Center for Women's Health - HOME


Center for Women's Health - JOURNAL WATCH Baylor College of Medicine

Return to Journal Watch Archives List

April, 1999 Review of Selected Scientific Publications

CONTENTS:


Grant News in Gender Differences:
"Gender Differences in Responses to Painful Stimuli."

Roger B. Fillingim. University of Alabama at Birmingham, Birmingham, Alabama.

DESCRIPTION: "Pain is characterized by complex physiological and perceptual responses, which appear to differ for females and males. For example, females show greater prevalence of many pain related disorders and enhanced perceptual responses to noxious stimuli compared to males, while males exhibit greater cardiovascular responses during painful tasks. However, the nature and clinical relevance of these gender differences in responses to painful stimuli remain unclear. The overall goal of these studies is to determine the nature of gender differences in physiological and perceptual responses to noxious stimuli, and to ascertain whether these responses are predictive of pain in the natural environment. In experiment 1, sensory (i.e., pain intensity) and affective (i.e., pain unpleasantness) responses to thermal, mechanical, pressure, ischemic, and cold pressor pain, as well as temporal summation of C fiber mediated pain in response to repetitive thermal stimuli will be compared in 75 females and 75 age matched males. In addition to these perceptual measures, physiological responses including salivary cortisol, cardiovascular and facial electromyographic response to thermal, ischemic, and cold pressor stimuli will be assessed. In Experiment 2, naturally occurring pain will be assessed over a 12 month period in subjects who complete Experiment 1, in order to determine whether laboratory pain responses predict the occurrence of pain in the natural environment. The results of this research will provide important information concerning the nature of gender differences in perceptual and physiological responses to painful stimuli. Additionally, the predictive validity of laboratory pain responses in females and males will be examined. The findings from these experiments in experimental and clinical pain responses, may ultimately lead to more effective diagnosis and treatment of gender related pain disorders." NIH GRANT NUMBER: 5R29DE12261-03. GRANT EXPIRES: June 13, 2001. PRINCIPLE INVESTIGATOR: Roger B. Fillingim. PERFORMING ORGANIZATION: University of Alabama at Birmingham, Birmingham, Alabama.

Women's Health Weekly: March 15, 1999 issue (excerpted with permission)


Protein in Tears, Urine of Pregnant Women Has Powerful Anti-HIV Effect

New York University School of Medicine and U.S. National Institutes of Health (NIH) researchers have identified an ordinary protein present in tears and saliva as the long-sought mystery substance in the urine of pregnant women that is a powerful anti-HIV agent.

The new finding helps explain why HIV cannot be transmitted through saliva, and opens the way to an entirely new class of anti-HIV medicines, according to a new study by the NYU and NIH scientists.

The researchers, led by Sylvia Lee-Huang, PhD, professor of Biochemistry at NYU, and Hao-Chia Chen, PhD, research chemist, National Institute of Child Health and Human Development, found that lysozyme, a well-known protein abundant in tears, is also present in the urine of pregnant women and is a potent anti-HIV agent. They also identified other potent anti-HIV agents in the urine, proteins called ribonucleases, enzymes that break apart the genetic material of RNA viruses, including HIV.

"These proteins are very promising anti-AIDS agents and likely will be well tolerated by the body, causing few side effects, because they occur naturally," said Lee-Huang. "We look forward to the next phase of our work, which will further determine how these proteins can best be used against HIV and other viruses."

Lysozyme, an enzyme first described in 1922 by Alexander Fleming, the discoverer of penicillin, breaks down the cell walls of bacteria, causing the cells to burst (or lyse) and die. The enzyme, which Fleming also discovered was abundant in tears, is produced in especially high levels during pregnancy and may play an important role protecting the body from foreign invaders like viruses and bacteria.

Although it isn't understood yet how the proteins actually inhibit HIV, Lee-Huang suspects that lysozyme and ribonuclease act together to inhibit HIV. In this scenario, the lysozyme may be acting to break down the outer membrane of the virus, potentially interfering with its ability to invade immune cells. The ribonucleases may target viral RNA, possibly affecting viral replication.

The new study, published in the March 16, 1999, issue of The Proceedings of the National Academy of Sciences, caps an intensive five-year search for the powerful anti-HIV and anti-cancer agent present in a most unusual source - the urine of pregnant women. Researchers had suspected that human chorionic gonadotropin (hCG), a pregnancy hormone produced by the placenta, was the agent because it inhibited HIV infected immune cells in the laboratory and in small clinical studies shrank Kaposi's sarcoma tumors in AIDS patients. Moreover, AIDS transmission rarely occurs during the first trimester of pregnancy when hCG levels are high. The main function of hCG is to stabilize pregnancy and protect the embryo from rejection by the mother's body.

However proof of hCG's effects wasn't straightforward. Although crude preparations of hCG inhibited the growth of Kaposi's sarcoma cells and HIV infected cells in the laboratory, Lee-Huang and many other scientists showed that highly purified extracts of hCG failed to have any affect on these cells. So it wasn't clear whether hCG itself or some other protein in the urine from which it was prepared was responsible. Lee-Huang's laboratory staff narrowed the search to a portion of the hormone called the beta subunit; but to her surprise, the culprits turned out to be other proteins also present in the urine and stick to the beta subunit.

In the new study, Lee-Huang and co-workers isolated the beta subunit from commercial preparations of hCG prepared from the urine of pregnant women. Then, using techniques such as electrophoresis, liquid chromatography, and amino acid sequencing, they painstakingly separated and purified the proteins present in the subunit and tested each against HIV infected cells, as well as analyzed their amino acid sequences. The entire process took about two years.

The amino acid sequences of the newly identified antiviral components associated with the beta core fragment of the beta subunit of hCG are identical to those of human lysozyme and ribonucleases. Why these compounds cling tightly to the pregnancy hormone is a fascinating question, said Lee-Huang. "Here again, it seems that Mother Nature knows best how to protect the earliest stages of human life," she said.

After the lysozyme and ribonuclease were identified, the researchers tested lysozymes found in mother's milk, white blood cells, and chicken egg white, as well as ribonuclease found in the pancreas of cows. All of these proteins inhibited HIV and were incredibly potent.

Women's Health Weekly: March 22, 1999 issue (excerpted with permission)


CWH Journal Watch: April 1999

Home
©1999 Baylor College of Medicine

E-Mail: cwh@bcm.tmc.edu
URL: http://www.bcm.tmc.edu/cwh/archive-0499.html (Modified: Apr-29-1999)