Venom Diet Pills

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 ALRI)

Cocoamine™ is trade marked 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% 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™ will show you how wrong you are. (Please start with only one capsule!)

Phenylethylamine (PEA) is an endogenous neuroamine that increases attention and activity in animals and has been studied for its ability to relieve depression in 60% 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 in that PEA improves mood as rapidly as amphetamine but does not produce tolerance. Okay, natural PEA is good. And synthetic 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.

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)

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), ALA (Alpha Lipoic Acid) to aid in insulin mediation,

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…and it is very dangerous. Better options?

It’s All About Synergy

A 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.

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 each substrate and that each 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 ALRI’s Venom™…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?

• ALRCocoamine 3.0+™ is a unique matrix standardized to yield nearly 98% active ingredients, which impact the body’s metabolism and energy system.  Isolate the euphoric and energy components of chocolate, strip away the fat and calories and you will have a natural extract that acts like a thermogenic sledgehammer. ALRCocoamine 3.0+™ acts like a metabolic turbo-charger ramping up fat utilization and calorie expenditure.   

-ALRCocoamine 3.0+™ contains:

• PEA – Phenylethylamine – A naturally occurring substance that increases attention and improves mood.  PEA is a powerful natural stimulant that boosts energy and mental focus and it also helps control hunger.

• Methylxanthines: (theobromine, caffeine, theophylline) - Group of powerful substances that supercharge the metabolism, stimulate thermogenesis and provide increased energy and alertness. 

• Tyramine, octopamine and methyl and other synephrines –Beta agonistic agents, which support fatty acid release and its utilization for energy, positively impact mood and help control hunger.  These substances provide much of the same beneficial effects as ephedrine.

Thyroid Support:

Rev up the metabolism; increase the burning of calories 24-hours per day by escalating the metabolic rate through natural thyroid support.

-Ingredients responsible for thyroid support:

• Tyrosine Ethyl Ester – This amino acid functions as a substrate in the production of thyroid hormone.  Hyperdrive 3.0+ contains esterified tyrosine to maximize oral bioavailability.

• Guggulsterones – Provide direct and indirect thyroid stimulation; rev up the metabolism and provide an increased thermogenic effect.

• Fat Mobilization:

Pull fat from the fat cells to allow the body to use fatty acids for energy (use stored fat as the preferred energy source):

-Ingredients responsible for fat mobilization:

• Propionyl-L-Carnitine Ethyl Ester – This amino acid positively affects the mitochondria or the cellular “power plants” of the cells of the body.  L-carnitine also acts as a “fat mobilizer”, thereby supporting fat oxidation and metabolism.   L-carnitine ensures that the body uses fat first for energy.

• Appetite Control:

-Ingredients responsible for appetite control:

• Hoodia Gordonii Concentrate- Research has demonstrated that Hoodia can suppress hunger, control appetite and increase satiety.

• R-ALA - Studies have shown that R-alpha lipoic acid (R-ALA) is a powerful anti-oxidant that ramps up mitochondrial function, increases metabolic rate and detoxifies cellular oxidative damage. 

• Rhodiola Rosea Concentrate – Known as an adaptogen, rhodiola supports serotonin optimization and increases ATP production (cellular energy).

*IN CONCLUSION:
Hyperdrive 3.0+™ is one of the strongest stand-alone comprehensive fat loss/energy and performance products available today.  Hyperdrive 3.0+™ is specifically designed for remarkable results & fat loss.  If this is your goal, there is no other choice.  Don’t you want to,” LIVE LIFE IN HYPERDRIVE!”?

Serving Size: 1 capsule

Servings per Container: 90

These statements have not been evaluated by the FDA. This product is not intended to diagnose, treat, or prevent any disease.

Please visit us at: www.alrindustries.com  

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. 

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, 168-71

5) 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.com 

11) 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.dk 

13) 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.

If you wish to read the abstracts of these references "click here"

• ALRI VENOM