D,L-Phenylalanine By Andrew Novick


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DATE: Sept. 3, 2020, 9:10 a.m.

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  1. D,L-Phenylalanine
  2. By Andrew Novick
  3. Antidepressant drugs that modulate the neurotransmitters serotonin and norepinephrine can often take up to 6 weeks to produce substantial response. This delayed response phenomenon is one of the most commonly cited flaws of the SSRI’s and related drugs. There are, however, other classes of drugs that are known to produce much more rapid relief of even the most severe depressions. Dopaminergic stimulants such as amphetamines as well as opiates like morphine are quite possibly the most powerful and fast acting antidepressants available. Their fast action lies in the modulation of the dopamine and opiate receptor complexes. Unfortunately, due to issues of tolerance and abuse potential, amphetamines and opiates are tightly controlled and not widely prescribed for depression.
  4. So, if the key to a quick antidepressant response lies within the dopamine and opiate systems, are there any natural supplements that have the ability to upregulate these systems? This is where DLPA comes in. DLPA plays an important role in providing the building blocks for dopamine and phenylethylamine (the body’s natural amphetamine) and has the ability to greatly increase the action of our endorphins (the body’s natural morphine).
  5. DLPA, is a 50:50 mixture of the D and L isomers of phenylalanine. It was found to be as effective as the tricyclic antidepressant imipramine in relieving depressive symptoms (17), can be used to treat ADHD (18) as well as potentiate opiate analgesia (16).
  6. L-Phenylalanine, the form that is found in most foods, is an essential amino acid that can be converted into L-tyrosine (the precursor to norepinephrine and dopamine, for more info see David Tolson’s article on Tyrosine). But unlike L-tyrosine, L-phenyalanine is a direct precursor to phenylethylamine (PEA). L-phenylalanine is converted to PEA at a rate similar to that of L-tyrosine to dopamine (1). PEA acts as an endogenous amphetamine in the brain that promotes energy, elevates mood, and favors aggression (2).A deficit of PEA is implicated in ADHD and depression while too much PEA might be a part of schizophrenia (3). When administered with the MAOI l-deprenyl, PEA improves mood similar to amphetamine but without tolerance (9).
  7. L-phenyalanine is readily absorbed across the brain-blood-barrier (4), and while there is conflicting evidence to as whether increases in dietary phenylalanine leads to increased levels of PEA in the brain (5,6), L-phenylalanine can improve mood and relieve depression when orally administered alone (7) and with the MAOI l-deprenyl (8).
  8. D-phenylalanine has similar nutritional value to L-phenylalanine (10) and can lead to increases in PEA, though a different pathway than the L enantiomer (11). What makes the D-phenylalanine remarkable is its ability to inhibit the enzyme enkephalinase and prevent the degradation of endorphins (13). Endorphins induce analgesia (pain relief) and probably play a role in DLPA’s mood enhancing effects. Although D-phenylalanine appears to be ineffective by itself for reducing chronic pain (14), it can greatly pontentiate the pain relieving effects of both acupuncture and narcotic drugs such as morphine (15,16).
  9. Dosages of DLPA used in most studies are usually considered very modest (200mg/day), and effective dosages are probably more in the range of 1g a day or more (19). Dosages should be divided up over the course of the day and taken in between meals. To treat depression, DLPA can be used alone or with l-deprenyl. For augmented pain relief, one can combine DLPA with prescribed narcotics. Those suffering from PKU (phenyketonuria) or schizophrenia should avoid DLPA supplementation as it might exacerbate the condition.
  10. *** Buy Life Extension brand D,L-Phenylalanine 500mg/cap: https://amzn.to/2ZD2s8n
  11. 1. Janssen PA, Leysen JE, Megens AA, Awouters FH. Does phenylethylamine act as an
  12. endogenous amphetamine in some patients? Int J Neuropsychopharmcol 1999 Sep; 2(3):229-240
  13. 2. Sabelli HC; Javaid JI. Phenylethylamine modulation of affect: therapeutic and diagnostic implications. J Neuropsychiatry Clin Neurosci 1995 Winter; 7(1):6-14
  14. 3. Wolf ME, Mosnaim AD. Phenylethylamine in neuropsychiatric disorders.
  15. Gen Pharmacol. 1983;14(4):385-90.
  16. 4. Momma S, Aoyagi M, Rapoport SI, Smith QR. Phenylalanine transport across the blood-brain barrier as studied with the in situ brain perfusion technique. J Neurochem. 1987 Apr;48(4):1291-300.
  17. 5. Silkaitis RP, Mosnaim AD. Pathways linking L-phenylalanine and 2-phenylethylamine with p-tyramine in rabbit brain. Brain Res. 1976 Sep 10;114(1):105-15.
  18. 6. Davis BA, O'Reilly RL, Placatka CL, Paterson IA, Yu PH, Durden DA. Effect of dietary phenylalanine on the plasma concentrations of phenylalanine, phenylethylamine and phenylacetic acid in healthy volunteers. Prog Neuropsychopharmacol Biol Psychiatry. 1991;15(5):611-23.
  19. 7. Sabelli HC, Fawcett J, Gusovsky F, Javaid JI, Wynn P, Edwards J, Jeffriess H, Kravitz H. Clinical studies on the phenylethylamine hypothesis of affective disorder: urine and blood phenylacetic acid and phenylalanine dietary supplements. J Clin Psychiatry. 1986 Feb;47(2):66-70.
  20. 8. Birkmayer W, Riederer P, Linauer W, Knoll J. L-deprenyl plus L-phenylalanine in the treatment of depression. J Neural Transm. 1984;59(1):81-7.
  21. 9. Sabelli H; Fink P; Fawcett J; Tom C Sustained antidepressant effect of PEA replacement. J Neuropsychiatry Clin Neurosci, 1996 Spr, 8:2, 168-71
  22. 10. Friedman M, Gumbmann MR. The nutritive value and safety of D-phenylalanine and D-tyrosine in mice. J Nutr. 1984 Nov;114(11):2089-96.
  23. 11. Borison RL, Maple PJ, Havdala HS, Diamond BI. Metabolism of an amino acid with antidepressant properties. Res Commun Chem Pathol Pharmacol. 1978 Aug;21(2):363-6.
  24. 13.Ehrenpreis S. Analgesic properties of enkephalinase inhibitors: animal and human studies. Prog Clin Biol Res. 1985;192:363-70.
  25. 14. Walsh NE, Ramamurthy S, Schoenfeld L, Hoffman J. Analgesic effectiveness of D-phenylalanine in chronic pain patients. Arch Phys Med Rehabil. 1986 Jul;67(7):436-9.
  26. 15. Kitade T, Odahara Y, Shinohara S, Ikeuchi T, Sakai T, Morikawa K, Minamikawa M, Toyota S, Kawachi A, Hyodo M, et al. Studies on the enhanced effect of acupuncture analgesia and acupuncture anesthesia by D-phenylalanine (2nd report)--schedule of administration and clinical effects in low back pain and tooth extraction. Acupunct Electrother Res. 1990;15(2):121-35.
  27. 16. Russell AL, McCarty MF. DL-phenylalanine markedly potentiates opiate analgesia - an example of nutrient/pharmaceutical up-regulation of the endogenous analgesia system. Med Hypotheses. 2000 Oct;55(4):283-8.
  28. 17. Beckmann H, Athen D, Olteanu M, Zimmer R. DL-phenylalanine versus imipramine: a double-blind controlled study. Arch Psychiatr Nervenkr. 1979 Jul 4;227(1):49-58.
  29. 18. Wood DR, Reimherr FW, Wender PH. Treatment of attention deficit disorder with DL-phenylalanine. Psychiatry Res. 1985 Sep;16(1):21-6.
  30. 19. Young SN. Behavioral effects of dietary neurotransmitter precursors: basic and clinical aspects. Neurosci Biobehav Rev. 1996 Summer;20(2):313-23.

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