Dostinex is a comparatively new medication used in the
treatment of Parkinson's disease and prolactinomas (tumors
of the pituitary gland). Because another medication used
for the treatment of the same conditions, bromocriptine,
can have a marked sexuality-enhancing effect if properly
used, I assume that Dostinex will work in the same
direction.
Cabergoline is a medication based on ergot alkaloids.
Ergot, of course, is the fungal disease of rye and other
grasses, and a potent neurotoxin. Ergot alkaloids heavily
interfere with neurotransmitter activity. Probably the
best-know ergot derivate is LSD, which strongly messes with
the neurotransmitter serotonin.
There are a good number of ergot alkaloids that are used in
conventional medicine. Usually, these medications are
developed for their dopaminergic capabilities. Such
medications are needed to treat the severe deficiency of
the neurotransmitter dopamine that leads to Parkinson's.
The ergot alkaloid bromocriptine can be used for its
sexuality enhancing properties. Actuality, of all
substances I have tested on myself for their
sexuality-enhancing properties, bromocriptine is among the
few for which I can attest effectiveness. However,
bromocriptine has to be taken in a specific manner to avoid
the nausea that otherwise would overshadow its
sexuality-enhancing properties. The topic is covered
extensively in my articles How to use bromocriptine in the
treatment of sexual dysfunction or for sexual enhancement
and How does bromocriptine feel - personal experience with
its use .
It's the pharmaceutical similarity to bromocriptine, which
makes Dostinex such an interesting substance. Of all
dopaminergic medications used for the treatment of
Parkinson's, Dostinex resembles bromocriptine the most,
with its double action of enhancing dopamine levels and
inhibiting the secretion of the hormone prolactin from the
anterior pituitary gland.
I am convinced that this dual action is crucial to sexual
enhancement. Prolactin, the hormone, which has been named
for its function of inducing lactation in women, directly
interferes with sex drive in both women and men. It
controls to a certain extend the secretion of gonadotropin,
the hormone which, one step further down the chain,
controls the secretion of testosterone in both men and
women. Regardless of which hormonal constellation in this
sequence is responsible for a lowered sex drive, the
reversal of the sequence through drugs like bromocriptine
clearly supports sexual desire.
As sexuality is the main source of happiness for
practically all forms of higher living, including man, and
as utmost sexual satisfaction can only be experience as a
sequence to sexual desire, it is a logical quest to provide
ourselves with a better long-term hormonal profile than
intended for by our genetic blueprints. Anti-sexual changes
of our hormonal levels as a consequence of the aging
process is an unacceptable provision, which nature, our
enemy, has designed in order to install the specific
generation turnover rate of humans (20 to 30 years).
Increasing prolactin levels and, at the same time,
decreasing testosterone levels are two inter-linked causes
why aging men don't have as much sex drive as younger men,
why they don't have orgasms as powerful as they used to
have, and why they don't get as much pleasure out of their
sex lives as when they were in their 20's.
To interfere with this chain of events isn't easy.
Testosterone supplementation often doesn't do the trick.
Each person's body has its own genetically set ideas what
the person's age-appropriate testosterone levels ought to
be. Supplying additional testosterone will, in healthy
subjects, just provoke the body to down-regulate its own
testosterone production, as well as to initiate other
measures by which the testosterone balance returns to the
aforementioned genetically set levels.
Willfully oversupplying testosterone, or supplementing with
synthetic steroids is usually useless, at least for men.
Women, if they don't mind the androgenic side effects
(increased muscle buildup), may be able to increase desire
and orgasmic capacity through both testosterone and
synthetic steroid supplementation.
But for men, forcing testosterone levels beyond the genetic
set points, mainly through the supplementation with
synthetic steroids, has some very counterproductive side
effects. It will, for example, result in shrinkage of the
male organ, as well as in problems to achieve an erection.
The prolactin reduction pathway doesn't seem to be
bedeviled in the same manner. I can attest from own
experience that bromocriptine enhances sexual functionality
as well as the intensity of orgasm. (Please see my articles
on bromocriptine for the finer points on how to dose the
drug for sexual enhancement, and how to avoid the nausea.)
On the other hand, my own experimentation with the
supplementation of testosterone (Andriol capsules) had no
measurable effect on sexual desire at all, not immediate
and not long-term.
There is an enormous number of compounds, both herbal and
synthetic, which can kill sex drive and interfere with
sexual performance. There are also a good number of
products, both herbal and synthetic, which are sold with
the promise that they help to overcome a lack of sexual
desire or so-called erectile dysfunction.
I have been writing about pharmacological sexual
enhancement for years, and I take the matter seriously. I
have tried almost everything that is available under the
sun, whether from below (ginseng) or above (ginkgo) the
grass line, and both natural and synthetic (such as
Viagra).
While Viagra definitely works for erections, I feel that
Viagra alone does not provide any kick in the desire or
orgasm departments. A combination with other drugs,
however, can bring out the best in Viagra.