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1.
RSC Adv ; 14(26): 18777-18786, 2024 Jun 06.
Artigo em Inglês | MEDLINE | ID: mdl-38867735

RESUMO

This study focuses on the synthesis and characterization of Ho3+ doped Ca3(VO4)2 phosphor for potential application in solid-state lighting technology. A citrate-based sol-gel process is optimized to achieve sheet-like morphologies in the phosphor material. The investigation reveals UV absorption at 371 nm, indicating a band gap of 3.28 eV. Emission transitions at (506, 541, and 651) nm are observed when excited at 451 nm, with an optimal Ho3+ concentration of 0.05 mol resulting in robust green emission at 541 nm. The concentration quenching in Ca3(VO4)2:xHo3+ phosphors is discussed in detail with Blesse's and Dexter's models. The concentration quenching effect found in the studied samples is due to the dipole-dipole interactions. Judd-Ofelt intensity parameters were calculated from the excitation bands, and for Ω 2, Ω 4, and Ω 6 are (0.16, 0.17, and 0.36) × 10-20 cm2, respectively. The emission properties for the (5S2 + 5F4) → 5I8 and 5F5 → 5I8 transitions are also estimated with J-O parameters. The higher magnitude of branching ratios (83%) and emission cross-sections (1.6 × 10-21 cm2) suggest that the Ca3(VO4)2:0.05Ho3+ phosphor materials may be suitable for efficient green-emitting device applications. The CIE coordinates confirm the potential of Ho3+-doped phosphors for green emissions, making them suitable for solid-state lighting and display technology.

2.
RSC Adv ; 13(40): 27782-27791, 2023 Sep 18.
Artigo em Inglês | MEDLINE | ID: mdl-37731831

RESUMO

A series of SrZrO3:xHo3+ (x = 0.01, 0.03, 0.05, 0.07, 0.09, and 0.11 mol) perovskite phosphors have been synthesized by using the sol-gel technique. The structural and optical characteristics of the prepared phosphors have been investigated through powder XRD, FT-IR, UV-visible diffuse reflectance, and photoluminescence analysis. The photoluminescence emission spectra showed a bright characteristic peak at 545 nm (5F4 + 5S2 → 5I8) under the 454 nm excitation, which exhibits emission in the green region of the electromagnetic spectrum. The emission intensity of the phosphors starts decreasing slowly beyond 3 mol% Ho3+ ions concentration due to concentration quenching, which is attributed to the dipole-dipole interaction between Ho3+ ions. The site symmetry of the Ho3+ ions has been studied by estimating the relative Judd-Ofelt intensity parameters (Ωλ, where λ = 2, 4, 6) from the photoluminescence excitation spectrum of the SrZrO3:0.03Ho3+ phosphor. The obtained findings suggest that the synthesized phosphors will be favorable for their bright green emission and thus, can be widely used for different optoelectronic applications.

3.
RSC Adv ; 13(6): 3592-3601, 2023 Jan 24.
Artigo em Inglês | MEDLINE | ID: mdl-36756577

RESUMO

The Ho3+-doped YVO4 phosphors were successfully prepared via a sol-gel process in which citric acid was used as a chelating agent. X-ray diffraction (XRD) confirmed the effective inclusion of Ho3+ ions into the host matrix with the formation of single phase YVO4. The surface morphology was observed using SEM, the results of which showed a grain growth propensity and the agglomeration of prepared phosphors. The V-O (VO4 3-) vibration mode was analyzed through Fourier transform infrared (FTIR) spectra. The spectroscopic properties were reported through UV-vis-NIR diffuse reflectance and photoluminescence (PL) spectra. The Judd-Ofelt (J-O) intensity parameters Ω 2 = 0.03 × 10-20 cm2, Ω 4 = 0.22 × 10-20 cm2, and Ω 6 = 0.23 × 10-20 cm2 obtained for the Y0.97VO4:0.03Ho3+ phosphors were used to obtain the total transition probabilities (A T), radiative lifetimes (τ rad) and branching ratios (ß) for the certain transitions of Ho3+ ions. Under 310 nm UV excitation, the visible emission spectra were measured, and an intense emission was observed around 541 nm (green region) for all the samples. The emission cross-section σ P(λ) was 3.22 × 10-21 cm2 and the branching ratio (ß) was 0.816; these were investigated to capture the optimal concentration of the Y0.97VO4:0.03Ho3+ phosphor. The estimated color coordinates were observed in the green region of CIE diagram. Ultimately, the superior properties (σ P(λ), ß, and color purity) of Y0.97VO4:0.03Ho3+ phosphor may make it suitable for green emitting devices.

4.
J Dent Res ; 102(4): 412-421, 2023 04.
Artigo em Inglês | MEDLINE | ID: mdl-36515317

RESUMO

Xerostomia is a common side effect of radiation therapy (RT) in patients with head and neck cancer. However, limited information is available on the temporal dynamics of parenchymal and vascular changes in salivary glands following RT. To address this gap in knowledge, we conducted experimental studies in mice employing ultrasound (US) with coregistered photoacoustic imaging (PAI) to noninvasively assess the early and late changes in salivary gland size, structure, vascularity, and oxygenation dynamics following RT. Multiparametric US-PAI of salivary glands was performed in immune-deficient and immune-competent mice before and after RT along with correlative sialometry and ex vivo histologic-immunohistochemical validation. US revealed reduction in gland volume and an early increase in vascular resistance postradiation. This was accompanied by a reduction in glandular oxygen consumption on PAI. Imaging data correlated strongly with salivary secretion and histologic evidence of acinar damage. The magnitude and kinetics of radiation response were impacted by host immune status, with immunodeficient mice showing early and more pronounced vascular injury and DNA damage response compared to immunocompetent animals. Our findings demonstrate the ability of noninvasive US-PAI to monitor dynamic changes in salivary gland hemodynamics following radiation and highlight the impact of the host immune status on salivary gland radiation injury.


Assuntos
Neoplasias de Cabeça e Pescoço , Lesões por Radiação , Lesões do Sistema Vascular , Xerostomia , Animais , Camundongos , Glândulas Salivares/diagnóstico por imagem , Glândulas Salivares/efeitos da radiação , Xerostomia/diagnóstico por imagem , Xerostomia/etiologia , Glândula Parótida
5.
Med J Armed Forces India ; 78(2): 123-124, 2022 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-35463545
7.
Spectrochim Acta A Mol Biomol Spectrosc ; 217: 315-321, 2019 Jun 15.
Artigo em Inglês | MEDLINE | ID: mdl-30954718

RESUMO

Sm3+-doped vanadate-based phosphors, Ca3-x (VO4)2:Smx(x = 0.005 ≤ x ≤ 0.095), were synthesized by the citrate-based sol-gel method. The samples were characterized with XRD, SEM, diffuse reflectance and photoluminescence spectroscopy, aiming at the development of phosphor-converted wLED applications. Using diffuse reflectance spectra and the Kubelka-Munk function, the band gap energy was calculated to be 3.28 eV for the Ca2.95(VO4)2:Sm0.05 phosphor. Observation of the photoluminescence excitation spectra revealed a broadband excitation from the distorted VO4 tetrahedron and a few narrow peaks from the 4f-4f intra-configuration transitions of the Sm3+ ions. Upon 404 nm excitation, 4G5/2 → 6H5/2 (564 nm), 4G5/2 → 6H7/2 (601 nm), 4G5/2 → 6H9/2 (648 nm) and 4G5/2 → 6H11/2 (701 nm) transitions were observed. The optimum Sm3+ concentration for the studied phosphor is 0.05 mol, and the estimated critical distance between Sm3+ ions (Rc) is 19.1 Å. The observed quenching of Sm3+ emission is attributed to the dipole-dipole interactions. The possible cross-relaxation process between neighboring Sm3+ ions was discussed in detail. The CIE coordinates were calculated for all the samples, and they set on the orange region of CIE diagram. In addition, pure orange color emission was observed under 365 nm UV lamp. The results suggest that the Ca3(VO4)2:Sm3+ phosphor could be a good candidate for the orange emitting component for wLED applications.

8.
Indian J Clin Biochem ; 34(1): 60-67, 2019 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-30728674

RESUMO

We investigated the combined effect of fluoride exposure and Vitamin D deficiency in causing bone damage as a precursor to development of Fluorotoxic Metabolic Bone Disease. Thirty-six male Sprague-Dawley rats were divided into 6 groups of six; 3 groups received a Vitamin D deficient diet whereas the other 3 received a Vitamin D adequate diet. Serum total 25-hydroxyvitamin D (25OHD), calcium, phosphorus, creatinine, Alkaline phosphatase (ALP), albumin, Parathyroid hormone (PTH), Osteocalcin and C terminal telopeptide (CTx) were measured following exposure to varying levels of fluoride in drinking water (< 1.0, 15 and 50 ppm). Full body Dual-energy X-ray Absorptiometry (DXA) scans were used to examine changes in bone morphology pre and post exposure to fluoride. Renal tubular function was assessed using serum creatinine and urine Cystatin C. Histopathological examination of sections of bone and kidney tissues were also performed. Prior to fluoride exposure, DXA scans revealed a significant decrease in Bone Mineral Density (BMD) and Bone Mineral content (BMC) (p < 0.05) but a significant increase in fat mass (p < 0.05) and fat percentage (p < 0.01) among Vitamin D deficient rats, with no significant change in biochemical parameters. Following exposure to fluoride, BMD was significantly increased (p < 0.05) in both groups with a corresponding increase in serum ALP, bone fluoride content, Osteocalcin, CTx and urine fluoride with increasing levels of fluoride exposure. Serum creatinine calcium and phosphate and urinary cystatin C levels showed no significant changes. Light microscopy examination revealed mild thickening and increased osteoid in 80% of the Vitamin D deficient rats exposed to high levels of fluoride but renal tubular changes were found only in one experimental and one control animal. Fluoride deposited in rat bone affects both osteoblastic and osteoclastic activity. Also, these effects are accentuated in the presence of Vitamin D deficiency.

10.
J Dent Res ; 97(11): 1268-1276, 2018 10.
Artigo em Inglês | MEDLINE | ID: mdl-29750890

RESUMO

Despite the recognized link between aging and cancer, most preclinical studies in experimental tumor models are conducted with 6- to 8-wk-old rodents. The goal of the present study was to examine the impact of age on tumor incidence, growth, and microenvironmental characteristics in mouse models of head and neck squamous cell carcinoma (HNSCC). Experimental studies were conducted with the 4-nitroquinoline-oxide (4NQO) oral carcinogenesis model and orthotopic FaDu HNSCC xenografts, established in young (7 to 12 wk of age) and old (65 to 70 wk of age) female C57BL/6 mice ( n = 44; 4NQO model) and severe combined immunodeficient mice ( n = 13; HNSCC xenografts). Noninvasive whole body magnetic resonance imaging revealed increased subcutaneous and visceral fat in aging animals of both strains. On histologic examination, a higher incidence ( P < 0.001) of severe dysplasia/invasive squamous cell carcinoma was observed in old mice (92%) as compared with young mice (69%). Old C57BL/6 mice exposed to 4NQO exhibited increased incidence of oral and extraoral (peritoneal masses) neoplasms (42%) versus their young counterparts ( P < 0.05). The incidence of extraoral neoplasms was significantly lower (16%) in the younger cohort. Interestingly, no difference in growth rate and oxygen saturation was observed between orthotopic FaDu xenografts established in old and young severe combined immunodeficient mice. Our observations suggest that host age may have an impact on the growth kinetics and progression of HNSCC in the immunocompetent 4NQO model. Further investigation into the impact of aging on tumor response to preventive and therapeutic intervention is warranted.


Assuntos
Neoplasias Bucais/patologia , Microambiente Tumoral , 4-Nitroquinolina-1-Óxido , Fatores Etários , Animais , Carcinoma de Células Escamosas/patologia , Progressão da Doença , Feminino , Neoplasias de Cabeça e Pescoço/patologia , Camundongos , Camundongos Endogâmicos C57BL , Camundongos SCID , Transplante de Neoplasias , Neoplasias Experimentais/patologia
11.
Luminescence ; 32(3): 443-451, 2017 May.
Artigo em Inglês | MEDLINE | ID: mdl-27546167

RESUMO

Nd3+ -doped lead-free zinc phosphate glasses with the chemical compositions (60-x) NH4 H2 PO4  + 20ZnO + 10BaF2  + 10NaF + xNd2 O3 (where x = 0.5, 1.0, 1.5, 2.0 and 2.5 mol%) were prepared using a melt quenching technique. Vibrational bands were assigned and clearly elucidated by Raman spectral profiles for all the glass samples. Judd-Ofelt (J-O) intensity parameters (Ωλ : λ = 2, 4, 6) were obtained from the spectral intensities of different absorption bands of Nd3+ ions. Radiative properties such as radiative transition probabilities (AR ), radiative lifetimes (τR ) and branching ratios (ßR ) for different excited states were calculated using J-O parameters. The near infrared (NIR) photoluminescence spectra exhibited three emission bands (4 F3/2 level to 4 I13/2 , 4 I11/2 and 4 I9/2 states) for all the concentrations of Nd3+ ions. Various luminescence properties were studied by varying the Nd3+ concentration for the three spectral profiles. Fluorescence decay curves of the 4 F3/2 level were recorded. The energy transfer mechanism that leads to quenching of the 4 F3/2 state lifetimes was discussed at higher concentration of Nd3+ ions. These glasses are suggested as suitable hosts to produce efficient lasing action in NIR region at 1.05 µm.


Assuntos
Vidro/química , Luminescência , Neodímio/química , Fosfatos/química , Compostos de Zinco/química , Neodímio/análise , Fosfatos/análise , Processos Fotoquímicos , Espectrometria de Fluorescência , Compostos de Zinco/análise
12.
J Assoc Physicians India ; 64(11): 90-91, 2016 11.
Artigo em Inglês | MEDLINE | ID: mdl-27805347

RESUMO

We report herein a patient who developed diclofenac-induced acute rhabdomyolysis and hypovolemic shock. Timely recognition and management led to rapid recovery. Awareness of this potentially life-threatening side-effect is very important to encourage sparing and selective use of this drug in clinical practice.


Assuntos
Diclofenaco/efeitos adversos , Rabdomiólise/induzido quimicamente , Humanos , Masculino , Pessoa de Meia-Idade , Rabdomiólise/diagnóstico
13.
Mutat Res ; 775: 59-65, 2015 May.
Artigo em Inglês | MEDLINE | ID: mdl-25879710

RESUMO

This study investigates whether peripheral blood mononuclear cells (PBMCs) from inhabitants of Kerala in southwest India, exposed to chronic low dose natural radiation in vivo (>1 mSv year(-1)), respond with a radioadaptive response to a challenging dose of gamma radiation. Toward this goal, PBMCs isolated from 77 subjects from high-level natural radiation areas (HLNRA) and 37 subjects from a nearby normal level natural radiation area (NLNRA) were challenged with 2 Gy and 4 Gy gamma radiation. Subjects from HLNRA were classified based on the mean annual effective dose received, into low dose group (LDG) and high dose group (HDG) with mean annual effective doses of 2.69 mSv (N=43, range 1.07 mSv year(-1) to 5.55 mSv year(-1)) and 9.62 mSv (N = 34, range 6.07 mSv year(-1) to 17.41 mSv year(-1)), respectively. DNA strand breaks and repair kinetics (at 7 min, 15 min and 30 min after 4 Gy) were evaluated using the alkaline single cell gel electrophoresis (comet) assay. Initial levels of DNA strand breaks observed after either a 2 Gy or a 4 Gy challenging dose were significantly lower in subjects of the HDG from HLNRA compared to subjects of NLNRA (2 Gy, P = 0.01; 4 Gy, P = 0.02) and LDG (2 Gy P = 0.01; 4 Gy, P=0.05). Subjects of HDG from HLNRA showed enhanced rejoining of DNA strand breaks (HDG/NLNRA, P = 0.06) during the early stage of repair (within 7 min). However at later times a similar rate of rejoining of strand breaks was observed across the groups (HDG, LDG and NLNRA). Preliminary results from our study suggest in vivo chronic low-level natural radiation provides an initial exposure that allows an adaptation to a subsequent higher radiation exposure, perhaps through improving DNA repair via an unknown mechanism. Therefore, further investigations would be necessary in this population to understand the biological and health effects of chronic low-level natural radiation exposures.


Assuntos
Radiação de Fundo/efeitos adversos , Ensaio Cometa , Dano ao DNA , Leucócitos Mononucleares/metabolismo , Lesões por Radiação/sangue , Adulto , Relação Dose-Resposta à Radiação , Humanos , Índia , Leucócitos Mononucleares/patologia , Masculino , Pessoa de Meia-Idade , Lesões por Radiação/mortalidade
14.
Horm Metab Res ; 47(2): 133-7, 2015 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-24977658

RESUMO

Determining the mutational status of susceptibility genes including RET, VHL, SDHx (SDHB, SDHC, SDHD) among patients with pheochromocytoma/paraganglioma (PCC/PGL) is gaining importance. These genes have not been systematically characterized among patients with PCC/PGL from India. The aim of the work was to screen the most frequently mutated genes among patients with PCC/PGL to determine the frequency and spectrum of mutations seen in this region. Fifty patients with PCC/PGL treated at our tertiary care hospital between January 2010 and June 2012 were screened for mutations in susceptibility genes using an algorithmic approach. Thirty-two percent (16/50) of patients were found to be positive for mutations including mutations among RET (n=4), VHL (n=6), SDHB (n=3), and SDHD (n=3) genes. None of these patients were positive for SDHC mutations. A significant association was found between young patients with bilateral tumors and VHL mutations (p=0.002). Two of the 3 patients with extra-adrenal SDHB associated tumors, had unique mutations, viz., c.436delT (exon 5) and c.788_857del (exon 8), one of which was malignant. High frequency of mutations seen among patients in this study emphasizes the need to consider mutational analysis among Indian patients with PCC/PGL.


Assuntos
Neoplasias das Glândulas Suprarrenais/genética , Predisposição Genética para Doença , Mutação , Proteínas de Neoplasias/genética , Feocromocitoma/genética , Adolescente , Adulto , Idoso , Criança , Feminino , Humanos , Índia , Masculino , Pessoa de Meia-Idade , Centros de Atenção Terciária
15.
Indian J Endocrinol Metab ; 18(4): 516-20, 2014 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-25143909

RESUMO

BACKGROUND: Medullary thyroid carcinoma (MTC) is a tumor arising from the para follicular (C) cells of the thyroid gland and can occur either sporadically or as part of an inherited syndrome. A proportion of these cases carry an autosomal dominant mutation in the RET (REarranged during Transfection) proto-oncogene. Screening for these mutations in the affected patients and the carriers "at risk" which includes the first-degree relatives is of utmost importance for early detection and prompt treatment including prophylactic thyroidectomy in cases that harbor these mutations. RESULTS: This report presents details of screening and subsequent follow-up of a large Indian family, where the index case was found to carry p. Cys634Ser mutation involving exon 11 of the RET gene. These data are of value considering the paucity of information within the region in context of screening large families affected by these mutations.

16.
Trop Doct ; 44(1): 33-5, 2014 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-24275360

RESUMO

Hypokalaemic periodic paralysis (HPP) is a life-threatening condition. Our aim was to study the clinical profile and laboratory parameters of HPP patients and to develop an algorithm to determine the causes of HPP. 84 patients presented with HPP over a 3 year period. 58 (69.0%) were found to have renal tubular acidosis (RTA). The other causes were idiopathic HPP (8 (9.5%)), acute gastroenteritis (4 (4.8%)), suspected primary hyperaldosteronism and familial HPP (2 each (2.4%)) and suspected Gitelman/Bartter Syndrome and thyrotoxic periodic paralysis (1 each (1.2%)). The number of cases peaks in the hot season. Over a third of the patients (35.7%) had recurrent episodes. 80% had secondary HPP and therefore a biochemical evaluation is mandatory. A simple algorithm was developed. Both health professionals and patients need further education regarding this problem in order to improve diagnosis and treatment and to improve compliance.


Assuntos
Acidose Tubular Renal/complicações , Paralisia Periódica Hipopotassêmica/diagnóstico , Paralisia Periódica Hipopotassêmica/etiologia , Administração Intravenosa , Adulto , Distribuição por Idade , Algoritmos , Diagnóstico Diferencial , Feminino , Humanos , Paralisia Periódica Hipopotassêmica/sangue , Paralisia Periódica Hipopotassêmica/tratamento farmacológico , Índia , Sulfato de Magnésio/administração & dosagem , Masculino , Pessoa de Meia-Idade , Cloreto de Potássio/administração & dosagem , Fatores de Risco , População Rural , Estações do Ano , Fatores Socioeconômicos , Resultado do Tratamento
17.
Indian J Endocrinol Metab ; 17(Suppl 1): S240-2, 2013 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-24251172

RESUMO

INTRODUCTION: We report a case of acute adrenal insufficiency (AAI) in a patient with antiphospholipid syndrome (APS). CASE REPORT: A 44-year-old female patient presented to us with acute abdominal pain associated with recurrent vomiting and giddiness. On examination, her blood pressure was 80/50 mm Hg. Systemic examination was normal. Further evaluation revealed hypocortisolemia with elevated plasma adrenocorticotropin hormone indicative of primary adrenal insufficiency. Her abdominal computed tomography scan showed features of evolving bilateral adrenal infarction. Etiological work-up revealed prolonged activated thromboplastin time, which didn't correct with normal plasma, her anti-cardiolipin antibody and lupus anticoagulant were also positive. She was diagnosed to have APS with adrenal insufficiency and she was started on intravenous steroids and heparin infusion. CONCLUSION: AAI due to the APS can present with acute abdominal pain followed by hypotension. A high index of suspicion is needed to make the correct diagnosis and to initiate appropriate treatment.

18.
J Community Genet ; 4(1): 21-31, 2013 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-22875746

RESUMO

Monitoring newborns for adverse outcomes like stillbirth and major congenital anomalies (MCA) is being carried out in government hospitals since 1995 in and around high-level natural radiation areas, a narrow strip of land on the southwest coast of Kerala, India. Natural deposits of monazite sand containing thorium and its daughter products account for elevated levels of natural radiation. Among 141,540 newborns [140,558 deliveries: 139,589 singleton, 957 twins (6.81 ‰), 11 triplets (0.078 ‰), and one quadruplet] screened, 615 (4.35 ‰) were stillbirth and MCA were seen in 1,370 (9.68 ‰) newborns. Clubfoot (404, 2.85 ‰) was the most frequent MCA followed by hypospadias (152, 2.10 ‰ among male newborns), congenital heart disease (168, 1.19 ‰), cleft lip/palate (149, 1.05 ‰), Down syndrome (104, 0.73 ‰), and neural tube defects (72, 0.51 ‰). Newborns with MCA among stillbirths were about 20-fold higher at 190.24 ‰ (117/615) compared to 8.89 ‰ (1,253/140,925) among live births (P < .001). Logistic regression was carried out to compare stillbirth, overall, and specific MCA among newborns from areas with dose levels of ≤1.5, 1.51-3.0, 3.01-6.0 and >6 mGy/year after controlling for maternal age at birth, gravida, consanguinity, ethnicity, and gender of the baby. Clubfoot showed higher prevalence of 3.26 ‰ at dose level of 1.51-3.0 mGy/year compared to 2.33 ‰ at ≤1.5 mGy/year (OR = 1.39; 95 % CI, 1.12-1.72), without indication of any clear dose-response. Prevalences of stillbirth, overall MCA, and other specific MCA were similar across different dose levels and were relatively lower than that reported elsewhere in India, probably due to better literacy, health awareness, and practices in the study population.

19.
Int J Radiat Biol ; 89(4): 259-67, 2013 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-23134065

RESUMO

PURPOSE: To study, characterize and compare chromosome aberrations and karyotype anomalies among newborns from high (> 1.5 mGy/y) and normal (≤ 1.5 mGy/y) level natural radiation areas of monazite-sand bearing southwest coast of Kerala in India. MATERIALS AND METHODS: Cord blood samples from newborns were collected from selected Government hospitals in heparinized vials and cultures were set up employing standard microculture techniques, slides were prepared, coded and stained with giemsa. Well spread metaphases were analyzed for chromosome aberrations and karyotype anomalies. RESULTS: A total of 1,267,788 metaphases from 27,295 newborns of mothers aged 17-45 years (17,298 from high and 9,997 from normal level radiation areas) were analyzed during 1986-2007. Frequencies of dicentrics in high and normal level radiation areas were 1.90 ± 0.14 and 2.01 ± 0.26 per 10,000 cells, respectively (Relative frequency [RF] = 0.94; 95% CI: 0.71-1.26). Karyotype anomalies had a frequency of 5.49‰ and 6.7‰, respectively (RF = 0.82; 95% CI: 0.60-1.12). No dose-related trend was observed in chromosome aberrations or karyotype anomalies. CONCLUSION: Frequencies of chromosomal aberration and karyotype anomalies between the newborns from the high level natural radiation area (HLNRA) and normal level natural radiation areas (NLNRA) were very similar.


Assuntos
Radiação de Fundo/efeitos adversos , Análise Citogenética , Adolescente , Adulto , Aberrações Cromossômicas/efeitos da radiação , Relação Dose-Resposta à Radiação , Feminino , Sangue Fetal/metabolismo , Sangue Fetal/efeitos da radiação , Humanos , Índia , Recém-Nascido , Cariótipo , Masculino , Pessoa de Meia-Idade , Polimorfismo Genético/efeitos da radiação , Fatores de Tempo , Adulto Jovem
20.
Mutat Res ; 751(2): 91-5, 2013 Mar 18.
Artigo em Inglês | MEDLINE | ID: mdl-23253487

RESUMO

To study the effect of chronic low level radiation, 4040 meiosis were screened at eight microsatellite and five minisatellite (2485 and 1555 meiosis respectively) marker loci in people residing in high and normal level natural radiation areas of Kerala. Variants in the repeat length of allele were considered as mutants. Mutation rates (expressed as the number of mutations observed in the total number of meiosis) were 6.4×10(-3) (16/2485) and 2.6×10(-3) (4/1555) at microsatellite and minisatellite respectively. The germline microsatellite mutation frequency of father was 1.78 times higher at 7.52×10(-3) (8/1064) compared to 4.22×10(-3) (6/1421) of mother (P=0.292, Fisher's Exact two-sided test). The paternal and maternal mutation rates at minisatellite loci were more or less similar at 2.78×10(-3) (2/719) and 2.39×10(-3) (2/836), respectively (P=1.0, Fisher's Exact two-sided test). Higher but statistically non-significant microsatellite mutation frequency was observed in HLNRA compared to NLNRA (7.25×10(-3) vs 3.64×10(-3); P=0.547). The apparent increase in the mutation rate of microsatellite loci with the increase in radiation dose was also not statistically significant. All the four minisatellite mutation observed were from HLNRA (1198 meiosis) and no mutation was observed among 357 meiosis screened from NLNRA families. All the markers used in the present study were in the non-coding region and hence mutations in these regions may not cause adverse health effects, but the study is important in understanding the effect of chronic low level radiation.


Assuntos
Radiação de Fundo , Mutação em Linhagem Germinativa/efeitos da radiação , Relação Dose-Resposta à Radiação , Humanos , Índia , Repetições de Microssatélites , Repetições Minissatélites , Testes de Mutagenicidade/métodos , Taxa de Mutação , Grupos Populacionais/genética
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