35S]Guanosine-5''-O-(3-thio)triphosphate binding as a measure of efficacy at human recombinant dopamine D4.4 receptors: actions of antiparkinsonian and antipsychotic agents

Great progress has been made in the last 10 years in the understanding of the various types of viral hepatitis, and new viruses, concepts, therapies, preventive measures, and control strategies have been recognized. Even more agents, vaccines, and drugs will be discovered or developed in the future, and pediatricians increasingly will be expected to provide guidance to patients and to the community on the importance and use of these new tools.     

Study of the neutral lipids of sunflower meal and isolates

Two types of sunflower protein isolates have been obtained from prepress and solvent extracted sunflower meal. The first was obtained by precipitation (at the isoelectric point) of the alkaline extract of the meal, and washing the curd with water. In the second, the alkaline extraction was carried out in the presence of sodium sulfite, and the curd was washed with water, ethanol and acetone. Both isolates were air-dried and then dried under vacuum at 50 C. From the total lipids, obtained with 86% ethanol, the neutral lipids were separated using a column of Florisil. The lipids studied were those of the two isolates mentioned above as well as those of the original meal. The following types of compounds were separated, identified and quantified: hydrocarbons, waxes, methyl esters, triglycerides, free fatty acids, diglycerides, free sterols, and hydroxy fatty acids.     

Mechanical effects of increases in the load applied in uniaxial and biaxial tensile testing: Part I. Calf pericardium

The authors analyzed the mechanical behavior of the calf pericardium employed in the construction of valve leaflets for cardiac bioprostheses. Forty samples of pericardium were subjected to uniaxial tensile testing, 20 as controls and 20 exposed to loads increasing stepwise until rupture, with a return to zero load between each new increment. Another 20 samples were used similarly in biaxial tensile tests involving loads increasing stepwise until rupture, again returning to zero load between steps. The ultimate stresses in the uniaxial study were very similar and were not influenced by the region of pericardial tissue being tested or the increments in load to which the tissue was exposed. The mean stresses at rupture in the stepwise biaxial assays were significantly greater (p<0.01). Using morphological and mechanical criteria for sample selection, it was possible to obtain mathematical fits for the stress/strain relationship in both types of assays, with excellent coefficients of determination (R ²>0.90). In uniaxial tests in which the selection criteria were not applied, the correlation improved as the load increased, a phenomenon that did not occur in the biaxial studies. The values varied throughout the different cycles, adopting exponential forms when the strain was greatest. These variations, which demonstrate that the increase in the energy consumed is a function of the stress applied and of the strain produced, should be good parameters for assessing the changes in the collagen fiber architecture of pericardial tissue subjected to cyclic stress, and may help to detect early failure.     

The dopamine D3 receptor antagonist, (+)-S 14297, blocks the cataleptic properties of haloperidol in rats

In contrast to haloperidol, the selective dopamine D3 receptor antagonist, (+)-S 11566 [(+/-)-[7-(N,N-dipropylamino)-5,6,7,8-tetrahydro- naphtho(2,3b)dihydro,2,3-furanel]] and its active isomer, (+)-S 14297, induced neither catalepsy nor reduced conditioned avoidance responses in rats. (+)-S 11566 and (+)-S 14297 did, however, dose-dependently abolish the cataleptic actions of haloperidol. This action was expressed stereospecifically inasmuch as (-)-S 17777, the inactive distomer of (+)-S 14297, was ineffective. Further, the influence of haloperidol upon conditioned avoidance responses was not affected by (+)-S 14297. These data suggest that blockade of dopamine D3 receptors may inhibit the extrapyramidal but not-as based on the conditioned avoidance response paradigm-antipsychotic actions of neuroleptics.     

An ON-resistance closed form for VDMOS devices

An analytical ON-resistance expression for different designs of VDMOS (vertically diffused metal-oxide-semiconductor) devices which takes into consideration the two-dimensional (2-D) nature of the current flow is obtained. This expression differs from other models that overestimate this resistance for large cell spacings. This formulation is in close agreement with experimental points obtained from the interdigitated fabricated structures and with 2-D simulations. Moreover, the effect of a two-level oxide thickness on the ON resistance has been investigated for the interdigitated case     

Reduction of self-heating effect on SOIM devices

The silicon-on-insulator (SOI) power devices have an inherent self-heating effect, which limits their operation at high current levels. This is a consequence of the very low thermal conductivity of the thick buried oxide layer. A novel solution to reduce the self-heating effect is proposed in this paper, based on silicon-over-insulator-multilayer (SOIM) emerging technology. A significant reduction of the insulator layer thermal resistance is achieved while keeping constant the electrical behaviour of integrated power devices in comparison to the conventional SOI counterparts. The effectiveness of the proposed solution has been corroborated with numerical simulations. Moreover, no additional steps in fabrication processes are required with regard to the conventional SOI technology.     

Poetry in Engineering Education

An important element of integrating disciplines and enhancing creativity in Drexel University's engineering curriculum is an assignment which combines poetry and engineering. For this assignment, students choose an artifact, research it, create a one-page annotated visual explaining how it works, and then write an original poem about it. Although the poetry instruction, based on a transactional model, takes place in the Humanities classroom, student poems become a component of a concurrent engineering assignment and are read aloud in an engineering lecture, attended by humanities faculty, designated as the “Poetry Reading.” Short in length and having a distinct design on the page, poetry is a particularly suitable literary medium for engineering students to explore. Students relinquish stereotypes about engineers when they see their engineering professor endorse poetry. They also begin to broaden their educational and professional goals.     

Contrasting effects of D- and L-(E)-4-(3-phosphono-2-propenyl)piperazine-2-carboxylic acid as anticonvulsants and as inhibitors of potassium-evoked increases in hippocampal extracellular glutamate and aspartate levels in freely moving rats

Microdialysis experiments performed in the dorsal hippocampus of freely moving rats showed that L-(E)-4-(3-phosphono-2-propenyl)piperazine-2-carboxylic acid (L-CPPene) is 10 times as potent as D-CPPene in inhibiting potassium-induced increases in extracellular levels of aspartate and glutamate. In control experiments, two 100 mM KCl stimuli (S1 and S2) applied for 10 min each (separated by a 40-min recovery period) produced substantial (300-500%) increases in the extracellular levels of aspartate, glutamate, taurine, and GABA and a 50% decrease in the glutamine level. S2/S1 ratios in the control groups were 0.67 (aspartate), 0.78 (glutamate), 0.83 (GABA), and 0.85 (taurine). In the experimental groups, D- or L-CPPene was applied via the probe during the second potassium stimulus (S2). L-CPPene (25 or 250 microM) produced selective suppression of potassium-induced increases of extracellular glutamate (S2/S1 ratio: 0.25) and aspartate (S2/S1 ratio: 0.20) levels, whereas 250 microM D-CPPene was required to inhibit the extracellular aspartate and glutamate increases. Neither enantiomer of CPPene affected the potassium-induced increases of GABA and taurine or the decrease in extracellular glutamine concentration. An additional study comparing the anticonvulsant potencies of D- and L-CPPene was performed using audiogenic DBA/2 mice. The anticonvulsant potency of D-CPPene, as assessed against sound-induced seizures in DBA/2 mice, was an order of magnitude higher than that of L-CPPene [ED50 clonic phase (intraperitoneal, 45 min): 1.64 mumol/kg and 16.8 mumol/kg, respectively]. We attribute the anticonvulsant action of D-CPPene to its antagonist action at the NMDA receptor.(ABSTRACT TRUNCATED AT 250 WORDS)     

Thin-film silicon-on-sapphire LDMOS structures for RF power amplifier applications

This work is addressed to the investigation of the electro-thermal performance of RF-LDMOS transistors integrated in TF-SOI, TF-SOS and thinned TF-SOS substrates by means of numerical simulations. Reported experimental trap density, carrier mobility and capture cross-section values have been used together with sapphire datasheet thermal properties, in order to provide accurate simulation results. It is found that subthreshold characteristics are the same for all the analysed substrates while blocking-state, on-state and power dissipation process depends on the substrate type.     

SR 144528, the first potent and selective antagonist of the CB2 cannabinoid receptor

Based on both binding and functional data, this study introduces SR 144528 as the first, highly potent, selective and orally active antagonist for the CB2 receptor. This compound which displays subnanomolar affinity (Ki = 0.6 nM) for both the rat spleen and cloned human CB2 receptors has a 700-fold lower affinity (Ki = 400 nM) for both the rat brain and cloned human CB1 receptors. Furthermore it shows no affinity for any of the more than 70 receptors, ion channels or enzymes investigated (IC50 > 10 microM). In vitro, SR 144528 antagonizes the inhibitory effects of the cannabinoid receptor agonist CP 55,940 on forskolin-stimulated adenylyl cyclase activity in cell lines permanently expressing the h CB2 receptor (EC50 = 10 nM) but not in cells expressing the h CB1 (no effect at 10 microM). Furthermore, SR 144528 is able to selectively block the mitogen-activated protein kinase activity induced by CP 55,940 in cell lines expressing h CB2 (IC50 = 39 nM) whereas in cells expressing h CB1 an IC50 value of more than 1 microM is found. In addition, SR 144528 is shown to antagonize the stimulating effects of CP 55,940 on human tonsillar B-cell activation evoked by cross-linking of surface Igs (IC50 = 20 nM). In vivo, after oral administration SR 144528 totally displaced the ex vivo [3H]-CP 55,940 binding to mouse spleen membranes (ED50 = 0.35 mg/kg) with a long duration of action. In contrast, after the oral route it does not interact with the cannabinoid receptor expressed in the mouse brain (CB1). It is expected that SR 144528 will provide a powerful tool to investigate the in vivo functions of the cannabinoid system in the immune response.