TY - JOUR
T1 - Mepirapim, a novel synthetic cannabinoid, induces Parkinson’s disease-related behaviors by causing maladaptation of the dopamine system in the brain
AU - Hur, Kwang Hyun
AU - Lee, Youyoung
AU - Donio, Audrey Lynn
AU - Lee, Jae Gyeong
AU - Lee, Bo Ram
AU - Kim, Seon Kyung
AU - Yoon, Seolmin
AU - Lee, Yong Sup
AU - Kim, Hyoung Chun
AU - Lee, Seok Yong
AU - Jang, Choon Gon
N1 - Publisher Copyright:
© 2022, The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.
PY - 2023/2
Y1 - 2023/2
N2 - Mepirapim is a novel synthetic cannabinoid that first appeared on the illicit drug market in 2013. In recent years, recreational abuse of Mepirapim has caused serious emergencies, posing a threat to public health. However, there are no legal regulations to prohibit the use of Mepirapim, as there is no scientific evidence for the dangerous pharmacological effects of the drug. In the present study, we investigated the dangerous neurotoxic effects of Mepirapim through behavioral and molecular experiments in mice (ICR/CD1, male, 25–30 g). In particular, based on a previous study that Mepirapim activates the dopamine system, we evaluated whether high-dose Mepirapim [single (15, 30, or 60 mg·kg−1, i.p.) or multiple (8, 15, or 30 mg·kg−1, i.p. × 4 at 2 h intervals)] treatment causes Parkinson’s disease-related symptoms through damage to the dopamine system. In the result, we found that Mepirapim treatment caused comprehensive Parkinson’s disease-related symptoms, including motor impairment, cognitive deficits and mood disorders. Furthermore, we confirmed the maladaptation in dopamine-related neurochemicals, including decreased dopamine levels, decreased tyrosine hydroxylase expression, and increased α-synuclein expression, in the brains of mice treated with Mepirapim. Taken together, these results indicate that Mepirapim has dangerous neurotoxic effects that induces Parkinson’s disease-related behaviors by causing maladaptation of the dopamine system in the brain. Based on these findings, we propose the strict regulation of recreational abuse and therapeutic misuse of Mepirapim.
AB - Mepirapim is a novel synthetic cannabinoid that first appeared on the illicit drug market in 2013. In recent years, recreational abuse of Mepirapim has caused serious emergencies, posing a threat to public health. However, there are no legal regulations to prohibit the use of Mepirapim, as there is no scientific evidence for the dangerous pharmacological effects of the drug. In the present study, we investigated the dangerous neurotoxic effects of Mepirapim through behavioral and molecular experiments in mice (ICR/CD1, male, 25–30 g). In particular, based on a previous study that Mepirapim activates the dopamine system, we evaluated whether high-dose Mepirapim [single (15, 30, or 60 mg·kg−1, i.p.) or multiple (8, 15, or 30 mg·kg−1, i.p. × 4 at 2 h intervals)] treatment causes Parkinson’s disease-related symptoms through damage to the dopamine system. In the result, we found that Mepirapim treatment caused comprehensive Parkinson’s disease-related symptoms, including motor impairment, cognitive deficits and mood disorders. Furthermore, we confirmed the maladaptation in dopamine-related neurochemicals, including decreased dopamine levels, decreased tyrosine hydroxylase expression, and increased α-synuclein expression, in the brains of mice treated with Mepirapim. Taken together, these results indicate that Mepirapim has dangerous neurotoxic effects that induces Parkinson’s disease-related behaviors by causing maladaptation of the dopamine system in the brain. Based on these findings, we propose the strict regulation of recreational abuse and therapeutic misuse of Mepirapim.
KW - Dopamine
KW - Mepirapim
KW - Parkinson’s disease
KW - Synthetic cannabinoid
UR - http://www.scopus.com/inward/record.url?scp=85141718149&partnerID=8YFLogxK
U2 - 10.1007/s00204-022-03414-y
DO - 10.1007/s00204-022-03414-y
M3 - Article
C2 - 36355181
AN - SCOPUS:85141718149
SN - 0340-5761
VL - 97
SP - 581
EP - 591
JO - Archives of Toxicology
JF - Archives of Toxicology
IS - 2
ER -