Head-to-nerve analysis of electromechanical impairments of diffuse axonal injury

Biomechanics and Modeling in Mechanobiology - The aim was to investigate mechanical and functional failure of diffuse axonal injury (DAI) in nerve bundles following frontal head impacts, by finite...     

Bidirectional potentiation between D1 and D2 dopamine agonists: effects of unilateral intra-accumbens injections on locomotor activity in mice.

We tested the effect of a single unilateral injection of a specific D1 agonist into the nucleus accumbens on the behavioral response to a subsequent unilateral intra-accumbens injection of a selective D2 agonist ten days later. The effect of the inverse order of presentation (D2 agonist followed ten days later by a D1 agonist) was also tested. No significant differences between the locomotor effects of the intra-accumbens injection of either SKF-38393 (3.5 micrograms) or LY-171555 (10 micrograms) were observed during the first test. Ten days later, during the second test, intra-accumbens injection of either the LY-171555 and SKF-38393 increased the percentage of contralateral rotations relative to the first test while LY-171555 also increased the total number of rotations. Control injections showed that these effects of LY-171555 and SKF-38393 were not due to a conditioning process. Rather, the results suggested that the locomotor changes observed during the second test were the result of behavioral sensitization due to the initial acute injection of the agonists.     

Anatomico-functional approach to the mechanisms of memory: analysis by deoxyglucose of the limbic activation induced by electric stimulation of the mouse entorhinal cortex

Previous behavioral studies using post-training electrical stimulation of the brain have suggested that the lateral entorhinal cortex (LEC) is involved in mnemonic processes. In an attempt to characterize in vivo the neural pathways activated by LEC stimulation, regional patterns of uptake of 14C-2-deoxy-D-glucose (2-DG) were assessed in BALB/c mouse brain. The animals were implanted with a bipolar electrode in the LEC and a catheter in the jugular vein. In addition, four animals received an electrolytic lesion of the perforant path (PP) in order to disconnect the LEC from the hippocampus. The LEC was stimulated at subconvulsive intensity for 5 min. before and 30 min. after an injection of 2-DG. Stimulation of the LEC produced significant increases in 2-DG radioactivity in the hippocampus (dentate gyrus, CA3, CA1), subiculum and pre-subiculum. Demonstrable labelling was found in brain areas, beyond the hippocampal formation: piriform cortex, amygdala, cingulate cortex, Diagonal Band of Broca, the medial and lateral septal nuclei and the medial forebrain bundle. After PP lesion, the metabolic activity disappeared ipsilaterally in subiculum, dorsal part of the hippocampus, in some thalamic nuclei and in mammillary bodies, but all other extra-hippocampal labelling was unchanged. These data considered along with our previous behavioral results, suggest that LEC stimulation may act on mnemonic processes by the recruitment of cortical and subcortical extra-hippocampal structures (e.g. amygdala and cingulate cortex) directly or indirectly connected to the entorhinal cortex.     

Paradoxical transitory facilitation of performance in the Hebb-Williams labyrinth after lesion of the cingulate cortex in mice

The effects of lesions of the anterior (Ant) or posterior (Post) regions of the cingulate cortex were tested using the closed-field maze tests of Hebb-Williams. Subjects were male BALB/c mice which had received restricted bilateral electrolytic lesions of the Ant or Post cingulate cortex. Their performances in acquisition or retention were compared to those of sham operated mice at different time intervals after the lesion. In a first series of experiments, naive animals were lesioned. The effects of lesions on acquisition were then tested at different time intervals (up to 45 days) after surgery. In a second series of experiments, the animals were lesioned only after prior complete acquisition of the maze tests and tested in a retention paradigm. The results show a differential effect of Ant versus Post cingulate lesions. Ant lesions had no significant effects whereas Post lesions induced a facilitation of performance at time intervals between 19 and 33 days (acquisition paradigm) or 11 and 25 days (retention paradigm). Conversely a reversal (impairment) of the effect was observed when Post animals were tested 28 days (acquisition) or 48 days (retention) after surgery. Taking into consideration the changing nature of the behavioral paradigm used, we suggest that the paradoxical and transitory facilitatory effects of the Post cingulate lesions may indicate that lesioned mice exhibited a greater degree of adaptability in each new learning situation. However, we can also postulate that these facilitatory effects resulted from a difficulty of lesioned mice in addressing long-term memory stores. This would therefore paradoxically protect them from interference generated by the high degree of familiarity in the behavioural testing apparatus.(ABSTRACT TRUNCATED AT 250 WORDS)     

Analysis of kinetics of consecutive metabolic cerebral activations induced by spatial discrimination testing, using (14C)-glucose, in an eight-arm radial maze in mice

Regional mapping of relative (14C)-glucose (GLU) uptake was analyzed in Balb/c mice at 3 time intervals (5 min., 1 hr., 3 hrs.) after either the first (Day 1) or the last (Day 9) daily sessions of a spatial discrimination testing procedure in an eight-arm radial maze. On Day 1, increased labelling was found 5 min. post-training in subcortical, hippocampal and cortical regions. Decreased GLU uptake was observed 1 hr. later in the same regions, followed at 3 hrs. post-training by a retarded activation in the above areas and particularly in thalamic and cortical structures. On Day 9, there was only an early (5 min.) post-training increase in metabolic activity followed by a subsequent monotonic decrease over 3 hrs. post-training period.     

Deficiencies in numerical models of anisotropic nonlinearly elastic materials

Incompressible nonlinearly hyperelastic materials are rarely simulated in finite element numerical experiments as being perfectly incompressible because of the numerical difficulties associated with globally satisfying this constraint. Most commercial finite element packages therefore assume that the material is slightly compressible. It is then further assumed that the corresponding strain-energy function can be decomposed additively into volumetric and deviatoric parts. We show that this decomposition is not physically realistic, especially for anisotropic materials, which are of particular interest for simulating the mechanical response of biological soft tissue. The most striking illustration of the shortcoming is that with this decomposition, an anisotropic cube under hydrostatic tension deforms into another cube instead of a hexahedron with non-parallel faces. Furthermore, commercial numerical codes require the specification of a ‘compressibility parameter’ (or ‘penalty factor’), which arises naturally from the flawed additive decomposition of the strain-energy function. This parameter is often linked to a ‘bulk modulus’, although this notion makes no sense for anisotropic solids; we show that it is essentially an arbitrary parameter and that infinitesimal changes to it result in significant changes in the predicted stress response. This is illustrated with numerical simulations for biaxial tension experiments of arteries, where the magnitude of the stress response is found to change by several orders of magnitude when infinitesimal changes in ‘Poisson’s ratio’ close to the perfect incompressibility limit of 1/2 are made.