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1.
Fig. 7.

Fig. 7. From: Increased colonic sodium absorption in rats with chronic renal failure is partially mediated by AT1 receptor agonism.

mRNA expression of AT1, AT2, and selected sodium transporters in the distal colon of control rats (CON), rats in CRF, and CRF rats treated with losartan (10 mg/kg) for 1 wk before study (+LOS). *Significant difference compared with control, P ≤ 0.05. †Significant difference compared with CRF, P ≤ 0.05. NHE, sodium-hydrogen exchanger; ENaC, epithelial sodium channel.

Marguerite Hatch, et al. Am J Physiol Gastrointest Liver Physiol. 2008 Aug;295(2):G348-G356.
2.
Fig. 5.

Fig. 5. From: Increased colonic sodium absorption in rats with chronic renal failure is partially mediated by AT1 receptor agonism.

Mucosal amiloride (10−4 M) partially reduces net sodium absorption and Isc in the distal colon of CRF rats (n = 7). Error bars represent ±1 SE above or below the mean of data in each group. An asterisk indicates a significant difference between Per I (CRF) and Per II (+Amiloride), using a paired t-test, P ≤ 0.05. Transepithelial conductance (GT) was not significantly changed in Per II (9.58 ± 1.09 mS/cm2) compared with Per I (10.13 ± 1.13 mS/cm2).

Marguerite Hatch, et al. Am J Physiol Gastrointest Liver Physiol. 2008 Aug;295(2):G348-G356.
3.
Fig. 3.

Fig. 3. From: Increased colonic sodium absorption in rats with chronic renal failure is partially mediated by AT1 receptor agonism.

Acute serosal losartan (10−4 M) does not alter sodium fluxes across distal colonic tissues removed from CON rats (n = 9), but Isc is significantly decreased. Error bars represent ±1 SE above or below the mean of data in each group. An asterisk indicates a significant difference between Per I (CON) and Per II (+LOS), using a paired t-test, P ≤ 0.05. Transepithelial conductance (GT) was not significantly changed in Per II (9.94 ± 1.05 mS/cm2) compared with Per I (10.37 ± 1.08 mS/cm2).

Marguerite Hatch, et al. Am J Physiol Gastrointest Liver Physiol. 2008 Aug;295(2):G348-G356.
4.
Fig. 8.

Fig. 8. From: Increased colonic sodium absorption in rats with chronic renal failure is partially mediated by AT1 receptor agonism.

Immunoblot analyses of Na+/H+ exchangers (NHE1, NHE2, NHE3), Na+ channel subunits (ENaC-α, ENaC-β, ENaC-γ), ATPase, and AT2 receptor in protein extracts of distal colon from CON, CRF, and + LOS rats. Membranes were reprobed for GAPDH as an internal loading control. Results were quantitated by densitometry from n = 4 to 6 tissues in each group and given in arbitrary units. Significant differences in CRF and + LOS from CON rats were established by a one-way ANOVA followed by Bonferroni's t-test and are indicated by an asterisk.

Marguerite Hatch, et al. Am J Physiol Gastrointest Liver Physiol. 2008 Aug;295(2):G348-G356.
5.
Fig. 2.

Fig. 2. From: Increased colonic sodium absorption in rats with chronic renal failure is partially mediated by AT1 receptor agonism.

Acute serosal losartan (10−4 M) reduces net sodium absorption and Isc across distal colonic tissues removed from CRF rats (n = 11). Error bars represent ±1 SE above or below the mean of data in each group. An asterisk indicates a significant difference between the control period of 45 min (Per I) (CRF) and the second 45-min flux period (Per II) (+LOS), using a paired t-test, P ≤ 0.05. Transepithelial conductance (GT) was not significantly changed in Per II (8.23 ± 0.66 mS/cm2) compared with Per I (9.00 ± 0.62 mS/cm2).

Marguerite Hatch, et al. Am J Physiol Gastrointest Liver Physiol. 2008 Aug;295(2):G348-G356.
6.
Fig. 4.

Fig. 4. From: Increased colonic sodium absorption in rats with chronic renal failure is partially mediated by AT1 receptor agonism.

Mucosal EIPA (50 μM) partially reduces net sodium absorption in the distal colon of CRF rats (n = 7). Indomethacin was present in this series (5 μM, serosal) to better resolve any changes in Isc that might result from EIPA inhibition of electrogenic Na+ absorption. Error bars represent ±1 SE above or below the mean of data in each group. An asterisk indicates a significant difference between Per I (CRF) and Per II (+EIPA), using a paired t-test, P ≤ 0.05. Transepithelial conductance (GT) was not significantly changed in Per II (7.82 ± 0.90 mS/cm2) compared with Per I (8.62 ± 0.77 mS/cm2).

Marguerite Hatch, et al. Am J Physiol Gastrointest Liver Physiol. 2008 Aug;295(2):G348-G356.
7.
Fig. 6.

Fig. 6. From: Increased colonic sodium absorption in rats with chronic renal failure is partially mediated by AT1 receptor agonism.

Angiotensin II (ANG II) stimulation of sodium transport by rat distal colon in vitro. ANG II (10−7 M) was added at the end of Per I (CON) to the serosal side of control rat colonic tissue (n = 7). Error bars represent ±1 SE above or below the mean of data in each group. An asterisk indicates a significant difference between Per I and II using a paired t-test, P ≤ 0.05. Transepithelial conductance (GT) was not significantly affected in Per II (8.00 ± 0.57 mS/cm2) compared with Per I (8.57 ± 0.48 mS/cm2).

Marguerite Hatch, et al. Am J Physiol Gastrointest Liver Physiol. 2008 Aug;295(2):G348-G356.
8.
Fig. 1.

Fig. 1. From: Increased colonic sodium absorption in rats with chronic renal failure is partially mediated by AT1 receptor agonism.

Comparison of Na+ transport and short-circuit current (Isc) across isolated, short-circuited distal colon from control rats with 2 intact kidneys (CON, n = 7), 5/6 nephrectomized rats with chronic renal failure (CRF, n = 11), and rats with renal failure that were treated with losartan (10 mg/kg) for 7 days before euthanasia (+LOS, n = 10). Error bars represent ±1 SE of the mean of data in each group. An asterisk indicates a significant difference compared with CON, and § indicates a significant difference from CRF in a one-way ANOVA (P ≤ 0.05). Transepithelial conductance (GT) was not significantly affected in CRF (9.00 ± 0.62 mS/cm2) or + LOS (8.23 ± 0.66 mS/cm2) compared with CON (8.79 ± 0.83 mS/cm2). The fluxes and electrical parameters measured in + LOS are not significantly different compared with CON. J, mucosal to serosal flux; J, serosal to mucosal flux; J, net flux.

Marguerite Hatch, et al. Am J Physiol Gastrointest Liver Physiol. 2008 Aug;295(2):G348-G356.

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