A comparative analysis of the potential of cannabinoids and ondansetron to suppress cisplatin-induced emesis in the Suncus murinus (house musk shrew)
- PMID: 14740147
- DOI: 10.1007/s00213-003-1739-9
A comparative analysis of the potential of cannabinoids and ondansetron to suppress cisplatin-induced emesis in the Suncus murinus (house musk shrew)
Abstract
Rationale: The 5-HT3 antagonist, ondansetron (OND), and the cannabinoid, delta9-tetrahydrocannabinol (delta9-THC), have been shown to interfere with emesis; however, their relative and/or combined effectiveness in suppressing vomiting produced by the chemotherapeutic agent, cisplatin, is unknown.
Objective: To evaluate the potential of: 1) a broad range of doses of delta9-THC and OND to prevent cisplatin-induced vomiting and retching in the Suncus murinus (house musk shrew), 2) combined treatment with ineffective individual doses of delta9-THC and OND to prevent cisplatin-induced vomiting and retching, 3) the CB1 receptor antagonist, SR141716, to reverse the antiemetic effects of OND, and 4) cannabidiol (CBD), the principal non-psychoactive component of marijuana, to reverse cisplatin-induced vomiting in the shrew.
Methods: Shrews were injected with various doses of OND (0.02-6.0 mg/kg), delta9-THC (1.25-10 mg/kg) and a combination of ineffective doses of each (0.02 mg/kg OND+1.25 mg/kg delta9-THC) prior to being injected with cisplatin (20 mg/kg) which induces vomiting. Shrews were also injected with CBD (5 mg/kg and 40 mg/kg) prior to an injection of cisplatin.
Results: OND and delta9-THC both dose-dependently suppressed cisplatin-induced vomiting and retching. Furthermore, a combined pretreatment of doses of the two drugs that were ineffective alone completely suppressed vomiting and retching. CBD produced a biphasic effect, suppressing vomiting at 5 mg/kg and potentiating it at 40 mg/kg.
Conclusions: A low dose of the non-intoxicating cannabinoid CBD may be an effective anti-emetic treatment and combined doses of OND and delta9-THC that are ineffective alone suppresses cisplatin-induced emetic reactions in shrews.
Similar articles
-
Effect of cannabinoids on lithium-induced vomiting in the Suncus murinus (house musk shrew).Psychopharmacology (Berl). 2004 Jan;171(2):156-61. doi: 10.1007/s00213-003-1571-2. Epub 2003 Sep 10. Psychopharmacology (Berl). 2004. PMID: 13680081
-
Delta-9-tetrahydrocannabinol differentially suppresses emesis versus enhanced locomotor activity produced by chemically diverse dopamine D2/D3 receptor agonists in the least shrew (Cryptotis parva).Pharmacol Biochem Behav. 2005 Jan;80(1):35-44. doi: 10.1016/j.pbb.2004.10.019. Epub 2004 Dec 8. Pharmacol Biochem Behav. 2005. PMID: 15652378
-
Synergy between cannabidiol, cannabidiolic acid, and Δ⁹-tetrahydrocannabinol in the regulation of emesis in the Suncus murinus (house musk shrew).Behav Neurosci. 2015 Jun;129(3):368-70. doi: 10.1037/bne0000057. Behav Neurosci. 2015. PMID: 26030435
-
[Use of ondansetron, a 5-HT3 receptor antagonist, as a new type of antiemetic in pediatric oncology].Orv Hetil. 1993 Jun 20;134(25):1363-7. Orv Hetil. 1993. PMID: 8332356 Review. Hungarian.
-
[Mechanisms of cytotoxic drug-induced emesis and its prevention].Yakugaku Zasshi. 1996 Sep;116(9):710-8. doi: 10.1248/yakushi1947.116.9_710. Yakugaku Zasshi. 1996. PMID: 8855716 Review. Japanese.
Cited by
-
Mechanisms of Broad-Spectrum Antiemetic Efficacy of Cannabinoids against Chemotherapy-Induced Acute and Delayed Vomiting.Pharmaceuticals (Basel). 2010 Sep 3;3(9):2930-2955. doi: 10.3390/ph3092930. Pharmaceuticals (Basel). 2010. PMID: 27713384 Free PMC article. Review.
-
Effects of the FAAH inhibitor, URB597, and anandamide on lithium-induced taste reactivity responses: a measure of nausea in the rat.Psychopharmacology (Berl). 2007 Feb;190(2):135-43. doi: 10.1007/s00213-006-0589-7. Epub 2006 Nov 17. Psychopharmacology (Berl). 2007. PMID: 17111174
-
Evidence For Cannabidiol Modulation of Serotonergic Transmission in a Model of Osteoarthritis via in vivo PET Imaging and Behavioral Assessment.Int J Innov Res Med Sci. 2022 Jun;7(6):254-271. doi: 10.23958/ijirms/vol07-i06/1418. Epub 2022 Jun 3. Int J Innov Res Med Sci. 2022. PMID: 37841504 Free PMC article.
-
Anxiogenic-like effects of chronic cannabidiol administration in rats.Psychopharmacology (Berl). 2012 May;221(2):239-47. doi: 10.1007/s00213-011-2566-z. Epub 2011 Nov 15. Psychopharmacology (Berl). 2012. PMID: 22083592
-
The nonpsychoactive cannabinoid cannabidiol inhibits 5-hydroxytryptamine3A receptor-mediated currents in Xenopus laevis oocytes.J Pharmacol Exp Ther. 2010 May;333(2):547-54. doi: 10.1124/jpet.109.162594. Epub 2010 Feb 16. J Pharmacol Exp Ther. 2010. PMID: 20160007 Free PMC article.
References
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical