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Datasets for Distribution of 2,2’,5,5’-Tetrachlorobiphenyl (PCB52) Metabolites in Adolescent Rats after Acute Nose-Only Inhalation Exposure
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Datasets for Distribution of 2,2’,5,5’-Tetrachlorobiphenyl (PCB52) Metabolites in Adolescent Rats after Acute Nose-Only Inhalation Exposure

Amanda J Bullert, Xueshu Li, Binita Gautam, Hui Wang, Andrea Adamcakova-Dodd, Kai Wang, Peter S Thorne and Hans-Joachim Lehmler
University of Iowa
03/22/2024
DOI: 10.25820/data.006680
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README13.38 kBDownloadView
READMELists creators of the dataset, preferred citation, an abstract, description of files, and methods.Open Data Commons Attribution (ODC-By) V1.0 Open Access
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D1_Animal_weights3.20 kBDownloadView
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D2_XAD_concentrations114.00 byteDownloadView
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D3_inhalation_notes2.61 kBDownloadView
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D4_PCB52_compiled_levels38.78 kBDownloadView
Open Data Commons Attribution (ODC-By) V1.0 Open Access

Abstract

This dataset summarized a study investigating the disposition of PCB52 and its metabolites in male and female rats following nose-only inhalation exposure to PCB52. Briefly, male and female Sprague-Dawley rats (50-58 days of age, 210 ± 27 g; n=6) were exposed for 4 h to PCB52 using a nose-only inhalation exposure system. Sham animals (n=6) were exposed to filtered lab air. Serum was collected immediately after removal of the animals from the nose-only apparatus by cardiac puncture under isoflurane anesthesia. Rats were perfused with saline, and organs were excised, weighed, and stored at -80°C. Based on gas chromatography-tandem mass spectrometry (GC-MS/MS) analysis, animals were exposed to 14 or 23 µg/kg body weight of PCB52. Levels of PCB52 and its hydroxylated metabolites, including 2,2',5,5'-tetrachlorobiphenyl-4-ol (4-OH-PCB52), were measured in tissues using GC-MS/MS. In addition, liquid chromatography-high resolution mass spectrometry (LC-HRMS) analysis was used to identify PCB52 metabolites, including sulfated, methoxylated, and dechlorinated PCB52 metabolites, in tissues.
Metabolites Acute exposure disposition PCB 52 Polychlorinated biphenyls

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