Evidence map›Paper›PMID 10822340›Full record

ArticleMolecular psychiatry2000

Effects of a novel corticotropin-releasing-hormone receptor type I antagonist on human adrenal function.

H S Willenberg, S R Bornstein, N Hiroi, G Päth, P E Goretzki, W A Scherbaum, G P Chrousos

Abstract read
PubMed Publisher
In one paragraph

Article in Molecular psychiatry, 2000. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 1 pooled it
1.9field-weighted citation impact, top 14% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

13 citing papers in PubMed, 1 synthesis or guideline pooled it, 56 citations in OpenAlex.

  1. Guideline
  2. Article
  3. Article
  4. Article
  5. Development of adrenal cortex zonation.Endocrinology and metabolism clinics of North America · 2015
    Review
  6. Article
  7. Article
  8. Effects of antalarmin, a CRF receptor 1 antagonist, on fright reaction and endocrine stress response in crucian carp (Carassius carassius).Journal of comparative physiology. A, Neuroethology, sensory, neural, and behavioral physiology · 2008
    Article
  9. Article
  10. Review
  11. Review
  12. Article
  13. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors at 2 institutions in 2 countries.

H S WillenbergDiabetes Research Institute at the University of Düsseldorf, Germany.
S R Bornstein
N Hiroi
G Päth
P E Goretzki
W A Scherbaum
G P Chrousos
Heinrich Heine University Düsseldorf · DEEunice Kennedy Shriver National Institute of Child Health and Human Development · US

Funding

Pathophysiology of The Hypothalamic-pituitary-adrenal & Gonadal AxesZIAHD000618 · NICHD · EUNICE KENNEDY SHRIVER NATIONAL INSTITUTE OF CHILD HEALTH & HUMAN DEVELOPMENT · PI KINO, TOMOSHIGE · 2009 to 2014
$2.0M
PHYSIOLOGY &PATHOPHYSIOLOGY OF THE HYPOTHALAMIC-PITUITARY-ADRENAL &GONADAL AXEZ01HD000618 · NICHD · EUNICE KENNEDY SHRIVER NATIONAL INSTITUTE OF CHILD HEALTH & HUMAN DEVELOPMENT · PI KINO, TOMOSHIGE · 1985 to 2008
$584k
6 · The paper itself

Abstract

Corticotropin-releasing hormone (CRH) is the principal regulator of the hypothalamic-pituitary-adrenal (HPA) axis and an activator of the sympathoadrenal (SA) and systemic sympathetic (SS) systems. Mental disorders, including major depression and, more recently, Alzheimer's disease have been associated with dysregulation of the HPA axis and the SA/SS systems. Treatment of rats or monkeys with the novel CRH receptor type 1 (CRH-R1) antagonist antalarmin inhibits the HPA and/or the SA/SS axes. This is the first study to examine the potential direct effect of antalarmin on human adrenal function. Adrenocortical and adrenomedullary cells were characterized by double-immunohistochemistry with anti-17 alpha hydroxylase (cortical cells) and anti-chromogranin A (chromaffin cells). Expression of CRH, ACTH, CRH type I and type II receptor mRNA were analyzed by reverse-transcription (RT) PCR. Human adrenal cortical and/or chromaffin cells in co-culture were incubated with CRH, antalarmin, and both CRH and antalarmin in vitro. Exposure of these cells to corticotropin or vehicle medium served as positive and negative controls, respectively. Cortical and chromaffin tissues were interwoven in the human adrenals, and both in situ and in the co-culture system the endocrine cell types were in close cellular contact. ACTH, CRH, and CRH-R1 and CRH-R2 mRNAs were expressed in the human adrenal as determined by RT-PCR. CRH (10-8 M) led to a moderate increase of cortisol release (145.7 +/- 20.0%) from cortical and chromaffin adrenal cells in co-culture. This effect corresponded to 41.8% of the maximal increase induced by ACTH (10-8 M). The action of CRH was completely inhibited by antalarmin. CRH, ACTH, and both CRH-R1 and CRH-R2 mRNAs are expressed in the adult human adrenal gland. CRH stimulates cortisol production in cortical and chromaffin cell co-cultures. This effect is blocked by antalarmin, a selective CRH-R1 receptor antagonist, suggesting that CRH-R1 receptors are involved in an intraadrenal CRH/ACTH control system in humans.

Indexed as

Adrenal CortexAdrenal MedullaAdrenocorticotropic HormoneAdultAnimalsCell LineCells, CulturedChromaffin CellsCoculture TechniquesCorticotropin-Releasing HormoneCRF Receptor, Type 1Gene Expression RegulationHaplorhiniHumansHydrocortisonePituitary GlandAdrenocorticotropic HormoneantalarminCorticotropin-Releasing HormoneCRF Receptor, Type 1CRF receptor type 2HydrocortisonePyrimidinesPyrrolesReceptors, Corticotropin-Releasing Hormone

Identifiers

PMID10822340
OpenAlexW2041636498

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.