The uptake mechanism of indocyanine green byrat isolated hepatocytes

Osamu Kamma, Kuniaki Saito, Yoichi Nagamura, Naomichi Ogitsu, Itaru Teshima, Isao Ishiguro, Madoka Ito

研究成果: Article

抄録

The uptake mechanisms of indocyanine green (ICG) were studied with rat native hepatocytes and denatured ones which were treated at 56°C for 10 minutes. The addition of several receptor blockers except aggregated IgG to the reaction system was not able to impair the uptake. Although metabolic inhibitors had no affect on the uptake, it was drastically reduced at low temperature. The denatured hepatocytes also eliminated ICG from reaction system rapidly rather than the native cells and it was inhibited at low temperature. The kinetic analysis of the ICG uptake by double reciprocal plots of Lineweaver-Burk showed the 4.76 nmol/min/106 cells of Vmax value and 0.15 mM of Km value for native hepatocytes but the line of denatured cells crossed at the origin, i. e., no Vmax and Km value was given as thesimple chemical binding of ICG. Subcellular fractionation of both the native and denatured hepatocytes after incubation with ICG indicated that ICG was distributed from membrane to lysosomal fraction in native cells but the most ICG was found in the membrane fraction in the case of denatured cells. Thus the uptake by denatured hepatocytes was not true one but the binding of ICG to the cell.

元の言語English
ページ(範囲)41-47
ページ数7
ジャーナルJapanese Journal of Clinical Chemistry
14
発行部数1
DOI
出版物ステータスPublished - 01-01-1985
外部発表Yes

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Indocyanine Green
Hepatocytes
Membranes
Temperature
Fractionation
Rats
Immunoglobulin G
Kinetics

All Science Journal Classification (ASJC) codes

  • Clinical Biochemistry

これを引用

Kamma, Osamu ; Saito, Kuniaki ; Nagamura, Yoichi ; Ogitsu, Naomichi ; Teshima, Itaru ; Ishiguro, Isao ; Ito, Madoka. / The uptake mechanism of indocyanine green byrat isolated hepatocytes. :: Japanese Journal of Clinical Chemistry. 1985 ; 巻 14, 番号 1. pp. 41-47.
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abstract = "The uptake mechanisms of indocyanine green (ICG) were studied with rat native hepatocytes and denatured ones which were treated at 56°C for 10 minutes. The addition of several receptor blockers except aggregated IgG to the reaction system was not able to impair the uptake. Although metabolic inhibitors had no affect on the uptake, it was drastically reduced at low temperature. The denatured hepatocytes also eliminated ICG from reaction system rapidly rather than the native cells and it was inhibited at low temperature. The kinetic analysis of the ICG uptake by double reciprocal plots of Lineweaver-Burk showed the 4.76 nmol/min/106 cells of Vmax value and 0.15 mM of Km value for native hepatocytes but the line of denatured cells crossed at the origin, i. e., no Vmax and Km value was given as thesimple chemical binding of ICG. Subcellular fractionation of both the native and denatured hepatocytes after incubation with ICG indicated that ICG was distributed from membrane to lysosomal fraction in native cells but the most ICG was found in the membrane fraction in the case of denatured cells. Thus the uptake by denatured hepatocytes was not true one but the binding of ICG to the cell.",
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Kamma, O, Saito, K, Nagamura, Y, Ogitsu, N, Teshima, I, Ishiguro, I & Ito, M 1985, 'The uptake mechanism of indocyanine green byrat isolated hepatocytes', Japanese Journal of Clinical Chemistry, 巻. 14, 番号 1, pp. 41-47. https://doi.org/10.14921/jscc1971b.14.1_41

The uptake mechanism of indocyanine green byrat isolated hepatocytes. / Kamma, Osamu; Saito, Kuniaki; Nagamura, Yoichi; Ogitsu, Naomichi; Teshima, Itaru; Ishiguro, Isao; Ito, Madoka.

:: Japanese Journal of Clinical Chemistry, 巻 14, 番号 1, 01.01.1985, p. 41-47.

研究成果: Article

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AU - Ishiguro, Isao

AU - Ito, Madoka

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N2 - The uptake mechanisms of indocyanine green (ICG) were studied with rat native hepatocytes and denatured ones which were treated at 56°C for 10 minutes. The addition of several receptor blockers except aggregated IgG to the reaction system was not able to impair the uptake. Although metabolic inhibitors had no affect on the uptake, it was drastically reduced at low temperature. The denatured hepatocytes also eliminated ICG from reaction system rapidly rather than the native cells and it was inhibited at low temperature. The kinetic analysis of the ICG uptake by double reciprocal plots of Lineweaver-Burk showed the 4.76 nmol/min/106 cells of Vmax value and 0.15 mM of Km value for native hepatocytes but the line of denatured cells crossed at the origin, i. e., no Vmax and Km value was given as thesimple chemical binding of ICG. Subcellular fractionation of both the native and denatured hepatocytes after incubation with ICG indicated that ICG was distributed from membrane to lysosomal fraction in native cells but the most ICG was found in the membrane fraction in the case of denatured cells. Thus the uptake by denatured hepatocytes was not true one but the binding of ICG to the cell.

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