Pregled bibliografske jedinice broj: 543
Regulation of AE1 anion exchanger and H+-ATPase in rat cortex by acute metabolic acidosis and alkalosis
Regulation of AE1 anion exchanger and H+-ATPase in rat cortex by acute metabolic acidosis and alkalosis // Kidney international. Supplement, 51 (1997), 1; 125-137 doi:10.1038/ki.1997.16 (međunarodna recenzija, članak, znanstveni)
CROSBI ID: 543 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Regulation of AE1 anion exchanger and H+-ATPase in
rat cortex by acute metabolic acidosis and alkalosis
Autori
Sabolić, Ivan ; Brown, Dennis ; Gluck, Stephen L. ; Alper, Seth L.
Izvornik
Kidney international. Supplement (0098-6577) 51
(1997), 1;
125-137
Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni
Ključne riječi
vacuolar H+-ATPase ; anion exchanger ; acidosis ; alkalosis ; renal tubule ; rat
Sažetak
Regulation of AE1 anion exchanger and H+-ATPase in rat cortex by acute metabolic acidosis and alkalosis. The cortical collecting duct (CCD) mediates net secretion or reabsorption of protons according to systemic acid/base status. Using indirect immunofluorescence, we examined the localization and abundance of the vacuolar H+- ATPase and the AE1 anion exchanger in intercalated cells (IC) of rat kidney connecting segment (CNT) and CCD during acute (6 hr) metabolic (NH4Cl) acidosis and respiratory (NaHCO3) alkalosis. AE1 immunostaining intensity quantified by confocal microscopy was elevated in metabolic acidosis and substantially reduced in metabolic alkalosis. AE1 immunostaining intensity was restricted to Type A IC in all conditions, and the fraction of AE1+ IC was unchanged in CNT and CCD. Metabolic acidosis was accompanied by redistribution of H+-ATPase immunostaining towards the apical surface of IC. Therefore, acute metabolic acidosis produced changes consistent with increased activity of Type A IC and decreased activity of Type B IC, whereas acute metabolic alkalosis produced changes corresponding to increased activity of Type B IC and decreased activity of Type A IC. These data demonstrate that acute systemic acidosis and alkalosis modulate the cellular distribution of two key transporters involved in proton secretion in the distal nephron.
Izvorni jezik
Engleski
Znanstvena područja
Temeljne medicinske znanosti
POVEZANOST RADA
Projekti:
00220101
Ustanove:
Institut za medicinska istraživanja i medicinu rada, Zagreb
Profili:
Ivan Sabolić
(autor)
Citiraj ovu publikaciju:
Časopis indeksira:
- Web of Science Core Collection (WoSCC)
- Science Citation Index Expanded (SCI-EXP)
- SCI-EXP, SSCI i/ili A&HCI
- Scopus
- MEDLINE