Literature DB >> 21747121

Morphologic aspects of rodent cardiotoxicity in a retrospective evaluation of National Toxicology Program studies.

Micheal P Jokinen1, Warren G Lieuallen, Michael C Boyle, Crystal L Johnson, David E Malarkey, Abraham Nyska.   

Abstract

The heart is increasingly recognized as a target for toxicity. As studies in laboratory rodents are commonly used to investigate the potential toxicity of various agents, the identification and characterization of lesions of cardiotoxicity is of utmost importance. Although morphologic criteria have been established for degenerative myocardial lesions in rats and mice, differentiation of spontaneously occurring lesions from toxin-induced or toxin-related lesions remains difficult. A retrospective light microscopic evaluation was performed on the hearts of F344 rats and B6C3F(1) mice from National Toxicology Program (NTP) studies of six chemicals identified in the NTP database in which treatment-induced myocardial toxicity was present. Two previously defined myocardial lesions were observed: "cardiomyopathy" that occurred spontaneously or as a treatment-related effect and "myocardial degeneration" that occurred as a treatment-related effect. Both lesions consisted of the same basic elements, beginning with myofiber degeneration and necrosis, with varying amounts of inflammation, interstitial cell proliferation, and eventual fibrosis. This observation is indicative of the heart's limited repertoire of responses to myocardial injury, regardless of the nature of the inciting agent. A prominent differentiating factor between spontaneous and treatment-induced lesions was distribution and lesion onset. Once the respective lesions had undergone fibrosis, however, they generally appeared morphologically indistinguishable.

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Year:  2011        PMID: 21747121     DOI: 10.1177/0192623311413788

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


  16 in total

1.  Data integration, analysis, and interpretation of eight academic CLARITY-BPA studies.

Authors:  Jerrold J Heindel; Scott Belcher; Jodi A Flaws; Gail S Prins; Shuk-Mei Ho; Jiude Mao; Heather B Patisaul; William Ricke; Cheryl S Rosenfeld; Ana M Soto; Frederick S Vom Saal; R Thomas Zoeller
Journal:  Reprod Toxicol       Date:  2020-07-16       Impact factor: 3.143

2.  Effects of bisphenol A on incidence and severity of cardiac lesions in the NCTR-Sprague-Dawley rat: A CLARITY-BPA study.

Authors:  Robin Gear; Jessica A Kendziorski; Scott M Belcher
Journal:  Toxicol Lett       Date:  2017-05-09       Impact factor: 4.372

3.  Protective Effect of Pycnogenol against Methotrexate-Induced Hepatic, Renal, and Cardiac Toxicity: An In Vivo Study.

Authors:  Faten Al-Abkal; Basel A Abdel-Wahab; Hanaa F Abd El-Kareem; Yasser M Moustafa; Dina M Khodeer
Journal:  Pharmaceuticals (Basel)       Date:  2022-05-27

Review 4.  Research-Relevant Conditions and Pathology of Laboratory Mice, Rats, Gerbils, Guinea Pigs, Hamsters, Naked Mole Rats, and Rabbits.

Authors:  Timothy K Cooper; David K Meyerholz; Amanda P Beck; Martha A Delaney; Alessandra Piersigilli; Teresa L Southard; Cory F Brayton
Journal:  ILAR J       Date:  2021-12-31       Impact factor: 1.521

Review 5.  Non-proliferative and Proliferative Lesions of the Cardiovascular System of the Rat and Mouse.

Authors:  Brian R Berridge; Vasanthi Mowat; Hirofumi Nagai; Abraham Nyska; Yoshimasa Okazaki; Peter J Clements; Matthias Rinke; Paul W Snyder; Michael C Boyle; Monique Y Wells
Journal:  J Toxicol Pathol       Date:  2016-07-29       Impact factor: 1.628

6.  Right Ventricular Epicardial Fibrosis in Mice With Sternal Segment Dislocation.

Authors:  H A Adissu; G A Medhanie; L Morikawa; J K White; S Newbigging; C McKerlie
Journal:  Vet Pathol       Date:  2014-10-03       Impact factor: 2.221

7.  Endocrine Disruption and Reproductive Pathology.

Authors:  Scott M Belcher; J Mark Cline; Justin Conley; Sibylle Groeters; Wendy N Jefferson; Mac Law; Emily Mackey; Alisa A Suen; Carmen J Williams; Darlene Dixon; Jeffrey C Wolf
Journal:  Toxicol Pathol       Date:  2019-12       Impact factor: 1.902

8.  Proceedings of the 2015 National Toxicology Program Satellite Symposium.

Authors:  Susan A Elmore; Cindy A Farman; James R Hailey; Ramesh C Kovi; David E Malarkey; James P Morrison; Jennifer Neel; Patricia A Pesavento; Brian F Porter; Kathleen A Szabo; Leandro B C Teixeira; Erin M Quist
Journal:  Toxicol Pathol       Date:  2016-04-12       Impact factor: 1.902

9.  Centrally administered angiotensin-(1-7) increases the survival of stroke-prone spontaneously hypertensive rats.

Authors:  Robert W Regenhardt; Adam P Mecca; Fiona Desland; Phillip F Ritucci-Chinni; Jacob A Ludin; David Greenstein; Cristina Banuelos; Jennifer L Bizon; Mary K Reinhard; Colin Sumners
Journal:  Exp Physiol       Date:  2013-10-18       Impact factor: 2.969

10.  Unexpected Cardiomyopathy and Cardiac Dysfunction after Administration of Sulfadiazine-trimethoprim Medicated Diet to ICR mice (Mus musculus).

Authors:  Nicole M Pach; Kerith R Luchins; Gene H Kim; George P Langan; Betty R Theriault
Journal:  Comp Med       Date:  2020-07-27       Impact factor: 0.982

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