Table 3.

Production of 14C-CO2 From D-[1-14C] Glucose in Normal and Deficient RPE

NPE NPE + MB RPE RPE + MB
Column  B  C  D  D-B  
Normal E  0.15 ± 0.06 3.92 ± 0.56  0.68 ± 0.21  5.27 ± 0.98  1.35 
 n  16  18  3  5  
P→  .001  .001  
P→→  .001  .001 
P↓  .001  .001  .166  .028 
Deficient E  0.05 ± 0.002  0.07 ± 0.04 0.33 ± 0.29  1.39 ± 0.37  1.32  
 No.  11 11  3  5  
P→  .001   .006 
P→→  .001  .001     
NPE NPE + MB RPE RPE + MB
Column  B  C  D  D-B  
Normal E  0.15 ± 0.06 3.92 ± 0.56  0.68 ± 0.21  5.27 ± 0.98  1.35 
 n  16  18  3  5  
P→  .001  .001  
P→→  .001  .001 
P↓  .001  .001  .166  .028 
Deficient E  0.05 ± 0.002  0.07 ± 0.04 0.33 ± 0.29  1.39 ± 0.37  1.32  
 No.  11 11  3  5  
P→  .001   .006 
P→→  .001  .001     

Production of 14C-CO2 is expressed as μmol/1010 cells/hour at 37°C. Mean values ± SD of 3 of 18 separate experiments (n) as indicated. RPE were separated from synchronized P falciparum cultures as detailed in Materials and Methods 14 to 18 hours after inoculum. 14C-CO2production values obtained with cultures containing 30% to 45% RPE were extrapolated to 100% RPE parasitemia as indicated in Materials and Methods. Nonparasitized E (NPE) were kept in culture and processed in the same way as parasitized E. MB, 135 μmol/L final, was used to maximally stimulate 14C-CO2 production. Column D-B: net maximal 14C-CO2 production by RPE after MB stimulation (see Results for details). P→ = significance to the first column to the right;P→→ = significance to the second column to the right; P↓ = significance within the same column. Significance of differences was assessed by t-test for paired samples.

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