
Yeah, I have one of the older version that I play from time to time, and I still love it.:) Btw, do you have DMPC Pro? I want to try it out, but I keep getting an error that keeps me from starting it up. Here you can download file DMPC_PRO_1.0.2. 2shared gives you an excellent opportunity to store your files here and share them.ĭoes not affect evading chance. (Surrender function not implemented yet) Light - Switch on/off light Heal - Heal digimon's sickness/injury Pause(Snowflake) - Freeze your digimon and pause the game Quit - Exit game Call - On when digimon is calling Evolution bar - It is on the right side of the main room and cannot be seen unless hovered by mouse. It shows the evolution path your digimon has followed.

Volume Bar - Press 'S' on your keyboard while in main room to toggle volume bar and disable ambient sound.

(activate it again, turning on or off the light) Right click or press 'S' again to disable it. Frame Color - Press 'C' on your keyboard to switch between different colors.Ĭhange Background - Press 'B' on your keyboard. Save the Game - Press 'F5' on your keyboard. These results support the hypothesis that acemetacin-induced gastric toxicity may be related to its effects on the protective phospholipid layers of the mucosal barrier.ID Card Generation - Press 'P' on your keyboard. In general, acemetacin decreased the temperature and the cooperativity of the lipid phase transition and induced changes in the packing and dynamics of the DMPC bilayer. Due to the higher affinity of neutral acemetacin, the drug effects on the phase transition and the structure and dynamics of the DMPC bilayer were more pronounced at lower pH values. The neutral (protonated) form of acemetacin had more affinity for the DMPC bilayer than the negatively charged form. The acemetacin–DMPC interactions were clearly pH-dependent. Various experimental techniques were combined to characterize the partitioning of acemetacin DMPC bilayers, and its effects on the phase transition behavior, as well as the structure and dynamics of DMPC bilayers. This pH range was chosen to mimic the pH gradient found in the gastric mucosa, and to ultimately gain insights into the mechanisms underlying the acemetacin-induced gastric toxicity. This work describes the interactions of acemetacin, a commercialized NSAID, with 1,2-dimyristoyl-sn-glycero-3-phosphocholine (DMPC) bilayers at pH 3.0, 5.0, and 7.4.

The NSAIDs topical actions on the protective phospholipid layers of the GI mucosa seem to be a central toxicity mechanism of these pharmaceuticals. Gastrointestinal (GI) toxicity is a major drawback of the chronic use of nonsteroidal anti-inflammatory drugs (NSAIDs).
