We studied the effect of 24 h of uninephrectomy and somatostatin analo
gue, an inhibitor of growth hormone secretion, in microdissected nephr
on segment H-ATPase, H-K ATPase and Na-K ATPase activities. Systemic a
cid-base status, plasma and tissue electrolytes, and aldosterone level
s in the uninephrectomized rats were similar to controls. Uninephrecto
my increased fractional sodium, potassium, and bicarbonate excretion (
p<0.05). After 24 h the solitary kidney weighed the same as the single
kidney from sham-operated controls. Protein content of the microdisse
cted nephron segments studied enzymatically did not differ from contro
l. Insulin-like growth factor-1 (IGF-1) levels in plasma and kidney we
re also similar. By contrast, ATPase values in uninephrectomized anima
ls were markedly elevated: H-ATPase was increased by 91+/-5% in proxim
al convoluted tubule (PCT) (p<0.005), 65+/-3% in medullary thick ascen
ding limb of Henle's loop (MTAL) (p<0.01), 92+/-9% in cortical collect
ing tubule (CCT) (p<0.005), and 94+/-8% in medullary collecting tubule
(MCT) (p<0.005). In these same animals, H-K ATPase activity was also
increased: 88+/-6% in CCT (p<0.005) and 92+/-5% in MCT (p<0.005). Unin
ephrectomy also decreased Na-K ATPase activity in PCT, MTAL and CCT, b
ut enzyme activity in MCT remained unchanged. Somatostatin analogue ad
ministration to animals with one kidney had no effect on metabolic par
ameters or plasma and kidney IGF-1 concentrations nor did it prevent t
he alterations in renal ATPase activities observed with uninephrectomy
done. The analogue alone had no effect in control animals. While the
mechanisms responsible for the increase in renal ATPases seen after un
inephrectomy are not known, they are independent of aldosterone, potas
sium, or IGF-1.