scholarly journals Biliary and Pancreatic Secretions in Abdominal Irradiation

1979 ◽  
Vol 18 (2) ◽  
pp. 145-154 ◽  
Author(s):  
A. Becciolini ◽  
L. Cionini ◽  
M. Cappellini ◽  
G. Atzeni
2021 ◽  
Vol 12 (1) ◽  
Author(s):  
Lydia Bensemmane ◽  
Claire Squiban ◽  
Christelle Demarquay ◽  
Noëlle Mathieu ◽  
Marc Benderitter ◽  
...  

Abstract Background The intestine is particularly sensitive to moderate-high radiation dose and the development of gastrointestinal syndrome (GIS) leads to the rapid loss of intestinal mucosal integrity, resulting in bacterial infiltration, sepsis that comprise patient survival. There is an urgent need for effective and rapid therapeutic countermeasures. The stromal vascular fraction (SVF) derived from adipose tissue is an easily accessible source of cells with angiogenic, anti-inflammatory and regenerative properties. We studied the therapeutic impact of SVF and its action on the intestinal stem cell compartment. Methods Mice exposed to the abdominal radiation (18 Gy) received a single intravenous injection of stromal vascular fraction (SVF) (2.5 × 106 cells), obtained by enzymatic digestion of inguinal fat tissue, on the day of irradiation. Mortality was evaluated as well as intestinal regeneration by histological analyses and absorption function. Results The SVF treatment limited the weight loss of the mice and inhibited the intestinal permeability and mortality after abdominal irradiation. Histological analyses showed that SVF treatment stimulated the regeneration of the epithelium by promoting numerous enlarged hyperproliferative zones. SVF restored CD24+/lysozyme− and Paneth cell populations in the ISC compartment with the presence of Paneth Ki67+ cells. SVF has an anti-inflammatory effect by repressing pro-inflammatory cytokines, increasing M2 macrophages in the ileum and anti-inflammatory monocyte subtypes CD11b+Ly6clowCX3CR1high in the spleen. Conclusions Through the pleiotropic effects that contribute to limiting radiation-induced lethality, SVF opens up attractive prospects for the treatment of emergency GIS.


1990 ◽  
Vol 36 (3) ◽  
pp. 327-330 ◽  
Author(s):  
David E. Linstadt ◽  
Jeffrey L. Stern ◽  
Jeanne M. Quivey ◽  
Steven A. Leibel ◽  
Conley G. Lacey

2008 ◽  
Vol 184 (3) ◽  
pp. 145-149 ◽  
Author(s):  
Nathalie Rochet ◽  
Florian Sterzing ◽  
Alexandra Jensen ◽  
Julien Dinkel ◽  
Klaus Herfarth ◽  
...  

1960 ◽  
Vol 199 (6) ◽  
pp. 1101-1104 ◽  
Author(s):  
W. S. Moos ◽  
H. C. Mason ◽  
M. Counelis

The physiological effects of high-intensity x-irradiation (2 x 105 r/min.) and dosages of 1 x 106 r on mice (head and abdomen) were investigated. An increase in pulmonary and heart rates were observed. Electrocardiographic recordings after irradiation demonstrated reversal of wave components and increase of amplitudes. Blood counts present no changes except for a drop in leukocyte counts. Hemoglobin remained unchanged. A considerable increase in serum potassium was noted and some indications of methemoglobin production. Head-irradiated animals yielded a higher incidence of auricular congestion and brain hemorrhage in contrast to animals receiving abdominal irradiation.


1975 ◽  
Vol 1 (1-2) ◽  
pp. 161-164
Author(s):  
Richard D. Marks ◽  
Hugh J. Scruggs ◽  
Keene M. Wallace ◽  
David F. Hottenstein

The Lancet ◽  
1977 ◽  
Vol 310 (8038) ◽  
pp. 615
Author(s):  
J.D. Khandekar ◽  
Laurie Neulist ◽  
Linda Dotson

PPAR Research ◽  
2010 ◽  
Vol 2010 ◽  
pp. 1-12 ◽  
Author(s):  
Christine Linard ◽  
Maâmar Souidi

The use of radiation therapy to treat cancer inevitably involves exposure of normal tissues. Although the benefits of this treatment are well established, many patients experience distressing complications due to injury to normal tissue. These side effects are related to inflammatory processes, and they decrease therapeutic benefit by increasing the overall treatment time. Emerging evidence indicates that PPARs and their ligands are important in the modulation of immune and inflammatory reactions. This paper discusses the effects of abdominal irradiation on PPARs, their role and functions in irradiation toxicity, and the possibility of using their ligands for radioprotection.


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