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Forces Necessary (force + necessary)
Selected AbstractsThe effects of partial and total interosseous membrane transection on load sharing in the cadaver forearmJOURNAL OF ORTHOPAEDIC RESEARCH, Issue 4 2001Michael F. Shepard This study was performed to examine the effects of partial and total transection of the interosseous membrane (IOM) on load transfer in the forearm. Twenty fresh frozen forearms were instrumented with custom designed load cells placed in the proximal radius and distal ulna. Simultaneous measurements of load cell forces, radial head displacement relative to the capitellum, and local tension within the central band of the IOM were made as the wrist was loaded to 134 N with the forearm at 90° of elbow flexion and in neutral pronation supination. For valgus elbow alignment (radial head contacting the capitellum), mean force carried by the distal ulna was 7.1% of the applied wrist force and mean force transferred from radius to ulna through the IOM was 4.4%. For varus elbow alignment (mean 2.0 mm gap between the radial head and capitellum), mean distal ulna force was 28% and mean IOM force was 51%. Section of the proximal and distal one-thirds of the IOM had no significant effect upon mean distal ulnar force or mean IOM force. Total IOM section significantly increased mean distal ulnar force for varus elbow alignment in all wrist positions tested. The mean level of applied wrist force necessary to close the varus gap (89 N) decreased significantly after both partial IOM section (71 N) and total IOM section (25 N). The IOM became loaded only when the radius displaced proximally relative to the ulna, closing the gap between the radius and capitellum. As the radius displaced proximally, the wrist becomes increasingly ulnar positive, which in turn leads to direct loading of the distal ulna. This shift of force to the distal ulna could present clinically as ulnar sided wrist pain or as ulnar impaction after IOM injury. © 2001 Orthopaedic Research Society. Punlished by Elsevier Science Ltd. All rights reserved. [source] Propagation of Tears in Pericardium From Young Bulls: Influence of the SutureARTIFICIAL ORGANS, Issue 3 2010José María García Páez Abstract The tearing of the collagen fibers of biological materials utilized in implants or bioprostheses is an important, and sometimes early cause of the failure of these devices. We studied the force necessary to propagate a tear in a biomaterial, pericardium from young bulls, and the influence of the suture. An Elmendorf pendulum capable of measuring the force necessary to tear a given length of tissue was employed. We analyzed 112 trials (70%) that proved valid after achieving the homogeneity of the samples according to their thickness, thus making the results comparable. Mean forces ranging between 19.87 and 150 N were required to propagate tears measuring from 0.25 to 2.0 cm. In the samples with a 1-cm-long suture, sewn using an edge-to-edge technique, the propagation of the tear required a mean force of 15.75 N when the suture was made of nylon and 28.73 N when Prolene was utilized. When these results were compared with the mean recorded in an unsutured control series (56.76 N), the loss of resistance was significant in both sutured series (P = 0.000 and P = 0.011, respectively). Finally, the equation that relates the force (y) with the length of the tear made in unsutured tissue (x) was also obtained: y = 58.14 + 9.62x2 (R2 = 0.924). The force necessary to produce a microtear, thus estimated, can be utilized as a parameter for comparison. [source] On the measurement of growth with applications to the modelling and analysis of plant growthFUNCTIONAL ECOLOGY, Issue 2 2000Roderick M. L. Abstract 1.,In this paper, a theoretical framework for the analysis of growth is described. Growth is equated with change in volume (V) and the growth rate is given by the equation; dV/dt = (dm/dt)(1/,) , (d,/dt)(m/,2) where m is the mass and , the density. The volume is inclusive of internal air spaces. 2.,The second term of the growth equation (see above) can be ignored if density is constant over time. Data for humans (and presumably other large animals) show that while composition changes over time, the density is approximately constant at about that of water. In that case, the growth rate can be estimated from measures of the rate of change of mass. However, the density of plants is variable (c. 0·4,1·2 g cm,3) and measures of mass and density are necessary to analyse plant growth. 3.,To use the theory as the basis of plant growth models, it is necessary to develop simple methods for estimating the surface area of roots, stems and leaves assuming that the mass and volume are known. A literature review found that the surface area to volume ratios of leaves and roots generally increase with the mass concentration of water. Theoretical arguments are used to predict that in woody stems, the situation should be reversed such that the surface area to volume ratio increases with the mass concentration of dry matter. Those relationships should be very useful in the development of plant growth models. 4.,Measures of plant dry mass and estimates of the rate of change in dry mass are shown to be very difficult to interpret because of differences in the mass concentration of dry matter between individuals and over time. 5.,It is concluded that measures of mass and density will be necessary before plant growth analysis can achieve its full potential. A framework for extending the theory to include the forces necessary for growth to occur is described. [source] Interactions between the L1 cell adhesion molecule and ezrin support traction-force generation and can be regulated by tyrosine phosphorylationJOURNAL OF NEUROSCIENCE RESEARCH, Issue 12 2008Takeshi Sakurai Abstract An Ig superfamily cell-adhesion molecule, L1, forms an adhesion complex at the cell membrane containing both signaling molecules and cytoskeletal proteins. This complex mediates the transduction of extracellular signals and generates actin-mediated traction forces, both of which support axon outgrowth. The L1 cytoplasmic region binds ezrin, an adapter protein that interacts with the actin cytoskeleton. In this study, we analyzed L1,ezrin interactions in detail, assessed their role in generating traction forces by L1, and identified potential regulatory mechanisms controlling ezrin,L1 interactions. The FERM domain of ezrin binds to the juxtamembrane region of L1, demonstrated by yeast two-hybrid interaction traps and protein binding analyses in vitro. A lysine-to-leucine substitution in this domain of L1 (K1147L) shows reduced binding to the ezrin FERM domain. Additionally, in ND7 cells, the K1147L mutation inhibits retrograde movement of L1 on the cell surface that has been linked to the generation of the traction forces necessary for axon growth. A membrane-permeable peptide consisting of the juxtamembrane region of L1 that can disrupt endogenous L1,ezrin interactions inhibits neurite extension of cerebellar cells on L1 substrates. Moreover, the L1,ezrin interactions can be modulated by tyrosine phosphorylation of the L1 cytoplasmic region, namely, Y1151, possibly through Src-family kinases. Replacement of this tyrosine together with Y1176 with either aspartate or phenylalanine changes ezrin binding and alters colocalization with ezrin in ND7 cells. Collectively, these data suggest that L1,ezrin interactions mediated by the L1 juxtamembrane region are involved in traction-force generation and can be regulated by the phosphorylation of L1. © 2008 Wiley-Liss, Inc. [source] A histomorphological study of tendon reconstruction to a hydroxyapatite-coated implant: Regeneration of a neo-enthesis in vivoJOURNAL OF ORTHOPAEDIC RESEARCH, Issue 6 2004C. J. Pendegrass The attachment of tendons and ligaments to massive endoprostheses remains a clinical challenge due to the difficulty in achieving a soft tissue implant interface with a mechanical strength sufficient to transmit the forces necessary for locomotion. We have used an in vivo animal model to study patellar tendon attachment to an implant surface. The interface generated when the patellar tendon was attached to a hydroxyapatite (HA) coated implant was examined using light microscopy and a quantitative histomorphological analysis was performed. In the Autograft Group, the interface was augmented with autogenous cancellous bone and marrow graft, and at six weeks an indirect-like insertion was observed. At twelve weeks, the interface was observed to be a layered neo-enthesis, whose morphology was similar to a normal direct tendon insertion. In the HA Group, the tendon,implant interface was not augmented, and the implant was enveloped by a dense collagenous fibrous tissue. This study shows that a tendon,implant neo,enthesis can develop in situ by employing a suitable implant surface in association with biological augmentation. © 2004 Orthopaedic Research Society. Published y Elsevier Ltd. All rights reserved. [source] | ||||||||||