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spelling paper:paper_07302312_v92_n3_p591_Zallocchi2023-06-08T15:43:47Z Adrenal gland involvement in the regulation of renal 11 β-hydroxysteroid dehydrogenase 2 Zallocchi, Marisa Laura Matkovic, Laura Beatriz Calvo, Juan Carlos Acidosis Corticosterone HSD2 Kidney Stress 11beta hydroxysteroid dehydrogenase chloride corticosterone glucocorticoid corticosterone adrenal gland adrenalectomy animal experiment animal model article body weight controlled study enzyme activity enzyme regulation feeding metabolic acidosis nonhuman priority journal radioimmunoassay rat stress Western blotting adrenal gland animal blood enzymology gene expression regulation kidney kinetics metabolism physiology Animalia 11-beta-Hydroxysteroid Dehydrogenase Type 2 Adrenal Glands Adrenalectomy Animals Corticosterone Gene Expression Regulation, Enzymologic Kidney Kinetics Models, Animal Rats Renal 11 β-hydroxysteroid dehydrogenase 2 (HSD2) catalyzes the conversion of active glucocorticoids to inert 11 β-keto compounds, thereby preventing the illicit binding of these hormones to mineralocorticoid receptors (MRs) and, thus, conferring aldosterone specificity. Absence or inhibition of HSD2 activity, originates a hypertensive syndrome with sodium retention and increased potassium elimination. Recent studies from our laboratory reported an increment of HSD2 activity in intact-stressed rats. To evaluate the adrenal involvement in this increase, we analyzed HSD2 activity and protein abundance in Intact, Sham-operated, and adrenalectomized rats under stress situations (gavage with an overload of 200 mM HCl (10 ml) and simulated gavage) or with corticosterone replacement. HSD2 activity was assessed in renal microsomal preparations obtained from different groups of animals. HSD2 protein abundance was measured by Western-blot. Circulating corticosterone was determined by radioimmunoassay. Sham-operated animals showed an increase in HSD2 activity and abundance compared to Intact and adrenalectomized rats suggesting the involvement of stress-related adrenal factors in HSD2 regulation. In the case of acidotic adrenalectomized animals, there was an increase in renal HSD2 activity when, along with the HCl overload, the rats were injected with corticosterone. This increment occurred without an increase in enzyme abundance. These results suggest the importance of circulating levels of glucocorticoids to respond to a metabolic acidosis, through regulation of HSD2 stimulation. The group subjected to a simulated gavage showed an increase in enzyme activity and protein abundance, thus demonstrating the need for both adrenal and extra-factors in the modulation of renal HSD2. The adrenalectomized animals injected with different doses of corticosterone, produced a progressive increase in enzyme activity and abundance, being significant for the dose of 68 ng corticosterone/100 g body weight. The highest dose (308 ng/100 g body weight) did not show any variation in activity and abundance compared to the control group. This biphasic effect of glucocorticoids could be explained taking into account their permissive and suppressive actions, depending on their blood levels. Knowing that stress induces multifactorial responses, it should not be suprising to observe a differential regulation in renal HSD2, confirming that different Stressors act through different factors of both, adrenal and extra-adrenal origin. © 2004 Wiley-Liss, Inc. Fil:Zallocchi, M.L. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Matkovic, L. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Calvo, J.C. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. 2004 https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_07302312_v92_n3_p591_Zallocchi http://hdl.handle.net/20.500.12110/paper_07302312_v92_n3_p591_Zallocchi
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-134
collection Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
topic Acidosis
Corticosterone
HSD2
Kidney
Stress
11beta hydroxysteroid dehydrogenase
chloride
corticosterone
glucocorticoid
corticosterone
adrenal gland
adrenalectomy
animal experiment
animal model
article
body weight
controlled study
enzyme activity
enzyme regulation
feeding
metabolic acidosis
nonhuman
priority journal
radioimmunoassay
rat
stress
Western blotting
adrenal gland
animal
blood
enzymology
gene expression regulation
kidney
kinetics
metabolism
physiology
Animalia
11-beta-Hydroxysteroid Dehydrogenase Type 2
Adrenal Glands
Adrenalectomy
Animals
Corticosterone
Gene Expression Regulation, Enzymologic
Kidney
Kinetics
Models, Animal
Rats
spellingShingle Acidosis
Corticosterone
HSD2
Kidney
Stress
11beta hydroxysteroid dehydrogenase
chloride
corticosterone
glucocorticoid
corticosterone
adrenal gland
adrenalectomy
animal experiment
animal model
article
body weight
controlled study
enzyme activity
enzyme regulation
feeding
metabolic acidosis
nonhuman
priority journal
radioimmunoassay
rat
stress
Western blotting
adrenal gland
animal
blood
enzymology
gene expression regulation
kidney
kinetics
metabolism
physiology
Animalia
11-beta-Hydroxysteroid Dehydrogenase Type 2
Adrenal Glands
Adrenalectomy
Animals
Corticosterone
Gene Expression Regulation, Enzymologic
Kidney
Kinetics
Models, Animal
Rats
Zallocchi, Marisa Laura
Matkovic, Laura Beatriz
Calvo, Juan Carlos
Adrenal gland involvement in the regulation of renal 11 β-hydroxysteroid dehydrogenase 2
topic_facet Acidosis
Corticosterone
HSD2
Kidney
Stress
11beta hydroxysteroid dehydrogenase
chloride
corticosterone
glucocorticoid
corticosterone
adrenal gland
adrenalectomy
animal experiment
animal model
article
body weight
controlled study
enzyme activity
enzyme regulation
feeding
metabolic acidosis
nonhuman
priority journal
radioimmunoassay
rat
stress
Western blotting
adrenal gland
animal
blood
enzymology
gene expression regulation
kidney
kinetics
metabolism
physiology
Animalia
11-beta-Hydroxysteroid Dehydrogenase Type 2
Adrenal Glands
Adrenalectomy
Animals
Corticosterone
Gene Expression Regulation, Enzymologic
Kidney
Kinetics
Models, Animal
Rats
description Renal 11 β-hydroxysteroid dehydrogenase 2 (HSD2) catalyzes the conversion of active glucocorticoids to inert 11 β-keto compounds, thereby preventing the illicit binding of these hormones to mineralocorticoid receptors (MRs) and, thus, conferring aldosterone specificity. Absence or inhibition of HSD2 activity, originates a hypertensive syndrome with sodium retention and increased potassium elimination. Recent studies from our laboratory reported an increment of HSD2 activity in intact-stressed rats. To evaluate the adrenal involvement in this increase, we analyzed HSD2 activity and protein abundance in Intact, Sham-operated, and adrenalectomized rats under stress situations (gavage with an overload of 200 mM HCl (10 ml) and simulated gavage) or with corticosterone replacement. HSD2 activity was assessed in renal microsomal preparations obtained from different groups of animals. HSD2 protein abundance was measured by Western-blot. Circulating corticosterone was determined by radioimmunoassay. Sham-operated animals showed an increase in HSD2 activity and abundance compared to Intact and adrenalectomized rats suggesting the involvement of stress-related adrenal factors in HSD2 regulation. In the case of acidotic adrenalectomized animals, there was an increase in renal HSD2 activity when, along with the HCl overload, the rats were injected with corticosterone. This increment occurred without an increase in enzyme abundance. These results suggest the importance of circulating levels of glucocorticoids to respond to a metabolic acidosis, through regulation of HSD2 stimulation. The group subjected to a simulated gavage showed an increase in enzyme activity and protein abundance, thus demonstrating the need for both adrenal and extra-factors in the modulation of renal HSD2. The adrenalectomized animals injected with different doses of corticosterone, produced a progressive increase in enzyme activity and abundance, being significant for the dose of 68 ng corticosterone/100 g body weight. The highest dose (308 ng/100 g body weight) did not show any variation in activity and abundance compared to the control group. This biphasic effect of glucocorticoids could be explained taking into account their permissive and suppressive actions, depending on their blood levels. Knowing that stress induces multifactorial responses, it should not be suprising to observe a differential regulation in renal HSD2, confirming that different Stressors act through different factors of both, adrenal and extra-adrenal origin. © 2004 Wiley-Liss, Inc.
author Zallocchi, Marisa Laura
Matkovic, Laura Beatriz
Calvo, Juan Carlos
author_facet Zallocchi, Marisa Laura
Matkovic, Laura Beatriz
Calvo, Juan Carlos
author_sort Zallocchi, Marisa Laura
title Adrenal gland involvement in the regulation of renal 11 β-hydroxysteroid dehydrogenase 2
title_short Adrenal gland involvement in the regulation of renal 11 β-hydroxysteroid dehydrogenase 2
title_full Adrenal gland involvement in the regulation of renal 11 β-hydroxysteroid dehydrogenase 2
title_fullStr Adrenal gland involvement in the regulation of renal 11 β-hydroxysteroid dehydrogenase 2
title_full_unstemmed Adrenal gland involvement in the regulation of renal 11 β-hydroxysteroid dehydrogenase 2
title_sort adrenal gland involvement in the regulation of renal 11 β-hydroxysteroid dehydrogenase 2
publishDate 2004
url https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_07302312_v92_n3_p591_Zallocchi
http://hdl.handle.net/20.500.12110/paper_07302312_v92_n3_p591_Zallocchi
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AT calvojuancarlos adrenalglandinvolvementintheregulationofrenal11bhydroxysteroiddehydrogenase2
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