Click
here to close Hello! We notice that
you are using Internet Explorer, which is not supported by Echinobase
and may cause the site to display incorrectly. We suggest using a
current version of Chrome,
FireFox,
or Safari.
Mar Drugs
2023 Nov 25;2112:. doi: 10.3390/md21120610.
Show Gene links
Show Anatomy links
Is Stress Relaxation in Sea Cucumber Dermis Chemoelastic?
Barbieri E
,
Gupta HS
.
???displayArticle.abstract???
Echinoderms, such as sea cucumbers, have the remarkable property of changing the stiffness of their dermis according to the surrounding chemical environments. When sea cucumber dermal specimens are constantly strained, stress decays exponentially with time. Such stress relaxation is a hallmark of visco-elastic mechanical behavior. In this paper, in contrast, we attempted to interpret stress relaxation from the chemoelasticity viewpoint. We used a finite element model for the microstructure of the sea cucumber dermis. We varied stiffness over time and framed such changes against the first-order reactions of the interfibrillar matrix. Within this hypothetical scenario, we found that stress relaxation would then occur primarily due to fast crosslink splitting between the chains and a much slower macro-chain scission, with characteristic reaction times compatible with relaxation times measured experimentally. A byproduct of the model is that the concentration of undamaged macro-chains in the softened state is low, less than 10%, which tallies with physical intuition. Although this study is far from being conclusive, we believe it opens an alternative route worthy of further investigation.
Figure 1. Finite element model of staggered fibrils of length LF, connected by an interfibrillar matrix. (a) Tissue specimen of length LT, with an applied constant strain ϵT and fibrillar microstructure; (b) fibril elements (cylinders), shear elements (blue lines) and node numbering (circled numbers); (c) The matrix cannot carry tensile loads, only shear stresses, τij.
Figure 2. Chemoelastic relaxation for tissue stress; the continuous lines are the numerical results, the dots are the mean of the experimental measures, and the error bar plots are the corresponding standard deviations.
Figure 3. Chemoelastic relaxation for the fibril strain; the continuous lines are the numerical results, the dots are the mean of the experimental measures, and the error bar plots are the corresponding standard deviations.
Figure 4. Chemoelastic relaxation parameters for the interfibrillar matrix.
Figure 5. Chemoelastic relaxation parameters for the fibrils.
Figure 6. Elastic fibrils made by collagen macromolecules: hypothesized reversible reaction of chain scission and recombination; A are macro-chains before scission and B are those after scission.
Figure 7. Interfibrillar matrix composed of crosslinked macro-chains (species A); the hypothesized reactions of chain scission, crosslink splitting, and recombination. Species B represents chains after chain scission and C is chains after chain scission and cross-link splitting.
Figure 8. The surfaces in Equation (A47). The intersection of the surfaces (red lines) is all the possible reaction rates.
Figure 9. Interfibrillar matrix reaction times for ASW, KASW, and CaFASW: in all three conditions, the fastest times are due to chain recombination, with crosslink splitting being around 10 times slower and chain scission being extremely slow.
Figure 10. Initial conditions of the chemical species for all the permissible reaction times.
Benedetto,
Production, characterization and biocompatibility of marine collagen matrices from an alternative and sustainable source: the sea urchin Paracentrotus lividus.
2014, Pubmed,
Echinobase
Benedetto,
Production, characterization and biocompatibility of marine collagen matrices from an alternative and sustainable source: the sea urchin Paracentrotus lividus.
2014,
Pubmed
,
Echinobase
Capadona,
Stimuli-responsive polymer nanocomposites inspired by the sea cucumber dermis.
2008,
Pubmed
,
Echinobase
Goh,
Collagenous Extracellular Matrix Biomaterials for Tissue Engineering: Lessons from the Common Sea Urchin Tissue.
2017,
Pubmed
,
Echinobase
Mo,
Interfibrillar stiffening of echinoderm mutable collagenous tissue demonstrated at the nanoscale.
2016,
Pubmed
,
Echinobase
Motokawa,
Mechanical mutability in connective tissue of starfish body wall.
2011,
Pubmed
,
Echinobase
Motokawa,
Dynamic mechanical properties of body-wall dermis in various mechanical states and their implications for the behavior of sea cucumbers.
2003,
Pubmed
,
Echinobase
Motokawa,
Contraction and stiffness changes in collagenous arm ligaments of the stalked crinoid Metacrinus rotundus (Echinodermata).
2004,
Pubmed
,
Echinobase
Roberts,
Chemorheology of phenylboronate-salicylhydroxamate crosslinked hydrogel networks with a sulfonated polymer backbone.
2008,
Pubmed
Takehana,
Softenin, a novel protein that softens the connective tissue of sea cucumbers through inhibiting interaction between collagen fibrils.
2014,
Pubmed
,
Echinobase
Takemae,
Low oxygen consumption and high body content of catch connective tissue contribute to low metabolic rate of sea cucumbers.
2009,
Pubmed
,
Echinobase
Tamori,
Evidence that water exudes when holothurian connective tissue stiffens.
2010,
Pubmed
,
Echinobase
Tipper,
Purification, characterization and cloning of tensilin, the collagen-fibril binding and tissue-stiffening factor from Cucumaria frondosa dermis.
2002,
Pubmed
,
Echinobase
Trotter,
Evidence that calcium-dependent cellular processes are involved in the stiffening response of holothurian dermis and that dermal cells contain an organic stiffening factor.
1995,
Pubmed
Wilkie,
Mutable collagenous tissue: overview and biotechnological perspective.
2005,
Pubmed
,
Echinobase
Wilkie,
Autotomy as a prelude to regeneration in echinoderms.
2001,
Pubmed
,
Echinobase