Evaluation of The Health Beneficial Properties of The Aromatic Ether Myristicin, A Volatile Oil Derived From Various Plants Sources

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Evaluation of the health beneficial properties of the aromatic ether

Myristicin, a volatile oil derived from various plants sources


Presented by:
Annie Mancha & Jerry Fuentes
The University of Texas-Pan American
1201 W. University Drive Edinburg, Texas 78539

Outline

Background

Information
Where is myristicin found?
What are the historical uses of myristicin?
In what capacity is myristicin currently used?
Are there drawbacks to myristicin?
What are the future uses of myristicin?

Background Information: Myristicin

An aromatic ether extracted from nutmeg,


parsley, and carrots
Molecular formula: C11H12O3
IUPAC: 4-Methoxy-6-prop-2-enylbenzo[1,3]dioxole
Other: 5-Allyl-1-methoxy-2,3(methylenedioxy)benzene
Many historical uses such as a diuretic
Chemopreventative, hepatoprotective, can
be psychotropic, can be toxic

Where can you find Myristicin?

Parsley
Nutmeg
Dill
Carrots
Broccoli
Coffee

Background Information: Parsley


Botanical Name: Carum petroselinum
Parts used: leaves, roots, and sometimes fruit
Habitat: Linnaeus stated its wild habitat to be Sardinia ;

eastern mediterranean regions


Aromatic oils of parsley make it an ideal breath freshener
High in vitamins A and C; Contains iron, iodine, and

copper
Two different varieties today: root parsley & leaf parsley
Many varieties such as plain-leaved, curled-leaved,

Hamburg
Curled-leaf parsley (Petroselinum crispum) is used

extensively for garnishing and seasoning foods

Constituents of Parsley

Many constituents; main is essential oil


Contains the volatile oils myristicin, apiole, beta-bisabolene,
flavanoids such as apiin, apigenin, and luteolin, and
furanocuoumarins such as psoralen
10-30% (in leaves and roots) are myristicin, limonene, and
menthatriene
Minor components are mono- and sesquiterpenes
Essential oil from fruits is dominated by myristicin (6080%)
Curly varieties are higher in myristicin

Historical Uses of Parsley

Romans were first to use parsley as food and also as a


garland
Greeks used parsley medicinally but did not eat it
Greek medicinal use of parsley spread to India where it
was used in Ayurvedic medicine
Carminative
Diuretic
Emmenagogue
expectorant
Spread to the Americas in the 17th century

Background Information: Nutmeg

Botanical name: Myristica fragrans


Parts used: dried kernel of the seeds
Origin: Banda Islands, Malayan Archipelago,
Molucca Islands, and cultivated in Sumatra, French
Guiana
Nutmegs have a strong, peculiar and delightful
fragrance and a very strong bitter warm aromatic
taste
oil of nutmeg, often termed 'oil of mace' or 'nutmeg
butter,' is made by bruising the nuts and treating
them with steam
The seed or nutmeg is firm, fleshy, whitish,
covered by red-brown veins and is abounding in oil

Constituents of Nutmeg
Many constituents:
lignin, stearin, volatile oil (myristicin), starch, and gum
By submitting nutmegs and water to distillation, a
volatile oil is obtained.
The powder of nutmegs, beaten to a pulp with water, then
pressed between heated plates, gives from 10 to 30 per cent
of orange colored scented concrete oil erroneously called
oil of mace

Historical Uses of Nutmeg

Oil of Nutmeg is used to conceal the taste of various drugs


Oil was also used as local stimulant to the
gastro-intestinal tract
Used for flatulence
Used to stop nausea and vomiting

Current Uses of Myristicin


Non-Medicinal
Most commonly used culinary
herb in the United States
Insecticidal agent
Used to flavor cigarettes
Medicinal
Still used as a botanical remedy
Chemopreventative
hepatoprotective

Myristicin and Cancer

Parsley leaf oil exhibited high biological activity that


warrants further study
Myristicin from Parsley leaf oil induces phase II enzymes
allowing for detoxification of carcinogens
Glutathione S-transferase: A phase II enzyme that detoxifies
xenobiotics and catalyzes the reaction of glutathione with
electrophiles including activated carcinogens to form less
toxic conjugates that are readily excreted.
NAD(P)H:Quinone oxidoreductase: Catalyzes the
obligatory two electron reduction of quinones and thus
shields the cells against the electrophilicity of quinones and
oxidative stress.

Myristicin and the Liver

Limited information is available to systematically


examine the effects of spices on liver injury
Screening of various compounds found potent activity
of nutmeg
A single oral administration of myristicin at a dose of
50, 100, or 200 mg/kg dose prohibited elevations of
serum ALT and AST activities in mice with liver injury
induced in the lab
This study shows that nutmeg, particularly myristicin
isolated from nutmeg, has a potent hepatoprotective
activity

Myristicin in Cigarettes

Bidi cigarettes: small hand-rolled cigarettes


produced primarily in India
Originated in India around 1905 as small
unflavored cigarettes
Made popular in America because of flavors
Clove cigarettes: kreteks another highly
flavored tobacco product that is popular in
America
Flavor-related compounds were found in
various brands at very high levels
Myristicin and elemicin showed consistent
levels in many of the tobacco-containing
bidis tested
Myristicin was also consistently present in
mainstream smoke from bidis

Drawbacks of Myristicin

Nutmeg seeds have been used as hallucinogenic narcotic, and many reports
have been issued on nutmeg poisoning.
Acute or chronic nutmeg or myristicin abuse has adverse effects on neuronal
cells.
The accumulation of myristicin from decreased oxidation may cause
psychopharmacological effects such as hallucination.
Myristicin has been shown to have anti-cholinergic and psychotropic effects.
3-methoxy-4,5-methylenedioxyamphetamine (MMDA), one of the metabolites
of myristicin, has a pronounced hallucinogenic effect resembling the
inebriation induced by mescaline.

Future Studies

Myristicin against benzo[a]pyrene-induced cancer


Determine the hepatoprotective properties of myristicin
Determine whether myristicin induces phase II enzymes in a
substrate-specific manner
Investigate which phase II enzymes myristicin can induce
Harfmul effects of inhalation of myristicin from cigarettes

Conclusion & Questions

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