Name: Development of a Preclinical Inhalation Model to Test Vaporized Cannabis Distillates (Video) | JoVE Journal
Uploaded: 2025-05-30T13:55:00.000+00:00
Duration: 6 min 9 s
Description: Learn a preclinical inhalation model to assess vaporized cannabis distillates using a murine exposure system. This method enables researchers to study THC vapor effects on lung epithelial cells and transcriptional changes.

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5 minutes

This work was supported by the Canadian Institutes for Health Research (CIHR) Project Grant 162273. CJB was supported by the Fonds de Recherche du Qu&#233;bec -Sant&#233; (FRQS).

The procedures below were approved by the McGill University Institutional Animal Care Committee (Protocol Number 8087) in accordance with the guidelines of the Canadian Council on Animal Care (CCAC).
1. Equipment preparation
NOTE: The following protocol applies to the SCIREQ inExpose system supported by the flexiWare 8 software.
<ol>
	<li>Ensure the correct assembly of all components of the system to resemble the example shown in Figure 1A. Ensure there is a closed tube inserted into the buffer chamber of the puffing pump to prevent system leakage, as shown in Figure 1B.</li>
	<li>Turn on the system and&#160;start the software. Select the Experimentation Sessions module.</li>
	<li>Select New Study and define the experimental groups and subjects to be studied. Select the experimental template that corresponds to the desired exposure regimen.</li>
	<li>In the Session Properties window, complete the Operator section to track equipment usage.</li>
	<li>To perform calibration, select the Desired Channel and follow the steps described in the operating software.</li>
	<li>(Critical step) To perform the system flow test, select the Desired Pump and follow the steps described in the operating software. Verify that the system flow is directed toward the rotameter. This calibration is to ensure there is no leakage in the system. If the system does not pass the flow test, clean the components and tubing before re-attempting the test.</li>
	<li>Cancel prompts to start data recording unless ready to start experiment.</li>
</ol>
2. Creation of Puff profiles
<ol>
	<li>Create a bias flow profile of 2 L/min to ensure adequate aeration of subjects throughout the experiment. To do so, refer to Technote 037: A Guide to Creating Profiles&#160;in an external document available from the manufacturer.</li>
	<li>Create a puff for e-cigarette profiles. To do so, refer to Technote 037. In the protocol described here, the technote was modified to deliver a 78 mL puff volume, with a 2.4 s puff duration, and 1, 2, or 4 puffs/min&#160;as previously published12,13,14,15,16,17.</li>
</ol>
3. Animal preparation
<ol>
	<li>Use both male and female C57BL/6 mice, aged 10-12 weeks and weighing approximately 20-30 g for this protocol. Acclimate mice to the system gradually over the course of 3 days.
	<ol>
		<li>Begin acclimation with the placement of the mice within the soft restraint, then start bias flow at 2 L/min with room air over a period that would match the length of their experimental exposure. Use an acclimation period of 10 min, 20 min, or 30 min to match the experimental exposures described here. These steps were taken to minimize any stress-induced impacts on outcomes of interest.</li>
		<li>To place animals in soft restraints, fully retract the mesh component, hold the entire restraint in front of the animal, and wait for the animal to move into the plunger component.</li>
		<li>Verify that the animal&#39;s nose is visible in the plunger component of the restraint, then secure a binder clip just behind the animal to prevent any movement out of the restraint. 
		NOTE: Younger, smaller animals can maneuver more easily within the restraint, so it is essential to verify that their nose remains visible outside the plunger component.</li>
	</ol>
	</li>
	<li>When working with mice of different sexes or genotypes, consider using color-coded binder clips to distinguish between animals.</li>
</ol>
4. Exposure of animals
<ol>
	<li>Place six restrained animals in the nose-only tower of the exposure system and initiate the bias flow at 2 L/min with room air to ensure sufficient airflow.</li>
	<li>In the task docker on the right-hand side of the screen, right-click on the E-cigarette Profile Created, then select Task Properties.</li>
	<li>Under Puff Frequency, input the desired frequency for initiating a puff. For example, a 2 puff/min regime requires an input of 30 s. Click OK, then Yes&#160;when the software asks for confirmation of this change. To save this puff regime for future use, at the end of the session follow the prompts to save it as a template.</li>
	<li>When ready to perform the exposure, double-click on the created and now modified E-Cigarette Profile. Be sure to start a timer to track the length of the exposure.</li>
	<li>To evaluate the dose over increasing exposure lengths, perform 10 min, 20 min, and 30 min exposures at 1 puff/min. Then, to evaluate increasing exposure intensity, maintain a 10 min exposure length and increase puff frequency to 1 puffs/min, 2 puffs/min, and 4 puffs/min.</li>
	<li>After the exposure is completed, re-initiate the bias flow while returning the animals to their cages.</li>
	<li>To remove animals from the restraints, detach the binder clip and retract the mesh fully to the plunger, allowing the animal to exit the restraint on its own. If the animal remains in the restraint, gently tug its tail to signal that it is free to move backward out of the restraint.</li>
</ol>
5. Hypo-locomotion test
<ol>
	<li>Immediately following the exposure, transfer the animals to a behavioral test suite to perform an open field test using the ANY-Maze software. To perform baseline recordings of animal behavior, ensure they are exposed only to bias flow.</li>
	<li>Ensure the room is well-lit and minimize noise levels to prevent unnecessary stress on the animals, as this could influence their behavior.</li>
	<li>Open the software and select New Empty Experiment. Under the Protocol tab at the top of the screen, select Add item, then click New Video Source from the dropdown list to add the camera source to be used for the experiment.</li>
	<li>On the menu on the left side of the screen, under the Tracking section, select Apparatus to define the open field in which the animal will be placed.</li>
	<li>Under the Protocol tab, select the Rectangle Tool to draw the open field area and input its dimensions into the software.</li>
	<li>On the menu on the left side of the screen, under the Tracking section, select Animal Color to specify whether the animal is lighter or darker than the background. This information assists the software to accurately track the animal&#39;s movement.</li>
	<li>In the left-hand menu, under the Testing section, select Stages to specify the test duration for the experiment. Input a 60 s test duration.</li>
	<li>Under the Experiment tab, define the experimental treatment and the number of animals per treatment.</li>
	<li>Now, to perform the test, click on the Tests tab. Place the animal into the open field, and click the Green Play Button above the recording of the open field to start the test.</li>
	<li>Upon completion of testing, in the left-hand menu, under the Analysis and Results section, select Results, Reports, and Data and select Total Distance traveled to include this information in the report.</li>
	<li>To generate the report, click the Results tab, and export the data in the desired format.</li>
</ol>
6. Collection of serum samples
<ol>
	<li>At 30 min after the exposure, anesthetize animals with an intraperitoneal injection of 250 mg/kg Avertin (2,2,2-tribromoethanol). To ensure proper anesthetization, stimulate the pedal withdrawal reflex by pinching the skin between the toes using blunt forceps. Once the reflex has disappeared completely, the animal is anesthetized deeply enough to be euthanized by exsanguination by cardiac puncture. The 30 min time point is selected to achieve peak serum THC-COOH concentrations post-exposure18.</li>
	<li>Collect blood by cardiac puncture in blood collection tubes, then centrifuge at 10,000 x g for 10 min to separate serum.</li>
	<li>Use serum samples to perform a THC Forensic ELISA to quantify THC-COOH levels as per manufacturer&#39;s instructions and as previously published19.</li>
</ol>

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<li>Chen, L. C., Lippmann, M. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((Inhalation+Toxicology+Methods%3A+The+Generation+and+Characterization+of+Exposure+Atmospheres+and+Inhalational+Exposures%5BTitle%5D)+AND+%22Curr+Protoc+Toxicol%22%5BJournal%5D)">Inhalation Toxicology Methods: The Generation and Characterization of Exposure Atmospheres and Inhalational Exposures.</a> Curr Protoc Toxicol. 63 (1), 24.24.21-24.24.23 (2015).</li>
<li>Wong, B. A. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((Inhalation+Exposure+Systems%3A+Design%2C+Methods+and+Operation%5BTitle%5D)+AND+%22Toxicologic+Pathol%22%5BJournal%5D)">Inhalation Exposure Systems: Design, Methods and Operation.</a> Toxicologic Pathol. 35 (1), 3-14 (2007).</li>
<li>Cousijn, J., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((Grey+matter+alterations+associated+with+cannabis+use%3A+results+of+a+VBM+study+in+heavy+cannabis+users+and+healthy+controls%5BTitle%5D)+AND+%22Neuroimage%22%5BJournal%5D)">Grey matter alterations associated with cannabis use: results of a VBM study in heavy cannabis users and healthy controls.</a> Neuroimage. 59 (4), 3845-3851 (2012).</li>
<li>Filbey, F. M., Schacht, J. P., Myers, U. S., Chavez, R. S., Hutchison, K. E. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((Marijuana+craving+in+the+brain%5BTitle%5D)+AND+%22Proc+Natl+Acad+Sci+U+S+A%22%5BJournal%5D)">Marijuana craving in the brain.</a> Proc Natl Acad Sci U S A. 106 (31), 13016-13021 (2009).</li>
<li>Sneider, J. T., Gruber, S. A., Rogowska, J., Silveri, M. M., Yurgelun-Todd, D. A. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((A+preliminary+study+of+functional+brain+activation+among+marijuana+users+during+performance+of+a+virtual+water+maze+task%5BTitle%5D)+AND+%22J+Addict%22%5BJournal%5D)">A preliminary study of functional brain activation among marijuana users during performance of a virtual water maze task.</a> J Addict. 2013, 461029(2013).</li>
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</ol>

The authors declare they have no conflicts of interest related to this work to disclose.

Cannabis distillate vape products contain high concentrations of cannabinoids, including up to 85% THC for the product utilized in this protocol. As the cannabis flower currently reaches only as high as 36% THC7, the potency of cannabis distillate vape products provides challenges when developing a model for inhalation exposure. The objective was to determine an exposure regime that could effectively deliver relevant doses of cannabinoids to mice without causing adverse effects from excessive THC ...

With the legalization of cannabis occurring throughout the world, cannabis use is increasing. Significant changes in the retail cannabis market are not only boosting accessibility, but these changes are also driving the development and production of new types of cannabis products for consumption1. Vaporizers, which heat cannabis products without combustion, are becoming an increasingly popular consumption method2,3. Vaporizers include cannabis vape cartridges that utilize e-cigarette technology to heat and aerosolize cannabis distillates. These distillates are extracted from the Cannabis sativa flower to produce a viscous liquid with high concentrations of cannabinoids such as &#916;9-tetrahydrocannabinol (THC), the primary psychoactive component of cannabis4. These devices are easy to use and conceal, making them attractive to novice users5. In Canada, where cannabis was legalized for recreational purposes in 2018, survey data obtained shows an increase in the perceived social acceptability of vaping cannabis as well as significant increases in cannabis vape pen/cartridge usage6.
Cannabis consumers may believe that vaping cannabis distillates is safer than smoking the dried flower in the form of a joint, contributing to its rising popularity2. Despite the possible reduction in exposure to inhaled combustion products when using cannabis vape distillates, these products may not be risk-free. One concern is the exposure to high doses of cannabinoids that are present in commercial vape cartridges. The dried cannabis flower can be purchased with up to 36% THC, whereas the THC concentration in cannabis distillate cartridges can reach as high as 96%7. Aerosols from cannabis distillate cartridges contain approximately twice the THC concentrations compared to cannabis smoke8,9. It is not yet known what effects these elevated THC concentrations have on the respiratory tract. Furthermore, the high concentrations of THC provide challenges in establishing effective dosing for preclinical murine studies, as excessive THC exposure itself may have adverse effects on mice10. It is essential to begin with minimal exposure levels and gradually increase until physiologically relevant doses are achieved to ensure that these exposures are relevant.
To date, there are no studies examining the potential effects of inhaled vaporized cannabis distillates. This is due, in part, to the lack of existing standardized preclinical models. Research challenges are compounded in regions where these products remain illegal, prompting researchers to produce in-house distillates that may not accurately reflect commercial products11. Additionally, the wide array of available products complicates standardization. To bridge this gap, this study was initiated using legal, commercially available products accessible to Canadian consumers. Products and devices listed as top sellers on the Ontario Cannabis Store were selected for use. The goal of this protocol is to establish an easy-to-use murine exposure regimen that delivers THC doses comparable to physiologically relevant human levels, creating a foundation for researchers to conduct additional studies on the respiratory and systemic effects of vaporized cannabis distillates.

<table><tbody><tr><td>2,2,2-Tribromoethanol</td><td>Sigma-Aldrich</td><td>T48402-5G</td><td>Avertin</td></tr><tr><td>inExpose</td><td>SCIREQ</td><td>sales@scireq.com</td><td>www.scireq.com</td></tr><tr><td>Microtainer Serum Separator Tubes</td><td>BD</td><td>365967</td><td></td></tr><tr><td>Pax Era Vape Pen</td><td>PAX</td><td></td><td>Purchased from Ontario Cannabis Store</td></tr><tr><td>Pineapple Express Pax Pod</td><td>Good Supply</td><td></td><td>Purchased from Ontario Cannabis Store</td></tr><tr><td>SoftRestraints</td><td>SCIREQ</td><td>IX-XN1-SR-AL</td><td>www.scireq.com</td></tr><tr><td>THC Forensic ELISA Kit</td><td>Neogen</td><td>131019</td><td></td></tr></tbody></table>

development of a preclinical inhalation model to test vaporized cannabis distillates

Development of a Preclinical Inhalation Model to Test Vaporized Cannabis Distillates

Despite their growing popularity, cannabis vape products remain understudied. Cannabis vape cartridges are used with battery-powered devices that aerosolize cannabis flower extracts containing high concentrations of cannabinoids such as THC. These types of products are commonly known as cannabis distillates. The potency of these products presents challenges in establishing effective dosing for preclinical studies. Currently, there are no established, standardized preclinical models for testing the safety and efficacy of these products in ways analogous to human use patterns. Thus, the in vivo cannabis distillate exposure regime required to achieve physiologically relevant doses in comparison to what is achieved in humans remains undetermined. To address this gap, a standardized preclinical murine model for inhalation of vaporized cannabis distillates has been developed using a computer-controlled delivery system. This protocol details procedures to administer cannabis vape distillates using a regimented puff topography to mice by a nose-only exposure tower. Methods to monitor mouse behavioral outcomes post-exposure and the utilization of a semi-quantitative ELISA to confirm THC delivery into the systemic circulation are also provided. This protocol will allow for the investigation of the pulmonary and systemic responses to cannabis vape distillate products by researchers interested in exploring the impact of cannabis vaping using real-world delivery protocols, thereby providing an opportunity for rigorous safety and therapeutic evaluation.

The initial objective was to determine an exposure regime that could deliver physiologically relevant levels of THC to the blood in comparison to humans. Thus, a key component to selecting exposure parameters was to use features that mimicked human use patterns20,21. Male and female C57BL/6 mice were exposed to a Pineapple Express Pax Era Pod containing ~85% THC for 10 min, 20 min, and 30 min at 1 puff/min with a 78 mL puff volume...

Cannabis distillate vape cartridges are battery-powered devices that aerosolize extracts containing high concentrations of cannabinoids. The absence of established preclinical models for these products creates challenges in studying their physiological effects. To address this gap, a standardized preclinical inhalation murine model for vaporized cannabis distillates has been developed.

Despite their growing popularity, cannabis vape products remain understudied. Cannabis vape cartridges are used with battery-powered devices that ...

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This protocol describes a method for exposing rodents to electronic cigarette vapor (E-vapor) and cigarette smoke. Exposure chambers are constructed by modifying anesthesia chambers with an automated pumping system that delivers E-vapor or cigarette smoke to rodents. This system can easily be modified to accommodate many experimental endpoints.

Comparing the Effects of Electronic Cigarette Vapor and Cigarette Smoke in a Novel In Vivo Exposure System

Here, we describe a programmable laboratory device that can be used to create extracts of conventional cigarette smoke and electronic cigarette aerosol. This method provides a useful tool for making direct comparisons between conventional cigarettes and electronic cigarettes, and is an accessible entry point into electronic cigarette research.

A Microcontroller Operated Device for the Generation of Liquid Extracts from Conventional Cigarette Smoke and Electronic Cigarette Aerosol

Electronic cigarette (e-cig) users are increasing worldwide. Little, however, is known about the health effects induced by inhaled e-cig aerosols. This article describes an e-cig aerosol generation technique suitable for animal exposures and subsequent toxicological studies. Such protocols are required to establish experimentally reproducible and standardized e-cig exposure systems.

Generation of Electronic Cigarette Aerosol by a Third-Generation Machine-Vaping Device: Application to Toxicological Studies

We present a robust, transferable and predictive in vitro exposure system for the screening and monitoring of airborne particles concerning their acute pulmonary cytotoxicity by exposing cultivated human lung cells at the air-liquid interface (ALI).

Assessment of the Acute Inhalation Toxicity of Airborne Particles by Exposing Cultivated Human Lung Cells at the Air-Liquid Interface

The protocol describes the settings and use of a capillary aerosol generator for continuous production of controlled aerosol from a multispecies liquid solution, suitable for steady large-volume aerosol delivery (e.g., in vivo inhalation studies).

Use of Capillary Aerosol Generator in Continuous Production of Controlled Aerosol for Non-Clinical Studies

The present protocol provides instructional information for using tobacco hornworm Manduca sexta in cannabinoid research. The method described here includes all necessary supplies and protocols to monitor physiological and behavioral changes of the insect model in response to cannabidiol (CBD) treatment.

Tobacco Hornworm as an Insect Model System for Cannabinoid Pre-clinical Studies

We establish a standardized in vitro model for studying cannabis vapor exposure at the air-liquid interface. This model provides a systematic approach to examine the impacts of vaporized cannabis, addressing the growing interest in cannabis vaporizers as an alternative to smoking.

In vitro Cannabis Exposures of Lung Epithelial Cells at the Air-Liquid Interface

Oral administration via gavage in rodents can induce distress associated with restraint. We explored oromucosal/buccal administration of CBD-enriched Cannabis extract, where rats were treated for 15 days with the extract at 3 mg/kg/day. Treatments were administered orally with a micropipette, using an affectionate touch technique to handle the animals.

Oromucosal as an Alternative Method for Administration of Cannabis Products in Rodents

As legislative restrictions change, resulting in increased accessibility of cannabinoid products, it is critically important to develop models to study the impact of these exposures, particularly during pregnancy. A preclinical model of moderate prenatal cannabinoid exposure through voluntary ingestion has been developed, enabling more in-depth investigations.

Preclinical Model of Prenatal Delta-9-Tetrahydrocannabinol Exposure to Assess Its Impact on Neurodevelopmental Outcomes

Δ9-tetrahydrocannabinol (THC) is the intoxicating constituent in cannabis and a controlled substance in the United States. This article outlines standard procedures for obtaining, storing, and administering THC to mice complying with current legal regulations and briefly introduces a method to assess basic pharmacodynamic effects of THC in rodents.

Administration of &#916;9-Tetrahydrocannabinol (THC) in Adolescent and Adult Mice

Learn a preclinical inhalation model to assess vaporized cannabis distillates using a murine exposure system. This method enables researchers to study THC vapor effects on lung epithelial cells and transcriptional changes.

Development of a Preclinical Inhalation Model to Test Vaporized Cannabis Distillates

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