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
. 2022 Jul 22:9:895368.
doi: 10.3389/fvets.2022.895368. eCollection 2022.

Serum Cannabinoid 24 h and 1 Week Steady State Pharmacokinetic Assessment in Cats Using a CBD/CBDA Rich Hemp Paste

Affiliations

Serum Cannabinoid 24 h and 1 Week Steady State Pharmacokinetic Assessment in Cats Using a CBD/CBDA Rich Hemp Paste

Tongxin Wang et al. Front Vet Sci. .

Abstract

Hemp based cannabinoids have gained popularity in veterinary medicine due to the potential to treat pain, seizure disorders and dermatological maladies in dogs. Cat owners are also using hemp-based products for arthritis, anxiety and neoplastic disorders with no studies assessing hemp cannabinoids, namely cannabidiol efficacy, for such disorders. Initial twenty-four pharmacokinetic and chronic dosing serum concentration in cats are sparse. The aim of our study was to assess 8 cats physiological and 24 h and 1-week steady state pharmacokinetic response to a cannabidiol (CBD) and cannabidiolic acid (CBDA) rich hemp in a palatable oral paste. Using a standard dose of paste (6.4 mg/CBD + CBDA 5.3 mg/gram) across 8 cats weighing between 4.2 and 5.4 kg showed an average maximal concentration of CBD at 282.0 ± 149.4 ng/mL with a half-life of ~2.1 ± 1.1 h, and CBDA concentrations of 1,011.3 ± 495.4 ng/mL with a half-life of ~2.7 ± 1.4 h, showing superior absorption of CBDA. After twice daily dosing for 1 week the serum concentrations 6 h after a morning dosing showed that the acidic forms of the cannabinoids were approximately double the concentration of the non-acidic forms like CBD and Δ9- tetrahydrocannabinol (THC). The results of this study compared to two other recent studies suggest that the absorption in this specific paste product may be superior to oil bases used previously, and show that the acidic forms of cannabinoids appear to be absorbed better than the non-acidic forms. More importantly, physical and behavioral examinations every morning after dosing showed no adverse events related to neurological function or behavioral alterations. In addition, bloodwork after 1 week of treatment showed no clinically significant serum biochemical alterations as a reflection of hepatic and renal function all remaining within the reference ranges set by the diagnostic laboratory suggesting that short-term treatment was safe.

Keywords: cannabidiol; cannabidiolic acid; cannabinoid; feline; hemp (Cannabis sativa L.).

PubMed Disclaimer

Conflict of interest statement

JW and WS are paid consultants for Ellevet Sciences. The remaining authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Figures

Figure 1
Figure 1
Twenty-four hour graphic representation of CBD, CBDA and metabolite 7-COOH-CBD serum concentrations (mean and standard deviation at each time point).
Figure 2
Figure 2
Twenty-four hour graphic representation of THC, THCA, CBG and CBGA serum concentrations (mean and standard deviation at each time point).
Figure 3
Figure 3
All cannabinoids at 6-h post 13th dose showing observed steady state concentrations in serum of cats compared to predicted steady state after 5 half-life of administration based on the 24-h pharmacokinetic analysis (Mean and standard deviation). * represents a statistically significant difference (P < 0.05).

Similar articles

Cited by

References

    1. Crippa JA, Guimarães FS, Campos AC, Zuardi AW. Translational investigation of the therapeutic potential of cannabidiol (CBD): toward a new age. Front Immun. (2018) 9:2009. 10.3389/fimmu.2018.02009 - DOI - PMC - PubMed
    1. Jin J-J, Yang M-Q, Fritsch PW, van Velzen R, Li D-Z, Yi T-S. Born migrators: historical biogeography of the cosmopolitan family Cannabaceae. J System Evol. (2020) 58:461–73. 10.1111/jse.12552 - DOI
    1. Pollio A. The name of cannabis: a short guide for nonbotanists. Cann Cannabin Res. (2016) 1:234–8. 10.1089/can.2016.0027 - DOI - PMC - PubMed
    1. ElSohly MA, Radwan MM, Gul W, Chandra S, Galal A. Phytochemistry of cannabis sativa L. Prog Chem Org Nat Prod. (2017) 103:1–36. 10.1007/978-3-319-45541-9_1 - DOI - PubMed
    1. National National Academies of Sciences E Division HM Practice Practice B on PH PH Agenda Agenda C on the HE of MAER R. Therapeutic Effects of Cannabis and Cannabinoids. National Academies Press. (2017). Available online at: https://www.ncbi.nlm.nih.gov/books/NBK425767/ (accessed October 5, 2021).