{"title":"评估 Omega-7 对小鼠骨髓细胞中甲氨蝶呤遗传毒性的保护作用","authors":"Zahraa Hasani, Ali F. Hassan","doi":"10.32007/jfacmedbagdad.2116","DOIUrl":null,"url":null,"abstract":"Background: A substance that can affect DNA or chromosomes is defined as a genotoxin. DNA damage in a somatic cell may result in a somatic mutation (cancer). In contrast, damage to a germ cell (germline mutation) may result in a heritable changed characteristic.Omega-7 is a non-essential monounsaturated free fatty acid with anti-inflammatory, anti-obesity, and antidiabetic effects.\nObjectives: Evaluation of the possible protective effects of omega seven against methotrexate genotoxicity.\nMethod: Two major equal groups were obtained from seventy mice, and five subgroups (each of seven) were created from these groups as follows: Group I received liquid paraffin orally for seven successive days. Group II: received liquid paraffin orally for seven successive days, followed by a single intraperitoneal dose of methotrexate (20 mg/kg) on the eighth day. Group III: received omega-7 (50mg/kg) orally for seven successive days, followed by a single intraperitoneal dose of methotrexate (20 mg/kg) on the eighth day. Group IV: received omega-7 (100mg/kg) orally for seven successive days, followed by a single intraperitoneal dose of methotrexate (20 mg/kg) on the eighth day. Group V: received omega-7 (100mg/kg) orally for seven successive days. The first major group was intraperitoneally injected with 1mg/kg colchicine, and then after two hours, all mice were killed by spinal dislocation. Bone marrow cells from the first major group were used to measure the mitotic index and chromosomal aberrations, and bone marrow cell of the second group was used to measure the appearance of the micronucleus. Statistical Package for Social Sciences (SPSS) and ANOVA test were used to compare groups.\nResults: Treatment of mice with omega-7 led to a significant decline in chromosomal aberration and micronucleus aberrance with a significant elevation of the mitotic index.\nConclusion: Omega-7 has been shown to have a protective role against methotrexate genotoxicity.\nReceived: April, 2023\nAccepted: July, 2023\nPublished: Jan.2024","PeriodicalId":516152,"journal":{"name":"Journal of the Faculty of Medicine Baghdad","volume":"121 21","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Evaluation of the protective effect of Omega-7 against Methotrexate Genotoxicity in bone marrow Cells of Mice\",\"authors\":\"Zahraa Hasani, Ali F. Hassan\",\"doi\":\"10.32007/jfacmedbagdad.2116\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Background: A substance that can affect DNA or chromosomes is defined as a genotoxin. DNA damage in a somatic cell may result in a somatic mutation (cancer). In contrast, damage to a germ cell (germline mutation) may result in a heritable changed characteristic.Omega-7 is a non-essential monounsaturated free fatty acid with anti-inflammatory, anti-obesity, and antidiabetic effects.\\nObjectives: Evaluation of the possible protective effects of omega seven against methotrexate genotoxicity.\\nMethod: Two major equal groups were obtained from seventy mice, and five subgroups (each of seven) were created from these groups as follows: Group I received liquid paraffin orally for seven successive days. Group II: received liquid paraffin orally for seven successive days, followed by a single intraperitoneal dose of methotrexate (20 mg/kg) on the eighth day. Group III: received omega-7 (50mg/kg) orally for seven successive days, followed by a single intraperitoneal dose of methotrexate (20 mg/kg) on the eighth day. Group IV: received omega-7 (100mg/kg) orally for seven successive days, followed by a single intraperitoneal dose of methotrexate (20 mg/kg) on the eighth day. Group V: received omega-7 (100mg/kg) orally for seven successive days. The first major group was intraperitoneally injected with 1mg/kg colchicine, and then after two hours, all mice were killed by spinal dislocation. Bone marrow cells from the first major group were used to measure the mitotic index and chromosomal aberrations, and bone marrow cell of the second group was used to measure the appearance of the micronucleus. Statistical Package for Social Sciences (SPSS) and ANOVA test were used to compare groups.\\nResults: Treatment of mice with omega-7 led to a significant decline in chromosomal aberration and micronucleus aberrance with a significant elevation of the mitotic index.\\nConclusion: Omega-7 has been shown to have a protective role against methotrexate genotoxicity.\\nReceived: April, 2023\\nAccepted: July, 2023\\nPublished: Jan.2024\",\"PeriodicalId\":516152,\"journal\":{\"name\":\"Journal of the Faculty of Medicine Baghdad\",\"volume\":\"121 21\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2024-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of the Faculty of Medicine Baghdad\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.32007/jfacmedbagdad.2116\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of the Faculty of Medicine Baghdad","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.32007/jfacmedbagdad.2116","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
摘要
背景:能影响 DNA 或染色体的物质被定义为基因毒性物质。体细胞的 DNA 受损可能导致体细胞突变(癌症)。与此相反,生殖细胞受损(生殖突变)可能会导致遗传性改变特征。欧米伽-7 是一种非必需的单不饱和游离脂肪酸,具有抗炎、抗肥胖和抗糖尿病作用:评估欧米伽 7 对甲氨蝶呤基因毒性的可能保护作用:方法:从七十只小鼠中分成两大组,每组七只小鼠,再从中分成以下五个亚组:第一组:连续七天口服液体石蜡。第二组:连续七天口服液体石蜡,第八天腹腔注射甲氨蝶呤(20 毫克/千克)。第三组:连续七天口服欧米伽-7(50 毫克/千克),第八天腹腔注射一次甲氨蝶呤(20 毫克/千克)。第四组:连续七天口服欧米伽-7(100 毫克/千克),第八天腹腔注射一次甲氨蝶呤(20 毫克/千克)。第五组:连续七天口服欧米伽-7(100 毫克/千克)。第一大组小鼠腹腔注射 1 毫克/千克秋水仙碱,两小时后,所有小鼠均被脊柱脱臼处死。第一大组的骨髓细胞用于测量有丝分裂指数和染色体畸变,第二大组的骨髓细胞用于测量微核的出现。采用社会科学统计软件包(SPSS)和方差分析对各组进行比较:结果:用欧米茄-7治疗小鼠后,染色体畸变和微核畸变显著下降,有丝分裂指数显著上升:结论:欧米茄-7对甲氨蝶呤的遗传毒性具有保护作用:接受:2023年4月接受:2023年7月发表:2024年1月2024年1月
Evaluation of the protective effect of Omega-7 against Methotrexate Genotoxicity in bone marrow Cells of Mice
Background: A substance that can affect DNA or chromosomes is defined as a genotoxin. DNA damage in a somatic cell may result in a somatic mutation (cancer). In contrast, damage to a germ cell (germline mutation) may result in a heritable changed characteristic.Omega-7 is a non-essential monounsaturated free fatty acid with anti-inflammatory, anti-obesity, and antidiabetic effects.
Objectives: Evaluation of the possible protective effects of omega seven against methotrexate genotoxicity.
Method: Two major equal groups were obtained from seventy mice, and five subgroups (each of seven) were created from these groups as follows: Group I received liquid paraffin orally for seven successive days. Group II: received liquid paraffin orally for seven successive days, followed by a single intraperitoneal dose of methotrexate (20 mg/kg) on the eighth day. Group III: received omega-7 (50mg/kg) orally for seven successive days, followed by a single intraperitoneal dose of methotrexate (20 mg/kg) on the eighth day. Group IV: received omega-7 (100mg/kg) orally for seven successive days, followed by a single intraperitoneal dose of methotrexate (20 mg/kg) on the eighth day. Group V: received omega-7 (100mg/kg) orally for seven successive days. The first major group was intraperitoneally injected with 1mg/kg colchicine, and then after two hours, all mice were killed by spinal dislocation. Bone marrow cells from the first major group were used to measure the mitotic index and chromosomal aberrations, and bone marrow cell of the second group was used to measure the appearance of the micronucleus. Statistical Package for Social Sciences (SPSS) and ANOVA test were used to compare groups.
Results: Treatment of mice with omega-7 led to a significant decline in chromosomal aberration and micronucleus aberrance with a significant elevation of the mitotic index.
Conclusion: Omega-7 has been shown to have a protective role against methotrexate genotoxicity.
Received: April, 2023
Accepted: July, 2023
Published: Jan.2024