Liver microsomal FMO activities of LPS-treated rats were decreased significantly. Hepatic content of FMO1 mRNA and tile liver microsomal content of FMO I (the major form in rat liver) in LPS-treated rats were significantly decreased also, However. the expression of inducible NO synthase (iNOS) and plasma nitrate/nitrite (NOx) concentration were increased. In rats cotreated with NOS inhibitors such as aminoguanidine and nitro L-arginine. the ativities and content of FMO1 in liver microsomes were restored. These results suggest that NO is an important mediator involved in the suppression of FMO1 activity in vivo.
机构:Inha Univ, Dept Pharmacol, Med Toxicol Res Ctr, Coll Med, Inchon 400103, South Korea
Ryu, SD
Yi, HG
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机构:Inha Univ, Dept Pharmacol, Med Toxicol Res Ctr, Coll Med, Inchon 400103, South Korea
Yi, HG
Cha, YN
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机构:Inha Univ, Dept Pharmacol, Med Toxicol Res Ctr, Coll Med, Inchon 400103, South Korea
Cha, YN
Kang, JH
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机构:Inha Univ, Dept Pharmacol, Med Toxicol Res Ctr, Coll Med, Inchon 400103, South Korea
Kang, JH
Kang, JS
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机构:Inha Univ, Dept Pharmacol, Med Toxicol Res Ctr, Coll Med, Inchon 400103, South Korea
Kang, JS
Jeon, YC
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机构:Inha Univ, Dept Pharmacol, Med Toxicol Res Ctr, Coll Med, Inchon 400103, South Korea
Jeon, YC
Park, HK
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机构:Inha Univ, Dept Pharmacol, Med Toxicol Res Ctr, Coll Med, Inchon 400103, South Korea
Park, HK
Yu, TM
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机构:Inha Univ, Dept Pharmacol, Med Toxicol Res Ctr, Coll Med, Inchon 400103, South Korea
Yu, TM
Lee, JN
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机构:Inha Univ, Dept Pharmacol, Med Toxicol Res Ctr, Coll Med, Inchon 400103, South Korea
Lee, JN
Park, CS
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Inha Univ, Dept Pharmacol, Med Toxicol Res Ctr, Coll Med, Inchon 400103, South KoreaInha Univ, Dept Pharmacol, Med Toxicol Res Ctr, Coll Med, Inchon 400103, South Korea