First published online September 19, 2006
Journal of Experimental Biology 209, 3719-3728 (2006)
Published by The Company of Biologists 2006
doi: 10.1242/jeb.02436
Dietary acidification enhances phosphorus digestibility but decreases H+/K+-ATPase expression in rainbow trout
Shozo H. Sugiura,
Prabir K. Roy and
Ronaldo P. Ferraris*
Department of Pharmacology and Physiology, UMDNJ-New Jersey Medical
School, 185 South Orange Avenue, Newark, NJ 07103, USA

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Fig. 1. Postprandial gastric luminal pH of fish and rats. The post-prandial hours
(x axis) are in log scale (0 h is the pre-prandial value), and
gastric luminal pH (y axis) is shown as mean ± s.e.m. (as
error bars, N=8 for fish and N=4 for rats). Fish studied
were four 2-month-old rainbow trout (10.24±0.54 g; mean body mass
± s.e.m.) and four 15-month-old rainbow trout (211.4±2.4 g).
Since there was no significant difference between these small and mid-sized
fish, they were pooled for statistical comparison with rats. Rats studied were
four 1-2-month-old rats (120.3±3.2 g). Difference between fish and rats
in gastric luminal pH at each postprandial hour is shown with asterisks:
*P<0.05; **P<0.01. Gastric
luminal pH of rats was much lower than that of fish at 1-6 h postprandial.
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Fig. 2. Phylogenic kinship of trout gastrin-like EST (A) and trout ATP4A-like EST
(B) to those of other species. Based on the translated amino acid sequence,
trout gastrin-like EST has 64% homology with halibut gastrin, and trout
ATP4A-like EST is 98% homologous to flounder ATP4A. Gastrin and CCK belong to
the same peptide family, but the trout gastrin-like EST belongs to a gastrin
cluster that is sufficiently removed from the trout CCK cluster (not shown).
Gas, gastrin; CCK: cholecystokinin; ATP4A: H+/K+-ATPase;
ATP1A: Na+/K+-ATPase. Trout EST1 (gi:42752688) and trout
EST2 (gi:42817423) in B are 97% homologous to one another in nucleotide base
sequence.
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Fig. 3. Effects of various dietary acids (x axis) on relative gene
expression (y axis) in the antral and corpus (body) regions of
rainbow trout stomach. One of the following acids or antacid was added to the
basal diet (No acid) (w/w). HCl: 12 mol 1-1 HCl 5.0%;
H2SO4h, 18 mol l-1
H2SO4 3.5%; H2SO4L: 18 mol
l-1 H2SO4 1.0%; acetic: glacial acetic acid
5.0%; antacid: CaCO3 5.0%. No acid: basal diet (see
Table 1). Gray bars represent
data of corpus stomach; white bars represent data of antral stomach. Each
column represents the average (+ s.e.m. as error bar) of four fish. Columns
within each stomach region labeled with different letters are significantly
different (P<0.05). ATP4A, H+/K+-ATPase;
SST, somatostatin; NBC, Na+/bicarbonate cotransporter). Differences
of mRNA abundance between antral and corpus stomach (all treatments inclusive)
were as follows: Gastrin-like gene (P=0.8); ATP4A
(P=0.0003); SST1 (P=0.02); SST2 (P=0.002); SST2-2
(P=0.8); NBC (P=0.0007).
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Fig. 4. Correlation between ATP4A (H+/K+-ATPase, the proton
pump) and NBC (Na+/bicarbonate cotransporter) mRNA abundance in the
antral and corpus stomach of rainbow trout. Each dot represents one sample.
One antral and one corpus sample was collected from each fish. In the antrum
(open diamonds), ATP4A mRNA is nearly absent, whereas small amounts of NBC
mRNA are present. In the corpus (filled diamonds), both ATP4A mRNA and NBC
mRNA are abundant and their abundances are correlated to one another
(regression of corpus ATP4A to corpus NBC: y=0.86x+0.36;
R2=0.40). Units of x and y axes are
relative (average of all data points is 1).
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Fig. 5. Dietary acidification increases phosphorus digestibility (A) but decreases
H+/K+-ATPase mRNA expression (B) in rainbow trout. Each
dot represents the mean (± s.e.m.) of six fish for phosphorus
digestibility measurements, and four fish for
H+/K+-ATPase mRNA measurements. Legend shows dietary
treatments (acids used). Significance of dietary acidification on phosphorus
digestibility (P<0.0001) and H+/K+-ATPase
mRNA expression (P<0.0001) was evaluated by linear regression.
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© The Company of Biologists Ltd 2006