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Hyperdrive 3.0 Plus NEW FORMULA! F ALRI Industries
Hyperdrive 3.0 Plus NEW FORMULA! F ALRI Industries - Click here for more info
ALR Venom Hyperdrive 3. 0 available at World Class Nutrition is for Adults 21 or over only!Okay, before anyone stresses out and sends us mean e-mails, Venom Hyperdrive 3. 0 by ALR Industries has the exact same ingredients and amounts as the original Venom plus two exception new ingredients. Of course it is a better product, but the other big plus is that, due to our ability to produce much larger volume, we have been able to make it more cost effective and pass the savings on to our customers. In short, thanks for loving the product. With World Class Nutrition offer of Venom Hyperdrive burn fat now. Venom Hyperdrive 3. 0™ from ALR Industries is a weight loss supplement designed for adults age 21 or over only. This is a diet product created for those adults who need the best environment for effective energy and fat metabolism for dramatic results through responsible application of a highly advanced formula. Directions: As a supplement begin by taking one (1) capsule first thing in the morning with food for first 2-3 days before progressing to one to two (1-2) capsules once daily(preferably in the morning…unless you are working the night shift) Always take this supplement with food and do not exceed recommended supplemental dosages. *Most report a single morning dosage with food is all they need for optimal energy levels and fat modulation synergy the entire day. So What Sets Venom™ Apart From the Rest?Anyone can mix a bunch of compounds or herbs together and shove it into a capsule. All too often this is followed by ads that promise the world but deliver next to nothing. This is not to say that all products in this category are bad, just that “some” create doubt upon those that perform as intended. So let’s look at the research supporting the value of the synergistic ingredients formulated for Venom™. Cocoamine™ (Only From ALR Industries)Cocoamine™ is trademarked and patent pending proprietary unique cocoa extract that provides the health benefits of chocolate without any of the unhealthy ingredients (you know, like sugar and fat). Please do not confuse Cocoamine™ with the patented ingredient Chocomine™. Our Cocoamine™ is a unique matrix standardized for nearly 98 percent actives. Try it before you judge it!Cocoamine™ contains several natural occurring substrates, including methylxanthines (theobromine, caffeine, and theophylline), biogenic-amines (phenylethylamine, tyramine, octopamine and synephrines), amino acids (phenylalanine, tryptophan, tyrosine, others), minerals (with a high content of magnesium) and several beneficial antioxidants. *You may think you have used a product similar to this, but one dose of Venom Hyperdrive 3. 0™ will show you how wrong you are. (Please start with only one capsule!)Phenylethylamine (PEA) is a naturally occurring endogenous neuroamine that increases attention and activity in animals as well as humans and has been studied for its ability to relieve depression in 60 percent of depressed patients. It has been proposed that PEA deficit may be the cause of a common form of depression. It is also your body’s most powerful natural stimulant. Interesting is that PEA improves mood as rapidly as amphetamine but does not produce tolerance. Okay, natural PEA good and amphetamine is bad. Though they share many common positive affects, the latter is not a good option due its own negative affects. Got it?Another interesting reality found in PEA research is its unique ability to stimulate striatal acetylcholine release. Big deal? Well, this neurotransmitter positively affects everything from libido to the sense of hunger with benefits to mood, focus and stress. Okay, and a positive effect upon erectile function has been noted in other studies. Big deal? You call it. Caffeine is an interesting and well know compound, certainly nothing new to the supplement industry. But there is some valuable research that shows a lot of potential benefits. Yes, everyone already knows that it is noted as a compound that increases energy significantly. In one rat study and several human studies, caffeine has show to have appetite suppressive value. Naturally most dieters cheat and can use all the will power they can get. Another study has shown caffeine to decrease fat redeposit and aid thermogenesis through fat oxidation. In part this appears to result in suppressed leptin (you know, the fat regulating hormone)Tyramine, Octopamine and Synephrines all have a positive effect upon beta-3 receptors thus increasing the rate of thermogenesis and metabolic rate. Many have compared the affects to those of ephedra mostly in a positive sense. Let me explain that a little better. Several studies have found that patients who achieve only a small weight loss during dietary therapy, and have a tendency for weight regain, are characterized by lower energy expenditure, lower sympathetic activity, and a reduced ability to mobilize fat stores, compared with patients who are more successful at losing weight. (gee, really?)It is reasonable to improve or normalize these traits by supporting the dietary approach with pharmacological/nutracuetical manipulation of central and peripheral pathways. Agents that stimulate adrenergic neurons are particularly suitable because they offer mechanisms for temporarily inhibiting hunger and for stimulating energy expenditure, lipolysis and fat oxidation. Interesting enough is that our bodies and diet can do this in a minimal way already…which means minimal results for your efforts. Supplementing these pathways with Venom Hyperdrive 3. 0™ has the obvious affect…super charged results. How (Science Geek Answer)?Sympathomimetic compounds can reduce appetite and increase energy expenditure. Energy expenditure can be increased by 5-10 percent via stimulation of a combination of beta-adrenoceptors; beta3-adrenoceptors may predominate during chronic use. This increased energy expenditure increases the relative proportion of fat oxidation; as this is not fully compensated by increased energy intake, a negative energy balance occurs. This mechanism may be responsible for the long-term weight loss efficiency of agents like, ephedra, octopamine, tyramine and synephrines. Noteworthy, the elevated plasma insulin of obese rats was lowered by octopamine. One study showed that octopamine can reduce body weight gain in obese rats, without apparent adverse effects, but with less efficacy than beta3-AR agonists. Both individually and combined the combination of these multiple ingredients produces a unique effect. Research has substantiated the many positive user feed-back factoids about Cocoamine™, including increased energy, appetite suppression, lipolysis (fat burning), improved mood, improved concentration, increased alertness, improved physical performance, aphrodisiac properties, and health benefits. When correctly processed, all of these benefits become a reality. Naturally this discussion is based upon the research sites listed at the end. (When I am done babbling)So What Else Is In It?The need for extreme appetite suppression seems to be a large factor in the out come of any diet intended to help lose body fat. So we added hoodia. One study appears to have explained why people report long term hunger suppression with the use of hoodia. It seems likely that increased ATP content/production in the hypothalamus may be a signal for energy-sensing of satiety. Next we included 5-HTP which acts as a precursor for serotonin (mood enhancement), R-ALA (R-Alpha Lipoic Acid) to aid in insulin mediation, guggul sterone extracts to support thyroid activity, Rhodiola to increase support for ATP and cAMP production, B vitamins to support energy pathways and capsiate for thermogenesis, lypolysis and anti-oxidant value. Okay, Capsiate is kind of cool so I want to say a little more about it. Everyone in hard core bodybuilding has heard of the fat loss compound DNP. Well, it works by making the mitochondria burn more calories in effort to make ATP by uncoupling the process with a compound called UCP-1 and UPC-2 thus dramatically increasing calorie expenditure…and it is very dangerous. Better options?It’s All About SynergyA single dose of capsiate temporarily raised both UCP1 mRNA in brown adipose tissue and UCP3 mRNA in skeletal muscle. These results suggest that UCP1 and UCP2 may contribute to the promotion of energy metabolism by capsiate, but that thyroid hormones do not. In short, a smarter and naturally occurring option. Yes, both human and rat studies. What Did We Add To The Original Intense Formula?Propionyl-L-Carnitine Ethyl Ester: Regular L-carnitine is a wonderful amino acid that positively affects mitochondrial function and supports fat oxidation via carnitine shuttle. However, propionyl-l-carnitine (PLC) is a completely new animal with much more far reverying potential for ergogenic benefits than its more basic cousin. Used medically to treat heart problems and improve blood flow in the body, PLC has been shown to increase mental function, enhance overall energy, hasten oxidation of both glucose and lactate, push more glycogen into muscles, and lengthen the time to muscular fatigue. These effects mean just one thing to the hard training bodybuilder or athlete and dieting world…you can train harder, longer, and will recover better from every gut-busting workout! Ok, so that’s a few things…but even better! Oh yeah, did I mention Ethyl Ester technology? Duh. Esters can increase oral bioavailability by as much as 400 percent and propionyl-l-carnitine needed to be far more oral friendly…so we created Propionyl-L-Carnitine Ethyl Ester and added it to our energy oriented goodies. Tyrosine Ethyl Ester: This is an obvious one. Tyrosine is an amino acid your body uses as a substrate to make active fat burning, metabolic rate governing thyroid hormones. When you diet your thyroid hormone production decreases which means it is harder to lose fat but you have muscle wastes away. Tyrosine for thyroid hormone function support is a no-brainer. Unfortunately oral tyrosine administration has poor bioavailability…did I mention esters having up to 400 percent better oral bioavailability?Sum It Up?Sometimes all of the right ingredients can be in a product but the correct amounts and standardization can blow the whole out come. It is all about the correct amounts of every substrate and that every acts in synergy with one another…without counteracting another…that makes the product gold or a rip-off. Get what you pay for and try ALR Industries Venom Hyperdrive 3. 0™…but please follow directions. We do things right. Let Us Know How We did!By The Way…Why Do Almost All Fat Loss Systems Fail?Pretty simple really…Come on now. Everyone wants to see what’s under that extra fat layer, but when we first start dieting (restricting our calorie intake) and augment the amount of calories we burn (by increasing exercise), everything goes great…for about the first week. Then, like most human’s on the planet, we start getting hungry (like eating a whole wedding cake at 3 AM type hungry) and run out of energy. So, in short, you crave food and have no interest in doing anything that requires any energy unless it somehow involves that wedding cake and a gallon of milk. (ya, I know, no fat people jokes)So What Do We Need To Succeed?First, we need to clean up our diets by dropping sugars, alcohol, and excessive fatty foods (Okay, at least consume them only in moderation). Second, we need to put together a training program that increases the number of calories we burn per day. *See our sites at www. ALRindustries. com or www. AnabolicBeast. com for all the best diet and training info you could need!Last, we need to do something about that “Commit felonies for a wedding cake but too lazy to do so” feeling that always hits us like a ton of lard after the first week of lower calories! And a dramatic increase in metabolic rate (increased calorie expenditure) certainly would make the whole deal more worth while, huh?ALR Industries Venom Hyperdive 3. 0 has that covered!VenomHyperdrive 3. 0 IngredientsThese statements have not been evaluated by the FDA. This product is not intended to diagnose, treat, or prevent any disease. NOT FOR USE BY INDIVIDUALS UNDER THE AGE OF 21 YEARS. DO NOT USE IF PREGNANT OR NURSING. Consult a Physician before using this or any product if you have, or have a family history of, including but not limited to high blood pressure, cardiac arrhythmias, heart, liver, kidney, thyroid, or psychiatric disease, phenochromacytoma, diabetes, asthma, recurrent head aches, anemia, nervousness, anxiety, depression or other psychiatric condition, peptic ulcers, Parkinson’s disease, glaucoma, difficulty in urinating, prostate enlargement, or seizure disorder, or if you are using a monoamine oxidase inhibitor (MAOI) or any other dietary supplement, prescription drug, or over-the-counter drug containing ephedrine, pseudoephedrine, or phenylpropanolamine (ingredients found in certain allergy, asthma, cough or cold, and weight control products). Do not exceed recommended serving. Exceeding recommended serving may cause serious adverse health effects, including heart attack and stroke. Discontinue use and call a physician or licensed qualified health care professional immediately if you experience rapid heartbeat, dizziness, severe headache, shortness of breath, or other similar symptoms. Individuals who consume caffeine with this product may experience serious adverse health effects and those that are sensitive to the effects of caffeine should consult a Physician before consuming this product. Improper use of this product may be hazardous to a person’s health. Do not use during strenuous activity in high temperature conditions (Greater than 80 degrees Fahrenheit). Drink at least 2 liters of water daily and consume adequate calories when using this product. To report any adverse events call 1-800-332-1088. † These statements have not been evaluated by the Food and Drug Administration. This product is not intended to diagnose, treat, cure or prevent disease. References:1) J Neurochem. 2004 Oct;91(2):362-73. Dopamine transporter-dependent and -independent actions of trace amine beta-phenylethylamine. Sotnikova TD, Budygin EA, Jones SR, Dykstra LA, Caron MG, Gainetdinov RR. 2) Song DK, Suh HW, Jung JS, Wie MB, Son KH, Kim YH. Antidepressant-like effects of p-synephrine in mouse models of immobility tests. Neurosci Lett. 1996 Aug 23;214(2-3):107-10. 3) Brown CM, McGrath JC, Midgley JM, Muir AG, O'Brien JW, Thonoor CM, Williams CM, Wilson VG. Activities of octopamine and synephrine stereoisomers on alpha-adrenoceptors. Br J Pharmacol. 1988 Feb;93(2):417-29. 4) Sustained antidepressant effect of PEA replacement Sabelli H; Fink P; Fawcett J; Tom C Rush University and the Center for Creative Development, Chicago, Illinois, USA. J Neuropsychiatry Clin Neurosci, 1996 Spr, 8:2, 168-715) Does phenylethylamine act as an endogenous amphetamine in some patients? Janssen PA, Leysen JE, Megens AA, Awouters FH. Centre for Molecular Design, Janssen Research Foundation, B-2340 Beerse, Belgium. Int J Neuropsychopharmcol 1999 Sep; 2(3):229-240 6) Atherosclerosis. 2005 Jan;178(1):25-32. Nobiletin, a citrus flavonoid isolated from tangerines, selectively inhibits class A scavenger receptor-mediated metabolism of acetylated LDL by mouse macrophages. Whitman SC, Kurowska EM, Manthey JA, Daugherty A. 7) Planta Med. 2002 Jan;68(1):76-9. Biflavones of Ginkgo biloba stimulate lipolysis in 3T3-L1 adipocytes. Department of Pharmacological Sciences, Faculty of Pharmacy, University of Milan, Milan, Italy. 8) Int J Obes Relat Metab Disord. 1993 Jun;17(6):343-7. Effect of ephedrine and theophylline on weight loss, resting energy expenditure and lipoprotein lipase activity in obese over-fed rats. Department of Pediatric Endocrinology, Silesian Medical Academy, Katowice, Poland. 9) Obes Res. 2005 Jul;13(7):1195-204. Body weight loss and weight maintenance in relation to habitual caffeine intake and green tea supplementation. Department of Human Biology, Maastricht University, PO Box 616, NL-6200 MD Maastricht, The Netherlands. m. westerterp@hb. unimaas. nl. 10) Yakugaku Zasshi. 2004 Nov;124(11):841-6. [Effects of long-term administration of caffeine on fat storage in ovariectomized rats] Department of Environmental and Symbiotic Sciences, Prefectural University of Kumamoto, Kumamoto 862-8502, Japan. hanlikun@hotmail. com11) Am J Clin Nutr. 2004 Jul;80(1):22-8. Caffeine ingestion increases the insulin response to an oral-glucose-tolerance test in obese men before and after weight loss. 12) Exp Clin Endocrinol Diabetes. 1998;106 Suppl 2:29-34. What do pharmacological approaches to obesity management offer? Linking pharmacological mechanisms of obesity management agents to clinical practice. Research Department of Human Nutrition, The Royal Veterinary and Agricultural University, Copenhagen, Denmark. ast@kvl. dk13) J Physiol Biochem. 2003 Sep;59(3):175-82. Moderate weight-lowering effect of octopamine treatment in obese Zucker rats. Institut National de la Sante et de la Recherche Medicale, U586, CHU Rangueil, Universite Paul Sabatier, 31043 Toulouse, France. 14) Biol Pharm Bull. 2005 Sep;28(9):1626-9. Beta-phenylethylamine stimulates striatal acetylcholine release through activation of the AMPA glutamatergic pathway. Department of Pharmacotherapeutics, Showa Pharmaceutical University, Tokyo, Japan. 15) J Comp Neurol. 2005 Nov 7;492(1):34-49. Dopamine D5 receptor localization on cholinergic neurons of the rat forebrain and diencephalon: A potential neuroanatomical substrate involved in mediating dopaminergic influences on acetylcholine release. Institute for Neuroscience, The University of Texas at Austin, Austin, Texas 78712. 16) J Am Geriatr Soc. 1988 Jan;36(1):54-62. Erectile failure in the aged: evaluation and treatment. Medical College of Virginia, Richmond. 17) Increased ATP content/production in the hypothalamus may be a signal for energy-sensing of satiety: studies of the anorectic mechanism of a plant steroidal glycoside. Brain Res. 2004 Sep 10;1020(1-2):1-11. 18) Altern Med Rev. 2005 Sep;10(3):216-21. The potential of 5-hydryoxytryptophan for hot flash reduction: a hypothesis. Research Associate, Southwest College Research Institute Correspondence address: Southwest College of Naturopathic Medicine, 2140 E. Broadway Road, Tempe, AZ 85282. Email: j. curcio@scnm. edu. 19) Circ Res. 2005 Sep 15; Protective Effect of {alpha}-Lipoic Acid in Lipopolysaccharide-Induced Endothelial Fractalkine Expression. Renal Regeneration Laboratory and Departments of Internal Medicine and Pathology, Research Institute of Clinical Medicine, Chonbuk National University Medical School, Jeonju; and Biomedical Research Center and Department of Biological Sciences, Korea Advanced Institute of Science and Technology, Daejeon, South Korea. 20) Upregulation of uncoupling proteins by oral administration of capsiate, a nonpungent capsaicin analog. J Appl Physiol. 2003 Dec;95(6):2408-15. Epub 2003 Sep 5. 21) Antioxidant activity of capsinoids. J Agric Food Chem. 2002 Dec 4;50(25):7396-401. 22) Effect of PLC on functional parameters and oxidative profile in type 2 diabetes-associated PAD. Diabetes Res Clin Pract. 2006 Jan 27;23) Acetyl-L-carnitine plus propionyl-L-carnitine improve efficacy of sildenafil in treatment of erectile dysfunction after bilateral nerve-sparing radical retropubic prostatectomy. 24) Uptake of L-carnitine and its short-chain ester propionyl-L-carnitine in the isolated perfused rat liver. J Pharmacol Exp Ther. 2005 Oct;315(1):118-24. Epub 2005 Jun 10. 25) Preliminary observations on the use of propionyl-L-carnitine in combination with sildenafil in patients with erectile dysfunction and diabetes. Curr Med Res Opin. 2004 Sep;20(9):1377-84. 26) Exploratory open label, randomized study of acetyl- and propionylcarnitine in chronic fatigue syndrome. Psychosom Med. 2004 Mar-Apr;66(2):276-82. 27) Control of thyroid hormone action in the developing rat brain. Thyroid. 2003 Nov;13(11):1039-56. Review. 28) Primary congenital hypothyroidism: defects in iodine pathways. Eur J Endocrinol. 2003 Oct;149(4):247-56. Review. 29) Sulfated tyrosines of thyroglobulin are involved in thyroid hormone synthesis. Biochem Biophys Res Commun. 1999 Aug 19;262(1):193-7. 30) [Thyroid hormone production and its regulation] Rev Prat. 1998 Nov 15;48(18):1987-91. Hyperdrive 3. 0 Plus NEW FORMULA! From ALRI Supplement Info: Ingredients Serving Size: 1 Capsule Servings Per Container: 90 Amount Per Serving: Vitamin B12 (cyanocobalamin): 200mcg Unique Proprietary Matrix: 400mg Cocoamine 3. 0 (cocoa extract), Guarana extract (99 percent xanthines), Hoodia gordonii, R-Alpha Lipoic Acis, 5-Hydroxy L-Tryptophan, Guggul Extract (Commiphoria mukul) (2. 5 percent Guggulsterones), Rhodiola rosea root extract, Tyrosine Ethyl Ester, Propionyl-Carnitine Ethyl Ester, Vitaberine (thiamine trisulfide), Red Pepper Extract (Capsiate). Other Ingredients: Modified cellulose (vegetable capsule), Microcrystalline Cellulose, Modified Cornstarch, Magnesium Stearate, Silica. Suggested Use: As a dietary supplement test your tolerance by taking one (1) capsule in the morning with food for the first 7 to 10 days. After tolerance test, you may consider taking one (1) to two (2) capsules, one (1) time daily with eight (8) ounces of water with food. Do not take after 5 P. M. May cause sleeplessness. Do not exceed two (2) capsules daily. Warnings: Not for use by individuals under the age of 21 years. Do not use if pregnant or nursing. Keep out of revery of children. Do NOT consume this product if you have a medical condition and/or taking any prescription medication. Do not exceed recommended serving. Discontinue use and call a physician or licensed qualified health care professional immediately if you experience rapid heartbeat, dizziness, severe headache, or other similar symptoms. This product is not intended to diagnose, treat, cure, or prevent any disease.
- Category: Personal Care - Exercise Wellness - SUPPLEMENT BRANDS - SUPPLEMENT BRANDS - Item: 461157261
- Hyperdrive 3.0 Plus NEW FORMULA! F ALRI Industries
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