Short-Term Radioprotective Effects of WR-2721 on the Rat Parotid Glands

1978 ◽  
Vol 75 (2) ◽  
pp. 317 ◽  
Author(s):  
M. Sodicoff ◽  
A. D. Conger ◽  
P. Trepper ◽  
N. E. Pratt
1993 ◽  
Vol 24 (1) ◽  
pp. 205-210 ◽  
Author(s):  
Hiroyuki Fujinami ◽  
Takao Komabayashi ◽  
Tetsuya Izawa ◽  
Takayuki Nakamura ◽  
Kazuhiro Suda ◽  
...  

Author(s):  
Hiroyuki Fujinami ◽  
Takao Komabayshi ◽  
Tetsuya Izawa ◽  
Takayuki Nakamura ◽  
Kazuhiro Suda ◽  
...  

1998 ◽  
Vol 31 (3) ◽  
pp. 211-216 ◽  
Author(s):  
Chan Young Lee ◽  
Takashi Muramatsu ◽  
Masaki Shimono

2001 ◽  
Vol 80 (5) ◽  
pp. 283-290 ◽  
Author(s):  
Shigeru Takahashi ◽  
Shiro Nakamura ◽  
Reiko Suzuki ◽  
Takanori Domon ◽  
Tsuneyuki Yamamoto ◽  
...  

1987 ◽  
Vol 66 (2) ◽  
pp. 537-540 ◽  
Author(s):  
K.T. Izutsu ◽  
D.E. Johnson ◽  
M. Goddard

Electron probe x-ray micro-analysis was used to study the elemental concentration changes that occur during pilocarpine-stimulated saliva secretion. Quantitative x-ray micro-analysis of elemental concentrations in intracellular compartments of rat parotid glands stimulated in vivo with pilocarpine showed that Na concentration was significantly increased, while K concentration was significantly reduced. The magnitude of these changes was consistent with values obtained in other tissues with the x-ray micro-analysis method, and in the same tissue with other experimental methods. Comparisons with results from studies utilizing dispersed acini suggest that acinar dispersion procedures may affect intracellular elemental concentrations. Total electrolyte concentrations in cytoplasm and secretory granules were estimated to increase on a dry-weight basis following pilocarpine stimulation. The former change is consistent with the notion of a trans-cellular route of salivary fluid flow, while the latter change may be important in the exocytosis of secretory granules.


1990 ◽  
Vol 70 (3) ◽  
pp. 143-152 ◽  
Author(s):  
Gérard Coffe ◽  
Marie-Noëlle Raymond

1991 ◽  
Vol 100 (3) ◽  
pp. 641-647
Author(s):  
D.K. Ann ◽  
A. Wechsler ◽  
H.H. Lin ◽  
E. Wang

Statin, a 57 kilodalton (kDa) nuclear protein, is characteristically found in nonproliferating cells in culture as well as nondividing cells of a wide range of highly differentiated tissues. Moreover, cells in culture that are statin positive lose this statin expression when re-entering the cell-cycle traverse. In this work, statin expression was investigated in the parotid gland of untreated rats and those treated with isoproterenol (IPR), a proliferation-inducing catecholamine. Indirect immunofluorescence microscopy revealed specific nuclear staining with anti-statin monoclonal antibody (S-44) in the acinar and ducts cells of the untreated rats but significantly reduced in those induced with isoproterenol. To characterize the protein recognized by S-44, protein extracts from both tissues were immunoblotted and incubated with S-44. The antibody reacted specifically with a 48 kDa protein in the extract of the parotid glands from untreated rats while no reaction was detected in that of the proliferation-induced ones. These observations along with the result that a statin-like (S1) transcript is downregulated by isoproterenol in the parotid glands further support the notion that the disappearance of statin-related expression is associated with the IPR-induced proliferation in the rat parotid glands. The discrepancy between the apparent molecular mass of the protein identified by S-44 in nonproliferating parotid cells and that of statin originally found in fibroblasts, suggests that either a modified form of statin may be present in the parotid gland, or this 48 kDa protein may be a member of the nonproliferative statin-like family.


1987 ◽  
Vol 43 ◽  
pp. 204
Author(s):  
Hiroko Nomura ◽  
Masakatsu Tachibana ◽  
Takahide Nomura ◽  
Yasumichi Hagino

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