Universal
Nutrition Zero G. It's the weightlessness only a select group of individuals who
travel to space experience. Imagine if you could feel
"weightless" right here at home. With new Zero G, you can. Zero
G is a proven fat burner that contains powerful ingredients like
Ginsenoside Rgb, 7-Keto and Cordia Salicifolia. This proprietary formula
will help you feel light and weightless by reducing body fat and overall
weight while helping to manage cholesterol and blood sugar levels. How?
Zero G uses a proprietary four-action system: (1) thermogenesis causes the
body to burn more calories than normal via heat production; (2) diuresis
sheds excess water weight for a smoother, more defined look; (3) appetite
suppression inhibits food cravings to stop weight gain before it begins;
and (4) thyroid support helps promote thyroid function for faster
metabolism. This unique four-action system in Zero G helps provide maximum results
in minimal time. Zero G also utilizes the new Wait-Less technology which
speeds up absorption for even quicker results and energy. Zero G becomes
activated right after your first dose, no waiting. How will you know it's
working? Because you'll experience a rise in body temperature and a slight
warming sensation within an hour of taking it. So what are you waiting
for? Experience what "weightlessness" is about today. Frequently
Asked Questions: Recommended
Use: Take 2 capsules before breakfast or morning exercise, and another 2
capsules during the afternoon. Do not exceed four capsules in any 24 hour
period. Please read label prior to use. Study Excerpts Sources: 1) Current
Therapeutic Research Vol. 61(7), and pp 435-442, Copyright 2000 by Excerpta
Medica, Inc. “Let me begin by saying THANK YOU. Now here is my story: I was
overweight and very depressed. I couldn’t bring myself to go out in
public unless it was late and there were no people around. I lost my job
as a computer technician because my state of depression made me very lazy
and I couldn’t get a woman to even look at me let alone date me. This
was no way to live and I knew I had to do something about it fast. One
night I was passing by a local vitamin shop on my way to the supermarket
and I decided to stop in, there I saw your Zero G™ fat loss product. I
am normally very skeptical of anything that’s a pill and promises to do
anything significant for me, but out of desperation I decided to try it.
To my amazement Zero G™ worked. It seemed like it was working with my
body to reduce my appetite and burn fat. I was eating less and feeling
more energized than ever before. I am no scientist and don’t take
supplements regularly, but somehow this thing works, that is all I know
and all I care to know. My increased energy and new leaner physique have
allowed me to turn my life around. I have found a new job and I can walk
out in public again. I have even started dating. There is no better gift
you can give a man than getting his self-respect back and you and your
product did that for me. Thanks again.”
How will Zero G™ help me lose weight?
Zero G™ uses a 4 action system to help you lose weight: Thermogenesis,
diuresis, appetite suppression and thyroid support. Thermogenesis causes
the body to burn more calories than normal via heat production. Diuresis
helps the body shed excess water weight for a smoother, more defined look.
Appetite suppression inhibits food cravings to stop weight gain before it
begins. Thyroid support helps promote thyroid function for faster
metabolism.
What is 7-Keto™, I have seen the name allot lately?
7-Keto™ is 3-acetyl-7-oxo-dehydroepiandrosterone (7-oxo-DHEA). It is a
natural metabolite of dehydroepiandrosterone (DHEA) and has been shown to
be very effective in enhancing weight loss.
What is Ginsenoside Rgb™?
Ginsenoside Rgb™ is an herb that has been shown to help promote lower
cholesterol levels and decreased weight by reducing appetite and
increasing activity levels.
How many capsules are in a serving of Zero G™ and what is the
recommended use?
Each serving of Zero G™ contains 2 capsules. We suggest you take two
servings daily, one serving before breakfast or morning exercise and the
second serving in the late afternoon.
Does Zero G™ contain any ephedra?
Zero G™ is an ephedra free fat burner, so you do not have to worry about
any side effects that ephedra use can tend to produce.
What is the Wait-Less technology in Zero G™?
Wait-Less™ technology speeds up the absorption and delivery of the Zero
G™ formula and produces noticeable physical effects within an hour of
consumption.
1) A study by Kalman noted a 1.8% reduction in body fat vs. 0.57% reduction in
the placebo group and a loss of 2.88kg of body weight vs. 0.97kg in the placebo
group using a twice daily serving of 100mg of 7-Keto™.
2) Another study registered remarkable effects on the thyroid. In this study
triiodothyronine (T3) activity increased significantly in the group receiving
7-Keto™ and not the placebo (+17.88 ng/dl vs. 2.75 ng/dl; p<0.05) T3 is
secreted by the thyroid and is used to regulate metabolism. When there is an
increase in the T3 released this will speed up the metabolism and allow the
person to drop weight faster.
3) Ginsenoside Rgb's™ main components have been studied by scientists at the
University of Chicago and the results were published in the June 2002 issue of
the world-renowned journal, Diabetes. Researchers noted that this ingredient
completely normalized blood glucose levels, improved sensitivity to insulin,
lowered cholesterol levels, and decreased weight by reducing appetite and
increasing activity levels in the test subjects.
4) An 8 week randomized, double blind placebo controlled study of guarana was
commenced with twenty-four subjects in each group completing the study. Active
treatment produced significantly (P<0.006) greater loss of weight (X+/-s.d.,-4.0+/-3.4
kg) and fat (-2.1+/-3.0% fat) over the 8-week treatment period than did placebo
(-0.8+/-2.4 kg and 0.2+/-2.3% fat). Active treatment also produced greater
reductions in hip circumference and serum triglyceride levels. Guarana
effectively promoted short-term weight and fat loss.
5) The effect of powdered green tea on the lipid metabolism was studied in male
subjects fed a 50% sucrose diet containing 15% butter. The oral treatment of 130
mg powdered green tea per day depressed body weight increase and various adipose
tissue weights but food intake was unaffected. The treatment also slightly
increased the plasma triglycerides. These effects were likely mediated by the
inhibition of lipogenesis in the adipose tissues. The experimental group had a
higher concentration of liver total lipid, triglycerides and plasma protein, and
lower liver weights than the controls. This may be due to lipid deposition in
the liver because of the reduction in adipose tissue weights. It was found that
powdered green tea lowered the plasma total cholesterol but liver total
cholesterol was unaffected.
6) Dandelions have long been used in herbal medicine for their choleretic,
diuretic, antiinflammatory, appetite-stimulating and laxative properties. An
antioxidant property can be supposed as a basis of their-therapeutic effects. To
understand the mechanism of the drug's action, the effects of natural extracts
on a microsomal fraction of rat liver were examined. The extracts diminished the
enzymatically induced-lipid peroxidation and reduced the cytochrome c with and
without NADPH in a concentration dependent manner.
7) The resin of the Commiphora mukul tree has been used in Ayurvedic medicine
for more than 2000 years to treat a variety of ailments. Studies in both animal
models and humans have shown that this resin, termed gum guggul, can decrease
elevated lipid levels. The stereoisomers E- and Z-guggulsterone have been
identified as the active agents in this resin. Recent studies have shown that
these compounds are antagonist ligands for the bile acid receptor FXR, which is
an important regulator of cholesterol homeostasis. It is likely that this effect
accounts for the hypolipidemic activity of these phytosteroids.
2) Journal of Exercise Physiology online, ISSN 1097-9751, Volume 2, Number 4,
October 1999.
3) Presented at Experimental Biology 98, April 19-22, 1998, San Francisco, CA.
4) Proc. Natl. Acad. Sci., Vol. 92, pp. 6617-6619, July 1995.
5) Archives of Biochemistry and Biophysics, Vol. 341, No. 1, May 1, pp. 122-128,
1997
6) Steroids 63:158-165, 1998
7) Presented at The 5th Conference on Retroviruses and Opportunistic Infections,
February 1-5, 1998, Chicago, IL.
8) Biochemical and Biophysical Research Communications 254, 124-126, 1999
9) Proc Natl Acad Sci, Vol 95, pp 11083-11088, Sept 98
10) http://www.rain-tree.com/chadebugre.htm
11) Biochemical and Biophysical Research Communications 254, 120-123, 1999
12) Diabetes 2002 June; 51(6):1851-8
13) Int J Obes Relat Metab Disord (England), Mar 2001, 25(3) p316-24
14) Phytother Res (England), May 2003, 17(5) p477-805
15) Phytother Res (England), Feb 2000, 14(1) p43-44
16) Annu Rev Nutr 2003 Feb 26; pS0199-9885
Eric M from Brooklyn