T1778 Reciprocal Modulation of Smooth Muscle Cell Contractility in TH1 and Th2 Dominant Environments Using Murine Model of Early Post Inflammatory Gut Dysfunction

2009 ◽  
Vol 136 (5) ◽  
pp. A-578 ◽  
Author(s):  
Hiroyuki Murao ◽  
Hirotada Akiho ◽  
Takahiro Mizutani ◽  
Mariko Yamada ◽  
Noriko Tokunaga ◽  
...  
2019 ◽  
Vol 9 (1) ◽  
Author(s):  
Natalija Bogunovic ◽  
Jorn P. Meekel ◽  
Dimitra Micha ◽  
Jan D. Blankensteijn ◽  
Peter L. Hordijk ◽  
...  

2019 ◽  
Vol 220 (1) ◽  
pp. S372
Author(s):  
Joy Vink ◽  
Sudip Dahal ◽  
Hongyu Li ◽  
Mirella Mourad ◽  
Chioma Ndubisi ◽  
...  

Author(s):  
Ramji Venkatasubramanian ◽  
Wim Wolkers ◽  
Charles Soule ◽  
Paul Iaizzo ◽  
John Bischof

Applications involving freeze-thaw in arteries such as cryoplasty and cryopreservation alter the arterial biomechanics significantly [1]. Tissue dehydration or bulk water loss is observed following freeze-thaw in native arteries as well as other artificial tissues [1, 2]. It is hypothesized that tissue dehydration observed during freeze-thaw is an important mechanism underlying the biomechanical changes in arteries. In order to test this hypothesis, dehydration was induced in arteries (without changing temperature or phase) by treating them with different concentrations of hyperosmotic mannitol solutions. Changes to smooth muscle cell (SMC) contractility, collagen matrix structure and overall artery biomechanics were studied following tissue dehydration. SMC contractility and relaxation were measured by studying the response of arteries to norepinephrine (NE) and acetylcholine (AC) respectively. Collagen matrix structure was assessed by studying the thermal denaturation of collagen due to heating using Fourier transform infrared (FTIR) spectroscopy and the overall artery biomechanics through uniaxial tensile tests.


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