•DHEA & Pregnenolone skin Gel
•Resveratrol & 7,8-Benzoflavone prevent estrogenic side effects
•Enhances athletic performance, recovery and strength
•Increases GH & IGF-1 to support muscle growth and fat reduction
•Pregnenolone provides hair-loss protection
The primary hormone in Dermacrine is DHEA (dehydroepiandrosterone) - the precursor to all anabolic/andrognic hormones in the body. Although DHEA has been available for years, and is found in many other hormonal supplements, Dermacrine offers a distinct advantage that makes it up to 20x more effective than regular pill or tablet based products. You see, with the rapidly absorbing Liqua-Vade technology, Dermacrine delivers DHEA to the blood stream within seconds. Within minutes, the body begins converting DHEA to other more anabolic hormones such as androstenediol, androstenedione and testosterone. This is where Dermacrine gets it's anabolic & androgenic horsepower - for increasing strength and lean muscle beyond your natural limit.
The DHEA is also converted to more powerful fat burning hormones such as 7-oxo-DHEA and 7-beta-DHEA. These are powerful thermogenic hormones that increase the rate of fat loss, helping you shed fat as you gain muscle.
The second hormone in Dermacrine is pregnenolone. This hormone was added in a precise ratio with the DHEA to balance and control conversion to DHT (dihydrotestosterone), which may cause hair loss in men prone to androgenic alopecia. Those sensitive to DHT who are concerned with hair-loss need not worry; Dermacrine won't cost you the hair-line! Pregnenolone is also a powerful neurosteroid, which can enhance cognitive focus and memory.
Since certain anabolic & androgenic hormones can convert to estrogen, Dermacrine was fortified with an anti-estrogen complex which consists of resveratrol, 7,8 benzoflavone. These are natural plant based compounds that block estrogenic effects such as gyno and fat storage. Resveratrol, 7,8 benzoflavone have also been proven to have potent fertility stimulating properties, which can help promote increased sexual desire, erectile function and stamina.
1. Administer lotion every morning, after a shower
2. 150-190 lbs : 3 pumps, 191-230 lbs : 4 pumps, 231+ lbs ; 5 pumps
3. Allow 4-5 minutes to dry
*Apply to shoulders and upper-back for best conversion
Only apply the product to clean, dry skin. Shaving off body hair is recommended, but not required. Also, avoid swimming, bathing or tanning for at least 6 hours after application.
Pumps per bottle: 130
7,8-Benzoflavone (99%) 36mg**
Resveratrol (99%) 36mg**
Other Ingredients: Water, ethyl alcohol (organic), dimethyl isosorbide, ethoxydiglycol, propylene glycol monolaurate, Dehydroepiandrosterone (DHEA), Trans-resveratrol (98%), 7,8,benzoflavone (98%), tiethanolamine, carbomer, pregnenelone, tetrahydropiperine..
* Certified Organic
† US Patent 6,849,645
Product may transfer to others by direct skin contact. Avoid direct skin contact with new born children. Product is not recommended for women, elderly, anyone under the age of 18 or anyone diagnosed with a serious health condition including but not limited to cancer, BPH, epilepsy, depression, diabetes, cardiovascular disease or high blood pressure. Always consult your physician before using this product with any over-the-counter or prescription medication.
Fast drying gel lotion, possessing fresh citrus scent.
Sustain Alpha can be a natural testosterone boosting cream that may stimulate your body's own production of testosterone. This can support vitality, libido, and erectile function. The formula dries within minutes, leaving the skin clean and moisturized. At five pumps Sustain Alpha will last 23 applications, at 6 pumps it will last 19 applications.
Sustain Alpha can be used safely, as a legal male or female enhancement formula. By increasing the "testosterone-production-signal" from the brain, Sustain Alpha may increase the production of testosterone from the testes, in males. More testosterone can lead to more strength, confidence and sexual prowess.
Consider Sustain Alpha a more natural alternative to Dermacrine. Sustain Alpha can also be used as or in conjunction with a post cycle therapy (PCT), for Dermacrine or products that may be suppressive to natural testosterone production.
Sustain Alpha may increase GrRH release, by preventing the negative feedback of hormones on the hypothalamus through GABAergic modulation and estrogen blockage.
In other words, Sustain Alpha can offset the suppression of hormones in the brain, allowing the body to produce more testosterone than it normally would, by potentially up-regulating GnRH and LH & FSH.
Sustain Alpha may push LH & FSH even higher by direct aromatic stimulation of the hypothalamic and pituitary cells. This should be accomplished with natural volatile oils that absorb and penetrate directly into the hypothalamic region upon inhalation.
* Remember, maintaining normal levels of estrogen is an important part of maintaining libido, muscle recovery, and testicular function. Therefore, it is undesirable to overly suppress estrogen levels. The natural anti-estrogens in Sustain Alpha may gently balance and control estrogen levels, without overly suppressing them.
What sort of results should I expect?
As testosterone climbs to its maximum potential, the following results may become noticeable -
More frequent & harder erections
Increased ejaculatory volume
Improved sense of well-being & social confidence
More prominent gains in the gym
What are the ingredients and how may they work?
The first ingredient in Sustain Alpha, that has recently become well known for its heart-health and life-extending benefits, is resveratrol. Aside from the noteworthy health benefits, resveratrol is an "estrogen blocker" because of its unique chemical structure which can bind to the estrogen receptor, thus blocking estrogenic activity. As discussed before, blocking estrogen can help increase LH & FSH levels.
The estrogen modulating effects of resveratrol have been proven to dramatically increase testosterone levels, fertility, and erection strength in several animal studies, without any side-effects. Other research with resveratrol has uncovered its supportive role in healthy blood vessel function - a great benefit for any male interested in improving his heart-health and erection fullness.
The second ingredient in Sustain Alpha is 7,8 Benzoflavone. This neuro-active flavone has the ability to pass the blood brain barrier and block the suppression GnRH release through modulation of the GABAergic receptor complex.
Research has shown 7,8 benzoflavone to have positive effects on libido due to its aphrodisiac and anxiolytic (anxiety-relieving) effects.
Ingredients: Ethyl Alcohol (Organic), Water (Aqua/Eau), Dimethyl Isosorbide, Ethoxydiglycol, Propylene Glycol Monolaurate, PEG-15 Cocoamine, Trans-Resveratrol (98%), 7,8-Benzoflavone (98%), 3-Aminopropanoic Acid, Carbomer, Triethanolamine, Tetrahydropiperine*, Salvia Sclarea (Clary Sage) Essential Oil. *US Patent 6,849,645
BPS' EndoSurge: Dramatically Increase Free Testosterone!
Free testosterone is the most important form of testosterone in the body. Free testosterone is the bioavailable and “useful” form that triggers all the benefits associated with High T – libido, strength, stamina, recovery and mood enhancement. The other, more prevalent form of testosterone in the body is Bound Testosterone, in which T is bound to SHBG (sex hormone binding globulin). When testosterone is bound to SHBG it cannot be used by the body like free testosterone – Bound Testosterone is essentially inactive. So even though your body may produce more testosterone on a particular supplement, it is useless unless FREE testosterone is increased and made available for use.
In short, Free T is the testosterone that has the most physiological effects.
When it comes to increasing free testosterone there is only one ingredient that has been used over and over successfully – nettle root extract. This ingredient has the ability to bind to SHBG itself causing less testosterone to bind. The result? More testosterone left as FREE unbound testosterone in the body.
Our stinging nettle root extract is a high yield for 3,4-divanillyltetrahydrofuran, the most active compound in nettle root.
Increase Total Testosterone
So now you know how important free testosterone is and you know that EndoSurge Turbo will be working to free up more of your total testosterone into free testosterone. But now let’s make it even better. By increasing total testosterone there is more testosterone available in the body to be freed up by the process above.
EndoSurge Turbo contains Mucuna Pruriens, a proven and well research ingredient extracted for natural L-Dopa. L-dopa has a number of powerful benefits, and the high purity, 98% extract used in EndoSurge Turbo provides a potent stimulus for these physiological effects. A primary mechanism of MP is to to increase the body’s level of LH (luteinizing hormone). This hormone signals the Leydig cells of the testes to produce more testosterone. More LH = more testosterone.
Additionally, EndoSurge Turbo now includes Maca extract. Maca has been shown in multiple clinical trials to increase libido, sperm count, sexual and social performance and may increase testosterone production as well. EndoSurge Turbo contains a whopping 750mg a day dose of 20:1 Maca; a powerful dose for even more powerful effects.
Finally, Vitamin D3, as Cholecalciferol, has been included to ensure healthy hormone and mineral levels. Vitamin D deficiency is rampant in modern Western society, and results in loss of bone density, serum electrolytes and mineral concentrations, and can even result in the impairment of endocrine (including testosterone) signaling. By including 400iu Vitamin D3 in each dose of EndoSurge Turbo, BPS ensures your body is primed and ready to upregulate Testosterone – to maximize EndoSurge Turbo’s other effects. This can even be further enhanced with proper supplementation of said electrolytes, including Zinc, Magnesium, Cobalt and Selenium.
L-dopa, the key extract in Mucuna Pruriens, has been shown to increase HGH levels. We all know the importance of HGH not only in bodybuilding but for many anti-aging benefits. EndoSurge Turbo’s high yield extract potently elicits increases in HGH.
No man likes prolactin. Prolactin is the libido killer. After an orgasm prolactin levels sky-rocket, immediately killing libido. Having high circulating prolactin levels throughout the day will decrease your libido as well. On top of that, popular supplement ingredients like DAA have been shown to increase prolactin production.
If you like having a libido, prolactin needs to be down! Lucky, for you through the combination of MP extracts in EndoSurge Turbo, your prolactin will stay DOWN and your libido UP.
EndoSurge Turbo was designed with the intention of drastically increasing ones libido. Through the combined pathways of increasing both free and total testosterone on top of decreasing prolactin, EndoSurge Turbo is a force to be reckoned with!
No Propriety Blend
Don’t bother with being unsure if you are getting enough of the essential ingredients in a formula. Taking a fraction of the amount of these ingredients is not going to give true results. You need the full and optimal dose. EndoSurge Turbo does not hide itself.
25 day Supply
You got it – 2 capsules 3 times per day, delivers the maximum and full dose of the powerful ingredients of this formula.
The supplement industry is full of testosterone boosters. Some contain magical ingredients and some contain huge blends of ingredients at undetermined amounts.
At BPS we aren’t trying to reinvent the wheel. We are just here to put the parts together right.
Combustion is a new and exciting fat burning/fat prevention formula from BPS. It works to increase lipolysis and adrenergic stimulation, all while working to prevent redeposition of fat (fat gain) in the body.
Combustion will decrease appetite, improve mood, burn fat, and allow for rapid body recomposition.
Sourced from a specific mulberry tree native to China, Morus Alba is an exciting ingredient backed by quite a bit of research elucidating several potential benefits.
We'll start with direct implications on fat loss. MA has been shown to lower blood glucose, while reducing oxidative stress in the liver (1). Decreasing glucose encourages the body to be in a better metabolic position to access stored fat as a fuel source. It has since been shown in multiple studies to have a direct effect on fat loss by upregulating beta oxidation, by increasing expression of PPARa and COMT1, while simultaneously decreasing expression of Fatty Acid Synthase (FAS) (2–5). In simple terms, this means an increase in fat burning with a concurrent decrease in fat storage.
Recently, researchers discovered that MA had the ability of preventing pre-adipocytes from becoming mature fat cells (6). Intrigued by these results, those same researchers performed a follow up study to see how that actually played out as far as fat loss. What they found, was that when two groups were overfed, the group treated with MA gained 27% less weight, 15% less visceral (deep) fat, and the existing visceral fat cells reduced in size by almost 50% (7). It also appears that MA helps regulate adipokine functioning, preventing dysregulation that can potentially lead to increased fat gain due to excessive signaling of the fat storage cytokines, so basically "cleaning house" in the fat cells (8).
In addition to the fat loss benefits, MA has quite a bit of supportive data backing it as an effective regulator of blood lipids. It has been shown to be anti-hyperlipidemic, enhance the function of the LDL receptors (decreased function tends to upregulate LDL cholesterol production), increase the blood clearance of LDL cholesterol, and decrease actual production of LDL (9). Far more important than lowering LDL-C (which is nice, but doesn't necessarily reduce risk for heart disease), MA has been shown to lower LDL oxidation and foam cell formation (10). Foam cells are the immune derived cells that come in help and "patch things up" and swallow up oxidized LDL cholesterol at the damaged sites of fatty buildup in the arterial wall. Foam cells are more of a marker for arterial damage than they are the cause of damage, but they also can be dangerous themselves when they accumulate at one site. Another similar study noted that MA was able to significantly reduce susceptibility to LDL oxidation as well as decrease atherosclerotic lesion area (think of a wound in the arterial wall), by over 50% (11).
Alstonia scholaris is a specific tree from the Apocynaceae family, native to Southern parts of Asia. Several studies have demonstrated potential mechanisms of AS to aid in fat loss, as well as improve general health, and even boost performance.
AS has been identified as a b2 adrenergic receptor agonist, acting on the same fat cell receptor as clenbuterol to aid in fat loss (12). This also gives it bronchodilatory, anti-asthmatic and anti-tussive properties (13). Multiple other studies have confirmed this b2-AR mediated effect while also favorably modulating nitric oxide an prostaglandins, making it a solid choice for potential fat loss and performance enhancement (14,15).
A recent study found that AS acted as an adaptogen, aiding in the body's return to equilibrium from stress by regulating various catecholamines and neurotransmitters. The researchers even referred to it as having nootropic properties due to its ability to improve memory during stress. It also demonstrated free radical savaging abilities and helped to normalize stress induced cholesterol elevations (16).
In addition to confirming its antioxidant status, a 2012 review supported the use of AS for blood sugar/insulin reduction as an anti-diabetic agent, which has been used for this purpose in traditional medicine in certain communities for decades (14). Again, better blood sugar management sets the stage for better access to stored body fat. Aside from the b2-agonism, free radical scavenging, lipid regulation, cognitive enhancement and blood sugar management, a recent review of Alstonia also noted anti-anxiety, anti-inflammatory, hepatoprotective, anti-diabetic and analgesic properties (17). It would appear that Alstonia has quite a bit up its sleeve.
Also known as norcoclaurine, Higenamine is a major active component from aconite root, but can be found in at least seven different plants. Initial research on Higenamine was promising as it appeared to have similar effects to everybody's favorite fat burner ephedrine, but not until recently (literally just a few months ago as of the time of this publication) did we have legitimate human data. Previous data earned it a classification as a beta2-AR agonist (like the asthma drug and popular fat burner clenbuterol), which awarded it some attention from physique athletes in the past few years (18). Now we have some interesting real world data showing that a higenamine based combination product increased blood free fatty acids (FFA's) as well as energy expenditure after an overnight fast, versus the placebo group (19). It is important to remember that increasing blood FFA's is only the first step in fat burning (lipolysis), but the study did also note an actual increase in calories burned. Also recognize that this study was done with a combination product where the other ingredients (caffeine and yohimbine) more than likely contributed to the effect. However, caffeine is included in Combustion and we feel the other ingredients in our formula can more than match the effect of yohimbine without the possible undesirable elevation in heart rate and blood pressure common to many users.
It's no secret that forskolin has been widely recognized in the research as an effective lipolytic for over 30 years. Although we will not be taking an exhaustive appraisal of the research, as far back as 1987, we have data showing forskolin to be effective at reducing subcutaneous fat when applied transdermally (20). One of the main mechanisms of action is through activating adenylate cyclase which upregulates cyclic AMP production in fat cells, although other mechanisms are thought to exist (21,22).
So what does that actually mean for fat loss? One unpublished study out of Japan in 2001 showed a modest decrease in body fat in the subjects taking a forskolin product, which, while interesting, probably didn't serve much purpose other than to spawn further research due to several uncontrolled variables. Another study in 2005 showed that 12 weeksk of forskolin supplementation favorably altered body composition while boosting free testosterone and bone density in males (23). And a brand new (Feb. 2014) study attempted to fatten up rats and track the effects of various compounds on weight gain. The researchers found that forskolin was indeed able to prevent weight gain compared to controls (24).
While the research on b-PEA has traditionally focused on neurochemistry, it does possess some potentially potent benefits as a fat loss aid while concurrently improving mood. Through elevation of catecholamines like epinephrine and norepinephrine, b-PEA can contribute to activating beta adrenergic receptors in fat cells to kick start lipolysis while increasing expression of HSL (25). b-PEA anecdotally tends to act as an appetite suppressant in most users, making it easier to stick to a hypocaloric eating plan, which has been verified in rats (26). It is also widely recognized to improve mood even at low doses, however the effect is short lived without the presence of a MAO-b inhibitor. Combustion does include piperine, a nonselective MAOI, which while not nearly as potent as a prescription selective MAO-b inhibitor, will help to keep the mood enhancing effect of b-PEA active longer, coupled with the recommended protocol of taking three doses per day (27).
Caffeine is one of the most thoroughly researched compounds available for fat loss and performance enhancement. Here's some bullet points to summarize the immense data:
· Increased cellular oxygen uptake during exercise.
· Allows ability to perform more exercise with no increased sensation of effort
· Moderate doses improve performance just as much as high doses
· Blunts perceived exertion and pain perception, provides a more positive subjective experience while training .
· Shown to be ergogenic in intense exercise ranging from 4-180 seconds, and improves performance in single and multiple sprint intervals .
· Redosing caffeine six hours later not necessary to maintain increased performance in two-a-day workouts .
· Significantly improves time to exhaustion during exercise, even when taken four hours prior to workout .
· Increased thermogenesis
· Retention of muscle while hypocaloric
· Increased fat oxidation
You'll see piperine included in many ergogenic supplements these days, mainly to enhance the absorption and concentration in the bloodstream of other nutrients, which it does a great job of assuming the nutrient in question is broken down by a particular class of liver enzymes .
We've included piperine for this purpose, but also it's potential effects to increase fat loss and blood lipids on its own, according to recent research. While most of the current research has been using animal studies, the results are compelling.
In two recent studies, when attempting to fatten up mice, researchers found that piperine was able to improve insulin sensitivity and favorably modulate AMPK and adiponectin (37,38). Another very recent study overfed rats a bunch of carbs and fat for 16 weeks, and found that piperine was able to prevent damage over the control group to just about everything you can imagine; blood pressure, inflammation, oxidative stress, liver enzymes, and heart function (39). Multiple other studies have shown improvements in general health parameters like oxidative stress and dyslipidemia during overfeeding when compared to non-piperine controls (40,41). Another study using carbohydrate and fat overfeeding showed that piperine was able to significantly decrease body weight and visceral fat compared to controls (42).
As well, Piperine has been included in the formula for its Monoamine-Oxidase inhibitory properties. Monoamine Oxidade (also known as MAO) is an enzyme responsible for the rapid breakdown of biactive amines (dopamine, etc) and Catecholamines. It is also the enzyme responsible for the breakdown of b-PEA. Inhibition of this enzyme allows for the b-PEA to remain active for longer periods of time.
1. Katsube T, Yamasaki M, Shiwaku K, Ishijima T, Matsumoto I, Abe K, et al. Effect of flavonol glycoside in mulberry (Morus alba L.) leaf on glucose metabolism and oxidative stress in liver in diet-induced obese mice. J Sci Food Agric [Internet]. 2010 Nov [cited 2014 Mar 13];90(14):2386–92. Available from: http://www.ncbi.nlm.nih.gov/pubmed/20648552
2. Kobayashi Y, Miyazawa M, Kamei A, Abe K, Kojima T. Ameliorative effects of mulberry (Morus alba L.) leaves on hyperlipidemia in rats fed a high-fat diet: induction of fatty acid oxidation, inhibition of lipogenesis, and suppression of oxidative stress. Biosci Biotechnol Biochem [Internet]. 2010 Jan [cited 2014 Mar 13];74(12):2385–95. Available from: http://www.ncbi.nlm.nih.gov/pubmed/21150120
3. Lee J, Chae K, Ha J, Park B-Y, Lee HS, Jeong S, et al. Regulation of obesity and lipid disorders by herbal extracts from Morus alba, Melissa officinalis, and Artemisia capillaris in high-fat diet-induced obese mice. J Ethnopharmacol [Internet]. 2008 Jan 17 [cited 2014 Mar 13];115(2):263–70. Available from: http://www.ncbi.nlm.nih.gov/pubmed/18023310
4. Peng C-H, Liu L-K, Chuang C-M, Chyau C-C, Huang C-N, Wang C-J. Mulberry water extracts possess an anti-obesity effect and ability to inhibit hepatic lipogenesis and promote lipolysis. J Agric Food Chem [Internet]. 2011 Mar 23 [cited 2014 Mar 13];59(6):2663–71. Available from: http://www.ncbi.nlm.nih.gov/pubmed/21361295
5. Ou T-T, Hsu M-J, Chan K-C, Huang C-N, Ho H-H, Wang C-J. Mulberry extract inhibits oleic acid-induced lipid accumulation via reduction of lipogenesis and promotion of hepatic lipid clearance. J Sci Food Agric [Internet]. 2011 Dec [cited 2014 Mar 13];91(15):2740–8. Available from: http://www.ncbi.nlm.nih.gov/pubmed/22002411
6. Hong Y, Kim M-Y, Yoon M. The anti-angiogenic herbal extracts Ob-X from Morus alba, Melissa officinalis, and Artemisia capillaris suppresses adipogenesis in 3T3-L1 adipocytes. Pharm Biol [Internet]. 2011 Aug [cited 2014 Mar 13];49(8):775–83. Available from: http://www.ncbi.nlm.nih.gov/pubmed/21449830
7. Yoon M, Kim M-Y. The anti-angiogenic herbal composition Ob-X from Morus alba, Melissa officinalis, and Artemisia capillaris regulates obesity in genetically obese ob/ob mice. Pharm Biol [Internet]. 2011 Jun [cited 2014 Mar 13];49(6):614–9. Available from: http://www.ncbi.nlm.nih.gov/pubmed/21554004
8. Sugimoto M, Arai H, Tamura Y, Murayama T, Khaengkhan P, Nishio T, et al. Mulberry leaf ameliorates the expression profile of adipocytokines by inhibiting oxidative stress in white adipose tissue in db/db mice. Atherosclerosis [Internet]. 2009 Jun [cited 2014 Mar 13];204(2):388–94. Available from: http://www.ncbi.nlm.nih.gov/pubmed/19070857
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10. Liu LK, Lee HJ, Shih YW, Chyau CC, Wang CJ. Mulberry anthocyanin extracts inhibit LDL oxidation and macrophage-derived foam cell formation induced by oxidative LDL. J Food Sci [Internet]. 2008 Aug [cited 2014 Mar 13];73(6):H113–21. Available from: http://www.ncbi.nlm.nih.gov/pubmed/19241587
11. Enkhmaa B, Shiwaku K, Katsube T, Kitajima K, Anuurad E, Yamasaki M, et al. Mulberry (Morus alba L.) leaves and their major flavonol quercetin 3-(6-malonylglucoside) attenuate atherosclerotic lesion development in LDL receptor-deficient mice. J Nutr [Internet]. 2005 Apr [cited 2014 Mar 13];135(4):729–34. Available from: http://www.ncbi.nlm.nih.gov/pubmed/15795425
12. Hou Y, Cao X, Dong L, Wang L, Cheng B, Shi Q, et al. Bioactivity-based liquid chromatography-coupled electrospray ionization tandem ion trap/time of flight mass spectrometry for β₂AR agonist identification in alkaloidal extract of Alstonia scholaris. J Chromatogr A [Internet]. 2012 Mar 2 [cited 2014 Mar 19];1227:203–9. Available from: http://www.ncbi.nlm.nih.gov/pubmed/22269170
13. Shang J-H, Cai X-H, Zhao Y-L, Feng T, Luo X-D. Pharmacological evaluation of Alstonia scholaris: anti-tussive, anti-asthmatic and expectorant activities. J Ethnopharmacol [Internet]. 2010 Jun 16 [cited 2014 Feb 19];129(3):293–8. Available from: http://www.ncbi.nlm.nih.gov/pubmed/20381600
14. Rahmatullah M, Azam MNK, Khatun Z, Seraj S, Islam F, Rahman MA, et al. Medicinal plants used for treatment of diabetes by the Marakh sect of the Garo tribe living in Mymensingh district, Bangladesh. Afr J Tradit Complement Altern Med [Internet]. 2012 Jan [cited 2014 Mar 13];9(3):380–5. Available from: http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=3746667&tool=pmcentrez&rendertype=abstract
15. Channa S, Dar A, Ahmed S, Atta-ur-Rahman. Evaluation of Alstonia scholaris leaves for broncho-vasodilatory activity. J Ethnopharmacol [Internet]. 2005 Mar 21 [cited 2014 Mar 13];97(3):469–76. Available from: http://www.ncbi.nlm.nih.gov/pubmed/15849877
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17. Pankti K, Payal G, Manodeep C, Jagadish K. A PHYTOPHARMACOLOGICAL REVIEW OF ALSTONIA SCHOLARIS : A PANORAMIC HERBAL MEDICINE. 2012;3(3):367–71.
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27. Kong LD, Cheng CHK, Tan RX. Inhibition of MAO A and B by some plant-derived alkaloids, phenols and anthraquinones. J Ethnopharmacol [Internet]. 2004 Apr [cited 2014 Mar 13];91(2-3):351–5. Available from: http://www.ncbi.nlm.nih.gov/pubmed/15120460
28. Westerterp-Plantenga MS. Green tea catechins, caffeine and body-weight regulation. Physiol Behav [Internet]. 2010 Feb; Available from: http://www.ncbi.nlm.nih.gov/pubmed/20156466
29. Laurence G, Wallman K, Guelfi K. Effects of caffeine on time trial performance in sedentary men. J Sports Sci [Internet]. 2012 Jan [cited 2013 Oct 3];30(12):1235–40. Available from: http://www.ncbi.nlm.nih.gov/pubmed/22647089
30. Desbrow B, Biddulph C, Devlin B, Grant GD, Anoopkumar-Dukie S, Leveritt MD. The effects of different doses of caffeine on endurance cycling time trial performance. J Sports Sci [Internet]. 2011 Dec 6 [cited 2011 Dec 12];30(2):115–20. Available from: http://www.ncbi.nlm.nih.gov/pubmed/22142020
31. Davis JK, Green JM. Caffeine and anaerobic performance: ergogenic value and mechanisms of action. Sports Med [Internet]. 2009 Jan [cited 2013 Oct 7];39(10):813–32. Available from: http://www.ncbi.nlm.nih.gov/pubmed/19757860
32. Bellar D, Kamimori GH, Glickman EL. The effects of low-dose caffeine on perceived pain during a grip to exhaustion task. J Strength Cond Res [Internet]. 2011 May [cited 2013 Oct 7];25(5):1225–8. Available from: http://www.ncbi.nlm.nih.gov/pubmed/21522070
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