1993•The Korean Journal of Nuclear MedicineRequires access

Genotoxicity of Therapeutic Dose of $^{131}I$ Analyzed by Micronuclei Test in the Mouse Bone Marrow

Hee‐Seung Bom, Ji-Yeul Kim

Open publisher page 1 citations

Abstract

Background Radioiodine (), a major component of nuclear fallout and a valuable therapeutic agent for thyrotoxicosis and thyroid cancer, has been regarded as a mutagen or a carcinogen without any convincing evidence. To evaluate the genotoxicity of radioiodine () we performed a micronuclei test in mice bone marrow. Materials and methods : Mice (ICR strain, ) were divided to 4 groups: control, group 1 (0.17 mCi/kg, usual therapeutic dose for thyrotoxicosis), group 2 (1.67 mCi/kg, usual therapeutic dose for thyroid cancer), and group 3 (16.67 mCi/kg, usual accumulated dose causing bone marrow suppression). was administered intraperitoneally. Ten mice of each group were sacrificed at days 1 and 3. Bone marrow were smeared and stained with May-Grunwald Giemsa method. One thou-sand polychromatic erythrocytes (PCE) and normochromatic erythrocytes (NCE) were counted under the light microscope, and the number of micronucleated PCEs were recorded. Results : The frequency of micronuclei in PCE (and NCE in parenthesis) in the control group was ()% in day 1 and ()% in day 3. Those in group 1 was ()% in day 1 and ()% in day 3. Micronuclei was noted in ()% in day 1 and ()% in day 3 in group 2, and in ()% in day 1 and ()% in day 3 in group 3. There was no difference in the frequency of micronuclei between each groups (p> 0.05). Conclusion : Radioiodine () did not cause any genotoxicity in mice bone marrow even at the large dose (16.67 mCi/kg).

About this research paper

What this paper is about

Background Radioiodine (), a major component of nuclear fallout and a valuable therapeutic agent for thyrotoxicosis and thyroid cancer, has been regarded as a mutagen or a carcinogen without any convincing evidence. To evaluate the genotoxicity of radioiodine () we performed a micronuclei test in mice bone marrow. Materials and methods : Mice (ICR strain, ) were divided to 4 groups: control, group 1 (0.17 mCi/kg, usual therapeutic dose for thyrotoxicosis), group 2 (1.67 mCi/kg, usual therapeutic dose for thyroid cancer), and group 3 (16.67 mCi/kg, usual accumulated dose causing bone marrow suppression). was administered intraperitoneally. Ten mice of each group were sacrificed at days 1 and 3. Bone marrow were smeared and stained with May-Grunwald Giemsa method. One thou-sand polychromatic erythrocytes (PCE) and normochromatic erythrocytes (NCE) were counted under the light microscope, and the number of micronucleated PCEs were recorded. Results : The frequency of micronuclei in PCE (and NCE in parenthesis) in the control group was ()% in day 1 and ()% in day 3. Those in group 1 was ()% in day 1 and ()% in day 3. Micronuclei was noted in ()% in day 1 and ()% in day 3 in group 2, and in ()% in day 1 and ()% in day 3 in group 3. There was no difference in the frequency of micronuclei between each groups (p> 0.05). Conclusion : Radioiodine () did not cause any genotoxicity in mice bone marrow even at the large dose (16.67 mCi/kg).

Why it matters

OpenAlex reports 1 citations for this work. Citation counts describe recorded attention and do not establish research quality.

Key contribution

A contribution statement is not available in the OpenAlex record.

Method / approach

Method details are not available in the OpenAlex metadata.

Main findings

Findings are not separately available in the OpenAlex metadata.

Limitations

Limitations are not available in the OpenAlex metadata.

Applications

Application details are not available in the OpenAlex metadata.

Available abstract

Background Radioiodine (), a major component of nuclear fallout and a valuable therapeutic agent for thyrotoxicosis and thyroid cancer, has been regarded as a mutagen or a carcinogen without any convincing evidence. To evaluate the genotoxicity of radioiodine () we performed a micronuclei test in mice bone marrow. Materials and methods : Mice (ICR strain, ) were divided to 4 groups: control, group 1 (0.17 mCi/kg, usual therapeutic dose for thyrotoxicosis), group 2 (1.67 mCi/kg, usual therapeutic dose for thyroid cancer), and group 3 (16.67 mCi/kg, usual accumulated dose causing bone marrow suppression). was administered intraperitoneally. Ten mice of each group were sacrificed at days 1 and 3. Bone marrow were smeared and stained with May-Grunwald Giemsa method. One thou-sand polychromatic erythrocytes (PCE) and normochromatic erythrocytes (NCE) were counted under the light microscope, and the number of micronucleated PCEs were recorded. Results : The frequency of micronuclei in PCE (and NCE in parenthesis) in the control group was ()% in day 1 and ()% in day 3. Those in group 1 was ()% in day 1 and ()% in day 3. Micronuclei was noted in ()% in day 1 and ()% in day 3 in group 2, and in ()% in day 1 and ()% in day 3 in group 3. There was no difference in the frequency of micronuclei between each groups (p> 0.05). Conclusion : Radioiodine () did not cause any genotoxicity in mice bone marrow even at the large dose (16.67 mCi/kg).

Key concepts: Micronucleus test, Bone marrow, Genotoxicity, Micronucleus, Medicine, Carcinogen, Internal medicine, Toxicology

Related papers

Back to paper searchBrowse research topicsOriginal source
Genotoxicity of Therapeutic Dose of $^{131}I$ Analyzed by Micronuclei Test in the Mouse Bone Marrow — Research Paper | ScholarLens