Angiotensin II modulates ion transport in rat proximal tubules through CVP metabolites

Alicia Sánchez-Mendoza, Pedro López-Sánchez, Beatriz Vázquez-Cruz, Amelia Rios, Sonia Martínez-Ayala, Bruno Escalante

Research output: Contribution to journalArticle

20 Citations (Scopus)

Abstract

To assess the effect of angiotensin II on ion transport in rat isolated proximal tubules and establish the arachidonic acid cytochrome P450 metabolites' role mediating angiotensin II effect and to analyze whether corticosteroids play a role modulating this effect, we studied the effect of low (10 and 100 pM) and high (0.1-1 μM) angiotensin II concentrations on proximal tubule ion transport, measured as 86Rb uptake. Low angiotensin II produced a stimulation on the 86Rb uptake (195.79 ± 35, 377.9 ± 81, and 300 ± 49 pg 86Rb/μg protein/2 min, for control and 10 and 100 pM angiotensin II, respectively). High angiotensin II concentration inhibited ion transport (0.1 μM, 57.9 ± 5 and 1 μM, 47.3 ± 4 pg 86Rb/μg protein/2 min), this effect was prevented by 17-ODYA and by losartan, while indomethacin had no effect. Dexamethasone treatment increased angiotensin II-induced 86Rb uptake inhibition and arachidonic acid metabolism (19-, 20-HETE and 12-HETE), while adrenalectomy partly prevented angiotensin II-induced inhibition and decreased cytochrome P450-dependent arachidonic acid metabolism. In conclusion, high doses of angiotensin II produce inhibition of ion transport in rat isolated proximal tubules; this effect is mediated by AT1 receptors, involves cytochrome P450-dependent arachidonic acid metabolites, and is upregulated by corticosteroids. (C) 2000 Academic Press.
Original languageAmerican English
Pages (from-to)423-430
Number of pages379
JournalBiochemical and Biophysical Research Communications
DOIs
StatePublished - 7 Jun 2000
Externally publishedYes

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angiotensins
metabolites
Ion Transport
Metabolites
Angiotensin II
rats
Rats
Ions
Enzyme inhibition
Acids
Metabolism
Arachidonic Acid
ions
cytochromes
Proteins
corticosteroids
Cytochrome P-450 Enzyme System
acids
metabolism
Adrenal Cortex Hormones

Cite this

Sánchez-Mendoza, Alicia ; López-Sánchez, Pedro ; Vázquez-Cruz, Beatriz ; Rios, Amelia ; Martínez-Ayala, Sonia ; Escalante, Bruno. / Angiotensin II modulates ion transport in rat proximal tubules through CVP metabolites. In: Biochemical and Biophysical Research Communications. 2000 ; pp. 423-430.
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Angiotensin II modulates ion transport in rat proximal tubules through CVP metabolites. / Sánchez-Mendoza, Alicia; López-Sánchez, Pedro; Vázquez-Cruz, Beatriz; Rios, Amelia; Martínez-Ayala, Sonia; Escalante, Bruno.

In: Biochemical and Biophysical Research Communications, 07.06.2000, p. 423-430.

Research output: Contribution to journalArticle

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AU - Sánchez-Mendoza, Alicia

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AU - Martínez-Ayala, Sonia

AU - Escalante, Bruno

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N2 - To assess the effect of angiotensin II on ion transport in rat isolated proximal tubules and establish the arachidonic acid cytochrome P450 metabolites' role mediating angiotensin II effect and to analyze whether corticosteroids play a role modulating this effect, we studied the effect of low (10 and 100 pM) and high (0.1-1 μM) angiotensin II concentrations on proximal tubule ion transport, measured as 86Rb uptake. Low angiotensin II produced a stimulation on the 86Rb uptake (195.79 ± 35, 377.9 ± 81, and 300 ± 49 pg 86Rb/μg protein/2 min, for control and 10 and 100 pM angiotensin II, respectively). High angiotensin II concentration inhibited ion transport (0.1 μM, 57.9 ± 5 and 1 μM, 47.3 ± 4 pg 86Rb/μg protein/2 min), this effect was prevented by 17-ODYA and by losartan, while indomethacin had no effect. Dexamethasone treatment increased angiotensin II-induced 86Rb uptake inhibition and arachidonic acid metabolism (19-, 20-HETE and 12-HETE), while adrenalectomy partly prevented angiotensin II-induced inhibition and decreased cytochrome P450-dependent arachidonic acid metabolism. In conclusion, high doses of angiotensin II produce inhibition of ion transport in rat isolated proximal tubules; this effect is mediated by AT1 receptors, involves cytochrome P450-dependent arachidonic acid metabolites, and is upregulated by corticosteroids. (C) 2000 Academic Press.

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