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1Division of Hypertension and Vascular Research, Henry Ford Hospital, Detroit; and 2Department of Physiology, Wayne State University, Detroit, Michigan
Submitted 25 November 2008 ; accepted in final form 21 February 2009
We have shown that increased luminal flow induces O2– and nitric oxide (NO) production in thick ascending limbs (TALs). However, the interaction of flow-stimulated NO and O2– in TALs is unclear. We hypothesized that NO inhibits flow-induced O2– production in TALs via cGMP-dependent protein kinase (PKG). We measured flow-stimulated O2– production in rat TALs using dihydroethidium in the absence and presence of L-arginine (0.3 mM), the substrate for NO synthase. The addition of L-arginine reduced flow-induced net O2– production from 68 ± 9 to 17 ± 4 AU/s (P < 0.002). The addition of the NO synthase inhibitor NG-nitro-L-arginine methyl ester (L-NAME; 5 mM) in the presence of L-arginine stimulated production (L-arginine: 15 ± 4 AU/s vs. L-arginine + L-NAME: 63 ± 7 AU/s; P < 0.002). The guanylate cyclase inhibitor LY-83583 (10 µM) also enhanced flow-induced net O2– production in the presence of L-arginine (L-arginine: 7 ± 4 AU/s vs. L-arginine + LY-83583: 53 ± 7 AU/s; P < 0.01). In the presence of LY-83583, L-arginine only reduced flow-induced net O2– by 36% (LY-83583: 80 ± 7 AU/s vs. LY-83583 + L-arginine: 51 ± 3 AU/s; P < 0.006). The cGMP analog dibutyryl (db)-cGMP reduced flow-induced net O2– from 39 ± 9 to 7 ± 3 AU/s (P < 0.03). The PKG inhibitor KT-5823 (5 µM) partially restored flow-induced net O2– in the presence of L-arginine (L-arginine: 4 ± 4 AU/s vs. L-arginine + KT-5823: 32 ± 9 AU/s; P < 0.03) and db-cGMP (db-cGMP: 9 ± 7 AU/s vs. db-cGMP + KT-5823: 54 ± 5 AU/s; P < 0.01). Phosphodiesterase II inhibition had no effect on arginine-inhibited O2– production. We conclude that 1) NO reduces flow-stimulated O2– production, 2) this occurs primarily via the cGMP/PKG pathway, and 3) O2– scavenging by NO plays a minor role.
reactive oxygen species; soluble guanylate cyclase; phosphodiesterase; scavenging
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