EvoMuse BRITE™ Writeup

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There is still one ingredient we are trying to finalize that we have left off of the writeup. Ingredients should arrive soon, and we will have around 100 beta units available. The product will come as an oil suspension in an 8 ounce bottle, with a pointed dispenser tip with 270 000-sized (1cc) capsules. It should take but a few seconds to shake the bottle and fill 9 capsules for the day. Final product will be in softgel form. And here we go:

Brite Write Up


Brite Cell Overview

In order to fully understand the concept of EvoMuse Brite, a bit of background science will be beneficial before we get into the specific ingredients.

Many years ago, it was thought that adult mammalian fat cells (adipocytes) were all basically the same. Under a microscope, they appeared white (white adipose tissue, or WAT), and they did a great job at storing fat in case it needed to be used later during periods of hunger or famine. While much maligned by fitness enthusiasts, WAT is essential to our functioning and survival, and is actually quite beneficial when it works as intended. However, sometimes WAT becomes dysfunctional, and gets too good at storing fat, for various genetic and/or dietary reasons, leading to conditions of overweight and obesity.

Then came the discovery of brown fat (BAT) it rodents, which appeared to act quite differently from traditional WAT. Behaving in a contradictory fashion, BAT was actually shown to be dense in mitochondria, and therefore thermogenic. It was determined that these cells primary function was something called "non-shivering thermogenesis", involving a futile cycle of shuttling protons to the mitochondria to generate heat (1).

This got researchers excited, and they began to study BAT for anti-obesity purposes. Several years later, this was all but abandoned, due to the initial apparent lack of BAT cells in humans past infancy.

Fast forward to recent years, and it was discovered that adult humans actually do have a significant amount of BAT cells. The quantity is small in comparison to WAT cells, but as it turns out, you don't need a large volume of these fat-burning cells to instigate a significant metabolic effect. So researchers revisited BAT upregulation as an avenue to treat obesity.

Based on the most current research, we have now discovered another player in the adipocyte continuum. These are called "Brite" cells. At a microscopic level, brite cells display a color in-between BAT and WAT cells, although they behave similar if not almost the same as BAT. And unlike BAT, they are actually created within WAT cells.

These cells are currently referred to in the research by several names; brite, beige, inducible, recruitable-brown, and brown adipocyte-like cells. For the purpose of this write up, we will be referring to them as "brite"; a name derived from a combination of the words "brown-in-white".

While the research on brite cells is in its infancy, we do know enough about these fascinating metabolically active fat depots to take steps to encourage their activation and therefore fat burning potential. EvoMuse Brite has been developed with the goal of shifting those with the unfortunate fat storing phenotype to a more genetically lean, fat burning phenotype.

The goal is to convince the WAT cells currently in your body, to trigger the intracellular production of brite cells, so that instead of just being fat storage depots and adipokine factories, they will also actually burn fat.

Research has shown that the hormone irisin (endogenous or exogenous), might trigger brite cell formation, as well as cold therapy, but the evidence is quite often contradictory as far as effectiveness. One of the current lines of thought is that not all white cells have this potential to turn brite, but those that do are located in specific places in humans, particularly along the spine and around the collarbone. But like BAT cells, we don't need many of them to have a big effect. And it turns out; people genetically prone to fatness are likely to express less of these cells.

BAT mitochondria respond to something called UCP1 (uncoupling protein 1) to burn fat and generate heat, while brite cells seem to express lower levels of UCP1. However, brite cells potentially burn fat independently of UCP1 signaling, and furthermore, with the proper triggers, brite fat can actually turn on high levels of UCP1 (2). Multiple ingredients in the Brite formula will encourage WAT cells to upregulate UCP1 levels.

The research shows that once developed, these brite cells directly correlate with leanness and can likely reduce metabolic disease and obesity in humans (3).

With that background in mind, the next thing we want to look at is a fatty acid called CLnA.
Conjugated Linolenic Acid (CLnA)

By now most people are well aware of conjugated linoleic acid (CLA), and while a similar fatty acid, conjugated linolenic acid (CLnA) functions quite differently. CLnA is found naturally in several seed oils, but can also be produced in small amounts endogenously by gut bacteria.

Current research has demonstrated CLnA's unique potential for fat loss from multiple angles. We have multiple sources of CLnA in the Brite formula, but first lets look at a little background on the overall CLnA research.

In a recent review published in the journal Lipids, CLnA was found to exhibit anti-obeseogenic properties, as well as reducing inflammation, boosting immune function, and improving overall cardiovascular health (4).

The worst thing a WAT cell can do is become dysfunctional, which will reduce it's ability to become a brite cell and cause it to become highly efficient at excessive fat storage and poor at releasing stored fatty acids to be oxidized. Normal cellular functioning involves low oxidative stress, low lipid peroxidation, and low inflammation, with optimal levels of superoxide dismutase (SOD). CLnA administration has been shown to support all of these (5,6).

In a study comparing CLnA to CLA, animals had a higher beta-oxidation rate and lost more fat in the CLnA group (7). Another study showed that CLnA had an apoptotic effect on proliferating pre-adipocytes (8). From a general health perspective, CLnA has also been shown to protect LDL cholesterol from oxidation (9).

 
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Tung Oil
TUNG OIL HAS BEEN REMOVED. THE DOSAGE OF BMSO HAS BEEN INCREASED TO COVER THE AEA REQUIREMENT.

has been included in Brite as a major source of CLnA, as well as the specific isomer a-Eleostearic Acid (AEA). Aside from all of the above cellular browning benefits from CLnA, researchers looking directly at the effects of Tung Oil found that when they added it to the diet of hens, they demonstrated a remarkably small amount of adipose tissue weight compared to non-Tung fed counterparts. They also noted reduced tryglyceride levels in heart and adipose tissue (10).

Also another point of interest, research shows that a portion of ingested AEA converts to CLA in the body (11). And while the body of research supporting the fat loss potential of CLA has been inconclusive, a 2013 study published in the journal Lipids found that a combination of CLA and alpha linoleic acid (see Perilla Oil below) blocked adipogenesis (12).

Additionally, AEA has been shown to act as a Selective Estrogen Receptor Modulator (SERM), thereby potentially reducing some of the negative effects of excess estrogen (13).
Bitter Melon Seed Oil

Bitter Melon Seed Oil (BMSO) is a another source of CLnA as well as AEA. In addition to the previously stated benefits of CLnA and AEA, Bitter Melon has also been shown to be a direct PPAR-a activator, which is one of the most important players in all three stages of fat burning (14). It has also been shown to cause apoptosis in undifferentiated adipocytes, thereby inhibiting the creation of new fat cells (15).

BMSO has also been shown in multiple studies to upregulate mitochondrial biogenesis and UCP1 (16),(27). And in an exciting study published in 2013, BMSO was shown to have a direct browning effect on WAT cells (17).
Korean Pine Nut Oil

Korean Pine Nut Oil (PNO) has been shown to upregulate UCP1 levels via its Pinolenic Acid content, as well as activate PPAR alpha and delta. Based on these findings, the researchers concluded PNO may have potential to counteract obesity (18).

In addition, a recent study showed that mice supplemented with PNO, when overfed, gained significantly less weight vs. the control group, demonstrating potential as an anti-obesity agent (19).
Perilla Seed Oil

Perilla Seed Oil (PO) is rich in Alpha Linoleic Acid (ALA), which has been shown to upregulate UCP1 levels and improve glucose metabolism (20). As discussed above, it also has an anti-adipogenic effect when coupled with CLA, for which Tung Oil is a precursor.

In comparison to feeding of olive oil or beef fat, Perilla Seed Oil (PO) was shown to reduce body fat and lower serum triglycerides, as well as suppress the late phase of adipocyte differentiation (21,22).

ALA has also been shown to decrease several fat storing enzymes and upregulate fatty acid oxidation (23).
Peppermint Oil

Peppermint oil activates a cellular protein called TRPM8, also known as the cold and menthol receptor (24). Upon activation we see an increased expression of UCP1 in WAT cells, causing a direct browning effect (25).
Borage Oil

Borage Oil is a rich source of Gamma Linoleic Acid (GLA), a fatty acid with a long list of benefits. For our purposes, GLA has been shown to increase expression of UCP1, decrease body fat storage, and increase fat oxidation (26).


Carnitine has been shown to increase UCP1 levels in rats (30). Acetyl-l-Carnitine also plays an important role in optimizing fat oxidation in browned adipocytes (31).
Phytol

Phytol is an organic alcohol that converts to phytanic acid during metabolism. Phytanic acid has been shown to cause a browning effect in pre-adipocytes as well as activate UCP1 in existing brown fat cells, enhancing their fat burning function (32,33).
Trans-Retinoic Acid

Trans-Retinoic Acid, from botanicals such as Rosehip Oil, has been included in the formula due to its potential ability to encourage adipocyte browning, again through UCP1 activation (34–36). It has also been shown to decrease cellular triglyceride content, while upregulating lipolysis and fatty acid oxidation, therefore shifting WAT to behave in a more metabolically oxidative fashion (37).

Product Usage

Brite comes in a liquid suspension, and should be consumed three times daily (preferably with meals). While acute fat loss effects can and should be expected, the most pronounced benefits will likely be achieved over continued use due to the gradual conversion of WAT to Brite cells, helping those that are typically efficient at fat storage adopt a more naturally lean, fat burning phenotype.



1. Rosenwald M, Wolfrum C. The origin and definition of brite versus white and classical brown adipocytes. Adipocyte [Internet]. 2014 Jan 1 [cited 2014 Apr 19];3(1):4–9. Available from: http://www.pubmedcentral.nih.gov/art...rtype=abstract
2. Nakamura Y, Sato T, Shiimura Y, Miura Y, Kojima M. FABP3 and brown adipocyte-characteristic mitochondrial fatty acid oxidation enzymes are induced in beige cells in a different pathway from UCP1. Biochem Biophys Res Commun [Internet]. 2013 Nov 8 [cited 2014 Apr 19];441(1):42–6. Available from: http://www.ncbi.nlm.nih.gov/pubmed/24129192
3. Harms M, Seale P. Brown and beige fat: development, function and therapeutic potential. Nat Med [Internet]. 2013 Oct [cited 2014 Mar 20];19(10):1252–63. Available from: http://www.ncbi.nlm.nih.gov/pubmed/24100998
4. Hennessy AA, Ross RP, Devery R, Stanton C. The health promoting properties of the conjugated isomers of α-linolenic acid. Lipids [Internet]. 2011 Feb [cited 2014 Apr 18];46(2):105–19. Available from: http://www.ncbi.nlm.nih.gov/pubmed/21161605
5. Saha SS, Ghosh M. Antioxidant and anti-inflammatory effect of conjugated linolenic acid isomers against streptozotocin-induced diabetes. Br J Nutr [Internet]. 2012 Sep 28 [cited 2014 Apr 18];108(6):974–83. Available from: http://www.ncbi.nlm.nih.gov/pubmed/22182422
6. Dhar P, Bhattacharyya D, Bhattacharyya DK, Ghosh S. Dietary comparison of conjugated linolenic acid (9 cis, 11 trans, 13 trans) and alpha-tocopherol effects on blood lipids and lipid peroxidation in alloxan-induced diabetes mellitus in rats. Lipids [Internet]. 2006 Jan [cited 2014 Apr 18];41(1):49–54. Available from: http://www.ncbi.nlm.nih.gov/pubmed/16555471
7. Koba K, Akahoshi A, Yamasaki M, Tanaka K, Yamada K, Iwata T, et al. Dietary conjugated linolenic acid in relation to CLA differently modifies body fat mass and serum and liver lipid levels in rats. Lipids [Internet]. 2002 Apr [cited 2014 Apr 18];37(4):343–50. Available from: http://www.ncbi.nlm.nih.gov/pubmed/12030314
8. Chou Y-C, Su H-M, Lai T-W, Chyuan J-H, Chao P-M. cis-9, trans-11, trans-13-Conjugated linolenic acid induces apoptosis and sustained ERK phosphorylation in 3T3-L1 preadipocytes. Nutrition [Internet]. 2012 Jul [cited 2014 Apr 14];28(7-8):803–11. Available from: http://www.ncbi.nlm.nih.gov/pubmed/22465903
9. Dhar P, Chattopadhyay K, Bhattacharyya D, Roychoudhury A, Biswas A, Ghosh S. Antioxidative effect of conjugated linolenic acid in diabetic and non-diabetic blood: an in vitro study. J Oleo Sci [Internet]. 2006 Jan [cited 2014 Apr 18];56(1):19–24. Available from: http://www.ncbi.nlm.nih.gov/pubmed/17693694
10. Lee J-S, Takai J, Takahasi K, Endo Y, Fujimoto K, Koike S, et al. Effect of dietary tung oil on the growth and lipid metabolism of laying hens. J Nutr Sci Vitaminol (Tokyo) [Internet]. 2002 Apr [cited 2014 Apr 14];48(2):142–8. Available from: http://www.ncbi.nlm.nih.gov/pubmed/12171435
11. Tsuzuki T, Tokuyama Y, Igarashi M, Nakagawa K, Ohsaki Y, Komai M, et al. Alpha-eleostearic acid (9Z11E13E-18:3) is quickly converted to conjugated linoleic acid (9Z11E-18:2) in rats. J Nutr [Internet]. 2004 Oct [cited 2014 Apr 24];134(10):2634–9. Available from: http://www.ncbi.nlm.nih.gov/pubmed/15465759
12. Kim Y, Kelly OJ, Ilich JZ. Synergism of α-linolenic acid, conjugated linoleic acid and calcium in decreasing adipocyte and increasing osteoblast cell growth. Lipids [Internet]. 2013 Aug [cited 2014 Mar 31];48(8):787–802. Available from: http://www.ncbi.nlm.nih.gov/pubmed/23757205
13. Tran HNA, Bae S-Y, Song B-H, Lee B-H, Bae Y-S, Kim Y-H, et al. Pomegranate (Punica granatum) seed linolenic acid isomers: concentration-dependent modulation of estrogen receptor activity. Endocr Res [Internet]. 2010 Jan [cited 2014 Mar 26];35(1):1–16. Available from: http://www.ncbi.nlm.nih.gov/pubmed/20136514
14. Chuang C-Y, Hsu C, Chao C-Y, Wein Y-S, Kuo Y-H, Huang C. Fractionation and identification of 9c, 11t, 13t-conjugated linolenic acid as an activator of PPARalpha in bitter gourd (Momordica charantia L.). J Biomed Sci [Internet]. 2006 Nov [cited 2013 Nov 7];13(6):763–72. Available from: http://www.ncbi.nlm.nih.gov/pubmed/16955349
15. Nishimura K, Tsumagari H, Morioka A, Yamauchi Y, Miya****a K, Lu S, et al. Regulation of apoptosis through arachidonate cascade in mammalian cells. Appl Biochem Biotechnol [Internet]. [cited 2014 May 12];102-103(1-6):239–50. Available from: http://www.ncbi.nlm.nih.gov/pubmed/12396127
16. Chan LLY, Chen Q, Go AGG, Lam EKY, Li ETS. Reduced adiposity in bitter melon (Momordica charantia)-fed rats is associated with increased lipid oxidative enzyme activities and uncoupling protein expression. J Nutr [Internet]. 2005 Nov [cited 2014 Apr 26];135(11):2517–23. Available from: http://www.ncbi.nlm.nih.gov/pubmed/16251604
17. Hsieh C-H, Chen G-C, Chen P-H, Wu T-F, Chao P-M. Altered White Adipose Tissue Protein Profile in C57BL/6J Mice Displaying Delipidative, Inflammatory, and Browning Characteristics after Bitter Melon Seed Oil Treatment. PLoS One [Internet]. 2013 Jan [cited 2013 Oct 16];8(9):e72917. Available from: http://www.pubmedcentral.nih.gov/art...rtype=abstract
18. Le NH, Shin S, Tu TH, Kim C-S, Kang J-H, Tsuyoshi G, et al. Diet enriched with korean pine nut oil improves mitochondrial oxidative metabolism in skeletal muscle and brown adipose tissue in diet-induced obesity. J Agric Food Chem [Internet]. 2012 Dec 5 [cited 2014 Apr 14];60(48):11935–41. Available from: http://www.ncbi.nlm.nih.gov/pubmed/23140571
19. Park S, Lim Y, Shin S, Han SN. Impact of Korean pine nut oil on weight gain and immune responses in high-fat diet-induced obese mice. Nutr Res Pract [Internet]. 2013 Oct [cited 2014 Apr 14];7(5):352–8. Available from: http://www.pubmedcentral.nih.gov/art...rtype=abstract
20. Takahashi Y, Ide T. Dietary n-3 fatty acids affect mRNA level of brown adipose tissue uncoupling protein 1, and white adipose tissue leptin and glucose transporter 4 in the rat. Br J Nutr [Internet]. 2000 Aug [cited 2014 Apr 14];84(2):175–84. Available from: http://www.ncbi.nlm.nih.gov/pubmed/11029968
21. Okuno M, Kajiwara K, Imai S, Kobayashi T, Honma N, Maki T, et al. Perilla oil prevents the excessive growth of visceral adipose tissue in rats by down-regulating adipocyte differentiation. J Nutr [Internet]. 1997 Sep [cited 2014 Apr 14];127(9):1752–7. Available from: http://www.ncbi.nlm.nih.gov/pubmed/9278555
22. Kim H-K, Choi H. Stimulation of acyl-CoA oxidase by alpha-linolenic acid-rich perilla oil lowers plasma triacylglycerol level in rats. Life Sci [Internet]. 2005 Aug 5 [cited 2014 Apr 14];77(12):1293–306. Available from: http://www.ncbi.nlm.nih.gov/pubmed/15894339
23. Fukumitsu S, Villareal MO, Onaga S, Aida K, Han J, Isoda H. α-Linolenic acid suppresses cholesterol and triacylglycerol biosynthesis pathway by suppressing SREBP-2, SREBP-1a and -1c expression. Cytotechnology [Internet]. 2013 Dec [cited 2014 Mar 23];65(6):899–907. Available from: http://www.ncbi.nlm.nih.gov/pubmed/23138267
24. Kim S-H, Nam J-H, Park E-J, Kim B-J, Kim S-J, So I, et al. Menthol regulates TRPM8-independent processes in PC-3 prostate cancer cells. Biochim Biophys Acta [Internet]. 2009 Jan [cited 2014 May 12];1792(1):33–8. Available from: http://www.ncbi.nlm.nih.gov/pubmed/18955132
25. Rossato M, Granzotto M, Macchi V, Porzionato A, Petrelli L, Calcagno A, et al. Human white adipocytes express the cold receptor TRPM8 which activation induces UCP1 expression, mitochondrial activation and heat production. Mol Cell Endocrinol [Internet]. 2014 Mar 5 [cited 2014 May 1];383(1-2):137–46. Available from: http://www.ncbi.nlm.nih.gov/pubmed/24342393
26. Takahashi Y, Ide T, Fujita H. Dietary gamma-linolenic acid in the form of borage oil causes less body fat accumulation accompanying an increase in uncoupling protein 1 mRNA level in brown adipose tissue. Comp Biochem Physiol B Biochem Mol Biol [Internet]. 2000 Oct [cited 2013 Oct 16];127(2):213–22. Available from: http://www.ncbi.nlm.nih.gov/pubmed/11079375
27. Shi L, Shi L, Song G, Zhang H, Hu Z, Wang C, et al. Oxymatrine attenuates hepatic steatosis in non-alcoholic fatty liver disease rats fed with high fructose diet through inhibition of sterol regulatory element binding transcription factor 1 (Srebf1) and activation of peroxisome proliferator activated recep. Eur J Pharmacol [Internet]. 2013 Aug 15 [cited 2014 Apr 14];714(1-3):89–95. Available from: http://www.ncbi.nlm.nih.gov/pubmed/23791610
28. Shi L, Shi L, Zhang H, Hu Z, Wang C, Zhang D, et al. Oxymatrine ameliorates non-alcoholic fatty liver disease in rats through peroxisome proliferator-activated receptor-α activation. Mol Med Rep [Internet]. 2013 Aug [cited 2014 Apr 14];8(2):439–45. Available from: http://www.ncbi.nlm.nih.gov/pubmed/23754536
29. Guo C, Zhang C, Li L, Wang Z, Xiao W, Yang Z. Hypoglycemic and hypolipidemic effects of oxymatrine in high-fat diet and streptozotocin-induced diabetic rats. Phytomedicine [Internet]. 2014 Mar 25 [cited 2014 Apr 18]; Available from: http://www.ncbi.nlm.nih.gov/pubmed/24680614
30. Couturier A, Ringseis R, Mooren F-C, Krüger K, Most E, Eder K. Carnitine supplementation to obese Zucker rats prevents obesity-induced type II to type I muscle fiber transition and favors an oxidative phenotype of skeletal muscle. Nutr Metab (Lond) [Internet]. 2013 Jul 10 [cited 2014 May 12];10(1):48. Available from: http://www.nutritionandmetabolism.com/content/10/1/48
31. Hahn P, Skala J. Carnitine and brown adipose tissue metabolism in the rat during development. Biochem J [Internet]. 1972 Mar [cited 2014 May 12];127(1):107–11. Available from: http://www.pubmedcentral.nih.gov/art...rtype=abstract
32. Schlüter A, Barberá MJ, Iglesias R, Giralt M, Villarroya F. Phytanic acid, a novel activator of uncoupling protein-1 gene transcription and brown adipocyte differentiation. Biochem J [Internet]. 2002 Feb 15 [cited 2014 May 12];362(Pt 1):61–9. Available from: http://www.pubmedcentral.nih.gov/art...rtype=abstract
33. Schluter A, Giralt M, Iglesias R, Villarroya F. Phytanic acid, but not pristanic acid, mediates the positive effects of phytol derivatives on brown adipocyte differentiation. FEBS Lett [Internet]. 2002 Apr 24 [cited 2014 May 12];517(1-3):83–6. Available from: http://www.ncbi.nlm.nih.gov/pubmed/12062414
34. Kiefer FW, Vernochet C, O’Brien P, Spoerl S, Brown JD, Nallamshetty S, et al. Retinaldehyde dehydrogenase 1 regulates a thermogenic program in white adipose tissue. Nat Med [Internet]. 2012 Jun [cited 2014 Mar 20];18(6):918–25. Available from: http://www.pubmedcentral.nih.gov/art...rtype=abstract
35. Mercader J, Palou A, Bonet ML. Induction of uncoupling protein-1 in mouse embryonic fibroblast-derived adipocytes by retinoic acid. Obesity (Silver Spring) [Internet]. 2010 Apr [cited 2014 Apr 18];18(4):655–62. Available from: http://www.ncbi.nlm.nih.gov/pubmed/19834471
36. Del Mar Gonzalez-Barroso M, Pecqueur C, Gelly C, Sanchis D, Alves-Guerra MC, Bouillaud F, et al. Transcriptional activation of the human ucp1 gene in a rodent cell line. Synergism of retinoids, isoproterenol, and thiazolidinedione is mediated by a multipartite response element. J Biol Chem [Internet]. 2000 Oct 13 [cited 2014 Mar 23];275(41):31722–32. Available from: http://www.ncbi.nlm.nih.gov/pubmed/10921912
37. Mercader J, Madsen L, Felipe F, Palou A, Kristiansen K, Bonet ML. All-trans retinoic acid increases oxidative metabolism in mature adipocytes. Cell Physiol Biochem [Internet]. 2007 Jan [cited 2014 Apr 18];20(6):1061–72. Available from: http://www.ncbi.nlm.nih.gov/pubmed/17975308
31. http://www.sciencedirect.com/science...56464613000133
 
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Nice
 
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*science boner*
 
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This is a VERY new and exciting angle on phenotype enhancement/long term change. This product will change your body over the long term to be far more efficient at using fat stores to generate heat, rather than just being stored/generating inflammatory adipokines.
 

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This is a VERY new and exciting angle on phenotype enhancement/long term change. This product will change your body over the long term to be far more efficient at using fat stores to generate heat, rather than just being stored/generating inflammatory adipokines.
Would being on a keto diet for a period of time help, or would it not matter?
 
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Would being on a keto diet for a period of time help, or would it not matter?
It doesn't seem to matter, though the acute fatloss will most definitely be more pronounced on a keto type diet.
 
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It doesn't seem to matter, though the acute fatloss will most definitely be more pronounced on a keto type diet.
That's great for someone looking for some more "instant" (term used loosely) results.

But I really love the products that EvoMuse is bringing out that are increasingly beneficial over long-term dosing/usage.
 
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For those interested, I will be making up a few test betas of a Topical BRITE™. This will be applied to the spot where a lot of people, like me, hold fat - notably the upper scapular region.

You will need some help applying this.
 
Dewey99

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Very interesting as always, Matt. I will have to try this when it's ready.
 
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Very interesting as always, Matt. I will have to try this when it's ready.
I tried to pick up domestic TUNG oil, but none of it was a high enough grade. Had to get this custom made overseas.
 
cubs1987

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really looking forward to this!!! Can't wait!
 
dsade

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I know how disappointed I was in straight CLA.

It did take me a while to dial in the dosage. I went too high and ended up with a few unpleasant experiences, so WARNING: FOLLOW LABEL DIRECTIONS FOR DOSAGE.
 

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For those interested, I will be making up a few test betas of a Topical BRITE(TM). This will be applied to the spot where a lot of people, like me, hold fat - notably the upper scapular region.

You will need some help applying this.
Interested in testing while in keto!

Could it also be used on the abs, glutes and legs just as effectively?
 
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Interested in testing while in keto!

Could it also be used on the abs, glutes and legs just as effectively?
I don't think so, no. For those areas you will want to stick, at least initially, with the Abliderate or Eviscerate series.

With the Upper scapular region already containing decent amounts of brown fat, application of a topical here might not only help activate thermogenesis there, but encourage the quicker formation of BRITE cells from the WAT content.
 

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I don't think so, no. For those areas you will want to stick, at least initially, with the Abliderate or Eviscerate series.

With the Upper scapular region already containing decent amounts of brown fat, application of a topical here might not only help activate thermogenesis there, but encourage the quicker formation of BRITE cells from the WAT content.
That'll work. I just ordered some Eviscerate BFF to melt away the man handles.
 
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The cold exposure/TRPM8 section is brushed on in the writeup.
 
AdelV

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Matt when is this ready? I want this too! Haha, loving all the releases.
 

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I know how disappointed I was in straight CLA.

It did take me a while to dial in the dosage. I went too high and ended up with a few unpleasant experiences, so WARNING: FOLLOW LABEL DIRECTIONS FOR DOSAGE.

Aside from the obvious near ****ting yourself experience a little too much fat tends to give you, what else did you experience? Also, how dependent is the success of Brite on the current fatty acid profile of your diet? Does it matter if you consume mainly saturated fat? Will this offset some of the results considering the fats in Brite are polyunsaturated?

This also looks like it'll give those that do dabble in cold exposure a serious boost. This product looks like it was worth the wait!
 
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Is there any truth to cold exposure and increased BAT?
Cold exposure does appear to be effective, as long as you keep doing it. It might even be something for the overachievers out there to consider kickstarting Brite supplementation with 2hrs/day of cold therapy. 60-ish degrees Fahrenheit is what is recommended in the current research, too cold and you activate shivering thermogenesis, which you don't want. Cold exposure also appears to be less effective in obese vs. lean subjects. You could always do it the first couple of weeks of supplementation to speed up browning then just let Brite take it from there. Seems like kind of a pain in the ass to do long-term.
 
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Also, as Matt alluded to, the peppermint oil in Brite activates TRPM8, which mimics cold therapy.
 

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My understanding is that this would be NOT useful to tackle the abdominal area. Not really a product for those who already fairly lean?
 
tyga tyga

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Something you could supplement year around?
 

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Will this product make the user feel warmer? I am usually cold at night, and I am going to move a place that will get quite cold in the winter (and I hate the cold) so it would be a good product for me if it created a feeling of warmth.
 
dsade

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Will this product make the user feel warmer? I am usually cold at night, and I am going to move a place that will get quite cold in the winter (and I hate the cold) so it would be a good product for me if it created a feeling of warmth.
I did notice a warming sensation initially, but it wasn't dramatic.
 
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Something you could supplement year around?
Definitely the design for it...a long term phenotype shifting product. Cause Brite cells to proliferate (wrong word), and WAT to turn beige, what you will do is increase the amount of fatty acids you burn doing even the most ordinary, mundane things. Overall, without specialized effort, you will remain leaner.

The effects should grow even stronger the longer you take it.
 
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My understanding is that this would be NOT useful to tackle the abdominal area. Not really a product for those who already fairly lean?
This really won't specially target any area in particular. This product WILL work for those that are fairly lean - especially if they want to stay that way with less effort.
 
Misfit28

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Wow, I may just have to pick up some of this!
 
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I did just find a place that is offering low minimum softgels, but that means many different things to many different people. Just waiting on a phone call back.
 

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This really won't specially target any area in particular. This product WILL work for those that are fairly lean - especially if they want to stay that way with less effort.
Stay lean with less effort... I'm sold! Would this allow me to increase calories and/or cheat meals while maintaining base weight?

Any stacking suggestions?
 
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There are two products I would stack this with for INCREDIBLE results....

First would be KetoForce. Second would be the upcoming product by Antaeus Labs. They have decided to try a variation of the BRITE product using a couple of different angles, which should be complementary
 
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There are two products I would stack this with for INCREDIBLE results....

First would be KetoForce. Second would be the upcoming product by Antaeus Labs. They have decided to try a variation of the BRITE product using a couple of different angles, which should be complementary
would you suggest using ketoforce even if not doing keto?
 
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would you suggest using ketoforce even if not doing keto?
I don't do keto, and I found KetoForce to be effective right before bed...especially if stacked with something like Slintensity and a single capsule of Defuse.

I have even designed a nighttime keto inducer product, but there are some pre-arranged ingredient agreements between Prototype and someone else for what I wanted to use.
 
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Is there a reason it can't be taken in liquid form/needs to be capped?
The other option is an oil squirter. The dosage wouldn't be very accurate, and the suspended powders could clog the sprayer. It's also not bad, but not wonderful tasting.
 
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The other option is an oil squirter. The dosage wouldn't be very accurate, and the suspended powders could clog the sprayer. It's also not bad, but not wonderful tasting.
I was thinking oral syringe.
 
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I was thinking oral syringe.
Big pain in the ass. Full dosage of 9g per day means I'm having to use 8 ounce bottles. I used to be in charge of the manufacturing for the SesaThin and the whole capping/syringe thing is a huge pain.

Ultimately, to ever see viable sales volume, this will have to be softgelled.
 
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Big pain in the ass. Full dosage of 9g per day means I'm having to use 8 ounce bottles. I used to be in charge of the manufacturing for the SesaThin and the whole capping/syringe thing is a huge pain.

Ultimately, to ever see viable sales volume, this will have to be softgelled.
Gotcha. Is the 9g taken all at once or spread out? Would you consider the dosing weight dependent?
 
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Gotcha. Is the 9g taken all at once or spread out? Would you consider the dosing weight dependent?
DEFINITELY spread out. You will regret taking over 3g of Tung oil at once time, trust me.

You could probably get away with 6-7g.
 

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DEFINITELY spread out. You will regret taking over 3g of Tung oil at once time, trust me.

You could probably get away with 6-7g.
What kind of 'side effects' can one expect from taking Brite all at once?
 
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