acth-(7-38) and 9-(tetrahydro-2-furyl)-adenine

acth-(7-38) has been researched along with 9-(tetrahydro-2-furyl)-adenine* in 2 studies

Other Studies

2 other study(ies) available for acth-(7-38) and 9-(tetrahydro-2-furyl)-adenine

ArticleYear
Orexin A stimulates cortisol secretion from human adrenocortical cells through activation of the adenylate cyclase-dependent signaling cascade.
    The Journal of clinical endocrinology and metabolism, 2001, Volume: 86, Issue:2

    Orexins A and B are two hypothalamic peptides that increase food intake and body weight and probably play a role in the sleep regulation. They act through two subtypes of G protein-coupled receptors, called OX1-R and OX2-R. OX1-R selectively binds orexin-A, whereas OX2-R is nonselective for both orexins. Orexins did not affect the in vitro secretion of either catecholamine or aldosterone from human adrenals. Conversely, orexin A, but not orexin B, concentration dependently increased basal cortisol secretion from dispersed adrenocortical cells; the maximal effective concentration was 10(-8) mol/L. Orexin A (10(-8) mol/L) enhanced the cortisol response to maximal effective concentrations (10(-9) mol/L) of angiotensin II and endothelin-1, but only to low concentrations of ACTH (10(-12)/10(-11) mol/L). Orexin A (10(-8) mol/L) increased basal cAMP release by dispersed adrenocortical cells, and the effect was blocked by the adenylate cyclase inhibitor SQ-22536. The cortisol response to 10(-8) mol/L orexin A was unaffected by the ACTH receptor antagonist corticotropin-inhibiting peptide, but was abolished by either SQ-22536 or the protein kinase A inhibitor H-89. RT-PCR demonstrated high levels of OX1-R messenger ribonucleic acid and very low levels of OX2-R messenger ribonucleic acid in human adrenal zona fasciculata-reticularis and adrenal medulla. Collectively, our findings suggest that orexins selectively stimulate glucocorticoid secretion from human adrenocortical cells, acting through OX1-R coupled with the adenylate cyclase-dependent signaling pathway.

    Topics: Adenine; Adenylyl Cyclases; Adrenal Cortex; Adrenocorticotropic Hormone; Adult; Carrier Proteins; Cells, Cultured; Cyclic AMP; Enzyme Activation; Enzyme Inhibitors; Hormone Antagonists; Humans; Hydrocortisone; Intracellular Signaling Peptides and Proteins; Middle Aged; Neuropeptides; Neurotransmitter Agents; Orexins; Peptide Fragments; Reverse Transcriptase Polymerase Chain Reaction; Signal Transduction

2001
PTH and PTH-related peptide enhance steroid secretion from human adrenocortical cells.
    American journal of physiology. Endocrinology and metabolism, 2001, Volume: 280, Issue:2

    Parathyroid hormone (PTH) and PTH-related peptide (PTH-RP) are two hypercalcemic hormones that share a common receptor subtype, the PTH/PTH-RP receptor. PTH and PTH-RP concentration dependently enhanced basal aldosterone and cortisol secretion from dispersed human adrenocortical cells, with a maximal effective concentration (approximately 2-fold increase) of 10(-8) M. The secretagogue effect of 10(-8) M PTH or PTH-RP was abolished by the PTH/PTH-RP receptor antagonist [Leu11,D-Trp12]-PTH-RP-(7-34)-amide (10(-6) M). PTH and PTH-RP (10(-8) M) raised cAMP and inositol-triphosphate release by dispersed adrenocortical cells, and these effects were blocked by the adenylate cyclase inhibitor SQ-22536 (10(-4) M) and the phospholipase C (PLC) inhibitor U-73122 (10(-5) M), respectively. SQ-22536 (10(-4) M) and U-73122 (10(-5) M) partially inhibited aldosterone and cortisol response to 10(-8) M PTH and PTH-RP; when added together, they abolished it. Similar results were obtained by using the protein kinase (PK)A and PKC inhibitors H-89 and calphostin C (10(-5) M). It is concluded that PTH and PTH-RP exert a sizeable secretagogue action on the human adrenal cortex, probably acting through the PTH/PTH-RP receptor coupled with both adenylate cyclase/PKA- and PLC/PKC-dependent signaling cascades.

    Topics: Adenine; Adrenal Cortex; Adrenocorticotropic Hormone; Aldosterone; Cyclic AMP; Enzyme Inhibitors; Estrenes; Humans; Hydrocortisone; Inositol 1,4,5-Trisphosphate; Parathyroid Hormone; Parathyroid Hormone-Related Protein; Peptide Fragments; Proteins; Pyrrolidinones

2001