Adolescent exposure to sucrose increases cocaine-mediated behaviours in adulthood via Smad3

IF 3.1 3区 医学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY
Amy M. Gancarz, Raveena Parmar, Treefa Shwani, Moriah M. Cobb, Michelle N. Crawford, Jacob R. Watson, Lisa Evans, Michael A. Kausch, Craig T. Werner, David M. Dietz
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Abstract

Adolescence, a critical period of developmental period, is marked by neurobiological changes influenced by environmental factors. Here, we show how exposure to sucrose, which is ubiquitously available in modern diets, results in changes in behavioural response to cocaine as an adult. Rats were given daily access to either 10% sucrose or water during the adolescent period (PND28–42). Following this period, rats are left undisturbed until they reach adulthood. In adulthood, rats were tested for (i) acquisition of a low dose of cocaine, (ii) progressive ratio (PR) test, and (iii) resistance to punished cocaine taking. Sucrose exposure resulted in significant alterations in all behavioural measures. To determine the neurobiological mechanisms leading to such behavioural adaptations, we find that adolescent sucrose exposure results in an upregulation of the transcription factor Smad3 in the nucleus accumbens (NAc) when compared with water-exposed controls. Transiently blocking the active form of this transcription factor (HSV-dnSmad3) during adolescence mitigated the enhanced cocaine vulnerability-like behaviours observed in adulthood. These findings suggest that prior exposure to sucrose during adolescence can heighten the reinforcing effects of cocaine. Furthermore, they identify the TGF-beta pathway and Smad3 as playing a key role in mediating enduring and long-lasting adaptations that contribute to sucrose-induced susceptibility to cocaine. Taken together, these results have important implications for development and suggest that adolescent sucrose exposure may persistently enhance the susceptibility to substance abuse.

Abstract Image

青少年接触蔗糖会通过Smad3增加成年期可卡因介导的行为
青春期是人类发育的关键时期,受环境因素的影响,神经生物学发生变化。在这里,我们展示了现代饮食中无处不在的蔗糖暴露如何导致成人对可卡因的行为反应发生变化。在青春期,每天给大鼠喂食10%的蔗糖或水(PND28-42)。在这段时间之后,老鼠不受干扰,直到它们成年。在成年期,对大鼠进行了(i)获得低剂量可卡因的测试,(ii)递进比(PR)测试,以及(iii)对惩罚可卡因服用的抗性测试。蔗糖暴露导致所有行为测量的显著改变。为了确定导致这种行为适应的神经生物学机制,我们发现,与暴露于水的对照组相比,青春期蔗糖暴露会导致伏隔核(NAc)中转录因子Smad3的上调。在青春期短暂阻断这种转录因子(HSV-dnSmad3)的活性形式,可以减轻在成年期观察到的增加的可卡因易感性行为。这些发现表明,在青春期之前接触蔗糖可以增强可卡因的强化作用。此外,他们确定tgf - β途径和Smad3在介导持久和持久的适应中发挥关键作用,这些适应有助于蔗糖诱导对可卡因的易感性。综上所述,这些结果对发育具有重要意义,并表明青少年接触蔗糖可能会持续增加对药物滥用的易感性。
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来源期刊
Addiction Biology
Addiction Biology 生物-生化与分子生物学
CiteScore
8.10
自引率
2.90%
发文量
118
审稿时长
6-12 weeks
期刊介绍: Addiction Biology is focused on neuroscience contributions and it aims to advance our understanding of the action of drugs of abuse and addictive processes. Papers are accepted in both animal experimentation or clinical research. The content is geared towards behavioral, molecular, genetic, biochemical, neuro-biological and pharmacology aspects of these fields. Addiction Biology includes peer-reviewed original research reports and reviews. Addiction Biology is published on behalf of the Society for the Study of Addiction to Alcohol and other Drugs (SSA). Members of the Society for the Study of Addiction receive the Journal as part of their annual membership subscription.
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