Human colonic short-chain fatty acid (SCFA) absorption is associated with increased luminal pH and HCO3- and enhanced Na+ absorption. Therefore, the mechanism of colonic SCFA transport, its dependence on Na+ and HCO3- and interactions with Cl-/HCO3- and Na+/H+ exchangers were characterized. Luminal membrane vesicles (LMV) isolated by divalent cation precipitation from organ donor colons were used for n-butyrate transport. Uptake of n-butyrate into the human colonic LMV was minimal even in the presence of an inward pH gradient, but an outward HCO3- gradient significantly increased uptake rates. HCO3(-)-stimulated butyrate uptake was saturable with an apparent Michaelis constant of 1.5 +/- 0.2 mM and maximal velocity of 105 +/- 3 nmol.mg protein-1.3 s-1. Intravesicular butyrate resulted in trans-stimulation of n-[1-14C]butyrate uptake. Butyrate uptake was inhibited approximately 25-40% by C2-C5 SCFAs and approximately 40% by niflumic acid. Butyrate uptake was not affected by extravesicular Na+, and 22Na uptake was unaltered by extravesicular butyrate. Butyrate uptake was independent of extra- or intravesicular CI-, and butyrate loading produced no changes in 36Cl uptake. We conclude that the predominant mechanism of n-butyrate transport across the human colonic luminal membrane appears to be via a HCO3-/SCFA antiport system independent of Cl-/HCO3- exchange and Na+ transport.

The MARS code is under continuous development and has recently undergone substantial improvements that further increase its reliability and predictive power in numerous shielding, accelerator, detector and space applications. The major developments and new features of the MARS15 (2004) version described in this paper concern an extended list of elementary particles and arbitrary heavy ions and their interaction cross-sections, inclusive and exclusive nuclear event generators, module for modelling particle electromagnetic interactions, enhanced geometry and histograming options, improved MAD-MARS Beam Line Builder, enhanced Graphical-User Interface, and an MPI-based parallelization of the code. Abstract -The MARS code is under continuous development and has recently undergone substantial improvements that further increase its reliability and predictive power in numerous shielding, accelerator, detector and space applications. The major developments and new features of the MARS15 (2004) version described in this paper concern an extended list of elementary particles and arbitrary heavy ions and their interaction cross-sections, inclusive and exclusive nuclear event generators, module for modelling particle electromagnetic interactions, enhanced geometry and histograming options, improved MAD-MARS Beam Line Builder, enhanced Graphical-User Interface, and an MPI-based parallelization of the code. __________________________

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This paper will present a solution to eliminate the requirements of sorting by prefix length in IP forwarding devices using Ternary Content Addressable Memories (TCAMs). This will do away with delays arising from inserting into a sorted list. To achieve this, the routing table entries in the TCAM are split by output port. This solution requires slight modifications to current TCAMs including the elimination of the built-in encoder. Overall, the solution presented reduces the insertion problem to lookup speed while maintaining similar clock rates and storage requirements of traditional TCAMs.

We present a solution to eliminate the requirements of routing table sorting by prefix length in IP lookup devices using Ternary Content Addressable Memories (TCAMs). This will reduce delays arising from routing table updates from linear to constant time. This solution introduces slight modifications to the organization of the routing table including the elimination of the built-in priority encoder. The routing table entries are split by output port to remove their dependence on length. Overall, the solution presented reduces the insertion problem to lookup speed while maintaining similar clock rates and storage requirements of traditional designs.