» Articles » PMID: 20386492

Angiotensin II Regulates NOS Expression in Afferent Arterioles of the Developing Porcine Kidney

Overview
Journal Pediatr Res
Specialties Biology
Pediatrics
Date 2010 Apr 14
PMID 20386492
Citations 5
Authors
Affiliations
Soon will be listed here.
Abstract

NO protection is crucial against angiotensin II (ANG II) mediated vasoconstriction in postnatal preglomerular resistance vessels. Although whole kidney NOS is developmentally regulated, NOS regulation in developing renal resistance vessels is unknown. The hypothesis was NOS expression and function in developing afferent arterioles are regulated by ANG II through AT1 and AT2 receptors. Afferent arterioles from porcine kidneys, ages newborn, 7, 21 d, and adult, were dissected using a polybead perfusion technique. Dissected afferent arterioles were treated with ANG II and with either the AT1 receptor inhibitor candesartan or the AT2 receptor inhibitor PD 123319 and evaluated for NOS isoform expression and NOS enzymatic activity. Although NOS activity and neuronal NOS (nNOS) expression were greater in the newborn than in the adult, endothelial NOS (eNOS) expression was greater in the adult. ANG II increased NOS activity and eNOS expression at all ages, but nNOS expression only in developing afferents. AT1 and AT2 receptor blockade significantly attenuated NOS activity and eNOS expression at all ages, but nNOS expression only in developing afferents. ANG II regulates nNOS and eNOS expression and NOS activity in afferent arterioles of the developing kidney via AT1 and AT2 receptors.

Citing Articles

Glomerular and tubular effects of nitric oxide (NO) are regulated by angiotensin II (Ang II) in an age-dependent manner through activation of both angiotensin receptors (AT1Rs and AT2Rs) in conscious lambs.

Vinturache A, Smith F Pflugers Arch. 2017; 470(2):249-261.

PMID: 28861607 DOI: 10.1007/s00424-017-2053-4.


Renal effects of angiotensin II in the newborn period: role of type 1 and type 2 receptors.

Vinturache A, Smith F BMC Physiol. 2016; 16:3.

PMID: 27090941 PMC: 4835895. DOI: 10.1186/s12899-016-0022-3.


Serotonin uptake rates in platelets from angiotensin II-induced hypertensive mice.

Singh P, Fletcher T, Li Y, Rusch N, Kilic F Health (Irvine Calif). 2013; 5(4A):31-39.

PMID: 24163726 PMC: 3806217. DOI: 10.4236/health.2013.54A005.


Identification and characterization of a functional mitochondrial angiotensin system.

Abadir P, Foster D, Crow M, Cooke C, Rucker J, Jain A Proc Natl Acad Sci U S A. 2011; 108(36):14849-54.

PMID: 21852574 PMC: 3169127. DOI: 10.1073/pnas.1101507108.


Targeting the angiotensin II type 2 receptor (AT2R) in colorectal liver metastases.

Ager E, Chong W, Wen S, Christophi C Cancer Cell Int. 2010; 10:19.

PMID: 20584290 PMC: 2902462. DOI: 10.1186/1475-2867-10-19.

References
1.
Mattson D, Wu F . Nitric oxide synthase activity and isoforms in rat renal vasculature. Hypertension. 2000; 35(1 Pt 2):337-41. DOI: 10.1161/01.hyp.35.1.337. View

2.
Wallace K, Hook J, BAILIE M . Postnatal development of the renin-angiotensin system in rats. Am J Physiol. 1980; 238(5):R432-7. DOI: 10.1152/ajpregu.1980.238.5.R432. View

3.
Michell B, Chen Zp , Tiganis T, Stapleton D, Katsis F, Power D . Coordinated control of endothelial nitric-oxide synthase phosphorylation by protein kinase C and the cAMP-dependent protein kinase. J Biol Chem. 2001; 276(21):17625-8. DOI: 10.1074/jbc.C100122200. View

4.
Bachmann S, Bosse H, Mundel P . Topography of nitric oxide synthesis by localizing constitutive NO synthases in mammalian kidney. Am J Physiol. 1995; 268(5 Pt 2):F885-98. DOI: 10.1152/ajprenal.1995.268.5.F885. View

5.
Evan Jr A, Stoeckel J, Loemker V, Baker J . Development of the intrarenal vascular system of the puppy kidney. Anat Rec. 1979; 194(2):187-99. DOI: 10.1002/ar.1091940202. View