| Project/Area Number |
17590500
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| Research Category |
Grant-in-Aid for Scientific Research (C)
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| Allocation Type | Single-year Grants |
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| Section | 一般 |
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| Research Field |
Laboratory medicine
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| Research Institution | Aichi Medical Univrsity |
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Principal Investigator |
HASEGAWA Takaaki Aichi Medical University, School of Medicine, Professor, 医学部, 教授 (80198720)
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| Co-Investigator(Kenkyū-buntansha) |
FENG G.G. Aichi Medical University, School of Medicine, Research Associate, 医学部, 助手 (70351111)
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| Project Period (FY) |
2005 – 2006
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| Project Status |
Completed (Fiscal Year 2006)
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| Budget Amount *help |
¥3,500,000 (Direct Cost: ¥3,500,000)
Fiscal Year 2006: ¥700,000 (Direct Cost: ¥700,000)
Fiscal Year 2005: ¥2,800,000 (Direct Cost: ¥2,800,000)
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| Keywords | Endotoxin / Drug transporter / Organic anion transport system / Renal excretion / Biliary excretion / Breast cancer resistant protein / Bcrp / 有機アニオン輸送担体 / TNF-α / 6-メルカプトプリン |
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| Research Abstract |
The effect of Klebsiella pneumoniae endotoxin on the function and expression of hepatic breast cancer resistance protein (BCRP) remains unknown. In the present study, we investigated the effect of K.pneumoniae endotoxin on the hepatobiliary excretion of mitoxantrone, a typical substrate of BCRP in mice at different times after intraperitoneal injection of endotoxin (10mg/kg of body weight). The biliary clearance of mitoxantrone significantly decreased by 40% and 70% 6 and 24 h after endotoxin injection, respectively. Both Western blot and immunofluorescence analyses revealed that BCRP expression decreased 6 and 24 h after injection of endotoxin, which were consistent with the results from in vivo experiments. These results suggest that endotoxin-induced decrease in BCRP-mediated hepatobiliary excretion is caused, in part, by down-regulation of hepatic BCRP expression. Endotoxin significantly induced the production of cytokines including interleukin-6 (IL-6) and IL-1β. Pretreatment with IL-1β did not decrease the hepatobiliary excretion of mitoxantrone and down-regulate hepatic BCRP expression. However, pretreatment with IL-6 significantly decreased the hepatobiliary excretion of mitoxantrone. Western blot and immunofluorescence analyses also revealed that pretreatment with IL-6 decreased the expression of BCRP, which is in line with in vivo experiments. These findings suggest that K.pneumoniae endotoxin decreases BCRP-mediated hepatobiliary excretion of mitoxantrone by decreasing the expression of hepatic BCRP, which is likely due to increased plasma IL-6 levels.
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