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Blog – Redcon1 Online Official https://redcon1online.com The Highest State of Readiness Fri, 18 Aug 2017 17:59:31 +0000 en-US hourly 1 https://wordpress.org/?v=6.5.2 HIIT VS Steady State https://redcon1online.com/hiit-vs-steady-state/ Fri, 18 Aug 2017 16:00:32 +0000 https://redcon1online.com/?p=4610

Head Trainer at Redcon1, Joe Bennett, better known as The Hypertrophy Coach, is back today to tell us which form of cardio is best: HIIT vs. Steady State. High Intensity Interval Training (HIIT) is much more metabolic on the body, meaning it has a greater impact on your total energy expenditure and calorie burn over the course of the entire day when compared to steady state cardio. If done properly, HIIT is not taxing on the body. Joe gives three options for HIIT exercises: Spin bike, sled push, high incline hills. The biggest factor in determining if you should do HIIT on a given day is how much glycogen have you consumed and currently have stored in your body. If you are on low carbohydrates and depleted, HIIT is not your best option. Start with 3-5 sets of intervals at 15-20 seconds duration for each. Joe recommends picking exercises that you enjoy doing and are more likely to stick to.

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Fat loss through Redcon1’s Double Tap burner https://redcon1online.com/fat-loss-double-tap-burner/ Thu, 10 Aug 2017 16:24:15 +0000 https://redcon1online.com/?p=4487 The goal of losing weight can be a daunting one. Be it for contest prep for a bodybuilding show or just general fitness goals, weight loss is often difficult to achieve. At some point in our lives, we’ve all looked at the scale and decided it was time to lose a few pounds. Likewise, we’ve all experienced the monotony of dieting and wondered if there was any easier way to accomplish what we set out to do. Fortunately just such a shortcut exists. Double Tap is a powder supplement containing numerous ingredients conducive to weight loss. If you’re seeking increased fat burning ability, extra drive in the gym, or increased mental clarity then Double Tap has got everything you’re looking for. In order to get a better idea of just how Double Tap works let’s examine the primary ingredients it contains, and how they work their magic.

Acetyl l-carnitine is the primary ingredient contained inside Double Tap, and is an amino acid. Commonly used as a component in fat loss products, acetyl l-carnitine has seen widespread use in supplements for many years. The primary means through which it accomplishes this task is by encouraging the uptake of fatty acids (hydrocarbon chains typically found in fats and oils) into your cells. From this point, cellular mitochondria utilize these fatty acids in what is known as the Krebs Cycle, which ultimately causes the output of energy. One gram of acetyl l-carnitine is contained in the recommended dose from Double Tap, and it is important to follow this dosing carefully. Excessive use will cause buildup of a molecule known as acetyl-CoA (coenzyme A) which causes carbohydrates to be used instead of fatty acids.

Next on the ingredients listed in Double Tap comes choline bitartrate, a water-soluble vitamin-like nutrient. When used for their fat loss capabilities, choline supplements rely on their ability to slightly elevate the body’s rate of lipolysis in order to bring about change. Lipolysis is a complex process involving the metabolism of lipids (fats) and is typically induced by certain hormones. Double Tap’s inclusion of choline into its formula speeds up the rate that this process happens at, allowing you to burn fat even sooner.

The third substance listed on the Double Tap label (green tea extract) may surprise you. Green tea however has long been known to possess some simple basic weight loss benefits, due to its makeup. Green tea contains a class of antioxidants known as catechins, which are the source of the tea extract’s fat loss properties. Simply put, catechins work by slightly increasing the typical rate at which your body utilizes energy. This causes increased need for energy output, and translates to more fats being metabolized. Furthermore, the caffeine inherent in the green tea extract acts (as caffeine always does) as a mild stimulant, serving to depress the consumer’s appetite. It is worth noting however that green tea’s ability to promote fat loss depends highly on the user not being caffeine-resistant prior to consumption, so it’s a good idea for consumers of Double Tap to cut back on their caffeine intake. Also ensure proper hydration during use, as caffeine is a natural diuretic.

Lastly we’ll discuss 2-aminoisoheptane, another stimulant. Aminoisoheptane is a somewhat newer ingredient, having very little exposure on the supplement market thus far. Relatively little is known about it, but it is believed to function in a method similar to tuaminoheptane. Its value is due to its ability to support high energy levels while simultaneously reducing appetite among users.

Through these ingredients, Double Tap covers multiple bases with its formula. Mental focus and improved physical drive are key to increased performance in the gym (especially to athletes on a reduced diet). Its ability to reduce appetite combined with its fat loss components greatly assist the athlete who utilizes it. Double Tap comes in powder form, making it easily combinable with preworkout supplements or just as simple to take on its own.

Overall, Double Tap is one of the most potent fat burning products on the market. Few others can match its overall potential to aid the user in their weight loss goals through the use of multiple different pathways and ingredients. Commonly, rival fat loss products will base their formula on one or two individually weak substances. Contrast this to Double Tap’s ingredient list, which is a veritable laundry list of components to bring you that much closer to your goals. In an industry swamped with outdated and non-scientific backed products, Double Tap stands out even more. The second-to-none potential contained in this powerhouse leaves it as the clear choice for bodybuilders and fitness athletes across the world.

Written by Trent Wozniak

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The Forgotten Vitamin K https://redcon1online.com/vitamin-k/ Fri, 04 Aug 2017 04:00:42 +0000 https://redcon1online.com/?p=4378 With pre-workouts and amino acid products flooding the market, the basic health supplements sadly take a back seat. Don’t get me wrong, ergogenic aids like pre workouts and amino acid products are heavily stocked on my supplement shelf because those are the products that will directly help you build muscle and lose body fat, but what about indirectly? If you’re not functioning and operating at 100%, why would your body spend valuable energy and resources to build muscle? Your body only cares about survival, not how lean you are or how much muscle you can hold on your frame…this is where health supplements like the forgotten vitamin k come into play!

Vitamin K is an essential vitamin that is one of the four fat-soluble vitamins. Vitamin K comes in different forms (vitamers) that are either phylloquinones (vitamin K1) or menaquinones (vitamin K2 which is abbreviated as MK-x.) The three forms of vitamin K that can be utilized by the body are vitamin K1 and dual forms of K2 (MK-4 and MK-7.) The health benefits of vitamin k seem endless and include regression of preformed arterial calcification, maintenance of bone density, and promotion of a healthy heart and vascular system. As with all of my articles, I do not feel making claims on a product or ingredient is good enough. Instead, we must dig into the research…and luckily for us. vitamin k has well over 400 studies that I have personally read over the years. The first one I wish to look at is from Knapen et al and looked at a three-year low-dose menaquinone-7 supplementation and how it helps decrease bone loss. The results were that MK-7 intake significantly improved vitamin K status and decreased the age-related decline in BMC and BMD at the lumbar spine and femoral neck, but not at the total hip. Bone strength was also favorably affected by MK-7. MK-7 significantly decreased the loss in vertebral height of the lower thoracic region at the mid-site of the vertebrae. This lead to their conclusion that MK-7 supplements may help  to prevent bone loss (1.)

But even more importantly that aiding in bone mineral density is its ability to fight atherosclerosis (as this is my main reason for recommending this vitamin to bodybuilders that are using potentially harsh supplements that can cause atherosclerosis over time.) Jennifer Ming has talked extensively on this topic stating that “numerous studies have demonstrated that people with higher intakes of vitamin K2 have a reduced risk for cardiovascular disease.  Intrigued by this connection, Polish researchers from the Medical University at Lodz teamed up with researchers from Maastricht University in the Netherlands and Poland’s International Science and Health Foundation to determine if vitamin K2 supplementation could reduce the progression of existing atherosclerosis. The scientists evaluated the progression of atherosclerosis in a group of 42 patients with chronic kidney disease. These patients were ideal for this type of study because they are known to experience a rapid reduction in bone mineral density (a measure of bone strength) as a result of calcium losses from bone. They are also subject to equally excessive deposits of calcium in tissues where it doesn’t belong—particularly in the walls of major arteries. For the study, the subjects were divided into two groups. One group received vitamin K2 (90 mcg per day) plus vitamin D3 (400 IU per day). The second group received only vitamin D3 (400 IU per day). After nine months, it was already evident that the subjects taking the combination of vitamins K2 and D3 experienced a slower progression of the Common Carotid Intima Media Thickness, which is a good indicator of atherosclerosis, as well as a predictor of cardiovascular episodes and death. Specifically, the thickness of the carotid (major neck) arteries increased by 13.73% in the group taking vitamin D3, but in the group taking both vitamins, it only increased by 6.32%. Remember that the group of subjects in this study have a tendency for an increased carotid intima media thickness as a result of calcium losses from bone. In addition, subjects taking the combination of vitamins K2 and D3 showed a reduction in carotid artery calcification score in all patients except those with the highest scores at baseline. This indicates that calcium was staying in the bones, where it belongs, and out of the arteries. These results clearly indicated that vitamin K2 does indeed reduce the progression of atherosclerosis” (2, 3, 4.)

Vitamin K clearly has a place on everyone’s health supplement shelf and has more than enough literature and actual application to back that statement up. In terms of practical application, we need to look at a few different minimum effective dosages for the various forms of vitamin k. For phylloquinone (vitamin K1), the minimum effective dosage is 50mcgs. For short chain menaquinones (MK-4), the minimum effective dosage is 1500mcgs. For the longer chain menaquinones (MK-7, MK-8, and MK-9), the minimum effective dose is around 100-250mcgs. So be sure to purchase a vitamin k product that contains the effective forms of vitamin k and in the proper dosages.

Alex Kikel

MS, PES, CPT, Speed and Explosion Specialist Level II

Owner of www.theprepcoach.com

References

  1. Three-year low-dose menaquinone-7 supplementation helps decrease bone loss in healthy postmenopausal women. M. H. J. Knapen, N. E. Drummen, E. Smit, C. Vermeer, E. Theuwissen. Osteoporos Int. 2013 (https://www.ncbi.nlm.nih.gov/pubmed/23525894)
  2. Dietary intake of menaquinone is associated with a reduced risk of coronary heart disease: the Rotterdam Study. Johanna M. Geleijnse, Cees Vermeer, Diederick E. Grobbee, Leon J. Schurgers, Marjo H. J. Knapen, Irene M. van der Meer, Albert Hofman, Jacqueline C. M. Witteman. J Nutr. 2004 (https://www.ncbi.nlm.nih.gov/pubmed/15514282)
  3. Effect of vitamin K2 on progression of atherosclerosis and vascular calcification in nondialyzed patients with chronic kidney disease stages 3-5. Ilona Kurnatowska, Piotr Grzelak, Anna Masajtis-Zagajewska, Magdalena Kaczmarska, Ludomir Stefańczyk, Cees Vermeer, Katarzyna Maresz, Michał Nowicki. Pol Arch Med Wewn. 2015 (https://www.ncbi.nlm.nih.gov/pubmed/26176325)
  4. Is Coronary Artery Calcification Associated with Vertebral Bone Density in Nondialyzed Chronic Kidney Disease Patients? Filgueira, A., Carvalho, A. B., Tomiyama, C., Higa, A., Rochitte, C. E., Santos, R. D., & Canziani, M. E. F. (2011). Clinical Journal of the American Society of Nephrology. (https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3109944/)
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Super Berberine https://redcon1online.com/super-berberine/ Thu, 03 Aug 2017 04:00:59 +0000 https://redcon1online.com/?p=4375 Berberine is a very popular glucose disposal agent (GDA) on the market that has caught the interest of many. Berberine is an alkaloid extracted from various plants that plays a role in reducing inflammation, improving intestinal health, possibly reducing cholesterol, as well as being a diabetic aid due to its ability to reduce glucose production in the liver. Its main mechanism os through activation of Adenosine Monophosphate-Activated Protein Kinase (AMPK) while inhibiting Protein-Tyrosine Phosphatase 1B (PTP1B). As it works through AMPK inhibition, it will only reduce blood sugar levels if they are elevated. We typically see berberine being used mainly for its glucose disposal effects so we will focus on that aspect during this article, please note however it has a host of other benefits.

A randomized, parallel controlled, open-label clinical trial was conducted to evaluate the effect of a botanic compound berberine (BBR) on NAFLD from Yan et al. A total of 184 eligible patients with NAFLD were enrolled and randomly received (i) lifestyle intervention (LSI), (ii) LSI plus pioglitazone (PGZ) 15mg qd, and (iii) LSI plus BBR 0.5g tid, respectively, for 16 weeks. Hepatic fat content (HFC), serum glucose and lipid profiles, liver enzymes and serum and urine BBR concentrations were assessed before and after treatment. We also analyzed hepatic BBR content and expression of genes related to glucose and lipid metabolism in an animal model of NAFLD treated with BBR. As compared with LSI, BBR treatment plus LSI resulted in a significant reduction of HFC (52.7% vs 36.4%, p = 0.008), paralleled with better improvement in body weight, HOMA-IR, and serum lipid profiles (all p<0.05). BBR was more effective than PGZ 15mg qd in reducing body weight and improving lipid profile. BBR-related adverse events were mild and mainly occurred in digestive system. Serum and urine BBR concentrations were 6.99ng/ml and 79.2ng/ml, respectively, in the BBR-treated subjects. Animal experiments showed that BBR located favorably in the liver and altered hepatic metabolism-related gene expression. BBR ameliorates NAFLD and related metabolic disorders. The therapeutic effect of BBR on NAFLD may involve a direct regulation of hepatic lipid metabolism (1.)

The second study I wanted us to look at was one from Zhang et al. The objective of the study was to evaluate the efficacy and safety of berberine in the treatment of type 2 diabetic patients with dyslipidemia. One hundred sixteen patients with type 2 diabetes and dyslipidemia were randomly allocated to receive berberine (1.0 g daily) and the placebo for 3 months. The primary outcomes were changes in plasma glucose and serum lipid concentrations. Glucose disposal rate (GDR) was measured using a hyperinsulinemic euglycemic clamp to assess insulin sensitivity. In the berberine group, fasting and postload plasma glucose decreased from 7.0 +/- 0.8 to 5.6 +/- 0.9 and from 12.0 +/- 2.7 to 8.9 +/- 2.8 mm/liter, HbA1c from 7.5 +/- 1.0% to 6.6 +/- 0.7%, triglyceride from 2.51 +/- 2.04 to 1.61 +/- 1.10 mm/liter, total cholesterol from 5.31 +/- 0.98 to 4.35 +/- 0.96 mm/liter, and low-density lipoprotein-cholesterol from 3.23 +/- 0.81 to 2.55 +/- 0.77 mm/liter, with all parameters differing from placebo significantly (P < 0.0001, P < 0.0001, P < 0.0001, P = 0.001, P < 0.0001, and P <0.0001, respectively). The glucose disposal rate was increased after berberine treatment (P = 0.037), although no significant change was found between berberine and placebo groups (P = 0.063). Mild to moderate constipation was observed in five participants in the berberine group. They concluded stating that “Berberine is effective and safe in the treatment of type 2 diabetes and dyslipidemia” (2.)

Now that we know from a literary standpoint that berberine itself is a very potent glucose disposal agent, I wanted to look specifically at Super Berberine, also known as Berberine-Cyclodextrin Complex (this just means that the berberine is complexed with cyclodextrins.) Cyclodextrins are sugar molecules bound into a ring- or doughnut-shape, which can be used to increase the solubility of other compounds by the formation of inclusion complexes. The insoluble compound is held in the hydrophobic cavity, and the cyclodextrin acts as a water-soluble “carrier” molecule. This makes berberine more soluble leading to a greater bioavailabliltiy than normal berberine and also makes it less bitter because the complexed molecules do not interact as fully with our taste buds (3, 4, 5.) As this form of berberine is enhanced, that typically means its a trademarked ingredient (which this is.) That means its typically only found in higher end GDAs. Partition-Elite from Prime Nutrition contains super berberine at a very effective dosage of 50mgs (due to the fact that the bioavailability is enhanced and is combined with eight other GDAs.) So if you’re looking to implement Super Berberine, try out Partition-Elite with a higher carbohydrate meal and monitor as it will increase insulin sensitivity, promotes a positive partitioning environment where you store more calories in muscle cells instead of fat cells, and helps in keeping you growing leaner.

Alex Kikel

MS, PES, CPT, Speed and Explosion Specialist Level II

Owner of www.theprepcoach.com

References

  1. Efficacy of Berberine in Patients with Non-Alcoholic Fatty Liver Disease. Hong-Mei Yan, Ming-Feng Xia, Yan Wang, Xin-Xia Chang, Xiu-Zhong Yao, Sheng-Xiang Rao, Meng-Su Zeng, Yin-Fang Tu, Ru Feng, Wei-Ping Jia, Jun Liu, Wei Deng, Jian-Dong Jiang, Xin Gao. PLoS One. 2015 (https://www.ncbi.nlm.nih.gov/pubmed/26252777)
  2. Treatment of type 2 diabetes and dyslipidemia with the natural plant alkaloid berberine. Yifei Zhang, Xiaoying Li, Dajin Zou, Wei Liu, Jialin Yang, Na Zhu, Li Huo, Miao Wang, Jie Hong, Peihong Wu, et al. J Clin Endocrinol Metab. 2008 (https://www.ncbi.nlm.nih.gov/pubmed/18397984)
  3. Study on the Interaction of β-Cyclodextrin and Berberine Hydrochloride and Its Analytical Application. Jia, B., Li, Y., Wang, D., & Duan, R. (2014). (https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4014474/)
  4. A simple fluorescence quenching method for berberine determination using water-soluble CdTe quantum dots as probes. Ming Cao, Meigui Liu, Chun Cao, Yunsheng Xia, Linjun Bao, Yingqiong Jin, Song Yang, Changqing Zhu. Spectrochim Acta A Mol Biomol Spectrosc. 2010 (https://www.ncbi.nlm.nih.gov/pubmed/20093069)
  5. Significant fluorescence enhancement by supramolecular complex formation between berberine chloride and cucurbit(n=7)uril and its analytical application. Nan Dong, Li-na Cheng, Xiu-lin Wang, Qin Li, Chuan-yu Dai, Zhu Tao. Talanta. 2011 (https://www.ncbi.nlm.nih.gov/pubmed/21482268)
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Grow While You Sleep https://redcon1online.com/grow-while-you-sleep/ Wed, 26 Jul 2017 04:00:29 +0000 https://redcon1online.com/?p=4326 I’ve written articles in the past for how important sleep is for your physique to develop. But now, I want to take things a step further and look specifically at how we can maximize our sleep to increase growth and development as a whole. This takes into consideration that fact that you’re getting a minimum of seven hours of sleep and will be utilizing the follow supplement ingredients to simply enhance an already optimal sleeping regimen. The ingredients we will be discussing are GABA, Taurine, and Mucuna Puriens.

First off, lets look into GABA! GABA is known as the ‘downer’ neurotransmitter that counters glutamate and has a tough time crossing the blood brain barrier. GABA is the main inhibitory neurotransmitter of the CNS. It is well established that activation of GABA(A) receptors favors sleep. Three generations of hypnotics are based on these GABA(A) receptor-mediated inhibitory processes. The first and second generation of hypnotics (barbiturates and benzodiazepines respectively) decrease waking, increase slow-wave sleep and enhance the intermediate stage situated between slow-wave sleep and paradoxical sleep, at the expense of this last sleep stage. The third generation of hypnotics (imidazopyridines and cyclopyrrolones) act similarly on waking and slow-wave sleep but the slight decrease of paradoxical sleep during the first hours does not result from an increase of the intermediate stage. It has been shown that GABA(B) receptor antagonists increase brain-activated behavioral states (waking and paradoxical sleep: dreaming stage). Recently, a specific GABA(C) receptor antagonist was synthesized and found by i.c.v. infusion to increase waking at the expense of slow-wave sleep and paradoxical sleep. Since the sensitivity of GABA(C) receptors for GABA is higher than that of GABA(A) and GABA(B) receptors, GABA(C) receptor agonists and antagonists, when available for clinical practice, could open up a new era for therapy of troubles such as insomnia, epilepsy and narcolepsy. They could possibly act at lower doses, with fewer side effects than currently used drugs (1.)

Second, we look into taurine. Taurine is an organic acid which acts as a lipid/membrane stablilizer in the body and is one of the major inhibitory amino acid neurotransmitters in the brain along with the previously mentioned GABA. When Taurine reaches the brain, it interacts with GABA receptors in the thalamus which is involved in controlling how much sensory information is forwarded to the processing cortex of the brain. Its in this way that taurine is more like a depressant than a stimulant and results in a suppression of excitatory activity. Lin et al stated in a paper entitled the “Effect of taurine and caffeine on sleep–wake activity in Drosophila melanogaster” thatTaurine is a GABA receptor agonist, which is inhibitory to neuronal firing. We show here that flies receiving a low dose of caffeine (0.01%) increase locomotor activity by 25%, and decrease total sleep by 15%. Treatment with taurine at 0.1% to 1.5% reduces locomotor activity by 28% to 86%, and shifts it from diurnal to nocturnal. At 0.75%, taurine also increases total sleep by 50%. Our results show that taurine increases sleep, while caffeine, as previously reported, attenuates sleep. Flies treated with both caffeine and taurine exhibit two differential effects which depend upon the ratio of taurine to caffeine. A high taurine:caffeine ratio promotes sleep, while a low ratio of taurine:caffeine inhibits sleep to a greater extent than the equivalent amount of caffeine alone” (2.)

Last, we look into Mucuna Puriens. Mucuna Pruriens are beans that are a good source of L-DOPA. One of the main reasons I’m a big fan of mucuna pruriens is because of their ability to induce a feeling of well being which aids in cortisol reductions and clearly is a good choice when looking at improving your quality of sleep. Shukla et al stated “This study included 60 subjects who were undergoing infertility screening and were found to be suffering from psychological stress, assessed on the basis of a questionnaire and elevated serum cortisol levels. Age-matched 60 healthy men having normal semen parameters and who had previously initiated at least one pregnancy were included as controls. Infertile subjects were administered with M. pruriens seed powder (5 g day(-1)) orally. For carrying out morphological and biochemical analysis, semen samples were collected twice, first before starting treatment and second after 3 months of treatment. The results demonstrated decreased sperm count and motility in subjects who were under psychological stress. Moreover, serum cortisol and seminal plasma lipid peroxide levels were also found elevated along with decreased seminal plasma glutathione (GSH) and ascorbic acid contents and reduced superoxide dismutase (SOD) and catalase activity. Treatment with M. pruriens significantly ameliorated psychological stress and seminal plasma lipid peroxide levels along with improved sperm count and motility. Treatment also restored the levels of SOD, catalase, GSH and ascorbic acid in seminal plasma of infertile men. On the basis of results of the present study, it may be concluded that M. pruriens not only reactivates the anti-oxidant defense system of infertile men but it also helps in the management of stress and improves semen quality” (3.)

There are obviously more tremendous sleep aids when it comes to supplementation but GABA, Taurine, and Mucuna Puriens are three that are easily in my top ten favorite sleep ingredients along with melatonin, l-theanine, and a few others. Luckily, GABA, Mucuna Puriens, melatonin, and l-theanine are all in RedCon1’s sleep product Fade Out which also contains other ingredients to aid in growth hormone support, getting you into a deeper REM sleep, as well as to improve muscle recovery!

Alex Kikel

MS, PES, CPT, Speed and Explosion Specialist Level II

Owner of www.theprepcoach.com

References

  1. GABA mechanisms and sleep. Claude Gottesmann. Neuroscience. 2002 (https://www.ncbi.nlm.nih.gov/pubmed/11983310)
  2. Effect of taurine and caffeine on sleep–wake activity in Drosophila melanogaster. Lin, F. J., Pierce, M. M., Sehgal, A., Wu, T., Skipper, D. C., & Chabba, R. (2010).  Nature and Science of Sleep. (https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3630960/)
  3. Mucuna pruriens Reduces Stress and Improves the Quality of Semen in Infertile Men, Kamla Kant Shukla, Abbas Ali Mahdi, Mohammad Kaleem Ahmad, Shyam Pyari Jaiswar, Satya Narain Shankwar, Sarvada Chandra Tiwari. Evid Based Complement Alternat Med. 2010 (https://www.ncbi.nlm.nih.gov/pubmed/18955292)
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Is Beta Alanine In YOUR Preworkout?! https://redcon1online.com/beta-alanine-preworkout/ Mon, 24 Jul 2017 17:11:05 +0000 https://redcon1online.com/?p=4320 Beta Alanine is an ingredient that is very popular in the supplement community but really isn’t discussed very much (and sadly usually isn’t dosed properly in many formulas on the market.) I think you should not only know what beta alanine is but also what it does, why you want it, and which products actually have clinical dosages (or proper dosages for lack of a better term.) Beta-alanine, the building block of carnosine, helps buffer acid in muscles and increases physical performance in the 60–240-second range. When beta-alanine is ingested, it turns into carnosine, which acts as that acid buffer. Carnosine is stored in cells and released in response to drops in pH. Paresthesia, the tingling feeling, can be caused by bigger dosages of beta alanine but it is simply a harmless side effect that usually disappears with usage. Beta Alanine has been shown to aid in increasing power, endurance, and reducing time to fatigue (along with a number of other benefits.)

Increased power output from muscle carnosine was shown by one of the more popular studies from Baguet et al in rowing performance. Chronic oral β-alanine supplementation is shown to elevate muscle carnosine content and improve anaerobic exercise performance during some laboratory tests, mainly in the untrained. It remains to be determined whether carnosine loading can improve single competition-like events in elite athletes. The aims of the present study were to investigate if performance is related to the muscle carnosine content and if β-alanine supplementation improves performance in highly trained rowers. Eighteen Belgian elite rowers were supplemented for 7 wk with either placebo or β-alanine (5 g/day). Before and following supplementation, muscle carnosine content in soleus and gastrocnemius medialis was measured by proton magnetic resonance spectroscopy ((1)H-MRS) and the performance was evaluated in a 2,000-m ergometer test. At baseline, there was a strong positive correlation between 100-, 500-, 2,000-, and 6,000-m speed and muscle carnosine content. After β-alanine supplementation, the carnosine content increased by 45.3% in soleus and 28.2% in gastrocnemius. Following supplementation, the β-alanine group was 4.3 s faster than the placebo group, whereas before supplementation they were 0.3 s slower (P = 0.07). Muscle carnosine elevation was positively correlated to 2,000-m performance enhancement (P = 0.042 and r = 0.498). It can be concluded that the positive correlation between baseline muscle carnosine levels and rowing performance and the positive correlation between changes in muscle carnosine and performance improvement suggest that muscle carnosine is a new determinant of rowing performance (1.)

Hobson et al conducted a very important bit of literature on beta alanine supplementation and its direct effects on exercise performance in a meta analysis. They stated that “due to the well-defined role of β-alanine as a substrate of carnosine (a major contributor to H+ buffering during high-intensity exercise), β-alanine is fast becoming a popular ergogenic aid to sports performance. There have been several recent qualitative review articles published on the topic, and here we present a preliminary quantitative review of the literature through a meta-analysis. A comprehensive search of the literature was employed to identify all studies suitable for inclusion in the analysis; strict exclusion criteria were also applied. Fifteen published manuscripts were included in the analysis, which reported the results of 57 measures within 23 exercise tests, using 18 supplementation regimes and a total of 360 participants [174, β-alanine supplementation group (BA) and 186, placebo supplementation group (Pla)]. BA improved (P=0.002) the outcome of exercise measures to a greater extent than Pla [median effect size (IQR): BA 0.374 (0.140-0.747), Pla 0.108 (-0.019 to 0.487)]. Some of that effect might be explained by the improvement (P=0.013) in exercise capacity with BA compared to Pla; no improvement was seen for exercise performance (P=0.204). In line with the purported mechanisms for an ergogenic effect of β-alanine supplementation, exercise lasting 60-240 s was improved (P=0.001) in BA compared to Pla, as was exercise of >240 s (P=0.046). In contrast, there was no benefit of β-alanine on exercise lasting <60 s (P=0.312). The median effect of β-alanine supplementation is a 2.85% (-0.37 to 10.49%) improvement in the outcome of an exercise measure, when a median total of 179 g of β-alanine is supplemented” (2.)

Finally, we’ll conclude on its ability to reduce fatigue from the works of Hoffman et al. The purpose of this study was to examine the effect of 30 days of beta-alanine supplementation in collegiate football players on anaerobic performance measures. Subjects were randomly divided into a supplement (beta-alanine group [BA], 4.5 g x d(-1) of beta-alanine) or placebo (placebo group [P], 4.5 g x d(-1) of maltodextrin) group. Supplementation began 3 weeks before preseason football training camp and continued for an additional 9 days during camp. Performance measures included a 60-second Wingate anaerobic power test and 3 line drills (200-yd shuttle runs with a 2-minute rest between sprints) assessed on day 1 of training camp. Training logs recorded resistance training volumes, and subjects completed questionnaires on subjective feelings of soreness, fatigue, and practice intensity. No difference was seen in fatigue rate in the line drill, but a trend (P = .07) was observed for a lower fatigue rate for BA compared with P during the Wingate anaerobic power test. A significantly higher training volume was seen for BA in the bench press exercise, and a trend (P = .09) for a greater training volume was seen for all resistance exercise sessions. In addition, subjective feelings of fatigue were significantly lower for BA than P. In conclusion, despite a trend toward lower fatigue rates during 60 seconds of maximal exercise, 3 weeks of beta-alanine supplementation did not result in significant improvements in fatigue rates during high-intensity anaerobic exercise. However, higher training volumes and lower subjective feelings of fatigue in BA indicated that as duration of supplementation continued, the efficacy of beta-alanine supplementation in highly trained athletes became apparent (3.)

It is clear that beta alanine is a supplement that is beyond beneficial for any athletic endeavor! In these studies, we see a wide array of dosages from 2 grams all the way up to 5 grams. It has been concluded that 3.2 grams of beta alanine is the accepted clinical dosage. If your taking a pre workout that has LESS than that clinical amount then you’re pretty much wasting your money as you will not reap the full benefits. Luckily, supplements like Total War from RedCon1 provide the full 3.2 gram clinical dosage of beta alanine along with other great ergogenic aids like citrulline malate, agmatine sulfate, and a number of others ALL having the correct clinical dosage.

Alex Kikel

MS, PES, CPT, Speed and Explosion Specialist Level II

Owner of www.theprepcoach.com

References

  1. Important role of muscle carnosine in rowing performance. Audrey Baguet, Jan Bourgois, Lander Vanhee, Eric Achten, Wim Derave. J Appl Physiol (1985) 2010 (https://www.ncbi.nlm.nih.gov/pubmed/20671038)
  2. Effects of β-alanine supplementation on exercise performance: a meta-analysis. R. M. Hobson, B. Saunders, G. Ball, R. C. Harris, C. Sale. Amino Acids. 2012 (https://www.ncbi.nlm.nih.gov/pubmed/22270875)
  3. Short-duration beta-alanine supplementation increases training volume and reduces subjective feelings of fatigue in college football players. Jay R. Hoffman, Nicholas A. Ratamess, Avery D. Faigenbaum, Ryan Ross, Jie Kang, Jeffrey R. Stout, John A. Wise. Nutr Res. 2008 (https://www.ncbi.nlm.nih.gov/pubmed/19083385)
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Which Squat is Right For YOU? https://redcon1online.com/which-squat-is-right-for-you/ Fri, 21 Jul 2017 13:30:18 +0000 https://redcon1online.com/?p=4306
In this instructional video by Redcon1’s Head Trainer Joe Bennett, Joe discusses the three different squat variations and how they should be utilized around your ideal goal. For hip dominant squatters, the focus should lay on the glutes and hamstrings to carry the bulk of the load. Range of motion is import, but you do not want to go below parallel as that can cause you to lose a considerable amount of strength out of the bottom position. The second variation is a quad dominant squat (front squat or high bar back squat). Keep the body upright and knees forward. You should be going for full knee flexion. And finally, a competitors squat, or someone who’s sport is squatting. This variation of squat should be a combination of the two variances above. Again, Bennett emphasizes selecting exercises based around your individual goal, not just blindly following a program that isn’t suited for you.
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What nonsense is in your gym bag? With Lawrence Chappe https://redcon1online.com/whats-gym-bag-lawrence-chappe/ Wed, 05 Jul 2017 21:23:02 +0000 https://redcon1online.com/?p=4147

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Meal Prep- Mommy’s Corner https://redcon1online.com/meal-prep-mommys-corner/ Thu, 29 Jun 2017 21:52:11 +0000 https://redcon1online.com/?p=4103
6am wake up. 
Baby cries.
You have an appointment at 7am. 
Your rushing like crazy to get out the door. Shower, skip it. Change baby, feed baby, grab diaper bag and whatever else you need and your out the door. 
What did you forget? 
Your food. Now what. Maybe you figured you would stop while out. So, stop at a drive through? No. Coffee shop? Sure they might have a better option. Sound like a typical scenario? 
You will never get where you want to be if you keep yourself stuck in scenarios like this. Meal planning. It sounds overwhelming and scary but if you plan accordingly you can be prepared for these type of situations. The biggest excuse I hear is I don’t have time, but just like everything else you have to make time.  It truly doesn’t take that long to do a quick prep for the whole family. It just consists of buying in bulk. I’ll give you an example of what my family does. 
I buy about 5lbs of each protein. Ground beef, ground turkey, and chicken. We also buy salmon and shrimp at times when costs allow. The fastest and easiest way to prep this to grill. Make pattys. That way your portions are already sized as well. If your just doing a basic plan and not too concerned about weighing your food and what not just have one patty or chicken breast for a meal. Men have two. I use a scale though for all meals. I also bake at this time little white potatoes that come in a 4 lb bag and after those are done I switch the oven to broil and roast broccoli. To have more variety I’ll also do brussel sprouts or zucchini. When asparagus is on sale I go for that as well. Rice I prep while oven is on and make about two servings which when cooked is about 8 cups, depending on which rice you buy. Now if you want this to last just portion small meals into bags and throw in the freezer and take out what’s needed day to day. Otherwise you can leave the food in big containers in the fridge and just take out what you need each meal and it will last about 5 days in the fridge. For little extras you can buy avocado or fruit or whatever other little side dish like pickles (my daughter loves pickles!) or lettuce and have that with your meal. This way food is cooked for the week, your not scrambling for meals and you have no excuse not to eat clean. For condiments (be careful here since this is a lot of empty calories) read labels. We like hot sauce in our house. My husband likes soy sauce and mustard as well. Walden farms is a no calorie alternative. The issue with people eating clean is consistency. You can get creative with foods and things when you choose but what’s nice is all main food is cooked. If you choose to make pasta one night then add some of the ground beef to your sauce and ta da meal is done. I don’t always have time to cook a full dinner or lunch so it’s nice to grab and go. As for the munchies or snack attack, popcorn is a great alternative for when you just need that treat while relaxing watching your favorite show. Everything in moderation. Eating clean doesn’t have to be miserable. I’ll give you an example of my family’s day below. 
Breakfast for all of us is eggs, slice of grained bread (my husband has two slices and baby has Cheerios or pancake or puffs or oatmeal.) 
Snack. I have a small meal here. Chicken with some veggies and either rice or some potatoes. Baby has some cheese, fruit, and more egg if she didn’t eat much for breakfast
Lunch. For myself is again chicken with veggie or salad and baby had chicken and rice and a veggie. Craig eats the same just more. Chicken, rice, veggie. 
Snack. Baby has a all natural nutrigrain bar or fruit and puffs.
Dinner. I have a ground beef patty here with rice and veggie of choice. Baby will have a quesadilla I use ground beef and cheese or something else creative for her. Pickles are her favorite with dinner. Craig eats again same as I do unless he wants something else. This is where I make him the same as baby just more. I’ll do burritos (meat already cooked), fajitas just add more stir fry veggies, pasta or whatever he is in the mood for. 
Snack. For me since I’m on a plan I have my ground turkey with veggies. This is where Craig will have popcorn in down time and I have a tea to help with cravings. Baby is sleeping by this point. 
The point is, the main bulk of food/protein is cooked. I don’t have to stress what am I going to make. Some days I don’t feel like cooking so it’s nice to have meals ready on hand. 
Remember there is NO EXCUSE when you want a result bad enough. 
XOXO
 
-Wendy Lee Govoni Capurso    
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Sulforaphane to Inhibit Myostatin? 3 https://redcon1online.com/sulforaphane-inhibit-myostatin-3/ Sat, 24 Jun 2017 16:29:22 +0000 https://redcon1online.com/?p=4055 In closing, lets bring in its ability to act as a significant anti-inflammatory and anti-cancer agent. I would like to look at three pieces of literature. The first is on the inhibition of histone deacetylase 6 acetylates and disrupts the chaperone function of heat shock protein 90: a novel basis for antileukemia activity of histone deacetylase inhibitors by Bali et al. The second is on  histone deacetylase inhibitors: signalling towards p21cip1/waf1 from Matthias Ocker. The third and final is entitled “A novel mechanism of chemoprotection by sulforaphane: inhibition of histone deacetylase” from Myzak et al. The hydroxamic acid (HAA) analogue pan-histone deacetylase (HDAC) inhibitors (HDIs) LAQ824 and LBH589 have been shown to induce acetylation and inhibit the ATP binding and chaperone function of heat shock protein (HSP) 90. This promotes the polyubiquitylation and degradation of the pro-growth and pro-survival client proteins Bcr-Abl, mutant FLT-3, c-Raf, and AKT in human leukemia cells. HDAC6 is a member of the class IIB HDACs. It is predominantly cytosolic, microtubule-associated alpha-tubulin deacetylase that is also known to promote aggresome inclusion of the misfolded polyubiquitylated proteins. Here we demonstrate that in the Bcr-abl oncogene expressing human leukemia K562 cells, HDAC6 can be co-immunoprecipitated with HSP90, and the knock-down of HDAC6 by its siRNA induced the acetylation of HSP90 and alpha-tubulin. Depletion of HDAC6 levels also inhibited the binding of HSP90 to ATP, reduced the chaperone association of HSP90 with its client proteins, e.g. Bcr-Abl, and induced polyubiquitylation and partial depletion of Bcr-Abl. Conversely, the ectopic overexpression of HDAC6 inhibited LAQ824-induced acetylation of HSP90 and alpha-tubulin and reduced LAQ824-mediated depletion of Bcr-Abl, AKT, and c-Raf. Collectively, these findings indicate that HDAC6 is also an HSP90 deacetylase. Targeted inhibition of HDAC6 leads to acetylation of HSP90 and disruption of its chaperone function, resulting in polyubiquitylation and depletion of pro-growth and pro-survival HSP90 client proteins including Bcr-Abl. Depletion of HDAC6 sensitized human leukemia cells to HAA-HDIs and proteasome inhibitors (9.) Chromatin-modifying enzymes such as histone deacetylases (HDAC) facilitate a closed chromatin structure and hence transcriptional repression. HDAC are commonly affected in human cancer diseases. Thus, inhibition of HDAC represents a novel therapeutic approach. Several studies have shown that HDAC inhibitors strongly activate the expression of the cyclin-dependent kinase inhibitor p21(cip1/waf1) through (i) enhanced histone acetylation around the p21(cip1/waf1) promoter and (ii) the Sp1 sites on the p21(cip1/waf1) promoter releasing the repressor HDAC1 from its binding. p21(cip1/waf1) expression is regulated in a p53-dependent and p53-independent manner. The decision if p21(cip1/waf1) up-regulation results in cell cycle arrest or apoptosis, decides about the therapeutic efficacy of an anti-cancer treatment with HDAC inhibitors (10.) Sulforaphane (SFN), a compound found at high levels in broccoli and broccoli sprouts, is a potent inducer of phase 2 detoxification enzymes and inhibits tumorigenesis in animal models. SFN also has a marked effect on cell cycle checkpoint controls and cell survival and/or apoptosis in various cancer cells, through mechanisms that are poorly understood. We tested the hypothesis that SFN acts as an inhibitor of histone deacetylase (HDAC). In human embryonic kidney 293 cells, SFN dose-dependently increased the activity of a beta-catenin-responsive reporter (TOPflash), without altering beta-catenin or HDAC protein levels. Cytoplasmic and nuclear extracts from these cells had diminished HDAC activity, and both global and localized histone acetylation was increased, compared with untreated controls. Studies with SFN and with media from SFN-treated cells indicated that the parent compound was not responsible for the inhibition of HDAC, and this was confirmed using an inhibitor of glutathione S-transferase, which blocked the first step in the metabolism of SFN, via the mercapturic acid pathway. Whereas SFN and its glutathione conjugate (SFN-GSH) had little or no effect, the two major metabolites SFN-cysteine and SFN-N-acetylcysteine were effective HDAC inhibitors in vitro. Finally, several of these findings were recapitulated in HCT116 human colorectal cancer cells: SFN dose-dependently increased TOPflash reporter activity and inhibited HDAC activity, there was an increase in acetylated histones and in p21(Cip1/Waf1), and chromatin immunoprecipitation assays revealed an increase in acetylated histones bound to the P21 promoter. Collectively, these findings suggest that SFN may be effective as a tumor-suppressing agent and as a chemotherapeutic agent, alone or in combination with other HDAC inhibitors currently undergoing clinical trials (11.)

Sulforaphane’s ability to do everything we just discussed should make you want to start eating your broccoli as well as possibly supplementing with a good sulforaphane product (which is very few and fair between.) In terms of an applicable dosage, it seems that right around the 30mg per day mark is proven in literature to be beneficial (with some even dosing it up to double based on their body weight being higher.) Sulforaphane’s benefits are endless and is a must have health AND ergogenic aid supplement for any serious competitor (or at least it is in my eyes.)

References

  1. Protein oxidation and aging. E. R. Stadtman. Science. 1992 (https://www.ncbi.nlm.nih.gov/pubmed/1355616)
  2. Sulforaphane Activates Heat Shock Response and Enhances Proteasome Activity through Up-regulation of Hsp27. Nanqin Gan, Yu-Chieh Wu, Mathilde Brunet, Carmen Garrido, Fung-Lung Chung, Chengkai Dai, Lixin Mi. J Biol Chem. 2010 (https://www.ncbi.nlm.nih.gov/pubmed/20833711)
  3. Role of increased expression of the proteasome in the protective effects of sulforaphane against hydrogen peroxide-mediated cytotoxicity in murine neuroblastoma cells. Mi-Kyoung Kwak, Jeong-Min Cho, Bo Huang, Soona Shin, Thomas W. Kensler. Free Radic Biol Med. 2007 (https://www.ncbi.nlm.nih.gov/pubmed/17664144)
  4. Sulforaphane induced adipolysis via hormone sensitive lipase activation, regulated by AMPK signaling pathway. Ju-Hee Lee, Myung-Hee Moon, Jae-Kyo Jeong, Yang-Gyu Park, You-Jin Lee, Jae-Won Seol, Sang-Youel Park. Biochem Biophys Res Commun. 2012 (https://www.ncbi.nlm.nih.gov/pubmed/22982310)
  5. Identification and role of the basal phosphorylation site on hormone-sensitive lipase. A. J. Garton, S. J. Yeaman. Eur J Biochem. 1990 (https://www.ncbi.nlm.nih.gov/pubmed/2165906)
  6. 5-Aminoimidazole-4-carboxamide-1-beta-D-ribofuranoside-induced AMP-activated protein kinase phosphorylation inhibits basal and insulin-stimulated glucose uptake, lipid synthesis, and fatty acid oxidation in isolated rat adipocytes. Mandeep Pinky Gaidhu, Sergiu Fediuc, Rolando Bacis Ceddia. J Biol Chem. 2006 (https://www.ncbi.nlm.nih.gov/pubmed/16816404)
  7. Sulforaphane causes a major epigenetic repression of myostatin in porcine satellite cells. Huitao Fan, Rui Zhang, Dawit Tesfaye, Ernst Tholen, Christian Looft, Michael Hölker, Karl Schellander, Mehmet Ulas Cinar. Epigenetics. 2012 (https://www.ncbi.nlm.nih.gov/pubmed/23092945)
  8. Sulforaphane attenuates hepatic fibrosis via NF-E2-related factor 2-mediated inhibition of transforming growth factor-β/Smad signaling. Chang Joo Oh, Joon-Young Kim, Ae-Kyung Min, Keun-Gyu Park, Robert A. Harris, Han-Jong Kim, In-Kyu Lee. Free Radic Biol Med. 2012 (https://www.ncbi.nlm.nih.gov/pubmed/22155056)
  9. Inhibition of histone deacetylase 6 acetylates and disrupts the chaperone function of heat shock protein 90: a novel basis for antileukemia activity of histone deacetylase inhibitors. Purva Bali, Michael Pranpat, James Bradner, Maria Balasis, Warren Fiskus, Fei Guo, Kathy Rocha, Sandhya Kumaraswamy, Sandhya Boyapalle, Peter Atadja, et al. J Biol Chem. 2005 (https://www.ncbi.nlm.nih.gov/pubmed/15937340)
  10. Histone deacetylase inhibitors: signalling towards p21cip1/waf1. Matthias Ocker, Regine Schneider-Stock. Int J Biochem Cell Biol. 2007 (https://www.ncbi.nlm.nih.gov/pubmed/17412634)
  11. A novel mechanism of chemoprotection by sulforaphane: inhibition of histone deacetylase. Melinda C. Myzak, P. Andrew Karplus, Fung-Lung Chung, Roderick H. Dashwood. Cancer Res. 2004 (https://www.ncbi.nlm.nih.gov/pubmed/15313918)
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