Announcement of NTP Workshop on “Animal Models for the NTP Rodent Cancer Bioassay: Strains and Stocks—Should We Switch?”

National Institute of Environmental Health Sciences, Research Triangle Park, North Carolina 27709, USA.
Toxicologic Pathology (Impact Factor: 2.14). 02/2006; 34(6):802-5. DOI: 10.1080/01926230600935938
Source: PubMed


The National Toxicology Program (NTP) hosted a workshop, "Animal Models for the NTP Rodent Cancer Bioassay: Strains and Stocks--Should We Switch?" on June 16-17, 2005, at the National Institute of Environmental Health Sciences (NIEHS) in Research Triangle Park, North Carolina. The workshop's objectives were to determine (1) whether the currently used models, the F344/N rat and B6C3F1/N mouse, continue to be appropriate to identify substances that may pose a carcinogenic hazard for humans and (2) whether the NTP should consider conducting cancer bioassays using multiple strains of rats and/or mice to better capture the range of genetic variability. Workshop participants advised the NTP to discontinue using the current F344/N strain due to the recent issues with fertility, seizure activity, and chylothorax and provided several options on how the program should approach identifying and selecting a new rat model. Participants believed that the B6C3F1/N mouse is still appropriate for use by the NTP, but suggested the NTP take steps to better understand and address increases in background rates of liver tumors in this strain. Finally, the participants supported the NTP exploring the use of the multiple strain approach, although they raised many questions concerning data interpretation and feasibility. This article also outlines the NTP's next steps in pursuing the workshop recommendations.

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Available from: Kristina Thayer, Jul 05, 2014
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    • "Sprague-Dawley (SD) rats are a common choice for regulatory toxicology studies, but recently the Wistar Han (WH) strain has been increasingly used. The growing popularity of the Wistar strain can be attributed to their reduced size, which requires less test material, as well as a higher survival rates (longer lifespan) and lower incidence of background tumors relative to the more traditionally used Sprague-Dawley strain, which make them more desirable for use in carcinogenicity studies [1]. In addition to these differences, there have also been anecdotal reports based on reproductive performance data that the male WH rat attains sexual maturity about 2 weeks later than the Sprague-Dawley strain. "
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    ABSTRACT: Given the increasing use of Wistar Han (WH) rats in regulatory toxicology studies, these studies were performed to characterize the onset of sexual maturation in maturing WH rats as compared to Sprague-Dawley (SD) rats. Beginning on postnatal day (PND) 38 through PND 91 groups (n=8) of untreated WH rats were evaluated for maturation of the male reproductive system. Testicular spermatid head counts increased beginning on PND 42 until PND 70. Sperm were detected in the caput, corpus, and cauda epididymis on PND 45, 49, and 49, respectively, and counts increased through PND 91. Sperm motility was at adult levels by PND 63. The morphology of the testis/epididymis of all animals at day 70 or older was consistent with qualitative sexual maturity. Based on these endpoints, WH rats were determined to be sexually mature at PND 70, and many of these endpoints evaluated in SD rats exhibited nearly identical trends.
    Reproductive Toxicology 02/2013; 38. DOI:10.1016/j.reprotox.2013.02.003 · 3.23 Impact Factor
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    • "Wistar Hannover GALAS rats (GALAS rats) have recently been used in toxicity studies in Japan because of their beneficial characteristics such as a higher survival rate and a lower body weight than other ordinary strains, such as Sprague-Dawley and Fisher 3441. In GALAS rats, it has been reported that vacuolar change of thyroid follicular cells sometimes occurs as a spontaneous lesion2. "
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    ABSTRACT: Incidences and morphological features of thyroid proliferative lesions induced by carcinogens in Wistar Hannover GALAS rats (GALAS rats) showing normal growth with or without thyroid dysplasia were examined. All thyroid tissue samples were obtained from our recently conducted study using male GALAS rats treated with 5 carcinogens according to the medium-term multiorgan carcinogenicity bioassay protocol (called DMBDD treatment). In the DMBDD-treated rats, thyroid dysplasia was found in 9 out of 114 rats. Follicular cell adenomas were found in 5 out of 9 rats with thyroid dysplasia and in 7 out of 105 rats without thyroid dysplasia. The incidence of adenoma was significantly increased in rats with thyroid dysplasia (55.6%) compared with that in rats without thyroid dysplasia (6.7%). Adenomas in rats with thyroid dysplasia were observed as single or multiple nodules, well demarcated and composed of variously sized vacuolated cells or unvacuolated cells. These histopathological features and staining profiles of luminal colloid for PAS and thyroglobulin, together with PCNA-positive cells, were fundamentally similar to those of rats without thyroid dysplasia. On the other hand, the luminal colloid in adenomas of rats with thyroid dysplasia had a tendency to be poorly stained for T(4) compared with that of rats without thyroid dysplasia. From these findings, it appears that dysplastic thyroids of rats showing normal growth are more sensitive to carcinogens than normal thyroids. In addition, the morphological features of carcinogen-induced thyroid proliferative lesions in GALAS rats with thyroid dysplasia were fundamentally similar to those of rats without thyroid dysplasia, except for the vacuoles and T(4) staining profile.
    Journal of Toxicologic Pathology 03/2012; 25(1):11-7. DOI:10.1293/tox.25.11 · 0.94 Impact Factor
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    • "In many institutes including our laboratory in Japan, CD(SD) (Sprague-Dawley) rats are used predominantly as experimental models in toxicity studies, and F344 (Fischer) rats have been used as traditional animal models for assessing carcinogenic potential of various kinds of compounds. However, an epoch-making decision was made by NTP (National Toxicology Program), that is, the animal model in rat carcinogenicity studies was changed from F344 rats to Wistar Hannover rats1. This decision exerted an impact to a certain extent on researchers in the field of toxicology, and Wistar Hannover rats began to be used in toxicity studies in Japan, but relatively little data are available. "
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    ABSTRACT: Recently, RccHan(TM):WIST (Wistar Hannover) rats were introduced to toxicity studies in Japan. The present study was performed to obtain control data for general toxicological parameters as an aid for interpretation of results in toxicity studies using this strain of rats. Four test groups comprising of 25 male and 25 female RccHan(TM):WIST rats were housed for 2, 4, 13 or 26 weeks from 6 weeks of age and observed and examined for clinical observation, body weight, food consumption, urinalysis, hematology, blood chemistry, organ weight, necropsy and/or histopathology. Ophthalmological examination was not conducted in this study, and the data in this report were obtained from an ongoing 104-week background study in RccHan(TM):WIST rats. These data were compared with the historical control data of CD(SD) (Sprague-Dawley) and/or F344 (Fischer) rats. The body weights of RccHan(TM):WIST rats were lower than those of CD(SD) rats and higher than those of F344 rats. The ophthalmological examination revealed a greater incidence of focal corneal opacity. Histopathology revealed focal mineralization of the cornea and Berlin blue-positive pigmentation in the epididymal interstitium as well as hepatocytes. Other than the above, some minor differences were found in urinalysis, hematology, blood chemistry and organ weights as compared with CD(SD) rats.
    Journal of Toxicologic Pathology 12/2011; 24(4):195-205. DOI:10.1293/tox.24.195 · 0.94 Impact Factor
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