Neonatal juxtamedullary proximal convoluted tubules (PCTs) transport b
icarbonate at one-third the rate of adult rabbit PCTs. The lower rate
of bicarbonate transport could be due to a greater permeability of the
neonatal PCT to bicarbonate or to a lower rate of active bicarbonate
transport. This review discusses potential factors which could result
in a lower rate of bicarbonate transport by the neonatal PCT. In isola
ted perfused PCT, bicarbonate permeability is lower in neonatal than a
dult PCT, and thus it does not account for the lower rate of bicarbona
te transport in neonatal PCT. In the adult PCT, apical proton secretio
n occurs via the Na+/H+ antiporter and H+-ATPase; basolateral bicarbon
ate exit occurs via the Na(HCO3)(3) symporter. The activity of transpo
rters can be ascertained by measuring intracellular pH with the fluore
scent dye BCECF. Apical Na+/H+ antiporter, apical H+-ATPase and basola
teral Na(HCO3)(3) symporter activity are all significantly lower in ne
onatal PCT. The factors which stimulate PCT maturation are unknown, ho
wever glucocorticoids have been postulated to play an important role i
n this process. Administration of dexamethasone to pregnant does resul
ts in higher rates of PCT volume absorption, bicarbonate transport, Na
+/H+ antiporter and Na(HCO3)(3) symporter activities than in PCT from
vehicle-treated controls. Thus, the lower rate of neonatal PCT bicarbo
nate transport is due to lower activities of the apical Na+/H+ antipor
ter, apical H+-ATPase and basolateral Na(HCO3)(3) symporter. Glucocort
icoids may be an important factor in the maturation of PCT acidificati
on.