The Impacts of Adolescent Cannabinoid Exposure on Striatal Anxiety- and Depressive-Like Pathophysiology Are Prevented by the Antioxidant N-Acetylcysteine

Marta De Felice , Hanna J. Szkudlarek , Taygun C. Uzuneser , Mar Rodríguez-Ruiz , Mohammed H. Sarikahya , Mathusha Pusparajah , Juan Pablo Galindo Lazo , Shawn N. Whitehead , Ken K.-C. Yeung , Walter J. Rushlow , Steven R. Laviolette
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Abstract

Background

Exposure to Δ9-tetrahydrocannabinol (THC) is an established risk factor for later-life neuropsychiatric vulnerability, including mood- and anxiety-related symptoms. The psychotropic effects of THC on affect and anxiogenic behavioral phenomena are known to target the striatal network, particularly the nucleus accumbens, a neural region linked to mood and anxiety disorder pathophysiology. THC may increase neuroinflammatory responses via the redox system and dysregulate inhibitory and excitatory neural balance in various brain circuits, including the striatum. Thus, interventions that can induce antioxidant effects may counteract the neurodevelopmental impacts of THC exposure.

Methods

In the current study, we used an established preclinical adolescent rat model to examine the impacts of adolescent THC exposure on various behavioral, molecular, and neuronal biomarkers associated with increased mood and anxiety disorder vulnerability. Moreover, we investigated the protective properties of the antioxidant N-acetylcysteine against THC-related pathology.

Results

We demonstrated that adolescent THC exposure induced long-lasting anxiety- and depressive-like phenotypes concomitant with differential neuronal and molecular abnormalities in the two subregions of the nucleus accumbens, the shell and the core. In addition, we report for the first time that N-acetylcysteine can prevent THC-induced accumbal pathophysiology and associated behavioral abnormalities.

Conclusions

The preventive effects of this antioxidant intervention highlight the critical role of redox mechanisms underlying cannabinoid-induced neurodevelopmental pathology and identify a potential intervention strategy for the prevention and/or reversal of these pathophysiological sequelae.

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抗氧化剂 N-乙酰半胱氨酸可预防青少年大麻素暴露对纹状体焦虑和抑郁样病理生理学的影响
背景接触Δ9-四氢大麻酚(THC)是导致晚年神经精神疾病(包括情绪和焦虑相关症状)的一个既定风险因素。众所周知,四氢大麻酚对情感和焦虑行为现象的精神作用以纹状体网络为目标,尤其是与情绪和焦虑症病理生理学相关的神经区域--伏隔核。四氢大麻酚可能会通过氧化还原系统增加神经炎症反应,并使包括纹状体在内的各种大脑回路中的抑制性和兴奋性神经平衡失调。因此,可诱导抗氧化作用的干预措施可能会抵消暴露于 THC 对神经发育的影响。方法在本研究中,我们使用了一个已建立的临床前青少年大鼠模型,研究青少年暴露于 THC 对与情绪和焦虑症易感性增加相关的各种行为、分子和神经元生物标志物的影响。此外,我们还研究了抗氧化剂 N-乙酰半胱氨酸对四氢大麻酚相关病理学的保护作用。结果我们证明,青少年暴露于四氢大麻酚会诱发长期焦虑和抑郁样表型,同时在伏隔核的两个亚区(外壳和核心)出现不同的神经元和分子异常。结论 这种抗氧化剂干预的预防效果突出了氧化还原机制在大麻素诱导的神经发育病理学中的关键作用,并确定了预防和/或逆转这些病理生理后遗症的潜在干预策略。
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来源期刊
Biological psychiatry global open science
Biological psychiatry global open science Psychiatry and Mental Health
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4.00
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审稿时长
91 days
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