September 5, 2012
Black Doctor.Org
Author: By Ellis Moore, BDO Staff Writer
A hormone-free drug tested in male mice might someday prove viable for men who want their own birth-control pill, according to new research.
The compound stifles sperm production but not s*xual activity, fertility returns once treatment stops and males can go on to father healthy offspring, the researchers say.
Strictly speaking, the new drug is not yet a male “pill,” explained lead researcher Dr. James Bradner, of the Dana-Farber Cancer Institute and Harvard Medical School in Boston.
“The molecule used in this study, JQ1, is a prototype drug,” Bradner said, explaining it is not intended for human use. “We have successfully administered the agent to animals by mouth, but notably in this research, JQ1 was injected into the belly of the mice and rats studied.”
JQ1 works by targeting a protein called BRDT that functions in the testes and is vital for fertility. Unlike previous drugs, JQI can physically reach the cells that make sperm. Sperm cell production drops in number and surviving sperm don’t work as well.
Researchers injected the rodents over an 18-month period and found they were mating as much as ever, but were completely infertile at higher does of JQ1. After treatment ended, they were again able to sire apparently healthy offspring.
“Mice can only report a few obvious symptoms,” Bradner said, “but with that caveat we do not observe any developmental or behavioral effects on offspring.”
The results have implications for men as well as mice.
“Humans do indeed have the BRDT gene, and human genetics suggests a similar role for BRDT in sperm production,” Bradner said. “We therefore tested activity against the human BRDT protein and found that JQ1 is a highly potent inhibitor of human BRDT.”
The study is published in the Aug. 17 issue of the journal Cell.
The researchers note that studies in animals often fail to provide similar results in humans, and this new form of birth control won’t be ready for humans in the near future.
“The development of a drug-like derivative of JQ1 will require at least a few years of dedicated chemistry and biology, though we may derive early insights from cancer clinical trials of structurally similar agents,” Bradner said.
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Wednesday, September 5th 2012 at 11:04AM
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