Adrenal gland involvement in the regulation of renal 11 β-hydroxysteroid dehydrogenase 2
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...
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2004
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| LEADER | 17966caa a22015977a 4500 | ||
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| 001 | PAPER-4316 | ||
| 003 | AR-BaUEN | ||
| 005 | 20230518203351.0 | ||
| 008 | 190411s2004 xx ||||fo|||| 00| 0 eng|d | ||
| 024 | 7 | |2 scopus |a 2-s2.0-16544364369 | |
| 024 | 7 | |2 cas |a 11beta hydroxysteroid dehydrogenase, 9041-46-7; chloride, 16887-00-6; corticosterone, 50-22-6; 11-beta-Hydroxysteroid Dehydrogenase Type 2, EC 1.1.1.146; Corticosterone, 50-22-6 | |
| 040 | |a Scopus |b spa |c AR-BaUEN |d AR-BaUEN | ||
| 030 | |a JCEBD | ||
| 100 | 1 | |a Zallocchi, M.L. | |
| 245 | 1 | 0 | |a Adrenal gland involvement in the regulation of renal 11 β-hydroxysteroid dehydrogenase 2 |
| 260 | |c 2004 | ||
| 270 | 1 | 0 | |m Zallocchi, M.L.; Facultad de Ciencias Exactas y Naturales, Ciudad Universitaria-Núnez, (1428) Buenos Aires, Argentina; email: mzallo@qb.fcen.uba.ar |
| 506 | |2 openaire |e Política editorial | ||
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| 504 | |a Ye, S., Zhong, H., Yanamadala, V., Campese, V., Renal injury caused by intrarenal injection of phenol increases afferent and efferent renal sympathetic nerve activity (2002) Am J Hyper, 15, pp. 717-724 | ||
| 520 | 3 | |a 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. |l eng | |
| 593 | |a Department of Biological Chemistry, Facultad de Ciencias Exactas y Naturales, Universidad de Buenos Aires and PRHOM-CONICET, Buenos Aires, Argentina | ||
| 593 | |a Instituto de Biología y Medicina Experimental (CONICET), Buenos Aires, Argentina | ||
| 593 | |a Facultad de Ciencias Exactas y Naturales, Ciudad Universitaria-Núnez, (1428) Buenos Aires, Argentina | ||
| 690 | 1 | 0 | |a ACIDOSIS |
| 690 | 1 | 0 | |a CORTICOSTERONE |
| 690 | 1 | 0 | |a HSD2 |
| 690 | 1 | 0 | |a KIDNEY |
| 690 | 1 | 0 | |a STRESS |
| 690 | 1 | 0 | |a 11BETA HYDROXYSTEROID DEHYDROGENASE |
| 690 | 1 | 0 | |a CHLORIDE |
| 690 | 1 | 0 | |a CORTICOSTERONE |
| 690 | 1 | 0 | |a GLUCOCORTICOID |
| 690 | 1 | 0 | |a CORTICOSTERONE |
| 690 | 1 | 0 | |a ADRENAL GLAND |
| 690 | 1 | 0 | |a ADRENALECTOMY |
| 690 | 1 | 0 | |a ANIMAL EXPERIMENT |
| 690 | 1 | 0 | |a ANIMAL MODEL |
| 690 | 1 | 0 | |a ARTICLE |
| 690 | 1 | 0 | |a BODY WEIGHT |
| 690 | 1 | 0 | |a CONTROLLED STUDY |
| 690 | 1 | 0 | |a ENZYME ACTIVITY |
| 690 | 1 | 0 | |a ENZYME REGULATION |
| 690 | 1 | 0 | |a FEEDING |
| 690 | 1 | 0 | |a METABOLIC ACIDOSIS |
| 690 | 1 | 0 | |a NONHUMAN |
| 690 | 1 | 0 | |a PRIORITY JOURNAL |
| 690 | 1 | 0 | |a RADIOIMMUNOASSAY |
| 690 | 1 | 0 | |a RAT |
| 690 | 1 | 0 | |a STRESS |
| 690 | 1 | 0 | |a WESTERN BLOTTING |
| 690 | 1 | 0 | |a ADRENAL GLAND |
| 690 | 1 | 0 | |a ANIMAL |
| 690 | 1 | 0 | |a BLOOD |
| 690 | 1 | 0 | |a ENZYMOLOGY |
| 690 | 1 | 0 | |a GENE EXPRESSION REGULATION |
| 690 | 1 | 0 | |a KIDNEY |
| 690 | 1 | 0 | |a KINETICS |
| 690 | 1 | 0 | |a METABOLISM |
| 690 | 1 | 0 | |a PHYSIOLOGY |
| 690 | 1 | 0 | |a ANIMALIA |
| 690 | 1 | 0 | |a 11-BETA-HYDROXYSTEROID DEHYDROGENASE TYPE 2 |
| 690 | 1 | 0 | |a ADRENAL GLANDS |
| 690 | 1 | 0 | |a ADRENALECTOMY |
| 690 | 1 | 0 | |a ANIMALS |
| 690 | 1 | 0 | |a CORTICOSTERONE |
| 690 | 1 | 0 | |a GENE EXPRESSION REGULATION, ENZYMOLOGIC |
| 690 | 1 | 0 | |a KIDNEY |
| 690 | 1 | 0 | |a KINETICS |
| 690 | 1 | 0 | |a MODELS, ANIMAL |
| 690 | 1 | 0 | |a RATS |
| 700 | 1 | |a Matkovic, L. | |
| 700 | 1 | |a Calvo, J.C. | |
| 700 | 1 | |a Damasco, M.C. | |
| 773 | 0 | |d 2004 |g v. 92 |h pp. 591-602 |k n. 3 |p J. Cell. Biochem. |x 07302312 |t Journal of Cellular Biochemistry | |
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| 856 | 4 | 0 | |u https://hdl.handle.net/20.500.12110/paper_07302312_v92_n3_p591_Zallocchi |y Handle |
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