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1.
Phys Rev Lett ; 124(10): 102501, 2020 Mar 13.
Artículo en Inglés | MEDLINE | ID: mdl-32216444

RESUMEN

Interaction cross sections for ^{42-51}Ca on a carbon target at 280 MeV/nucleon have been measured for the first time. The neutron number dependence of derived root-mean-square matter radii shows a significant increase beyond the neutron magic number N=28. Furthermore, this enhancement of matter radii is much larger than that of the previously measured charge radii, indicating a novel growth in neutron skin thickness. A simple examination based on the Fermi-type distribution, and mean field calculations point out that this anomalous enhancement of the nuclear size beyond N=28 results from an enlargement of the core by a sudden increase in the surface diffuseness of the neutron density distribution, which implies the swelling of the bare ^{48}Ca core in Ca isotopes beyond N=28.

3.
Int J Hematol ; 73(3): 383-5, 2001 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-11345207

RESUMEN

We report a case of concomitant mantle cell lymphoma (MCL) and multiple myeloma (MM) in which we investigated the possibility of a clonal relationship. A 76-year-old man was diagnosed with MCL [immunoglobulin (Ig)M,D-kappa; stage IVB] and MM (IgG-kappa; stage I). Ig heavy chain (IgH) gene complementarity-determining region 3 in DNA from both the MCL tumor and from single MM cells from bone marrow smears was amplified to investigate whether there was a clonal relationship between MCL and MM. Sequence analysis revealed no clonal relationship between MCL and MM in our patient.


Asunto(s)
Neoplasias del Íleon/patología , Válvula Ileocecal/patología , Linfoma de Células del Manto/patología , Mieloma Múltiple/patología , Neoplasias Primarias Múltiples/patología , Células Madre Neoplásicas/patología , Reacción en Cadena de la Polimerasa/métodos , Anciano , Médula Ósea/patología , Cromosomas Humanos Par 11/genética , Cromosomas Humanos Par 11/ultraestructura , Cromosomas Humanos Par 14/genética , Cromosomas Humanos Par 14/ultraestructura , Células Clonales/química , Células Clonales/patología , ADN de Neoplasias/análisis , Genes de Inmunoglobulinas , Humanos , Neoplasias del Íleon/genética , Inmunoglobulina G/genética , Cadenas Pesadas de Inmunoglobulina/genética , Cadenas kappa de Inmunoglobulina/genética , Linfoma de Células del Manto/genética , Masculino , Mieloma Múltiple/genética , Proteínas de Mieloma/genética , Proteínas de Neoplasias/genética , Neoplasias Primarias Múltiples/genética , Células Madre Neoplásicas/química , Translocación Genética
4.
Cancer Genet Cytogenet ; 126(1): 8-12, 2001 Apr 01.
Artículo en Inglés | MEDLINE | ID: mdl-11343772

RESUMEN

We describe very uncommon phenotypic and cytogenetic findings in a 40-year-old female with blast phase of Philadelphia chromosome (Ph)-positive CML. In addition to the t(9;22)(q34;q11) that was detected in all metaphases, a t(11;17)(q23;q21) was identified in 15 of 20 metaphases. Reverse transcription-polymerase chain reaction showed the major and minor bcr/abl fusion transcripts in the cells from a bone marrow (BM) sample. Fluorescence in situ hybridization (FISH) analysis also showed that fusion signals of the bcr and abl probes were found in 95% of blastic cells and in 64% of neutrophils. MLL gene rearrangement was also detected in some blastic cells but not in neutrophils by FISH analysis. Phenotypically, blastic cells expressed mixed lineage antigens such as CD34, CD33, CD13, CD19, CD7, and CD41. Immunogenotypically, some population of BM cells showed monoclonal rearrangements of immunoglobulin heavy chain and T-cell receptor gamma chain genes by Southern blot analysis. Clinical course was aggressive, and therapy was poorly tolerated. Such findings seem to support an association between Ph and an abnormality of 11q23 with poor prognosis, and suggest that the expression of both abnormal genes may be related to this mixed lineage antigen-expressing leukemia.


Asunto(s)
Antígenos/inmunología , Cromosomas Humanos Par 11 , Cromosomas Humanos Par 17 , Leucemia Mielógena Crónica BCR-ABL Positiva/genética , Proto-Oncogenes , Factores de Transcripción , Translocación Genética , Adulto , Protocolos de Quimioterapia Combinada Antineoplásica/uso terapéutico , Southern Blotting , Trasplante de Médula Ósea , Terapia Combinada , Proteínas de Unión al ADN/genética , Femenino , Proteínas de Fusión bcr-abl/genética , Genotipo , N-Metiltransferasa de Histona-Lisina , Humanos , Inmunofenotipificación , Hibridación Fluorescente in Situ , Cariotipificación , Leucemia Mielógena Crónica BCR-ABL Positiva/inmunología , Leucemia Mielógena Crónica BCR-ABL Positiva/terapia , Proteína de la Leucemia Mieloide-Linfoide , Reacción en Cadena de la Polimerasa de Transcriptasa Inversa
6.
Am J Pathol ; 158(1): 131-45, 2001 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-11141486

RESUMEN

To examine the role of granulocyte/macrophage colony-stimulating factor (GM-CSF) in inflammatory granuloma formation, we injected GM-CSF-deficient (GM-CSF(-/-)) mice and wild-type (GM-CSF(+/+)) mice intravenously with 2 mg of zymocel, and mice were killed at various intervals for examination. In GM-CSF(-/-) mice, we demonstrated a marked delay of zymocel-induced hepatic granuloma formation until 5 days after zymocel injection with a rapid reduction in numbers of granulomas at 10 days until their disappearance. In the early phase of granuloma formation, monocyte infiltration and differentiation of monocytes into macrophages were impaired in GM-CSF(-/-) mice compared with GM-CSF(+/+) mice. The percentages of [(3)H]thymidine-labeled macrophages at 2 days after zymocel injection were lower in the GM-CSF(-/-) mice than in the GM-CSF(+/+) mice. The DNA nick-end-labeling method demonstrated increased numbers of apoptotic cells in and around hepatic granulomas of GM-CSF(-/-) mice from 8 days after zymocel injection, and electron microscopy detected apoptotic bodies. Granuloma macrophage digestion of glucan particles and activation of macrophages were similar in the two types of mice. In situ hybridization demonstrated expression of GM-CSF mRNA in the endothelial cells, hepatocytes, and some granuloma cells in the GM-CSF(+/+) mice but not in the GM-CSF(-/-) mice. These results provide evidence that GM-CSF is important for the influx of monocytes into hepatic granulomas, for differentiation of monocytes into macrophages, and for proliferation and survival of macrophages within hepatic granulomas.


Asunto(s)
Enfermedad Hepática Inducida por Sustancias y Drogas , Glucanos/efectos adversos , Factor Estimulante de Colonias de Granulocitos y Macrófagos/fisiología , Granuloma/inducido químicamente , Animales , Muerte Celular/efectos de los fármacos , División Celular/efectos de los fármacos , Femenino , Regulación de la Expresión Génica/efectos de los fármacos , Genotipo , Glucanos/administración & dosificación , Factor Estimulante de Colonias de Granulocitos y Macrófagos/deficiencia , Factor Estimulante de Colonias de Granulocitos y Macrófagos/genética , Granuloma/genética , Inyecciones Intravenosas , Recuento de Leucocitos , Hígado/efectos de los fármacos , Hígado/metabolismo , Hígado/patología , Hepatopatías/genética , Recuento de Linfocitos , Activación de Macrófagos , Macrófagos/citología , Macrófagos/fisiología , Macrófagos/ultraestructura , Masculino , Ratones , Ratones Endogámicos C57BL , Ratones Mutantes , Microscopía Electrónica , Monocitos/citología , Monocitos/efectos de los fármacos , Mutación , Fagocitosis/efectos de los fármacos , Fagocitosis/genética , ARN Mensajero/efectos de los fármacos , ARN Mensajero/genética , ARN Mensajero/metabolismo , Factores de Tiempo
8.
Arch Dis Child ; 83(2): 172-3, 2000 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-10906031

RESUMEN

An 8 year old girl was admitted to hospital with the typical clinical features of Guillain-Barré syndrome (GBS) after recovering from varicella. Onset of the disease was just two weeks after the onset of varicella in her young sister. Examination of cerebrospinal fluid and nerve conduction studies showed typical findings of GBS. Although serum from both the patient and sister were analysed for autoantibodies to gangliosides and myelin P0 protein, IgM anti-GM1 antibody and anti-GD1b antibody were only detected in the patient. HLA DR haplotypes were quite different between the two subjects. This suggests that these autoantibodies may play an important role in the pathogenesis of GBS after varicella zoster virus infection.


Asunto(s)
Autoanticuerpos/inmunología , Varicela/inmunología , Gangliósidos/inmunología , Síndrome de Guillain-Barré/inmunología , Varicela/complicaciones , Niño , Femenino , Antígenos HLA-DR/inmunología , Humanos , Inmunoglobulina M/inmunología , Proteína P0 de la Mielina/inmunología
9.
Food Chem Toxicol ; 37(8): 869-79, 1999 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-10506011

RESUMEN

Phenobarbital sodium (PB) was administered at dietary levels of 0 (control), 8, 30, 125 and 500 ppm to groups of 20 male F344/DuCrj rats for 104 weeks. There were no treatment-related clinical signs or adverse effects on survival rate, body weights, food consumption, and haematology or blood biochemistry data. Statistically significant increases of relative liver weights were found in the 500 and 125 ppm, but not the 30 and 8 ppm groups. Quantitative analysis of glutathione S-transferase placental form positive (GST-P+) hepatocyte foci/areas revealed clear increases limited to the 500 and 125 ppm groups. Western blotting revealed CYP2B1, 2C6 and 3A2 proteins to be also increased only with these high doses. In addition, significant increase of regenerative hepatocellular hyperplasias was noted in the 500 ppm group. No hepatocellular adenomas were observed, but a hepatocellular carcinoma arose in single rats of the 8 ppm and 125 ppm groups. No treatment-related changes were found in any other organs or tissues. Thus, under the experimental conditions used, the highest dose of PB (500 ppm) was not carcinogenic in male F344 rats. Furthermore, increase in putative preneoplastic proliferative hepatocytic lesions was only noted with 500 and 125 ppm.


Asunto(s)
Carcinógenos/toxicidad , Hígado/efectos de los fármacos , Fenobarbital/toxicidad , Lesiones Precancerosas/inducido químicamente , Administración Oral , Animales , Peso Corporal , Carcinógenos/administración & dosificación , Carcinoma Hepatocelular/inducido químicamente , Dieta , Relación Dosis-Respuesta a Droga , Ingestión de Alimentos , Enzimas/sangre , Gutatión-S-Transferasa pi , Glutatión Transferasa/análisis , Pruebas Hematológicas , Hiperplasia , Inmunohistoquímica , Isoenzimas/análisis , Hígado/enzimología , Hígado/patología , Neoplasias Hepáticas/inducido químicamente , Masculino , Tamaño de los Órganos/efectos de los fármacos , Fenobarbital/administración & dosificación , Lesiones Precancerosas/sangre , Ratas , Ratas Endogámicas F344 , Tasa de Supervivencia , Hormonas Tiroideas/sangre , Factores de Tiempo
12.
Rinsho Shinkeigaku ; 39(10): 1071-4, 1999 Oct.
Artículo en Japonés | MEDLINE | ID: mdl-10655773

RESUMEN

A 50-year-old man noticed a mass in the right cervical region and presented to our hospital. He underwent biopsy of a cervical lymph node, which revealed non-Hodgkin's lymphoma (diffuse large B cell, lymphoblastic type) histologically. He was treated with chemotherapy (CHOP) and radiation, and achieved complete remission. Two months later, he was admitted because of distal pain and extensive numbness of the lower limb as well as weakness of the left leg. Lumbar MRI showed an area of abnormal intensity in the cauda equina. Cytological examination of cerebrospinal fluid showed class V (lymphoma cells), so he was diagnosed as having recurrent malignant lymphoma of the spinal cord. He was treated with intrathecal chemotherapy and irradiation. After the treatment the mass in the cauda equina disappeared and the neurological symptoms in his legs resolved. It is rare for malignant lymphoma to recur in the spinal cord, particularly the cauda equina. It is well known that cauda equina syndrome can be caused by vertebral lesions and primary spinal cord tumors, but it is also necessary to keep malignant lymphoma of the cauda equina in mind.


Asunto(s)
Linfoma de Células B/complicaciones , Linfoma de Células B Grandes Difuso/complicaciones , Polirradiculopatía/etiología , Neoplasias de la Médula Espinal/complicaciones , Anciano , Cauda Equina , Terapia Combinada , Humanos , Linfoma de Células B/terapia , Linfoma de Células B Grandes Difuso/terapia , Imagen por Resonancia Magnética , Masculino , Polirradiculopatía/diagnóstico , Neoplasias de la Médula Espinal/terapia , Resultado del Tratamiento
13.
Prostate ; 31(1): 9-13, 1997 Apr 01.
Artículo en Inglés | MEDLINE | ID: mdl-9108880

RESUMEN

BACKGROUND: Our previous data suggest that estrogen plays an important role in rat prostate carcinogenesis, particularly in promotion by testosterone. Therefore, in the present experiment, effects of an antiestrogen, tamoxifen (TAM), were investigated. METHODS: Male F344 rats initially received 3,2'-dimethyl-4-aminobiphenyl (DMAB) at 50 mg/kg bw every 2 weeks for 20 weeks and then TAM in Silastic tubes was subcutaneously given alone or together with testosterone propionate (TP) for 40 weeks. RESULTS: TAM significantly suppressed prostate weights, suggesting an estrogenic action, but the development of preneoplastic and/or neoplastic lesions of the prostate or seminal vesicles in rats given DMAB alone or DMAB and TP was not altered. TAM reversed the suppression of development of ventral atypical hyperplasias by TP. CONCLUSIONS: These findings suggest that estrogen, which is derived from testosterone by the action of aromatase, is not involved in the strong promotion by TP of DMAB prostate carcinogenesis.


Asunto(s)
Antagonistas de Estrógenos/farmacología , Neoplasias de la Próstata/inducido químicamente , Tamoxifeno/farmacología , Testosterona/toxicidad , 9,10-Dimetil-1,2-benzantraceno , Animales , Carcinógenos , Línea Celular Transformada , Masculino , Tamaño de los Órganos/efectos de los fármacos , Próstata/efectos de los fármacos , Próstata/patología , Hiperplasia Prostática/inducido químicamente , Ratas , Vesículas Seminales/efectos de los fármacos , Vesículas Seminales/patología , Células Tumorales Cultivadas
14.
Rinsho Shinkeigaku ; 37(10): 876-80, 1997 Oct.
Artículo en Japonés | MEDLINE | ID: mdl-9490896

RESUMEN

A 72-year-old female patient, hospitalized for parkinsonism, suffered cardiopulmonary arrest without any certain causes. The patient was successfully resuscitated and her life was sustained by artificial ventilator for 100 days. All brainstem reflexes were absent, and flat electroencephalogram and no response of brainstem auditory evoked potentials were confirmed twice with an interval of over 6 hours. Flexion of the arm induced reflex rectus abdominis muscle contraction, resembling expiratory movement. Muscle stretch reflexes on rectus abdominis were hyperactive. The expiration-like movement appeared in an apnea test seven minutes after a cessation of artificial ventilation. Electrical stimuli on femoral nerve induced complex action potentials with a 70.2 +/- 6.9 msec latency and 300 msec duration in rectus abdominis muscle, which were similar to the spino-bulbo-spinal reflex. Single photon emission tomography showed only slight cerebral cortical blood flow. The expiration-like movements observed in this case suggest a relationship not only with the spinal cord reflex but also with polysynaptic reflexes to reticular formation in the medulla oblongata.


Asunto(s)
Apnea/fisiopatología , Coma/fisiopatología , Hipoxia Encefálica/complicaciones , Bulbo Raquídeo/fisiología , Reflejo Abdominal , Reflejo de Estiramiento , Médula Espinal/fisiología , Anciano , Apnea/etiología , Coma/etiología , Femenino , Humanos , Enfermedad de Parkinson Secundaria/fisiopatología
15.
Food Chem Toxicol ; 34(6): 537-46, 1996 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-8690313

RESUMEN

2,2'-[(4-aminophenyl)imino]bisethanol sulfate (4APE) was administered at dietary levels of 0 (control), 300, 1000 and 3000 ppm to groups of 50 male and 50 female Fischer 344/DuCrj rats for 104 wk. As slight body weight retardation was observed in the male 3000 ppm group in the preliminary 13-wk feeding study, this dose was selected for the highest exposure level. Mean body weights of both sexes in the 3000 ppm group were lower than those of the controls from wk 2 to termination. However, there were no treatment-related clinical signs or adverse effects on survival rate, food consumption or haematology data. Very slight but statistically significant increases in relative thyroid weights were found in males of the 3000 ppm group, but there was no significant treatment-related increase in the incidence of any non-neoplastic or neoplastic lesions. Thus, under the experimental conditions used, 4APE was not carcinogenic in Fischer 344 rats of either sex.


Asunto(s)
Tinturas para el Cabello/toxicidad , Fenilendiaminas/toxicidad , Glándula Tiroides/efectos de los fármacos , Neoplasias de la Tiroides/inducido químicamente , Animales , Peso Corporal/efectos de los fármacos , Pruebas de Carcinogenicidad , Femenino , Masculino , Neoplasias/inducido químicamente , Tamaño de los Órganos/efectos de los fármacos , Ratas , Ratas Endogámicas F344 , Estadísticas no Paramétricas , Tasa de Supervivencia , Glándula Tiroides/patología
16.
Food Chem Toxicol ; 34(5): 463-7, 1996 May.
Artículo en Inglés | MEDLINE | ID: mdl-8655095

RESUMEN

The carcinogenic potential of tamarind seed polysaccharide was examined in both sexes of B6C3F1 mice. Groups of 50 male and 50 female animals were given diets containing 0, 1.25 and 5% of tamarind seed polysaccharide for 78 wk. Body weight retardation was exhibited by the females in the 1.25 and 5% groups from 34 wk to termination. However, there were no treatment-related clinical signs or adverse effects on survival rate, food and water consumption, haematology findings or organ weights. Detailed histopathological examination also revealed no treatment-related increase in the incidence of any non-neoplastic or neoplastic lesions. These results demonstrated that tamarind seed polysaccharide is not carcinogenic in B6C3F1 mice of either sex.


Asunto(s)
Polisacáridos/toxicidad , Semillas , Animales , Peso Corporal/efectos de los fármacos , Femenino , Frutas/química , Masculino , Ratones , Ratones Endogámicos , Neoplasias/inducido químicamente , Tamaño de los Órganos/efectos de los fármacos , Semillas/química , Tasa de Supervivencia , Pruebas de Toxicidad , Árboles
17.
Rinsho Shinkeigaku ; 35(3): 225-30, 1995 Mar.
Artículo en Japonés | MEDLINE | ID: mdl-7614741

RESUMEN

Magnetic resonance imaging (MRI) is useful for detecting spinal cord lesions in multiple sclerosis (MS). In this study, we have examined MRI for 14 patients (26 cases) with clinically definite MS and investigated the correlations between neurological and MRI findings before and after high-dose corticosteroid therapy (pulse therapy). High signal intensity areas on T2-weighted images (T2WI) were found in 25 of 26 cases. In 22 cases spinal level of clinically suspected lesions were involved in these high intensity areas. T1-weighted images (T1WI) after intravenous gadolinium with diethylenetriamine pentaacetic acid (Gd-DTPA) were also obtained and in 12 of 17 cases before pulse therapy, the symptoms and enhancement of lesions correlated well. The symptoms regressed in all cases after pulse therapy, and high-intensity areas in T2WI became less distinct. Gd-DTPA enhanced areas disappeared in 6 cases and became smaller in 3 of 12 cases. Additional pulse therapy in 3 cases effectively diminished the enhanced areas in these cases. In one patient who had repeated pulse therapy, MRI showed no enhancement. In two other patients who continued on decreased steroid dose had relapses, pulse therapy was therefore started again, providing a good recovery both clinically and radiologically. The changes of MRI findings and clinical course suggest that the pathological changes in spinal MS may be caused not only by demyelination but also by parenchymal edema. Clinical and MRI concordance was significantly better with Gd-DTPA enhanced T1WI than the high-intensity areas in T2WI. Contrast enhancement gives more information about disease activity and the reaction to therapy.


Asunto(s)
Imagen por Resonancia Magnética , Metilprednisolona/administración & dosificación , Esclerosis Múltiple/diagnóstico , Enfermedades de la Médula Espinal/diagnóstico , Enfermedad Aguda , Adolescente , Adulto , Anciano , Femenino , Gadolinio DTPA , Humanos , Masculino , Persona de Mediana Edad , Esclerosis Múltiple/tratamiento farmacológico , Compuestos Organometálicos , Ácido Pentético/análogos & derivados , Médula Espinal/patología , Enfermedades de la Médula Espinal/tratamiento farmacológico
18.
Appl Opt ; 34(22): 4848-56, 1995 Aug 01.
Artículo en Inglés | MEDLINE | ID: mdl-21052325

RESUMEN

The x-ray properties of multinested thin-foil mirror x-ray telescopes (XRT's) on board ASCA, the Advanced Satellite for Cosmology and Astrophysics, were fully evaluated with an x-ray pencil beam.Scanning over the telescope aperture of 35 cm in diameter with an x-ray pencil beam, we found the effective area of a set of XRT's to be 325, 200, and 113 cm(2) at energies of 1.5, 4.5, and 8.0 keV, respectively. We derive the point-spread functions (PSF's) of the XRT's by measuring the image profile at the focal plane with an x-ray CCD. The PSF is found to exhibit a sharp core concentrated within 30 arcsec and a broad wing extended to 3 arcmin in half-power diameter. We also evaluate the contribution of stray light, which is caused by the single reflection of x rays by primary or secondary mirrors and by the backside reflection of the mirrors. To obtain the characteristics of the XRT in the energy region of 0.5-10.0 keV, incorporated with the measurements at discrete energies, we develop a ray-tracing method with the telescope design parameter, the PSF, and optical constants. In particular, we obtain the optical constants around the gold-atom M shell (Au-M) absorption-edge energies by measuring the reflectivity of our mirror sample, with monochromatized x-rays in the energy range of 2.0-3.5 keV from synchrotron radiation. Taking into account the PSF's and optical constants, we find that our ray-tracing program can reproduce all these XRT performances.

19.
Carcinogenesis ; 15(5): 1037-41, 1994 May.
Artículo en Inglés | MEDLINE | ID: mdl-8200065

RESUMEN

Potential synergism between 10 carcinogenic heterocyclic amines [3-amino-1,4-dimethyl-5H-pyrido[4,3-b]indole (Trp-P-1), 3-amino-1-methyl-5H-pyrido[4,3-b]indole (Trp-P-2), 2-amino-6 methyldipyrido[1,2-a:3',2'-d]imidazole (Glu-P-1), 2-amino-dipyrido[1,2-a:3',2'-d]imidazole (Glu-P-2), 2-amino-3-methylimidazo[4,5-f]quinoline (IQ), 2-amino-3,4-dimethyl-imidazo[4,5-f]quinoline (MeIQ), 2-amino-3,8-dimethyl-imidazo[4,5-f]quinoxaline (MeIQx), 2-amino-3-methyl-9H-pyrido[2,3-b]indole (MeA alpha C), 2-amino-9H-pyrido[2,3-b]indole (A alpha C) and 2-amino-1-methyl-6-phenylimidazo[4,5-b]pyridine (PhIP)] in rat liver carcinogenesis was examined. Male F344 rats were initially given diethylnitrosamine (200 mg/kg, i.p.) and beginning 2 weeks later received heterocyclic amines individually at doses 1/10 of that proven to be carcinogenic or in combination at 1/10 or 1/100 doses for 6 weeks. All animals were subjected to partial hepatectomy at week 3 and killed at week 8. The induction of immunohistochemically demonstrable placental glutathione S-transferase positive foci was significantly increased in rats given all 10 chemicals in combination at the 1/10 dose level while values were almost the same as in controls with the 1/100 dose mixture and the individual chemicals, except for Glu-P-1 which significantly increased foci development and Glu-P-2 and A alpha c which significantly decreased levels of foci at the 1/10 dose level. Thus apparent synergism was observed with the 1/10 dose level combination. When the data are considered together with our previous results obtained with five heterocyclic amines using 1/1, 1/5 and 1/25 dose levels, combined effects were found to be related to the number of chemicals included and the dose levels of each, with a possible isoadditive influence being common. The findings are of particular significance since heterocyclic amines and other carcinogenic agents might be simultaneously generated during cooking.


Asunto(s)
Aminas/toxicidad , Carcinógenos/toxicidad , Compuestos Heterocíclicos/toxicidad , Neoplasias Hepáticas Experimentales/inducido químicamente , Animales , Peso Corporal/efectos de los fármacos , Relación Dosis-Respuesta a Droga , Sinergismo Farmacológico , Glutatión Transferasa/metabolismo , Hígado/anatomía & histología , Hígado/efectos de los fármacos , Hígado/enzimología , Neoplasias Hepáticas Experimentales/enzimología , Masculino , Tamaño de los Órganos/efectos de los fármacos , Ratas , Ratas Endogámicas F344
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