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Abstract

Bay leaf is a popular household spice used in flavoring foodstuff. The true bay leaf is derived from the bay laurel or sweet bay tree, Laurus nobilis, native to the Mediterranean region. However, leaves of several other species including Cinnamomum tamala (Indian bay leaf), Litsea glaucescens (Mexican bay leaf), Pimenta racemosa (West Indian bay leaf), Syzygium polyanthum (Indonesian bay leaf) and Umbellularia californica (Californian bay leaf) are also often sold as 'bay leaves' and are commonly substituted, adulterated or mistaken for the true bay leaves (Laurus nobilis) due to their similarity in appearance, aroma and flavor [1]. Thus, the name 'bay leaf' in herbal commerce may mean any of these botanicals [2]. The present work provides a detailed morpho-anatomical study of different types of bay leaves for correct identification of the true bay leaf and its substitutes. Acknowledgements: This research is supported by Science Based Authentication of Dietary Supplements and Botanical Dietary Supplement Research funded by the Food and Drug Administration grant # 1U01FD004246 – 05. References: [1] Tabanca N, Avonto C, et al. (2013)J Agric Food Chem 61: 12283 – 12291. [2] Leung AY, Foster S (2003) Encyclopedia of Common and Natural Ingredients used in Food, Drugs and Cosmetics. Wiley & Sons, Hoboken.

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The California bay laurel or Umbellularia californica (Hook. & Arn.) Nutt., is known as the 'headache tree' because the inhalation of its vapours can cause severe headache crises. However, the underlying mechanism of the headache precipitating properties of Umbellularia californica is unknown. The monoterpene ketone umbellulone, the major volatile constituent of the leaves of Umbellularia californica, has irritating properties, and is a reactive molecule that rapidly binds thiols. Thus, we hypothesized that umbellulone stimulates the transient receptor potential ankyrin 1 channel in a subset of peptidergic, nocioceptive neurons, activating the trigeminovascular system via this mechanism. Umbellulone, from µM to sub-mM concentrations, selectively stimulated transient receptor potential ankyrin 1-expressing HEK293 cells and rat trigeminal ganglion neurons, but not untransfected cells or neurons in the presence of the selective transient receptor potential ankyrin 1 antagonist, HC-030031. Umbellulone evoked a calcium-dependent release of calcitonin gene-related peptide from rodent trigeminal nerve terminals in the dura mater. In wild-type mice, umbellulone elicited excitation of trigeminal neurons and released calcitonin gene-related peptide from sensory nerve terminals. These two responses were absent in transient receptor potential ankyrin 1 deficient mice. Umbellulone caused nocioceptive behaviour after stimulation of trigeminal nerve terminals in wild-type, but not transient receptor potential ankyrin 1 deficient mice. Intranasal application or intravenous injection of umbellulone increased rat meningeal blood flow in a dose-dependent manner; a response selectively inhibited by systemic administration of transient receptor potential ankyrin 1 or calcitonin gene-related peptide receptor antagonists. These data indicate that umbellulone activates, through a transient receptor potential ankyrin 1-dependent mechanism, the trigeminovascular system, thereby causing nocioceptive responses and calcitonin gene-related peptide release. Pharmacokinetics of umbellulone, given by either intravenous or intranasal administration, suggest that transient receptor potential ankyrin 1 stimulation, which eventually results in meningeal vasodilatation, may be produced via two different pathways, depending on the dose. Transient receptor potential ankyrin 1 activation may either be caused directly by umbellulone, which diffuses from the nasal mucosa to perivascular nerve terminals in meningeal vessels, or by stimulation of trigeminal endings within the nasal mucosa and activation of reflex pathways. Transient receptor potential ankyrin 1 activation represents a plausible mechanism for Umbellularia californica-induced headache. Present data also strengthen the hypothesis that a series of agents, including chlorine, cigarette smoke, formaldehyde and others that are known to be headache triggers and recently identified as transient receptor potential ankyrin 1 agonists, utilize the activation of this channel on trigeminal nerves to produce head pain.
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Umbellularia californica, a shrub or tree indigenous to southwestern Oregon and northern California, is commonly known as headache tree, probably because it is reported that its scent can cause headache. Here, we report the case of a 69-year-old Italian gardener, affected during his young adult age by cluster headache, who, 10 years from his last cluster episode, developed shorter-lasting cluster-like headache attacks after and at any time he was exposed to U. californica scent. The present case indicates that, even though endogenous mechanisms causing the cluster headache were no longer present, susceptibility to exogenous triggers remains active in this patient, and suggests that identification of the constituent(s) of U. californica responsible for triggering cluster headache-like attacks may help in the understanding of the hitherto elusive mechanism of cluster headache.
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A, E -in transverse sectional view; all others in surface view
  • G -Normal Light Microscopy
B, C, F, G -normal light microscopy. A, E -in transverse sectional view; all others in surface view; all unstained). A L. nobilis;
Mc: mucilage cell, Oa: oil cell attachment, Oc: oil cell, Oi: oil cell content, Ow: oil cell wall, Pa: palisade tissue, Sk: stalk of oil cell
  • H U Californica Lo
H U. californica. Lo: lower epidermis, Mc: mucilage cell, Oa: oil cell attachment, Oc: oil cell, Oi: oil cell content, Ow: oil cell wall, Pa: palisade tissue, Sk: stalk of oil cell, St: stomata, Up: upper epidermis. Bars: A, H = 20 µm;