The effect of aging on the status of macrominerals and trace elements in ti
ssues was studied using two strains (SAMP1 and SAMR1) of senescence acceler
ated mouse. Two-month-old, 6-mo-old, and 10-mo-old female SAMP1 and SAMR1 m
ice were fed a commercial diet. Iron, zinc, copper, calcium, magnesium, pho
sphorus, sulfur, sodium, and potassium concentrations in blood, liver, kidn
ey, brain, and tibia of the mice were determined. The copper concentration
in the brain was significantly increased with age in SAMP1 and SAMR1. In ad
dition, the brain copper levels in SAMP1 were significantly higher than tha
t in SAMR1 at respective ages. The calcium concentration in the kidney was
significantly increased with age, but the copper and phosphorus concentrati
ons significantly decreased with age in SAMP1 and SAMR1. In the liver of SA
MR1, all minerals measured in this study except for sodium and potassium we
re significantly decreased with age. In addition, all mineral concentration
s in the liver of 2-mo-old mice in SAMR1 except for copper and sodium were
markedly higher than those in SAMP1 of the same age. These results suggest
that the genetic factor is related to the age-associated mineral changes in
tissues.