Literature DB >> 23475558

Interpreting stress responses during routine toxicity studies: a review of the biology, impact, and assessment.

Nancy E Everds1, Paul W Snyder, Keith L Bailey, Brad Bolon, Dianne M Creasy, George L Foley, Thomas J Rosol, Teresa Sellers.   

Abstract

Stress often occurs during toxicity studies. The perception of sensory stimuli as stressful primarily results in catecholamine release and activation of the hypothalamic-pituitary-adrenal (HPA) axis to increase serum glucocorticoid concentrations. Downstream effects of these neuroendocrine signals may include decreased total body weights or body weight gain; food consumption and activity; altered organ weights (e.g., thymus, spleen, adrenal); lymphocyte depletion in thymus and spleen; altered circulating leukocyte counts (e.g., increased neutrophils with decreased lymphocytes and eosinophils); and altered reproductive functions. Typically, only some of these findings occur in a given study. Stress responses should be interpreted as secondary (indirect) rather than primary (direct) test article-related findings. Determining whether effects are the result of stress requires a weight-of-evidence approach. The evaluation and interpretation of routinely collected data (standard in-life, clinical pathology, and anatomic pathology endpoints) are appropriate and generally sufficient to assess whether or not changes are secondary to stress. The impact of possible stress-induced effects on data interpretation can partially be mitigated by toxicity study designs that use appropriate control groups (e.g., cohorts treated with vehicle and subjected to the same procedures as those dosed with test article), housing that minimizes isolation and offers environmental enrichment, and experimental procedures that minimize stress and sampling and analytical bias. This article is a comprehensive overview of the biological aspects of the stress response, beginning with a Summary (Section 1) and an Introduction (Section 2) that describes the historical and conventional methods used to characterize acute and chronic stress responses. These sections are followed by reviews of the primary systems and parameters that regulate and/or are influenced by stress, with an emphasis on parameters evaluated in toxicity studies: In-life Procedures (Section 3), Nervous System (Section 4), Endocrine System (Section 5), Reproductive System (Section 6), Clinical Pathology (Section 7), and Immune System (Section 8). The paper concludes (Section 9) with a brief discussion on Minimizing Stress-Related Effects (9.1.), and a final section explaining why Parameters routinely measured are appropriate for assessing the role of stress in toxicology studies (9.2.).

Entities:  

Keywords:  endocrine system.; epinephrine; glucocorticoid; hypothalamic-pituitary-adrenal (HPA) axis; immune system; stress; toxicity

Mesh:

Year:  2013        PMID: 23475558     DOI: 10.1177/0192623312466452

Source DB:  PubMed          Journal:  Toxicol Pathol        ISSN: 0192-6233            Impact factor:   1.902


  56 in total

1.  Impact of Environmental Enrichment Devices on NTP In Vivo Studies.

Authors:  Sheba R Churchill; Daniel L Morgan; Grace E Kissling; Gregory S Travlos; Angela P King-Herbert
Journal:  Toxicol Pathol       Date:  2016-02-12       Impact factor: 1.902

2.  Phyllanthus emblica leaf extract ameliorates testicular damage in rats with chronic stress.

Authors:  Supatcharee Arun; Jaturon Burawat; Supataechasit Yannasithinon; Wannisa Sukhorum; Akgpol Limpongsa; Sitthichai Iamsaard
Journal:  J Zhejiang Univ Sci B       Date:  2018 Dec.       Impact factor: 3.066

3.  Recommendations for harmonization of data collection and analysis of developmental neurotoxicity endpoints in regulatory guideline studies: Proceedings of workshops presented at Society of Toxicology and joint Teratology Society and Neurobehavioral Teratology Society meetings.

Authors:  Abby A Li; Larry P Sheets; Kathleen Raffaele; Virginia Moser; Angela Hofstra; Alan Hoberman; Susan L Makris; Robert Garman; Brad Bolon; Wolfgang Kaufmann; Roland Auer; Edmund Lau; Thomas Vidmar; Wayne J Bowers
Journal:  Neurotoxicol Teratol       Date:  2017-07-27       Impact factor: 3.763

4.  Protective effects of Andrographis paniculata extract and pure andrographolide against chronic stress-triggered pathologies in rats.

Authors:  Ajit Kumar Thakur; Upendra Kumar Soni; Geeta Rai; Shyam Sunder Chatterjee; Vikas Kumar
Journal:  Cell Mol Neurobiol       Date:  2014-07-18       Impact factor: 5.046

5.  Retrospective mining of toxicology data to discover multispecies and chemical class effects: Anemia as a case study.

Authors:  Richard S Judson; Matthew T Martin; Grace Patlewicz; Charles E Wood
Journal:  Regul Toxicol Pharmacol       Date:  2017-02-24       Impact factor: 3.271

6.  Scientific and Regulatory Policy Committee (SRPC) Points to Consider: Histopathology Evaluation of the Pubertal Development and Thyroid Function Assay (OPPTS 890.1450, OPPTS 890.1500) in Rats to Screen for Endocrine Disruptors.

Authors:  Kevin A Keane; George A Parker; Karen S Regan; Catherine Picut; Darlene Dixon; Dianne Creasy; Dipak Giri; Renee R Hukkanen
Journal:  Toxicol Pathol       Date:  2015-05-06       Impact factor: 1.902

7.  Optimization of Glioblastoma Mouse Orthotopic Xenograft Models for Translational Research.

Authors:  Susan M Irtenkauf; Susan Sobiechowski; Laura A Hasselbach; Kevin K Nelson; Andrea D Transou; Enoch T Carlton; Tom Mikkelsen; Ana C deCarvalho
Journal:  Comp Med       Date:  2017-08-01       Impact factor: 0.982

8.  Development of a step-down method for altering male C57BL/6 mouse housing density and hierarchical structure: Preparations for spaceflight studies.

Authors:  David C Scofield; Jeffrey D Rytlewski; Paul Childress; Kishan Shah; Aamir Tucker; Faisal Khan; Jessica Peveler; Ding Li; Todd O McKinley; Tien-Min G Chu; Debra L Hickman; Melissa A Kacena
Journal:  Life Sci Space Res (Amst)       Date:  2018-03-07

9.  Comparison of Submental Blood Collection with the Retroorbital and Submandibular Methods in Mice (Mus musculus).

Authors:  Rainy D Regan; Judy E Fenyk-Melody; Sam M Tran; Guang Chen; Kim L Stocking
Journal:  J Am Assoc Lab Anim Sci       Date:  2016       Impact factor: 1.232

10.  Genistein modulation of streptozotocin diabetes in male B6C3F1 mice can be induced by diet.

Authors:  Tai L Guo; Yunbiao Wang; Tao Xiong; Xiao Ling; Jianfeng Zheng
Journal:  Toxicol Appl Pharmacol       Date:  2014-08-30       Impact factor: 4.219

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