Abstract:
The 11β-hydroxysteroid dehydrogenase type 2 (11βHSD-2) enzyme is thought to confer aldosterone specificity upon mineralocorticoid target tissues by protecting the mineralocorticoid receptor from binding by the more abundant glucocorticoids, corticosterone and cortisol. We have developed a Chinese hamster ovary cell line stably transfected with a plasmid containing the rat 11βHSD-2 complementary DNA. This cell line has expressed the enzyme consistently for many generations. The 11βHSD-2 was located primarily in the microsomes, but significant amounts also existed in the nuclei and mitochondria. The enzymatic reaction was unidirectional, oxidative, and inhibited by the product, 11-dehydrocorticosterone, with an IC50 of approximately 200 nM. The K(m) for corticosterone was 9.6 ± 3.1 nM, and that for NAD+ was approximately 8 μM. The enzyme did not convert dexamethasone to 11-dehydrodexamethasone. Tunicamycin, an N-glycosylation inhibitor, had no effect on enzyme activity, 11α-Hydroxyprogesterone (11αOH-P) was an order of magnitude more potent a competitive inhibitor of the 11βHSD-2 than was glycyrrhetinic acid (GA) (approximate IC50 0.9 vs. 15 nM). 11βOH-P, progesterone, and GA were almost equipotent (IC50 = 10 and 6 nM, respectively), and 5α-pregnandione and 5β-pregnandione were less potent (IC50 = 100 and 500 nM, respectively) inhibitors of the enzyme. When the inhibitory activities were examined with intact transfected cells, 11αOH-P was more potent than GA (IC50 = 5 and 150 nM, respectively). 11αOH-P was not metabolized by 11βHSD-2. We were unable to demonstrate the presence of 11αOH-P in human urine. In conclusion, a cell line stably transfected with the rat 11βHSD-2 was created, and the enzyme kinetics, including inhibition, were characterized. 11αOH-P was found to be a potent relatively specific inhibitor of the 11βHSD-2 enzyme. Its potential importance is that it is the most specific inhibitor of the 11βHSD-2 so far encountered and would aid in the study of the physiological importance of the isoenzyme.
Registro:
Documento: |
Artículo
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Título: | 11β-Hydroxysteroid dehydrogenase type 2 complementary deoxyribonucleic acid stably transfected into Chinese hamster ovary cells: Specific inhibition by 11α-hydroxyprogesterone |
Autor: | Morita, H.; Zhou, M.; Foecking, M.F.; Gomez-Sanchez, E.P.; Cozza, E.N.; Gomez-Sanchez, C.E. |
Filiación: | Div. Endocrinol., Diabet., Metab., Department of Internal Medicine, University of Missouri, Columbia, MO 65212, United States Harry S Truman Mem. Vet. Hospital, Columbia, MO 65201, United States Dept. of Vet. Biomedical Sciences, University of Missouri, Columbia, MO 65211, United States Fac. de Ciencias Exactas y Naturales, Universidad de Buenos Aires, Buenos Aires, Argentina Div. of Endocrinology and Metabolism, Harry S. Truman Mem. Vet. Hospital, University of Missouri, 800 Hospital Drive, Columbia, MO 65201, United States
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Palabras clave: | 11alpha hydroxyprogesterone; 11beta hydroxysteroid dehydrogenase; animal cell; article; Chinese hamster; competitive inhibition; enzyme activity; enzyme inhibition; enzyme kinetics; genetic complementation; genetic transfection; glycosylation; nonhuman; potassium excretion; priority journal; sodium retention |
Año: | 1996
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Volumen: | 137
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Número: | 6
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Página de inicio: | 2308
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Página de fin: | 2314
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DOI: |
http://dx.doi.org/10.1210/endo.137.6.8641180 |
Título revista: | Endocrinology
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Título revista abreviado: | ENDOCRINOLOGY
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ISSN: | 00137227
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CODEN: | ENDOA
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CAS: | 11alpha hydroxyprogesterone, 80-75-1; 11beta hydroxysteroid dehydrogenase, 9041-46-7
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PDF: | https://bibliotecadigital.exactas.uba.ar/download/paper/paper_00137227_v137_n6_p2308_Morita.pdf |
Registro: | https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_00137227_v137_n6_p2308_Morita |
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Citas:
---------- APA ----------
Morita, H., Zhou, M., Foecking, M.F., Gomez-Sanchez, E.P., Cozza, E.N. & Gomez-Sanchez, C.E.
(1996)
. 11β-Hydroxysteroid dehydrogenase type 2 complementary deoxyribonucleic acid stably transfected into Chinese hamster ovary cells: Specific inhibition by 11α-hydroxyprogesterone. Endocrinology, 137(6), 2308-2314.
http://dx.doi.org/10.1210/endo.137.6.8641180---------- CHICAGO ----------
Morita, H., Zhou, M., Foecking, M.F., Gomez-Sanchez, E.P., Cozza, E.N., Gomez-Sanchez, C.E.
"11β-Hydroxysteroid dehydrogenase type 2 complementary deoxyribonucleic acid stably transfected into Chinese hamster ovary cells: Specific inhibition by 11α-hydroxyprogesterone"
. Endocrinology 137, no. 6
(1996) : 2308-2314.
http://dx.doi.org/10.1210/endo.137.6.8641180---------- MLA ----------
Morita, H., Zhou, M., Foecking, M.F., Gomez-Sanchez, E.P., Cozza, E.N., Gomez-Sanchez, C.E.
"11β-Hydroxysteroid dehydrogenase type 2 complementary deoxyribonucleic acid stably transfected into Chinese hamster ovary cells: Specific inhibition by 11α-hydroxyprogesterone"
. Endocrinology, vol. 137, no. 6, 1996, pp. 2308-2314.
http://dx.doi.org/10.1210/endo.137.6.8641180---------- VANCOUVER ----------
Morita, H., Zhou, M., Foecking, M.F., Gomez-Sanchez, E.P., Cozza, E.N., Gomez-Sanchez, C.E. 11β-Hydroxysteroid dehydrogenase type 2 complementary deoxyribonucleic acid stably transfected into Chinese hamster ovary cells: Specific inhibition by 11α-hydroxyprogesterone. ENDOCRINOLOGY. 1996;137(6):2308-2314.
http://dx.doi.org/10.1210/endo.137.6.8641180