Free Content Ziprasidone decreases cortisol excretion in healthy subjects

Authors: Meier, Andreas1; Neumann, Anna-Catharina1; Jordan, Wolfgang1; Huether, Gerald1; Rodenbeck, Andrea1; Rüther, Eckart1; Cohrs, Stefan

Source: British Journal of Clinical Pharmacology, Volume 60, Number 3, September 2005 , pp. 330-336(7)

Publisher: Blackwell Publishing

Key:
Free Content - Free Content
New Content - New Content
Subscribed Content - Subscribed Content
Free Trial Content - Free Trial Content

Abstract:

Aims

To determine the influence of the atypical antipsychotic ziprasidone on cortisol excretion. Methods

In a double-blind, placebo-controlled, randomized cross-over design 11 healthy male subjects were studied twice for 2 consecutive nights (N1, undisturbed sleep conditions; N2, exposure to acoustic stress) 5 days apart. Placebo or ziprasidone 40 mg was administered orally 2 h before bedtime on N1 and N2. Urine was collected during three fractionated collection periods (evening; night; morning) for the later determination of cortisol concentrations by standard radioimmunoassays. Results

Ziprasidone decreased the total amount of cortisol excreted by 4.9 (95% CI 3.3, 6.5) µg during N1 and by 10.8 (95% CI 5.7, 15.8) µg during N2 (P < 0.002). This effect was still detectable in the morning (P < 0.02), with decreases of 5.8 (95% CI -2.8, 14.4) µg after N1 and by 12.1 (95% CI 2.8, 21.4) µg after N2. The effect subsided in the evening. A significant intervention–condition interaction (P < 0.02), was found. The significant increase in cortisol excretion during acoustic stress observed with placebo was absent after treatment with ziprasidone. Conclusions

The significant decrease in nocturnal cortisol excretion following ziprasidone reflects a decreased activity of the HPA-axis in healthy subjects. This effect may be an important contributor to the mode of action of ziprasidone in different patient populations, particularly in the treatment of depression and in cognitive impairment in schizophrenia.

Keywords: antipsychotics; cortisol; HPA-axis; urinary excretion; ziprasidone

Document Type: Research article

DOI: 10.1111/j.1365-2125.2005.02431.x

Affiliations: 1: Department of Psychiatry and Psychotherapy, Georg-August-University of Göttingen, von-Siebold Strasse 5, D-37075 Göttingen, Germany

You have access to the full text article on a website external to Ingentaconnect.

Please click here to view this article on InterScience.

You may be required to register and activate access on InterScience before you can obtain the full text. If you have any queries please contact onlinehelp@oxon.blackwellpublishing.com

Back to top

Key:
Free Content - Free Content
New Content - New Content
Subscribed Content - Subscribed Content
Free Trial Content - Free Trial Content
Share this item with others: These icons link to social bookmarking sites where readers can share and discover new web pages.
Page Help Click here for Page Help
Shopping cart
Tools
Sign in






Need to register?
Sign up here
Text size: A | A | A | A