DNA Damaging Effects, Oxidative Stress Responses and Cholinesterase Activity in Blood and Brain of Wistar Rats Exposed to Δ<sup>9</sup>-Tetrahydrocannabinol

Currently we are faced with an ever-growing use of &#916;<sup>9</sup>-tetrahydrocannabinol (THC) preparations, often used as supportive therapies for various malignancies and neurological disorders. As some of illegally distributed forms of such preparations, like cannabis oils and b...

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Main Authors: Nevenka Kopjar, Nino Fuchs, Suzana Žunec, Anja Mikolić, Vedran Micek, Goran Kozina, Ana Lucić Vrdoljak, Irena Brčić Karačonji
Format: Article
Language:English
Published: MDPI AG 2019-04-01
Series:Molecules
Subjects:
Online Access:https://www.mdpi.com/1420-3049/24/8/1560
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author Nevenka Kopjar
Nino Fuchs
Suzana Žunec
Anja Mikolić
Vedran Micek
Goran Kozina
Ana Lucić Vrdoljak
Irena Brčić Karačonji
author_facet Nevenka Kopjar
Nino Fuchs
Suzana Žunec
Anja Mikolić
Vedran Micek
Goran Kozina
Ana Lucić Vrdoljak
Irena Brčić Karačonji
author_sort Nevenka Kopjar
collection DOAJ
description Currently we are faced with an ever-growing use of &#916;<sup>9</sup>-tetrahydrocannabinol (THC) preparations, often used as supportive therapies for various malignancies and neurological disorders. As some of illegally distributed forms of such preparations, like cannabis oils and butane hash oil, might contain over 80% of THC, their consumers can become intoxicated or experience various detrimental effects. This fact motivated us for the assessments of THC toxicity in vivo on a Wistar rat model, at a daily oral dose of 7 mg/kg which is comparable to those found in illicit preparations. The main objective of the present study was to establish the magnitude and dynamics of DNA breakage associated with THC exposure in white blood and brain cells of treated rats using the alkaline comet assay. The extent of oxidative stress after acute 24 h exposure to THC was also determined as well as changes in activities of plasma and brain cholinesterases (ChE) in THC-treated and control rats. The DNA of brain cells was more prone to breakage after THC treatment compared to DNA in white blood cells. Even though DNA damage quantified by the alkaline comet assay is subject to repair, its elevated level detected in the brain cells of THC-treated rats was reason for concern. Since neurons do not proliferate, increased levels of DNA damage present threats to these cells in terms of both viability and genome stability, while inefficient DNA repair might lead to their progressive loss. The present study contributes to existing knowledge with evidence that acute exposure to a high THC dose led to low-level DNA damage in white blood cells and brain cells of rats and induced oxidative stress in brain, but did not disturb ChE activities.
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spelling doaj.art-971c22e17ba944429cb5b8f196d0f4712022-12-21T20:34:54ZengMDPI AGMolecules1420-30492019-04-01248156010.3390/molecules24081560molecules24081560DNA Damaging Effects, Oxidative Stress Responses and Cholinesterase Activity in Blood and Brain of Wistar Rats Exposed to Δ<sup>9</sup>-TetrahydrocannabinolNevenka Kopjar0Nino Fuchs1Suzana Žunec2Anja Mikolić3Vedran Micek4Goran Kozina5Ana Lucić Vrdoljak6Irena Brčić Karačonji7Institute for Medical Research and Occupational Health, Zagreb HR-10001, CroatiaUniversity Hospital Centre Zagreb, Zagreb HR-10000 CroatiaInstitute for Medical Research and Occupational Health, Zagreb HR-10001, CroatiaInstitute for Medical Research and Occupational Health, Zagreb HR-10001, CroatiaInstitute for Medical Research and Occupational Health, Zagreb HR-10001, CroatiaUniversity Centre Varaždin, University North, Varaždin HR-42000, CroatiaInstitute for Medical Research and Occupational Health, Zagreb HR-10001, CroatiaInstitute for Medical Research and Occupational Health, Zagreb HR-10001, CroatiaCurrently we are faced with an ever-growing use of &#916;<sup>9</sup>-tetrahydrocannabinol (THC) preparations, often used as supportive therapies for various malignancies and neurological disorders. As some of illegally distributed forms of such preparations, like cannabis oils and butane hash oil, might contain over 80% of THC, their consumers can become intoxicated or experience various detrimental effects. This fact motivated us for the assessments of THC toxicity in vivo on a Wistar rat model, at a daily oral dose of 7 mg/kg which is comparable to those found in illicit preparations. The main objective of the present study was to establish the magnitude and dynamics of DNA breakage associated with THC exposure in white blood and brain cells of treated rats using the alkaline comet assay. The extent of oxidative stress after acute 24 h exposure to THC was also determined as well as changes in activities of plasma and brain cholinesterases (ChE) in THC-treated and control rats. The DNA of brain cells was more prone to breakage after THC treatment compared to DNA in white blood cells. Even though DNA damage quantified by the alkaline comet assay is subject to repair, its elevated level detected in the brain cells of THC-treated rats was reason for concern. Since neurons do not proliferate, increased levels of DNA damage present threats to these cells in terms of both viability and genome stability, while inefficient DNA repair might lead to their progressive loss. The present study contributes to existing knowledge with evidence that acute exposure to a high THC dose led to low-level DNA damage in white blood cells and brain cells of rats and induced oxidative stress in brain, but did not disturb ChE activities.https://www.mdpi.com/1420-3049/24/8/1560acetylcholinesteraseantioxidative enzymesbrain cellsbutyrylcholinesterasegenotoxicityglutathionecomet assaylipid peroxidationwhite blood cells
spellingShingle Nevenka Kopjar
Nino Fuchs
Suzana Žunec
Anja Mikolić
Vedran Micek
Goran Kozina
Ana Lucić Vrdoljak
Irena Brčić Karačonji
DNA Damaging Effects, Oxidative Stress Responses and Cholinesterase Activity in Blood and Brain of Wistar Rats Exposed to Δ<sup>9</sup>-Tetrahydrocannabinol
Molecules
acetylcholinesterase
antioxidative enzymes
brain cells
butyrylcholinesterase
genotoxicity
glutathione
comet assay
lipid peroxidation
white blood cells
title DNA Damaging Effects, Oxidative Stress Responses and Cholinesterase Activity in Blood and Brain of Wistar Rats Exposed to Δ<sup>9</sup>-Tetrahydrocannabinol
title_full DNA Damaging Effects, Oxidative Stress Responses and Cholinesterase Activity in Blood and Brain of Wistar Rats Exposed to Δ<sup>9</sup>-Tetrahydrocannabinol
title_fullStr DNA Damaging Effects, Oxidative Stress Responses and Cholinesterase Activity in Blood and Brain of Wistar Rats Exposed to Δ<sup>9</sup>-Tetrahydrocannabinol
title_full_unstemmed DNA Damaging Effects, Oxidative Stress Responses and Cholinesterase Activity in Blood and Brain of Wistar Rats Exposed to Δ<sup>9</sup>-Tetrahydrocannabinol
title_short DNA Damaging Effects, Oxidative Stress Responses and Cholinesterase Activity in Blood and Brain of Wistar Rats Exposed to Δ<sup>9</sup>-Tetrahydrocannabinol
title_sort dna damaging effects oxidative stress responses and cholinesterase activity in blood and brain of wistar rats exposed to δ sup 9 sup tetrahydrocannabinol
topic acetylcholinesterase
antioxidative enzymes
brain cells
butyrylcholinesterase
genotoxicity
glutathione
comet assay
lipid peroxidation
white blood cells
url https://www.mdpi.com/1420-3049/24/8/1560
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