HARMINE

'Harmine'
Harmine
Systematic name	7-MeO-1-Me-9H-pyrido[3,4-b]-indole
Chemical formula	C13H12N2O
Molecular mass	212.25 g/mol
Melting point	321 °C (·HCl)
	262 °C (·HCl·2H2O)[1]
CAS number	[442-51-3]
SMILES	CC1=NC=CC2=C1NC3=C2C=CC(=C3)OC

'Harmine' is an alkaloid belonging to the Beta-carboline family of compounds. It occurs in a number of different plants, most notably the Middle Eastern plant harmal or Syrian rue (''Peganum harmala'') and the South American vine ''Banisteriopsis caapi'' ('yage', 'ayahuasca'). Harmine is a reversible monoamine oxidase inhibitor (MAO inhibitor or MAOI) and CNS stimulant. It inhibits MAO-A but has no effect MAO-B.^[2]

Contents

Uses

Adverse effects

Natural sources

References

See also

Categorization

Uses

As a MAO inhibitor, harmine inhibits the breakdown of monoamines by enzymes called monoamine oxidases. Monoamines include neurotransmitters (serotonin, dopamine), hormones (melatonin) and drugs, including many hallucinogens (psilocybin, dimethyltryptamine (DMT), mescaline). By slowing the breakdown of neurotransmitters, MAOIs can help to replenish the body's supply of these chemicals, and many MAOIs are used as antidepressants. Harmine has not been the subject of much clinical research in the treatment of depression, which could be due in part to its restricted legal status in many countries, as well as the existence of synthetic MAOIs with fewer side effects.
''P. harmala'' and ''B. caapi'' are both traditionally used for their psychoactive effects. ''B. caapi'' has a tradition of use in conjunction with plants containing the drug DMT. Traditionally, ''B. caapi'' is consumed as a drink, with or without the DMT-bearing plants (see Ayahuasca). Ordinarily, DMT is not active when taken orally, but users report very different effects when DMT is present in such beverages. Harmine and substances containing it have been used in conjunction with many other drugs by modern experimenters. Many hallucinogens appear to exhibit increased potency when used in this way.
Harmine is also a useful fluorescent pH indicator. As the pH of its local environment increases, the fluorescence emission of harmine decreases.

Adverse effects

It is important to note that unlike synthetic pharmaceutical MAOIs such as Phenelzine, harmine is reversible and selective meaning it does not have nearly as high a risk for the "cheese syndrome" caused by consuming tyramine-containing foods, which is a risk associated with pharmaceutical MAOIs sometimes (mistakenly) applied to all MAO inhibitors.^[3] Harmine, and plants containing significant amounts of harmine and other harmala alkaloids are generally not considered safe treatments for depression within the medical community.^[4]

Natural sources

Harmine is found in a wide variety of different organisms, most of which are plants. Shulgin (1997)^[5] lists about thirty different species known to contain harmine, including seven species of butterfly in the Nymphalidae family. The harmine-containing plants listed include tobacco, two species of passion flower/passion fruit, and numerous others.
In addition to ''B. caapi'', at least three members of the Malpighiaceae contain harmine, including two more ''Banisteriopsis'' species and the plant ''Cabi paraensis''. Callaway, Brito and Neves (2005)^[6] found harmine levels of 0.31-8.43% in ''B. caapi'' samples.
The Zygophyllacae family, which harmal belongs to, contains at least two other harmine-bearing plants: ''Peganum nigellastrum'' and ''Zygophyllum fabago''.

References

1. The Merck Index (1996). 12th edition
2. Abstract Gerardy J, "Effect of moclobemide on rat brain monoamine oxidase A and B: comparison with harmaline and clorgyline.", Department of Pharmacology, University of Liège, Sart Tilman, Belgium.
3. McKenna, Callaway, & Grb. "Scientific Investigation of Ayahuasca", Scientific Investigation of Ayahuasca, retrieved 2007-06-03.
4. Eric Yarnell, Kathy Abascal. 2001, Botanical Treatments for Depression, 7(3): 138-143.
5. Shulgin, Alexander and Shulgin, Ann (1997). TiHKAL: The Continuation. pp. 713-14
6. Callaway JC, Brito GS & Neves ES (2005). Phytochemical analyses of Banisteriopsis caapi and Psychotria viridis. Journal of Psychoactive Drugs 37(2): 145-150.

See also

★ Beta-carboline

★ Harmala alkaloid

Categorization