Peer-Reviewed Journal Details
Mandatory Fields
Houghton, BL,Huang, CL,Johns, EJ;
2010
January
Experimental Physiology
Influence of dietary sodium on the blood pressure and renal sympathetic nerve activity responses to intracerebroventricular angiotensin II and angiotensin III in anaesthetized rats
Validated
()
Optional Fields
SPONTANEOUSLY HYPERTENSIVE-RATS HIGH-SALT DIET ARGININE-VASOPRESSIN AMINOPEPTIDASE-A AT(1) RECEPTOR GENE-EXPRESSION CONSCIOUS SHEEP SYSTEM RELEASE NEURONS
95
282
295
The regulation of blood pressure and sympathetic outflow by the brain renin-angiotensin system in animals subjected to raised or lowered dietary Na+ intake is unclear. This study compared the mean arterial pressure (MAP) and renal sympathetic nerve activity (RSNA) responses to intracerebroventricular (I.C.V.) infusion of angiotensin II (AngII) and III (AngIII) before and after peripheral V-1 receptor blockade (V1B) in alpha-chloralose-urethane-anaesthetized rats fed a low (0.03%, LNa+), normal (0.3%, NNa+) or high Na+ diet (3.0%, HNa+) from 4 to 11 weeks of age. The rise in MAP 2 min post AngII i.c.v. was greater in HNa+ (14 +/- 3 mmHg) versus LNa+ (8 +/- 1 mmHg, P < 0.05) and after AngIII i.c.v. in HNa+ (14 +/- 3 mmHg) versus NNa+ (6 +/- 1 mmHg, P < 0.05) and LNa+ (7 +/- 1 mmHg, P < 0.05). The MAP responses to AngII and AngIII i.c.v. were abolished after V1B in LNa+, but were only attenuated in HNa+. In NNa+, V1B blunted the MAP responses to AngII and abolished those to AngIII. The MAP remained elevated 30 min after AngII in all groups, but returned to baseline levels 15 min after AngIII in NNa+ and HNa+ (P < 0.01). Twenty minutes after i.c.v. AngII, RSNA rose above baseline in HNa+ (112 +/- 1%), a response not observed in the LNa+ and NNa+ groups. Twenty minutes post AngIII i.c.v., RSNA was elevated in both HNa (109 +/- 2%) and NNa+ (109 +/- 2%). After V1B, RSNA rose only in the HNa+ group 15 min post AngIII infusion (109 +/- 1%). Together, these findings: (1) suggest that HNa+ intake augments the MAP and RSNA responses to i.c.v. AngII and AngIII; (2) highlight an important role for peripheral V-1 receptors during these responses; and (3) differentiate the effects of AngII and AngIII on blood pressure and RSNA.
DOI 10.1113/expphysiol.2009.049833
Grant Details