Korean J Physiol Pharmacol.
1999 Apr;3(2):183-189.
Acute pulmonary responses in vivo to silica complexed with H+, Zn2+, or
Fe3+
- Affiliations
-
- 1Department of Physiology, College of Medicine, Division of Cell
Biology, Ewha Womans University, South Korea.
Abstract
-
This investigation is to determine whether the surface complexation of
iron influence acute pulmonary responses induced by silica. For this
study, three varieties of cation complexed silica were used: silica-H+,
-Zn2+, and -Fe3+, since the first two are not active in the transport
of electrons and generate little free radicals relative to the dust
with the surface iron. Rats (270 to 280 g) were intratracheally (IT)
instilled with saline, silica-H+, -Zn2+, or -Fe3+ (5 mg in 0.5 ml
saline). After 4 h, cell number, type, and differentiation were
analysed in the bronchoalveolar lavage cells, and the levels of lactate
dehydrogenase (LDH) and total protein were determined in the lavage
fluid. In addition, bronchoalveolar lavage cells were cultured, and
nitric oxide production was measured using nitrate assay. Inducible
nitric oxide synthase (iNOS) mRNA in the bronchoalveolar lavage cells
was also determined by northern blot analysis. Differential counts of
the lavage cells showed that red blood cells were increased by 9-, 8-,
and 13-fold and total leukocytes (lymphocytes plus polymorphonuclear
neutrophils) by 48-, 36-, and 33-fold, following IT silica- H+, -Zn2+,
and -Fe3+, respectively compared with the saline group. Meanwhile,
there were no significant differences in red blood cells and total
leukocytes among any of the cation complexed silica groups. The levels
of LDH and total protein in the lavage fluid were significantly
increased by 3- to 4-fold. However, compared among these silica groups,
Fe3+ complexation did not significantly change the LDH activity and
total protein. NO production in cultured bronchoalveolar lavage cells
was elevated by 2-fold, following IT any of the silica treatments
compared with the saline group. Furthermore, the steady-state levels of
iNOS mRNA in the lavage cells were greatly increased. There were any
differences in iNOS mRNA expression among the silica-treated groups as
with NO production. These findings suggest that surface complexed iron
may not influence the acute pulmonary responses resulted from 4h
exposure to silica.