Key result
Vascular cells modulate arterial Poisson's ratio in vivo by influencing circumferential compliance.
Why the study?
There is no consensus on the degree of arterial anisotropy or its relationship to vascular cell function, necessitating reliable measures of biaxial displacements in vivo.
Biaxial rat artery data may refine elasticity models; leaves open anisotropy consensus and cell-function links in humans.
There is no consensus as to the degree of arterial anisotropy or to its relationship to vascular cell function. Given the relevance of the isotropic assumption in formulating elasticity models, reliable measures of biaxial displacements are needed. In this study, a video motion analyzer (VMA) was used to describe the biaxial in vivo dynamic elasticity of 22 carotid arteries and 5 abdominal aortas in 27 rats. The influence of vascular cell function was also examined by subjecting six rats to a photosensitive drug, chloroaluminum sulfonated phthalocyanine (CASPc), which is focally cytotoxic on activation by laser. Circumferential compliance (Ccirc) was greater than longitudinal compliance (Clong) for all vessels. Compliance pressure curves were nonlinear, and biaxial displacements were in phase. The circumferential elastic modulus was less than the longitudinal modulus at common stresses. CASPc + laser reduced Ccirc but not Clong, thus altering Poisson's ratio. In conclusion, rat arteries are biaxially, nonlinearly elastic and anisotropic in vivo. Vascular cells modulate Poisson's ratio by influencing Ccirc.
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L'Italien et al. (1994) studied Arterial elasticity and anisotropy (n=27). Chloroaluminum sulfonated phthalocyanine (CASPc) + laser was evaluated on Biaxial in vivo dynamic elasticity (circumferential and longitudinal compliance). Rat arteries are biaxially, nonlinearly elastic and anisotropic in vivo, with vascular cells modulating Poisson's ratio by influencing circumferential compliance.
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