First published online August 8, 2003
Urea transport in kidney brush-border membrane vesicles from an elasmobranch, Raja erinacea
Robyn L. Morgan,
Patricia A. Wright* and
James S. Ballantyne
Department of Zoology, University of Guelph, Guelph, Ontario, Canada,
N1G 2W1

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Fig. 1. (A) Rates of urea uptake at various urea concentrations in dorsal BBMV from
the kidney of the little skate Raja erinacea. The regression is
y=0.3309x, r2=0.9708. Values are means ±
S.E.M., N=5. (B) Expansion of the lower end of the urea
concentration range, subtracting the linear rate from A. The regression is
y=0.563x, r2=0.8413. Values are means ±
S.E.M., N=6.
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Fig. 2. (A) Rates of urea uptake at various urea concentrations in ventral BBMV
from the kidney of the little skate Raja erinacea. The regression is
y=0.3312x, r2=0.9724. Values are means ±
S.E.M., N=5. (B) Expansion of the lower end of the urea
concentration range, subtracting the linear rate from A. The regression is
y=1.3941x/(0.9016+x),
r2=0.9561. Values are means ± S.E.M.,
N=6. (C) LineweaverBurk transformation of the relationship
between urea concentration and urea uptake V (µmol
h1 mg1 protein) by BBMV. The regression is
y=0.5988x+0.8308, r2=0.9330. Values are
means ± S.E.M., N=6.
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Fig. 3. Inhibition of urea uptake by phloretin (0.50 mmol l1),
mercury chloride (HgCl2; 0.30 mmol l1) and
phloretin (0.50 mmol l1) + HgCl2 (0.30 mmol
l1) in dorsal and ventral BBMV from the kidney of the little
skate Raja erinacea. Urea concentration in the incubation medium was
0.5 mmol l1. Control urea uptake rates are 1.42±0.14
and 1.41±0.18 µmol h1 mg1
protein, for dorsal and ventral sections, respectively. Values are means
± S.E.M., N=57. *Significant
difference from respective control; significant difference
from dorsal phloretin (ANOVA on log-transformed data, TukeyKramer
multiple comparison test, P<0.05).
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Fig. 4. Effect on urea uptake in the dorsal and ventral BBMV from the kidney of the
little skate Raja erinacea, by the urea analogs acetamide,
N-methylurea (370 mmol l1) and nitrophenylthiourea
(NPTU; 0.08 mmol l1). Urea concentration in the incubation
medium was 0.5 mmol l1. Control rates are 1.32±0.19
and 0.97±0.09 µmol h1 mg1
protein, for dorsal and ventral sections, respectively. Values are means
± S.E.M., N=5. *Significant difference
from dorsal control (ANOVA on log-transformed data, TukeyKramer
multiple comparison test, P<0.05); significant
difference from dorsal acetamide (Student t-test on log-transformed
data, P<0.05).
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Fig. 5. The effect of Na+ and K+ on the rate of urea
transport in the dorsal and ventral BBMV from the kidney of the little skate
Raja erinacea, presented as percentage of control (no ion gradient).
Urea concentration in the incubation medium was 4 mmol l1.
Control rates are 1.53±0.32 and 1.56±0.29 µmol
h1 mg1 protein, for the dorsal section
Na+ and K+, respectively, and 1.77±0.44 and
1.42±0.35 µmol h1 mg1 protein,
for the ventral section Na+ and K+ respectively. Values
are means ± S.E.M., N=4. *Significant
difference from ventral sodium control (Student t-test,
P<0.05).
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© The Company of Biologists Ltd 2003