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Subtilisin Increases Macromolecular Efflux from the Oral Mucosa

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ABSTRACTThe purpose of this study was to determine whether subtilisin, a potent serine proteinase derived fromBacillusspecies contaminating smokeless tobacco, increases macromolecular efflux from the oral mucosa and, if so, whether local elaboration of bradykinin mediates this response. Using intravital microscopy, I found that suffusion of subtilisin elicits significant, concentration-dependent leaky site formation and an increase in the clearance of fluorescein isothiocyanate-labeled dextran (molecular mass, 70 kDa) from the in situ hamster cheek pouch (P< 0.05). Heat-inactivated subtilisin had no significant effects on macromolecular efflux. Subtilisin-induced responses were significantly attenuated by Hoe 140 and NPC 17647, two structurally distinct selective bradykinin B2receptor antagonists, but not by des-Arg9-[Leu8]bradykinin, a selective bradykinin B1receptor antagonist, or CP-96,345, a selective neurokinin-1 receptor antagonist. Aprotinin, but not leupeptin, significantly attenuated subtilisin-induced increase in macromolecular efflux. Indomethacin had no significant effects on subtilisin-induced responses. Collectively, these data indicate that subtilisin increases the macromolecular efflux from the in situ hamster cheek pouch in a catalytic-site-dependent fashion through local elaboration of bradykinin. This response does not involve the stimulation of local afferent nerves or the production of prostaglandins.
Title: Subtilisin Increases Macromolecular Efflux from the Oral Mucosa
Description:
ABSTRACTThe purpose of this study was to determine whether subtilisin, a potent serine proteinase derived fromBacillusspecies contaminating smokeless tobacco, increases macromolecular efflux from the oral mucosa and, if so, whether local elaboration of bradykinin mediates this response.
Using intravital microscopy, I found that suffusion of subtilisin elicits significant, concentration-dependent leaky site formation and an increase in the clearance of fluorescein isothiocyanate-labeled dextran (molecular mass, 70 kDa) from the in situ hamster cheek pouch (P< 0.
05).
Heat-inactivated subtilisin had no significant effects on macromolecular efflux.
Subtilisin-induced responses were significantly attenuated by Hoe 140 and NPC 17647, two structurally distinct selective bradykinin B2receptor antagonists, but not by des-Arg9-[Leu8]bradykinin, a selective bradykinin B1receptor antagonist, or CP-96,345, a selective neurokinin-1 receptor antagonist.
Aprotinin, but not leupeptin, significantly attenuated subtilisin-induced increase in macromolecular efflux.
Indomethacin had no significant effects on subtilisin-induced responses.
Collectively, these data indicate that subtilisin increases the macromolecular efflux from the in situ hamster cheek pouch in a catalytic-site-dependent fashion through local elaboration of bradykinin.
This response does not involve the stimulation of local afferent nerves or the production of prostaglandins.

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