| First Author | Wang T | Year | 2002 |
| Journal | Am J Physiol Renal Physiol | Volume | 283 |
| Issue | 4 | Pages | F658-62 |
| PubMed ID | 12217856 | Mgi Jnum | J:113614 |
| Mgi Id | MGI:3687093 | Doi | 10.1152/ajprenal.00243.2001 |
| Citation | Wang T (2002) Role of iNOS and eNOS in modulating proximal tubule transport and acid-base balance. Am J Physiol Renal Physiol 283(4):F658-62 |
| abstractText | Our laboratory has previously shown that mice lacking neuronal nitric oxide synthase (nNOS) are defective in fluid absorption (J(v)) and HCO absorption (J(HCO3)) in the proximal tubule and develop metabolic acidosis. The present study examined the transport of fluid and HCO in the proximal tubule and acid-base status in mice lacking two other isoforms of NOS, inducible NOS (iNOS) and endothelial NOS (eNOS). Proximal tubules were microperfused in situ in wild-type and NOS knockout mice by methods previously described (Wang T, Yang C-L, Abbiati T, Schultheis PJ, Shull GE, Giebisch G, and Aronson PS. Am J Physiol Renal Physiol 277: F298-F302, 1999). [(3)H]inulin and total CO(2) concentrations were measured in the perfusate and collected fluid, and net J(v) and J(HCO3) were analyzed. These data show that J(HCO3) was 35% lower (71.7 +/- 6.4 vs. 109.9 +/- 7.3 pmol x min(-1) x mm(-1), n = 13, P < 0.01) and J(v) was 38% lower (0.95 +/- 0.15 vs. 1.54 +/- 0.17 nl. min(-1) x mm(-1), n = 13, P < 0.05) in iNOS knockout mice compared with their wild-type controls. Addition of the iNOS-selective inhibitor L-N(6)-(1-iminoethyl) lysine, reduced both J(v) and J(HCO3) significantly in wild-type, but not in iNOS knockout, mice. In contrast, both J(HCO3) (93.3 +/- 7.9 vs. 110.6 +/- 6.18 pmol x min(-1) x mm(-1)) and J(v) (1.56 +/- 0.17 vs. 1.55 +/- 0.16 nl. min(-1) x mm(-1)) did not change significantly in eNOS knockout mice. These results indicated that iNOS upregulates Na(+) and HCO transport, whereas eNOS does not directly modulate Na(+) and HCO transport in the kidney proximal tubules. |
