Enhanced intestinal 2-deoxy-2-[18F]fluoro-D-glucose uptake under metformin is not fully suppressed by loperamide

Objective. This study investigated whether the metformin (Met)-induced enhanced intestinal uptake of 2-deoxy-2-[18F]fluoro-D-glucose (18F-FDG) is reduced by loperamide, a long-acting anti-diarrheal agent. Methods. Mean 18F-FDG uptake in the mouse small intestine and colon with Met exposure was compa...

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Autores principales: Nobashi Tomomi, Saga Tsuneo, Nakamoto Yuji, Shimizu Yoichi, Koyasu Sho, Ishimori Takayoshi, Watanabe Masao, Kimura Hiroyuki, Togashi Kaori
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Publicado: Sciendo 2018
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Acceso en línea:https://doaj.org/article/427e471973cc4c0a94fd8ba174835275
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spelling oai:doaj.org-article:427e471973cc4c0a94fd8ba1748352752021-12-02T19:07:36ZEnhanced intestinal 2-deoxy-2-[18F]fluoro-D-glucose uptake under metformin is not fully suppressed by loperamide1336-032910.2478/enr-2018-0023https://doaj.org/article/427e471973cc4c0a94fd8ba1748352752018-10-01T00:00:00Zhttps://doi.org/10.2478/enr-2018-0023https://doaj.org/toc/1336-0329Objective. This study investigated whether the metformin (Met)-induced enhanced intestinal uptake of 2-deoxy-2-[18F]fluoro-D-glucose (18F-FDG) is reduced by loperamide, a long-acting anti-diarrheal agent. Methods. Mean 18F-FDG uptake in the mouse small intestine and colon with Met exposure was compared with that in control mice. In the Met group, high-dose (1.0 mg/kg body weight) and low-dose (0.1 mg/kg body weight) loperamide were introduced, and 18F-FDG uptake in the small intestine and colon was compared with that of control mice administered high-dose loperamide. The percent injected dose of 18F-FDG per gram of tissue (%ID/g) in the extracted tissues was then determined. Results. 18F-FDG uptake increased significantly in the small intestine (0.64±0.06 vs. 1.01±0.15, p=0.040) and, especially, the colon (0.46±0.13 vs. 2.16±0.51, p<0.001) after Met exposure. Neither high-dose nor low-dose loperamide significantly reduced 18F-FDG uptake in the small intestine (0.82±0.31 vs. 0.84±0.22, p=0.93 and 0.78±0.25 vs. 0.70±0.15, p=0.13, respectively) or colon (2.13±0.41 vs. 1.67±0.55, p=0.063 and 1.77±0.39 vs. 1.80±0.25, p=0.56, respectively). The colonic %ID/g was significantly higher in Met groups irrespective of loperamide introduction than in control group, whereas the significant difference in the small intestine was observed only between Met and control groups. Conclusion. Metformin increased 18F-FDG uptake in intestines especially in colon. Loperamide administration partially, but not sufficiently, suppresses the Met-induced increased colonic uptake of 18F-FDG.Nobashi TomomiSaga TsuneoNakamoto YujiShimizu YoichiKoyasu ShoIshimori TakayoshiWatanabe MasaoKimura HiroyukiTogashi KaoriSciendoarticle18f-fdgpet/ctmetforminloperamideintestinephysiologicalDiseases of the endocrine glands. Clinical endocrinologyRC648-665ENEndocrine Regulations, Vol 52, Iss 4, Pp 185-191 (2018)
institution DOAJ
collection DOAJ
language EN
topic 18f-fdg
pet/ct
metformin
loperamide
intestine
physiological
Diseases of the endocrine glands. Clinical endocrinology
RC648-665
spellingShingle 18f-fdg
pet/ct
metformin
loperamide
intestine
physiological
Diseases of the endocrine glands. Clinical endocrinology
RC648-665
Nobashi Tomomi
Saga Tsuneo
Nakamoto Yuji
Shimizu Yoichi
Koyasu Sho
Ishimori Takayoshi
Watanabe Masao
Kimura Hiroyuki
Togashi Kaori
Enhanced intestinal 2-deoxy-2-[18F]fluoro-D-glucose uptake under metformin is not fully suppressed by loperamide
description Objective. This study investigated whether the metformin (Met)-induced enhanced intestinal uptake of 2-deoxy-2-[18F]fluoro-D-glucose (18F-FDG) is reduced by loperamide, a long-acting anti-diarrheal agent. Methods. Mean 18F-FDG uptake in the mouse small intestine and colon with Met exposure was compared with that in control mice. In the Met group, high-dose (1.0 mg/kg body weight) and low-dose (0.1 mg/kg body weight) loperamide were introduced, and 18F-FDG uptake in the small intestine and colon was compared with that of control mice administered high-dose loperamide. The percent injected dose of 18F-FDG per gram of tissue (%ID/g) in the extracted tissues was then determined. Results. 18F-FDG uptake increased significantly in the small intestine (0.64±0.06 vs. 1.01±0.15, p=0.040) and, especially, the colon (0.46±0.13 vs. 2.16±0.51, p<0.001) after Met exposure. Neither high-dose nor low-dose loperamide significantly reduced 18F-FDG uptake in the small intestine (0.82±0.31 vs. 0.84±0.22, p=0.93 and 0.78±0.25 vs. 0.70±0.15, p=0.13, respectively) or colon (2.13±0.41 vs. 1.67±0.55, p=0.063 and 1.77±0.39 vs. 1.80±0.25, p=0.56, respectively). The colonic %ID/g was significantly higher in Met groups irrespective of loperamide introduction than in control group, whereas the significant difference in the small intestine was observed only between Met and control groups. Conclusion. Metformin increased 18F-FDG uptake in intestines especially in colon. Loperamide administration partially, but not sufficiently, suppresses the Met-induced increased colonic uptake of 18F-FDG.
format article
author Nobashi Tomomi
Saga Tsuneo
Nakamoto Yuji
Shimizu Yoichi
Koyasu Sho
Ishimori Takayoshi
Watanabe Masao
Kimura Hiroyuki
Togashi Kaori
author_facet Nobashi Tomomi
Saga Tsuneo
Nakamoto Yuji
Shimizu Yoichi
Koyasu Sho
Ishimori Takayoshi
Watanabe Masao
Kimura Hiroyuki
Togashi Kaori
author_sort Nobashi Tomomi
title Enhanced intestinal 2-deoxy-2-[18F]fluoro-D-glucose uptake under metformin is not fully suppressed by loperamide
title_short Enhanced intestinal 2-deoxy-2-[18F]fluoro-D-glucose uptake under metformin is not fully suppressed by loperamide
title_full Enhanced intestinal 2-deoxy-2-[18F]fluoro-D-glucose uptake under metformin is not fully suppressed by loperamide
title_fullStr Enhanced intestinal 2-deoxy-2-[18F]fluoro-D-glucose uptake under metformin is not fully suppressed by loperamide
title_full_unstemmed Enhanced intestinal 2-deoxy-2-[18F]fluoro-D-glucose uptake under metformin is not fully suppressed by loperamide
title_sort enhanced intestinal 2-deoxy-2-[18f]fluoro-d-glucose uptake under metformin is not fully suppressed by loperamide
publisher Sciendo
publishDate 2018
url https://doaj.org/article/427e471973cc4c0a94fd8ba174835275
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