Involvement of Endogenous Nitric Oxide in the Regulation of K〔+〕 Channel Activity in Cultured Human Proximal Tubule Cells

DOI Web Site 被引用文献4件 参考文献56件
  • Nakamura Kazuyoshi
    Department of Physiology II, Iwate Medical University School of Medicine
  • Habano Wataru
    Division of DNA Laboratory, Iwate Medical University School of Medicine
  • Kojo Toshiyuki
    Department of Physiology II, Iwate Medical University School of Medicine
  • Komagiri You
    Department of Physiology II, Iwate Medical University School of Medicine
  • Kubota Takahiro
    Department of Physiology, Osaka Medical College
  • Kubokawa Manabu
    Department of Physiology II, Iwate Medical University School of Medicine

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  • Involvement of Endogenous Nitric Oxide in the Regulation of K+ Channel Activity in Cultured Human Proximal Tubule Cells

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Nitric oxide (NO) modulates the activity of an inwardly rectifying K+ channel in cultured human proximal tubule cells. In this study, we investigated which NO synthase (NOS) isoform(s) was involved in the endogenous production of NO and hence the regulation of channel activity. The patch-clamp experiments using the cell-attached mode showed that a nonselective NOS inhibitor, Nω-nitro-L-arginine methyl ester (L-NAME; 100 μM), suppressed channel activity, whereas a NOS substrate, L-arginine (500 μM), stimulated it. A neuronal NOS (nNOS)/inducible NOS (iNOS)-selective inhibitor, 1-(α,α,α-trifluoro-o-tolyl)-imidazole (TRIM; 100 μM), suppressed channel activity to the same extent as L-NAME. TRIM also blocked the stimulatory effect of L-arginine. In contrast, an NO donor, sodium nitroprusside (10 μM) or 8-bromoguanosine 3′,5′-cyclic monophosphate (100 μM) stimulated channel activity even in the presence of TRIM. RT-PCR revealed that iNOS mRNA alone was expressed in most of the cultures, i.e., 34 out of 40. In the other 6 cases, endothelial NOS (eNOS) and iNOS mRNA were simultaneously expressed. This finding was confirmed at the protein level by Western blotting. Indeed, in the patch-clamp experiments TRIM sometimes failed to suppress the channel activity, but the following addition of L-NAME suppressed it. However, since the suppressive effect of TRIM was usually similar to that of L-NAME, the involvement of eNOS in K+ channel regulation would be relatively low. These results suggest that iNOS plays a pivotal role in the endogenous production of NO under the basal condition, which is involved in the activity of the inwardly rectifying K+ channel in cultured human proximal tubule cells.<br>

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