Investigating brain-derived neurotrophic factor (BDNF) changes in three main rodent models of autism spectrum disorder (ASD): a systematic review.

IF 3.3 3区 医学 Q2 NEUROSCIENCES
Marzieh Jalalian-Javadpour, Mahdi Khaledian, Hamed Moradi, Hamidreza Behnoud, Mandana Sajjadi, Batool Ghorbani Yekta, Salar Vaseghi
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Abstract

Autism spectrum disorder (ASD) is a neurodevelopmental disorder characterized by social impairments, and repetitive and aggressive behaviors. The pathophysiology of ASD still remains unclear, while the population with ASD is 1/36 in children in the USA in 2024. Evidence suggests a wide range of inconsistent changes in brain-derived neurotrophic factor (BDNF), the most important neurotrophin in the central nervous system, in ASD. The present systematic review investigated studies that examined BDNF levels in three main ASD-like models in rodents [induced by valproic acid (VPA) and propionic acid (PPA), and in the BTBR mouse strain] in accord with PRISMA guidelines and in PubMed database. Forty-two studies were included. Most studies used male rats/mice. The results showed ASD model induced by VPA often leads to decreased BDNF, although unchanged or increased BDNF levels were also reported. ASD model induced by PPA leads to both increased and decreased BDNF. BDNF changes in BTBR mouse strain were also inconsistent. We found that the type of molecular assay appears to be important in evaluating BDNF. Also, few evidence showed a role for postnatal day and sex difference in BDNF changes in ASD-like rodent models. In addition, some studies have shown the potential role of the brain region in BDNF changes in different ASD-like models. In conclusion, it was suggested that inconsistencies in BDNF changes in rodent models of ASD may be related to the type of the molecular assay, the brain region, ASD model, sex, or even the postnatal day. However, evidence is still insufficient.

研究脑源性神经营养因子(BDNF)在三种主要的自闭症谱系障碍(ASD)啮齿动物模型中的变化:系统综述。
自闭症谱系障碍(ASD)是一种以社交障碍、重复性和攻击性行为为特征的神经发育障碍。ASD的病理生理学尚不清楚,而2024年美国儿童中有1/36患有ASD。有证据表明,脑源性神经营养因子(BDNF)是中枢神经系统中最重要的神经营养因子,在ASD中存在广泛而不一致的变化。本系统综述根据PRISMA指南和PubMed数据库,对三种主要的asd样动物模型(丙戊酸(VPA)和丙酸(PPA)诱导的啮齿类动物和BTBR小鼠品系)中BDNF水平的研究进行了调查。纳入了42项研究。大多数研究使用雄性大鼠/小鼠。结果显示,VPA诱导的ASD模型经常导致BDNF下降,尽管也有BDNF水平不变或升高的报道。PPA诱导的ASD模型BDNF均升高或降低。BDNF在BTBR小鼠品系中的变化也不一致。我们发现,分子检测的类型在评估BDNF中似乎很重要。此外,很少有证据表明出生日期和性别差异在asd样啮齿动物模型中BDNF变化中的作用。此外,一些研究表明,在不同的asd样模型中,大脑区域在BDNF变化中的潜在作用。综上所述,ASD啮齿动物模型中BDNF变化的不一致性可能与分子检测的类型、脑区、ASD模型、性别甚至出生后日期有关。然而,证据仍然不足。
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来源期刊
Neurotoxicity Research
Neurotoxicity Research 医学-神经科学
CiteScore
7.70
自引率
5.40%
发文量
164
审稿时长
6-12 weeks
期刊介绍: Neurotoxicity Research is an international, interdisciplinary broad-based journal for reporting both basic and clinical research on classical neurotoxicity effects and mechanisms associated with neurodegeneration, necrosis, neuronal apoptosis, nerve regeneration, neurotrophin mechanisms, and topics related to these themes. Published papers have focused on: NEURODEGENERATION and INJURY Neuropathologies Neuronal apoptosis Neuronal necrosis Neural death processes (anatomical, histochemical, neurochemical) Neurodegenerative Disorders Neural Effects of Substances of Abuse NERVE REGENERATION and RESPONSES TO INJURY Neural Adaptations Neurotrophin mechanisms and actions NEURO(CYTO)TOXICITY PROCESSES and NEUROPROTECTION Excitatory amino acids Neurotoxins, endogenous and synthetic Reactive oxygen (nitrogen) species Neuroprotection by endogenous and exogenous agents Papers on related themes are welcome.
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