Hs. Mackenzie et al., NEPHRON SUPPLY IS A MAJOR DETERMINANT OF LONG-TERM RENAL-ALLOGRAFT OUTCOME IN RATS, The Journal of clinical investigation, 94(5), 1994, pp. 2148-2152
The effects of augmenting the nephron supply on indices of allograft i
njury were assessed in a rat model of ''chronic rejection.'' Orthotopi
c renal allotransplantation into uninephrectomized rats was followed b
y excision (allograft-alone group) or preservation of the remaining na
tive kidney (allograft + native kidney group) such that the total kidn
ey complement was either the allograft alone, or the allograft plus on
e retained native kidney. After 18 wk, values for GFR (1.85+/-0.3 ml/m
in) and kidney weights (2.3+/-0.2 g) in allograft-alone rats were far
in excess of corresponding values in the allograft of allograft + nati
ve kidney rats (0.88+/-0.1 ml/min and 1.1+/-0.5 g, respectively). Prot
einuria (35+/-2 mg/d) and allograft glomerulosclerosis (24+/-8%) also
characterized allograft-alone but not allograft + native kidney rats,
in whom glomerular structure (allograft glomerulosclerosis, 4+/-1%; na
tive kidney glomerulosclerosis, 0%) and glomerular functional integrit
y (proteinuria 7+/-0.7 mg/d) were well preserved. Thus, the observed a
llograft protection derived from the presence of a retained recipient
native kidney supports the hypothesis that a single renal allograft co
ntains insufficient nephrons to prevent progressive renal injury, impl
icating nephron supply as a major determinant of long-term allograft o
utcome.