The effects of 12-week exposure to zidovudine (AZT) at 400, 500, and 600 mg/kg/d were examined on expression of 542 mitochondria-related genes and mitochondrial DNA (mtDNA) copy number in the liver of male and female B6C3F(1) mice to understand mitochondrial role in sex-related differences in development of lactic acidosis. Plasma lactate levels and hematologic parameters were also examined. Results indicated increased red blood cell (RBC) count in vehicle-treated controls, whereas a dose-related decline in the RBC count was noted in AZT-treated mice compared to the basal levels before treatments began. These decreases were associated with significant dose-related increases in mean corpuscular volume and mean corpuscular hemoglobin levels. This effect was greater in AZT-treated females compared to males. In both sexes, 12-week AZT or vehicle exposure significantly reduced plasma lactate levels compared to the basal levels. Results also showed modest, but significant, changes in the expression of genes associated with apoptosis and lipid metabolism at 600 mg/kg/d AZT. Neither drug nor sex influenced hepatic mtDNA copy number. Altogether, 12-week AZT exposure as high as 600 mg/kg/d did not impair hepatic mitochondria or induce lactic acidosis in B6C3F(1) mice. However, AZT-mediated hematologic toxicity appeared to be greater in females compared to males.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3321529PMC
http://dx.doi.org/10.1155/2012/317695DOI Listing

Publication Analysis

Top Keywords

b6c3f1 mice
12
hepatic mitochondria
8
mtdna copy
8
copy number
8
lactic acidosis
8
plasma lactate
8
lactate levels
8
rbc count
8
compared basal
8
basal levels
8

Similar Publications

Identification and characterization of spontaneous AA amyloidosis in CD-1 mice used in toxicity studies: implications of SAA1 and SAA2 copy number variations.

J Toxicol Pathol

January 2025

Laboratory of Veterinary Pathology, School of Veterinary Medicine, Azabu University, 1-17-71 Fuchinobe, Chuo-ku, Sagamihara-shi, Kanagawa 252-5201, Japan.

Amyloidosis is characterized by the extracellular deposition of insoluble protein fibrils that cause cellular damage and dysfunction in organs and tissues. Multiple types of amyloidosis and their causative precursor proteins have been identified in humans and animals. In toxicological studies, a high incidence of spontaneous amyloidosis has been reported in CD-1 mice; however, the precursor protein responsible remains unclear.

View Article and Find Full Text PDF

Investigation of mutagenicity of styrene in tumor target and non-target tissues of transgenic Big Blue® mice.

Environ Mol Mutagen

November 2024

General and Genetic Toxicology, Charles River Laboratories, Ashland, Ohio, USA.

Article Synopsis
  • - A study investigated if styrene, known to cause lung tumors in mice but not in rats, contributes to genotoxicity as a potential first step in tumor development.
  • - Transgenic mice were treated with varying doses of styrene for 28 days, and the frequency of mutations in lung and non-lung tissues was measured.
  • - Results showed no increase in mutations in treated mice, indicating that styrene is unlikely to act as a mutagen in vivo and does not initiate lung tumors in this model.
View Article and Find Full Text PDF

Does environmental enrichment mitigate the adverse effects of chronic low dose-rate radiation exposure on mice?

Radiat Prot Dosimetry

November 2024

Department of Radiobiology, Institute for Environmental Sciences, 2-121 Hacchazawa, Rokkasho, Aomori 039-3213, Japan.

The purpose of the study was to determine whether environmental enrichments (EE) can mitigate the adverse effects of chronic low-dose-rate radiation exposure in mice. Female B6C3F1 mice were continuously exposed to 20 mGy d-1 gamma-rays under specific-pathogen-free conditions since 8 weeks of age for 400 d. After completion of the radiation exposure, OV3121 cells, derived from an ovarian granulosa cell tumor, were inoculated subcutaneously alongside age-matched non-irradiated control mice.

View Article and Find Full Text PDF

Toxicity study of Stachybotrys chartarum (CASRN 67892-26-6) administered by inhalation to B6C3F1/N mice.

Toxic Rep Ser

October 2024

Division of Translational Toxicology, National Institute of Environmental Health Sciences, Research Triangle Park, North Carolina, USA.

Stachybotrys chartarum, also known as "black mold," is a cellulolytic saprophyte with a worldwide distribution. Public concern for potential illnesses associated with water-damaged indoor environments has been heightened since the report of pediatric acute idiopathic pulmonary hemorrhage/hemosiderosis cases in the United States and following recent natural disasters. Although mycotoxicosis and pulmonary immunological endpoints have been previously examined, the systemic toxicity following subchronic inhalation of viable S.

View Article and Find Full Text PDF
Article Synopsis
  • The study investigates the effects of chronic low dose radiation exposure during prenatal and postnatal stages on neurological health, specifically focusing on potential links to neuropsychiatric disorders and changes in the hippocampus in mice.
  • Findings show no significant cellular or cognitive impairments in the irradiated mice, but there were noticeable reductions in body weight and exploratory behavior, alongside changes in organ weights without abnormal pathology.
  • Molecular analysis revealed specific genes and microRNAs were altered in the hippocampus and blood of irradiated mice, indicating a biological response to radiation exposure despite the absence of major neurological symptoms.
View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!