TY - JOUR
T1 - Cilostazol strengthens the endothelial barrier of postcapillary venules from the rat mesentery in situ
AU - Sugiura, Yasoo
AU - Morikawa, Takayuki
AU - Takenouchi, Toshiki
AU - Suematsu, Makoto
AU - Kajimura, Mayumi
N1 - Funding Information:
This work was supported by Japan Society for the Promotion of Science, Grant-in-Aid for Scientific Research 24500448 from the Japan Society for the Promotion of Science (to M. K.), Grant-in-Aid for Creative Scientific Research, Leading Project for Biosimulation from the Ministry of Education, Culture, Sports, Science and Technology in Japan (to M.S.) and the ERATO (Exploratory Research for Advanced Technology) Gas Biology Project from Japan Science and Technology Agency (to M.S.). We would like to thank the Otsuka Pharmaceutical Co., Ltd. for generous gift of cilostazol.
PY - 2014/10
Y1 - 2014/10
N2 - Objective: Although cilostazol, a phosphodiesterase 3 inhibitor, has been suggested to strengthen the endothelial barrier using cultured endothelial monolayers, its effect has not been tested in vivo. We, therefore, investigated effects of cilostazol on barrier properties of postcapillary venules of the rat in situ. Methods: Cilostazol was administered to the rats through oral gavage at 4 hours before the measurements. The hydraulic permeability (Lp) and the effective osmotic pressure ((Formula presented.)), molecular sieving properties of microvascular walls, were estimated in single mesenteric postcapillary venules by a micro-occlusion technique, first during control perfusion and then in the presence of histamine. Results: When the vessels were inflamed with histamine, cilostazol attenuated a transient increase in Lp and prevented (Formula presented.) from falling. Furthermore, it reduced baseline Lp under a control state. Conclusion: Cilostazol appears to tighten the endothelial barrier in situ, at least in part by inhibiting the cAMP-degrading enzyme in the endothelium.
AB - Objective: Although cilostazol, a phosphodiesterase 3 inhibitor, has been suggested to strengthen the endothelial barrier using cultured endothelial monolayers, its effect has not been tested in vivo. We, therefore, investigated effects of cilostazol on barrier properties of postcapillary venules of the rat in situ. Methods: Cilostazol was administered to the rats through oral gavage at 4 hours before the measurements. The hydraulic permeability (Lp) and the effective osmotic pressure ((Formula presented.)), molecular sieving properties of microvascular walls, were estimated in single mesenteric postcapillary venules by a micro-occlusion technique, first during control perfusion and then in the presence of histamine. Results: When the vessels were inflamed with histamine, cilostazol attenuated a transient increase in Lp and prevented (Formula presented.) from falling. Furthermore, it reduced baseline Lp under a control state. Conclusion: Cilostazol appears to tighten the endothelial barrier in situ, at least in part by inhibiting the cAMP-degrading enzyme in the endothelium.
KW - Microvascular permeability
KW - antiplatelet drugs
KW - phosphodiesterase 3
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U2 - 10.1177/0268355513497361
DO - 10.1177/0268355513497361
M3 - Article
C2 - 23858026
AN - SCOPUS:84906880528
SN - 1433-3031
VL - 29
SP - 594
EP - 599
JO - Phlebology
JF - Phlebology
IS - 9
ER -