Enhancement of Ultrasonically Induced Cell Damage by a Gallium‐Porphyrin Complex, ATX‐70
Enhancement of ultrasonically induced cell damage by a gallium‐porphyrin complex [ATX‐70, 2,4‐ bis(l‐decyloxyethyl)‐Ga(III)‐1,3,5,8‐tetramethylporphyrin‐6,7‐dipropionyl diaspartic acid] was investigated. The rate of damage to isolated sarcoma 180 cells in air‐saturated suspension induced by 2 MHz ul...
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Published in | Cancer science Vol. 84; no. 5; pp. 582 - 588 |
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Main Authors | , , |
Format | Journal Article |
Language | English |
Published |
Oxford, UK
Blackwell Publishing Ltd
01.05.1993
Japanese Cancer Association John Wiley & Sons, Inc |
Subjects | |
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Abstract | Enhancement of ultrasonically induced cell damage by a gallium‐porphyrin complex [ATX‐70, 2,4‐ bis(l‐decyloxyethyl)‐Ga(III)‐1,3,5,8‐tetramethylporphyrin‐6,7‐dipropionyl diaspartic acid] was investigated. The rate of damage to isolated sarcoma 180 cells in air‐saturated suspension induced by 2 MHz ultrasound irradiation was enhanced more than four times by 80 μM ATX‐70 in contrast to only twice by the same concentration of hematoporphyrin (Hp). The enhancement was almost completely inhibited in the presence of 10 mM histidine in the suspension, but not at all by 100 mM mannitol, which suggests that the enhanced cell damage was mostly mediated by singlet oxygen. Ultrasonically induced active oxygen generation in an air‐saturated aqueous solution of ATX‐70 was studied by detecting the electron spin resonance signals of 2,2,6,6,‐tetramethyl‐4‐piperidone‐N‐oxyl produced by the reaction of 2,2,6,6‐tetramethyl‐4‐piperidone with the generated active oxygen species. The rate of ultrasonically induced nitroxide generation was enhanced five times by 80 μM ATX‐70 in contrast to only twice by Hp. The enhancement was inhibited significantly in the presence of 10 mM histidine in the suspension, but not at all by 100 mM mannitol. The singlet oxygen generation in air‐saturated aqueous solution was further confirmed by the bleaching of N, N‐dimethyl‐4‐nitrosoaniline in the presence of imidazole. The ultrasonically induced bleaching rate was enhanced six times by ATX‐70, in contrast to only twice by Hp. |
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AbstractList | Enhancement of ultrasonically induced cell damage by a gallium‐porphyrin complex [ATX‐70, 2,4‐ bis(l‐decyloxyethyl)‐Ga(III)‐1,3,5,8‐tetramethylporphyrin‐6,7‐dipropionyl diaspartic acid] was investigated. The rate of damage to isolated sarcoma 180 cells in air‐saturated suspension induced by 2 MHz ultrasound irradiation was enhanced more than four times by 80
μM
ATX‐70 in contrast to only twice by the same concentration of hematoporphyrin (Hp). The enhancement was almost completely inhibited in the presence of 10
mM
histidine in the suspension, but not at all by 100
mM
mannitol, which suggests that the enhanced cell damage was mostly mediated by singlet oxygen. Ultrasonically induced active oxygen generation in an air‐saturated aqueous solution of ATX‐70 was studied by detecting the electron spin resonance signals of 2,2,6,6,‐tetramethyl‐4‐piperidone‐N‐oxyl produced by the reaction of 2,2,6,6‐tetramethyl‐4‐piperidone with the generated active oxygen species. The rate of ultrasonically induced nitroxide generation was enhanced five times by 80
μM
ATX‐70 in contrast to only twice by Hp. The enhancement was inhibited significantly in the presence of 10 m
M
histidine in the suspension, but not at all by 100 m
M
mannitol. The singlet oxygen generation in air‐saturated aqueous solution was further confirmed by the bleaching of N, N‐dimethyl‐4‐nitrosoaniline in the presence of imidazole. The ultrasonically induced bleaching rate was enhanced six times by ATX‐70, in contrast to only twice by Hp. Enhancement of ultrasonically induced cell damage by a gallium-porphyrin complex [ATX-70, 2,4-bis(1-decyloxyethyl)-Ga(III)-1,3,5,8- tetramethylporphryin-6,7-dipropionyl diaspartic acid] was investigated. The rate of damage to isolated sarcoma 180 cells in air-saturated suspension induced by 2 MHz ultrasound irradiation was enhanced more than four times by 80 microM ATX-70 in contrast to only twice by the same concentration of hematoporphyrin (Hp). The enhancement was almost completely inhibited in the presence of 10 mM histidine in the suspension, but not at all by 100 mM mannitol, which suggests that the enhanced cell damage was mostly mediated by singlet oxygen. Ultrasonically induced active oxygen generation in an air-saturated aqueous solution of ATX-70 was studied by detecting the electron spin resonance signals of 2,2,6,6,-tetramethyl-4-piperidone-N-oxyl produced by the reaction of 2,2,6,6-tetramethyl-4-piperidone with the generated active oxygen species. The rate of ultrasonically induced nitroxide generation was enhanced five times by 80 microM ATX-70 in contrast to only twice by Hp. The enhancement was inhibited significantly in the presence of 10 mM histidine in the suspension, but not at all by 100 mM mannitol. The singlet oxygen generation in air-saturated aqueous solution was further confirmed by the bleaching of N,N-dimethyl-4-nitrosoaniline in the presence of imidazole. The ultrasonically induced bleaching rate was enhanced six times by ATX-70, in contrast to only twice by Hp. Enhancement of ultrasonically induced cell damage by a gallium‐porphyrin complex [ATX‐70, 2,4‐ bis(l‐decyloxyethyl)‐Ga(III)‐1,3,5,8‐tetramethylporphyrin‐6,7‐dipropionyl diaspartic acid] was investigated. The rate of damage to isolated sarcoma 180 cells in air‐saturated suspension induced by 2 MHz ultrasound irradiation was enhanced more than four times by 80 μM ATX‐70 in contrast to only twice by the same concentration of hematoporphyrin (Hp). The enhancement was almost completely inhibited in the presence of 10 mM histidine in the suspension, but not at all by 100 mM mannitol, which suggests that the enhanced cell damage was mostly mediated by singlet oxygen. Ultrasonically induced active oxygen generation in an air‐saturated aqueous solution of ATX‐70 was studied by detecting the electron spin resonance signals of 2,2,6,6,‐tetramethyl‐4‐piperidone‐N‐oxyl produced by the reaction of 2,2,6,6‐tetramethyl‐4‐piperidone with the generated active oxygen species. The rate of ultrasonically induced nitroxide generation was enhanced five times by 80 μM ATX‐70 in contrast to only twice by Hp. The enhancement was inhibited significantly in the presence of 10 mM histidine in the suspension, but not at all by 100 mM mannitol. The singlet oxygen generation in air‐saturated aqueous solution was further confirmed by the bleaching of N, N‐dimethyl‐4‐nitrosoaniline in the presence of imidazole. The ultrasonically induced bleaching rate was enhanced six times by ATX‐70, in contrast to only twice by Hp. |
Author | Umemura, Shin‐ichiro Yumita, Nagahiko Nishigaki, Ryuichiro |
AuthorAffiliation | 1 Advanced Research Laboratory, Hitachi, Ltd., 2520 Akanuma, Hatoyama, Saitama 350‐03 2 School of Pharmaceutical Science, Toho University, 2‐2‐1 Miyama, Funabashi, Chiba 274 |
AuthorAffiliation_xml | – name: 2 School of Pharmaceutical Science, Toho University, 2‐2‐1 Miyama, Funabashi, Chiba 274 – name: 1 Advanced Research Laboratory, Hitachi, Ltd., 2520 Akanuma, Hatoyama, Saitama 350‐03 |
Author_xml | – sequence: 1 givenname: Shin‐ichiro surname: Umemura fullname: Umemura, Shin‐ichiro – sequence: 2 givenname: Nagahiko surname: Yumita fullname: Yumita, Nagahiko – sequence: 3 givenname: Ryuichiro surname: Nishigaki fullname: Nishigaki, Ryuichiro |
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Cites_doi | 10.2530/jslsm1980.10.3_225 10.1093/jnci/55.1.115 10.1378/chest.81.3.269 10.1111/j.1751-1097.1978.tb06972.x 10.1002/jcu.1870070410 10.1111/j.1349-7006.1989.tb02295.x 10.1111/j.1349-7006.1990.tb02565.x 10.3191/thermalmedicine.3.175 10.1111/j.1349-7006.1990.tb02674.x 10.1080/09553008814552351 |
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Keywords | Oxygen Sonochemistry Rodentia Malignant tumor Sarcoma 180 Biological activity Vertebrata Experimental disease Mammalia Treatment Mouse Porphyrin Animal Established cell line Singlet Gallium complex Ultrasound |
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References | 1988; 54 1987; 3 1978; 28 1982 1975; 55 1989; 10 1982; 81 1990 1989; 80 1990; 81 1979; 7 Yumita N. (e_1_2_1_11_2) Umemura S. (e_1_2_1_10_2) 1990 e_1_2_1_6_2 e_1_2_1_7_2 e_1_2_1_4_2 e_1_2_1_5_2 Lele P. P. (e_1_2_1_2_2) 1982 e_1_2_1_3_2 e_1_2_1_12_2 e_1_2_1_13_2 e_1_2_1_14_2 e_1_2_1_8_2 e_1_2_1_9_2 |
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SubjectTerms | Animals Antineoplastic Agents - pharmacology Aqueous solutions ATX‐70 Biological and medical sciences Bleaching Cell damage Electron spin resonance Gallium Histidine Histidine - pharmacology Imidazole Male Mannitol Mannitol - pharmacology Medical sciences Mice Mice, Inbred ICR Nitric Oxide - metabolism Nitroxide Other treatments Oxygen Oxygen - metabolism Porphyrins - pharmacology Radiation Sarcoma Sarcoma 180 - metabolism Sarcoma 180 - pathology Sarcoma 180 - therapy Singlet Oxygen Sonochemical activity Treatment. General aspects Tumor Cells, Cultured Tumors Ultrasonic Therapy Ultrasound |
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Title | Enhancement of Ultrasonically Induced Cell Damage by a Gallium‐Porphyrin Complex, ATX‐70 |
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