Unbound MEDLINE

Prenatal programming of rat thick ascending limb chloride transport by low-protein diet and dexamethasone. American journal of physiology. Regulatory, integrative and comparative physiology [Am J Physiol Regul Integr Comp Physiol] Journal article

 
TitlePrenatal programming of rat thick ascending limb chloride transport by low-protein diet and dexamethasone.
Author(s)Dagan A, Habib S, Gattineni J, Dwarakanath V, Baum M 
InstitutionDepartment of Pediatrics, University of Texas Southwestern Medical Center at Dallas, Dallas, Texas 75390-9063, USA.
SourceAm J Physiol Regul Integr Comp Physiol 2009 Jul; 297(1):R93-9.
MeSHAging
Animals
Antihypertensive Agents
Biological Transport
Blood Pressure
Chlorides
Dexamethasone
Diet, Protein-Restricted
Female
Furosemide
Gestational Age
Glucocorticoids
Hypertension
Injections, Intraperitoneal
Kinetics
Loop of Henle
Male
Maternal Nutritional Physiological Phenomena
Pregnancy
Prenatal Exposure Delayed Effects
Rats
Rats, Sprague-Dawley
Sodium Potassium Chloride Symporter Inhibitors
Sodium-Potassium-Chloride Symporters
AbstractPrenatal administration of dexamethasone and a low-protein diet has been shown to result in hypertension in the offspring when they are adults. The cause for the hypertension is unknown. The purpose of this study was to examine whether there was prenatal programming of thick ascending limb transport. Rats were administered either dexamethasone for 4 days (0.2 mg/kg body wt) by intraperitoneal injection daily between the 15th and 18th day of gestation, or they were fed a low-protein diet (6% protein) or an isocaloric normal protein diet (20% protein) from day 12 gestation until birth. The offspring were studied as adults. Prenatal dexamethasone and dietary protein deprivation resulted in an increase in blood pressure. Offspring of mothers fed a low-protein diet had an increase in medullary but not cortical bumetanide-sensitive Na-K-2Cl cotransporter (NKCC2) protein abundance (P < 0.01). There was not a statistically significant increase in medullary NKCC2 by prenatal dexamethasone (P = 0.07). Both prenatal administration of dexamethasone and a low-protein diet resulted in an increase in medullary thick ascending limb chloride transport compared with control (298 +/- 33 pmoles x mm(-1) x min(-1), 280 +/- 26 pmoles x mm(-1) x min(-1), and 191 +/- 21 pmoles x mm(-1) x min(-1), respectively P < 0.05). There was a higher lumen-positive transepithelial potential difference in the prenatal dexamethasone and low-protein group compared with control as well. Administration of furosemide for 24 h resulted in a decrease in blood pressure in the low-protein group but not the control group. This study demonstrates that insults administered to the fetus can program altered sodium transport. Increased tubular sodium transport is a likely cause for the hypertension by prenatal programming.
Languageeng
Pub Type(s)Journal Article
Research Support, N.I.H., Extramural
PubMed ID19403862
  
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