Medical Forum / Diseases and Disorders / Prostate Cancer / June 2007
Help Is Here!!!
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Seyhan - 10 Jun 2007 11:46 GMT DO YOU KNOW ANYONE THAT IS SUFFERING FROM...
HEART DISEASE, STROKES, HIGH BLOOD PRESSURE, ANY FORM OF CANCER, DIABETEAS, ASTHMA, ANY FORM OF SKIN DISEASE (ACHNY, ECZEMA,ECT), CARDIOVASCULAR DISEASE, UMNIPETANT, HAY FEVER, VARICOSE VAINS, ACHES & PAINS, MEMORY DISORDERS, BONE PROBLEMS, OBESITY, HAIR LOSS, TIREDNESS, ETC?
A UNIQUELY FORMULATED PRODUCT
There is a product that may help these symptoms. This product has a unique formula one ingredient in it is Arginine when taking the pink drink reacts with the liver to produce nitric oxide.
On October 12th 1998, a team of scientists won the Nobel Prize in medicine for their discoveries about a gas molecule called Nitric Oxide. Nitric Oxide (labelled as the miracle molecule) is a powerful vasodilator, which simply means, it helps to keep your arteries open and helps maintain their smooth, Teflon like texture so blood can flow normally, which has so many positive affects it's unbelievable. Only in the UK at the moment.
Message me back if you are interested. Look forward to hearing from you shortly
I.P. Freely - 10 Jun 2007 22:53 GMT > DO YOU KNOW ANYONE THAT IS SUFFERING FROM... > > HEART DISEASE, STROKES, HIGH BLOOD PRESSURE, ANY FORM OF CANCER, > DIABETEAS, ASTHMA, ANY FORM OF SKIN DISEASE (ACHNY, ECZEMA,ECT), > CARDIOVASCULAR DISEASE, UMNIPETANT, HAY FEVER, VARICOSE VAINS, ACHES & > PAINS, MEMORY DISORDERS, BONE PROBLEMS, OBESITY, HAIR LOSS, TIREDNESS, You forgot buck teeth, global warming, political rhetoric, and spam.
I.P.
california_chief - 10 Jun 2007 23:15 GMT > DO YOU KNOW ANYONE THAT IS SUFFERING FROM... (ACHNY,> What is this "achny" thing? The product of an uneducated spammer/onager?
> On October 12th 1998, a team of scientists won the Nobel Prize in medicine Who were they?
> Only in the UK at the moment. Because the US FDA won't approve it?
california_chief - 11 Jun 2007 00:24 GMT Path: be06.lga!hwmnpeer02.lga!hw-filter.lga!hwmnpeer01.lga!news.highwinds-media.co m!news.glorb.com!border1.nntp.dca.giganews.com!nntp.giganews.com!postnews.go ogle.com!q75g2000hsh.googlegroups.com!not-for-mail From: Seyhan <seyhan__mustafa@hotmail.com> Newsgroups: sci.med.prostate.cancer Subject: Help Is Here!!! Date: Sun, 10 Jun 2007 10:46:46 -0000 Organization: http://groups.google.com Lines: 25 Message-ID: <1181472406.443456.82510@q75g2000hsh.googlegroups.com> NNTP-Posting-Host: 82.40.182.80 Mime-Version: 1.0 Content-Type: text/plain; charset="iso-8859-1" X-Trace: posting.google.com 1181472406 21249 127.0.0.1 (10 Jun 2007 10:46:46 GMT) X-Complaints-To: groups-abuse@google.com NNTP-Posting-Date: Sun, 10 Jun 2007 10:46:46 +0000 (UTC) User-Agent: G2/1.0 X-HTTP-UserAgent: Mozilla/4.0 (compatible; MSIE 7.0; Windows NT 5.1; (R1 1.5); .NET CLR 1.1.4322),gzip(gfe),gzip(gfe) Complaints-To: groups-abuse@google.com Injection-Info: q75g2000hsh.googlegroups.com; posting-host=82.40.182.80; posting-account=v2UyTA0AAABUuhviyKw-hB0iEk39RPRX Xref: Hurricane-Charley sci.med.prostate.cancer:2761 X-Received-Date: Sun, 10 Jun 2007 03:46:47 MST (be06.lga)
> DO YOU KNOW ANYONE THAT IS SUFFERING FROM... > A UNIQUELY FORMULATED PRODUCT > Message me back if you are interested. Better yet, message to numbnutz' ISP 82.40.182.80:
inetnum: 82.32.0.0 - 82.47.255.255 org: ORG-CIL2-RIPE netname: UK-CABLEINET-20030131 descr: PROVIDER Local Registry descr: Cable Internet Ltd country: GB org-name: Cable Internet Ltd org-type: LIR address: Telewest Broadband, address: 4 Bankhead Avenue address: Bankhead Industrial Estate address: KY7 6JG address: Glenrothes, Fife address: United Kingdom phone: +44 (0)2920305411 fax-no: +44 (0)2920305377 e-mail: hostmaster@cableinet.net e-mail: david.lumb@telewest.co.uk e-mail: Planninginformation.management@ntl.com
role: Telewest Broadband NCMC address: Communications House address: Mayfair Business Park address: Broad Lane address: Bradford address: BD4 8PW e-mail: capacity@telewest.co.uk
role: Telewest Broadband IP Network Services address: Genesis Business Park address: Albert Drive address: Woking address: Surrey UK address: GU21 5RW address: remarks: Report abuse to www.virginmedia.com/netreport remarks: +44(0)1633 710142 e-mail: ripe@telewest.net
descr: Telewest Broadband descr: UK Broadband ISP remarks: report abuse to www.virginmedia.com/netreport remarks: +44(0)1633 710142
Seyhan - 11 Jun 2007 20:13 GMT What would you do if you had a product that will change lives? Would you stay quiet about it or try and give it to as many people as you could? What if your family members are sick would you starve them from or help them?
c palmer - 11 Jun 2007 23:49 GMT From: seyhan__mustafa@hotmail.com (Seyhan) who belched and pushed out the forgoing thought:
What would you do if you had a product that will change lives? Would you stay quiet about it or try and give it to as many people as you could? What if your family members are sick would you starve them from or help them? ===> love the guilt touch. trying to appeal to the person's senses in trying to sell the product. but it doesn't cut it here.
if you can provide hard core, documented proof that it can cure cancer. post it! otherwise, anything else you say would be construed as a spammer.
~curtis
knowledge is power - growing old is mandatory - growing wise is optional "Many more men die with prostate cancer than of it. Growing old is invariably fatal. Prostate cancer is only sometimes so." http://community.webtv.net/PALMER_ENT/doc
california_chief - 12 Jun 2007 02:40 GMT > What would you do if you had a product that will change lives? I wouldn't write "message me," dork.
> Would you stay quiet about it or try and give it to as many people as > you could? You're giving it away. FREE? NO COST?
But you won't state what it is, will you?
> What if your family members are sick would you starve them from or > help them? Where did you learn English grammar? Or are you still in kindergarten?
Do mommy and daddy know you're pounding on the keyboard, little boy?
Seyhan - 12 Jun 2007 15:21 GMT hay chef your very funny..... I like your sence of humour. c.palmer I would love to say there is a cure for cancer.... But because it is found in your genetics, it cannot be cured. This is somthing Allah s.w.t had prescribed for us. But what this product does is it treats the cause rather than the symptom. You want some scientific proof. I hope you enjoy this.
Nitric Oxide: Nitric Oxide (NO) is a very important signaling molecule that acts in many tissues to regulate a wide range of physiological processes. It was first discovered several years ago by a group that was attempting to identify the agent responsible for promoting blood vessel relaxation and the regulation of vascular tone. This particular agent was named endothelium-derived relaxing factor (EDRF), and was initially assumed to be a protein like most of the other signaling factors previously discovered. The discovery that EDRF was in fact nitric oxide, a small gaseous molecule, has led to many publications over the years including our NOSTM discovery. Our scientist found that besides promoting blood vessel relaxation and the regulation of vascular tone, NO plays a key role in many biological processes including immune defense, neurotransmission, and the regulation of cell death (apoptosis). Since NO is such a very small molecule, it is able to diffuse rapidly across cell membrane and depending on the conditions, is able to travel several hundred microns. Nitric oxide is produced by enzymes known as nitric oxide syntheses (NOS). Nitric Oxide Syntheses: Nitric Oxide (NO) is produced by a group of enzymes called nitric oxide syntheses (NOS). These enzymes (present in body) convert the Arginine in our Arginine alpha- Ketoglutarate (AKG) into citrulline, producing NO in the process. Oxygen and NADPH are necessary co-factors. The pure and simple science starts with the correct form of AKG. There are three isoforms of NOS which have been named according to their activity. They are neuronal NOS (nNOS), endothelial NOS (eNOS), and inducible NOS (iNOS). Our scientists commonly refer to these enzymes by number so that nNOS is known as NOS1, iNOS is NOS2, and eNOS is NOS3. Although there are three names, these isoforms can be found in a variety of tissues and cell types working toward the same biological functions. The general function of NO production from NOS is illustrated below in figure 1. Figure 1: L- Arginine-alpha- Ketoglutarate NO nNOS NADPH iNOS NADP eNOS O2 L-citrulline nNOS & eNOS synthesizes nitric oxide in response to intracellular calcium levels. In other words, like all NOS isoforms, its activity is dependent on the binding of calmodulin. Increases in cellular calcium leads to increases in levels of calmodulin and the increased binding of calmodulin to eNOS and nNOS which then leads to an increase in NO production by these enzymes. The binding of calmodulin is required for the activity of all the NOS isoforms to convert our Arginine alpha-Ketoglutarate to nitric oxide. Physiological Roles of Nitric Oxide: Since the initial discovery that NO is able to induce vasodilation, a large number of other roles have also been found, as described below. Role in immune system: NO can be produced by numerous cells involved in immune response. In particular cytokine-activated macrophages can produce high levels of NO in order to kill targeted cells such as tumors and bacteria. Role in inflammation: NO has shown to act as a mediator of inflammatory processes. This process has enhanced the effect of cyclooxygenases and stimulates the production of pro-inflammatory eiconosoids. Role in nervous system: NO behaves as a neurotransmitter in the central and peripheral nervous systems, and because of this function, is has shown to be involved in regulating apoptosis in neurons. Role in blood flow: NO relaxes the smooth muscle in the walls of the arterioles. At each systole, the complex endothelial cells that line the blood vessels, will release a puff of NO, which then diffuses into the underlying smooth muscle cells. This process causes these cells to relax, which permits the surge of blood to pass through easily. L-Arginine-alpha-Ketoglutarate: This amino acid compound was discovered by Rocky Mountain Chemical Company (RMC), back in the 1980's, as being a superior form for delivering L- Arginine to the human system. RMC is the only domestic manufacture for this compound, along with 21 other amino acids that are bound to alpha-Ketoglutarate. Our research scientist discovered that L-Arginine-alpha-Ketoglutarate was a fuel for nitric oxide synthases (NOS). In laymen's terms, we discovered a natural, non-drug method of creating nitric oxide in the human body. This mechanism is complex, but the trigger-mechanism is very elemental. In order to stimulate or produce nitric oxide in the body, a terminal nitrogen atom must combine with an oxygen molecule in the blood. An enzyme called nitric oxide synthase controls this reaction and NADPH (a niacincontaining redox-active electron storage compound), mediates the reaction. The reaction is accomplished and controlled by oral ingestion of L- Arginine-alpha- Ketoglutarate. The left-handed molecule, called L-Arginine, is the primary source for nitric oxide in humans. When NO is produced in the body by this process, scientists have referred to this as ADNO or Arginine-Derived-Nitric-Oxide. Additional clinically proven benefits of pure Arginine are: *Improved blood flow in men with elevated serum cholesterol and early coronary artery disease. Circulation *Reduced pathological increases in the thickness of plaque-lined walls in people with elevated cholesterol. *Lowered plasma cholesterol levels in subjects with advanced hypertension. New England Journal of Medicine *Elderly patient's oral treatments resulted in significant improvement in lipid profiles, with no side effects. Journal of Perenteral & Enternal Nutrition *Enhanced coronary artery blood flow in heart patients. Journal of the American College of Cardiology *Improved blood-vessel relaxation Circulation L-Arginine-alpha-Ketoglutarate has several other important functions besides the above. Remember biology 101, which taught that this compound is essential to the metabolism of ammonia that is generated from protein breakdown and the transportation of nitrogen used in muscle metabolism. L-Arginine also influences several hormone functions, like the stimulation to the pituitary gland for the production of growth hormone. Human growth hormone helps in muscle building, leading to increased muscle size, strength, tone, along with strengthening tendons and ligaments. Growth hormone, in general, decreases body fat and increases metabolism which results in more energy. Back in the 1980's a book called Life Extension (Pearson & Shaw) proved that adequate amounts of the amino acid L-Arginine did stimulate growth hormone production. References: 1).Barbul, Fishel, Shimazu, Wasserkrug, Yoshimura, Tao, And Efron, Intravenous Alimentation with High Arginine levels Improves Would Healing and Immune Function., Journal of Surgical Research, 38 (1985), 228-334. 2).Jay Lombard, board Certified Neurologist; The Brain Wellness Plan, Breakthrough Medical, Nutritional, and Immune-Boosting Therapies, 1998. 3). Bath PMW, Willmont M, Leonardi-Bee, Bath FJ, Nitric oxide donors, L-Arginine, or nitric oxide synthase inhibitors for acute stroke, Cochrane Review, March 2002. 4).R.M.J. Palmer, A.G. Ferrige, S. Moncada, "Nitric Oxide release accounts for the biological activity of endotheliumderived relaxing factor," Nature, 327:524-526, 1987. 5). S. Monada, R.M.J. Palmer, E.A. Higgs, "Nitric oxidephysiology, pathophysiology, and pharmacology," Pharmacological Reviews, 43:109-142, 1992. 6). R.M.J. Palmer, D.S. Ashton, S. Monada, "Vascular endothelial cells synthesize nitric oxide from l-Arginine," Nature, 333:664-666, 1988. 7).Monada, S. , Higgs A., "The L-Arginine-nitric oxide pathway, New England J. Med, 329:2002-2012, 1993. 8).Hishikawa, Nakaki, Tsuda, Esumi, Ohshima, Suzuli, Saruta and Kato, Effect of Systemic L-Arginine administration on hemodynamis and nitric oxide release in men, Japan Heart Journal, 33:41-48, 1992. 9).1998 FDA Public records department. 10).M.W. Radomski, S. Moncada, R.M.J. Palmer,"The role of nitric oxide and cGMP in platelet adhesion to vascular endothelium," Biochem. Biophys. Res. Comml, 148:1482- 1489, 1987. 11).S.Moncada, "L-Arginine-nitric oxide pathway," Acta Physiological Scandinavia, 145:201-227, 1992. 12).M.R.Shaffer, U. Tatry, R.A. Van Wesep, A. Brabul, "Nitric oxide metabolism in wounds. Journal Surgical Res, 71:25:31, 1997. 13).Schmidt, Hofman, Shindler, Shutenkl, "NO from NO synthases, Proc Nati Aad Sil, 93:14492-14497, 1997. 14).D. D. Rees, R.M.J. Palmer, S. Moncads, "Role of endothelium-derived nitric oxide in the regulation of blood pressure", Proceedings of the National Academy of Sciences, 86:3375-3378, 1989. 15).R.J. Gryglewski, S. Moncada, R.M.J. Palmer, "Superoxide anion is involved in the breakdown of endothelium-derived vascular relaxing factor", Nature, 320:454-456, 1986.
Seyhan - 12 Jun 2007 15:29 GMT One Min. That is explaining NO. But now is a explaination on L- Arginine.
A Report On Arginine By Harry Elwardt, N.D., PhD. "... A few grams of prevention is worth a ton of cure." 1 So just what is Nitric Oxide (NO)? Over 20,000 articles in the medical literature since 1980 attest that "absolutely everything in the body depends on it." Its function in human physiology is so important that the American Academy of Science named Nitric Oxide the "Molecule of the year" in 1992. The Nobel Peace prize in Medicine was awarded to scientists who began the research on Nitric Oxide in 1998 and now NO has been referred to as "The Molecule of the Millennium". Dr. Jonathan S. Stamler, a professor of medicine at Duke University Medical Center, put it best when he said of Nitric Oxide: "It does everything, everywhere. You cannot name a major cellular response or physiological effect in which [Nitric Oxide] is not implicated today. It's involved in complex behavioral changes in the brain, airway relaxation, beating of the heart, dilation of blood vessels, regulation of intestinal movement, function of blood cells, the immune system, even how fingers and arms move." There are three types of NO. Endothelial-derived NO diffuses out of endothelial cells (cells lining arteries and veins) and into smooth muscle cells of arteries enhancing relaxation and other properties of vascular physiology. Endothelial-derived NO also functions in platelets (blood cells responsible for blood clots) to inhibit aggregation or blood clotting. Brain-derived NO affects several types of nerve cells and appears to be important in neurotransmitter pathways in both the central as well as peripheral nervous system and regulates the production and release of many hormones. Macrophage-derived NO is important in the immune system. This type of NO helps macrophages (a type of immune cell) kill bacteria and tumor cells. So, NO is important to the nervous system, the immune system and the vascular system, which supplies nutrients to all parts of the body. Arginine, when combined with Oxygen, forms NO. Arginine, as found in Ark1? is the source of all forms of NO.2, 3 NO decreases with age 4, 5, 6, various age related conditions and many medications7,8. Among the most common disease states to affect NO and therefore sexual function are: ? Diabetes ? Heart disease ? Hypertension (high blood pressure) ? Peripheral Vascular Disease ? Neurological Damage ? Peptic Ulcer ? Arthritis ? Allergy ? Low HDL 2 ? Some of the most common drugs affecting NO and/or sexual functions are antidepressants - many common drugs like Elavil?, Prozac?. Paxil?, Zoloft?, etc. ? Anti-anxiety drugs, including Xanax? and Valium? ? Anti-psychotic drugs ? Blood Pressure medications ? Other Cardiac drugs, like lanoxin or other drugs that affect cardiac rhythm ? Anti-heartburn drugs like Tagamet? and Zantac? ? Opioids especially chronic use of legal (e.g., Lortab?, codeine, etc.) and illegal (e.g., heroin) narcotics and pain medicines ? Alcohol, especially chronic use ? Tobacco The use of many of these drugs and the incidence of most of this disease conditions increase after the age of 40. Obviously it is also the age group most likely to benefit from the use of Ark1?, though any age group can benefit. The 40 and above age group is also the most likely age group (both men and women) to want to use Ark1? for the treatment of sexual dysfunction. In the genital tissue, NO triggers the release of c-GMP, which is a molecule that causes engorgement of this tissue. The arginine found in Ark1? releases NO to make sure there is plenty of c-GMP. Viagra, on the other hand, is a drug that blocks an enzyme to make sure there is plenty of c-GMP. Arginine has been shown to be a safe and effective alternative to Viagra?. Viagra? has been reported to be safe; however, the FDA public records suggest the opposite. These records reported that between April of 1998 and May of 1999 there were 1,473 adverse events including 255 serious heart rhythm disturbances, 53 episodes of congestive heart failure (weakened heart) 119 strokes, 517 heart attacks and 522 deaths.9 Every major disease process today is directly or indirectly related to lack of NO. Diabetes, Hypertension, Hyperlipidemia, Hypercholesterolemia, Cancer, Peripheral Vascular Disease, Coronary Artery Disease, Sickle Cell, Scleroderma, Renal Failure, Pulmonary Hypertension and Atherosclerosis are all associated with decreased levels of NO. (With the exception of cancer, where NO functions in the immune system, most of these disease processes involve the vascular system and endothelial derived NO). The primary function of endothelial derived NO is vascular homeostasis, or balance. NO maintains vascular health by enhancing endothelial reactivity. The endothelium is the inner lining of the blood vessels and as long as the endothelium remains reactive, they are supple, pliable and flexible. They are able to respond appropriately to the various changes that occur in blood vessels in the course of normal and abnormal physiology, when NO decreases, the vessels become stiff and rigid. This is called atherosclerosis or hardening of the arteries. When we develop atherosclerosis, the results are high blood pressure, heart attack and stroke and ultimately death. As long as we have plenty of NO, as can be supplied by the arginine in Ark1?, our blood pressure remains low and we have protection from many of the consequences of the aging process. To date arginine has been shown in animal as well as human trials that it may be effective in the following: 3 ? Decreasing and reversing atherosclerosis by decreasing intimal thickening and monocyte accumulation 9,10,11,12,13,14 ? Restore normal endothelial function in hypercholesterolemia 14,15,16,17,18,19,20,21 ? Reversing consequences of coronary artery disease 22,23,24,25,26,27,28,29,30 ? Decreasing cholesterol and triglycerides 32 ? Improves walking distance in peripheral vascular disease 31,33,34,35,36 ? Improves pain in interstitial cystitis 37,38 ? Prolonged administration of arginine reverses adverse effects of high blood pressure 39,40,41,42 ? Decreases high blood pressure 43 ? Decreases post operative infection and length of stay 44 ? Increases human growth hormone 45,46,47,48,49,50,116 ? Improves outcome after bypass surgery 51 ? Improves sexual function 52 ? Improves exercise tolerance 53,54 ? Improves renal function 55,56,57,58,59,60 ? Improves glucose uptake in muscle cells 61 ? Improves asthma 61,62,63,64,65,66 ? Improves cell mediated immunity 67,68,69,70,71 ? Improves pituitary responsiveness and modulates hormonal control 72,73,74 ? Improves muscle performance 75 ? Improves diabetes and reverses damage 76,77,78,79 ? May prevent diabetes 78 ? Reduces blood clots and strokes 80,81,82 ? Helps prevent restenosis after angioplasty and bypass 83,84,85 ? Helps prevent post surgical damage after intestinal manipulation 86 ? May improve irritable bowel syndrome 87 ? Improves osteoporosis 88 ? May improve prostate function 89 ? May give protection against size of heart attack 90 ? Helps protect in cardiac transplants 91,92 ? Improve scleroderma 93 ? Improve sickle cell disease 94 ? Prevent pre-eclampsia 95 ? Improves exercise capacity in pulmonary hypertension 96,117,118 ? Improves wound healing 97,98,99 ? Reduces ulcers 101,102 ? Improves peripheral vascular disease 103,104 ? Improves outcome in sepsis 105 ? Improves heart failure 106 ? Improves outcome of cancer treatment 107,108 ? Improve alzheimer's 109,110,111,112 ? Improves memory and cognitive functions 113,114,115 ? L-arginine has been shown to safe in the above studies as well as others 100,116 To summarize, arginine by virtue of being a safe and natural Nitric Oxide donor can be an extremely significant factor in the treatment and reversal of most major diseases. 4 The impact of the arginine in Ark1? on preventative healthcare and anti-aging is profound, not to mention that it is a safe and effective replacement for the Viagra? type drugs. References 1. Fried R, Merrell WC. The Arginine Solution. New York, NY. Warner Books, 1999. 2. Coffee, C J: Metabolism. Madison, Ct: Fence Creek Publishing, 1998.pp388-389 3. Catt KJ: Molecular Mechanisms of Hormone Action. In Endocrinology and Metabolism, 3rd ed. Edited by Felig P, Baxter JD, Frohman LA. New York, NY: McGraw-Hill, 1995, pp 138-139 4. Gerhard M, et al. Aging progressively impairs endothelium-dependent vasodilation in forearm resistance vessels of humans. Hypertension 1996 Apr;27(4):849-53 5. Toprakci M, et al. Age-associated changes in nitric oxide metabolites, nitrite and nitrate. Int J Clin Lab Res 2000;30(2):83-5 6. Sakuma I, et al. Identification of arginine as a precursor of endothelium-derived relaxing factor. Proc Natl Acad Sci USA 1988 Nov;85(22):8664-7 7.Vallance P, Moncada S. Nitric Oxide-from mediator to medicines. J R Coll Physicians Lond 1994 May-Jun;28 (3): 209-219 8. Kam PC, Govender G. Nitric oxide: basic science and clinical applications. Anaesthesia 1994 Jun;49(6): 515-21 9. Sinha G. Viagra: ups and downs. Popular Science 2000 July: page 35 10. Boger RH, Bode-Boger SM, Kienke S, et al. Dietary L-arginine decreases myointimal cell proliferation and vascular monocyte accumulation in cholesterol-fed rabbits.Atherosclerosis 1998 Jan;136(1) 67-77 11. Cheng JW, Balwin SN. L-Arginine in the management of cardiovascular diseases. Ann Pharmacother 2001 Jun;35(6):755-64 12. Tentolouris C, Tousoulis D, et al. L-Arginine in coronary atherosclerosis. Int J Cardiol 2000 Sep 15;75(2-3):123-8 13. Wang B, Ho HV, et al. Regression of atherosclerosis. Circulation 1999;99(9):1236-41 14. Boger RH, Bode-Boger SM, et al. Dietary L-arginine reduces the progression of atherosclerosis in cholesterol fed rabbits: comparison with lovastatin. Circulation 1997; 96(4):1282-90 15. Schuschke DA, Miller FN, Lominadze DG, Feldhoff RC. L-arginine restores cholesterol-attenuated micro vascular responses in the rat cremaster. Int J Micricirc Clin Exp 1994 Jul-Aug; 14(4): 204-11 16. Orlandi A, Marcellini M Spagnoli LG. Aging influences development and progression of earl aortic atherosclerosis lesions in cholesterol-fed rabbits. Arterioscler Thromb Vasac Biol 2000 Apr;20 17. Chong PH, Bachenheimer BS. Current, New and future treatments in dyslipidemia and atherosclerosis. Drugs 2000 Jul;60(1):55-93 18. Phivthong-ngam L, Bode-Boger SM, Boger RH, et al. Dietary L- arginine normalizes endothelial induced vascular contractions in cholesterol-fed rabbits. J Cardiovasc Pharmacol 1998 Aug;32(2): 300-7 19. Maxwell AJ, Anderson B Zapien MP, Cooke JP. Endothelial dysfunction in hypercholesterolemia is reversed by: nutritional product designed to enhance nitric oxide activity. Cardiovasc Drugs Ther 2000 Jun;14(3):309-16 20. Clarkson P, Adams MR, Powe AJ, et al. Oral L-arginine improves endothelial-dependent dilation in hypercholesterolemic young adults. J Clin Invest 1996 April; 97(8): 1989-94 21. Cooke JP, Dzau J, Creager A. Endothelial dysfunction in hypercholesterolemia is corrected by L-arginine. Basic Res Cardiol 1991; 86 Suppl 2: 173-81 22. Fraser GE. Diet and coronary heart disease: beyond dietary fats and low-density-lipoprotein cholesterol. Am J Clin Nutr 1994 May;59(5 Suppl) 1117s-1142sand atherosclerosis. Drugs 2000 Jul;60(1):55-93 23. Quyyumi AA. Does acute improvement of endothelial dysfunction in coronary arterydisease improve myocardial ischemia? J Am Coll Cardiol 1998 Oct;32(4):904-11 24. Lerman A, Burnett JC Jr, Higano ST, et al. Long-term L-arginine supplementation improves small vessel coronary endothelial function in humans. Circulation 1998 Jun 2;97(21):1648-9 25. Ceremuzynski L, Chamiec T, Herbaczynska-Cedro K. Effect of supplemental oral L-arginine on exercise capacity in patients with stable angina pectoris. Am J Cardiol 1997 Aug 1; 80(3):331-3 26. Desrois M, Sciaky M, Lan C, et al. L-arginine during long-term ischemia: effects on cardiac function, energetic metabolism and endothelial damage. J Heart Lung Transplant 2000 April; 19(4): 367-76 27. Quyyumi AA, Dakak N, Dodati JG, et al. Effect of L-arginine on human coronary endothelium-dependent and physiologic vasodilation, J AM Coll Cardiol 1997 Nov 1; 30(5):1220-7 28. Egashira K, et al. Effects of L-arginine supplementation on endothelium-dependent coronary vasodilation in patients with angina pectoris and normal coronary arteriograms. Circulation 1996;94(2):130-4 29. Tentoluris C, et al. L-arginine in coronary atherosclerosis. Int J Cardiol 2000 Sep15;75(2-3):123-8 5 30. Tretjakovs P, Kalnins U, Dabina I, et al. Plasma HDL-cholesterol has an effect on nitric oxide production and arachidonic production in the platelet membranes of coronary artery disease patients without LDLhypercholesterolemia. Med Sci Monitor 2000 May- Jun;6(3):507-11 31. Bode-Boger SM, Boger RH, Galland A, Tsikas D Frolich JC. L- arginine induced vasodilatation in healthy humans: pharmacokinetic-pharmacodynamic relationship. Br J Clin Pharmacol 1998 Nov; 46(5): 489-97 32. Khedara A, Kawai Y Kayashita J Kato N. Feeding rats the nitric oxide synthase inhibitor, L-N(omega) nitroarginine, elevates serum triglycerides and cholesterol and lowers hepatic fatty acid oxidation. J Nutr 1996 Oct;126(10):2563- 7 33. Boger RH, Bode-Boger SM, Theil W, et al. Restoring vascular nitric oxide formation by L-arginine improves symptoms of intermittent claudication in patients with Peripheral arterial occlusive disease. J Am Col Cardiol 1998 Nov;32(5):1336-44 34. Maxwell AJ, Anderson BE Cooke JP. Nutritional therapy for peripheral artery disease. Vasc Med 2000;5(1):11-19 35. Hiatt WR. New treatment options in intermittent claudication: the US experience. Int J Clin Pract Suppl 2001 Apr;(119):20-27 36. Creager MA. Medical management of peripheral artery disease. Cardiol Rev 2001 Jul-Aug;9(4):238-45 37. Korting GE, Smith SD, Wheeler MA, Weiss RM, Foster HE. A randomized double-blind study of oral L-arginine for treatment of interstitial cystitis. J Urol 1999 Feb; 161(2):558-65 38. Cartledge JJ, Davies AM, Eardley I. A randomized double-blind placebo-controlled crossover trial of the efficacy of L-arginine in the treatment of interstitial cystitis. BJU Int 2000 Mar; 85(4):421-6 39. Sisic D, Francishetti A, Frolich ED. Prolonged L-arginine on cardiovascular mass and myocardial hemodynamics and collagen in aged spontaneously hypertensive and normal rats. Hypertension 1999 Jan;33(1 Pt 2):451-5 40. Higashi Y, et al. Effects of L-arginine infusion on renal hemodynamics in patients with mild hypertension. Hypertension1995;25(4):898-902 41. Hishikawa K, et al. Role of L-arginine-nitric oxide pathway in hypertension. J Hypertens 1993 Jun; 11(6):639-45 42. Dominiczak AF, Bohr DF. Nitric oxide and its' putative role in hypertension. Hypertension 1995;25(6):1202-11 43. Nakaki T, et al. L-arginine induced hypotension. Lancet 1990Oct 20; 336(8721):1016-7 44. Braga M, Gianotti L Raedelli G, et al. Perioperative immunonutrition in patients undergoing cancer surgery: results of a randomized double-blind phase 3 trial. Arch Surg 1999 Apr;134(4): 428-33 45. Ghigo E, Aimaretti G, Cornelli G, et al. Diagnosis of GH deficiency in adults. Growth Hormone IGF Res 1998 Feb;8 Suppl A:55-8 46. Wideman L Weltman JY, Patrie JY, et al. Synergy of L-arginine and GHRP-2 stimulation of growth hormone in men and women: modulation by exercise. Am J Physiol Regul Integr Comp Physiol 2000 Oct;279(4):R1467-77 47. Gianotti L, Macario M, Lanfranco F, et al. Arginine counteracts the inhibitory effect of recombinant human insulinlike growth factor I on the somatotroph responsiveness to growth hormone- releasing hormone in humans. J Clin Endocrinol Metab 2000 Oct;85(10):3604-8 48. Mauras N, Walton P, Nicar M, et al. Growth hormone stimulation testing in both short and normal statured children. Pediatr Res 2000 Nov;48(5):579-80 49. Ghigo E, Arvat E, Gianotti L, et al. Hypothalamic growth hormone- insulin-like growth facto-1 axis across the human life span. J Pediatr Endocrinol Metab 2000;13 Suppl 6:1493-502 50. Korbonits M, Kaltsas G, Perry LA, et al. The growth hormone secretagogue hexarelin stimulates the hypothalamopituitary- adrenal axis via arginine vasopressin. J Clin Endocrinol Metab 1999 Jul;84(7):2489-95 51. Wallace AW, Ratcliffe MB, Galindez D, Kong JS. L-arginine infusion dilates coronary vasculature in patients undergoing coronary bypass surgery Aenesthesiology 1999 Jun;90(6): 1577-8 52. Chen J, Wollman Y, Chernichovsky T, et al. Effect of high dose nitric oxide donor L-arginine in men with organic erectile dysfunction. BJU Int 1999 Feb;83(3):269-73 53. Kobayashi N, Nakamura M, Hiramori K. Effects of infusion of L- arginine on exercise-induced myocardial ischemic changes and capacity to exercise of patients with stable angina pectoris. Coron Artery Dis 1999 Jul;10(5):321-6 54. Bednarz B, Wolk R, Chamiec T, et al. Effects of oral L-arginine supplementation on exercised induced QT dispersion and exercise tolerance in stable angina pectoris.Int J Cardiol 2000 Sep 15; 75(2-3): 205-10 55. De Nicola L, Bellizzi V, Minutolo R, et al. Randomized, double- blind, placebo controlled study of arginine supplementation in chronic renal failure. 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Diabetes 1999 Sep; 48(9): 1815-21 6 62. De Gouw HW, Verbruggen MB, Twiss IM, Sterk PJ. Effect of oral L- arginine on airway hyper-responsiveness to histamine in asthma. Thorax 1999 Nov;54(11):1033-5 63. De Gouw HW, Marshall-Partridge SJ, et al. Role of nitric oxide in the airway response to exercise in healthy and asthmatic subjects. J Appl Physiol 2001 Feb;90(2):586-92 64. Boer J, et al. Role of L-arginine deficiency of nitric oxide and airway hyperreactivity after allergen-induced early asthmatic reaction in guinea-pigs. Br J Pharmacol 1999 Nov;128(5): 1114-20 65. Blease K, Kunkel SL, Hogaboam CM. Acute inhibition of nitric oxide exacerbates airway hyperresponsiveness, eosinophilia and C-C chemokine generation in a murinemodel of fungal asthma. Inflamm Res 2000 Jun; 49(6):297- 304 66. Du J, Cui D, Tian D. [ The role of nitric oxide in the pathogenesis of asthma.] [ Full text in Chinese] Zhonghua Jie He He Hu Xi Za Zhi 1997 Jun;20(3):153-6 67. Gionotti L, Braga M, Fortis C, et al. A prospective, randomized clinical trial on perioperative feeding with an arginine-, omega-3 fatty acid-, and RNA enriched enteral diet: effect on host response and nutritional status. J Parenter Enteral Nutr1999 Nov- Dec;23(6):314-20 68. Efron D, Barbul A. Role of arginine in immunonutrition. J Gastroentol 2000;35 Suppl 12:20-3 69.Lewis B, Langkamp-Henken B. Arginine enhances in vivo immune responses in young, adult and aged mice. J Nutri 2000;130(7):1827-30 70. Mannick JB, et al. Nitric oxide produced by human B lymphocytes inhibits apoptosis and Epstein-Barr virus reactivation. Cell 1994 Dec 30;79(7):1137-46 71.Ochoa JB, et al. Effects of L-arginine on the proliferation of T- lymphocyte subpopulations. J Parenter Enteral Nutr 2001 Jan- Feb;25(1):23-9 72. di Luigi L, Guidetti L, Pigozzi F, et al. Acute amino acid supplementation enhances pituitary responsiveness in athletes. Med Sci Sports Exerc 1999 Dec;31(12):1748-54 73. Lawecki J et al. Serum insulin, pancreatic glucagons and growth hormone levels in response to intravenous infusion of L-arginine in patients with recently detected juvenile diabetes. Pol Med Sci Hist Bull 1976 Apr- Jun;15(2):177-82 74. Valcenti S, et al Biphasic effect of nitric oxide on testosterone and cyclic GMP productionby purified rat Leydig cells cultured in vivo. Int J Androl 1999 Oct; 22(5):336-41 75. Stevens BR, Godfrey MD, Kaminski TW, Braith RW. High intensity dynamic human muscle performance enhanced by a metabolic intervention. Med Sci Sports Exerc 2000 Dec;32(12): 2102-8 76. Piatti PM, Monti LD, Valsecchi G, et al. Long term oral L-arginine administration improves peripheral and hepatic insulin sensitivity in type 2 diabetes. Diabetes Care 2001 MAY;24(5): 875-80 77. Giugliana D, et al. Vascular effects of acute hyperglycemia are reversed by L-arginine. Circulation 1997; 95(7):1783-90 78. Mohan IK, Cas UN. Effects of L-arginine-nitric oxide system on chemical induced diabetes mellitus. Free Radic Biol Med 1998 Nov 1;25(7):757-65 79. Mendez JD, Balderas F. Regulation of hyperglycemia and dyslipidemia by exogenous L-arginine in Diabetic rats. Biochemie 2001 May;83(5):453-8 80. Kaposzta Z, et al. L-arginine and S-nitroglutathione reduce embolization in Humans. Circulation 2001;103(19):2371-75 81. Bode-Boger SM, Boger RH, et al. Differential inhibition of human platelet aggregation and thromboxane A 2 formation by L-arginine in vivo and in vitro. Arch Pharmacol 1998; 357:143-150 82. Wolf A, et al. Dietary L-arginine supplementation normalizes platelet aggregation in hypercholesterolemic humans. J Am Coll Cardiol 1997 Mar 1; 29(3):479 83. Le Yorneau T, Van Belle E, Corseaux D, et al . Role of nitric oxide in re-stenosis after experimental balloon angioplasty in the hypercholesterolemic rabbit. J Am CollCardiol 1999 Mar;33(3):876-82 84. Janero DR, Ewing JF. Nitric Oxide and Postangioplasty re-stenosis: Pathologicalcorrelates and therapeutic potential. Free Radic Biol Med 2000 Dec 15;29(12):1199-221 85. Severin P, et al. Local intramural delivery of l-arginine enhances nitric oxide generation and inhibits lesion formation after balloon angioplasty. Circulation 1997;95(7):1863-9 86. Thomas S, Ramachandran A, Patra S, et al. Nitric oxide protects the intestine from the damage induced by laparotomy and gut manipulation. J Surg Res 2001 Jul;99(1):25-32 87.Sahin AS, Atalik KE, Gunel E, Dogan N. Nonadrenergic, noncholinergic responses of the human colon smooth muscle and the role of K+channels in these responses.. Methods Find Exp Clin Pharmacol 2001 Jan-Feb;23(1):13- 7 88. Fini M, et al. Effect of l-lysine and L-arginine on primary osteoblast cultures from normal and osteopenic rats Biomed Pharmacother 2001 May;55(4):213-21 89. Aikawa K, Yokota T, et al. Endogenous nitric oxide-mediated relaxation and nitrinergic innervation in the rabbit prostate: the change with aging. Prostate 2001 Jun 15;48(1):40-6 90. Suematsu Y, Ohtsuka T, et al. L-Arginine given after ischemic preconditioning can enhance cardioprotection in isolated rat hearts. Eur J Cardiothorac Surg 2001, Jun;19(6):873-9 7 91. Koglin J. Pathogenetic mechanisms of cardiac allograft vasculopathy-impact of nitric oxide. Z Kardiol 2000;89 Suppl 9:IX/24-7 92. Kown MH, Van Der Steenhoven T, Uemura S, et al. L-Arginine polymer mediated inhibition of graft coronary artery disease after cardiac transplantation. Transplantation 2001 June 15;71(11):1542-8 93. Freedman RR, Girgis R, Mayers MD. Acute effect if nitric oxide on Raynaud's phenomenon in scleroderma. Lancet 1999 Aug 28:354;739 94. Morric CR, Kuypers FA, et al. Patterns of arginine and nitric oxide in patients with sickle cell disease with vasoocclusive crisis and acute chest syndrome. J Ped Hemat/Onc 2000 Nov-Dec;22(6): 515-20 95. Kumar CA, Das UN. Lipid peroxides, antioxidants and nitric oxide in patients with pre-eclampsia and essential hypertension. Med Sci Monitor 2000 Sep-Oct;6(5):901-7 96. Nagaya N, Uematsu M, et al. Short term oral administration of l- arginine improves hemodynamics and exercise capacity in patients with precapillary pulmonary hypertension. Am J Resp Crit Care Med 2001 April;163(4):887-91 97. Barbul A, et al. Arginine enhances wound healing and lymphocyte immune responsesin humans. Surgery 1990 Aug;108(2):331-6; discussion 336-7 98. Kirk SJ, et al Arginine stimulates wound healing and immune function in elderly humans. Surgery 1993 Aug;114(2):155-9; discussion 160 99. De-Souza DA, Greene LJ. Pharmacological nutrition after burn injury. J of Nutri 1998 May;128(5):797-803 100.Blum A, Cannon RO, Costello R, et al. Endocrine and lipid effects of oral L-arginine treatment in healthy postmenopausal women. J Lab Clin Med 2000 Mar;135(3):231-7 101.Ohta Y, Nishida K., Protective effect of l-arginine against stress- induced gastric mucosal lesions in rats and its relation to nitric acid-mediated inhibition of neutrophil infiltration. Pharmacal Res 2001 Jun;43(6):535-41 102.Khattab MM, Gad MZ, Abdallah D. Protective role of nitric oxide in indomethacin- induced gastric ulceration by a mechanism independent of gastric acid secretion. Pharmacol Res 2001 May;43(5):463-7 103.Calver A, Collier J, Vallance P. Dilator actions of arginine in human peripheral vasculature. Clin Sci 1991 Nov;81(5):695-700 104.Bode-Boger SM, Boger RH,et al. L-arginine induces nitric oxide- dependent vasodilation in patients with critical limb ischemia. A randomized, controlled study. Circulation 1996 Jan 1; 93(1):85-90 105.Vallet B. Microthrombosis in sepsis. Minerva Anestesiol 2001 Apr; 67(4):298-301. 106.Hambrecht R, et al. Correction of endothelial dysfunction in chronic heart failure: additional effects of exercise training and oral L-arginine supplementation. J Am Coll Cardiol 2000 Mar 1; 35(3):706-13 107.Heys SD, et al. Dietary supplementation with L-arginine: Modulation of tumor infiltrating lymphocytes in patients with colo-rectal cancer. Br J Surg 1997 Feb;84(2):238-41 108.Brittenden J, et al. Dietary supplementation with L-arginine in patients with breast cancer(> 4cm.) receiving multimodality treatment: report of a feasibility study. Br J Cancer 1994 May;69(5): 918-21 109.McCarty MF. Vascular nitric oxide, sex hormone replacement, and fish oil may help to prevent Alzheimer's disease by suppressing synthesis of acute-phase cytokines. Med Hypotheses 1999 Nov;53(3):369-74 110.Tarkowski E, et al. Intrathecal release of nitric oxide in Alzheimer's disease and vascular dementia. Dement Geriatr Cogn Disord 2000 Nov- Dec;11(6):322-6 111.de la Torre JC, Stefano GB. Evidence that Alzheimer's disease is a microvascular disorder: the role of constitutive nitric oxide. Brain Res Brain Res Rev 2000 Dec;34(3):119-36 112.Kuiper MA, et al. Decrease cerebrospinal fluid nitrate levels in Parkinson's disease, Alzheimer's disease and multiple system atrophy patients. J Neurol Sci 1994 Jan; 121(1):46-9 113.Pautler EL. The possible role and treatment of deficient microcirculation regulation in age-associated memory impairment. Med Hypotheses 1994 Jun;42(6):363-6 114.Pandhi P, Balakrishnan S. Cognitive dysfunction induced by phenytoin and valproate in rats: effect of nitric oxide. Indian J Physiol Pharmacol 1999 Jul; 43(3):378-82 115.Pendergast MA, et al. Nitric oxide synthase inhibition impairs delayed recall in mature monkeys. Pharmacol Biochem Behav 1997 Jan;56(1):81-7 116.Fideieff HL,et al. Reproducibility and safety of the arginine test in normal adults.Medicina (B Aires) 1999; 59(3):249-53 117.Fagan JM, et al. L-arginine reduces right heart hypertrophy in hypoxia-induced pulmonary hypertension. Biochem Biophys Res Commun 1999 Jan 8; 254(1):100-3 118.Nitric oxide and pulmonary hypertension. Coron Artery Dis 1999 Jul; 10(5):287-94
This is what I was Saying..................................... Now are you interested in changing lives???????????????????
I.P. Freely - 13 Jun 2007 00:12 GMT > The Nobel Peace prize in Medicine was awarded to scientists who > began the research on Nitric Oxide The entire Nobel prize concept was forever and irrevocably tainted beyond all credibility by its awards to Jimmy Carter and Yasser Arafat.
> NO has been referred to as "The Molecule of the Millennium" The molecule N-methyl-1-phenyl-propan-2-amine has had an infinitely greater impact on our nation than has nitric oxide. Its common name is meth, and we ain't seen nothing yet.
HOWEVER . . .
> 118.Nitric oxide and pulmonary hypertension. Coron Artery Dis 1999 > Jul; 10(5):287-94 We gotta admit, this is probably the first time a spammer has responded to a reference challenge with 118 of 'em. Hell, this will give Steve Jordan an orgasm . . . and a whole lot of homework to do. ;-)
I.P.
Seyhan - 13 Jun 2007 01:03 GMT This what you say meth is a drug. What does that mean? It means there is two things wrong with it, there will aways be side effects and secondly you can over dose. Now you may say no. But here is the proof for meth or chemically known as Methamphetamine.
Methamphetamine is a potent central nervous system stimulant which affects neurochemical mechanisms responsible for regulating heart rate, body temperature, blood pressure, appetite, attention, mood and responses associated with alertness or alarm conditions. The acute effects of the drug closely resemble the physiological and psychological effects of an epinephrine-provoked fight-or-flight response, including increased heart rate and blood pressure, vasoconstriction (constriction of the arterial walls), bronchodilation, and hyperglycemia (increased blood sugar). Users experience an increase in focus, increased mental alertness, and the elimination of fatigue, as well as a decrease in appetite.
Users must also take caution and avoid being showered by cold water, riding high-speed roller coasters, consuming caffeine powered drinks, or exercising and weight lifting, as these actions can trigger hypertension, nervousness, extreme rapid heartbeat, dilated heartbeat, or sudden death.
The methyl group is responsible for the potentiation of effects as compared to the related compound amphetamine, rendering the substance on the one hand more lipid soluble and easing transport across the blood brain barrier, and on the other hand more stable against enzymatic degradation by MAO. Methamphetamine causes the norepinephrine, dopamine and, serotonin(5HT) transporters to reverse their direction of flow. This inversion leads to a release of these transmitters from the vesicles to the cytoplasm and from the cytoplasm to the synapse (releasing monoamines in rats with ratios of about NE:DA = 1:2, NE:5HT= 1:60), causing increased stimulation of post- synaptic receptors. Methamphetamine also indirectly prevents the reuptake of these neurotransmitters, causing them to remain in the synaptic cleft for a prolonged period (inhibiting monoamine reuptake in rats with ratios of about: NE:DA = 1:2.35, NE:5HT = 1:44.5[10]).
Recent research published in the Journal of Pharmacology And Experimental Therapeutics (2007)[1], indicates that methamphetamine binds to a group of receptors called TAAR. TAAR is a newly discovered receptor system which seems to be affected by a range of amphetamine- like substances called trace amines.
Range of Effects Common immediate side effects.:[17]
Euphoria Increased energy and attentiveness Diarrhea, nausea Loss of appetite, insomnia, tremor, jaw-clenching (Bruxism) Agitation, compulsive fascination with repetitive tasks (Punding) Talkativeness, irritability, panic attacks Increased libido Dilated pupils Side effects associated with chronic use:
Drug craving Weight loss Withdrawal-related depression and anhedonia Rapid tooth decay ("meth mouth") Amphetamine psychosis, mainly due to sleep deprivation Side effects associated with overdose:
Brain damage (Neurotoxicity) Formication (sensation of flesh crawling with bugs, with possible associated compulsive picking and infecting sores) Paranoia, delusions, hallucinations Rhabdomyolysis (Muscle breakdown) which leads to Kidney failure Death from over dose is usually due to stroke or heart failure, but can also be caused by hyperthermia or kidney failure.
Meth Mouth
Methamphetamine addicts may lose their teeth abnormally quickly, a condition known as "meth mouth". This effect is not caused by any corrosive effects of the drug itself, as per commonly repeated myth. According to the American Dental Association, meth mouth "is probably caused by a combination of drug-induced psychological and physiological changes resulting in xerostomia (dry mouth), extended periods of poor oral hygiene, frequent consumption of high calorie, carbonated beverages and tooth grinding and clenching."[18] Similar, though far less severe symptoms have been reported in clinical use of other amphetamines, where effects are not exacerbated by a lack of oral hygiene for extended periods.[19]
Like other substances which stimulate the sympathetic nervous system, methamphetamine causes decreased production of acid-fighting saliva and increased thirst, resulting in increased risk for tooth decay, especially when thirst is quenched by high-sugar drinks.[20]
Sexual Behaviour
Users may exhibit sexually compulsive behaviour while under the influence. This disregard for the potential dangers of unprotected sex or other reckless sexual behavior may contribute to the spread of sexually transmitted infections (STIs) or sexually transmitted diseases (STDs).
Among the effects reported by methamphetamine users is an increase in the need and urgency for sex, the ability to have sex for extended periods of time, and an inability to ejaculate or reach orgasm or physical release. In addition to increasing the need for sex and enabling the user to engage in marathon sex sessions, methamphetamine lowers inhibitions and may cause users to behave recklessly or to become forgetful. Additionally, many chronic users find themselves engaging in excessive and repeated masturbation. This type of behavior often includes the use of fetish type pornography and also may include experimentation with dangerous behaviors such as auto-erotic asphyxiation.
According to a recent San Diego study[citation needed], methamphetamine users often engage in unsafe sexual activities, and forget or choose not to use condoms. The study found that methamphetamine users were six times less likely to use condoms. The urgency for sex combined with the inability to achieve release (ejaculation) can result in tearing, chafing, and trauma (such as rawness and friction sores) to the sex organs, the rectum and mouth, dramatically increasing the risk of transmission of HIV and other sexually transmitted diseases. Methamphetamine also causes erectile dysfunction due to vasoconstriction.
Addiction
In an article about his son's addiction to methamphetamine, California writer and former methamphetamine user David Schiff said:
" This drug has a unique, horrific quality. "
In an interview, Stephan Jenkins, the singer in the band Third Eye Blind, said that methamphetamine makes you feel 'bright and shiny.'
" It also makes you paranoid, incoherent and both destructive and pathetically and relentlessly self-destructive. Then you will do unconscionable things in order to feel bright and shiny again.[21] "
Methamphetamine is potentially addictive, particularly when injected or smoked.[22] While not life-threatening, withdrawal is often intense and, as with all addictions, relapse is common. To combat relapse, many recovering addicts attend 12 Step meetings, such as Crystal Meth Anonymous.
Former users have noted that they feel stupid or dull when they quit using methamphetamine. This is because the brain is adapting a need for methamphetamine to think faster, or at what seems to be a higher level. It is possible that daily administration of the amino acids L- Tyrosine and L-5HTP/Tryptophan can aid in the recovery process by making it easier for the body to reverse the depletion of Dopamine, Norepinephrine, and Serotonin. Although studies involving the use of these amino acids have shown some success, this method of recovery has not been shown to be consistently effective.
It is shown that taking ascorbic acid prior to using methamphetamine may help reduce acute toxicity to the brain, as rats given the human equivalent of 5-10 grams of ascorbic acid 30 minutes prior to methamphetamine dosage had toxicity mediated, yet this will likely be of little avail in solving the serious behavioral problems associated with methamphetamine use that create many of the problems the users experience ________________________________________________________________________________________
United Kingdom As of 18 January 2007,[30] methamphetamine is classified as a Class A drug under the Misuse of Drugs Act 1971 following a recommendation made by the Advisory Council on the Misuse of Drugs in June 2006.[31] It had previously been classified as a Class B drug, except when prepared for injection
New Zealand Methamphetamine is a Class A controlled drug under the New Zealand Misuse of Drugs Act 1500. The maximum penalty for production and distribution is imprisonnment for life. While in theory a doctor could prescribe it for an appropriate indication, this would require case-by- case approval by the director-general of public health. In New Zealand, Methamphetamine is most commonly referred to by the street name P[27] (short for "pure methamphetamine"[28]).
The Netherlands Methamphetamine is not approved for medical use in The Netherlands. It falls under Schedule I of the Opium Act. Although production and distribution of this drug are prohibited, few people who were caught with a small amount for personal use have been prosecuted.
Australia The medical use of methamphetamine is recognised in Australia. It is also known as Ice and has become the focus of a nation-wide crackdown. As of 2007, this has become part of the election agenda for both major political parties.
Canada Methamphetamine is not approved for medical use in Canada. The maximum penalty for the production and distribution is imprisonment for life.
And your right that it has had an infinatly greater impact on our nation. You are also right that we have not seen nothing yet. It just gets worse.
My product is all natural and organic which means you can have as much of it as you like with no overdose and there are only positive side effects. Why? Because you are feeding the body with what it already has but it is starving for more. AND IT IS HELPING PEOPLE - NOT KILLING PEOPLE. You be the judge.
Seyhan - 14 Jun 2007 02:52 GMT I nearly forgot. The people that won the Nobel Science Prize were three american pharmacologists here are there names: Robert Furchgott, Ferid Murad, and Louis Ignarro
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