“…: Personal commun., 1980], Why should chloroquine facilitate the release of these excess por phyrins from hepatocytes in nonuremic PCT cases, but not in patients on dialysis? The simplest answer, again, is that the bulk of these urinary porphyrins in nonuremic PCT originates in the kidney and, as chloroquine is known to accumulate in the kidney as well as in the liver [27], the former is the organ where it has its major porphyrinmobilizing effect. Hence, in dialysis patients, insignificant renal porphyrin synthesis occurs because the organs are not functional, whilst only slight quantities of porphyrin leak into the plasmas of these patients from their hepato cytes since, as in the HCB-poisoned rats described earlier [14], most of the excess porphyrins synthesized in the liver accumulate without excretion.…”