Endothelin and nitric oxide mediate adaptation of the cortical collecting duct t - 《American Journal of Physiology》美国生理学杂志干细胞之家



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发表于 2009-4-22 08:35 |只看该作者 |倒序浏览 |打印

作者：Shuichi Tsuruoka, Seiji Watanabe, Jeffrey M. Purkerson, Akio Fujimura, and George J. Schwartz作者单位：1 Department of Pharmacology, Jichi Medical School, Tochigi, Japan; and 2 Department of Pediatrics, University of Rochester School of Medicine, Rochester, New York 4 X5 D: x8 I& p* e& X( E

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      【摘要】
   Endothelin (ET) and nitric oxide (NO) modulate ion transport in the kidney. In this study, we defined the function of ET receptor subtypes and the NO guanylate cyclase signaling pathway in mediating the adaptation of the rabbit cortical collecting duct (CCD) to metabolic acidosis. CCDs were perfused in vitro and incubated for 3 h at pH 6.8, and bicarbonate transport or cell pH was measured before and after acid incubation. Luminal chloride was reversibly removed to isolate H and HCO 3 - secretory fluxes and to raise the pH of -intercalated cells. Acid incubation caused reversal of polarity of net HCO 3 - transport from secretion to absorption, comprised of a 40% increase in H secretion and a 75% decrease in HCO 3 - secretion. The ET B receptor antagonist BQ-788, as well as the NO synthase inhibitor, N G -nitro- L -arginine methyl ester ( L -NAME), attenuated the adaptive decrease in HCO 3 - secretion by 40%, but only BQ-788 inhibited the adaptive increase in H secretion. There was no effect of inactive D -NAME or the ET A receptor antagonist BQ-123. Both BQ-788 and L -NAME inhibited the acid-induced inactivation (endocytosis) of the apical Cl - /HCO 3 - exchanger. The guanylate cyclase inhibitor LY-83583 and cGMP-dependent protein kinase inhibitor KT-5823 affected HCO 3 - transport similarly to L -NAME. These data indicate that signaling via the ET B receptor regulates the adaptation of the CCD to metabolic acidosis and that the NO guanylate cyclase component of ET B receptor signaling mediates downregulation of Cl - /HCO 3 - exchange and HCO 3 - secretion. 5 k2 U5 a4 g' k4 _( G" w- Y
      【关键词】 tubule microperfusion endothelin receptor antagonist nitric oxide synthase inhibitor cyclic GMP cyclic GMPdependent protein kinase. c+ X. x2 t& r$ T" I( J
   ENDOTHELINS (ET) were first described as vasoactive peptides that regulate regional vascular tone by signaling cells in the cardiovascular system via members of the G protein-coupled receptor family ( 15a, 45 ). Since the early 1990s, it has become apparent that ET also regulates sodium-water balance and pH homeostasis in the kidney by directly signaling renal epithelial cells. ET promotes water diuresis by acting to inhibit the hydroosmotic action of vasopressin ( 22 ). Several studies implicate ET in the regulation of acid-base homeostasis in the proximal tubule ( 41 ) as well as the distal nephron ( 42, 43 ). ET modulates NHE3 activity in the proximal tubule and thereby regulation of proton secretion by this segment ( 13 ). In the distal nephron, ET-1 is abundantly expressed by collecting ducts ( 12 ), as are ET B receptors ( 29 ). ET stimulates distal tubular acidification in the rat ( 42, 43 ), and the expression of ET in the kidney is stimulated by metabolic acidosis ( 44 ). Mice having a genetically disrupted ET B receptor experience a more severe acidosis than normal mice in response to acid loading ( 13 ). However, a detailed assessment of the regulation of proton vs. bicarbonate transport in the cortical collecting duct (CCD) is lacking.
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In many cases, the effects of ET on ion transport processes in nephron segments are mediated by the generation of nitric oxide (NO) resulting from activation of a NO synthase (NOS) ( 9, 10, 17 ). In vivo studies suggest that NO induces a natriuresis and diuresis, which is mediated by activation of guanylate cyclase. In the proximal tubule, Wang et al. ( 41 ) reported that tubules from neuronal NOS knockout mice exhibited lower fluid and HCO 3 - absorption rates compared with tubules from wild-type mice. Thus NO produced by neuronal NOS in the proximal tubule is likely to stimulate fluid and HCO 3 - absorption. In the CCD NO inhibits Na absorption and vasopressin-stimulated osmotic water permeability ( 5, 17 ). The effect of NO on osmotic water permeability is blocked by guanylate cyclase and cGMP-dependent protein kinase (PKG) inhibitors, indicating that the effect of NO is mediated by activation of soluble guanylate cyclase and subsequent activation of PKG by cGMP ( 6, 17 ). This cascade results in inhibition of vasopressin-stimulated osmotic water permeability ( 6, 17 ).

In the thick ascending limb, endogenous NO inhibits chloride transport ( 20 ), and a comparable inhibition is observed using exogenous ET-1 ( 19 ). The ET effect is blocked by inhibiting NOS with N G -nitro- L -arginine methyl ester ( L -NAME) ( 19 ), suggesting that the effects of ET-1 are mediated by NOS in the thick ascending limb of Henle's loop ( 9 )., a6 d2 }/ e% k( z7 @1 \7 f+ z5 b

NO also regulates pH homeostasis in the distal nephron. In freshly isolated CCDs, NO donors decrease bafilomycin-sensitive H -ATPase activity ( 31 ). Such inhibition is likely mediated by cGMP because cGMP analogs also inhibit H -ATPase activity ( 31 ). However, this finding would lead to an expectation of decreased H secretion in the CCD, which could be life threatening in a setting of metabolic acidosis. In contrast, mice deficient in neuronal (n)NOS develop metabolic acidosis ( 41 ). In rats inhibition of NO by administration of L -NAME impairs urinary acid excretion after acute NH 4 Cl loading ( 35 ). CCDs taken from such treated rats showed that net bicarbonate absorption was reduced by 40%. These studies strongly suggest that NO is involved in the maintenance of acid-base homeostasis in the distal nephron; however, it has not been established whether NO regulates proton and/or bicarbonate flux by intercalated cells.# M3 }4 J1 D4 @, h

In this study, we examine whether the changes in H /HCO 3 - secretion fluxes induced by acidosis are regulated by ET receptor signaling via the NO-guanylate cyclase pathway. We made use of in vitro acid incubation of CCDs that recapitulates the findings of 3 days of in vivo acid loading ( 21 ). CCDs taken from normal rabbits secrete net HCO 3 -, and this net flux is made up of a small H secretory flux that is outstripped by a much larger HCO 3 - secretory flux ( 26, 33 ). The adaptation to acidosis is associated with both a modest increase in H secretory flux and a large decrease in HCO 3 - secretory flux, with the resultant sum of fluxes being the secretion of net protons ( 26, 33 ); that is, a reversal in polarity of net HCO 3 - transport., b9 `" u5 i( J) U
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METHODS% L* @8 i; P8 W

Animals. Female New Zealand white rabbits ( n = 49) weighing 1.6-2.5 (mean 2.04) kg were maintained on standard laboratory chow (Japan Clea) with free access to water ( 33 ). Animals were killed by intracardiac injection of 130 mg pentobarbital sodium after premedication with ketamine (44 mg/kg) and xylazine (5 mg/kg). Urine was obtained postmortem by bladder tap; urine pH averaged 7.96 ± 0.02 (SE, n = 49).
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Microperfusion of CCDs. CCDs were microdissected and microperfused as performed in this laboratory ( 26, 33 ). The average tubule length was 0.9 ± 0.1 mm. Equilibration and transport were performed using Burg's solution in the perfusate and bath, containing (in mM) 120 NaCl, 25 NaHCO 3, 2.5 K 2 HPO 4, 2 CaCl 2, 1.2 MgSO 4, 5.5 D -glucose, 1 trisodium citrate, 4 sodium lactate, and 6 L -alanine, 290 ± 2 mosmol/kgH 2 O, and gassed with 94% O 2 -6% CO 2, yielding a pH of 7.4 at 37°C ( 26, 33, 34 ). Bath was continually exchanged at 14 ml/h by a peristaltic pump. Luminal perfusion rate was maintained at 1.5-2.1 nl/min.' T0 l+ t% }5 f$ u# T
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Incubation for 3 h at low pH (pH 6.8 in both luminal and bathing solutions) has been previously described ( 21 ). Briefly, the luminal solution contained DMEM without NaHCO 3 (GIBCO, BRL, Gaithersburg, MD), Burg's solution, and dissection solution (Burg's solution with 25 mM NaHCO 3 replaced by NaCl) in a ratio of 3:2:4, respectively. The bathing solution was similar except that it also contained 30 U/ml penicillin, 30 µg/ml streptomycin, and 3.3% fetal calf serum (GIBCO, BRL) ( 21, 33, 46 ). Incubation at pH 6.8 in vitro yields a physiology comparable to 3 days of acidosis in vivo and reverses the polarity of HCO 3 - flux from net secretion to net absorption ( 21, 26, 33 ).6 n3 @0 [9 w3 u1 r: D

Bicarbonate transport. Triplicate collections of 12-15 nl of tubular fluid were made under water saturated mineral oil and analyzed for HCO 3 - using a Nanoflo (WPI, Sarasota, FL) ( 26, 33, 35, 36 ). Net HCO 3 - was calculated as J HCO3 = (C O - C L ) x (V L / L ), where C O and C L are the HCO 3 - concentrations of perfused and collected fluid, respectively, V L is the rate of collected fluid, and L is the length of the tubule (mm) ( 26, 33 ). When HCO 3 - transport ( J HCO3 0, there is net HCO 3 - absorption; when J HCO3 is * |7 x- `. c2 e) w2 T5 n" o+ a# \# Y
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Measurements were repeated after the 3-h incubation and compared with preincubation values. In most of the experiments, an agent was introduced in the bath for 30 min at pH 7.4 before being added to the pH 6.8 bathing solution for the 3-h incubation ( 21, 26 ). The agents included BQ-788 (1 µM, Sigma, ET B receptor antagonist) ( 8 ), BQ-123 (1-10 µM, Sigma, ET A receptor antagonist) ( 2 ), L -NAME (1 mM, Sigma, St. Louis, MO and Tokyo, Japan, NOS inhibitor) ( 39 ), D -NAME (1 mM, Sigma, inactive enantiomer control), LY-83583 (or 6-anilino-5,8-quinolinedione, 10 µM, Biomol, Plymouth Meeting, PA, guanylate cyclase inhibitor) ( 39 ), and KT-5823 (2 µM, Sigma, specific cell-permeant cGMP-dependent protein kinase inhibitor) ( 16 ).

Transepithelial voltage (mV) was measured using the luminal perfusion pipette as an electrode. The voltage difference between calomel cells connected via 3 M KCl agar bridges to perfusate and bath was measured with a high-impedance electrometer.+ I# W5 i! m* p6 J$ R0 M
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Cell pH studies. Cell pH was measured by excitation ratio fluorometry (490 nm/445-nm excitation; 520-nm emission) using 5-10 µM BCECF (Molecular Probes, Eugene, OR) ( 26, 36 ). Fluorescence was detected in multiple intercalated cells and corrected for background (Photon Technology, London, Ontario). Movement and contaminating fluorescent signals were minimized by examining cells in focus close to the perfusion pipette and in the wall of the tubule. Duplicate readings were averaged in Burg's solution, after the reversible removal of luminal Cl - and subsequently after the reversible removal of basolateral Cl -. The sequence of readings was repeated in the same identified intercalated cells after 3-h incubation.4 h- H$ n/ U# \% v
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Agents were dissolved in 0.1% DMSO (vehicle) and added to the bathing solution 3-15 min before and during the 3-h incubation at pH 6.8. These agents included BQ-788 (1 µM, the ET B receptor antagonist) and L -NAME (1 mM).
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Statistics. Data are presented as means ± SE. Standard paired and unpaired comparisons were performed on spreadsheets using Excel 2003 (Microsoft, Bellvue, WA). One-way ANOVA, box plots, and post hoc Duncan and Scheffé's multiple comparison tests were used to examine the acid-incubated/basal H /HCO 3 - flux ratios and the acid-induced changes in net HCO 3 - flux using NCSS 6.0 statistical software (Kaysville, UT). Significance was asserted if P % K% @6 D. F+ h+ C. ]0 w: I

RESULTS9 ]& Z8 B, m! X
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Incubation at pH 6.8 induces a reversal in polarity of net HCO 3 - flux. To study the adaptation of intercalated cells, we utilized the model of in vitro acid incubation ( 21 ) and examined the effect of 3-h incubation of each CCD at pH 6.8 in both luminal and bathing solutions. In three CCDs taken from normal rabbits, the mean rate of bicarbonate transport before acid incubation was -3.18 ± 0.51 pmol·min -1 ·mm -1, indicating net HCO 3 - secretion. After 3-h incubation at pH 6.8, the solutions were restored to pH 7.4 and HCO 3 - transport was remeasured in the same tubule. After acid incubation the net flux was  3.07 ± 0.28 pmol·min -1 ·mm -1 ( P * ]* Q; y! N: c7 h, P2 b: l
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To dissect out the unidirectional fluxes of HCO 3 - and H comprising the net flux, we incubated five CCDs at pH 6.8 and added a period in which luminal Cl - was removed (and replaced by gluconate) to the pre- and postacid-incubation measurements. Bicarbonate transport in the absence of luminal Cl - reflects the secretion of protons by -intercalated cells, because HCO 3 - secretion is simultaneously inhibited in the -intercalated cells. Figure 1 shows that the mean rate of net HCO 3 - transport was -3.81 ± 0.21 pmol·min -1 ·mm -1, which was comprised of an H secretion rate of 3.69 ± 0.16 pmol·min -1 ·mm -1 and a HCO 3 - secretion rate of -7.50 ± 0.36 pmol·min -1 ·mm -1 ( Table 1 ). After 3-h incubation at pH 6.8 in the presence of vehicle, the net HCO 3 - flux reversed polarity to net H secretion ( 3.27 ± 0.14 pmol·min -1 ·mm -1, P
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Fig. 1. Changes in H /HCO 3 - flux induced by incubation of cortical collecting duct (CCD) at pH 6.8 ( n = 5 CCDs). Left : net bicarbonate transport. Middle : H secretory fluxes obtained from luminal Cl - removal (which inhibits HCO 3 - secretion). Right : HCO 3 - secretory fluxes obtained from the difference between the net and H secretion flux. Each flux is presented before and following acid incubation. *Significantly different ( P
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Table 1. Basal and acid incubation net and H /HCO 3 - fluxes

Fig. 2. Inhibition of ET B receptor signaling blocks adaptive changes in net bicarbonate flux induced by acid incubation. The difference between acid-incubated and basal net bicarbonate flux in pmol·min -1 ·mm -1 under various treatments is shown in box plots. Treatments include vehicle ( n = 5), BQ-788 ( n = 5), BQ-123 ( n = 5), L -NAME ( n = 4), D -NAME ( n = 4), LY-83583 ( n = 6), and KT-5823 ( n = 6). The horizontal line represents the median, the top and bottom of the box represent the 75th and 25th percentiles, respectively, and the length of the box is the interquartile range; the T-shaped lines represent upper and lower adjacent values, wherein the former is the largest observation that is less than or equal to the 75th percentile plus 1.5 times the interquartile range and the latter is the smallest observation that is greater than or equal to the 25th percentile minus 1.5 times the interquartile range. The change in net bicarbonate flux is positive, indicating a shift from net secretion to zero net flux or to net HCO 3 - absorption. Because 1-way ANOVA was highly significant ( P + y0 F- h$ ^) S7 }# m8 Y$ e

Fig. 3. Antagonism of ET B receptor blocks increases in H secretion induced by low pH. The ratio of acid-incubated/basal H secretory fluxes under the various treatments is shown. The median and 75th and 25th percentiles are presented as in Fig. 2. The dashed horizontal line denotes the ratio of one, indicating no significant increase in H secretion. ANOVA was highly significant ( P ; E+ v1 y* j8 K5 a8 F- v* D# J
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Fig. 4. Inhibition of ET B receptor signaling blocks adaptive changes in HCO 3 - secretion induced by acid incubation. The ratio of acid-incubated/basal HCO 3 - secretory fluxes under the various treatments is shown. The median and 75th and 25th percentiles are presented as in Fig. 2. ANOVA was highly significant ( P

Adaptive changes in H /HCO3- secretion fluxes induced by low pH are inhibited by ET B receptor antagonism. Because ET secretion is induced by acidosis ( 42, 44 ) and ET receptor signaling regulates ion transport processes along the nephron ( 13, 32, 43 ), we examined the effect of ET receptor antagonism on the changes in H /HCO 3 - secretory fluxes induced by incubation at low pH. Acid incubation with BQ-788 failed to reverse the polarity of the net HCO 3 - flux ( Table 1 ); that is, net HCO 3 - secretion was reduced to no significant HCO 3 - transport (-4.03 ± 0.29 to 0.047 ± 0.16 pmol·min -1 ·mm -1, P 3 B% [* z& Q$ \
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Time control. To ensure the stability of the isolated CCD preparation, we performed four timed control experiments with a 3-h incubation at pH 7.4; three of these experiments utilized 1 µM BQ-788 and the fourth used no inhibitor. Net bicarbonate secretion was unchanged by the incubation (or inhibitor): -3.89 ± 0.16 before and -3.83 ± 0.17 pmol·min -1 ·mm -1 after incubation ( P = NS). There was no change in H secretory flux (3.44 ± 0.05 to 3.68 ± 0.21 pmol·min -1 ·mm -1, P = NS) or in HCO 3 - secretory flux (-7.33 ± 0.13 to -7.51 ± 0.29 pmol·min -1 ·mm -1, P = NS). In agreement with the stability of the H secretory flux, there was no change in transepithelial voltage (-2.1 ± 0.1 to -2.1 ± 0.1 mV, P = NS). Similar data have been reported previously ( 33 ).3 a$ j; |, I' ?8 Q# y. o

Adaptive decrease in HCO3- secretion flux induced by low pH requires NO synthesis. ET receptor signaling induces activation of NOS activity ( 9, 10 ). Therefore, we examined whether NO production was required for adaptation of the CCD to low pH. To detect the effect of NOS inhibition, we incubated five CCDs in 1 µM L -NAME just before and during the pH 6.8 incubation. Net HCO 3 - secretion before the acid incubation averaged -3.22 ± 0.22 pmol·min -1 ·mm -1 and after acid incubation was only slightly greater than zero, 0.59 ± 0.02 pmol·min -1 ·mm -1. Whereas the change in net HCO 3 - flux was significant ( P

We further examined the effect of NOS inhibition on the adaptation to low pH (in vitro acidosis) by measuring HCO 3 - transport in the presence and absence of luminal Cl -. Table 1 shows that acid incubation with L -NAME resulted in a significant reduction, but not a reversal in polarity, of net HCO 3 - transport (-3.66 ± 0.37 to 0.16 ± 0.19 pmol·min -1 ·mm -1, P ! D# Z3 d4 ]  m  }

ET B receptor antagonism and L -NAME block the effect of acidosis on chloride-dependent cell pH changes. To confirm the changes in HCO 3 - transport, we examined -intercalated cell pH changes in response to removal of Cl - from the lumen or bath. Previously, we showed that -intercalated cells express apical Cl - /HCO 3 - exchangers and basolateral Cl - conductances ( 21, 25 ). Figure 5 A shows that when luminal Cl - was removed, intercalated cell pH rose by 0.40 ± 0.04 pH U, but that after acid incubation, there was no alkalinization of cell pH with this maneuver (delta pH = -0.01 ± 0.03, P ; u+ I$ x, v  W! f0 M) H
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Fig. 5. ET B receptor signaling is required for loss of luminal Cl - /HCO 3 - exchange activity stimulated by low pH. Cell pH changes in response to Cl - removal in basal state and after acid incubation are shown. A, C, and E : intercalated cell pH changes resulting from luminal Cl - removal. B, D, and F : cell pH changes resulting from bath Cl - removal. A and B : vehicle ( n = 25 cells from 3 CCDs). C and D : BQ-788 ( n = 40 cells from 5 CCDs). E and F : L -NAME ( n = 66 cells from 7 CCDs). *Significantly different from basal value ( P 9 F. W- c4 U. Y2 S# ]- x$ n

BQ-788 added to the pH 6.8 incubation prevented the adaptive reduction in apical Cl - /HCO 3 - exchange (0.46 ± 0.02 to 0.46 ± 0.01 pH U, P = NS; Fig. 5 C ) and in sensitivity to basolateral Cl - removal (-0.44 ± 0.03 to -0.44 ± 0.04, P = NS; Fig. 5 D ). Similarly, L -NAME added to the pH 6.8 incubation clearly prevented the reduction in apical Cl - /HCO 3 - exchange (0.47 ± 0.03 to 0.45 ± 0.03 pH U, P = NS; Fig. 5 E ) and in sensitivity to basolateral Cl - removal (-0.48 ± 0.04 to -0.51 ± 0.05 pH U, P = NS; Fig. 5 F ). These results confirm that ET B receptor signaling and NO synthesis are required for the adaptive decrease in HCO 3 - secretion (presumably by endocytosis of apical Cl - /HCO 3 - exchangers) induced by incubation at low pH.7 }8 _! D3 X' E; ]5 y
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cGMP generation and subsequent activation of PKG are required for acid-induced changes in H /HCO 3 - fluxes. Many of the effects of the signaling molecule NO are mediated by stimulation of NO-sensitive guanylate cyclase resulting in cGMP formation and the subsequent activation of cGMP-dependent protein kinase (PKG) ( 7, 15 ). We tested the effect on HCO 3 - transport of 10 µM LY-83583, an inhibitor of soluble guanylate cyclase, during acid incubation ( Fig. 2 ). LY-8353 markedly attenuated the reversal of polarity of net HCO 3 - flux in response to low pH, and there was no net HCO 3 - flux (-3.76 ± 0.17 to 0.18 ± 0.09 pmol·min -1 ·mm -1, P 7 B& I. l! N5 S; q
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The role of PKG in the acid-induced adaptation was tested by examining the effect of 2 µM KT-5823, a specific cell-permeant inhibitor of PKG, on H /HCO 3 - fluxes. KT-5823 substantially prevented the reversal of polarity of HCO 3 - flux in response to low pH, so that there was no net flux after acid incubation (-4.22 ± 0.15 to 0.08 ± 0.05 pmol·min -1 ·mm -1, P

Taken together, these data indicate that the adaptive decrease in HCO 3 - secretion in response to acidosis is mediated in large part by ET-ET B -NO-guanylate cyclase-PKG signaling pathway. In contrast, the adaptive increase in H secretion, which may be directly stimulated by ET-ET B signaling, tends to be less affected by the NO-signaling pathway.% Y; X5 K/ l4 ]
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DISCUSSION6 z0 p) r4 z" M. a% c* f6 K
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To investigate the role of ET and NO in intercalated cells of the CCD, we made use of our in vitro acidosis model in which incubation of a CCD for 3 h at pH 6.8 induces a change in polarity of net HCO 3 - flux from net secretion to net absorption ( 21, 26 ). This model recapitulates the pathophysiological condition of 3 days of NH 4 Cl loading (in the drinking water) that results in metabolic acidosis in vivo ( 21, 25 ). The adaptation to acid treatment is accomplished by two adjustments: increased H secretion, presumably by existing and perhaps recruited -intercalated cells, and decreased HCO 3 - secretion by -intercalated cells ( 23, 24, 33 ). The rabbit CCD contains both - and -intercalated cells, and both types are active under normal conditions. Previously, we showed that luminal bafilomycin, by inhibiting the apical H -ATPase of -intercalated cells of CCDs from normal rabbits, reduces H secretion and thereby makes the net HCO 3 - flux more negative (higher rate of secretion under basal conditions). When bafilomycin was used after acid incubation, the basal and adaptive increases in H secretion were inhibited, such that net HCO 3 - transport was not significantly different from zero ( 33 ). The effect of inhibiting the H -K -ATPase was previously shown ( 33 ) to be much smaller than that of inhibiting the H -ATPase in acid-adapted CCDs, indicating a limited role for the H -K -ATPase in adapting to metabolic acidosis. These data show that there is a substantial amount of HCO 3 - secretion in CCDs from normal rabbits, but after they are incubated at low pH, the HCO 3 - secretion rate is greatly diminished, such that when the offsetting H secretion by -intercalated cells is inhibited by bafilomycin, there is virtually no net HCO 3 - transport. These data also show that there are partially offsetting H secretory fluxes in CCDs from normal rabbits but after acid incubation, the basal and adaptive increase in H secretion are entirely inhibited by a vacuolar H -ATPase inhibitor. In this study, we extended these observations by demonstrating that ET B receptor signaling in response to low pH mediated the decreased HCO 3 - secretion as well as the adaptive increase in H secretion. It is not surprising that the ET B receptor antagonist entirely inhibited the adaptive increase in H secretion, because Wesson's group showed inhibition of B- but A-type ET receptors blunts not only the decreased HCO 3 - secretion but also the increased H secretion in the distal tubule of rats given dietary acid ( 42 ). Thus ET, via the ET B receptor, regulates adaptive changes in H /HCO 3 - fluxes during metabolic acidosis.0 W7 t9 x4 l8 ?) X: h9 _

NO has been found to play an important role in mediating salt and water transport, in addition to hemodynamics and tubuloglomerular feedback in the kidney ( 17 ). Less is known about how NO affects acid-base transport. Mice lacking nNOS have defective proximal tubule HCO 3 - reabsorption and develop metabolic acidosis ( 41 ). Mice lacking inducible NOS, but not endothelial NOS, also show reduced proximal HCO 3 - reabsorption ( 40 ). These studies show that inducible and nNOS stimulate proximal HCO 3 - reabsorption. Also, acidosis stimulates NO synthesis in rat lung ( 18 ) and canine heart ( 11 ), perhaps because the cellular acidosis increases cellular calcium levels ( 4, 38 ), and calcium activates NOS ( 15 ).
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The CCD is known to express endothelial, inducible, and nNOS ( 1, 14, 30, 31, 37 ) and NO has important actions in the CCD. NO inhibits ADH-stimulated osmotic water permeability in the CCD ( 5, 6 ). Also, in M-1 cultured CCD cells, NO inhibits sodium transport at the apical membrane sodium channel ( 27 ). The present study adds modulation of -intercalated cell HCO 3 - secretory fluxes in response to acidosis to the actions of NO on ion transport in the CCD. There are no reports of NO stimulating H secretion in the CCD; and furthermore, results of this study fail to demonstrate a pivotal role for NO guanylate cyclase in upregulating H secretion. However, Tojo et al. ( 31 ) showed that exogenous donors of NO inhibit bafilomycin-sensitive H -ATPase activity in microdissected rat CCDs, suggesting that an inducible form of NOS downregulates H secretion by -intercalated cells. It is possible that ET-ET B signaling to control H secretion works via another pathway that predominates over the NO-guanylate cyclase system.7 h8 f$ ?& k& R6 ]5 ^/ Z
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Activation of soluble guanylate cyclase leading to the production of cGMP is a key function of NO as a signal generator. cGMP has several targets, with the major one being PKG ( 7 ). cGMP has recently been shown to cause the membrane insertion of aquaporin-2 in renal epithelial cells ( 3 ). Results presented in the present study demonstrate that activation of guanylate cyclase and subsequent stimulation of PKG are critical for the adaptation of the -intercalated cell to acidosis. Based on the analysis of HCO 3 - flux and cell pH changes in response to luminal Cl - removal, we suggest that cGMP activation of PKG stimulates endocytosis of apical Cl - /HCO 3 - exchangers, leading to a decrease in HCO 3 - secretion in response to acidosis. Identification of substrates of PKG that directly or indirectly influence endocytic pathways is an important area for further investigation.+ p7 @* h# Q) V. D
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GRANTS

This work was supported in part by a Grant-in-Aid from the American Heart Association (0455829T) New York State Affiliate (G. J. Schwartz) and by grants from the Ministry of Education, Culture, Sports, Science and Technology, and Ministry of Health, Labor and Welfare of Japan (S. Tsuruoka).8 Z) [9 N* d) ?
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Garcia NH, Pomposiello SI, and Garvin JL. Nitric oxide inhibits ADH-stimulated osmotic water permeability in cortical collecting ducts. Am J Physiol Renal Fluid Electrolyte Physiol 270: F206-F210, 1996.8 C; T8 c8 I0 x7 p; O

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