Force Feedback is Noticeably Different for Linear versus Nonlinear Elastic Tissue Models

2007 ◽  
Author(s):  
Sarthak Misra ◽  
Allison M. Okamura ◽  
K. T. Ramesh
Keyword(s):  
Force Feedback ◽  
Elastic Tissue ◽  
Nonlinear Elastic ◽  
Tissue Models

Strain Energy Descriptions of Biological Swelling II: Multiple Fluid Compartment Models

1987 ◽  
Vol 109 (3) ◽  
pp. 257-262 ◽  
Author(s):  
D. K. Bogen
Keyword(s):  
Volume Expansion ◽  
Strain Energy ◽  
Elastic Tissue ◽  
Significant Determinant ◽  
Tissue Elasticity ◽  
Energy Functions ◽  
Compartment Models ◽  
Fluid Compartment ◽  
Strain Energy Functions ◽  
Tissue Models

A series of multicompartmental, biphasic elastic tissue models is developed. In its most general form, the models consist of multiple tubular networks, each with an internal spring network. In addition, another spring network occupies the extratubular compartment. Strain energy functions are derived for the models, as well as expressions for the fluid pressures in each compartment arising from volume expansion or swelling. Calculations also show that the distribution of fluid among compartments is a significant determinant of tissue elasticity.

Ultrastructure and Staining of Developing Elastic Tissue

1971 ◽  
Vol 29 ◽  
pp. 244-245
Author(s):  
E. N. Albert
Keyword(s):  
Fine Structure ◽  
Phosphotungstic Acid ◽  
Staining Method ◽  
Rat Aorta ◽  
Uranyl Acetate ◽  
The Other ◽  
Elastic Fibers ◽  
Elastic Tissue ◽  
Lead Citrate ◽  
New Born

Silver tetraphenylporphine sulfonate (Ag-TPPS) was synthesized in this laboratory and used as an electron dense stain for elastic tissue (Fig 1). The procedures for the synthesis of tetraphenylporphine sulfonate and the staining method for mature elastic tissue have been described previously.The fine structure of developing elastic tissue was observed in fetal and new born rat aorta using tetraphenylporphine sulfonate, phosphotungstic acid, uranyl acetate and lead citrate. The newly forming elastica consisted of two morphologically distinct components. These were a central amorphous and a peripheral fibrous. The ratio of the central amorphous and the peripheral fibrillar portion changed in favor of the former with increasing age.It was also observed that the staining properties of the two components were entirely different. The peripheral fibrous component stained with uranyl acetate and/or lead citrate while the central amorphous portion demonstrated no affinity for these stains. On the other hand, the central amorphous portion of developing elastic fibers stained vigorously with silver tetraphenylporphine sulfonate, while the fibrillar part did not (compare figs 2, 3, 4). Based upon the above observations it is proposed that developing elastica consists of two components that are morphologically and chemically different.

Immunoelectron microscopic localization of elastic tissue in archival material using an improved method

1990 ◽  
Vol 48 (3) ◽  
pp. 794-795
Author(s):  
J. C. Fanning ◽  
J. F. White ◽  
R. Polewski ◽  
E. G. Cleary
Keyword(s):  
Normal Animal ◽  
Animal Tissue ◽  
Elastic Tissue ◽  
Human Tissues ◽  
Improved Method ◽  
Tissue Samples ◽  
Archival Material ◽  
Immuno Electron Microscopy ◽  
Arteries And Veins ◽  
Biochemical Examination

Elastic tissue is an important component of the walls of arteries and veins, of skin, of the lungs and in lesser amounts, of many other tissues. It is responsible for the rubber-like properties of the arteries and for the normal texture of young skin. It undergoes changes in a number of important diseases such as atherosclerosis and emphysema and on exposure of skin to sunlight.We have recently described methods for the localizationof elastic tissue components in normal animal and human tissues. In the study of developing and diseased tissues it is often not possible to obtain samples which have been optimally prepared for immuno-electron microscopy. Sometimes there is also a need to examine retrospectively samples collected some years previously. We have therefore developed modifications to our published methods to allow examination of human and animal tissue samples obtained at surgery or during post mortem which have subsequently been: 1. stored frozen at -35° or -70°C for biochemical examination; 2.

Loss of dermal elastic tissue in solar elastosis

1980 ◽  
Vol 116 (4) ◽  
pp. 474b-475 ◽  
Author(s):  
T. Tsuji
Keyword(s):  
Elastic Tissue
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