Increased activity of cGMP-specific phosphodiesterase (PDE5) contributes to resistance to atrial natriuretic peptide natriuresis in the pregnant rat

• Published in: Journal of the American Society of Nephrology Vol. 15; no. 5; pp. 1254 - 1260
• Main Authors: NI, Xi-Ping, SAFAI, Massy, RISHI, Rahul, BAYLIS, Chris, HUMPHREYS, Michael H
• Format: Journal Article
• Language: English
• Published: Hagerstown, MD Lippincott Williams & Wilkins 01-05-2004
• Subjects: 3',5'-Cyclic-GMP Phosphodiesterases - metabolism; Animals; Atrial Natriuretic Factor - blood; Biological and medical sciences; Cyclic GMP - urine; Cyclic Nucleotide Phosphodiesterases, Type 5; Female; Kidney Tubules, Collecting - enzymology; Medical sciences; Natriuresis - physiology; Nephrology. Urinary tract diseases; Pregnancy; Pregnancy, Animal - metabolism; Rats; Rats, Sprague-Dawley; Sodium - metabolism; Nephrology; Rat; Rodentia; 3',5'-GMP; Atrial natriuretic peptide; Urology; Specific activity; Pregnancy; Resistance; Vertebrata; Natriuretic hormone; Mammalia; Animal
• ISSN: 1046-6673; 1533-3450
• DOI: 10.1097/01.ASN.0000125613.96927.38

Increased cGMP-specific phosphodiesterase (PDE5) activity in renal inner medullary collecting duct (IMCD) cells contributes to resistance to atrial natriuretic peptide (ANP) and the excessive sodium retention seen in experimental nephrotic syndrome and liver cirrhosis. Normal pregnancy is also accompanied by sodium retention and plasma volume expansion, and pregnant rats are resistant to the natriuretic action of ANP. The authors investigated a possible role of increased renal PDE5 activity in the physiologic sodium retention of normal rat pregnancy. The natriuresis and increased urinary cGMP excretion (U(cGMP)V) evoked by acute volume expansion (a measure of renal responsiveness to endogeneous ANP) was blunted in 16-d pregnant versus virgin rats, despite equivalent increases in circulating ANP in pregnants and virgins. The ANP-dependent cGMP accumulation in isolated IMCD cells from pregnants was blunted versus virgins and restored by the PDE5-selective antagonist DMPPO (10(-7) mol/L). PDE5 activity in vitro and PDE5 protein abundance in IMCD were greater in pregnants. Four days postpartum, volume expansion natriuresis, U(cGMP)V, and PDE5 protein levels in IMCD cell homogenates had returned to virgin values. These results demonstrate that normal rat pregnancy leads to in vivo and in vitro renal resistance to ANP, in association with heightened activity of the cGMP-specific PDE5 in IMCD. This may contribute to the physiologic sodium retention of normal pregnancy.