Short-term vs sustained inhibition of proximal tubule Na,K-ATPase activity by dopamine: Cellular mechanisms

• Type: Article in International Scientific Journal
• Date: 1997

Authors

Perpetua Pinto do O (Author) Other; Chibalin, AV (Author) Other; Katz, AI (Author) Other; soares-da-silva, p (Author) FMUP; Bertorello, AM (Author) Other

Journal

Title: Clinical and Experimental Hypertension

Vol. 19

Pages: 73-86

ISSN: 1064-1963

Publisher: Taylor & Francis

Indexing

ISI Web of Knowledge - 19 Citations

Scopus - 18 Citations

Other information

Authenticus ID: P-001-C8T

DOI: 10.3109/10641969709080805

Abstract (EN): Dopamine (DA) produces a natriuresis attributed in part to inhibition of Na,K-ATPase activity (NKA) in the proximal tubule (PCT), and impairment in this inhibition has been linked to several forms of hypertension in animals. Here we examined whether the intracellular signaling mechanisms involved are the same in the early and late phases of this phenomenon. DA (1 mu M) inhibited NKA similarly after 15 min (by 38%) or 180 min (by 36%) incubation, taken to represent short-term (ST) and sustained (Sd) pump regulation, respectively. Calphostin C, a specific inhibitor of protein kinase C (PKC), completely blocked the ST action of DA on NKA, whereas IP20, a specific inhibitor of protein kinase (PKA), had no effect. In contrast, IP20 completely abolished the Sd (180 min) inhibition by DA, whereas calphostin C had only a partial or variable effect. The DA-1 agonist fenoldopam (which does not activate PKC but increases cAMP) alone failed to inhibit the pump at 180 min (as it does also in the short-term in PCT), suggesting that ST inhibition is required for the Sd effect to occur. Furthermore, PTH1-34, a known ST inhibitor of NKA suppressed the pump at 180 min (by 46%), but unlike in the short-term, this effect was completely prevented by IP20. In contrast, PTH3-34, which does not stimulate adenylyl cyclase or activate PHA, caused only a small (19%) and variable Sd inhibition. In conclusion, short-term inhibition of the PCT pump by dopamine is mediated via PKC, whereas the sustained inhibition requires the PKA pathway in addition to the ongoing PMC-mediated effect.

Language: English

Type (Professor's evaluation): Scientific

No. of pages: 14