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Department of Medicine, University of Illinois at Chicago, and West Side Department of Veterans Affairs Medical Center, Chicago, Illinois 60612
Received 8 July 1996; accepted in final form 7 March 1997.
Gao, Xiao-pei, Hideyuki Suzuki, Christopher O. Olopade,
Sergei Pakhlevaniants, and Israel Rubinstein. Purified ACE attenuates smokeless tobacco-induced increase in macromolecular efflux
from the oral mucosa. J. Appl.
Physiol. 83(1): 74-81, 1997.
The purpose of this
study was to determine whether purified angiotensin I-converting enzyme
(ACE) attenuates smokeless tobacco extract (STE)-induced increase in
macromolecular efflux from the in situ oral mucosa. By
using intravital microscopy, we found that suffusion of an aqueous
extract of smokeless tobacco elicited significant concentration-dependent leaky site formation and increase in clearance of fluorescein isothiocyanate-labeled dextran (mol mass, 70 kDa) from
the hamster cheek pouch (P < 0.05). Suffusion of purified rabbit lung ACE
significantly attenuated these responses in a concentration-dependent
fashion (P < 0.05). These effects
were specific because purified ACE also significantly attenuated the increase in macromolecular efflux elicited by bradykinin, which is
produced in the cheek pouch during suffusion of STE, but did not
attenuate the increase elicted by adenosine. Moreover,
suffusion of heat-inactivated purified ACE and purified superoxide
dismutase had no significant effects on STE- and
bradykinin-induced responses. Collectively, these data suggest
that exogenous ACE attenuates STE-induced increase in macromolecular
efflux from the in situ oral mucosa, in part, by promoting local
bradykinin catabolism.
inflammation; microcirculation; plasma exudation; bradykinin; angiotensin-I converting enzyme; hamster
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