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Tyrosine

Common Name: Tyrosine
Synonyms: L-tyrosine

Overview:

Tyrosine is classified as a conditionally essential amino acid. Although under normal circumstances the body can make all of the tyrosine that it needs, when certain conditions such as phenylketonuria exist, tyrosine must come from dietary sources. L-tyrosine is manufactured in the body from phenylalanine and is found in soy, chicken turkey nuts, dairy, legumes (beans and peas), avocados, bananas and pumpkin seeds.

Tyrosine, as with all amino acids, is involved in protein synthesis. Protein synthesis is not the only role it plays. Tyrosine is a precursor of not only the thyroid hormones thyroxine and triiodothyronine but the fight or flight hormone, epinephrine as well as the neurotransmitters, norepinephrine and dopamine. Tyrosine is also used by the body to manufacture melanin, the substance that gives hair and skin their color.

Tyrosine also has the ability to bind unstable free radicals and is considered to be a mild antioxidant. Because of its antioxidant capabilities, tyrosine may be helpful for people who have been exposed to harmful chemicals (such as from smoking) or radiation.

Low levels of tyrosine have been associated with:

  1. Low blood pressure
  2. Low body temperature
  3. An under active thyroid
  4. Depression
  5. Edema
  6. Fatigue
  7. Lethargy
  8. Liver damage
  9. Loss of pigment of the hair and skin

Benefits

Tyrosine is essential in those who suffer from phenylketonuria (a genetic condition where people cannot metabolize phenylalanine). By eliminating all sources of phenylalanine, the brain damage and mental retardation that results can be avoided. The tyrosine deficiency that develops is because phenylalanine is necessary for the manufacture of tyrosine.

Preliminary studies of tyrosine’s benefits have shown that:

  1. Tyrosine may help in the body’s ability to handle stress. This is because of the fact that it is the precursor for epinephrine and norepinephrine, the body’s two main stress related hormones. Taken ahead of time, tyrosine can help some people ward off the body’s reactions to such stressful situations as surgery, emotional upset, and sleep deprivation. A small study of marines showed that they were better able to handle and recovered faster from sleep deprivation when they took supplements of tyrosine.
  2. In combination with conventional treatment, tyrosine appears to help in the successful treatment of cocaine abuse and withdrawal. It is usually used in conjunction with tryptophan (an essential amino acid) and imipramine ( an antidepressant). It has also proven helpful in caffeine and nicotine withdrawal.
  3. Tyrosine may be helpful in the treatment of depression as tyrosine levels are often low in people who suffer from depression. Early studies showed that when used in conjunction with 5-HTP (5-hydroxytryptophan). However, more studies are needed to confirm the benefit of tyrosine supplements in the treatment of mild to moderate depression.
  4. Tyrosine may prove helpful in the treatment of vitiligo (depigmentation of random areas of skin). This is an assumption made because tyrosine is involved the making of melanin and the fact that phenylalanine and ultra violet light are used to treat this condition.
  5. Because tyrosine is a precursor to dopamine and preliminary studies have shown that tyrosine can cause an increase in the levels of dopamine in the brain, it has been speculated that tyrosine may be helpful in the treatment of Parkinson’s disease. This theory however has never been proven.
  6. Body builders supplement with tyrosine in order to better tolerate stress and to increase muscle mass. These uses however have never been studied.

Recommended Dosage:

  1. Therapeutic doses range from 7-30gms daily
  2. This dosage should be divided into three doses taken 30 minutes before a meal
  3. Doses of tyrosine should also be taken with a multivitamin tablet as vitamin B6, folate )B9) and copper are helpful in converting tyrosine into the neurotransmitters, norepinephrine and dopamine.
  4. Total dietary intake of tyrosine should never exceed 12,000mg
  5. Children who need supplementation of tyrosine should do so only under the direct care of their healthcare practioner.

Precautions

  1. Those who suffer from migraine headaches should avoid tyrosine. It has been known to trigger migraine headaches and gastrointestinal upset in those who suffer from this condition.
  2. tyrosine taken with MAOIs, antidepressant medications like phenelzine, tranylcypromine, pargyline and selegiline, may cause a severe increase in blood pressure. This hypertensive crisis can lead to a heart attack or stroke. Because of this people who are taking MAOI’s should avoid tyrosine supplements and even foods that contain a high amount tyrosine.
  3. In animal studies, tyrosine increased the appetite suppressing effects of several medications including phenypropanolamine, ephedrine and amphetamine. Human studies are now needed to see if this characteristic of tyrosine is also seen in human beings.
  4. Again animal studies have shown that tyrosine increases the pain relieving effects of morphine.
  5. Levodopa (a medication used to treat Parkinson’s disease) may interfere with the absorption of tyrosine.
  6. Those who suffer from melanoma should avoid tyrosine
  7. Those with inborn errors of metabolism such as alkaptonuria and tyrosinemia type I and II should not take tyrosine

Women who are pregnant or breastfeeding should consult a health care provider before using any supplements. The affects of this supplement has not been tested on children and those suffering from liver or kidney disease. It is recommended that in people with liver or kidney disease this supplementation not be used.

Web References

  1. http://www.umm.edu/altmed/ConsSupplements/Tyrosinecs.html
  2. http://healthlibrary.epnet.com/GetContent.aspx?token=e0498803-7f62-4563-8d47-5fe33da65dd4&chunkiid=21794
  3. http://www.pdrhealth.com/drug_info/nmdrugprofiles/nutsupdrugs/lty_0256.shtml

Printed Reference Material

  1. Awad AG. Diet and drug interactions in the treatment of mental illness – a review. Can J Psychiatry. 1984;29:609-613.
  2. Banderet LE, Lieberman HR. Treatment with tyrosine, a neurotransmitter precursor, reduces environmental stress in humans. Brain Res Bull. 1989; 22:759-762.
  3. Camacho F, Mazuecos J. Treatment of vitiligo with oral and topical phenylalanine: 6 years of experience. Arch Dermatol. 1999;135:216-217
  4. Chakraborty DP, Roy S, Chakroborty AK. Vitiligo, psoralen, and meanogenesis: some observations and understanding. Pigment Cell Res. 1996;9(3):107-116.
  5. Chiaroni P, Azorin JM, Bovier P, et al. A multivariate analysis of red blood cell membrane transports and plasma levels of L-tyrosine and L-tryptophan in depressed patients before treatment and after clinical improvement. Neuropsychobiology. 1990;23(1):1-7.
  6. Deijen JB, Orlebeke JF. Effect of tyrosine on cognitive function and blood pressure under stress. Brain Res Bull. 1994;33(3):319-323.
  7. Elwes RD, Crewes H, Chesterman LP, et al. Treatment of narcolepsy with L-tyrosine: double-blind, placebo-controlled trial. Lancet. 1989; 2(8671):1067-1069.
  8. Fernstrom JD. Can nutrient supplements modify brain function? Am J Clin Nutr. 2000;71(6 Suppl):1669S-1675S.
  9. Fugh-Berman A, Cott JM. Dietary supplements and natural products as psychotherapeutic agents. Psychosom Med. 1999;61:712-728.
  10. Gelenberg AJ, Gibson CJ. Tyrosine for the treatment of depression. Nutr Health. 1984; 3:163-173.
  11. Gelenberg AJ, Wojcik JD, Falk WE, et al. Tyrosine for depression: a double-blind trial. J Affect Disord. 1990; 19:125-132.
  12. Gelenberg AJ, Wojcik JD, Gibson CJ, Wurtman RJ. Tyrosine for depression. J Psychiatr Res. 1982-83; 17:175-180.
  13. Growdon JH, Melamed E, Logue M, et al. Effects of oral L-tyrosine administration on CSF tyrosine and homovanillic acid levels in patients with Parkinson's disease. Life Sci. 1982;30:827-832,
  14. Hull KM, Maher TJ. L-Tyrosine potentiates the anorexia induced by mixed-acting sympathomimetic drugs in hyperphagic rats. J Pharmacol Exp Ther. 1990;255(2):403-409.
  15. Hull KM, Tolland DE, Maher TJ. L-tyrosine potentiation of opioid-induced analgesia utilizing the hot-plate test. J Pharmacol Exp Ther. 1994;269(3):1190-1195.
  16. Kelly GS. Nutritional and botanical interventions to assist with the adaptation to stress. Altern Med Rev. 1999;4940;249-265.
  17. Kirschmann GJ and Kirschmann JD. Nutrition Almanac, 4th ed. New York, NY: McGraw-Hill;1966:304.
  18. Koch R. Tyrosine supplementation for phenylketonuria treatment. Am J Clin Nutr. 1996;64(6):974-975.
  19. Menkes DB, Coates DC, Fawcett JP. Acute tryptophan depletion aggravates premenstrual syndrome. J Affect Disord. 1994;3291):37-44.
  20. Meyers S. Use of neurotransmitter precursors for treatment of depression. Altern Med Rev. 2000;5(1):64-71.
  21. Neri DF, Wiegmann D, Stanny RR, Shappell SA, McCardie A, McKay DL. The effects of tyrosine on cognitive performance during extended wakefulness.
    Aviat Space Environ Med. 1995;66(4):313-319.
  22. Parry BL. The role of central serotonergic dysfunction in the aetiology of premenstrual dysphoric disorder: therapeutic implications. CNS Drugs2001;15(4):277-285.
  23. Pizzorno JE and Murray MT. Textbook of Natural Medicine, Vol 2. New York, NY: Churchill Livingstone; 1999:1049-1059.
  24. Poustie VJ, Rutherford P. Tyrosine supplementation for phenylketonuria. Cochrane Database Syst Rev. 2000;(2):CD001507.
  25. Reimherr FW, Wender PH, Wood DR, Ward M. An open trial of L-tyrosine in the treatment of attention deficit disorder, residual type. Am J Psychiatry. 1987; 144:1071-1073.
  26. Riederer P. L-Dopa competes with tyrosine and tryptophan for human brain uptake. Nutr Metab. 1980;24(6):417-423.
  27. Smith ML, Hanley WB, Clarke JT, et al. Randomised controlled trial of tyrosine supplementation on neuropsychological performance in phenylketonuria. Arch Dis Child. 1998;78(2):116-121.
  28. Smith ML, Hanley WB, Clarke JTR, et al. Randomised controlled trial of tyrosine supplementation on neuropsychological performance in phenylketonuria. Arch Dis Child. 1998; 78:116-121.
  29. van Spronsen FJ, van Rijn M, Bekhof J, Koch R, Smit PG. Phenylketonuria: tyrosine supplementation in phenylalanine-restricted diets. Am J Clin Nutr. 2001;73(2):153-157.
  30. Wagenmakers AJ. Amino acid supplements to improve athletic performance. Curr Opin Clin Nutr Metab Care. 1999;2(6):539-544.
  31. Yehuda S. Possible anti-Parkinson properties of N-(alpha-linolenoyl) tyrosine. A new molecule. Pharmacol Biochem Behav. 2002;72(1-2):7-11.
  32. Young SN. Behavioral effects of dietary neurotransmitter precursors: basic and clinical aspects. Neurosci Biobehav Rev. 1996; 20:313-323.

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