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Neurochemical and Behavioral Profiling in Male and Female Rats of the Psychedelic Agent 25I-NBOMe.

Cristina Miliano, Matteo Marti, Nicholas Pintori, Maria Paola Castelli, Micaela Tirri, Raffaella Arfè, Maria Antonietta De Luca

Frontiers in Pharmacology January 1, 2019 DOI: 10.3389/fphar.2019.01406 (opens in new tab) via PubMed

Summary

AI-generated from the abstract

25I-NBOMe (N-Bomb), a synthetic psychedelic often sold as fake LSD or as a substitute for MDMA, acts as a full agonist on serotonin 5-HT2A receptors. In rats, the drug alters dopamine transmission in the nucleus accumbens shell differently in males and females, impairs visual responses in both sexes, heavily affects core temperature in females, and at the highest dose tested produces an analgesic effect prominent in males. It also impairs startle amplitude and prepulse inhibition in both sexes. These findings highlight sex-specific risks of intoxication and overdose.

Study at a glance

Characteristics Preclinical study Peer reviewed
Population Male and female rats
Intervention 25I-NBOMe
Topics Serotonin
Keywords Behavior Dopamine Novel psychoactive substances Sex differences
Key finding 25I-NBOMe affects dopamine transmission in the nucleus accumbens shell differently in male and female rats, impairs visual responses in both sexes, heavily affects core temperature in females, and exerts an analgesic effect prominent in males.

Abstract

4-Iodo-2,5-dimethoxy-N-(2-methoxybenzyl)phenethylamine (25I-NBOMe), commonly called "N-Bomb," is a synthetic phenethylamine with psychedelic and entactogenic effects; it was available on the Internet both as a legal alternative to lysergic acid diethylamide (LSD) and as a surrogate of 3,4-methylenedioxy-methamphetamine (MDMA), but now it has been scheduled among controlled substances. 25I-NBOMe acts as full agonist on serotonergic 5-HT2A receptors. Users are often unaware of ingesting fake LSD, and several cases of intoxication and fatalities have been reported. In humans, overdoses of "N-Bomb" can cause tachycardia, hypertension, seizures, and agitation. Preclinical studies have not yet widely investigated the rewarding properties and behavioral effects of this compound in both sexes. Therefore, by in vivo microdialysis, we evaluated the effects of 25I-NBOMe on dopaminergic (DA) and serotonergic (5-HT) transmissions in the nucleus accumbens (NAc) shell and core, and the medial prefrontal cortex (mPFC) of male and female rats. Moreover, we investigated the effect of 25I-NBOMe on sensorimotor modifications as well as body temperature, nociception, and startle/prepulse inhibition (PPI). We showed that administration of 25I-NBOMe affects DA transmission in the NAc shell in both sexes, although showing different patterns; moreover, this compound causes impaired visual responses in both sexes, whereas core temperature is heavily affected in females, and the highest dose tested exerts an analgesic effect prominent in male rats. Indeed, this drug is able to impair the startle amplitude with the same extent in both sexes and inhibits the PPI in male and female rats. Our study fills the gap of knowledge on the behavioral effects of 25I-NBOMe and the risks associated with its ingestion; it focuses the attention on sex differences that might be useful to understand the trend of consumption as well as to recognize and treat intoxication and overdose symptoms.

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