Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2014 Aug;232(8):2511-34.
doi: 10.1007/s00221-014-3942-9. Epub 2014 May 4.

Anticipatory nausea in animal models: a review of potential novel therapeutic treatments

Affiliations

Anticipatory nausea in animal models: a review of potential novel therapeutic treatments

Erin M Rock et al. Exp Brain Res. 2014 Aug.

Abstract

Cancer patients undergoing chemotherapy continue to experience the debilitating side effect of nausea associated with their treatment. Although acute and delayed vomiting have become well managed with the advent of the 5-hydroxytryptamine-3 antagonists, such as ondansetron, and the neurokinin-1 receptor antagonists (such as aprepitant), nausea is still a relatively unmanaged adverse side effect of chemotherapy treatment. When nausea and vomiting are not properly managed, patients are at a greater risk of developing anticipatory nausea (AN)--a conditional association between chemotherapy-related treatment cues, such as the clinic environment, and the subsequent nausea experienced. Once it develops, AN is refractive to pharmacological treatment with classic antiemetics. Currently, non-specific antianxiety drugs (benzodiazepines) are prescribed; however, their sedating side effects are undesirable. Here, we review the animal models of AN that have been developed. These preclinical models have aided researchers in the evaluation of potentially efficacious pharmacological treatments for AN. Accumulating evidence using animal models demonstrates that cannabinoid compounds effectively reduce AN, without producing sedation. These results highlight the need for human clinical trials evaluating the efficacy of these compounds.

PubMed Disclaimer

Similar articles

Cited by

References

    1. Cancer. 2003 May 1;97(9):2290-300 - PubMed
    1. J Clin Oncol. 2011 Apr 10;29(11):1495-501 - PubMed
    1. Med J Aust. 1979 Dec 15;2(12):657-9 - PubMed
    1. J Pediatr Hematol Oncol. 2001 Dec;23(9):578-81 - PubMed
    1. Radiology. 1984 Feb;150(2):598-9 - PubMed

LinkOut - more resources