PubMed · 9002885
The source did not provide an abstract. Follow the original record for more information.
Explore connections, maps & timelines
M B Miller. 1995. Taking risks.. https://pubmed.ncbi.nlm.nih.gov/9002885/
Cite the original work for its findings. Save a collection to share your selection of sources.
KEEP EXPLORING
The resistances to sliding were studied as a function of five angulations (0 degrees, 3 degrees, 7 degrees, 11 degrees, and 13 degrees) using nine different couples made of stainless steel, single crystal sapphire, or polycrystalline alumina brackets against stainless steel, nickel titanium, or beta-titanium arch wires. After 22 mil brackets were mounted to fixtures and 21 x 25 mil arch wires were ligated with 10 mil stainless steel ligatures, the arch wires were slid through the brackets at 1 cm/minute in the dry state at 34 degrees C. The resistance to sliding was measured by one computer while five normal forces (nominally 0.2, 0.4, 0.6, 0.8, and 1.0 kg) were serially maintained by another computer. A second couple was prepared for each material combination with five normal forces that were each 0.1 kg less. Statistical fits of linear regressions were such that p <.001 for most tests. When couples were in the passive configuration at low angulations, all stainless steel wire-bracket couples once again had the least resistance to sliding. When the angulation exceeded about 3 degrees, however, the active configuration emerged and binding quickly dominated as the resistance to sliding increased over 100-fold. Under these conditions, the relative rankings among the materials transposed; couples of stainless steel had the most resistance to sliding, whereas, couples of the more compliant alloys, such as nickel titanium wire, had the least. Results suggested that the active configuration and subsequent binding emerged when no bracket clearance remained. This binding component increased in importance with angulation and was additive to the frictional component, that is, they followed the principle of superposition.
The goal of the present study was to determine whether alumina gel injections into temporal lobe structures cause complex partial seizures (CPS) and pathological changes observed in human temporal lobe epilepsy. Rhesus monkeys with alumina gel injections in the amygdala, perirhinal and entorhinal cortices, or Ammon's horn and dentate gyrus all initially displayed focal pathological electroencephalographic (EEG) slowing limited to the site of injection. After clinical seizures developed, they also displayed widespread pathological EEG slowing over both hemispheres, interictal and ictal epileptiform EEG abnormalities limited to the mesial-inferior temporal lobe on the side of injection, and different degrees of spread to other ipsilateral and contralateral structures. Noninjected control and nonepileptic monkeys with injections into the middle and inferior temporal gyri displayed no hippocampal neuronal loss or mossy fiber sprouting. When alumina gel was injected into the amygdala, CPS began within 3-6 weeks and degeneration of neurons and gliosis occurred in the perirhinal cortex or the hippocampus, with consequent sprouting of mossy fibers in the dentate gyrus. Dispersion of the granule cell layer was also observed. Other monkeys with alumina gel in the perirhinal and entorhinal cortices developed CPS within 2-3 weeks after the injections and displayed mossy fiber sprouting only after 4 weeks after the injections. Alumina gel in Ammon's horn and the dentate gyrus also induced CPS, but mossy fiber sprouting was limited to sites immediately adjacent to the injection, probably because none survived more than 4 weeks after the injections. This nonhuman primate model of CPS displayed similar anatomical, behavioral, and EEG features as observed in human temporal lobe epilepsy and provides opportunities to analyze the chronological sequence of epileptogenesis and to test potential therapies.
With water as the elution solvent, zwitterionic solutes and polyols were retained on HPLC columns, more than was water, by totally hydrophobic packing materials. Relative retentions were systematically affected by oxygen functional groups in the packing material, explicable as specific retention of water. Reproducible elution sequences of 20 solutes at a variety of hydrophobic surfaces (aromatic and both long- and short-alkyl aliphatic surfaces) showed there is a general process, consistent with interactions with hydration water at the surface having solvent properties distinct from bulk water. Early eluting solutes included glycine, sarcosine and taurine. Glycine betaine followed both these and N,N-dimethylglycine. The natural betaines propionobetaine and dimethylsulfoniopropionate also preceded glycine betaine. Dimethylsulfoxide was strongly retained, as (to a lesser extent) was proline betaine. Polyols eluted in the sequence sorbitol, trehalose, glycerol. Changes in the chemical nature of the surface or base material affected relative retentions of water and solutes. The presence of hydrogen-bonding functions increased retention of polyols, as well as water, relative to zwitterionic solutes. Specific effects retention, constraining models based on the formation of low-density water.