Affiliations 

  • 1 Cardiovascular and Renal Physiology Lab, School of Pharmaceutical Sciences, Universiti Sains Malaysia, Penang, 11800, Malaysia. samalik77@hotmail.com
  • 2 Cardiovascular and Renal Physiology Lab, School of Pharmaceutical Sciences, Universiti Sains Malaysia, Penang, 11800, Malaysia
  • 3 Department of Physiology, University College Cork, Cork, Ireland
  • 4 Department of Pharmacology, Universiti Malaya, Kuala Lumpur, 50603, Malaysia
J Physiol Biochem, 2016 Dec;72(4):593-604.
PMID: 27405250

Abstract

Adiponectin exerts vasodilatory effects. Irbesartan, an angiotensin receptor blocker, possesses partial peroxisome proliferator-activated receptor gamma (PPAR-γ) agonist activity and increases circulating adiponectin. This study explored the effect of irbesartan alone and in combination with adiponectin on blood pressure, renal hemodynamic excretory function, and vasoactive responses to angiotensin II and adrenergic agonists in spontaneously hypertensive rat (SHR). Irbesartan was given orally (30 mg/kg/day) for 28 days and adiponectin intraperitoneally (2.5 μg/kg/day) for last 7 days. Groups of SHR received either irbesartan or adiponectin or in combination. A group of Wistar Kyoto rats (WKY) served as controls. Metabolic data and plasma samples were taken on days 0, 21, and 28. In acute studies, the renal vasoconstrictor actions of angiotensin II (ANGII), noradrenaline (NA), phenylephrine (PE), and methoxamine (ME) were determined. SHR control rats had a higher mean blood pressure than the WKY (132 ± 7 vs. 98 ± 2 mmHg), lower plasma and urinary adiponectin, creatinine clearance, urine flow rate and sodium excretion, and oxidative stress markers compared to WKY (all P 

* Title and MeSH Headings from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.

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