Comparison of the transcellular transport of FDG and D-glucose by the kidney epithelial cell line, LLC-PK1
OBJECTIVESAlmost all D-glucose (GLU) filtered through the glomerulus is reabsorbed by the renal proximal tubules, whereas a high portion of 2-[F]fluoro-2-deoxy-D-glucose [(F)FDG] is excreted through the urine. However, [F]FDG is not entirely excreted in the urine suggesting that it may be partially...
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Veröffentlicht in: | Nuclear medicine communications 2010-02, Vol.31 (2), p.141-146 |
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creator | Kobayashi, Masato Shikano, Naoto Nishii, Ryuichi Kiyono, Yasushi Araki, Hiroyo Nishi, Kodai Oh, Myungmi Okudaira, Hiroyuki Ogura, Masato Yoshimoto, Mitsuyoshi Okazawa, Hidehiko Fujibayashi, Yasuhisa Kawai, Keiichi |
description | OBJECTIVESAlmost all D-glucose (GLU) filtered through the glomerulus is reabsorbed by the renal proximal tubules, whereas a high portion of 2-[F]fluoro-2-deoxy-D-glucose [(F)FDG] is excreted through the urine. However, [F]FDG is not entirely excreted in the urine suggesting that it may be partially reabsorbed by the proximal tubules. The purpose of this study was to compare the time course of transcellular transport of administered [C] labeled FDG ([C]FDG) with that of [C] labeled GLU ([C]GLU) using the kidney epithelial cell line, LLC-PK1.
METHODSTranscellular transport of [C]FDG and [C]GLU by LLC-PK1 cells was measured in Na-containing or Na-free Dulbeccoʼs phosphate-buffered saline [PBS(+) and PBS(−), respectively] in the presence or absence of phlorizin, phloretin, probenecid, or tetraethylammonium bromide inhibitors that predominantly inhibit sodium-dependent glucose transporters (SGLTs), sodium-independent glucose transporters, organic anion transporters, and organic cation transporters, respectively.
RESULTSWhen assayed in PBS(+), less [C]FDG than [C]GLU was reabsorbed by the proximal tubular cells over the entire incubation time. Reabsorption of [C]FDG was mediated mainly by SGLT at early time points in the incubation, whereas high reabsorption of [C]GLU was mediated by both SGLT and glucose transporter over 90 min of incubation. Secretion of [C]FDG also tended to be slightly higher than that of [C]GLU over 90 min of incubation.
CONCLUSIONTranscellular transport of [C]FDG over time by LLC-PK1 cells was clarified. The polarized distribution of transcellular transporters of [C]FDG and [C]GLU in LLC-PK1 cells differs. |
doi_str_mv | 10.1097/MNM.0b013e328333bcf5 |
format | Article |
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METHODSTranscellular transport of [C]FDG and [C]GLU by LLC-PK1 cells was measured in Na-containing or Na-free Dulbeccoʼs phosphate-buffered saline [PBS(+) and PBS(−), respectively] in the presence or absence of phlorizin, phloretin, probenecid, or tetraethylammonium bromide inhibitors that predominantly inhibit sodium-dependent glucose transporters (SGLTs), sodium-independent glucose transporters, organic anion transporters, and organic cation transporters, respectively.
RESULTSWhen assayed in PBS(+), less [C]FDG than [C]GLU was reabsorbed by the proximal tubular cells over the entire incubation time. Reabsorption of [C]FDG was mediated mainly by SGLT at early time points in the incubation, whereas high reabsorption of [C]GLU was mediated by both SGLT and glucose transporter over 90 min of incubation. Secretion of [C]FDG also tended to be slightly higher than that of [C]GLU over 90 min of incubation.
CONCLUSIONTranscellular transport of [C]FDG over time by LLC-PK1 cells was clarified. The polarized distribution of transcellular transporters of [C]FDG and [C]GLU in LLC-PK1 cells differs.</description><identifier>ISSN: 0143-3636</identifier><identifier>EISSN: 1473-5628</identifier><identifier>DOI: 10.1097/MNM.0b013e328333bcf5</identifier><identifier>PMID: 19949354</identifier><language>eng</language><publisher>England: Lippincott Williams & Wilkins, Inc</publisher><subject>Biological Transport - drug effects ; Cell Line ; Epithelial Cells - drug effects ; Epithelial Cells - metabolism ; Fluorodeoxyglucose F18 - metabolism ; Glucose - metabolism ; Glucose Transport Proteins, Facilitative - antagonists & inhibitors ; Glucose Transport Proteins, Facilitative - metabolism ; Kidney - cytology ; Kidney Tubules, Proximal - cytology ; Organic Anion Transporters - metabolism ; Organic Cation Transport Proteins - metabolism ; Radioisotopes ; Sodium-Glucose Transport Proteins - antagonists & inhibitors ; Sodium-Glucose Transport Proteins - metabolism ; Time Factors</subject><ispartof>Nuclear medicine communications, 2010-02, Vol.31 (2), p.141-146</ispartof><rights>2010 Lippincott Williams & Wilkins, Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4215-2bcfcca6f491cbd2583cfb507162eb3334d0e3d8d8ae1fa33789168779666e6f3</citedby><cites>FETCH-LOGICAL-c4215-2bcfcca6f491cbd2583cfb507162eb3334d0e3d8d8ae1fa33789168779666e6f3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,777,781,27905,27906</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19949354$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kobayashi, Masato</creatorcontrib><creatorcontrib>Shikano, Naoto</creatorcontrib><creatorcontrib>Nishii, Ryuichi</creatorcontrib><creatorcontrib>Kiyono, Yasushi</creatorcontrib><creatorcontrib>Araki, Hiroyo</creatorcontrib><creatorcontrib>Nishi, Kodai</creatorcontrib><creatorcontrib>Oh, Myungmi</creatorcontrib><creatorcontrib>Okudaira, Hiroyuki</creatorcontrib><creatorcontrib>Ogura, Masato</creatorcontrib><creatorcontrib>Yoshimoto, Mitsuyoshi</creatorcontrib><creatorcontrib>Okazawa, Hidehiko</creatorcontrib><creatorcontrib>Fujibayashi, Yasuhisa</creatorcontrib><creatorcontrib>Kawai, Keiichi</creatorcontrib><title>Comparison of the transcellular transport of FDG and D-glucose by the kidney epithelial cell line, LLC-PK1</title><title>Nuclear medicine communications</title><addtitle>Nucl Med Commun</addtitle><description>OBJECTIVESAlmost all D-glucose (GLU) filtered through the glomerulus is reabsorbed by the renal proximal tubules, whereas a high portion of 2-[F]fluoro-2-deoxy-D-glucose [(F)FDG] is excreted through the urine. However, [F]FDG is not entirely excreted in the urine suggesting that it may be partially reabsorbed by the proximal tubules. The purpose of this study was to compare the time course of transcellular transport of administered [C] labeled FDG ([C]FDG) with that of [C] labeled GLU ([C]GLU) using the kidney epithelial cell line, LLC-PK1.
METHODSTranscellular transport of [C]FDG and [C]GLU by LLC-PK1 cells was measured in Na-containing or Na-free Dulbeccoʼs phosphate-buffered saline [PBS(+) and PBS(−), respectively] in the presence or absence of phlorizin, phloretin, probenecid, or tetraethylammonium bromide inhibitors that predominantly inhibit sodium-dependent glucose transporters (SGLTs), sodium-independent glucose transporters, organic anion transporters, and organic cation transporters, respectively.
RESULTSWhen assayed in PBS(+), less [C]FDG than [C]GLU was reabsorbed by the proximal tubular cells over the entire incubation time. Reabsorption of [C]FDG was mediated mainly by SGLT at early time points in the incubation, whereas high reabsorption of [C]GLU was mediated by both SGLT and glucose transporter over 90 min of incubation. Secretion of [C]FDG also tended to be slightly higher than that of [C]GLU over 90 min of incubation.
CONCLUSIONTranscellular transport of [C]FDG over time by LLC-PK1 cells was clarified. The polarized distribution of transcellular transporters of [C]FDG and [C]GLU in LLC-PK1 cells differs.</description><subject>Biological Transport - drug effects</subject><subject>Cell Line</subject><subject>Epithelial Cells - drug effects</subject><subject>Epithelial Cells - metabolism</subject><subject>Fluorodeoxyglucose F18 - metabolism</subject><subject>Glucose - metabolism</subject><subject>Glucose Transport Proteins, Facilitative - antagonists & inhibitors</subject><subject>Glucose Transport Proteins, Facilitative - metabolism</subject><subject>Kidney - cytology</subject><subject>Kidney Tubules, Proximal - cytology</subject><subject>Organic Anion Transporters - metabolism</subject><subject>Organic Cation Transport Proteins - metabolism</subject><subject>Radioisotopes</subject><subject>Sodium-Glucose Transport Proteins - antagonists & inhibitors</subject><subject>Sodium-Glucose Transport Proteins - metabolism</subject><subject>Time Factors</subject><issn>0143-3636</issn><issn>1473-5628</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kEtPwzAQhC0EgvL4Bwj5xoWAnXUc54haXqIFDnCOHGdDA24c7ERV_z0prYTEgdNqtTOzmo-QU84uOcvSq9nT7JIVjANCrACgMFWyQ0ZcpBAlMla7ZMS4gAgkyANyGMIHY0yBTPfJAc8ykUEiRuRj7Bat9nVwDXUV7eZIO6-bYNDa3mq_2Vrnu_X5dnJHdVPSSfRue-MC0mL14_msywZXFNt62GytLV0HUFs3eEGn03H08siPyV6lbcCT7Twib7c3r-P7aPp89zC-nkZGxDyJ4qGIMVpWIuOmKONEgamKhKVcxlgMRUXJEEpVKo280gCpyrhUaZpJKVFWcETON7mtd189hi5f1D99dIOuD3kKIDOhYj4oxUZpvAvBY5W3vl5ov8o5y9eQ8wFy_hfyYDvbPuiLBZa_pi3VQaA2gqWzHfrwafsl-nyO2nbz_7O_AR86iy4</recordid><startdate>201002</startdate><enddate>201002</enddate><creator>Kobayashi, Masato</creator><creator>Shikano, Naoto</creator><creator>Nishii, Ryuichi</creator><creator>Kiyono, Yasushi</creator><creator>Araki, Hiroyo</creator><creator>Nishi, Kodai</creator><creator>Oh, Myungmi</creator><creator>Okudaira, Hiroyuki</creator><creator>Ogura, Masato</creator><creator>Yoshimoto, Mitsuyoshi</creator><creator>Okazawa, Hidehiko</creator><creator>Fujibayashi, Yasuhisa</creator><creator>Kawai, Keiichi</creator><general>Lippincott Williams & Wilkins, Inc</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>201002</creationdate><title>Comparison of the transcellular transport of FDG and D-glucose by the kidney epithelial cell line, LLC-PK1</title><author>Kobayashi, Masato ; Shikano, Naoto ; Nishii, Ryuichi ; Kiyono, Yasushi ; Araki, Hiroyo ; Nishi, Kodai ; Oh, Myungmi ; Okudaira, Hiroyuki ; Ogura, Masato ; Yoshimoto, Mitsuyoshi ; Okazawa, Hidehiko ; Fujibayashi, Yasuhisa ; Kawai, Keiichi</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4215-2bcfcca6f491cbd2583cfb507162eb3334d0e3d8d8ae1fa33789168779666e6f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>Biological Transport - drug effects</topic><topic>Cell Line</topic><topic>Epithelial Cells - drug effects</topic><topic>Epithelial Cells - metabolism</topic><topic>Fluorodeoxyglucose F18 - metabolism</topic><topic>Glucose - metabolism</topic><topic>Glucose Transport Proteins, Facilitative - antagonists & inhibitors</topic><topic>Glucose Transport Proteins, Facilitative - metabolism</topic><topic>Kidney - cytology</topic><topic>Kidney Tubules, Proximal - cytology</topic><topic>Organic Anion Transporters - metabolism</topic><topic>Organic Cation Transport Proteins - metabolism</topic><topic>Radioisotopes</topic><topic>Sodium-Glucose Transport Proteins - antagonists & inhibitors</topic><topic>Sodium-Glucose Transport Proteins - metabolism</topic><topic>Time Factors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kobayashi, Masato</creatorcontrib><creatorcontrib>Shikano, Naoto</creatorcontrib><creatorcontrib>Nishii, Ryuichi</creatorcontrib><creatorcontrib>Kiyono, Yasushi</creatorcontrib><creatorcontrib>Araki, Hiroyo</creatorcontrib><creatorcontrib>Nishi, Kodai</creatorcontrib><creatorcontrib>Oh, Myungmi</creatorcontrib><creatorcontrib>Okudaira, Hiroyuki</creatorcontrib><creatorcontrib>Ogura, Masato</creatorcontrib><creatorcontrib>Yoshimoto, Mitsuyoshi</creatorcontrib><creatorcontrib>Okazawa, Hidehiko</creatorcontrib><creatorcontrib>Fujibayashi, Yasuhisa</creatorcontrib><creatorcontrib>Kawai, Keiichi</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Nuclear medicine communications</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kobayashi, Masato</au><au>Shikano, Naoto</au><au>Nishii, Ryuichi</au><au>Kiyono, Yasushi</au><au>Araki, Hiroyo</au><au>Nishi, Kodai</au><au>Oh, Myungmi</au><au>Okudaira, Hiroyuki</au><au>Ogura, Masato</au><au>Yoshimoto, Mitsuyoshi</au><au>Okazawa, Hidehiko</au><au>Fujibayashi, Yasuhisa</au><au>Kawai, Keiichi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Comparison of the transcellular transport of FDG and D-glucose by the kidney epithelial cell line, LLC-PK1</atitle><jtitle>Nuclear medicine communications</jtitle><addtitle>Nucl Med Commun</addtitle><date>2010-02</date><risdate>2010</risdate><volume>31</volume><issue>2</issue><spage>141</spage><epage>146</epage><pages>141-146</pages><issn>0143-3636</issn><eissn>1473-5628</eissn><abstract>OBJECTIVESAlmost all D-glucose (GLU) filtered through the glomerulus is reabsorbed by the renal proximal tubules, whereas a high portion of 2-[F]fluoro-2-deoxy-D-glucose [(F)FDG] is excreted through the urine. However, [F]FDG is not entirely excreted in the urine suggesting that it may be partially reabsorbed by the proximal tubules. The purpose of this study was to compare the time course of transcellular transport of administered [C] labeled FDG ([C]FDG) with that of [C] labeled GLU ([C]GLU) using the kidney epithelial cell line, LLC-PK1.
METHODSTranscellular transport of [C]FDG and [C]GLU by LLC-PK1 cells was measured in Na-containing or Na-free Dulbeccoʼs phosphate-buffered saline [PBS(+) and PBS(−), respectively] in the presence or absence of phlorizin, phloretin, probenecid, or tetraethylammonium bromide inhibitors that predominantly inhibit sodium-dependent glucose transporters (SGLTs), sodium-independent glucose transporters, organic anion transporters, and organic cation transporters, respectively.
RESULTSWhen assayed in PBS(+), less [C]FDG than [C]GLU was reabsorbed by the proximal tubular cells over the entire incubation time. Reabsorption of [C]FDG was mediated mainly by SGLT at early time points in the incubation, whereas high reabsorption of [C]GLU was mediated by both SGLT and glucose transporter over 90 min of incubation. Secretion of [C]FDG also tended to be slightly higher than that of [C]GLU over 90 min of incubation.
CONCLUSIONTranscellular transport of [C]FDG over time by LLC-PK1 cells was clarified. The polarized distribution of transcellular transporters of [C]FDG and [C]GLU in LLC-PK1 cells differs.</abstract><cop>England</cop><pub>Lippincott Williams & Wilkins, Inc</pub><pmid>19949354</pmid><doi>10.1097/MNM.0b013e328333bcf5</doi><tpages>6</tpages></addata></record> |
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subjects | Biological Transport - drug effects Cell Line Epithelial Cells - drug effects Epithelial Cells - metabolism Fluorodeoxyglucose F18 - metabolism Glucose - metabolism Glucose Transport Proteins, Facilitative - antagonists & inhibitors Glucose Transport Proteins, Facilitative - metabolism Kidney - cytology Kidney Tubules, Proximal - cytology Organic Anion Transporters - metabolism Organic Cation Transport Proteins - metabolism Radioisotopes Sodium-Glucose Transport Proteins - antagonists & inhibitors Sodium-Glucose Transport Proteins - metabolism Time Factors |
title | Comparison of the transcellular transport of FDG and D-glucose by the kidney epithelial cell line, LLC-PK1 |
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