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本文引用的文献

1
Anxiolytic Effect of Exogenous Ketone Supplementation Is Abolished by Adenosine A1 Receptor Inhibition in Wistar Albino Glaxo/Rijswijk Rats.在Wistar白化Glaxo/Rijswijk大鼠中,腺苷A1受体抑制消除了外源性补充酮的抗焦虑作用。
Front Behav Neurosci. 2018 Feb 22;12:29. doi: 10.3389/fnbeh.2018.00029. eCollection 2018.
2
Disruption of A2AR-D2R Heteroreceptor Complexes After A2AR Transmembrane 5 Peptide Administration Enhances Cocaine Self-Administration in Rats.A2AR 跨膜 5 肽给药后 A2AR-D2R 异源受体复合物的破坏增强了大鼠可卡因的自我给药。
Mol Neurobiol. 2018 Aug;55(8):7038-7048. doi: 10.1007/s12035-018-0887-1. Epub 2018 Jan 30.
3
Ketogenic diet-induced extension of longevity in epileptic Kcna1-null mice is influenced by gender and age at treatment onset.生酮饮食诱导癫痫性Kcna1基因敲除小鼠寿命延长受治疗开始时的性别和年龄影响。
Epilepsy Res. 2018 Feb;140:53-55. doi: 10.1016/j.eplepsyres.2017.11.005. Epub 2017 Nov 21.
4
Non-ketogenic combination of nutritional strategies provides robust protection against seizures.非生酮营养策略的联合应用提供了针对癫痫发作的强大保护。
Sci Rep. 2017 Jul 14;7(1):5496. doi: 10.1038/s41598-017-05542-3.
5
An examination of biochemical parameters and their association with response to ketogenic dietary therapies.对生化参数及其与生酮饮食疗法反应的关联进行检查。
Epilepsia. 2017 May;58(5):893-900. doi: 10.1111/epi.13729. Epub 2017 Apr 3.
6
Ketogenic diet improves behaviors in a maternal immune activation model of autism spectrum disorder.生酮饮食可改善自闭症谱系障碍母体免疫激活模型中的行为。
PLoS One. 2017 Feb 6;12(2):e0171643. doi: 10.1371/journal.pone.0171643. eCollection 2017.
7
Ketogenic diets improve behaviors associated with autism spectrum disorder in a sex-specific manner in the EL mouse.生酮饮食以性别特异性方式改善了EL小鼠与自闭症谱系障碍相关的行为。
Physiol Behav. 2017 Jan 1;168:138-145. doi: 10.1016/j.physbeh.2016.10.023. Epub 2016 Nov 9.
8
Regulation of brain PPARgamma2 contributes to ketogenic diet anti-seizure efficacy.大脑中PPARγ2的调节有助于生酮饮食的抗癫痫疗效。
Exp Neurol. 2017 Jan;287(Pt 1):54-64. doi: 10.1016/j.expneurol.2016.08.006. Epub 2016 Aug 12.
9
Ketogenic diet prevents neuronal firing increase within the substantia nigra during pentylenetetrazole-induced seizure in rats.生酮饮食可防止大鼠在戊四氮诱导的癫痫发作期间黑质内神经元放电增加。
Brain Res Bull. 2016 Jul;125:168-72. doi: 10.1016/j.brainresbull.2016.07.001. Epub 2016 Jul 2.
10
Ibudilast attenuates expression of behavioral sensitization to cocaine in male and female rats.异丁司特可减轻雄性和雌性大鼠对可卡因行为敏化的表达。
Neuropharmacology. 2016 Oct;109:281-292. doi: 10.1016/j.neuropharm.2016.06.024. Epub 2016 Jun 22.

生酮饮食可减少青年雄性和雌性大鼠对可卡因行为反应。

A ketogenic diet diminishes behavioral responses to cocaine in young adult male and female rats.

机构信息

Neuroscience Program, Hartford, CT, 06106, USA.

Neuroscience Program, Hartford, CT, 06106, USA; Department of Psychology, Trinity College, Hartford, CT, 06106, USA.

出版信息

Neuropharmacology. 2019 May 1;149:27-34. doi: 10.1016/j.neuropharm.2019.02.001. Epub 2019 Feb 4.

DOI:10.1016/j.neuropharm.2019.02.001
PMID:30731137
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6712576/
Abstract

Ketogenic diets (KDs) are high fat, low carbohydrate formulations traditionally used to treat epilepsy; more recently, KDs have shown promise for a wide range of other neurological disorders. Drug addiction studies suggest that repeated exposure to drugs of abuse, including cocaine, results in a suite of neurobiological changes that includes neuroinflammation, decreased glucose metabolism, and disordered neurotransmission. Given that KDs positively regulate these factors, we addressed whether administration of a KD has potential as a novel therapy for drug addiction. In this study, male and female Sprague-Dawley rats were placed on a KD or a control diet (CD), beginning at five weeks of age and continuing through the end of behavioral testing. Three weeks after initiation of dietary treatments, rats received daily i.p. injections of cocaine (15 mg/kg) or saline vehicle for one week, were drug free for a subsequent week, and then all animals received a final challenge injection of 15 mg/kg cocaine. In the absence of cocaine injections, stereotyped locomotor responses were minimal and were unaffected by dietary treatment. In contrast, both males and females fed a KD exhibited decreased cocaine-induced stereotyped responses as compared to CD-fed rats. The sensitization of ambulatory responses was also disrupted in KD-fed rats. These results suggest that KDs directly impact dopamine-mediated behaviors, and hence may hold potential as a therapy for drug addiction.

摘要

生酮饮食(KDs)是一种高脂肪、低碳水化合物的配方,传统上用于治疗癫痫;最近,KDs 在一系列其他神经疾病方面显示出了前景。药物成瘾研究表明,反复接触包括可卡因在内的滥用药物会导致一系列神经生物学变化,包括神经炎症、葡萄糖代谢减少和神经递质传递紊乱。鉴于 KDs 对这些因素有积极的调节作用,我们研究了生酮饮食作为一种新型药物成瘾治疗方法的潜力。在这项研究中,雄性和雌性 Sprague-Dawley 大鼠从五周龄开始接受生酮饮食或对照饮食(CD),并持续进行行为测试。饮食治疗开始三周后,大鼠每天接受 15mg/kg 的可卡因腹腔注射或生理盐水载体注射一周,随后一周无药物治疗,然后所有动物接受最后一次 15mg/kg 可卡因挑战注射。在没有可卡因注射的情况下,刻板的运动反应很少,不受饮食处理的影响。相比之下,接受 KD 喂养的雄性和雌性大鼠的可卡因诱导的刻板反应都比接受 CD 喂养的大鼠减少。KD 喂养的大鼠的运动反应也出现了敏化作用的破坏。这些结果表明,KDs 直接影响多巴胺介导的行为,因此可能有潜力作为药物成瘾的治疗方法。