Yale Bulletin and Calendar

October 13, 2006|Volume 35, Number 6


BULLETIN HOME

VISITING ON CAMPUS

CALENDAR OF EVENTS

IN THE NEWS

BULLETIN BOARD

CLASSIFIED ADS


SEARCH ARCHIVES

DEADLINES

DOWNLOAD FORMS

BULLETIN STAFF


PUBLIC AFFAIRS HOME

NEWS RELEASES

E-MAIL US


YALE HOME PAGE


High testosterone kills nerve cells, says study

A School of Medicine study shows for the first time that ,a high level of testosterone, such as that caused by the use of steroids to increase muscle mass or for replacement therapy, can lead to a catastrophic loss of brain cells.

Taking large doses of androgens, or steroids, is known to cause hyperexcitability, a highly aggressive nature, and suicidal tendencies. These behavioral changes could be evidence of alterations in neuronal function caused by the steroids, says the senior author, Barbara Ehrlich, professor of pharmacology and physiology.

"Next time a muscle-bound guy in a sports car cuts you off on the highway, don't get mad, just take a deep breath and realize that it might not be his fault," says Ehrlich.

Testosterone is the main male hormone, and it plays fundamental roles in development, differentiation and cellular growth. In neurons, testosterone acts as a neurosteroid and can induce changes at the cellular level, which in turn lead to changes in behavior, mood and memory. Both neuroprotective and neurodegenerative effects of androgens have been reported.

The researchers showed that high levels of testosterone triggered programmed cell death in nerve cells in culture. Cell death, or apoptosis, is critical in many life processes, including development and disease. It is characterized by membrane instability, activation of caspases (the executioner proteins in apoptosis), change in membrane potential and DNA fragmentation.

"In the present study we have demonstrated for the first time that the treatment of neuroblastoma cells with elevated concentrations of testosterone for relatively short periods, 6 to 12 hours, induces a decrease in cell viability by activation of a cell death program," Ehrlich says. "Low concentrations of testosterone had no effects on cell viability, whereas at high concentrations the cell viability decreased with incremental increases in hormone concentration."

The testosterone-induced apoptosis described in this study occurs through overactivation of intracellular Ca2+ signaling pathways. Overstimulation of the apoptotic program in neurons has been associated with several neurological illnesses, such as Alzheimer disease and Huntington disease.

Co-authors include Manuel Estrada, now continuing his work at the University of Chile in Santiago, and Anurag Varshney, now working at Ranbaxy, a drug discovery company in New Delhi, India.

-- By Jacqueline Weaver


T H I SW E E K ' SS T O R I E S

Medical School receives $57.3 million NIH grant

Medical School receives $11.5 million to improve cancer diagnosis . . .

Museum technicians to show their own artworks at Open Studios

Student designs creative alternative to traditional construction fencing

MORE SCHOOL OF MEDICINE NEWS

Levin, Zedillo discuss the role of UNESCO at Paris event

'Women and Globalization' will be the topic of discussion . . .

Marketing executives and scholars to discuss latest trends

Australia's history and people are focus of film

Exhibit features paintings of England by Venetian artist 'Canaletto'

Lecture will examine the U.N. and 21st-century challenges

Lab talk

Play reading and talk will explore the romantic life of Benjamin Franklin

Tanner Lectures and related discussion to focus on humanities

'Crafting a Life' is the theme of this year's Law School reunions

Student research on early French songs culminates in . . .

Mutual interests

ALL gallery after-party celebrates artists in its newest exhibit and in CWOS

Campus Notes

Yale Books in Brief


Bulletin Home|Visiting on Campus|Calendar of Events|In the News

Bulletin Board|Classified Ads|Search Archives|Deadlines

Bulletin Staff|Public Affairs|News Releases| E-Mail Us|Yale Home