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Title: Influence of induction and flavones on lung microsomal oxygen metabolism

Conference · · Fed. Proc., Fed. Am. Soc. Exp. Biol.; (United States)
OSTI ID:5176951

NADPH oxidase activity, H/sub 2/O/sub 2/ production and O/sub 2/ production were studied using microsomes isolated from lungs of control rats and rats treated with phenobarbital (PB), 3-methylcholanthrene (3-MC), 5,6-benzoflavone (..beta..-NF), or chlordecone (CD). 3-MC, ..beta..-NF or Cd treatment resulted in induction of lung P-450 and P-450 reductase. NADPH oxidase activity was slightly higher in 3-MC or ..beta..-NF lung microsomes than in control, PB or CD microsomes. 5 mM metyrapone inhibited oxidase activity of these microsomes by 20-50% depending upon their source. The rates of H/sub 2/O/sub 2/ and O/sub 2/ production did not appear to vary significantly as a function of induction and metyrapone had only a marginal effect on these rates. The rates of H/sub 2/O/sub 2/ and O/sub 2/ production at 37/sup 0/ were 1.8 +/- 0.2 and 1.8 +/- 0.3 nmol/min/mg, respectively. 50 ..mu..M ..beta..-NF stimulated H/sub 2/O/sub 2/ production by about 2-fold regardless of microsomal source while the stimulation of O/sub 2/ production was marginal. In each case, the effect of ..beta..-NF was greater than a comparable amount of 7,8-benzoflavone (..cap alpha..-NF). NADPH oxidase activity was dramatically stimulated by ..beta..-NF. For example, at 37/sup 0/ 100 ..mu..M ..beta..-NF increased the oxidase activity of control lung microsomes by about 9-fold from 3.4 to 31.6 nmol/min/mg. Lung microsomes from induced rats were comparably stimulated by ..beta..-NF. This stimulation was concentration dependent although not hyperbolic. Metyrapone did not inhibit the ..beta..-NF stimulated NADPH oxidase activity.

Research Organization:
Virginia Tech, Blacksburg
OSTI ID:
5176951
Report Number(s):
CONF-8606151-
Journal Information:
Fed. Proc., Fed. Am. Soc. Exp. Biol.; (United States), Vol. 45:6; Conference: 76. annual meeting of the Federation of American Society for Experimental Biology, Washington, DC, USA, 8 Jun 1986
Country of Publication:
United States
Language:
English

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