Abstract | OBJECTIVE: To determine whether alterations in extracellular volume expansion observed during normal and hypertensive pregnancy run in parallel to changes in the mRNA expression of renal transporters. METHODS: Wistar rats were divided into four groups: control (C, n = 5); pregnancy (P, n = 5); N(omega)-nitro-l-arginine methyl ester ( L-NAME; 50 mg/kg/d)-treated control (H, n = 6); and pregnant rats (HP, n = 6). Hemodynamic studies were performed on day 14 of pregnancy, at which time we also analyzed of the sodium transporters (NHE3, Na/K/2Cl and Na/Cl), potassium channel (ROMK2) and water channel (AQP2). RESULTS: As expected, P rats presented high cardiac output (CO) and normal blood pressure (BP), whereas H rats presented lower CO and elevated BP. A significant (threefold) increase in total vascular resistance and a decrease in stroke volume were observed in the HP group. Hypertension resulting from nitric oxide (NO) synthesis inhibition blunted systemic hemodynamic adaptations during pregnancy. Compared with C rats, mRNA expression of ROMK2 in P rats was lower, whereas that of AQP2 was higher. Expression of AQP2 was significantly higher in H than in C or HP groups. Expression of BSC and NHE3 was lower in the HP than in the P group. The NO inhibition also provoked renal transporter alterations in HP. CONCLUSIONS: Our results suggest that tubule transporter variants may mediate the hemodynamic adaptations seen during pregnancy, although we cannot rule out the hypothesis that other factors are also mediating hemodynamic changes.
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Authors | Np Abreu, Joisse Caria Barboza Monerat Tardin, Mirian Aparecida Boim, Ruy R Campos, Cassia T Bergamaschi, Nestor Schor |
Journal | Hypertension in pregnancy
(Hypertens Pregnancy)
Vol. 27
Issue 1
Pg. 49-63
( 2008)
ISSN: 1064-1955 [Print] England |
PMID | 18293204
(Publication Type: Comparative Study, Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Aquaporin 2
- Ion Channels
- KCNJ1 protein, human
- Potassium Channels, Inwardly Rectifying
- RNA, Messenger
- SLC9A3 protein, human
- Slc9a3 protein, rat
- Sodium Chloride Symporters
- Sodium-Hydrogen Exchanger 3
- Sodium-Hydrogen Exchangers
- Sodium-Potassium-Chloride Symporters
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Topics |
- Animals
- Aquaporin 2
(metabolism)
- Disease Models, Animal
- Female
- Gene Expression
- Hypertension, Pregnancy-Induced
(physiopathology)
- Ion Channels
(metabolism)
- Kidney
(metabolism, physiopathology)
- Models, Animal
- Potassium Channels, Inwardly Rectifying
(metabolism)
- Pregnancy
(physiology)
- Pregnancy Complications, Cardiovascular
(physiopathology)
- RNA, Messenger
(biosynthesis)
- Rats
- Rats, Wistar
- Sodium Chloride Symporters
(metabolism)
- Sodium-Hydrogen Exchanger 3
- Sodium-Hydrogen Exchangers
(metabolism)
- Sodium-Potassium-Chloride Symporters
(metabolism)
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