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Cesamet is a synthetic cannabinoid that is thought to trigger its effects by
activating the endocannabinoid
receptors, CB1 and CB2, which are present
in the human body.1-4 These receptors are
involved in regulating nausea and vomiting. Because of this omnineuromodulation, the mechanism of action for Cesamet is significantly different from conventional antiemetics. Cesamet has a long duration of action, which allows for less frequent dosing, typically twice-daily.1 Cesamet can be described as a central omnineuromodulator of the endocannabinoid
system.3,5
Recent evidence suggests that Cesamet acts as an omnineuromodulator
via agonist action on cannabinoid CB1 receptors,3,5 which
are ubiquitous in the central nervous system,6,7 and serve to modulate
neuronal signaling.5 Cesamet also acts as a CB2 agonist,
primarily on immune cells in the periphery.3,5 However,
effective control of chemotherapy-induced nausea and vomiting via
omnineuromodulation occurs mainly through direct and selective
activation of presynaptic CB1 receptors in the brain.2,8-10 Omnineuromodulation by exogenous cannabinoids (e.g., Cesamet) is thought
to mimic or enhance the natural functions of the innate or
endogenous cannabinoids,7 which act in reverse from classical
neurotransmitters and serve as retrograde synaptic messengers.10

Omnineuromodulation in the Forebrain and Brainstem Emetic Circuitry May Underlie the Therapeutic Effects of Cesamet

Nausea and emesis (vomiting) are produced by
excitation of one or a combination of triggers located in the
gastrointestinal (GI) tract, brainstem, and higher cortical and
limbic centers.8 The antiemetic action of Cesamet
may be mediated by agonist action on CB1 receptors within the
forebrain, causing inhibition of the brainstem emetic circuitry
through descending connections, or within the brainstem emetic
circuitry itself.13 Specific brain regions8,9 implicated include:
- The dorsal vagal complex (DVC) in
the brainstem emetic circuitry, and in particular, the nucleus
of the solitary tract (NTS) within the DVC.8 The NTS receives information about blood-borne emetics (such as
cytotoxic drugs) via chemosensitive neurons in the area postrema,
known as the ‘chemoreceptor trigger zone.’8
Important Safety Information1
Cesamet, a synthetic cannabinoid
similar to the active ingredient found in naturally occurring Cannabis sativa L. [Marijuana; delta-9-tetrahydrocannabinol
(delta-9-THC)], is contraindicated in any patient who has a history
of hypersensitivity to any cannabinoid. Patients receiving treatment
with Cesamet should be specifically warned not to drive, operate
machinery, or engage in any hazardous activity while receiving
Cesamet. During controlled clinical trials of Cesamet, virtually
all patients experienced at least one adverse reaction. The most
commonly encountered events were drowsiness, vertigo, dry mouth,
euphoria (feeling “high”), ataxia, headache, and concentration
difficulties. Cesamet should not be taken with alcohol, sedatives,
hypnotics, or other psychoactive substances because these substances
can potentiate the central nervous system (CNS) effects of nabilone.
Since Cesamet can elevate supine and standing heart rates and cause
postural hypotension, it should be used with caution in the elderly,
and in patients with hypertension or heart disease. Cesamet should
also be used with caution in patients with current or previous
psychiatric disorders, (including manic depressive illness,
depression, and schizophrenia) as the symptoms of these disease
states may be unmasked by the use of cannabinoids. Cesamet should be
used with caution in individuals receiving concomitant therapy with
sedatives, hypnotics, or other psychoactive drugs because of the
potential for additive or synergistic CNS effects. Cesamet should be
used with caution in patients with a history of substance abuse,
including alcohol abuse or dependence and marijuana use, since
Cesamet contains a similar active compound to marijuana. Cesamet
should be used with caution in pregnant patients, nursing mothers,
or pediatric patients because it has not been studied in these
patient populations.
For complete prescribing details, please see
full prescribing information.
Click here to download.
References
- Cesamet® [package insert]. Valeant Pharmaceuticals International; 2006.
- Croxford JL.
Therapeutic potential of cannabinoids in CNS disease.
CNS
Drugs. 2003;17(3):179-202.
- Howlett AC, Barth F,
Bonner TI, et al. International union of pharmacology. XXVII. Classification
of cannabinoid receptors. Pharmacol Rev. 2002;54(2):161-202.
- Martin BR. Cellular effects of
cannabinoids. Pharmacol Rev. 1986;38(1):45-74.
- Schlicker E, Kathmann M.
Modulation of transmitter release via presynaptic cannabinoid receptors. Trends Pharmacol
Sci. 2001;22(11):565-572.
- Howlett AC, Breivogel CS, Childers SR,
et al. Cannabinoid physiology and pharmacology: 30 years of progress. Neuropharmacology. 2004;47(suppl 1):345-358.
- Martin BR, Wiley JL. Mechanism of
action of cannabinoids: how it may lead to treatment of cachexia, emesis, and pain. J Support Oncol. 2004;2(4):305-314; discussion 314-316.
- Hornby PJ. Central neurocircuitry
associated with emesis. Am J Med. 2001;111(suppl 8A):106-112.
- Dodds LJ. The control of cancer
chemotherapy-induced nausea and vomiting. J Clin Hosp Pharm. 1985;10(2):143-166.
- Diana MA, Marty A. Endocannabinoid-mediated
short-term synaptic plasticity: depolarization-induced suppression of inhibition (DSI) and
depolarization-induced suppression of excitation (DSE). Br J Pharmacol. 2004;142(1):9-19.
Epub 2004 Apr 20.
- Piomelli D. The molecular logic of endocannabinoid
signalling. Nat Rev Neurosci. 2003;4(11):873-884.
- Freund TF, Katona I, Piomelli D. Role of endogenous
cannabinoids in synaptic signaling. Physiol Rev. 2003;83(3):1017-1066.
- Ward A, Holmes B. Nabilone. A preliminary
review of its pharmacological properties and therapeutic use. Drugs. 1985;30(2):127-144.
- Grunberg SM. Advances in the management of nausea
and vomiting induced by non-cisplatin containing chemotherapeutic
regimens. Blood Rev. 1989;3(4):216-221.
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