaric stiffness. The effect of structural vessel wall alterations was confirmed using a genetic mouse model. This set‐up will contribute to a better understanding of how active vessel wall components and mechanical stimuli such as stretch frequency and amplitude regulate aortic mechanics.