Nitric oxide, superoxide and renal blood flow autoregulation in SHR after perinatal L-arginine and antioxidants

2007 ◽  
Vol 190 (4) ◽  
pp. 329-338 ◽  
Author(s):  
M. P. Koeners ◽  
S. Racasan ◽  
H. A. Koomans ◽  
J. A. Joles ◽  
B. Braam
Author(s):  
N.-H. Holstein-Rathlou ◽  
K. H. Chon ◽  
D. J. Marsh ◽  
V. Z. Marmarelis

1964 ◽  
Vol 207 (1) ◽  
pp. 123-127 ◽  
Author(s):  
Victor E. Nahmod ◽  
Alfredo Lanari

In order to study the mechanism of autoregulation of renal blood flow, 36 mongrel dogs were connected in parabiosis according to the Brull method. The following determinations were made: a) flow/pressure curves in innervated and denervated kidneys and b) acetylcholine and arterenol infusion in innervated kidneys. The critical closing pressure and the "run-off" index were also determined in all cases. The results of these experiments show the existence of renal blood flow autoregulation in innervated, denervated, and arterenol-infused kidneys, and the abolition of the autoregulatory mechanism in the acetylcholine-infused kidneys. The run-off index showed a better correlation with renal resistance than with critical closing pressure.


1964 ◽  
Vol 206 (4) ◽  
pp. 707-713 ◽  
Author(s):  
J. P. Gilmore

Experiments have been undertaken to determine the role which tissue pressure plays in renal blood flow autoregulation. The following results have been obtained: 1) During occlusion of the ureter of the dog undergoing mannitol diuresis renal blood flow changes little, or increases, while tissue and ureteral pressures may increase up to 70 and 100 mm Hg, respectively. 2) Rapid sustained increases in ureteral pressure are associated with a rapid initial decline in renal blood flow followed by a gradual return to or near the control value; during these blood flow changes the elevated needle and ureteral pressures are constant. 3) During ureteral occlusion vasodilator drugs have little effect on renal blood flow. 4) The decapsulated kidney autoregulates. These data indicate that renal blood flow autoregulation cannot be explained on the basis of the tissue pressure hypothesis, but rather give further support to the myogenic theory.


2014 ◽  
Vol 0 (0) ◽  
Author(s):  
Hitesh Soni ◽  
Randal K. Buddington ◽  
Adebowale Adebiyi

AbstractIntravascular pressure-induced vasoconstriction (myogenic constriction) is central to renal blood flow autoregulation. At term, kidney maturation is functionally incomplete. Premature neonates are at risk of kidney dysfunction. However, it is unclear whether renal artery myogenic constriction is altered after preterm birth. Here, we compared renal artery myogenic constriction in full-term and preterm pigs during the first week of life.We investigated myogenic constriction in small interlobular arteries isolated from the kidneys of pigs delivered at term and at 91% of term (with and without 96 h of neonatal intensive care).Cross-sectional area, media/lumen ratio, and luminal diameter measured under passive conditions were similar in arteries from full-term and preterm pig kidneys. An acute elevation in intravascular pressure from 20 to 100 mm Hg increased arterial wall tension and induced steady-state constriction of the arteries. However, arteries isolated from newly born preterm pigs (within 24 h) developed greater myogenic tone and lower active wall tension compared with arteries from full-term and 4-day-old preterm neonates. Pressure-induced elevation in intracellular CaMyogenic constriction is elevated in newly born preterm pigs. Our data also suggests that postnatal kidney maturation may modulate renal blood flow autoregulation.


2014 ◽  
Vol 120 (5) ◽  
pp. 1281-1281
Author(s):  
Arthur E. Schwartz

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