Prenatal Exposure to Azadiradione Leads to Developmental Disabilities.

IF 4.6 2区 医学 Q1 NEUROSCIENCES
Molecular Neurobiology Pub Date : 2025-03-01 Epub Date: 2024-09-23 DOI:10.1007/s12035-024-04493-x
Sudipta Jana, Sagarika Das, Bhaskarjyoti Giri, Raghavendra Archak, Sharba Bandyopadhyay, Nihar Ranjan Jana
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Abstract

Azadiradione is a brain-permeable phytochemical present in the seed of an Indian medicinal plant, Azadirachta Indica, well known as neem. Recently, this small bioactive molecule has been revealed to induce the expression of Ube3a, a ubiquitin ligase whose loss and gain of function are associated with two diverse neurodevelopmental disorders. Here, we report that in utero exposure to azadiradione in mice results in severe developmental disabilities. Treatment of a well-tolerated dose of azadiradione into the pregnant dam (at embryonic days 12 and 14) causes a substantial decrease in the body weight of the newborn pups during their early developmental periods along with significant cognitive, motor, and communication deficits and increased anxiety-like behaviors. As the animals grow from adolescence to adulthood, their body weight and many behavioral deficits are gradually restored to normalcy, although the cognitive deficit persists significantly. Biochemical analysis reveals that the azadiradione prenatally exposed mice brain exhibits about 2-3 fold increase in the level of Ube3a at postnatal day 25 along with a significant increase in some of its target proteins linked to synaptic function and plasticity, indicating the enduring effect of the drug on Ube3a expression. The prenatally azadiradione-exposed mice also display increased dendritic spines in the hippocampal and cortical pyramidal neurons. These results suggest that Ube3a might be one of the key players in azadiradione-induced developmental disabilities.

产前接触阿扎地拉二酮会导致发育障碍。
Azadiradione 是一种具有脑渗透性的植物化学物质,存在于印度药用植物 Azadirachta Indica(又称印楝)的种子中。最近,这种生物活性小分子被发现能诱导 Ube3a 的表达,Ube3a 是一种泛素连接酶,其功能的丧失和获得与两种不同的神经发育障碍有关。在这里,我们报告了小鼠在子宫内暴露于偶氮二酮会导致严重的发育障碍。在胚胎第 12 天和第 14 天,向妊娠母鼠施用耐受性良好的剂量的氮基二酮,会导致新生幼鼠在发育早期体重大幅下降,同时出现认知、运动和交流障碍以及焦虑行为增多。随着动物从青春期成长到成年期,它们的体重和许多行为缺陷逐渐恢复正常,但认知缺陷仍然显著存在。生化分析表明,产前暴露于偶氮二酮的小鼠大脑中的 Ube3a 水平在出生后第 25 天增加了约 2-3 倍,同时与突触功能和可塑性相关的一些靶蛋白也显著增加,这表明药物对 Ube3a 的表达具有持久影响。出生前暴露于偶氮二酮的小鼠海马和皮层锥体神经元的树突棘也有所增加。这些结果表明,Ube3a可能是偶氮二酮诱导发育障碍的关键因素之一。
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来源期刊
Molecular Neurobiology
Molecular Neurobiology 医学-神经科学
CiteScore
9.00
自引率
2.00%
发文量
480
审稿时长
1 months
期刊介绍: Molecular Neurobiology is an exciting journal for neuroscientists needing to stay in close touch with progress at the forefront of molecular brain research today. It is an especially important periodical for graduate students and "postdocs," specifically designed to synthesize and critically assess research trends for all neuroscientists hoping to stay active at the cutting edge of this dramatically developing area. This journal has proven to be crucial in departmental libraries, serving as essential reading for every committed neuroscientist who is striving to keep abreast of all rapid developments in a forefront field. Most recent significant advances in experimental and clinical neuroscience have been occurring at the molecular level. Until now, there has been no journal devoted to looking closely at this fragmented literature in a critical, coherent fashion. Each submission is thoroughly analyzed by scientists and clinicians internationally renowned for their special competence in the areas treated.
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