Abstract

Elastic fibers (90% elastin, 10% fibrillin-rich microfibrils) are synthesized only in early life and adolescence mainly by the vascular smooth muscle cells through the cross-linking of its soluble precursor, tropoelastin. Elastic fibers endow the large elastic arteries with resilience and elasticity. Normal vascular aging is associated with arterial remodeling and stiffening, especially due to the end of production and degradation of elastic fibers, leading to altered cardiovascular function. Several pharmacological treatments stimulate the production of elastin and elastic fibers. In particular, dill extract (DE) has been demonstrated to stimulate elastin production in vitro in dermal equivalent models and in skin fibroblasts to increase lysyl oxidase–like-1 (LOXL-1) gene expression, an enzyme contributing to tropoelastin crosslinking and elastin formation. Here, we have investigated the effects of a chronic treatment (three months) of aged male mice with DE (5% or 10% v/v, in drinking water) on the structure and function of the ascending aorta. DE treatment, especially at 10%, of aged mice protected pre-existing elastic lamellae, reactivated tropoelastin and LOXL-1 expressions, induced elastic fiber neo-synthesis, and decreased the stiffness of the aging aortic wall, probably explaining the reversal of the age-related cardiac hypertrophy also observed following the treatment. DE could thus be considered as an anti-aging product for the cardiovascular system.

Highlights

  • Elastic fibers, composed of an elastin core (90%) surrounded by fibrillin-rich microfibrils (10%), are essential extracellular matrix (ECM) macromolecules endowing extensible tissues with critical mechanical properties such as resilience, flexibility, and elasticity

  • Our results indicate that dill extract (DE) treatment reverses age-related cardiac hypertrophy, protects elastic lamellae (EL), reactivates elastin and elastic fiber synthesis, and improves the biomechanical properties of the aging aortic wall

  • We have shown that a 3-month treatment of aged male mice with DE reduces the aortic elastic lamella disruptions induced by ageing (5% and 10% DE), leads to elastic fiber neosynthesis and functional improvement of the ascending aorta (10% DE), and reverses the age-related cardiac hypertrophy

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Summary

Introduction

Elastic fibers, composed of an elastin core (90%) surrounded by fibrillin-rich microfibrils (10%), are essential extracellular matrix (ECM) macromolecules endowing extensible tissues with critical mechanical properties such as resilience, flexibility, and elasticity. The arterial wall elastic fibers, returning to their relaxed state, release the accumulated energy, applying pressure to the blood which forwards the stored blood volume to the peripheral circulation. This maintains a relatively elevated arterial blood pressure and flow during diastole. This cushioning phenomenon, called the Windkessel effect, helps to decrease the heart afterload, smoothens the pressure changes in the arterial circulation, and generates a more continuous peripheral blood flow [4,5,6,7,8,9]. Aging and genetic deficiency in elastin or microfibrils lead to serious alterations of the arterial physiology and/or pathologies such as Williams or Marfan syndromes [4,6,10,11,12,13]

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