Estrogen and Male Development
Posted: Mon Dec 09, 2013 10:45 pm
While there is a great deal of information on the Eunuch Archive about the effects of testosterone on males and on estrogen for Male-to-Female transitioning, there is relatively little on the role of estrogen in normal male development. This is a very brief introduction to some of the issues that need to be considered.
A first point is that all normal males produce estrogen as well as testosterone. The enzyme aromatase turns testosterone into estradiol in some parts of the body where it is essential for normal functioning. Some of this happens before birth, some at puberty, and some is part of normal functioning through the lifespan.
A very few males are born with a genetic mutation to the gene that produces aromatase and their bodies, while having the full male component of testosterone, have no estrogen in circulation. These males provide a natural experiment.
There are real structural differences between a normal "male brain" and a "female brain" that can be discerned with functional magnetic resonance imaging (fMRI). The blood-brain barrier prevents estrogen crossing into the developing brain of a fetus. It does not, however, prevent testosterone from crossing the barrier. In a male fetus, testosterone in the brain is converted to estrogen by the aromatase enzyme and it is crucial in creating a "male brain." The "female brain" is formed in the absence of estrogen!
An aromatase-deficient male goes through normal male puberty with the expected growth of penis, testicles, prostate gland, etc. He produces viable sperm. However, in the absence of estrogen in the testicles, the sperm are of low quality and tend not to be very motile, leading to low fertility. His libido, however, will be that of a normal male.
One critical role of estrogen that was discovered through these aromatase=deficient males was that they did not go through the normal adolescent growth spurt. Their long bones, though, continue to grow throughout their lifespan. What are termed "eunuchoid" body characteristics in macroskeletal development are a result of lack of estrogen, not lack of testosterone. Estrogen treatment for aromatase-deficient males causes their long bones to stop growing.
Some of the important changes that come as a result of castration of the adult male are a result of loss of estrogen, not loss of testosterone. The most important ones are hot flashes, osteoporosis, and some changes in memory and cognitive processing (e.g., spatial memory, mental rotation). A small dose of estrogen, to replace that which the male would normally produce by conversion from testosterone, can reverse these effects.
Some other changes are from loss of testosterone, however, such as loss of body hair below the neck, loss of muscle strength and gynocomastia (breast growth). Most Male-to-Female individuals are chagrined to learn that even massive doses of estrogen do not do much to aid breast growth beyond what lack of testosterone does in adult males. (Estrogen does have a major effect on breast growth during female puberty, however, just not after the completion of puberty.)
There is speculation that some of the "loss of energy" in castrated males is a result of loss of estrogen, rather than loss of testosterone. This is true for castrated male rats, though there is not yet sufficient data on human beings.
A few selected references for anyone who wishes to pursue the subject:
Finklestein, J.S., H. Lee, S.M. Burnett-Bowie, J.C. Pallais, E.W. Yu, L.F. Borges, B.F. Jones, C.V. Barry, K.E. Wulczyn, B.J. Thomas, and B. Z. Leder. 2013. Gonadal steroids and body composition, strength, and sexual function in men. New England Journal of Medicine 368:1011-1022.
McCarthy, M. M. 2008. Estradiol and the developing brain. Physiological Reviews 88 (1):91-124.
Rochira, V., and C. Carani. 2009. Aromatase deficiency in men: a clinical perspective. Nature Review Endocrinology 5 (10):559-68.
Scott, E., Q. G. Zhang, R. Wang, R. Vadlamudi, and D. Brann. 2012. Estrogen neuroprotection and the critical period hypothesis. Frontiers in Neuroendocrinology 33 (1):85-104.
Wibowo, E., S. Deurveilher, R. J. Wassersug, and K. Semba. 2012. Estradiol treatment modulates spontaneous sleep and recovery after sleep deprivation in castrated male rats. Behavioural Brain Research 226 (2):456-64.
A first point is that all normal males produce estrogen as well as testosterone. The enzyme aromatase turns testosterone into estradiol in some parts of the body where it is essential for normal functioning. Some of this happens before birth, some at puberty, and some is part of normal functioning through the lifespan.
A very few males are born with a genetic mutation to the gene that produces aromatase and their bodies, while having the full male component of testosterone, have no estrogen in circulation. These males provide a natural experiment.
There are real structural differences between a normal "male brain" and a "female brain" that can be discerned with functional magnetic resonance imaging (fMRI). The blood-brain barrier prevents estrogen crossing into the developing brain of a fetus. It does not, however, prevent testosterone from crossing the barrier. In a male fetus, testosterone in the brain is converted to estrogen by the aromatase enzyme and it is crucial in creating a "male brain." The "female brain" is formed in the absence of estrogen!
An aromatase-deficient male goes through normal male puberty with the expected growth of penis, testicles, prostate gland, etc. He produces viable sperm. However, in the absence of estrogen in the testicles, the sperm are of low quality and tend not to be very motile, leading to low fertility. His libido, however, will be that of a normal male.
One critical role of estrogen that was discovered through these aromatase=deficient males was that they did not go through the normal adolescent growth spurt. Their long bones, though, continue to grow throughout their lifespan. What are termed "eunuchoid" body characteristics in macroskeletal development are a result of lack of estrogen, not lack of testosterone. Estrogen treatment for aromatase-deficient males causes their long bones to stop growing.
Some of the important changes that come as a result of castration of the adult male are a result of loss of estrogen, not loss of testosterone. The most important ones are hot flashes, osteoporosis, and some changes in memory and cognitive processing (e.g., spatial memory, mental rotation). A small dose of estrogen, to replace that which the male would normally produce by conversion from testosterone, can reverse these effects.
Some other changes are from loss of testosterone, however, such as loss of body hair below the neck, loss of muscle strength and gynocomastia (breast growth). Most Male-to-Female individuals are chagrined to learn that even massive doses of estrogen do not do much to aid breast growth beyond what lack of testosterone does in adult males. (Estrogen does have a major effect on breast growth during female puberty, however, just not after the completion of puberty.)
There is speculation that some of the "loss of energy" in castrated males is a result of loss of estrogen, rather than loss of testosterone. This is true for castrated male rats, though there is not yet sufficient data on human beings.
A few selected references for anyone who wishes to pursue the subject:
Finklestein, J.S., H. Lee, S.M. Burnett-Bowie, J.C. Pallais, E.W. Yu, L.F. Borges, B.F. Jones, C.V. Barry, K.E. Wulczyn, B.J. Thomas, and B. Z. Leder. 2013. Gonadal steroids and body composition, strength, and sexual function in men. New England Journal of Medicine 368:1011-1022.
McCarthy, M. M. 2008. Estradiol and the developing brain. Physiological Reviews 88 (1):91-124.
Rochira, V., and C. Carani. 2009. Aromatase deficiency in men: a clinical perspective. Nature Review Endocrinology 5 (10):559-68.
Scott, E., Q. G. Zhang, R. Wang, R. Vadlamudi, and D. Brann. 2012. Estrogen neuroprotection and the critical period hypothesis. Frontiers in Neuroendocrinology 33 (1):85-104.
Wibowo, E., S. Deurveilher, R. J. Wassersug, and K. Semba. 2012. Estradiol treatment modulates spontaneous sleep and recovery after sleep deprivation in castrated male rats. Behavioural Brain Research 226 (2):456-64.