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Authors
Info
D.K. Park, Y. H. Yu, J.H. Kang,
K.H. Lee, D.Y. Yoo, K.H. Park
and D.S. Kim*
Department of Anatomy, Soonchunhyang
University, Cheonan, 31151, Republic of Korea
*Corresponding
Author Email :
dskim@sch.ac.kr
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Abstract
Aim: The present study
was conducted to investigate the distribution of nitric oxide synthase
isoforms (endothelial, neuronal, and inducible NOS) and changes in
endothelial NOS (eNOS) expression after intraperitoneal injection of
N(G)-Nitro-L-arginine methyl ester (L-NAME) in rats.
Methodology: Immunohistological
and immunoelectron microscopic study, using monoclonal mouse anti-endothelial
NOS, anti-neuronal NOS and anti-inducible NOS were performed on the exorbital
lacrimal glands of rats.
Results: eNOS-positive
immunoreactivities were observed in the intralobular ducts and interlobular
ducts of exorbital lacrimal gland of rats. One day after L-NAME
administration, the size of eNOS-positive immunoreactivities had
significantly decreased, however, after 3 and 5 days of L-NAME
administration, eNOS-positive immunoreactivities were restored. Neuronal
NOS-positive immunoreactivity was observed in nerve fibers of exorbital
lacrimal gland, but was not detected in the duct systems or in the acinar
cells. The inducible NOS was not detected in the exorbital lacrimal glands of
rats.
Interpretation: Expression of
nNOS in the nerves of lacrimal gland suggests that NO may play a role in
modulating tear production. eNOS and nNOS were expressed in the exorbital
lacrimal glands of rats, and the endogenously located eNOS was influenced by
NOS inhibitor (L-NAME). These results suggest that endogenous NOS may be
closely related with the direct or indirect regulation of glandular secretion
and blood flow in the exorbital lacrimal glands.
Key words: Exorbital lacrimal gland, N ω- Nitro-L-arginine
methyl ester hydrochloride, Nitric oxide synthase, Tear production
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