RESUMEN
Retinoic acid (RA) has been found to regulate hypothalamic function, but precisely where it acts is unknown. This study shows expression of retinaldehyde dehydrogenase (RALDH) enzymes in tanycytes that line the third ventricle in an area overlapping with the site of hypothalamic neural stem cells. The influence of RA was examined on the proliferation of progenitors lining the third ventricle using organotypic slice cultures. As has been shown in other regions of neurogenesis, RA was found to inhibit proliferation. Investigations of the dynamics of RALDH1 expression in the rat hypothalamus have shown that this enzyme is in tanycytes under photoperiodic control with highest levels during long versus short days. In parallel to this shift in RA synthesis, cell proliferation in the third ventricle was found to be lowest during long days when RA was highest, implying that RALDH1 synthesized RA may regulate neural stem cell proliferation. A second RA synthesizing enzyme, RALDH2 was also present in tanycytes lining the third ventricle. In contrast to RALDH1, RALDH2 showed little change with photoperiodicity, but surprisingly the protein was present in the apparent absence of mRNA transcript and it is hypothesized that the endocytic tanycytes may take this enzyme up from the cerebrospinal fluid (CSF).
Asunto(s)
Proliferación Celular/efectos de los fármacos , Hipotálamo/citología , Hipotálamo/enzimología , Fotoperiodo , Retinal-Deshidrogenasa/biosíntesis , Tretinoina/farmacología , Familia de Aldehído Deshidrogenasa 1 , Animales , Western Blotting , Células Cultivadas , Regulación Enzimológica de la Expresión Génica/efectos de los fármacos , Hipotálamo/efectos de los fármacos , Inmunohistoquímica , Hibridación in Situ , Isoenzimas/biosíntesis , Masculino , Ratones , Ratones Endogámicos C57BL , Células-Madre Neurales/efectos de los fármacos , Técnicas de Cultivo de Órganos , Reacción en Cadena de la Polimerasa , Ratas , Ratas Endogámicas F344 , Ratas Sprague-Dawley , Retinal-Deshidrogenasa/líquido cefalorraquídeo , Tercer Ventrículo/citología , Tercer Ventrículo/efectos de los fármacos , Tercer Ventrículo/metabolismo , Tretinoina/análisisRESUMEN
It has been reported that retinoids, such as retinoic acid (RA) and retinol (ROL), dissolved in aqueous solutions are susceptible to oxidative damage when exposed to light, air, and relatively high temperatures, conditions that are normal for culturing stem cells. Thus, questions arise regarding the interpretation of results obtained from studies of mouse embryonic stem cells exposed to retinoids because their isomerization state, their stability in culture conditions, and their interactions with other potential differentiation factors in growth media could influence developmental processes under study. Media samples were supplemented with retinoids and exposed to cell culture conditions with and without mouse embryonic stem cells (mESC), and retinoids were extracted and analyzed using HPLC. To determine whether retinoids are stable in media supplemented with fetal bovine serum (FBS) or in chemically-defined, serum-free media, mESC adapted to each type of growth media were investigated. Studies reported here indicate there was little loss or isomerization of at-RA, 9-cis-RA, 13-cis-RA, or ROL in cell cultures grown in serum-supplemented media when cell cultures were maintained in the dark and manipulated and observed under yellow light. In contrast, the stability of both at-RA and ROL were determined to be greatly reduced in serum-free media as compared with serum-supplemented media. Addition of 6 mg/ml bovine serum albumin was found to stabilize retinoids in serum-free media. It was also determined that ROL is less stable than RA in cell culture conditions.
Asunto(s)
Medios de Cultivo/análisis , Células Madre Embrionarias/citología , Tretinoina/análisis , Alitretinoína , Animales , Bovinos , Diferenciación Celular/efectos de los fármacos , Células Cultivadas , Cromatografía Líquida de Alta Presión , Medios de Cultivo/metabolismo , Medios de Cultivo/farmacología , Medios de Cultivo Condicionados/análisis , Medios de Cultivo Condicionados/metabolismo , Medio de Cultivo Libre de Suero/análisis , Medio de Cultivo Libre de Suero/metabolismo , Medio de Cultivo Libre de Suero/farmacología , Relación Dosis-Respuesta a Droga , Estabilidad de Medicamentos , Células Madre Embrionarias/efectos de los fármacos , Células Madre Embrionarias/metabolismo , Isotretinoína/análisis , Isotretinoína/metabolismo , Isotretinoína/farmacología , Ratones , Ratones Endogámicos C57BL , Suero/metabolismo , Tretinoina/metabolismo , Tretinoina/farmacologíaRESUMEN
In order to increase our knowledge about the distribution of vitamins in the mammalian brain, we have developed a highly specific antiserum directed against retinoic acid with good affinity (10(-8) M), as evaluated by ELISA tests. In the rat brain, no immunoreactive fibers containing retinoic acid were detected. Cell bodies containing retinoic acid were only found in the hypothalamus. This work reports the first visualization and the morphological characteristics of cell bodies containing retinoic acid in the mammalian paraventricular hypothalamic nucleus and in the dorsal perifornical region, using an indirect immunoperoxidase technique. The restricted distribution of retinoic acid in the rat brain suggests that this vitamin could be involved in very specific physiological mechanisms.
Asunto(s)
Hipotálamo/química , Tretinoina/análisis , Animales , Ensayo de Inmunoadsorción Enzimática , Hipotálamo/citología , Sueros Inmunes/inmunología , Técnicas para Inmunoenzimas , Inmunohistoquímica , Núcleo Hipotalámico Paraventricular/química , Núcleo Hipotalámico Paraventricular/citología , Ratas , Tretinoina/inmunologíaRESUMEN
The retinoid X receptor (RXR) is activated by its often elusive cognate ligand, 9-cis-retinoic acid (9-cis-RA). In flies and moths, molting is mediated by a heterodimer ecdysone receptor consisting of the ecdysone monomer (EcR) and an RXR homolog, ultraspiracle (USP); the latter is believed to have diverged from its RXR origin. In the more primitive insect, Locusta migratoria (Lm), RXR is more similar to human RXRs than to USPs. LmRXR was detected in early embryos when EcR transcripts were absent, suggesting another role apart from ecdysone signaling. Recombinant LmRXRs bound 9-cis-RA and all-trans-RA with high affinity (IC(50) = 61.2-107.7 nM; K(d) = 3 nM), similar to human RXR. To determine whether specific binding had functional significance, the presence of endogenous retinoids was assessed. Embryos were extracted by using modified Bligh and Dyer and solid-phase protocols to avoid the oily precipitate that makes this material unsuitable for assay. These extracts contained retinoids (5.4 nM) as assessed by RA-inducible Cyp26A1-promoter luciferase reporter cell lines. Furthermore, the use of HPLC and MS confirmed the presence of retinoids and identified in any embryo, 9-cis-RA, in addition to all-trans-RA. We estimate that whole embryos contain 3 nM RA, including 9-cis-RA at a concentration of 1.6 nM. These findings strongly argue for a functional role for retinoids in primitive insects and favor a model where signaling through the binding of 9-cis-RA to its RXR is established relatively early in evolution and embryonic development.
Asunto(s)
Locusta migratoria , Receptores X Retinoide/genética , Tretinoina/análisis , Alitretinoína , Animales , Clonación Molecular , ADN Complementario/genética , ADN Complementario/aislamiento & purificación , Embrión no Mamífero , Unión Proteica , Isoformas de Proteínas , Receptores X Retinoide/metabolismo , Receptores X Retinoide/fisiología , Tretinoina/metabolismoRESUMEN
BACKGROUND: Retinoids and alpha-hydroxy acids (AHAs) are major compounds in topical therapy. They exert distinct but potentially complementary activities. However, their association is limited by their respective irritating potential. Recently, the first association between a retinoid and an AHA has been achieved; this formulation (RALGA) associates retinaldehyde (RAL)--a precursor of retinoic acid (RA)--and glycolic acid (GA)--an AHA. OBJECTIVE: To study the pharmacological properties of RALGA. METHODS: The bioavailability of RAL into the skin after topical RALGA was studied by HPLC, and its bioconversion to RA was analysed by measuring the enzyme activity of retinaldehyde dehydrogenase and the RA content in the epidermis and dermis. The retinoid activity of RALGA was studied on the modulation of Hhb4 keratin mRNA on the tail of C57BL/6 mice, and its comedolytic properties on the size and density of dermal cysts and the morphology of sebaceous glands in hairless mice. RESULTS: Epidermal and dermal concentrations of RAL and RA were higher after RALGA treatment, as compared to both RAL 0.1% alone and RA 0.05% alone; this indicates that the presence of GA favours the bioavailability and biotransformation of RAL into RA. The retinoid activity of RALGA (suppression of Hhb4 mRNA keratin) was similar to that of RAL alone, indicating that the presence of GA does not interfere with specific retinoid activity; GA alone had no effect in this test, which confirms the specificity of Hhb4 mRNA keratin modulation for retinoid activity. The diameter and the density of dermal cysts as well as the size of sebaceous glands were significantly decreased by RALGA. CONCLUSION: These observations indicate that the addition of an AHA such as GA to a retinoid such as RAL results in a better bioavailability of the retinoid, thus a higher delivery of RA, which potentiates the biological activities of the retinoid. This combination allows a delivery of high amounts of RA in the skin while preventing the side-effects usually observed with high concentrations of topical RA.
Asunto(s)
Fármacos Dermatológicos/farmacología , Glicolatos/farmacología , Glicolatos/farmacocinética , Queratolíticos/farmacología , Retinaldehído/farmacología , Retinaldehído/farmacocinética , Aldehído Oxidorreductasas/análisis , Animales , Disponibilidad Biológica , Biotransformación , Cromatografía Líquida de Alta Presión , Quistes/tratamiento farmacológico , Fármacos Dermatológicos/farmacocinética , Dermis/enzimología , Dermis/metabolismo , Combinación de Medicamentos , Epidermis/enzimología , Epidermis/metabolismo , Femenino , Queratinas/efectos de los fármacos , Queratolíticos/farmacocinética , Ratones , Ratones Pelados , Ratones Endogámicos C57BL , Ratones Endogámicos , Retinal-Deshidrogenasa , Glándulas Sebáceas/efectos de los fármacos , Tretinoina/análisisRESUMEN
Chronic and excessive ethanol intake in rats results in low levels of hepatic retinoic acid (RA) either by inhibiting the biosynthesis of RA or by enhancing its catabolism of RA. Chronic ethanol intake also decreases both hepatic expression of insulin-like growth factor-I (IGF-I) and plasma IGF-I concentration in rats. It is not known whether RA supplementation in alcohol-fed rats can restore plasma IGF-I concentrations and hepatic IGF-I expression. In the present study, we examined both plasma IGF-I level and hepatic IGF-I mRNA expression in alcohol-fed rats with or without RA (100 microg/kg body weight) supplementation for 6 mo. Hepatic IGF-I mRNA levels and plasma IGF-I concentration were decreased (84 and 29%, respectively) significantly in alcohol-fed rats compared with the control. In contrast, RA supplementation in ethanol-fed rats partially restored both hepatic IGF-I mRNA levels and plasma IGF-I concentration compared with rats fed ethanol alone. These data suggest that alcohol-impaired hepatic RA status contributes to the decreased plasma IGF-I level and hepatic IGF-I expression in alcoholics.
Asunto(s)
Etanol/farmacología , Factor I del Crecimiento Similar a la Insulina/análisis , Hígado/química , Tretinoina/administración & dosificación , Animales , Peso Corporal , Suplementos Dietéticos , Etanol/efectos adversos , Expresión Génica/efectos de los fármacos , Factor I del Crecimiento Similar a la Insulina/genética , ARN Mensajero/análisis , Ratas , Ratas Sprague-Dawley , Tretinoina/análisis , Vitamina A/análisisRESUMEN
We investigated the capacity of Royal College of Surgeons (RCS) rat retinal pigment epithelial (RPE) cells to take up all-trans-retinol (ROL) (vitamin A) and to metabolize it into retinyl esters (RE). Cultures of RPE cells were established from RCS and control newborn rats. All-trans-ROL was delivered to the apical surface of the RPE monolayer. Retinoids were analyzed by high-performance liquid chromatography. The cellular retinol-binding protein type I (CRBP-I) was assessed by Western blotting. Before supplementation with ROL, RE were lower in RCS rats. After ROL supplementation, esters increased and reached values that were similar in the two strains, but the increase, expressed relative to the initial value, was higher in RCS rats. The uptake of ROL and the level of CRBP-I were greater in RCS rats. Our results provide evidence of a functional retinol esterifying enzyme in cultured RCS RPE cells and suggest that CRBP-I could play a role in the uptake and esterification of ROL in the RPE cells.
Asunto(s)
Células Epiteliales/metabolismo , Epitelio Pigmentado Ocular/metabolismo , Tretinoina/metabolismo , Animales , Western Blotting/métodos , Cromatografía Líquida de Alta Presión/métodos , Esterificación , Ratas , Ratas Endogámicas , Proteínas de Unión al Retinol/análisis , Proteínas Celulares de Unión al Retinol , Tretinoina/análisis , Tretinoina/farmacologíaRESUMEN
BACKGROUND: The biologic activity of vitamin A depends, in part, on its metabolism to active nuclear receptor ligands, chiefly retinoic acid. The cellular retinol-binding protein (CRBP) binds vitamin A with high affinity and is postulated to regulate its uptake and metabolism. In this report, we analyze the expression of CRBP in normal and malignant breast tissues. METHODS: We evaluated CRBP expression by in situ hybridization in six reduction mammoplasty specimens and 49 human breast carcinoma specimens by use of digoxigenin-labeled RNA probes and in nine cultured mammoplasty specimens by northern or western blot analysis. Statistical significance was evaluated with the chi(2) test or Fisher's exact test if the sample sizes were small. All P values are from two-sided tests. RESULTS: CRBP was expressed in all 15 mammoplasty specimens (normal breast tissue) and in 33 of 35 available specimens of normal tissue adjacent to carcinoma. In contrast, 12 (24%) of 49 carcinoma lesions were uniformly negative for CRBP (P =.023 for comparison with adjacent normal breast tissue). The loss of CRBP expression was as frequent in ductal carcinoma in situ (six [27%] of 22) as in invasive lesions (six [22%] of 27), suggesting that it is a relatively early event in carcinogenesis and not associated with patient age, tumor grade, and expression of steroid receptors or c-Myc. Preliminary experiments did not find an association between CRBP and retinoic acid receptor beta loss, but most (four of five) CRBP-negative tumors were also retinoic acid receptor beta negative. CONCLUSION: CRBP is underexpressed in 24% (95% confidence interval = 12.5%-36.5%) of human breast carcinomas, implying a link between cellular vitamin A homeostasis and breast cancer. We hypothesize that the loss of CRBP restricts the effects of endogenous vitamin A on breast epithelial cells.
Asunto(s)
Neoplasias de la Mama/química , Carcinoma in Situ/química , Carcinoma Ductal de Mama/química , Receptores de Ácido Retinoico/análisis , Proteínas de Unión al Retinol/análisis , Transducción de Señal , Tretinoina/análisis , Vitamina A/análisis , Northern Blotting , Mama/metabolismo , Neoplasias de la Mama/patología , Carcinoma in Situ/patología , Carcinoma Ductal de Mama/patología , ADN Complementario , Femenino , Regulación Neoplásica de la Expresión Génica , Genes myc , Humanos , Hibridación in Situ , Mamoplastia , ARN Neoplásico/química , Proteínas de Unión al Retinol/genética , Proteínas Celulares de Unión al RetinolRESUMEN
BACKGROUND: Epidemiologic studies have demonstrated that individuals who eat more fruits and vegetables and/or have high levels of serum beta-carotene have a lower risk of cancer, especially lung cancer. However, recent human intervention studies using beta-carotene supplements have shown an increase in the risk of lung cancer among smokers and asbestos workers. In this study, we used an animal model system to evaluate the hazard associated with a combination of high-dose beta-carotene supplementation and tobacco smoking. METHODS: Ferrets were given a beta-carotene supplement, exposed to cigarette smoke, or both for 6 months. Cell proliferation and squamous metaplasia in lung tissue were assessed by examination of proliferating-cell nuclear antigen expression and histopathologic examination, respectively. beta-Carotene and retinoid concentrations in lung tissue and plasma samples were analyzed by high-performance liquid chromatography. Expression of genes for retinoic acid receptors (RARs) and activator protein-1 (encoded by the c-Jun and c-Fos genes) in lung tissue specimens was examined by western blotting. RESULTS: A strong proliferative response in lung tissue and squamous metaplasia was observed in all beta-carotene-supplemented animals, and this response was enhanced by exposure to tobacco smoke. When compared with control groups, all three treatment groups had statistically significantly lower concentrations of retinoic acid in lung tissue, and they exhibited 18%-73% reductions in RARbeta gene expression; however, RARalpha and RARgamma gene expression was not reduced. Ferrets given a beta-carotene supplement and exposed to tobacco smoke had threefold to fourfold elevated expression of the c-Jun and c-Fos genes. CONCLUSIONS: Diminished retinoid signaling, resulting from the suppression of RARbeta gene expression and overexpression of activator protein-1, could be a mechanism to enhance lung tumorigenesis after high-dose beta-carotene supplementation and exposure to tobacco smoke.
Asunto(s)
Cocarcinogénesis , Regulación de la Expresión Génica/efectos de los fármacos , Neoplasias Pulmonares/inducido químicamente , Pulmón/patología , Nicotiana , Plantas Tóxicas , Lesiones Precancerosas/inducido químicamente , Receptores de Ácido Retinoico/efectos de los fármacos , Transducción de Señal/fisiología , Humo/efectos adversos , Factor de Transcripción AP-1/biosíntesis , beta Caroteno/toxicidad , Animales , División Celular/efectos de los fármacos , Diterpenos , Regulación hacia Abajo/efectos de los fármacos , Exposición a Riesgos Ambientales , Hurones , Genes fos , Genes jun , Humanos , Pulmón/química , Masculino , Metaplasia , Antígeno Nuclear de Célula en Proliferación/biosíntesis , Antígeno Nuclear de Célula en Proliferación/genética , Ésteres de Retinilo , Transducción de Señal/efectos de los fármacos , Factor de Transcripción AP-1/genética , Factor de Transcripción AP-1/fisiología , Tretinoina/análisis , Vitamina A/análogos & derivados , Vitamina A/análisis , beta Caroteno/análisisRESUMEN
We demonstrate that cultured human and bovine parathyroid cells incubated with all-trans-[11,12-3H]-retinol convert this tracer into all-trans- and 9-cis-retinoic acid. By using RT-PCR, cellular retinol-binding protein type I (CRBP I), cellular retinoic acid binding protein I and II (CRABP I and II), retinoic acid receptors (RARs) alpha, beta and gamma, and 9-cis-retinoic acid receptor (RXR) alpha transcripts were detected in human parathyroid cDNA. CRBP I and CRABP I expression was confirmed by immunohistochemistry. Both 9-cis- and all-trans-RA were found to suppress parathyroid hormone (PTH) secretion from dispersed human adenomatous parathyroid cells, which was augmented by combined treatment with 1mM RA and 100 nM 1,25 (OH)2D3. The present data establish parathyroid gland as a target for retinoids and as a site of synthesis of the hormonal forms of vitamin A (retinol), all-trans- and 9-cis-retinoic acid.
Asunto(s)
Glándulas Paratiroides/metabolismo , Tretinoina/análisis , Alitretinoína , Animales , Bovinos , Células Cultivadas , ADN Complementario/análisis , ADN Complementario/genética , HumanosRESUMEN
An isocratic reversed-phase high-performance liquid chromatographic procedure for the determination of all-trans-retinoic acid (all-trans-RA) and its metabolites, all-trans-4-oxo-RA, 5,6-epoxy-RA, 9-cis-RA and 13-cis-RA, in mouse plasma and embryo and in new in vitro potential test systems for developmental toxicology has been developed. These compounds, their biological precursor retinol (vitamin A) and the internal standard were resolved on a Spherisorb ODS-2 (5 microns) column (250 x 4.6 mm I.D.) with acetonitrile-water-methanol-n-butyl alcohol (56:37:4:3, v/v) containing 100 mM ammonium acetate and 70 mM acetic acid as the elution system, with a total run time of 23 min. The assay was linear over a wide range, with a lower limit of quantitation of 50 ng/ml or 10 ng/mg of protein for all-trans-RA, 13-cis-RA and 9-cis-RA and of 25 ng/ml or 5 ng/mg protein for the 4-oxo- and 5,6-epoxy-metabolites. At these concentrations, intra-assay coefficients of variation (C.V.) of the retinoids were 3-9%. Mean intra-assay C.V. averaged 5-7% in the tissues studied. Its use is discussed for RA measurements in some of the new test systems--Drosophila melanogaster, sea urchin embryos and cultured human keratinocytes--that have to be evaluated in toxicological testing, supplementary to standard assays in mammals.
Asunto(s)
Toxicología/métodos , Tretinoina/análisis , Animales , Células Cultivadas , Cromatografía Líquida de Alta Presión , Drosophila melanogaster , Femenino , Feto/metabolismo , Humanos , Queratinocitos/química , Modelos Lineales , Ratones , Embarazo , Reproducibilidad de los Resultados , Erizos de Mar/embriología , Sensibilidad y Especificidad , Espectrofotometría Ultravioleta , Estereoisomerismo , Tretinoina/química , Tretinoina/metabolismo , Vitamina A/análisisRESUMEN
Soon after [11-3H]retinoic acid (RA) (1.1 x 10(8) d.p.m.) was administered orally to rats either as a large dose (115 micrograms = 0.38 mumol/rat) or mixed with unlabelled RA as a huge dose (22 mg = 73.33 mumol/rat), retinoyl beta-glucuronide (RAG) was identified and characterized as a significant metabolite in the serum and small intestine. Of the administered dose, 70% remained unchanged as retinoic acid in the stomach up to 1 h. Significant amounts of 5,6-epoxyretinoic acid, 4-hydroxyretinoic acid, esters of retinoic acid and several polar retinoids, including 4-oxoretinoic acid, were also detected in the stomach. No significant difference was observed in the nature of the retinoids found after a large or a huge dose; however, the ratio of RAG/RA was higher after a huge dose than after a large dose. Thus RAG, which is biologically active in vivo and in vitro, is formed quickly in significant amounts in tissues after a dose of RA.
Asunto(s)
Tretinoina/análogos & derivados , Tretinoina/metabolismo , Administración Oral , Animales , Biotransformación , Cromatografía Líquida de Alta Presión , Femenino , Masculino , Embarazo , Técnica de Dilución de Radioisótopos , Ratas , Ratas Endogámicas , Factores de Tiempo , Distribución Tisular , Tretinoina/administración & dosificación , Tretinoina/análisis , Tretinoina/sangre , Tretinoina/farmacocinética , TritioRESUMEN
The incorporation of [2-3H]mannose into dolichyl phosphate mannose and glycoproteins is markedly reduced in livers of vitamin A-deficient hamsters. To determine whether vitamin A deficiency selectively alters the level of mannose incorporation into sugar phosphates and sugar nucleotides, we studied the in vivo incorporation of [2-3H]mannose, [5-3H]glucose, and [4,5-3H]galactose into sugar phosphates and sugar nucleotides. Male hamsters fed either a vitamin A-depleted or a retinoic acid-supplemented (3 micrograms/g) diet were used at 4, 6 and 8 wk of age; the animals were killed at various time points after an intraperitoneal injection of the radiolabeled sugar. A two- to threefold increase in the amount of [2-3H]mannose was found in liver of hamsters fed a vitamin A-depleted diet for 4 wk, resulting in enhanced incorporation into mannosyl-phosphate and guanosine diphosphate (GDP) mannose. As deficiency progressed, there was a smaller increase in [2-3H]mannose and a significant decrease in [3H]mannose-phosphate and GDP-[3H]mannose, suggesting a decreased mannose kinase activity. [5-3H]Glucose-labeled livers showed no difference in the total uptake of the label or its incorporation into uridine diphosphate glucose and galactose-phosphate during the 8-wk study. However, the synthesis of glucosyl-phosphate was reduced by 50 to 90% at 6 and 8 wk of deficiency, suggesting an impaired gluco-kinase activity. In hamsters injected with [4,5-3H]galactose only [3H]glucose was found within 5 min in the free sugar fraction. In contrast, as much as 70% of the label in the sugar phosphate and sugar nucleotide fraction remained as [3H]galactose even at 60 min. These effects on sugar, sugar phosphate and sugar nucleotide formation in part may explain the effects of vitamin A deficiency on glycoconjugate biosynthesis.
Asunto(s)
Dieta , Galactosa/metabolismo , Glucosa/metabolismo , Hígado/metabolismo , Manosa/metabolismo , Azúcares de Nucleósido Difosfato/biosíntesis , Fosfatos de Azúcar/biosíntesis , Deficiencia de Vitamina A/metabolismo , Animales , Cricetinae , Galactosa/administración & dosificación , Galactosa/análisis , Glucosa/administración & dosificación , Glucosa/análisis , Guanosina Difosfato Manosa/biosíntesis , Hígado/análisis , Hígado/efectos de los fármacos , Masculino , Manosa/administración & dosificación , Manosa/análisis , Mesocricetus , Modelos Biológicos , Factores de Tiempo , Tretinoina/administración & dosificación , Tretinoina/análisis , Uridina Difosfato Glucosa/biosíntesisRESUMEN
Retinoids have chemopreventive activity for epithelial tumors in a variety of systems, including the two-stage tumorigenesis system of mouse skin in which only the promotion stage is inhibited. We asked whether dietary vitamin A deficiency could affect the skin tumorigenic response, prior to major changes in body weight or general health of the animals. Two regimens were tested to induce vitamin A deficiency. SENCAR mice were either (a) fed a vitamin A-deficient diet from 4 or 9 weeks of age or (b) their mothers were fed the diet from the time of birth of the experimental animals which were then weaned on the same diet. The latter regimen produced typical symptoms of vitamin A deficiency in the offspring by Weeks 12-14 and all the mice died by Week 19; the former regimen permitted sufficient accumulation of retinol and its esters to sustain life for up to 45 and 75 weeks, respectively, in the majority of mice. For our experiments, vitamin A depletion was produced by placing the mothers on the deficient diet at birth of the experimental animals. A single topical dose of 20 micrograms of 7,12-dimethylbenz(a)anthracene (DMBA) was used as the initiator at 3 weeks of age and 1 to 2 micrograms of 12-O-tetradecanoylphorbol-13-acetate (TPA) once weekly as the tumor promoter for 10 weeks (from Week 4 through 13 of the experiment). Fifty-five % of mice (n = 40) on Purina laboratory chow (mean body weight, 31.4 g) developed skin tumors (2.58 per mouse) at 12 weeks, versus 2.5% (0.05 papillomas per mouse) of mice (n = 40) kept on the purified vitamin A-deficient diet (mean body weight, 30.3 g), a 98% decrease in tumor/mouse. Retinoic acid (RA) (1-3 micrograms/g diet) supplementation after Week 12 caused a rapid tumorigenic response in 95% of the mice by week 22. This tumor response occurred to a reduced extent in the absence of continued TPA treatment up to Week 13. Even though tumor incidence increased within 1 week of RA and 95% of the mice showed the tumorigenic response, the number of tumors per mouse was about 50% of that observed in mice maintained on standard Purina diet. This was confirmed in an experiment in which the mice were maintained for life either on Purina or on the RA (3 micrograms/g) containing purified diet, the latter being the control group for the effect of vitamin A deficiency on skin tumorigenesis.(ABSTRACT TRUNCATED AT 400 WORDS)
Asunto(s)
Carotenoides/administración & dosificación , Neoplasias Cutáneas/inducido químicamente , Tretinoina/administración & dosificación , Deficiencia de Vitamina A , 9,10-Dimetil-1,2-benzantraceno , Animales , Carotenoides/análisis , Cocarcinogénesis , Dieta , Femenino , Hígado/análisis , Masculino , Ratones , Neoplasias Experimentales/inducido químicamente , Neoplasias Experimentales/patología , Neoplasias Experimentales/prevención & control , Neoplasias Cutáneas/patología , Neoplasias Cutáneas/prevención & control , Acetato de Tetradecanoilforbol , Tretinoina/análisis , Deficiencia de Vitamina A/mortalidad , Deficiencia de Vitamina A/fisiopatología , Pérdida de Peso , beta CarotenoRESUMEN
The effect of feeding large amounts of beta-carotene and 13-cis-retinoic acid (RA) on plasma and liver levels of alpha-tocopherol, lipid peroxides and retinoids was studied. Groups of young male rats were fed semipurified diets supplemented with 0, 100 mg/kg beta-carotene, 20 and 100 mg/kg 13-cis-RA. After feeding the various diets for 11 weeks, rats were killed and the concentrations of lipid peroxides, alpha-tocopherol, and retinoids were measured in blood plasma and liver. Peroxide levels were increased and alpha-tocopherol levels were decreased in plasma as well as liver of rats fed diets containing 13-cis-RA; this effect seems to be dose dependent, beta-Carotene had no significant effect on either of the above parameters. There was a decrease in the liver and plasma concentrations of retinol in rats fed 13-cis-RA; the levels of RA were generally higher in these two groups. The results suggest that the mechanism whereby 13-cis-RA increases the tissue peroxide levels may be related to its ability to decrease alpha-tocopherol levels.