Published in

Springer Verlag, Pflügers Archiv European Journal of Physiology, 3(463), p. 399-404

DOI: 10.1007/s00424-011-1065-8

Links

Tools

Export citation

Search in Google Scholar

Haemodynamic responses to angiotensin II in conscious lambs: role of nitric oxide and prostaglandins

Journal article published in 2011 by Kesavarao Kumar Ebenezar, Andy Kin On Wong ORCID, Francine Gabriel Smith
This paper is available in a repository.
This paper is available in a repository.

Full text: Download

Green circle
Preprint: archiving allowed
Green circle
Postprint: archiving allowed
Red circle
Published version: archiving forbidden
Data provided by SHERPA/RoMEO

Abstract

It was hypothesized that nitric oxide (NO) and prostaglandins (PGs) play a synergistic role in modulating haemodynamic responses to angiotensin II (ANG II) in an age-dependent manner. To this end, experiments were carried out in conscious, chronically instrumented lambs aged ∼1 week (N = 9) and ∼6 weeks (N = 10) to evaluate the haemodynamic responses to ANG II, before and after treatment with the L: -arginine analogue, N-nitro-L: -arginine methyl ester (L: -NAME), as well as the cyclooxygenase inhibitor, indomethacin (INDO). Pressor and renal blood flow responses to ANG II were measured before (control) and after administration of L: -NAME (20 mg kg(-1)), following pretreatment with either vehicle (VEH) (experiment 1) or INDO (1 mg kg(-1), experiment 2). The two experiments were carried out at minimum intervals of 48 h. In both age groups, the pressor and renal vasoconstrictor responses to ANG II were augmented by pretreatment with INDO, the effects being similar at 1 and 6 weeks. The haemodynamic responses to ANG II were, however, not altered after L: -NAME following pretreatment with either VEH or INDO. These data provide new evidence that soon after birth, endogenously produced PGs, but not endogenously produced NO, balance the vasoconstrictor actions of ANG II. There is, however, no apparent interaction between PGs and NO in modulating the responses to ANG II postnatally.