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(Hypertension. 2009;54:248.)
© 2009 American Heart Association, Inc.
Original Articles |
From the Department of Physiology (P.M.O., M.L., A.W.C.), Medical College of Wisconsin, Milwaukee; and the Department of Physiology and Pathophysiology (L.L.), Shanghai Medical College, Fudan University, Shanghai, China.
Correspondence to Paul M. O'Connor, Department of Physiology, Medical College of Wisconsin, 8701 Watertown Plank Rd, Milwaukee, WI 53202. E-mail poconnor{at}mcw.edu
It has been reported previously that H+ efflux via the Na+/H+ exchange stimulates NAD(P)H oxidase-dependent superoxide (O2·–) production in medullary thick ascending limb. We have demonstrated recently that N-methyl-amiloride-sensitive O2·– production is enhanced in the thick ascending limb of Dahl salt-sensitive (SS) rats, suggesting that H+ efflux through Na+/H+ exchangers may promote renal oxidative stress and the development of hypertension in these animals. In the current study we demonstrate, using selective and potent inhibitors, that inhibition of Na+/H+ exchange does not mediate the ability of N-methyl-amiloride to inhibit thick ascending limb O2·– production. To determine the mechanism of action of N-methyl-amiloride, we examined H+ efflux and O2·– production in SS and SS.13BN thick ascending limbs of prehypertensive, 0.4% NaCl-fed rats. Tissue strips containing the medullary thick ascending limb were isolated from male SS and salt-resistant consomic SS.13BN rats, loaded with either dihydroethedium or 2',7'-bis-(2-carboxyethyl)-5-(and-6)-carboxyfluorescein, acetoxymethyl ester, and imaged in a heated tissue bath. In Na+-replete media, activation of Na+/H+ exchange using an NH4Cl prepulse did not stimulate thick ascending limb O2·– production. In Na+-free media containing BaCl2 in which Na+/H+ activity was inhibited, an NH4Cl prepulse stimulated O2·– production in medullary thick ascending limb renal tubular segments. This response was enhanced in medullary thick ascending limb of SS rats (slope
ethidium/
dihydroethedium=0.029±0.004) compared with SS.13BN rats (slope=0.010±0.004; P<0.04) and could be inhibited by N-methyl-amiloride (slope=0.005±0.002 and 0.006±0.002 for SS and SS.13BN, respectively). We concluded that only H+ efflux through a specific, as-yet-unidentified, amiloride-sensitive H+ channel promotes O2·– production in the medullary thick ascending limb and that this channel is upregulated in SS rats.
Key Words: amiloride blood pressure free radicals H+ transport kidney NAD(P)H oxidase pH
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