Beneficial Effects of Ankaferd Blood Stopper on Caustic Esophageal Injuries: An Experimental Model

2011 ◽  
Vol 140 (5) ◽  
pp. S-317
Author(s):  
Erdem Akbal ◽  
Erdem Koçak ◽  
Gökhan Karaca ◽  
Hesna M. Astarci ◽  
Adnan Tas ◽  
...  
2011 ◽  
Vol 25 (3) ◽  
pp. 188-194 ◽  
Author(s):  
E. Akbal ◽  
S. Köklü ◽  
G. Karaca ◽  
H. M. Astarcı ◽  
E. Koçak ◽  
...  

2003 ◽  
Vol 2 (1) ◽  
pp. 33-34
Author(s):  
B SHIVALKAR ◽  
B MEURIS ◽  
R VANBENEDEN ◽  
J KETESLEGERS ◽  
F BECKERS ◽  
...  

2015 ◽  
Vol 116 (02) ◽  
pp. 128-131
Author(s):  
O. Aydin ◽  
S. Tuncal ◽  
B. Kilicoglu ◽  
A. K. Onalan ◽  
M. A. Gonultas ◽  
...  

2012 ◽  
Vol 2012 ◽  
pp. 1-10 ◽  
Author(s):  
Youngjoo Kwon ◽  
Sung-Hwa Sohn ◽  
Gihyun Lee ◽  
Youngeun Kim ◽  
Hyejung Lee ◽  
...  

A mouse pulmonary hypersensitivity experimental model that mimics human asthma was developed, and electroacupuncture (EA) treatment was shown to reduce allergic inflammatory processes. In addition, we also assessed whether the beneficial effects of EA on allergic asthma could be correlated with CD4+CD25+Foxp3+regulatory T cells (Treg). Cellular profiles and histopathologic analysis demonstrated that peribronchial and perivascular inflammatory cell infiltrates were significantly decreased in the EA-treated groups when compared to the OVA and anti-CD25 Ab-injected (Treg depletion) groups. Furthermore, total BAL cells were reduced in the EA groups when compared to other groups. Interestingly, the population of CD4+CD25+Foxp3+Tregs in pneumonocytes increased in EA-treated group when compared to OVA and Treg depletion groups. These results imply that EA stimulation at ST 36 may affect CD4+CD25+Foxp3+Treg in an OVA-induced experimental model and may enhance Treg function by suppressing other T cells and limiting the immune response.


2012 ◽  
Vol 11 (1) ◽  
pp. 64-68 ◽  
Author(s):  
Cagri Akalin ◽  
Serdar Kuru ◽  
Aziz Mutlu Barlas ◽  
Kemal Kismet ◽  
Bugra Kaptanoglu ◽  
...  

2008 ◽  
Vol 75 (4) ◽  
pp. 497-504 ◽  
Author(s):  
Nadia Gobbato ◽  
Mirta Rachid ◽  
Gabriela Perdigón

Inflammatory bowel disease (IBD; Crohn′s disease and ulcerative colitis) is the clinical outcome of three interactive pathogenic factors: genetic susceptibility, environmental triggers and immune dis-regulation. At present, only the immune response is targeted by most therapeutic or preventive strategies. The beneficial effect of yoghurt on health as well as its immunomodulator effect on the gut immune system is well documented. The aim of this work was to study the possible beneficial effects of yoghurt consumption on an experimental model of IBD in mice. Balb/c mice were fed with yoghurt for 10 consecutive days. At the end of the feeding period the mice received three inoculations of 2, 4, 6-trinitrobenzene sulphonic acid (TNBS) solutions once a week for 3 consecutive weeks. After TNBS instillation the mice received yoghurt again for 10 consecutive days. IBD control received only TNBS. After treatments we analysed the number of IgA–secreting cells, CD4+, CD8+ T cells population and the number of apoptotic cells in the large intestine. The number of erythrocytes and leucocytes in peripheral blood mononuclear cells (PBMCs) was also determined. We demonstrated the antinflammatory effect of yoghurt in an experimental model of IBD induced by TNBS. The effect was mediated by an increase in the number of the IgA+cells, a decrease in CD8+ population and by the induction of apoptosis of the infiltrative cells in the large intestine.


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