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Biological Distribution of Orally Administered [123I]MIBG for Estimating Gastrointestinal Tract Absorption
https://repo.qst.go.jp/records/85039
https://repo.qst.go.jp/records/85039b7f6a6a4-7770-4d07-bf15-e161127203f4
Item type | 学術雑誌論文 / Journal Article(1) | |||||
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公開日 | 2022-01-14 | |||||
タイトル | ||||||
タイトル | Biological Distribution of Orally Administered [123I]MIBG for Estimating Gastrointestinal Tract Absorption | |||||
言語 | ||||||
言語 | eng | |||||
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資源タイプ識別子 | http://purl.org/coar/resource_type/c_6501 | |||||
資源タイプ | journal article | |||||
アクセス権 | ||||||
アクセス権 | metadata only access | |||||
アクセス権URI | http://purl.org/coar/access_right/c_14cb | |||||
著者 |
Kobayashi, Masato
× Kobayashi, Masato× Mizutani , Asuka× Muranaka , Yuka× Nishi , Kodai× Komori , Hisakazu× Ryuichi, Nishii× Shikano , Naoto× Nakanishi , Takeo× Tamai , Ikumi× Kawai , Keiichi× Ryuichi, Nishii |
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抄録 | ||||||
内容記述タイプ | Abstract | |||||
内容記述 | Gastrointestinal tract absorption of cationic anticancer drugs and medicines was estimated using whole-body imaging following oral [123I]MIBG administration. [123I]MIBG was added to cultures of human embryonic kidney (HEK)293 cells expressing human organic anion transporting polypeptide (OATP)2B1, carnitine/organic cation transporter (OCTN)1 and OCTN2, and organic cation transporter (OCT)1, OCT2, and OCT3 with and without cimetidine (an OCTN and OCT inhibitor) and L-carnitine (an OCTN inhibitor). Biodistribution analyses and single-photon emission computed tomography (SPECT) imaging in normal and dextran sodium sulfate (DSS)-induced experimental colitis mice were conducted using [123I]MIBG with and without cimetidine. [123I]MIBG uptake was significantly higher in HEK293/OCTN1, 2, and OCT1-3 cells than in mock cells. Uptake via OCTN was inhibited by L-carnitine, whereas OCT-mediated uptake was inhibited by cimetidine. Biodistribution analyses and SPECT imaging studies showed significantly lower accumulation of [123I]MIBG in the blood, heart, liver, and bladder in DSS-induced experimental colitis mice and mice with cimetidine loading compared with normal mice, whereas significantly higher accumulation in the stomach and kidney was observed after [123I]MIBG injection. [123I]MIBG imaging after oral administration can be used to estimate gastrointestinal absorption in the small intestine via OCTN and/or OCT by measuring radioactivity in the heart, liver, and bladder. | |||||
書誌情報 |
Pharmaceutics 巻 14, 号 1, p. 61, 発行日 2022-01 |
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出版者 | ||||||
出版者 | MDPI | |||||
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収録物識別子タイプ | ISSN | |||||
収録物識別子 | 1999-4923 | |||||
DOI | ||||||
識別子タイプ | DOI | |||||
関連識別子 | 10.3390/pharmaceutics14010061 | |||||
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識別子タイプ | URI | |||||
関連識別子 | https://www.mdpi.com/1999-4923/14/1/61 |