Medical Journals

Androgen Effects on Hippocampal Ca1 Spine Synapse Numbers Are Retained in Tfm Male Rats with Defective Androgen Receptors.

Authors:
  • MacLusky Neil J
  • Hajszan Tibor
  • Johansen Jamie A
  • Jordan Cynthia L
  • Leranth Csaba

From: Departments of Obstetrics, Gynecology and Reproductive Sciences, Yale University School of Medicine, New Haven, Connecticut 06520, USA. nmaclusk@uoguelph.ca

Endocrinology

  • Publish Date: May 2006
  • ISSN: 0013-7227
  • Volume: 147
  • Issue: 5
  • Pages: 2392-8
  • Medium: Print
  • Language: English
  • Citation (JAMA): MacLusky Neil J, Hajszan Tibor, Johansen Jamie A, et al. Androgen Effects on Hippocampal Ca1 Spine Synapse Numbers Are Retained in Tfm Male Rats with Defective Androgen Receptors.. Endocrinology May 2006;147:2392-8

Abstract

The effects of estradiol benzoate (EB), dihydrotestosterone (DHT), or the antiandrogen hydroxyflutamide on CA1 pyramidal cell dendritic spine synapses were investigated in adult male rats. To elucidate the contribution of the androgen receptor to the hormone-induced increase in hippocampal CA1 synapses, wild-type males were compared with males expressing the Tfm mutation, which results in synthesis of defective androgen receptors. Orchidectomized rats were treated with EB (10 microg/rat.d), DHT (500 mug/rat.d), hydroxyflutamide (5 mg/rat.d), or the sesame oil vehicle sc daily for 2 d and examined using quantitative electron microscopic stereological techniques, 48 h after the second injection. In wild-type males, DHT and hydroxyflutamide both induced increases in the number of spine synapses in the CA1 stratum radiatum, whereas EB had no effect. DHT almost doubled the number of synaptic contacts observed, whereas hydroxyflutamide increased synapse density by approximately 50%, compared with the vehicle-injected controls. Surprisingly, in Tfm males, the effects of EB, DHT, and hydroxyflutamide were all indistinguishable from those observed in wild-type animals. These observations demonstrate that Tfm male rats resemble normal males in having no detectable hippocampal synaptic response to a dose of EB that is highly effective in females. Despite the reduction in androgen sensitivity as a result of the Tfm mutation, hippocampal synaptic responses to both DHT and a mixed androgen agonist/antagonist (hydroxyflutamide) remain intact in Tfm males. These data are consistent with previous results suggesting that androgen effects on hippocampal spine synapses may involve novel androgen response mechanisms.

Mesh Headings (Keywords): Androgens, Animals, Dendrites, Dendritic Cells, Dihydrotestosterone, Estradiol, Flutamide, Genotype, Hippocampus, Male, Microscopy, Electron, Models, Statistical, Mutation, Neurons, Orchiectomy, Rats, Receptors, Androgen, Sesame Oil, Synapses, Time Factors


Check for Full Text / PubMed Unique Identifier (PMID): 16439462


This abstract is part of PubMed, a service of the U.S. National Library of Medicine. PubMed includes more than 17 million citations from MEDLINE and other life science journals for biomedical articles. See Copyright and Disclaimers.

Linked medical terms appearing on this page are added by Healia to help readers find more information and are not part of the original PubMed document.

The data herein was last updated on July 8th, 2008 and may not reflect the most current and accurate data available from NLM.


Advertisements

About | Privacy Policy | Business Solutions | Advertise | Contact | Add Healia to your site

©2012. Healia / Meredith Corporation  

Use of this site constitutes acceptance of our Terms of Service and Privacy Policy. All content on this Web site, including medical opinion and any other health-related information, is for informational purposes only and should not be used for a specific diagnosis or individual treatment plan for any situation. Use of this site and the information contained herein does not create a doctor-patient relationship. Always seek the direct advice of your doctor in connection with any questions or issues you may have regarding your own health or the health of others.