7-Keto-DHEA
Description:
7-Keto (3-Acetyl-7-Oxo-dehydroepiandrosterone) is a
naturally occurring metabolite of DHEA
(dehydroepiandrosterone). In the body, 7-Keto is not
converted into testosterone or estrogen to any
appreciable degree. 7-Keto, as a downstream metabolite
of DHEA, is produced in the body during the degradation
of DHEA. 7 Keto can be measured in the blood as a
ketosteroid.
Claims:
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Improves immune system function
-
Aids in weight reduction / Thermogenic
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Supports thyroid function
-
Non-androgenic or estrogenic
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Enhances memory
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Theory:
Because 7-Keto is a downstream metabolite of DHEA
it is promoted as being a
“non-androgenic” or
“estrogenic” version of DHEA. It is also
promoted as a weight loss aid for its supposed
thermogenic effect. Animal studies demonstrate that
it can enhance thermogenesis, which may translate
into weight loss. Because DHEA levels decline as we
age and ketosteroids are made from DHEA, all
conditions which may benefit from DHEA
supplementation, may also benefit from 7-Keto.
Scientific Support:
7-Keto supplements, at a dose of 200mg/day in
adults ~25 to 55 years of age has been shown in one
poorly designed trial to enhance weight loss, aid in
the reduction of body fat and effect thyroid hormone
levels. This two-month study also demonstrated that
7-Keto does not significantly effect blood sugar,
testosterone, estradiol, liver or kidney function,
but the “significant” weight loss
benefits were more do to an unbalanced study
designthan to any real benefit of the supplement
(the group receiving the supplement were
significantly heavier/fatter at the start of the
study compared to the control group). Another study
showed that 200mg/day of 7-Keto for 8 weeks does not
effect dihydrotestosterone (DHT), estradiol,
cortisol and insulin levels in men 18-49 years of
age. Several animal studies have demonstrated that
7-Keto, like other anabolic hormones, can induce
thermogenic enzymes. One trial with 7-Keto
demonstrated that it could bolster interleukin 2
production in lymphocytes, but this study was
conducted in cells (in vitro) and not in humans.
7-Keto has also been shown in mice to improve memory
(water maze procedure).
Safety:
7-Keto appears to be safe in doses of 200mg per
day. The two human trials to date have not shown any
androgenic or estrogenic effects of high dose
supplementation. Many of the claims for 7-Keto are
based on petri dish studies, animal research and
cell line studies, thus the data and findings cannot
be carried over to the human model.
Value:
The scientific evidence for using 7-Keto as either
an anabolic agent or for promoting weight loss is
quite weak and more research is needed to
substantiate if any of the popular claims made for
this supplement are indeed justified.
Dosage:
The few human trials have used a 200mg/day dose
– but commercial supplements typically provide
about 50mg/day.
References:
1. Bobyleva, Bellei, Kneer, and Lardy.The Effects
of the Ergosteroid
3-Acetyl-7-Oxo-Dehydroepiandrosterone on
mitochondrial membrane potential: possible
relationship to thermogenesis. Archives of
Biochemistry and Biophysics, Vol. 341, No. 1, May 1,
pp. 122-128, 1997
2. Colker, Torina, Swain, Kalman. Double-Blind,
Placebo-Controlled, Randomized Clinical Trial
Evaluating the Effects of Exercise Plus
3-Acetyl-7-oxo-dehydroepiandrosterone on Body
Composition and the Endocrine System in Overweight
Adults. Journal of Exercise Physiology online, ISSN
1097-9751, Volume 2, Number 4, October 1999.
3. Davidson, Weeks, Lardy, Maki, Umporowicz.
Clinical Safety and Endocrine Effects of
3-Acetyl-7-Oxo-Dehydroepiandrosterone. Presented at
Experimental Biology 98, April 19-22, 1998, San
Francisco, CA.
4. Lardy, Partridge, Kneer and Wei. Ergosteroids:
Induction of thermogenic enzymes in liver of rats
treated with steroids derived from DHEA. Proc. Natl.
Acad. Sci., Vol. 92, pp. 6617-6619, July
199-995.
5. Nelson, Herron, Weeks, and Lardy.
Dehydroepiandrosterone and
3-Acetyl-7-Oxo-Dehydroepiandrosterone Augment
Interleukin 2 (IL2) Production by Human Lymphocytes
In Vitro. Presented at The 5th Conference on
Retroviruses and Opportunistic Infections, February
1-5, 1998, Chicago, IL.
6. Shi and Lardy.
3-Acetyl-7-Oxo-Dehydroepiandrosterone Improves
Memory in Mice. Presented at Experimental Biology
98, April 19-22, 1998, San Francisco, CA.
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