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  1. 原著論文

Transport mechanism and affinity of [99mTc]Tc-mercaptoacetyltriglycine ([99mTc]MAG3) on the apical membrane of renal proximal tubule cells

https://repo.qst.go.jp/records/80274
https://repo.qst.go.jp/records/80274
ee5f4883-d096-40a3-92cb-343b32779ccb
Item type 学術雑誌論文 / Journal Article(1)
公開日 2020-08-04
タイトル
タイトル Transport mechanism and affinity of [99mTc]Tc-mercaptoacetyltriglycine ([99mTc]MAG3) on the apical membrane of renal proximal tubule cells
言語
言語 eng
資源タイプ
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

WEKO 885207

Kobayashi, Masato

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Nishi, Kodai

× Nishi, Kodai

WEKO 885208

Nishi, Kodai

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Mizutani, Asuka

× Mizutani, Asuka

WEKO 885209

Mizutani, Asuka

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Okudaira, Hiroyuki

× Okudaira, Hiroyuki

WEKO 885210

Okudaira, Hiroyuki

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Nakanishi, Takeo

× Nakanishi, Takeo

WEKO 885211

Nakanishi, Takeo

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Shikano, Naoto

× Shikano, Naoto

WEKO 885212

Shikano, Naoto

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Nishii, Ryuichi

× Nishii, Ryuichi

WEKO 885213

Nishii, Ryuichi

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Tamai, Ikumi

× Tamai, Ikumi

WEKO 885214

Tamai, Ikumi

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Kawai, Keiichi

× Kawai, Keiichi

WEKO 885215

Kawai, Keiichi

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Nishii, Ryuichi

× Nishii, Ryuichi

WEKO 885216

en Nishii, Ryuichi

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抄録
内容記述タイプ Abstract
内容記述 Technetium-99m-labeled mercaptoacetyltriglycine ([99mTc]MAG3) is widely used for evaluation of transplanted kidneys, diagnosis of tubular necrosis, and scintigraphic studies of tubular function. [99mTc]MAG3 is a substrate for organic anion transporter (OAT)1 and OAT3 on the basolateral membrane side for renal secretion. We investigated the transport mechanism and affinity of [99mTc]MAG3 on the apical membrane of renal proximal tubule cells for renal secretion. Adenosine triphosphate-binding cassette (ABC) transporters for renal secretion of [99mTc]MAG3 were examined using ABC transporter vesicles expressing multiple drug resistance 1 (MDR1), breast cancer resistance protein (BCRP), multidrug resistance-associated protein (MRP)2, and MRP4. MK-571, a MRP inhibitor, was applied to measure the Km and Vmax of MRP2 and MRP4 in a vesicle transport assay. Single photon emission computed tomography (SPECT) was performed in normal rats and MRP2-deficient Eisai hyperbilirubinuria rats (EHBR) using [99mTc]MAG3 with and without MK-571. [99mTc]MAG3 uptake in adenosine triphosphate was significantly higher than that in adenosine monophosphate in vesicles that highly expressed MRP2 and MRP4. The affinity of [99mTc]MAG3 for MRP4 was higher than that for MRP2. Renal secretion via MRP2 and MRP4 was identified by comparing normal and EHBR rats with and without MK-571 on SPECT. [99mTc]MAG3 is transported via MRP2 and MRP4 on the apical membrane of renal proximal tubule cells. The affinity of MRP4 is higher than that of MRP2.
書誌情報 Nuclear Medicine and Biology

巻 84-85, p. 33-37, 発行日 2020-08
ISSN
収録物識別子タイプ ISSN
収録物識別子 0969-8051
DOI
識別子タイプ DOI
関連識別子 10.1016/j.nucmedbio.2020.01.002
関連サイト
識別子タイプ URI
関連識別子 https://www.sciencedirect.com/science/article/pii/S0969805119305426
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