Case Study: He said 'Dr.Lin, So far your advise has helped me out. Many areas have had improvements. You were right about the seminal retention,' Why can semen or sperm retention cause pelvic pains, blue
balls, testicular pains, prostate pains, frequent urination, sleeping
disorders, short temper, anxiety, stress and premature ejaculation?
Reader: 6/27/2010>
Hey, Dr.Lin, So far your advise has helped me out. Many areas have had improvements. You were right about the seminal retention, because each week it would hit me on the 6th or 7th day. After which my frequency urinating would jump up. So, about two weeks ago I gave masturbation a temporary try to test and see if that would help relieve some tension in the pelvic region that had built up. It worked, as I slept great and frequency came down. I did the same this past friday with mixed results. I had high frequency and slight penile soreness. I think when I ejaculate I ejaculate too much at one time. How can I use self control to reduce the amount I ejaculae at a time? Would this help rid me of the bad sperm while retaining some in the tank for healing? I'm also going to exercise more on the 6th and 7th day as you were right about increasing exercise that helps out also. Thanks for your great advice.
Dr. Lin: 6/27/2010>
First, your have to do penile ballooning for 20-30 minutes to shift your
testicular function in the highest gear, so that you still have sufficient
testosterone and DHT to help you get recovery after ejaculating.
Secondarily, use anal breathing to reduce ejaculation when you are about to
common, so that we can retain about 50% of semen in your seminal vesicles to
help you get recovered faster.
Semen retention induced problems are not a result of bad sperms. The
problems can result from:
1. A lack of orgasm will accumulate excessive dopamine to trigger the release
and gene expression of dopamine betab-hydroxylase and phenylethanolamine-N-methyl
transferase gene for the homeostasis of the brain chemistry and you end up
excessive epinpehrine in the bloodstream to trigger the sympathetic eyes, lungs,
liver, kidney, heart, prostate and bladder fires and COX-2 over-expression for
the synthesis of inflammatory prostaglandin E-2 in the tissue. Excessive
prostaglandin E-2 and its 19-hydroxy-prostaglandin E-2 (due to the liver P450
enzyme 19-hydroxylase in semen) will also trigger
pelvic/prostate/testicles/seminal vesicles pains or inflammatory congestion. In
fact, prostaglandin E2 can overheat the brain and induce excessive
dopamine-norepinephrine conversion for sympathetic nervous fight or/and flight
responses. This will result in endless mutual enhancement between norepinephrine
and prostaglandin E2, until you get sufficient serotonin, GABA and melatonin
nervous action to cool down the central nervous system. Ejaculation or orgasm is
one of the method to solve the problems, but we can not fully empty your semen
and sperms in order to avoid andropause symptoms (male menopause) induced by
deficiency of androgen hormones, deficiency of testicular blood flow, deficiency
of the parasympathetic nervous nitric oxide release, excessive binding of
norepinephrine and epinephrine in the sympathetic nervous alpha adrenergic
receptors, and excessive prolactin, LH and FSH release.
One the other hands, the same conditions happen in the excessive orgasm or
over-ejaculation since the brain's nature response to orgasm or ejaculation is
the dopamine-norepinephrine-epinephrine conversion. You have to let the
epinephrine level in the bloodstream drops to a homeostasis level before you can
ejaculate again if you want to prevent the sympathetic eye, lung, liver, kidney,
heart, prostate and bladder fires and COX-2 over-expression.
The main differences between excessive orgasm/ejaculation and deficient orgasm:
A lack of orgasm trigger a natural homeostasis process for the
dopamine-epinephrine conversion while excessive orgasm/ejaculation forces the
dopamine-epinephrine conversion via the pituitary prolactin release. So, you
are in the non-winning condition unless you optimize your ejaculation frequency
or take proper nutrients.
2. If you don't ejaculate for a long time, the accumulative semen will
mechanically inflame the seminal vesicles and exert a pressure against your
prostate, bulbourethral glands and tailbone for pelvic pains, and the
accumulative sperms in the testicles will fill up your
seminiferous tubules,
rete
testis,
epididymis and
vas
deferens, leading to forced opening of the
blood-testis barrier to allow sperms and their
antigens to
seep through into the adjacent blood vessels where sperms and their antigen
trigger autoimmune inflammation and pains. Long-term sperm retention causes
blue balls, or disables the testicular sperm production mechanism and then slows
down the testicular testosterone and DHT synthesis. Vasectomy patients can
usually experience these problems as described in
http://action.love/extra/vascectomy.htm
3.
Accumulation of sperms inside the epididymis results in suppression of
testicular activin and inhibin release, and then in decreasing and deregulating
the pituitary FSH and LH release, leading to dropping the testicular
testosterone and DHT output. Releasing sperms will reactive the
pituitary-testicular axis for activin and FSH release which in turn uplift the
pituitary LH release for stimulation of the testicular function. On the other
hand, if you fully empty your epididymis by multiple ejaculation, you will get
too much activin and FSH release, resulting in post-ejaculation/post-orgasm
menopause hot flushing and testicular inflammatory pains induced by excessive
prolactin, norepinephrine and epinephrine release from your
hypothalamus-pituitary-adrenal axis and an abrupt drop of testosterone and DHT
in next days.
If you want a hard erection and balloon your penis, you will a high level of
testosterone and DHT to feed your erectile tissues and activate the nitric oxide
and prostaglandin E1 production.
By the way, the testis and epididymis are not the only sources of activin in the
male reproductive tract, associated with sperm and testosterone/DHT production,
and there are several reports of activin subunit mRNA and protein expression in
the prostate and seminal vesicles associated with semen production. This means
suppression of activin will result in seminal production disorders in the
prostate and seminal vesicles for watery ejaculation with a lack of semen. Ref:
http://ror.reproduction-online.org/cgi/reprint/5/2/99 ;
http://endo.endojournals.org/cgi/reprint/142/6/2178