The mechanisms of ammonia excretion at fish gills have been
studied for
decades but details remain unclear, with continuing
debate on the relative
importance of non-ionic NH
3 or ionic
NH
4+
permeation by various mechanisms. The presence of an apical
Na
+/NH
4+ exchanger has also been
controversial. The present study utilized
an
in vitro cultured gill
epithelium (double seeded insert,
DSI) of freshwater rainbow trout as a model
to investigate these
issues. The relationship between basolateral ammonia
concentration
and efflux to apical freshwater was curvilinear, indicative
of a
saturable carrier-mediated component (
Km=66 µmol
l
–1)
superimposed on a large diffusive linear component.
Pre-exposure
to elevated ammonia (2000 µmol l
–1) and
cortisol
(1000 ng ml
–1) had synergistic effects on the
ammonia
permeability of DSI, with significantly increased Na
+
influx
and positive correlations between ammonia efflux and Na
+
uptake.
This increase in ammonia permeability was bidirectional. It
could not
be explained by changes in paracellular permeability
as measured by
[
3H]PEG-4000 flux. The mRNA expressions of Rhbg,
Rhcg2,
H
+-ATPase and Na
+/H
+ exchanger-2 (NHE-2) were
up-regulated
in DSI pre-exposed to ammonia and cortisol, CA-2 mRNA was
down-regulated,
and transepithelial potential became more negative.
Bafilomycin
(1 µmol l
–1), phenamil (10 µmol
l
–1)
and 5-(
N,N-hexamethylene)amiloride (HMA, 10
µmol l
–1)
applied to the apical solution significantly
inhibited ammonia
efflux, indicating that H
+-ATPase, Na
+
channel and NHE-2 pathways
on the apical surface were involved in ammonia
excretion. Apical
amiloride (100 µmol l
–1) was similarly
effective,
while basolateral HMA was ineffective. Pre-treatment with apical
freshwater
low in [Na
+] caused increases in both Rhcg2 mRNA
expression
and ammonia efflux without change in paracellular permeability.
These
data suggest that Rhesus glycoproteins are important for ammonia
transport
in the freshwater trout gill, and may help to explain
in
vivo data where plasma ammonia stabilized at 50% below water levels
during
exposure to high environmental ammonia (

2300 µmol
l
–1).
We propose an apical
`Na
+/NH
4+ exchange complex' consisting
of
several membrane transporters, while affirming the importance
of non-ionic
NH
3 diffusion in ammonia excretion across freshwater
fish
gills.