coproporphyrin isomers
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2015 ◽  
pp. 172-177
Author(s):  
E. Ventura ◽  
E. Rocchi ◽  
F. Balli ◽  
P. Gibertini ◽  
V. Santunione ◽  
...  

1999 ◽  
Vol 282 (1-2) ◽  
pp. 45-58 ◽  
Author(s):  
A. Kühnel ◽  
U. Groß ◽  
K. Jacob ◽  
M.O. Doss

1995 ◽  
Vol 41 (9) ◽  
pp. 1315-1317 ◽  
Author(s):  
N R Badcock ◽  
D A Szep ◽  
G D Zoanetti ◽  
B D Lewis

1994 ◽  
Vol 13 (12) ◽  
pp. 839-847 ◽  
Author(s):  
Gonzalo G. García-Vargas ◽  
Luz M. Del Razo ◽  
Mariano E. Cebrián ◽  
Arnulfo Albores ◽  
Patricia Ostrosky-Wegman ◽  
...  

1 A detailed study of the urinary excretion pattern of porphyrins in humans chronically exposed to As via drinking water was performed using high performance liquid chromatography (HPLC) 2 Thirty-six individuals (15 men and 21 women) were selected from a town which had 0.400 mg L -1 of As in drinking water. The control group consisted of thirty-one individuals (13 men and 18 women) whose As concentration in drinking water was 0.020 mg L-1. 3 The major abnormalities in the urinary porphyrin excretion pattern observed in arsenic-exposed individuals were: (a) significant reductions in coproporphyrin III excretion resulting in decreases in the COPRO III/COPRO I ratio, and (b) significant increases in uroporphyrin excretion. Both alterations were responsible for the decrease in the COPRO/URO ratio. 4 No porphyrinogenic response was found in individuals with urinary As concentrations below 1,000 μg of As g-1 of creatinine, However, as arsenic concentrations exceeded this value, the excretion of porphyrins (except coproporphyrin III) increased proportionally. 5 The prevalence of clinical signs of arsenicism showed a direct relationship to both As concentration in urine and time-weighted exposure to As. A direct relationship between time-weighted exposure and alterations in urinary porphyrin excretion ratios was also observed. 6 The alterations found are compatible with a lower uroporphyrinogen decarboxylase activity in arsenic-exposed individuals. However, the similarities in the urinary porphyrin excretion pattern between As-exposed individuals and Dubin-Johnson syndrome patients suggest that impairments in the excretion of coproporphyrin isomers may also contribute to the pattern observed.


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