Gene/Protein Disease Symptom Drug Enzyme Compound
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Query: UMLS:C0085632 (apathy)
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The voluntary intake by male Sprague-Dawley rats of five calcium salts and eight mineral chlorides was assessed. Groups of 12-25 rats received a series of 48-h two-bottle tests with a choice between water and ascending concentrations of a mineral solution. Similar inverted U-shaped concentration-intake functions were obtained with each of the five calcium salts tested (hydroxide, gluconate, phosphate, lactate, and chloride): rats drank more calcium solution than water at concentrations between approximately 0.2 and 5 mM, showed indifference between 5 and 12 mM, and avoided higher concentrations. Inverted U-shaped concentration-intake functions were also obtained for ammonium chloride (peak at 100 mM), magnesium chloride (peak at 10 microM), potassium chloride (peak at 10 mM), ferrous chloride (peak at 4.64 microM), and rubidium chloride (peak at 2.15 mM). Rats drank slightly and nonsignificantly more 2.15 microM aluminum chloride than water and never drank more zinc chloride than water (range tested, 1 microM to 464 mM). These results illustrate that, as is the case for sodium, rats spontaneously ingest low concentrations of calcium and several other mineral solutions in preference to water. In general, the lower the cation's ionic charge, the greater the intake and higher the most accepted concentration.
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PMID:Voluntary intake of calcium and other minerals by rats. 806 56

Caspofungin (CAS) inhibits fungal cell wall synthesis. Sulfamethoxazole (SMX) inhibits folate biosynthesis and is active in vitro against Aspergillus spp. We studied the activities of the combination of CAS and SMX against 31 Aspergillus isolates and compared them with that of SMX combined with amphotericin B (AMB) or itraconazole (ITC). MICs and minimal effective concentrations (MECs) were determined by the NCCLS broth microdilution method. With MIC endpoints, the combination of SMX and CAS showed synergy or synergy to additivity against 29 of 31 isolates. With MEC endpoints, synergy to additivity was found against 12 of 31 isolates and indifference was displayed against the rest of them. SMX in combination with AMB or ITC was not truly synergistic, while synergy to additivity was found for SMX-AMB and SMX-ITC against 17 of 31 and 3 of 12 isolates, respectively. No antagonism was found with any of the drug combinations. Further analysis of the synergy of CAS and SMX was performed by detailed measurement of hyphal length by microscopy and time-dependent 2,3-bis(2-methoxy-4-nitro-5-[(sulfenylamino)carbonyl]-2H-tetrazolium hydroxide (XTT)-based hyphal damage experiments. With MEC endpoints, the combination of CAS and SMX was characterized by a greater than 50% decrease in hyphal length compared to the hyphal lengths achieved with double the concentration of each drug alone. The XTT-based hyphal damage studies showed a statistically significant (P < 0.05) reduction in viability with CAS and SMX in combination compared to the viabilities achieved with double the concentration of each drug alone. These findings support the synergy results found by using MIC endpoints and suggest that visual MEC measurements may not be sufficient to identify the synergistic interactions seen by more sensitive, quantitative methods. Animal models are required to validate the significance of the synergy of CAS and SMX against Aspergillus spp. observed in vitro.
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PMID:In vitro activity of caspofungin combined with sulfamethoxazole against clinical isolates of Aspergillus spp. 1532 85