scholarly journals Combined Intraperitoneal and Intrathecal Etanercept Reduce Increased Brain Tumor Necrosis Factor-Alpha and Asymmetric Dimethylarginine Levels and Rescues Spatial Deficits in Young Rats after Bile Duct Ligation

Author(s):  
Jiunn-Ming Sheen ◽  
Yu-Chieh Chen ◽  
Mei-Hsin Hsu ◽  
You-Lin Tain ◽  
Hong-Ren Yu ◽  
...  
2001 ◽  
Vol 120 (5) ◽  
pp. A362
Author(s):  
Gianfranco Alpini ◽  
Laur Tadlock ◽  
Shannon Glaser ◽  
Gene Lesage ◽  
Tushar Patel

1996 ◽  
Vol 270 (6) ◽  
pp. G987-G991 ◽  
Author(s):  
M. G. Swain ◽  
M. Maric

Tumor necrosis factor-alpha (TNF-alpha ) is capable of activating the hypothalamic-pituitary-adrenal (HPA) axis. We have recently documented altered activation of this axis by endotoxin and interleukin-1 in cholestatic rats. Therefore, in this study, we examined TNF-alpha-induced activation of the HPA axis, in rats with cholestasis due to bile duct resection, with the use of sham-resected rats as controls. Administration of TNF-alpha to bile duct- and sham-resected rats in vivo resulted in a similar increase in plasma adrenocorticotropic hormone levels in both groups of animals but significantly higher corticosterone levels in cholestatic rats, suggesting a direct steroidogenic effect of TNF-alpha in cholestatic rats. This suggestion was confirmed in further experiments by the demonstration of TNF-alpha-induced corticosterone secretion in hypophysectomized cholestatic but not control rats. Furthermore, a direct stimulatory effect of TNF-alpha on adrenal corticosterone secretion in vitro was noted only for cholestatic rats, possibly via augmented adrenal prostaglandin E2 (PGE2) production. These results indicate that TNF-alpha has a direct stimulatory effect on adrenal corticosterone secretion in cholestatic rats, possibly due to augmented adrenal PGE2 release.


2003 ◽  
Vol 285 (1) ◽  
pp. C183-C194 ◽  
Author(s):  
Gianfranco Alpini ◽  
Yoshiyuki Ueno ◽  
Laura Tadlock ◽  
Shannon S. Glaser ◽  
Gene LeSage ◽  
...  

Tumor necrosis factor (TNF)-α plays a critical role in epithelial cell injury. However, the role of TNF-α in mediating cholangiocyte injury under physiological or pathophysiological conditions is unknown. Thus we assessed the effects of TNF-α alone or following sensitization by actinomycin D on cell apoptosis, proliferation, and basal and secretin-stimulated ductal secretion in cholangiocytes from normal or bile duct-ligated (BDL) rats. Cholangiocytes from normal or BDL rats were highly resistant to TNF-α alone. However, presensitization by actinomycin D increased apoptosis in cholangiocytes following BDL and was associated with an inhibition of proliferation and secretin-stimulated ductal secretion. Thus TNF-α mediates cholangiocyte injury and altered ductal secretion following bile duct ligation. These observations suggest that cholestasis may enhance susceptibility to cytokine-mediated cholangiocyte injury.


2016 ◽  
Vol 18 (suppl_6) ◽  
pp. vi189-vi189
Author(s):  
Candice C. Poon ◽  
Susobhan Sarkar ◽  
Michael Blough ◽  
J. Gregory Cairncross ◽  
V. Wee Yong ◽  
...  

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