Welcome to the third and final part in this article series on how to safely and healthily lose weight fast.
In the first part of this series, we covered the diet and nutrition part of rapid, healthy weight loss.
In the second part, we discussed various exercise strategies you can use to speed up the fat loss.
In this part, we’re going to talk about what types of safe, effective supplements you can use to lose weight fast.
So, let’s start with a simple fact that the weight loss pill manufacturers don’t want you to know…
Weight Loss Supplements Aren’t Wonder Pills
No matter what the advertisements or sponsored athletes say, know this:
Weight loss supplements can only help speed the process if you’re maintaining a calorie deficit.
There is no such thing as a safe, natural substance that will cause you to lose fat if you’re not properly restricting your caloric intake (as discussed in part one). And ironically, many of the weight loss pills on the market won’t do anything at all, proper diet or not.
That said, there are a handful of natural supplements that, when combined with proper diet and exercise, you can use to safely speed up weight loss.
Personally, I use all of the supplements below when I’m dieting to lose weight. I’ve gotten to the 5 – 7% body fat range both with and without supplements, and there’s no question: it’s faster with.
The main reason why I want my “cutting” to go as quickly is possible is not impatience, but because it negatively affects my training. When you’re dieting for weight loss, you eventually begin to lose strength, and as time goes on, you can lose more and more muscle.
Thus, my goal when cutting is to use all the safe, natural, and effective methods I can to reach my target body fat percentage as quickly as possible.
So, let’s look at the natural weight loss supplements you can take to lose weight fast, and how to take them properly.
Weight Loss Supplements that Work
There aren’t many weight loss supplements that have been scientifically proven to help you lose fat, but here are the ones that we know work:
In the spirit of full disclosure, I want you to know that the supplements I recommend in this article are not just what I personally use but they are from my supplement line, LEGION.
As you probably know, the supplement industry is notorious for its lies and shenanigans. The truth is the majority of the supplements you see in the magazines and on the shelves aren’t going to help you reach your goals faster.
That’s why I decided to create the products I myself have always wanted: science-based formulations, clinically effective dosages of all ingredients, no fillers or unnecessary junk, and natural sweetening and flavoring.
You can learn more about LEGION and my goal to change the supplement industry for the better here.
And if you like what you see and decide to support my work…you’re awesome. 🙂 It’s because of people like you that I get to spend my time writing articles like this that help others get into the best shape of their lives.
Caffeine
As weight loss boils down to energy consumed vs. energy expended, caffeine helps you lose fat by increasing your body’s daily energy expenditure.
Caffeine also improves strength, muscle endurance, and anaerobic performance, and also reverses the “morning weakness” experienced by many weightlifters.
Part of maximizing the fat loss benefits of caffeine is preventing your body from building up too much of a tolerance, however. The best way to do this is to limit intake, of course.
Here’s what I recommend:
- Before training, supplement with 3 – 6 mg caffeine per kg of body weight. If you’re not sure of your caffeine sensitivity, start with 3 mg/kg and work up from there.
- Keep your daily. intake at or below 6 mg per kg of body weight. Don’t have 6 mg/kg before training and then drink a couple of coffees throughout the day.
- Do 1 – 2 low-caffeine days per week, and 1 no-caffeine day per week. A low day should be half your normal intake, and a no day means less than 50 mg of caffeine (you can have a cup or two of tea, but no coffee, caffeine pills, etc.).
Personally I get my caffeine from my pre-workout PULSE, which contains a dehydrated and concentrated form of caffeine (caffeine anhydrous) shown to be more effective for improving performance than what is naturally found in beverages like coffee.
PULSE also contains clinically effective dosages of 5 other ingredients scientifically proven to improve workout performance:
- Beta-Alanine. Beta-alanine is a naturally occurring amino acid that reduces exercise-induced fatigue, improves anaerobic exercise capacity, and can accelerate muscle growth.
- Citrulline Malate. Citrulline is an amino acid that improves muscle endurance, relieves muscle soreness, and improves aerobic performance.
- Betaine. Betaine is a compound found in plants like beets that improves muscle endurance, increases strength, and increases human growth hormone and insulin-like growth factor 1 production in response to acute exercise.
- Ornithine. Ornithine is an amino acid found in high amounts in dairy and meat that reduces fatigue in prolonged exercise and promotes lipid oxidation (the burning of fat for energy as opposed to carbohydrate or glycogen).
- Theanine. Theanine is an amino acid found primarily in tea that reduces the effects of mental and physical stress, increases the production of nitric oxide, which improves blood flow, and improves alertness, focus, attention, memory, mental task performance, and mood.
And what you won’t find in PULSE is equally special:
- No artificial sweeteners or flavors.
- No artificial food dyes.
- No unnecessary fillers, carbohydrate powders, or junk ingredients.
The bottom line is if you want to know what a pre-workout is supposed to feel like…if you want to experience the type of energy rush and performance boost that only clinically effective dosages of scientifically validated ingredients can deliver…then you want to try PULSE.
Yohimbine
Yohimbine is made from the Pausinystalia yohimbe plant, and it helps the body “tap into” fat stores.
(Not a very technical explanation, I know–if you want to know exactly how it works, check out this article of mine on how to lose stubborn fat.)
Yohimbine accelerates weight loss, but only works if you’re training in a fasted state. Elevated insulin levels negate yohimbine’s effects.
I’ve cut both with and without fasted training and yohimbine and I can say with absolutely certainty that with is noticeably faster. So much so that I think the biggest benefits of fasted training are that it lets you use yohimbine and it makes the other supplements discussed in this article more effective.
By itself, fasted training will make a slight difference in how quickly you lose fat. Combined with these supplements, however, it’s quite dramatic.
In terms of dosages, research has shown that .2 mg/kg of body weight is sufficient for fat loss purposes, and that ingesting it prior to exercise is particularly effective.
Some people get overly jittery from yohimbine, so I recommend you start with .1 mg/kg of body weight to assess tolerance. If you feel fine, then increase to the clinically effective dosage of .2 mg/kg.
Furthermore, yohimbine can raise blood pressure. If you have high blood pressure, I don’t recommend you use it.
In terms of which specific yohimbine supplement I recommend, you’re probably not surprised that I’ve included a clinically effective dosage in every serving of my pre-workout fat burner FORGE.
FORGE is a fat burner made specifically for use with fasted training and it contains clinically effective dosages of…
- HMB. β-Hydroxy β-Methylbutyrate (also known as HMB) is a substance formed when your body metabolizes the amino acid leucine.
Research shows that HMB is an extremely effective anti-catabolic agent, which means it’s very good at preventing muscle breakdown. And this means you will recover faster from your workouts and experience less muscle soreness.
- Yohimbine. Research shows that yohimbine enables your body to reduce fat stores faster, and it’s particularly useful as you get leaner and are battling with stubborn fat holdouts.
- Citicoline. CDP-choline (also known as citicoline) is a chemical that occurs naturally in the brain that increases levels of another chemical called phosphatidylcholine, which is vital for brain function.
Research shows that supplementation with CDP-choline improves attentional focus, and I included this in FORGE because most people find fasted training more mentally draining than fed training and CDP-choline can help counteract this.
The bottom line is FORGE helps you lose fat–and “stubborn” fat in particular–faster, preserve muscle, and maintain training intensity and mental sharpness.
PHOENIX Fat Burner
PHOENIX’s caffeine-free formulation is quite different from FORGE’s and is actually meant to be “stacked” with it (taken together).
PHOENIX helps you burn fat faster in three different ways:
- It dramatically increases metabolic speed.
- It amplifies the power of fat-burning chemicals produced by your body.
- It increases the feeling of fullness from food.
It accomplishes this through clinically effective dosages of several ingredients, including…
- Synephrine. This increases both basal metabolic rate and lipolysis, inhibits the activity of certain fat cell receptors that prevent fat mobilization, and increases the thermic effect of food (the “energy cost” of metabolizing food).
- Naringin. This stimulates the production of a hormone called adiponectin, which is involved in the breakdown of fat cells, and that it activates a type of receptor in fat cells that regulates fat mobilization (the PPARα receptor).
Through these mechanisms, naringin also works synergistically with synephrine and hesperidin to further accelerate the basal metabolic rate.
- Hesperidin. Like naringin, this also stimulates the production of adiponectin and activates the PPARa receptor. It also improves blood flow and reduces the inflammation of blood vessels.
- Epigallocatechin gallate (EGCG). This inhibits the activity of a different enzyme also responsible for breaking down neurotransmitters that induce lipolysis. It has also been shown to reduce abdominal fat in particular.
- Forskolin. This increases blood plasma and intracellular levels of a molecule known as cAMP. When cAMP is high, it signifies a lack of ATP (the most basic form of cellular energy in the body) and thus initiates a process to make more ATP by burning through energy reserves (body fat).
Research has show that supplementation with forskolin accelerates fat loss and increases testosterone levels.
- And more…
The bottom line is if you want to lose fat faster without pumping yourself full of stimulants or other potentially harmful chemicals…then you want to try PHOENIX.
Summary of Rapid Weight Loss Strategies
I want to wrap up this series of articles with a summary of everything covered, for easy reference and reminders. (Make sure to read parts one and two of this series if you haven’t already–the bullet points below won’t quite make sense if you don’t.)
- Maintain a mild-to-moderate calorie deficit, not a severe one
- Don’t just focus on calories, but on proper macronutritional ratios to maximize weight loss while preserving muscle
- Create an exact meal plan to follow and stick to it every day
- Don’t cheat on your meal plan as it will only slow things down
- Train with as high of a frequency as your body can take, which is likely no more than weightlifting 5 times per week and HIIT cardio 4 times per week
- Lift heavy weights, and focus on compound lifts
- Do high-intensity interval cardio
- Train in a fasted state
- Take supplements proven to accelerate fat loss.
- Limit and cycle caffeine consumption
Well, that’s really everything there is to say on the subject of safely and healthily losing weight fast.
If you use the strategies outlined in these articles, you will rapidly lose weight, and you won’t pay for it later in metabolic damage or muscle loss.
What do you think of these weight loss supplements? Have anything else you’d like to share? Let me know in the comments below!
Scientific References +
- Jagtap, M., Ravishankar, B., & Chandola, H. (2011). Clinical efficacy of Coleus forskohlii (Willd.) Briq. (Makandi) in hypertension of geriatric population. AYU (An International Quarterly Journal of Research in Ayurveda), 32(1), 59. https://doi.org/10.4103/0974-8520.85729
- Godard, M. P., Johnson, B. A., & Richmond, S. R. (2005). Body composition and hormonal adaptations associated with forskolin consumption in overweight and obese men. Obesity Research, 13(8), 1335–1343. https://doi.org/10.1038/oby.2005.162
- Walsh, D. A., & Van Patten, S. M. (1994). Multiple pathway signal tran sduction by the cAMP‐dependent protein kinase. The FASEB Journal, 8(15), 1227–1236. https://doi.org/10.1096/fasebj.8.15.8001734
- Maki, K. C., Reeves, M. S., Farmer, M., Yasunaga, K., Matsuo, N., Katsuragi, Y., Komikado, M., Tokimitsu, I., Wilder, D., Jones, F., Blumberg, J. B., & Cartwright, Y. (2009). Green tea catechin consumption enhances exercise-induced abdominal fat loss in overweight and obese adults. Journal of Nutrition, 139(2), 264–270. https://doi.org/10.3945/jn.108.098293
- Zhu, B. T., Shim, J. Y., Nagai, M., & Bai, H. W. (2008). Molecular modelling study of the mechanism of high-potency inhibition of human catechol-O-methyltransferase by (-)-epigallocatechin-3-O-gallate. Xenobiotica, 38(2), 130–146. https://doi.org/10.1080/00498250701744641
- Rizza, S., Muniyappa, R., Iantorno, M., Kim, J. A., Chen, H., Pullikotil, P., Senese, N., Tesauro, M., Lauro, D., Cardillo, C., & Quon, M. J. (2011). Citrus polyphenol hesperidin stimulates production of nitric oxide in endothelial cells while improving endothelial function and reducing inflammatory markers in patients with metabolic syndrome. Journal of Clinical Endocrinology and Metabolism, 96(5). https://doi.org/10.1210/jc.2010-2879
- Stohs, S. J., Preuss, H. G., Keith, S. C., Keith, P. L., Miller, H., & Kaats, G. R. (2011). Effects of p-synephrine alone and in combination with selected bioflavo-noids on resting metabolism, blood pressure, heart rate and self-reported mood changes. International Journal of Medical Sciences, 8(4), 295–301. https://doi.org/10.7150/ijms.8.295
- Liu, L., Shan, S., Zhang, K., Ning, Z. Q., Lu, X. P., & Cheng, Y. Y. (2008). Naringenin and hesperetin, two flavonoids derived from Citrus aurantium up-regulate transcription of adiponectin. Phytotherapy Research, 22(10), 1400–1403. https://doi.org/10.1002/ptr.2504
- Gougeon, R., Harrigan, K., Tremblay, J. F., Hedrei, P., Lamarche, M., & Morais, J. A. (2005). Increase in the thermic effect of food in women by adrenergic amines extracted from citrus aurantium. Obesity Research, 13(7), 1187–1194. https://doi.org/10.1038/oby.2005.141
- Brown, C. M., McGrath, J. C., Midgley, J. M., Muir, A. G. B., O’Brien, J. W., Thonoor, C. M., Williams, C. M., & Wilson, V. G. (1988). Activities of octopamine and synephrine stereoisomers on α‐adrenoceptors. British Journal of Pharmacology, 93(2), 417–429. https://doi.org/10.1111/j.1476-5381.1988.tb11449.x
- Haaz, S., Fontaine, K. R., Cutter, G., Limdi, N., Perumean-Chaney, S., & Allison, D. B. (2006). Citrus aurantium and synephrine alkaloids in the treatment of overweight and obesity: An update. In Obesity Reviews (Vol. 7, Issue 1, pp. 79–88). Obes Rev. https://doi.org/10.1111/j.1467-789X.2006.00195.x
- McGlade, E., Locatelli, A., Hardy, J., Kamiya, T., Morita, M., Morishita, K., Sugimura, Y., & Yurgelun-Todd, D. (2012). Improved Attentional Performance Following Citicoline Administration in Healthy Adult Women. Food and Nutrition Sciences, 03(06), 769–773. https://doi.org/10.4236/fns.2012.36103
- Millan, M. J., Newman-Tancredi, A., Audinot, V., Cussac, D., Lejeune, F., Nicolas, J. P., Cogé, F., Galizzi, J. P., Boutin, J. A., Rivet, J. M., Dekeyne, A., & Gobert, A. (2000). Agonist and antagonist actions of yohimbine as compared to fluparoxan at α2-adrenergic receptors (AR)s, serotonin (5-HT)(1A), 5-HT(1B), 5-HT(1D) and dopamine D2 and D3 receptors. Significance for the modulation of frontocortical monoaminergic transmission and depressive states. Synapse, 35(2), 79–95. https://doi.org/10.1002/(SICI)1098-2396(200002)35:2<79::AID-SYN1>3.0.CO;2-X
- Wilson, J. M., Lowery, R. P., Joy, J. M., Walters, J. A., Baier, S. M., Fuller, J. C., Stout, J. R., Norton, L. E., Sikorski, E. M., Wilson, S. M. C., Duncan, N. M., Zanchi, N. E., & Rathmacher, J. (2013). β-Hydroxy-β-methylbutyrate free acid reduces markers of exercise-induced muscle damage and improves recovery in resistance-trained men. British Journal of Nutrition, 110(3), 538–544. https://doi.org/10.1017/S0007114512005387
- Goldberg, M. R., Hollister, A. S., & Robertson, D. (1983). Influence of yohimbine on blood pressure, autonomic reflexes, and plasma catecholamines in humans. Hypertension, 5(5), 772–778. https://doi.org/10.1161/01.HYP.5.5.772
- McCarty, M. F. (2002). Pre-exercise administration of yohimbine may enhance the efficacy of exercise training as a fat loss strategy by boosting lipolysis. Medical Hypotheses, 58(6), 491–495. https://doi.org/10.1054/mehy.2001.1459
- GALITZKY, J., TAOUIS, M., BERLAN, M., RIVIÈRE, D., GARRIGUES, M., & LAFONTAN, M. (1988). α2‐Antagonist compounds and lipid mobilization: evidence for a lipid mobilizing effect of oral yohimbine in healthy male volunteers. European Journal of Clinical Investigation, 18(6), 587–594. https://doi.org/10.1111/j.1365-2362.1988.tb01272.x
- Ostojic, S. M. (2006). Yohimbine: The effects on body composition and exercise performance in soccer players. Research in Sports Medicine, 14(4), 289–299. https://doi.org/10.1080/15438620600987106
- Millan, M. J., Newman-Tancredi, A., Audinot, V., Cussac, D., Lejeune, F., Nicolas, J. P., Cogé, F., Galizzi, J. P., Boutin, J. A., Rivet, J. M., Dekeyne, A., & Gobert, A. (2000). Agonist and antagonist actions of yohimbine as compared to fluparoxan at α2-adrenergic receptors (AR)s, serotonin (5-HT)(1A), 5-HT(1B), 5-HT(1D) and dopamine D2 and D3 receptors. Significance for the modulation of frontocortical monoaminergic transmission and depressive states. Synapse, 35(2), 79–95. https://doi.org/10.1002/(SICI)1098-2396(200002)35:2<79::AID-SYN1>3.0.CO;2-X
- Haskell, C. F., Kennedy, D. O., Milne, A. L., Wesnes, K. A., & Scholey, A. B. (2008). The effects of l-theanine, caffeine and their combination on cognition and mood. Biological Psychology, 77(2), 113–122. https://doi.org/10.1016/j.biopsycho.2007.09.008
- Gomez-Ramirez, M., Kelly, S. P., Montesi, J. L., & Foxe, J. J. (2009). The effects of l-theanine on alpha-band oscillatory brain activity during a visuo-spatial attention task. Brain Topography, 22(1), 44–51. https://doi.org/10.1007/s10548-008-0068-z
- Foxe, J. J., Morie, K. P., Laud, P. J., Rowson, M. J., De Bruin, E. A., & Kelly, S. P. (2012). Assessing the effects of caffeine and theanine on the maintenance of vigilance during a sustained attention task. Neuropharmacology, 62(7), 2320–2327. https://doi.org/10.1016/j.neuropharm.2012.01.020
- Bryan, J. (2008). Psychological effects of dietary components of tea: Caffeine and L-theanine. In Nutrition Reviews (Vol. 66, Issue 2, pp. 82–90). Nutr Rev. https://doi.org/10.1111/j.1753-4887.2007.00011.x
- Siamwala, J. H., Dias, P. M., Majumder, S., Joshi, M. K., Sinkar, V. P., Banerjee, G., & Chatterjee, S. (2013). L-Theanine promotes nitric oxide production in endothelial cells through eNOS phosphorylation. Journal of Nutritional Biochemistry, 24(3), 595–605. https://doi.org/10.1016/j.jnutbio.2012.02.016
- Kimura, K., Ozeki, M., Juneja, L. R., & Ohira, H. (2007). l-Theanine reduces psychological and physiological stress responses. Biological Psychology, 74(1), 39–45. https://doi.org/10.1016/j.biopsycho.2006.06.006
- Sugino, T., Shirai, T., Kajimoto, Y., & Kajimoto, O. (2008). l-Ornithine supplementation attenuates physical fatigue in healthy volunteers by modulating lipid and amino acid metabolism. Nutrition Research, 28(11), 738–743. https://doi.org/10.1016/j.nutres.2008.08.008
- Apicella, J. M., Lee, E. C., Bailey, B. L., Saenz, C., Anderson, J. M., Craig, S. A. S., Kraemer, W. J., Volek, J. S., & Maresh, C. M. (2013). Betaine supplementation enhances anabolic endocrine and Akt signaling in response to acute bouts of exercise. European Journal of Applied Physiology, 113(3), 793–802. https://doi.org/10.1007/s00421-012-2492-8
- Lee, E. C., Maresh, C. M., Kraemer, W. J., Yamamoto, L. M., Hatfield, D. L., Bailey, B. L., Armstrong, L. E., Volek, J. S., McDermott, B. P., & Craig, S. A. S. (2010). Ergogenic effects of betaine supplementation on strength and power performance. Journal of the International Society of Sports Nutrition, 7. https://doi.org/10.1186/1550-2783-7-27
- Trepanowski, J. F., Farney, T. M., McCarthy, C. G., Schilling, B. K., Craig, S. A., & Bloomer, R. J. (2011). The effects of chronic betaine supplementation on exercise performance, skeletal muscle oxygen saturation, and associated biochemical parameters in resistance trained men. Journal of Strength and Conditioning Research, 25(12), 3461–3471. https://doi.org/10.1519/JSC.0b013e318217d48d
- Bendahan, D., Mattei, J. P., Ghattas, B., Confort-Gouny, S., Le Guern, M. E., & Cozzone, P. J. (2002). Citrulline/malate promotes aerobic energy production in human exercising muscle. British Journal of Sports Medicine, 36(4), 282–289. https://doi.org/10.1136/bjsm.36.4.282
- Pérez-Guisado, J., & Jakeman, P. M. (2010). Citrulline malate enhances athletic anaerobic performance and relieves muscle soreness. Journal of Strength and Conditioning Research, 24(5), 1215–1222. https://doi.org/10.1519/JSC.0b013e3181cb28e0
- Kern, B. D., & Robinson, T. L. (2011). Effects of β-alanine supplementation on performance and body composition in collegiate wrestlers and football players. Journal of Strength and Conditioning Research, 25(7), 1804–1815. https://doi.org/10.1519/JSC.0b013e3181e741cf
- Smith, A. E., Walter, A. A., Graef, J. L., Kendall, K. L., Moon, J. R., Lockwood, C. M., Fukuda, D. H., Beck, T. W., Cramer, J. T., & Stout, J. R. (2009). Effects of β-alanine supplementation and high-intensity interval training on endurance performance and body composition in men; a double-blind trial. Journal of the International Society of Sports Nutrition, 6. https://doi.org/10.1186/1550-2783-6-5
- Derave, W., Özdemir, M. S., Harris, R. C., Pottier, A., Reyngoudt, H., Koppo, K., Wise, J. A., & Achten, E. (2007). β-Alanine supplementation augments muscle carnosine content and attenuates fatigue during repeated isokinetic contraction bouts in trained sprinters. Journal of Applied Physiology, 103(5), 1736–1743. https://doi.org/10.1152/japplphysiol.00397.2007
- Goldstein, E. R., Ziegenfuss, T., Kalman, D., Kreider, R., Campbell, B., Wilborn, C., Taylor, L., Willoughby, D., Stout, J., Graves, B. S., Wildman, R., Ivy, J. L., Spano, M., Smith, A. E., & Antonio, J. (2010). International society of sports nutrition position stand: Caffeine and performance. In Journal of the International Society of Sports Nutrition (Vol. 7, Issue 1). J Int Soc Sports Nutr. https://doi.org/10.1186/1550-2783-7-5
- Mora-Rodríguez, R., Pallarés, J. G., López-Samanes, Á., Ortega, J. F., & Fernández-Elías, V. E. (2012). Caffeine ingestion reverses the circadian rhythm effects on neuromuscular performance in highly resistance-trained men. PLoS ONE, 7(4). https://doi.org/10.1371/journal.pone.0033807
- Beck, T. W., Housh, T. J., Schmidt, R. J., Johnson, G. O., Housh, D. J., Coburn, J. W., & Malek, M. H. (2006). The acute effects of a caffeine-containing supplement on strength, muscular endurance, and anaerobic capabilities. Journal of Strength and Conditioning Research, 20(3), 506–510. https://doi.org/10.1519/18285.1
- Astorino, T. A., Rohmann, R. L., & Firth, K. (2008). Effect of caffeine ingestion on one-repetition maximum muscular strength. European Journal of Applied Physiology, 102(2), 127–132. https://doi.org/10.1007/s00421-007-0557-x
- Astrup, A., Toubro, S., Cannon, S., Hein, P., Breum, L., & Madsen, J. (1990). Caffeine: A double-blind, placebo-controlled study of its thermogenic, metabolic, and cardiovascular effects in healthy volunteers. American Journal of Clinical Nutrition, 51(5), 759–767. https://doi.org/10.1093/ajcn/51.5.759
- Durrant, M. L., Garrow, J. S., Royston, P., Stalley, S. F., Sunkin, S., & Warwick, P. M. (1980). Factors influencing the composition of the weight lost by obese patients on a reducing diet. British Journal of Nutrition, 44(3), 275–285. https://doi.org/10.1079/bjn19800042