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Literature DB >> 5008732

The uptake of hydrocortisone in mouse brain and ependymoblastoma.

M L Schwartz, C H Tator, H J Hoffman.

Abstract

Entities: Chemical Disease Species

Mesh：

Substances：
Tritium
Hydrocortisone

Year: 1972 PMID： 5008732 DOI： 10.3171/jns.1972.36.2.0178

Source DB: PubMed Journal: J Neurosurg ISSN： 0022-3085 Impact factor: 5.115

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2 in total

1. Corticosteroid action on choroid plexus: reduction in Na+-K+-ATPase activity, choline transport capacity, and rate of CSF formation.

Authors: M Lindvall-Axelsson; P Hedner; C Owman
Journal: Exp Brain Res Date: 1989 Impact factor: 1.972

2. Acute Elevations in Cortisol Increase the In Vivo Binding of [¹¹C]NOP-1A to Nociceptin Receptors: A Novel Imaging Paradigm to Study the Interaction Between Stress- and Antistress-Regulating Neuropeptides.

Authors: Margaret Flanigan; Savannah Tollefson; Michael L Himes; Rehima Jordan; Katherine Roach; Clara Stoughton; Brian Lopresti; N Scott Mason; Roberto Ciccocioppo; Rajesh Narendran
Journal: Biol Psychiatry Date: 2019-09-25 Impact factor: 12.810

2 in total

The uptake of hydrocortisone in mouse brain and ependymoblastoma.

1. Corticosteroid action on choroid plexus: reduction in Na+-K+-ATPase activity, choline transport capacity, and rate of CSF formation.

2. Acute Elevations in Cortisol Increase the In Vivo Binding of [11C]NOP-1A to Nociceptin Receptors: A Novel Imaging Paradigm to Study the Interaction Between Stress- and Antistress-Regulating Neuropeptides.

2. Acute Elevations in Cortisol Increase the In Vivo Binding of [¹¹C]NOP-1A to Nociceptin Receptors: A Novel Imaging Paradigm to Study the Interaction Between Stress- and Antistress-Regulating Neuropeptides.