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جستجوی مقالات مرتبط با کلیدواژه « chromosome aberration » در نشریات گروه « پزشکی »

  • Prompt cytomolecular identification of chromosome aberration in irradiated blood cells
    Seyed Akbar Moosavi, Zahra Ghanbari, Ayoub Farhadi, Fariba Heshmati, Mohammad Mofid-Nakhaei
    Background
    understanding the genomic alteration induced by ionizing radiation still remains to be a methodological challenge in genetic field. The energy released from this type of radiation can potentially causes structural and numerical alterations in lymphocytes, which in turn converts them into abnormal tumor cells. Chromosomal abnormalities associated with specific type of hematological malignancies are determinant factors in evaluation of radiation dose and its potential in harming the body. None the less early detection of chromosomal aberration (CA) is crucial in prognosis and selection of therapy for the people exposed to irradiations. The aim of this study was to explore a swift and accurate genetic test that identifies CAs in radiologist exposed to X-rays. In addition synergistic effect of other clastogens in irradiated workers was also evaluated.
    Material and
    Methods
    thirty four heparinized blood samples were obtained from radiology workers exposed to X-rays. Blood samples were cultured in RPMI 1640 and F-10 Medias with and without PHA stimulation. Lymphocytes were harvested, separated and arrested at metaphase and their chromosomes were analyzed by solid and G-Banding techniques. Lymphocytic CA was also analyzed through whole chromosome painting FISH.
    Results
    of the 37 blood sample from workers, 60% had various structural aberrations in which both the frequency and type of CAs were intensified among tobacco smokers.
    Conclusion
    the results did not show any significant differences between the genders but other carcinogen like smoking can significantly increases the rate of CAs
    Keywords: Chromosome aberration, X-ray radiation, G-banding, Painting FISH}
  • Acharya Balkrishna, Hemanth Manikyam, Vinay Sharma, Niti Sharma
    Introduction
    The Picrorhiza kurroa rhizome has a long history of use in Indian Ayurvedic and Chinese system of medicine for the treatment of a wide spectrum of diseases. Today it is viewed as an important therapeutic target in both Western and Eastern medicinal systems. This work was aimed to study the clastogenic effect of Picrorhiza kurroa rhizome extract on cultured human peripheral blood lymphocytes.
    Methods
    Hydroalcoholic extract of rhizome was prepared and mammalian chromosomal aberration test was conducted using cultured human peripheral blood lymphocytes. The study was performed in two independent phases where the human peripheral blood lymphocytes were exposed to various of the extract in absence and presence of metabolic activation system for a continuous and short duration.
    Results
    Picrorhiza kurroa rhizome extract did not induce chromosome aberration up to 2500 μg/mL in final culture concentration in the presence (1% v/v) and absence of metabolic activation.
    Conclusion
    Picrorhiza kurroa rhizome extract is completely safe to be used as a medicine since it manifest its healing effects without causing genotoxicity.
    Keywords: Picrorhiza kurroa, Rhizome, Chromosome aberration, Human peripheral blood lymphocytes}
  • مصطفی نوری زاده تازه کند *، ممت تپاکتاش، ارکیده حاجی پور
    زمینه و هدف
    میرتازاپین یک داروی ضدافسردگی سروتونینی و نورواپینفرینی است که در درمان افسردگی شدید تجویز می شود. این مطالعه به منظور تعیین اثر ژنوتوکسیسیته و سیتوتوکسیسیته میرتازاپین با استفاده از روش های ناهنجاری های کروموزومی و شاخص میتوزی در لنفوسیت های خونی انجام شد.
    روش بررسی
    این مطالعه توصیفی تحلیلی روی لنفوسیت های خون 4 فرد (2 زن و 2 مرد) در محدوده سنی 26-23 سال با تیمارهای 24 و 48 ساعته در دوزهای 10، 25، 40 و 55 میکروگرم بر میلی لیتر به صورت in vitro و با روش Kocaman و Topaktas انجام گردید.
    یافته ها
    میرتازاپین موجب کاهش شاخص میتوزی در همه نمونه ها گردید؛ اما موجب افزایش معنی دار ناهنجاری های کروموزومی در تیمارهای 24 و 48 ساعته نگردید.
    نتیجه گیری
    میرتازاپین اثرات قابل توجه ژنوتوکسیک ندارد؛ ولی دارای ویژگی سیتوتوکسیک در لنفوسیت های خونی است.
    کلید واژگان: میرتازاپین, سیتوتوکسیسیتی, ژنوتوکسیسیتی, ناهنجاری کروموزومی, شاخص میتوزی, لنفوسیت}
    Norizadeh Tazehkand M. *, Topaktas M., Hajipour O
    Background And Objective
    Mirtazapine is a norepinephrine and serotonergic antidepressant that is used in the theraphy of major depressive disorders. This study was carried out to determine the genotoxic and cytotoxic effect of mirtazapine using chromosome aberration and mitotic index tests in human peripheral blood lymphocytes.
    Methods
    In this descriptive -analytic study genotoxic and cytotoxic effect of mirtazapine at 24 and 48 hours treatment periods on four concentration (10, 25, 40, and 55µg/ml) was performed on peripheral blood lymphocyte of four subjects.
    Results
    Mirtazapine significantly reduced the mitotic index in the all concentrations but it non-significantly increased the chromosome aberration at 24-hours and 48-hours treatment periods.
    Conclusion
    Mirtazapine has cytotoxic effect but it has no genotoxic effect on human lymphocyte.
    Keywords: Mirtazapine, Cytotoxicity, Genotoxicity, Chromosome Aberration, Mitotic index, Lymphocyte}
  • Vahid Changizi*, Mohammad Hossein Alizadeh, Akbar Mousavi
    Background
    CT scan and nuclear medicine exams deliver a great part of medical exposures. This study examined professional radiation hazards in CT scan and nuclear medicine workers.
    Methods
    In a cross sectional study 30 occupationally exposed workers and 7 controls (all from personnel of a laboratory) were selected. Physical dosimetry was performed for exposed workers. Blood samples were obtained from the experimental and control groups. Three culture mediums for each one were prepared in due to routine chromosome analysis using G-banding and solid stain.
    Results
    There were significant increased incidence of chromatid gap (ctg) and chromatid break (ctb) with mean±SD frequencies of 3±0.84 and 3.1±1.40 per 100 cells respectively in the nuclear medicine workers versus controls with mean±SD frequencies of 1.9±0.69 and 1.3±0.84 for ctg and ctb, respectively. Chromosome gaps (chrg) were higher significantly in the nuclear medicine population (2.47±0.91) than in controls (1.4±0.9) (p< 0.05). In CT scan group the ctg and ctb were increased with a mean±SD frequency of 2.7±0.79 and 2.6±0.91 per 100 cells respectively compared with control group. The mean±SD frequencies of the chrb were 2.0±0.75 and 0.86±0.690 per 100 cells for exposed workers and control group, respectively.
    Conclusion
    This study showed chromosome aberrations in peripheral lymphocytes using solid stain method are reasonable biomarker reflecting personnel radiation damage.
    Keywords: CT scan, Nuclear physics, Chromosome aberration, G, banding, Solid stain}
نکته
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