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Short-term toxicogenomics as an alternative approach to chronic in vivo studies for derivation of points of departure: A case study in the rat with a triazole fungicide.
- Source :
-
Regulatory toxicology and pharmacology : RTP [Regul Toxicol Pharmacol] 2020 Jun; Vol. 113, pp. 104655. Date of Electronic Publication: 2020 Apr 05. - Publication Year :
- 2020
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Abstract
- The derivation of an apical endpoint point of departure (POD) from animal-intensive testing programs has been the traditional cornerstone of human health risk assessment. Replacement of in vivo chronic studies with novel approaches, such as toxicogenomics, holds promise for future alternative testing paradigms that significantly reduce animal testing. We hypothesized that a toxicogenomic POD following a 14 day exposure in the rat would approximate the most sensitive apical endpoint POD derived from a battery of chronic, carcinogenicity, reproduction and endocrine guideline toxicity studies. To test this hypothesis, we utilized myclobutanil, a triazole fungicide, as a model compound. In the 14 day study, male rats were administered 0 (vehicle), 30, 150, or 400 mg/kg/day myclobutanil via oral gavage. Endpoints evaluated included traditional apical, hormone, and liver and testis transcriptomic (whole genome RNA sequencing) data. From the transcriptomic data, liver and testis biological effect POD (BEPOD) values were derived. Myclobutanil exposure for 14 days resulted in increased liver weight, altered serum hormones, liver histopathology, and differential gene expression in liver and testis. The liver and testis BEPODs from the short-term study were 22.2 and 25.4 mg/kg/day, respectively. These BEPODs were approximately an order of magnitude higher than the most sensitive apical POD identified from the two year cancer bioassay based on testis atrophy (1.4 mg/kg/day). This study demonstrates the promise of using a short-term study BEPOD to derive a POD for human health risk assessment while substantially reducing animal testing.<br />Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.<br /> (Copyright © 2020 Elsevier Inc. All rights reserved.)
- Subjects :
- Administration, Oral
Animals
Dose-Response Relationship, Drug
Fungicides, Industrial administration & dosage
Liver metabolism
Liver pathology
Male
Nitriles administration & dosage
No-Observed-Adverse-Effect Level
Organ Size drug effects
Rats
Rats, Sprague-Dawley
Testis metabolism
Testis pathology
Time Factors
Toxicity Tests, Subacute
Triazoles administration & dosage
Disease Models, Animal
Fungicides, Industrial toxicity
Liver drug effects
Nitriles toxicity
Testis drug effects
Toxicogenetics
Triazoles toxicity
Subjects
Details
- Language :
- English
- ISSN :
- 1096-0295
- Volume :
- 113
- Database :
- MEDLINE
- Journal :
- Regulatory toxicology and pharmacology : RTP
- Publication Type :
- Academic Journal
- Accession number :
- 32268158
- Full Text :
- https://doi.org/10.1016/j.yrtph.2020.104655