The secondary visual cortex mediated the enhancement of associative learning on methamphetamine self-administration behaviors.

IF 3.5 3区 医学 Q2 NEUROSCIENCES
Psychopharmacology Pub Date : 2024-09-01 Epub Date: 2024-05-03 DOI:10.1007/s00213-024-06597-7
Cai-Ling Wang, Dan-Ni Cao, Ning Wu, Ying-Jie Zhu, Jin Li
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引用次数: 0

Abstract

Rationale: Methamphetamine addiction is a persistent and intractable pathological learning and memory, whereas no approved therapeutics is available. However, few attentions have been paid to how associative learning participates in the formation of intractable memory related to drug addiction OBJECTIVES AND METHODS: To investigate the role of associative learning in methamphetamine addiction and the underlying neurobiological mechanism, methamphetamine self-administration, oral sucrose self-administration, chemogenetic neuromanipulation, and fiber photometry in mice were performed in this study.

Results: We reported that associative learning increased methamphetamine-induced self-administration, but not oral sucrose self-administration. In addition, the enhancement of methamphetamine-induced self-administration was independent of more methamphetamine consumption, and remained with higher drug-taking and motivation in the absence of visual cues, suggesting the direct effects of the associative learning that enhanced methamphetamine-induced self-administration. Moreover, chemogenetic inactivation of the secondary visual cortex (V2) reduced the enhancement of the drug-taking induced by associative learning but did not alter sucrose-taking. Further fiber photometry of V2 neurons demonstrated that methamphetamine-associative learning elicits V2 neuron excitation, and sucrose-associative learning elicits V2 neuron inhibition.

Conclusions: Therefore, this study reveals the neurobiological mechanism of V2 excitability underlying how associative learning participates in the formation of intractable memory related to drug addiction, and gives evidence to support V2 as a promising target for stimulation therapy for methamphetamine addiction.

Abstract Image

次级视觉皮层介导了联想学习对甲基苯丙胺自我给药行为的增强。
理由甲基苯丙胺成瘾是一种顽固而难治的病态学习和记忆,目前尚无经批准的治疗方法。目的和方法:为了研究联想学习在甲基苯丙胺成瘾中的作用及其潜在的神经生物学机制,本研究对小鼠进行了甲基苯丙胺自我给药、口服蔗糖自我给药、化学遗传神经操纵和纤维光度测定:结果:我们发现,联想学习能增强甲基苯丙胺诱导的自我给药,但不能增强口服蔗糖的自我给药。此外,甲基苯丙胺诱导的自我给药增强与更多的甲基苯丙胺摄入量无关,并且在没有视觉线索的情况下,甲基苯丙胺诱导的自我给药增强仍与更高的药物摄入量和动机有关,这表明联想学习的直接作用增强了甲基苯丙胺诱导的自我给药。此外,化学失活次级视觉皮层(V2)可降低联想学习对药物摄取的增强作用,但不会改变蔗糖摄取。对V2神经元的进一步纤维光度测定表明,甲基苯丙胺联想学习会引起V2神经元兴奋,而蔗糖联想学习会引起V2神经元抑制:因此,本研究揭示了联想学习如何参与形成与药物成瘾有关的难治性记忆的 V2 兴奋性神经生物学机制,并提供证据支持将 V2 作为刺激治疗甲基苯丙胺成瘾的一个有前途的靶点。
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来源期刊
Psychopharmacology
Psychopharmacology 医学-精神病学
CiteScore
7.10
自引率
5.90%
发文量
257
审稿时长
2-4 weeks
期刊介绍: Official Journal of the European Behavioural Pharmacology Society (EBPS) Psychopharmacology is an international journal that covers the broad topic of elucidating mechanisms by which drugs affect behavior. The scope of the journal encompasses the following fields: Human Psychopharmacology: Experimental This section includes manuscripts describing the effects of drugs on mood, behavior, cognition and physiology in humans. The journal encourages submissions that involve brain imaging, genetics, neuroendocrinology, and developmental topics. Usually manuscripts in this section describe studies conducted under controlled conditions, but occasionally descriptive or observational studies are also considered. Human Psychopharmacology: Clinical and Translational This section comprises studies addressing the broad intersection of drugs and psychiatric illness. This includes not only clinical trials and studies of drug usage and metabolism, drug surveillance, and pharmacoepidemiology, but also work utilizing the entire range of clinically relevant methodologies, including neuroimaging, pharmacogenetics, cognitive science, biomarkers, and others. Work directed toward the translation of preclinical to clinical knowledge is especially encouraged. The key feature of submissions to this section is that they involve a focus on clinical aspects. Preclinical psychopharmacology: Behavioral and Neural This section considers reports on the effects of compounds with defined chemical structures on any aspect of behavior, in particular when correlated with neurochemical effects, in species other than humans. Manuscripts containing neuroscientific techniques in combination with behavior are welcome. We encourage reports of studies that provide insight into the mechanisms of drug action, at the behavioral and molecular levels. Preclinical Psychopharmacology: Translational This section considers manuscripts that enhance the confidence in a central mechanism that could be of therapeutic value for psychiatric or neurological patients, using disease-relevant preclinical models and tests, or that report on preclinical manipulations and challenges that have the potential to be translated to the clinic. Studies aiming at the refinement of preclinical models based upon clinical findings (back-translation) will also be considered. The journal particularly encourages submissions that integrate measures of target tissue exposure, activity on the molecular target and/or modulation of the targeted biochemical pathways. Preclinical Psychopharmacology: Molecular, Genetic and Epigenetic This section focuses on the molecular and cellular actions of neuropharmacological agents / drugs, and the identification / validation of drug targets affecting the CNS in health and disease. We particularly encourage studies that provide insight into the mechanisms of drug action at the molecular level. Manuscripts containing evidence for genetic or epigenetic effects on neurochemistry or behavior are welcome.
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