Green Tea
Tablets - Green Tea has been a popular supplement in China
& the Far East for thousands of years - its role as an
Anti-Oxidant has been demonstrated in many studies,
recently however it has been found that taken in larger doses
Green Tea has significant benefits as a FAT BURNING WEIGHT
LOSS supplement.
According to the Daily Mail 28/11/06 Researchers at Taipei
Hospital in Taiwan found that drinking Green Tea
Speeds up
Body Fat Burning
Suppresses Appetite
Lowers Cholesterol
Balances Hormones
Further studies on its Weight Loss
potential suggest that green tea extract boosts metabolism
and helps to burn stored body fat, In November, 1999,
the American Journal of Clinical Nutrition published the
results of a study at the University of Geneva in Switzerland.
Researchers found that men who were given a combination of
caffeine and green tea extract burned more calories than those
given only caffeine or a placebo. Burning more calories =
GREATER WEIGHT LOSS.
The benefits of taking Green
Tea therefore are HUGE - often though it is just not practical
to drink the volume of tea required to achieve the desired
health & weight loss benefits - this is why EXTRA
STRENGTH GREEN TEA (500mg per serving) Tablets have proven to
be so hugely successful - rather than drinking pints of Green
Tea each day simply take 2 tablets twice a day & get
HUGE Health & Weight Loss Benefits.
Or for even FASTER FAT Burning check out Lipotrophin
AM
Applied
Nutriceuticals has developed a powerful new fat burning compound
through extensive research and application of the most modern
scientific principles. Our research team invested the last year and
a half in product development and testing, filtering through the
countless ingredients available on the market in order to find the
most effective product possible. The team finally concluded that the
active ingredients in this formula, when specially titrated and
synergistically proportioned to optimized dosage levels, creates the
most effective fat metabolizer available today without a
prescription. The result is Lipotrophin AM™.
Lipotrophin-AM contains methylxanthine anhydrous
caffeine (MXAC), a xanthine alkaloid compound that acts as a
metabolic stimulant that has been used by humans since the Stone Age
(1,2,3). Additionally, it incorporates Green Tea, a compound used in
China for thousands of years to promote health in the mind and
body. Green Tea has strong anti-oxidant properties, and its main
ingredient, EGCG, has been shown to have significant metabolic
benefits (5). Lipotrophin AM also contains Bacopa Monnieri, an
Ayurvedic herb that boosts thyroid function and conversion, which is
a potent fat-burning stimulus and also been shown to reduce stress
levels (22). Mucuna Pruriens, the final ingredient in Lipotrophin-AM,
contains large amounts of L-Dopa, a potent compound that allows for
greater growth hormone release (13). The combination of the
ingredients in Lipotrophin-AM are specially titrated into a powerful
synergistic compound, designed to turn your body into a fat-burning
machine!
Energy Metabolism, Caffeine, and Green
Tea
Methylxanthine anhydrous caffeine (MXAC) is a
central nervous system and metabolic stimulant that temporarily
restores alertness and reduces physical fatigue. It also improves
general body coordination and exerts many beneficial effects on the
body, such as fat loss and.energy metabolism. Methylxanthine
anhydrous caffeine has been shown to increase lipolysis (fat
burning), by liberating glycerol and free fatty acids from
triglycerides (stored fat). This is important because when free
fatty acids and glycerol enter the blood stream they can be readily
disposed of as energy. MXAC accomplishes lipolysis through a
multifaceted system, starting with an increase in norepinephrine
(NE), a neurotransmitter responsible for alertness and also for fat
loss. Once NE is activated, it allows cAMP (cyclic AMP, an energy
molecule necessary for fat liberation) to build up in cells. NE
begins this process of cAMP build-up by combining with beta
receptors on a target cell to inhibit cAMP-phosphodiesterase (PDE),
a process that allows cAMP levels to increase drastically in
cells. Increased levels of cAMP within the cell ultimately result
in greater amounts of fatty acids being liberated from triglycerides
through the following mechanism: Increased cAMP levels cause the
protein kinase enzyme PKA to activate production Hormone-Sensitive
Lipase (HSL), a hormone responsible for fat loss. HSL then
triggers the release of fatty acids from triglycerides (fat
tissue). These resulting fatty acid chains are broken down within
the fat cell, which are subsequently broken down even further into
acetyl-CoA. Acetyl-CoA is an important energy substrate that is
in a form that can be readily utilized during the Krebs Cycle, which
is active during aerobic exercise. This is am primary mechanism of
how fat is disbursed as fuel for the body, but is just one of the
many ways that Lipotrophin-AM facilitates fat metabolization
(1,2,3). Green Tea is a versatile herb used for many centuries for
a variety of maladies. Recent studies have determined Green Tea to
be a strong fat burner that works through several different
complementary mechanisms. It is composed mainly of catechins,
pheophytins, chlorophylls, carotenoids, theanine, and a small amount
of caffeine (1,2,4,5). EGCG, a catechin found in high amounts in
Lipotrophin, is the most relevant compound, because in exerts a
variety of important metabolic, nutrient partitioning, and
appetite-controlling effects that contribute to significant weight
loss. Green tea is a potent appetite suppressant, as the EGCG
triggers the brain to secrete higher amounts of cholecystokinin (CCK),
a peptide hormone that is vital in control of the appetite and the
digestion of fat and protein (3,7). Green Tea also seems to have a
nutrient-repartitioning quality, which means it has the ability to
allow for the metabolism and utilization of macronutrients
(carbohydrates and bound triglycerides as fuel), while disallowing
others (like dietary fat) to be digested and stored. This
nutrient-repartitioning quality is extremely important during weight
and body fat loss, as EGCG allows the body to preferentially
utilize fat as fuel over carbohydrates. Clinical studies on
human subjects have confirmed this, showing that increases of
preferential fatty acid oxidation over glucose have been noted in
the majority of subjects while taking Green Tea. Another important
piece of this puzzle has to do with the fact that the EGCG in Green
Tea has been shown to inhibit the production of
catechol-0-methyl-transferase (COMT). COMT is important to fat
loss, because it is the enzyme that breaks down norepinephrine;
therefore limiting the production of COMT allows norepinephrine to
exert much stronger effects on the fat-burning cascade (4,6,7).
Mucuna Pruriens and Bacopa Monnieri
Another important mechanism of action in the
Lipotrophin-AM fat loss arsenal is the release of L-Dopa-induced
growth hormone (GH) and L-Dopa-related control of carbohydrate
cravings and blood sugar (8,10,11,12). The mucuna pruriens
contained in Lipotrophin-AM is of the highest quality, and is
standardized to 25% L-Dopa. There is plentiful documentation of L-Dopa’s
potent neurotransmitter-boosting effects, including its conversion
to dopamine and its blood sugar controlling effects, both of which
are very noteworthy for weight loss. Low neurotransmitter levels
(mainly dopamine and serotonin) can result in cravings for sugars
and sweets and depression, to which to most common response is
“comfort eating”. Obviously, uncontrolled cravings can wreck any
diet or weight loss plan. Mucuna helps stem this problem due to its
properties that attenuate blood sugar levels, which is important
because high blood sugar triggers higher insulin secretion and which
results in high insulin levels. The inclusion of mucuna pruriens
allows for a greater control of cravings and glucose utilization,
benefiting the user by allowing for greater weight loss.
While mucuna limits blood sugar and controls
cravings, it positively effects GH levels as well. As mentioned
earlier, Lipotrophin-AM contains large amounts of L-Dopa, and L-Dopa
is the only form of Dopamine that can cross the blood/brain
barrier. Once L-Dopa is converted to Dopamine in the brain, it
allows for a greater stimulation of GHRH (growth hormone releasing
hormone), which directly stimulates increased growth hormone
production. Acting directly, GH mobilizes fats from fat depots and
decreases the rate of glucose intake and metabolism, and higher
dopamine levels allow for control of cravings. Growth Hormone
mobilizes fats through the regulation of HSL (Hormone Sensitive
Lipase), which we have discussed earlier (8,13,14,15,16). This is
extremely important part of the fat loss equation, as the more HSL
released to liberate fatty acids that can be burned as fuel, the
more significant your fat loss will be.
Bacopa Monnieri is the final ingredient in
Lipotrophin. Studies have shown that Bacopa can increase T4 (thyroxine,
a thyroid hormone) synthesis by up to 41% in mice, while allowing
the uninterrupted conversion of T4 to T3. This is noteworthy,
because thyroid hormone is metabolically active, and is an important
component of fat loss. Conversion of T4 to T3 is an important
aspect of this process, and is affected by increased levels of GH,
which occurs during the usage of Lipotrophin-PM. T4 is
synthesized from free tyrosine, and combined with iodine, and upon
stimulation by TSH (Thyroid Stimulating Hormone), T3 and T4 are
formed ((18,25). Thyroid hormone produced is about 90% T4 and 10%
T3, and T3 is considered the biologically active component of
thyroid, as T4 must be converted down to T3 for it to be active in
target tissues (12). The production of thyroxine is regulated by
TSH, and TSH is suppressed when T4 levels are high. GH decreases T4
levels due to heightened conversion to T3, and when T4 levels become
too low, thyroid function becomes altered. The mechanism of action
of Bacopa is crucial to this process, as it stimulates the continued
synthesis of T4, providing a constant and readily available source
of convertible material that will ultimately become T3 (25). This
is extremely important to fat loss, because T3 is roughly ten times
more biologically active than T4, and T3 increases basal metabolic
rate and body heat production, resulting in greater fat loss.
In summary, our exhaustive research into fat
metabolization has produced the creation of an effective, powerful
new fat burning formulation that outperforms the big brands,
providing you with a wide range of benefits from reducing physical
fatigue and restoring mental alertness to dramatic increases in fat
metabolism, even while at rest, allowing your body to use fat as
fuel.
Nehlig A, Daval JL, Debry, G (1992). Caffeine and the CNS:
Mechanisms of Action, biochemical, metabolic, and psychostimulant
effects. Brain Res Rev 17(2): 139-170.
Weinberg BA, Belar BK (2001). The World of Caffeine.
Routledge. ISBN 0-415-92722-6.
Bolton PHd. Sanford GN (1981). Caffeine: Psychological
Effects, Use and Abuse. Orthomolecular Psychiatry10(3): 202-211.
Nagua T, Komine Y, Soga S, Meguro S, Hase T, Tanaka Y,
Tokimitsu I (2004). Anti-obesity actions of green tea: possible
involvements in modulation of the glucose uptake system and
suppression of the adipogenesis-related transcription factors.
Biofactors22(1-4): 135-140.
Carlson A (2005). Ingestion of a tea rich in catchechins leads
to a reduction in body fat and malondialhyde-modified LDL in
men. Am J Clin Nutri81(1): 122-129.
Greenough A, Cole G, Lewis J, Lockton A, Blundell J (1998).
Untangling the effects of hunger, anxiety, and nausea on energy
intake during IV cholecystokinin octapeptide (CCK-8) infusion.
Physiol Behav65(2): 303-310.
Fink A, Rex A, Voits M, Voight JP (1999). Major biological
actions of CCK- a critical evaluation of research findings.
Exp Brain Res123(1-2): 77-83.
Chantre P, Lairon D (2002). Phytomedicine. Recent findings
of green tea extract AR 25 (Exolise) and its activity for the
treatment of obesity. Phytomedicine9(1):
3-8.
Dulloo AG, Seydoux J Girardier L, Chantre P (2000). Green tea
and thermogenesis: Interactions between catechin-polyphenols,
caffeine, and sympathetic activity. Int J Obes Relat Metab
Dis 24 (2): 252-258.
Kao YH, Hilpakka RA, Liao S (2000) Modulation of endocrine
systems and food intake by green tea epigallocatechin gallate.
Endocrinology141(3): 980-7.
Richelsen B (1999) Effect of growth hormone on adipose tissue
and skeletal muscle lipoprotein lipase activity in humans. J
Endocronol Invest. 22(5):10-15.
Dimaraka EV, Jaffe CA, Bowers CY, Marbach P (2003) Pulsatile
and nocturnal growth hormone secretions in men do not require
periodic declines of somatostatin. Am J Phsiol Endocrinol
Metab. 285(1): 163-170.
Jensen MD (2003) Effects of growth hormone administration on
human obesity. Obes. Res.11(2). 170-5.
The thyroid gland. Endocrinology: An Integrated Approach
by Stephen Nussey and Saffron Whitehead (2001). Published by
BIOS Scientific Publishers Inc.
Eggo MC, Bachrach LK, Burrow GN. (1990) Interaction of TSH,
insulin and insulin-like growth factors with thyroid growth and
function.Growth Factors. 2(2-3).
99-109.
Rathi SS, Grover JK, Vats V. (1999) The effect of momordica
charantia and Mucuna pruriens in experimental diabetes and their
effect on key metabolic enzymes involved in carbohydrate
metabolism. Department of Pharmacology, All India Institute of
Medical Sciences, Ansari Nagar, New Delhi.
Parikh et al, (1990) Indian Drugs. Chem Abs
27: 353. \
Ahmad S et al (1991) Conference of Pharmacology and Simposium
on Herbal Drugs (New Delhi), March 1991, 15:26.
Manyam BV (1995) J. Altern. Completment Med. Fall.
1(3) 244-255.
Takahashi Y, Kipnis M, Daughaday WH (1968) Growth hormone
secretion during sleep. J Clin Invest47(9):
2079-2090.
Kar A, Panda S, Bharti S (2002) Relative efficacy of three
medicinal plant extracts in the alteration of thyroid hormone
concentrations in male mice. J Ethnopharmacol 81(2):
281-85.
Rai D, Bhatia P, Palit G, Pal R, Singh S, Singh HK (2003)
Adaptogenic effect of Bacopa Monnieri. Pharmacol Biochem.
Behavior75(4): 823-830.
The Fittest Bodies in the World use GREEN TEA
supplements.