Transactivation via the human glucocorticoid and mineralocorticoid receptor by therapeutically used steroids in CV-1 cells: a comparison of their glucocorticoid and …

…, AF Pfeiffer, S Diederich, V Bahr - European journal of …, 2004 - academic.oup.com
Background Glucocorticoids (GCs) are commonly used for long-term medication in
immunosuppressive and anti-inflammatory therapy. However, the data describing gluco- and …

Severe hyponatremia due to hypopituitarism with adrenal insufficiency: report on 28 cases

S Diederich, NF Franzen, V Bähr… - European Journal of …, 2003 - academic.oup.com
Objective Severe hyponatremia due to hypopituitarism and adrenal insufficiency can be life-threatening,
and treatment with glucocorticoids is very effective once the diagnosis of the …

Comparison of low and high dose corticotropin stimulation tests in patients with pituitary disease

J Mayenknecht, S Diederich, V Bähr… - The Journal of …, 1998 - academic.oup.com
Tetracosactin [corticotropin-(1–24)] is used for clinical testing of adrenocortical responsiveness.
The usual dose [high dose test (HDT)] is 250 μg. With this test, patients with mild …

11β-Hydroxysteroid dehydrogenase types 1 and 2: an important pharmacokinetic determinant for the activity of synthetic mineralo-and glucocorticoids

S Diederich, E Eigendorff, P Burkhardt… - The Journal of …, 2002 - academic.oup.com
The 11β-hydroxysteroid dehydrogenase (11β-HSD) system plays a pivotal role in glucocorticoid
(GC) and mineralocorticoid (MC) action. Although 11β-HSD activities are important …

Torsemide inhibits aldosterone secretion in vitro

TL Goodfriend, DL Ball, W Oelkers, V Bähr - Life sciences, 1998 - Elsevier
Torsemide inhibited aldosterone secretion by adrenal cells from rats, cows, and guinea pigs
stimulated in vitro by potassium, angiotensin, dibutyryl cyclic AMP, ACTH, or corticosterone. …

[HTML][HTML] The flavones apigenin and luteolin induce FOXO1 translocation but inhibit gluconeogenic and lipogenic gene expression in human cells

C Bumke-Vogt, MA Osterhoff, A Borchert… - PloS one, 2014 - journals.plos.org
The flavones apigenin (4′,5,7,-trihydroxyflavone) and luteolin (3′,4′,5,7,-tetrahydroxyflavone)
are plant secondary metabolites with antioxidant, antiinflammatory, and anticancer …

Novel inactivating mutations of the calcium-sensing receptor: the calcimimetic NPS R-568 improves signal transduction of mutant receptors

R Rus, C Haag, C Bumke-Vogt, V Bähr… - The Journal of …, 2008 - academic.oup.com
Context and Objective: Inactivating mutations in the calcium-sensing receptor (CaSR) gene
cause neonatal severe hyperparathyroidism and familial hypocalciuric hypercalcemia (FHH). …

Progesterone metabolism in the human kidney and inhibition of 11β-hydroxysteroid dehydrogenase type 2 by progesterone and its metabolites

M Quinkler, S Johanssen, C Großmann… - The Journal of …, 1999 - academic.oup.com
Progesterone binds with high affinity to the mineralocorticoid (MC) receptor, but confers only
very low agonistic MC activity. Therefore, progesterone is a potent MC antagonist in vitro. …

Effect of exogenous glucocorticoid on osmotically stimulated antidiuretic hormone secretion and on water reabsorption in man

V Bähr, N Franzen, W Oelkers… - European journal of …, 2006 - academic.oup.com
Objective Glucocorticoids exert tonic suppression of antidiuretic hormone (ADH) secretion.
Hypocortisolism in secondary adrenocortical insufficiency can result in a clinical picture …

Metabolism of synthetic corticosteroids by 11β-hydroxysteroid-dehydrogenases in man

S Diederich, B Hanke, P Burkhardt, M Müller… - Steroids, 1998 - Elsevier
The presence of an 11β-hydroxyl group is essential for the anti-inflammatory and
immunosuppressive effects of glucocorticoids. Interconversion of the 11β-hydroxyl into the …