The image intensity in many contrast agent perfusion studies is design
ed to be a function of bulk tissue T-1, which is, in turn, a function
of the compartmental (vascular, interstitial, and cellular) T(1)s, and
the rate of proton exchange between the compartments. The goal of thi
s study was to characterize the compartmental tissue Gd-DTPA relaxivit
ies and to determine the proton exchange rate between the compartments
. Expressing [Gd-DTPA] as mmol/liter tissue water, the relaxivities at
8.45 T and room temperature were: saline, 3.87 +/- 0.06 (mM.s)(-1) (m
ean +/- SE; n = 29); plasma, 3.98 +/- 0.05 (mM.s)(-1) (n = 6); and con
trol cartilage (primarily an interstitium), 4.08 +/- 0.08 (mM.s)(-1) (
n = 17), none of which are significantly different. The relaxivity of
cartilage did not change with compression, trypsinization, or equilibr
ation in plasma, suggesting relaxivity is not influenced by interstiti
al solid matrix density, charge, or the presence of plasma proteins. T
-1 relaxation studies on isolated perfused hearts demonstrated that th
e cellular-interstitial water exchange rate is between 8 and 27 Hz, wh
ile the interstitial-vascular water exchange rate is less than 7 Hz. T
hus, for Gd-DTPA concentrations, which would be used clinically, the T
-1 relaxation rate behavior of intact hearts can be modeled as being i
n the fast exchange regime for cellular-interstitial exchange but slow
exchange for interstitial-vascular exchange. A measured relaxivity of
3.82 +/- 0.05 (mM.s)(-1) (n = 8) for whole blood (red blood cells and
plasma) and 4.16 +/- 0.02 (mM.s)(-1) (n = 3) for frog heart tissue (c
ells and interstitium) (with T-1 and Gd-DTPA concentration defined fro
m the total tissue water volume) supports the conclusion of fast cellu
lar-extracellular exchange. Knowledge of the Gd-DTPA relaxivity and ma
intaining Gd-DTPA concentration in the range so as to maintain fast ce
llular-interstitial exchange allows for calculation of bulk Gd-DTPA co
ncentration from bulk tissue T-1 within a calculable error due to slow
vascular exchange.