Evidence map›Paper›PMID 29502054›Full record

ArticleNan fang yi ke da xue xue bao = Journal of Southern Medical University2018

[Changes of cerebral cortical metabolomics in rats following benzo[a]pyrene exposure].

Jing Wang, Chun-Lin Li, Lu-Lu Bai, Qiang-Hu Tang, Rui-Yuan Zhang, Ting-Li Han, Yu-Ming Guo, Philip N Baker, Yin-Yin Xia, Bai-Jie Tu

Abstract read
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Article in Nan fang yi ke da xue xue bao = Journal of Southern Medical University, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

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3 · Its place in the literature

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0 citing papers in PubMed, 1 citations in OpenAlex.

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4 · The record

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5 · Who and what money

Authors and funding

10 authors at 1 institution in 1 country.

Jing WangDepartment of Occupational and Environmental Hygiene, School of Public Health and Management, Research Center for Medicine and Social Development, Innovation Center for Social Risk Governance in Health, Chongqing Medical University, Chongqing 400016, China. E-mail: jingwang.crystal@qq.com.
Chun-Lin Li
Lu-Lu Bai
Qiang-Hu Tang
Rui-Yuan Zhang
Ting-Li Han
Yu-Ming Guo
Philip N Baker
Yin-Yin Xia
Bai-Jie Tu
Chongqing Public Health Medical Center · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo analyze the changes in endogenous small molecule metabolites after benzo[a]pyrene (B[a]P) exposure in rat cerebral cortex and explore the mechanism of B[a]P neurotoxicity.

methodsFive-day-old SD rats were subjected to gavage administration of 2 mg/kg B[a]P for 7 consecutive weeks. After the exposure, the rats were assessed for spatial learning ability using Morris water maze test, ultrastructural changes of the cortical neurons under electron microscope, and metabolite profiles of the cortex using GC/MS. The differential metabolites between the exposed and control rats were identified with partial least squares discriminant analysis (PLS-DA) and the metabolic pathways related with the differential metabolites were analyzed using Cytoscape software.

resultsCompared with the control group, the rats exposed to B[a]P showed significantly increased escape latency (P<0.05) and decreased time spent in the target area (P<0.05). The exposed rats exhibited widened synaptic cleft, thickened endplate membrane and swollen cytoplasm compared with the control rats. Eighteen differential metabolites (VIP>1, P<0.05) in the cortex were identified between the two groups, and 9 pathways associated with B[a]P neurotoxicity were identified involving amino acid metabolism, tricarboxylic acid cycle and Vitamin B3 (niacin and nicotinamide) metabolism.

conclusionB[a]P can cause disturbance in normal metabolisms and its neurotoxicity is possibly related with disorders in amino acid metabolism, tricarboxylic acid cycle and vitamin metabolism.

Indexed as

MetabolomeAnimalsBenzo(a)pyreneCerebral CortexMaze LearningRatsRats, Sprague-DawleyBenzo(a)pyrene

Identifiers

PMID29502054
PMCPMC6743872
OpenAlexW2797164275

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.