Carcinogenicity study of the emulsifier TOSOM and the release agent TOS in Wistar rats

1993 ◽  
Vol 31 (11) ◽  
pp. 825-833 ◽  
Author(s):  
O. Meyer ◽  
E. Kristiansen ◽  
J. Gry ◽  
C. Madsen ◽  
P. Olsen ◽  
...  
1988 ◽  
Vol 26 (2) ◽  
pp. 159-167 ◽  
Author(s):  
C.F. Kuper ◽  
P.G.J. Reuzel ◽  
V.J. Feron ◽  
H. Verschuuren

1997 ◽  
Vol 40 (1) ◽  
pp. 75-89
Author(s):  
E. M. Bomhard ◽  
G. J. Krinke ◽  
W. M. Rossberg ◽  
Th. Skripsky

1991 ◽  
Vol 29 (1) ◽  
pp. 31-39 ◽  
Author(s):  
P.G.J. Reuzel ◽  
H.C. Dreef-van der Meulen ◽  
V.M.H. Hollanders ◽  
C.F. Kuper ◽  
V.J. Feron ◽  
...  

2019 ◽  
Vol 47 (4) ◽  
pp. 556-560 ◽  
Author(s):  
Tao Chen ◽  
Ke Chen ◽  
Shaung Qiu ◽  
Peter C. Mann

In a 2-year carcinogenicity study, we identified a spontaneous cholangiofibrosis in a control male Wistar rat. This lesion has long been considered as a compound-related change, with no spontaneous cases reported in the Wistar rat. In addition to routine hematoxylin and eosin stains evaluation, we applied Masson’s trichrome staining, Alcian blue-periodic acid–Schiff staining, and OV-6 immunohistochemistry staining. The special staining demonstrated the fibrous component in the interstitium and intestinal metaplasia of the epithelium (presence of goblet cells), while the positive anti-OV-6 reaction indicated the bile duct origin of the epithelium. These results help to confirm the diagnosis of cholangiofibrosis in this case. We report this rare case to alert pathologists that spontaneous cholangiofibrosis does occur in Wistar rats.


2011 ◽  
Vol 33 (7) ◽  
pp. 593-606 ◽  
Author(s):  
Darol Dodd ◽  
Gabrielle Willson ◽  
Horace Parkinson ◽  
Edilberto Bermudez

2008 ◽  
Vol 233 (2) ◽  
pp. 262-275 ◽  
Author(s):  
Adriana R. Oller ◽  
Daniel T. Kirkpatrick ◽  
Ann Radovsky ◽  
Hudson K. Bates

1980 ◽  
Vol 66 (2) ◽  
pp. 131-144 ◽  
Author(s):  
José R. Cabral ◽  
Lorenzo Rossi ◽  
Tommaso A. Dragani ◽  
Giuseppe Delia Porta

3-(5-nitro-2-furyl)-imidazo(1,2-α)pyridine was tested for carcinogenicity by long-term administration in the diet to CTM mice at 0.1, 0.2 and 0.4 % dose levels and to Wistar rats at 0.2 and 0.4 % dose levels, and by short-term intraperitoneal injections to suckling BALB/c mice. The compound was a strong carcinogen. In CTM mice it induced carcinomas of the esophagus and forestomach at all dose levels and thymic lymphosarcomas at the two highest doses. In male and female rats, esophagus and forestomach papillomas were observed at all dose levels, whereas esophagus and forestomach carcinomas and kidney tumors were observed only at the high dose. In female rats, an increased incidence of mammary tumors was seen at the high dose. The treatment of BALB/c suckling mice by intraperitoneal injections did not induce a clear carcinogenic response.


Author(s):  
D. J. McComb ◽  
J. Beri ◽  
F. Zak ◽  
K. Kovacs

Investigation of the spontaneous pituitary adenomas in rat have been limited mainly to light microscopic study. Furth et al. (1973) described them as chromophobic, secreting prolactin. Kovacs et al. (1977) in an ul trastructural investigation of adenomas of old female Long-Evans rats, found that they were composed of prolactin cells. Berkvens et al. (1980) using immunocytochemistry at the light microscopic level, demonstrated that some spontaneous tumors of old Wistar rats could contain GH, TSH or ACTH as well as PRL.


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