Umbellulone
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| Names | |
|---|---|
| IUPAC name
4-Methyl-1-(propan-2-yl)bicyclo[3.1.0]hex-3-en-2-one | |
| Other names
Thujenone; Thujen-2-one; Umbellulon | |
| Identifiers | |
24545-81-1  546-78-1 (1R,5S) | |
| ChemSpider | 82348 |
| Jmol 3D image | Interactive graph |
| PubChem | 91195 |
| |
| |
| Properties | |
| C10H14O | |
| Molar mass | 150.22 g·mol−1 |
| Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
| Infobox references | |
Umbellulone is a headache-inducing monoterpene ketone found in the leaves of the tree Umbellularia californica, sometimes known as the "headache tree".[1][2]
It is hypothesized to cause headaches by influencing the trigeminovascular system via TRPA1.[1]
History
The Umbellularia californica is a tree native to the coastal forest of California.
Menzies was the first to collect the oil at the end of the 18th century. In 1826 this tree was classified as a laurel, Laurus regia, by Douglass. He probably intended to indicate the beauty and splendor of the tree.
In 1833 the tree got another classification by Hooker and Arnott, Tetranthera californica. Shortly after that the present name was given by Nuttal, Umbellularia californica. In 1875 Heaney obtained a colorless liquid (Oreodaphenol) via fractionation under reduced pressure. This oil of the California laural possess a pungent odor.
Stillman (1880) did a fractionation at 215-216 °C. He discovered that inhalation of its fumes can lead to painful cold sensation and severe headaches. In earlier times the leaves of the tree were used for cures for headaches or stomachaches and even toothaches.
Powers and Lee did in 1904 another fractionation on the oil of the tree at 217-222 °C. The yielded different compounds: pinene, cineol, eugenol, methyl eugenol and a ketone called umbellulone. Umbellulone is the chemical responsible for the headaches induced by the tree. They gave umbellulone the following structural formula (Fig. 1).
In 1908 the structural formula was adapted by Tutin (Fig. 2A).
This was correct later that year by Semmller, he gave the structural formula which is accepted today (Fig. 2B).
Structure and reactivity
Umbellulone is a monoterpene ketone that is found in the leaves of the Umbellularia californica. The formula of umbellulone is C10H14O. There is only one isomer of umbellulone known. Umbellulone is a lipophilic, it's a liquid (oil) at room temperature. The boiling point of umbellulone is 220 °C and the vapor pressure is 0.159 mm/Hg. Due to this extremely low vapor pressure, umbellulone fumes are easily created. This makes the substance easily inhaled. Umbellulone has a high-affinity binding for thiols. The molecule is reactive with most of the thiols, but not with all.[1] The reaction between the thiol cysteamine and umbellulone, is given in figure 3. An European registered medicine called Cystagon® or Procysbi® contains cysteamine, which can interact with umbellulone.
Synthesis
A possible synthesis of Umbellulone is given by the following process[4]. Diazomethyl isopropyl ketone reacts with methyl methacrylate to give 1-carbo-methoxy-2-isobutyryl-1-methylcyclopropane. This reaction gives a yield of 35%. This is then hydrolyzed to a mixture of cis and trans 2-isobutyryl-1-methyl-1-cyclopropane. The trans isomer is isolated and reacts with the cadmium methyl Grignard reagent to 1-acetyl-2-isobutyryl-1-methylcyclopropane. This undergoes an aldol cyclization on treatment with dilute base to umbellulone.
Available forms
At room temperature umbellulone is an liquid (oil). Due to its low vapor pressure, umbellulone fumes are easily created. Physical contact with the substance can be accomplished by direct skin contact of the oil or inhalation of the vapors.
Mechanism of action
Umbellulone is known to be able to react on two ion channels, TRPA1 and TRPM8. Umbellulone has a high affinity to TRPA1 and a lower affinity to TRPM8.
TRPA1
Umbellulone can cause severe headaches by activating transient receptor potential cation channel, subfamily A, member 1 (TRPA1) and influencing the trigeminovascular system via calcitonin gene-related peptide (CGRP). Once inhaled umbellulone will diffuse from the nasal mucosa into the blood circulation. Because of the high lipid structure of umbellulone, the molecule will quickly pass through the epithelial cells and will quickly be absorbed in the blood. From there on, umbellulone is able to reach the perivascular sensory nerve endings of the meningeal vessels. Stimulation of these nerve fibers will eventually lead to the release of CGRP, an nociceptor known for its ability to induce migraine and cluster headache attacks.[1]
To activate TRPA1, umbellulone first has to bind the thiol cysteamine, this will produce a Michael-adduct (Fig. 4). As is seen in figure 4, cysteamine is bound to the first carbon atom of umbellulone. At low concentrations of umbellulone, this adduct molecule will be able to activate TRPA1, umbellulone will inhibit TRPA1 at high concentrations. Activation of TRPA1 will result in the opening of this ion channel. Calcium will enter the cell and the cell membrane will be depolarised. Depolarisation of the membrane will result in the release of CGRP1. Released CGRP can bind to its CGRP-receptor. This will induce a CGRP-dependent local vasodilatation (Fig. 4) of the cerebral blood vessels. Vasodilation of the cerebral blood vessels will increase the bloodflow to the brain outer membranes. CGRP binding to its receptor will also promote mast cell degranulation and infiltration by neutrophils and other immune cells. The increase in immune cells and its inflammatory response is thought to be the main cause of the occurrence of migraine. It’s is still being discussed if vasodilatation of the cerebral blood vessels contributes to the cause of the migraine and headaches. Still the vasodilatory effect and the blood flow increase can be used as an indirect indication for the release of CGRP and therefore for the presence of the migraine and headaches.
TRPM8
Transient receptor potential cation channel, subfamily M, member 8 (TRPM8) is an ion channel that is able to induce an intensely cold sensation when activated. Menthol is the primary ligand of TRPM8, but since umbellulone has some structural similarities with menthol, umbellulone is also able to activate TRPM8. But this is a weak interaction.
Indications
When a person got in contact with umbellulone, the person is likely to experience an intense cold sensation in the nasal cavity. In combination with a headache, an increase in plasma CGRP or irritation of the eyes, the possibility for the person to have been exposed to umbellulone increases.
Toxicity
The oil of the Umbellularia californica contains 40% to 60% of umbellulone. It possesses an effect similar to atropine on the nerves and muscle fibers. Contact with the oil, or even expose to the vapors, can cause:
-headache
-irritation to eyes
-irritation to the nose
-irritation of the mucous membrane
-loss of concentration
-lowering blood pressure
-difficulty with respiration
Umbellulone induces a rapid production of methemoglobine. Methemoglobine is a globin in the blood which mainly consists of ferric (Fe3+) haemoglobin instead of the usual ferrous (Fe2+) haemoglobin. Methemoglobin has a decreased ability to bind oxygen. But in combination with the 3 other ferrous irons on the hemoglobin unit, the oxygen release is also decreased. Red blood cells will be less able to nurture organs with oxygen. Therefore the probability for a hypoxia increases. Methemoglobin lethality is possible at higher concentrations than 50% of the substance in red blood cells.
The Umbellularia californica should not be mistaken for the conventional bay leaf (Laurus nobilis), which is devoid of these toxic effects.
Other applications
In 2013 a new possible application of Umbellulone californica came to light. The essential oil was used for its moquite biting deterrent and larvicidal activity. This encourages futher investigation of this oil. Not only as a natural repellent for other arthropods, but also for medical and veterinary importance. This could lead to a new molecular-based approach to ethnopharmacological investigation of essential oils for pest control.
References
- 1 2 3 4 Nassini, R.; Materazzi, S.; Vriens, J.; Prenen, J.; Benemei, S.; De Siena, G.; La Marca, G.; Andrè, E.; Preti, D.; Avonto, C.; Sadofsky, L.; Di Marzo, V.; De Petrocellis, L.; Dussor, G.; Porreca, F.; Taglialatela-Scafati, O.; Appendino, G.; Nilius, B.; Geppetti, P. (2011). "The 'headache tree' via umbellulone and TRPA1 activates the trigeminovascular system". Brain 135 (Pt 2): 376–390. doi:10.1093/brain/awr272. PMID 22036959.
- ↑ Rachel Ehrenberg (November 3, 2011). "Headache tree is a pain in the brain: Bay laurel swells cranial blood vessels". ScienceNews. Retrieved 2011-11-07.
3. Drake, M.; Stuhr, E.; (1934) "Some pharmacological and bactericidal properties of umbellulone" . Retrieved 2016-03-10.
4. Synthesis of an Isomer of Umbellulone (1956) . Retrieved 2016-03-10.