StabilimaxNZ) versus simulated fusion: evaluation of adjacent-level effects. (1/162)

Rationale behind motion preservation devices is to eliminate the accelerated adjacent-level effects (ALE) associated with spinal fusion. We evaluated multidirectional flexibilities and ALEs of StabilimaxNZ and simulated fusion applied to a decompressed spine. StabilimaxNZ was applied at L4-L5 after creating a decompression (laminectomy of L4 plus bilateral medial facetectomy at L4-L5). Multidirectional Flexibility and Hybrid tests were performed on six fresh cadaveric human specimens (T12-S1). Decompression increased average flexion-extension rotation to 124.0% of the intact. StabilimaxNZ and simulated fusion decreased the motion to 62.4 and 23.8% of intact, respectively. In lateral bending, corresponding increase was 121.6% and decreases were 57.5 and 11.9%. In torsion, corresponding increase was 132.7%, and decreases were 36.3% for fusion, and none for StabilimaxNZ ALE was defined as percentage increase over the intact. The ALE at L3-4 was 15.3% for StabilimaxNZ versus 33.4% for fusion, while at L5-S1 the ALE were 5.0% vs. 11.3%, respectively. In lateral bending, the corresponding ALE values were 3.0% vs. 19.1%, and 11.3% vs. 35.8%, respectively. In torsion, the corresponding values were 3.7% vs. 20.6%, and 4.0% vs. 33.5%, respectively. In conclusion, this in vitro study using Flexibility and Hybrid test methods showed that StabilimaxNZ stabilized the decompressed spinal level effectively in sagittal and frontal planes, while allowing a good portion of the normal rotation, and concurrently it did not produce significant ALEs as compared to the fusion. However, it did not stabilize the decompressed specimen in torsion.  (+info)

Evaluation of the debonding strength of orthodontic brackets using three different bonding systems. (2/162)

The aim of this work was to investigate the stability of the bracket-adhesive-enamel interface, as a function of adhesive material and of debonding procedure, in order to assess which debonding technique is the least detrimental to the enamel. Ninety lower adult bovine incisors were selected and metallic orthodontic brackets were bonded using three adhesive systems: Concise, Transbond, and Fuji Ortho. Three different debonding procedures were used based on tensile, shear, and torsional stresses. One-way analysis of variance statistical analysis was employed to compare mechanical properties, while the adhesive remnant index was used to evaluate fracture properties. Each adhesive material used showed a statistical difference in tensile failure. The difference between shear and torsion failure loads was statistically significant only for the Fuji GC sample (P < 0.01). The shear test was the most damaging to the enamel surface. Transbond luting resulted in greater adhesion than the Concise or Fuji Ortho systems. Fuji Ortho was more prone to accidental debonding, while Transbond tended to cause enamel lesions, since high loads were required to debond the bracket. Of the three modes examined, torsional debonding stress resulted in the least enamel damage.  (+info)

A virtual ophthalmotrope illustrating oculomotor coordinate systems and retinal projection geometry. (3/162)

Eye movements are kinematically complex. Even when only the rotational component is considered, the noncommutativity of 3D rotations makes it hard to develop good intuitive understanding of the geometric properties of eye movements and their influence on monocular and binocular vision. The use of at least three major mathematical systems for describing eye positions adds to these difficulties. Traditionally, ophthalmotropes have been used to visualize oculomotor kinematics. Here, we present a virtual ophthalmotrope that is designed to illustrate Helmholtz, Fick, and rotation vector coordinates, as well as Listing's extended law (L2), which is generalized to account for torsion with free changing vergence. The virtual ophthalmotrope shows the influence of these oculomotor patterns on retinal projection geometry.  (+info)

Ventricular untwisting: a temporal link between left ventricular relaxation and suction. (4/162)

Left ventricular (LV) untwisting starts early during the isovolumic relaxation phase and proceeds throughout the early filling phase, releasing elastic energy stored by the preceding systolic deformation. Data relating untwisting, relaxation, and intraventricular pressure gradients (IVPG), which represent another manifestation of elastic recoil, are sparse. To understand the interaction between LV mechanics and inflow during early diastole, Doppler tissue images (DTI), catheter-derived pressures (apical and basal LV, left atrial, and aortic), and LV volume data were obtained at baseline, during varying pacing modes, and during dobutamine and esmolol infusion in seven closed-chest anesthetized dogs. LV torsion and torsional rate profiles were analyzed from DTI data sets (apical and basal short-axis images) with high temporal resolution (6.5 +/- 0.7 ms). Repeated-measures regression models showed moderately strong correlation of peak LV twisting with peak LV untwisting rate (r = 0.74), as well as correlations of peak LV untwisting rate with the time constant of LV pressure decay (tau, r = -0.66) and IVPG (r = 0.76, P < 0.0001 for all). In a multivariate analysis, peak LV untwisting rate was an independent predictor of tau and IVPG (P < 0.0001, for both). The start of LV untwisting coincided with the beginning of relaxation and preceded suction-aided filling resulting from elastic recoil. Untwisting rate may be a useful marker of diastolic function or even serve as a therapeutic target for improving diastolic function.  (+info)

Domain motions of Argonaute, the catalytic engine of RNA interference. (5/162)

BACKGROUND: The Argonaute protein is the core component of the RNA-induced silencing complex, playing the central role of cleaving the mRNA target. Visual inspection of static crystal structures already has enabled researchers to suggest conformational changes of Argonaute that might occur during RNA interference. We have taken the next step by performing an all-atom normal mode analysis of the Pyrococcus furiosus and Aquifex aeolicus Argonaute crystal structures, allowing us to quantitatively assess the feasibility of these conformational changes. To perform the analysis, we begin with the energy-minimized X-ray structures. Normal modes are then calculated using an all-atom molecular mechanics force field. RESULTS: The analysis reveals low-frequency vibrations that facilitate the accommodation of RNA duplexes - an essential step in target recognition. The Pyrococcus furiosus and Aquifex aeolicus Argonaute proteins both exhibit low-frequency torsion and hinge motions; however, differences in the overall architecture of the proteins cause the detailed dynamics to be significantly different. CONCLUSION: Overall, low-frequency vibrations of Argonaute are consistent with mechanisms within the current reaction cycle model for RNA interference.  (+info)

Kinking the double helix by bending deformation. (6/162)

DNA bending and torsional deformations that often occur during its functioning inside the cell can cause local disruptions of the regular helical structure. The disruptions created by negative torsional stress have been studied in detail, but those caused by bending stress have only been analyzed theoretically. By probing the structure of very small DNA circles, we determined that bending stress disrupts the regular helical structure when the radius of DNA curvature is smaller than 3.5 nm. First, we developed an efficient method to obtain covalently closed DNA minicircles. To detect structural disruptions in the minicircles we treated them by single-strand-specific endonucleases. The data showed that the regular DNA structure is disrupted by bending deformation in the 64-65-bp minicircles, but not in the 85-86-bp minicircles. Our results suggest that strong DNA bending initiates kink formation while preserving base pairing.  (+info)

Resurrection of the flagellar rotary motor near zero load. (7/162)

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The effect of aging on torsional optokinetic nystagmus. (8/162)

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