Products

Lipotrophin-AM™ 

Lipotrophin AM®

Applied Nutriceuticals™ has developed a powerful new two-stage fat burning system designed to keep your body in fat-burning mode 24 hours a day. Most fat-burners give you that “crank and crash” effect; wiring you up for a few hours only to leave you feeling tired and fatigued later. When taken as recommended, Lipotrophin AM™ can reduce physical fatigue and restore mental alertness all day long while dramatically increasing fat metabolism – even during inactivity. For maximum results, take with Lipotrophin PM™ for non-stop fat metabolization.

Frequently Asked Questions

Lipotrophin AM®

Q: When is the best time to take Lipotrophin AM?

A: Take on an empty stomach first thing in the morning, and in the early afternoon.  It can be taken with food, but it will not be as effective

 

Q: How long before I will notice the energy boosting and weight control benefits of Lipotrophin-AM? 

A: From the first day your energy level will increase and you will notice a “warming” sensation about fifteen minutes after it is first ingested. This is a natural sensation experienced with most thermogenics. The fat-burning effects begin immediately, with visible reduction in weight and inches visible after the first week. The effects of Lipotrophin-AM can be increased when stacked with Lipotrophin-PM™ providing you with 24-hour fat burning effects. 

Q: What makes Lipotrophin-AM different from other fat burners? 

A: Lipotrophin-AM has been specially formulated to deliver full effective dosages of each compound delivering maximum results in shorter time. All of our ingredients are derived from natural extracts, standardized to consistent quality, purity and potency. We use no fillers so all you are getting is pure fat-melting performance. Our products work well for both males and females with a variety types of body types. When maintaining a proper diet and exercise program, Lipotrophin-AM will make weight management easy and fun as you watch those unwanted pounds melt away. 

Q: How long can I use this product? 

A: There have been no documented cases of our products having long term negative effects. All ingredients are found naturally are safe. However, it is always best to consult your physician when taking any medications long term.

Q: What is MXAC and how does it increase the fat burning process? 

A: has been shown to increase lipolysis leading to elevated glycerol and free fatty acid levels in the blood.    MXAC does this through a multifaceted system by increasing norepinephrine, inhibiting cAMP-phosphodiesterase release which allows cAMP to build up in cells.  Subsequent increase in cAMP by the cAMP-PDE enzyme leads to the activation of the Protein Kinase enzyme PKA, which in turn phosphorylates and activates Hormone-Sensitive Lipase (HSL).HSL liberates fatty acids from adipose (which is fat tissue) Fatty acid chains are hydrolyzed within the fat cell from triaglycerols, and the resulting diaglycerols are substrates (fuel) that are then broken down into acetyl-CoA, where they can be readily utilized by the Krebs cycle of aerobic metabolism and burned off as energy.  

Q: Does Lipotrophin-AM control appetite? 

A: EGCG (epigallocatechin gallate) and MXAC (methylxanthine anhydrous caffeine) are well known appetite suppressants because they elevate your CCK (cholecystokinin) levels. CCK is a peptide hormone that is vital in control of the appetite and the digestion of fat and protein, and triggers satiety signals in the brain. 

Q: How does Lipotrophin AM help control my cravings? 

A: The mucuna pruriens in Lipotrophin AM help curb cravings by stabilizing blood sugar and insulin levels. Mucuna pruriens has been documented to have potent neurotransmitter-boosting effects along with blood sugar controlling effects, both of which promote fat metabolization. Low neurotransmitter levels (mainly dopamine and serotonin) can result in cravings for sugars and sweets and in some cases even depression, which leads to “comfort eating”.  

Q: What is Bacopa Monnieri and what role does it play? 

A: Bacopa Monnieri is extremely important to the fat-burning process. It stimulates the continued synthesis of the thyroid hormone T4, providing a constant, readily available source of convertible material that later converts to T3.  This is extremely important in fat loss because T3 is biologically more active than T4, and radically increases your basal metabolic rate and increases body heat production (thermogenesis) which results in greater fat loss.

Condensed Write Up

Lipotrophin AM®

The Applied Nutriceuticals™ research team is proud to introduce Lipotrophin-AM™, THE most effective thermogenic available. Period.

 

This highly effective formulation was developed through our extensive research into nearly one-hundred different ingredients currently used in various weight-loss products on the market, along with an in-depth analysis of the potential benefits of several newly discovered compounds. Lipotrophin-AM is the result of that research.

 

Lipotrophin-AM contains metabolic activators that boost energy levels while reducing physical fatigue; improving general body coordination and mental focus. This unique formulation accelerates the process of lipolysis (fat-burning) by increasing cAMP, a biochemical messenger that signals cells to commence the fat-burning process. cAMP also drives protein kinase and hormone sensitive lipase (HSL) to become active, breaking down triglycerides in fat cells into fatty acids, which are then metabolized by mitochondria into fuel in a process call thermogenesis. Additionally, Lipotrophin-AM promotes the release of adenosine receptors in the brain, resulting in the increased levels of norepinephrine. Norepinephrine is extremely important as it signals receptors in the brain that trigger the release of metabolic energy from fat cells. In a nutshell, Lipotrophin-AM gets your body to turn fat into energy!

 

Lipotrophin-AM induces another dynamic and hugely beneficial biochemical mechanism.  L-Dopa is converted in the body into the hormone dopamine, which stimulates the pituitary’s secretion of growth hormone (GH). GH directly mobilizes fats from deposits and inhibits the formation of new fat cells by blocking their ability to divide. It also helps stabilize blood sugar levels and plays a primary role in triggering muscle hypertrophy through a variety of mechanisms; all of which contribute to synergistic effects of this amazing product.

 

Lipotrophin-AM attacks fat cells from yet another angle; by stimulating thyroid production of T4 and its subsequent conversion to T3 - two powerful hormones that play a direct role in increasing your metabolic rate. It also suppresses the production of the stress hormone cortisol, which promotes the deposit of fat in the midsection while having catabolic effects on lean muscle. On top of it all, by maintaining consistent blood sugar levels (especially in the evening) Lipotrophin-AM helps prevent those dreaded late-day hunger cravings that can ruin an entire day of otherwise healthy dieting.

 

Another benefit of Lipotrophin-AM™ is that it is an extremely effective appetite suppressant. It curbs hunger and cravings through increased CCK, a hormone that works with the central nervous system to signal satiety. It also allows less fat to be digested by slowing the release of pancreatic lipase, which is an enzyme that digests dietary fat that would otherwise be stored as adipose tissue (body fat). On the contrary, Lipotrophin-AM increases the use of fat for fuel over carbohydrates, so you burn more fat and store less, while feeling less hungry.

 

Lastly, Lipotrophin-AM is a powerful anti-catabolic; it helps you maintain and grow lean muscle that is often sacrificed when dieting due to elevated GH levels. Regular use of Lipotrophin-AM will shift your body’s energy source from using glycogen and protein to using fat for fuel instead. This helps preserve skeletal muscle, which would otherwise be relied upon more heavily for fuel without the use of Lipotrophin-AM. The result is a leaner, stronger, healthier you.

Technical Write Up

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. 

 

  1. 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.
  2. Weinberg BA, Belar BK (2001).  The World of Caffeine.  Routledge. ISBN 0-415-92722-6.
  3. Bolton PHd.  Sanford GN (1981).  Caffeine:  Psychological Effects, Use and Abuse.  Orthomolecular Psychiatry 10(3): 202-211.
  4. 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.  Biofactors 22(1-4): 135-140.
  5. 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 Nutri 81(1): 122-129.
  6. 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 Behav 65(2): 303-310.
  7. Fink A, Rex A, Voits M, Voight JP (1999). Major biological actions of CCK- a critical evaluation of research findings.  Exp Brain Res 123(1-2): 77-83.
  8. Chantre P, Lairon D (2002).  Phytomedicine.  Recent findings of green tea extract AR 25 (Exolise) and its activity for the treatment of obesity.  Phytomedicine 9(1): 3-8.
  9. 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.
  10. Kao YH,  Hilpakka RA, Liao S  (2000)  Modulation of endocrine systems and food intake by green tea  epigallocatechin gallate.  Endocrinology 141(3): 980-7.
  11. 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.
  12. 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.
  13. Jensen MD (2003) Effects of growth hormone administration on human obesity. Obes. Res. 11(2). 170-5.
  14. The thyroid gland. Endocrinology: An Integrated Approach by Stephen Nussey and Saffron Whitehead (2001).   Published by BIOS Scientific Publishers Inc.
  15. 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.
  16. 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.
  17. Parikh et al, (1990) Indian Drugs.  Chem Abs 27: 353.  \
  18. Ahmad S et al (1991) Conference of Pharmacology and Simposium on Herbal Drugs (New Delhi), March 1991, 15:26.
  19. Manyam BV (1995) J. Altern. Completment Med. Fall. 1(3) 244-255.
  20. Takahashi Y, Kipnis M, Daughaday WH (1968) Growth hormone secretion during sleep.  J Clin Invest 47(9): 2079-2090.
  21. 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.
  22. Rai D, Bhatia P, Palit G, Pal R, Singh S, Singh HK (2003) Adaptogenic effect of Bacopa Monnieri. Pharmacol Biochem. Behavior 75(4): 823-830.

Fat Burning Stack

The Lipotrophin-AM/Lipotrophin-PM Stack: 

 

Is your fat burner only working half the time? Destroy Fat 24 Hours a Day! 

 

The Lipotrophin-AM/Lipotrophin-PM stack will turn your body into a metabolic machine, allowing you maintain at the highest levels of lipolysis* possible, 24 hours a day, while actually helping you get a deeper, more restful sleep!!!  Forget about dangerous crash diets or other “fad” programs that promise results - they only work on TV! The powerful blend of herbal components in the Lipotrophin fat-melting matrix is specifically designed to mobilize fat as fuel, turning your body into fat-burning furnace - giving you more energy during the day while helping you sleep better at night! 

 

*Lipolysis (lĭ-pŏl'ĭ-sĭs, lī-) n., pl. -ses (-sēz'). The breakdown of fats into lipids (fatty acids) to where they can be easily metabolized as energy. 

 

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