RESUMEN
Biochemical studies have demonstrated the presence of ouabain-sensitive Na-K-ATPase in lens epithelium. The development of certain experimental cataracts has been associated with the decrease in the level of activity of this enzyme. Cytochemical investigations at the ultrastructural level to localize this important enzyme in the ocular lens are needed to exhibit the site of Na-K-ATPase action. In this investigation cytochemical methods originally described by Ernst for the localization of Na-k-atpase through K-NPPase reaction have been used for normal and cataractous ocular lens. The reaction product was observed to be present on the lateral and apical portion of the epithelial cell membranes. Mooreover, the membranes of the cortical fibers in the anterior polar and equatorial region of the lens also exhibited reaction product of Na-k-atpase. The presence of ouabain reduced the reaction product of Na-K-ATPase; however, continuous exposure to ouabain during preincubation fixation, and incubation demonstrated greater reduction in enzyme action in the lens. The Na-K-ATPase activity in the lenses of animals fed galactose decreased with increase in time on galactose diet. In this study, using ultrastructural cytochemistry, we have demonstrated gradual decrease in Na-K-ATPase activity in the lenses of galactose-fed animals.
Asunto(s)
Catarata/enzimología , Cristalino/enzimología , ATPasa Intercambiadora de Sodio-Potasio/metabolismo , Animales , Dieta , Femenino , Galactosa/metabolismo , Histocitoquímica , Nitrofenoles/análisis , Compuestos Organofosforados/análisis , Ouabaína/farmacología , Ratas , ATPasa Intercambiadora de Sodio-Potasio/antagonistas & inhibidoresRESUMEN
The effects of fluvastatin treatment on lipid profile and apolipoproteins were assessed in a group of 31 Chinese patients with hypercholesterolemia, maintained on a constant low-fat diet. Some patients had the additional cardiovascular risk factors of hypertension and non-insulin-dependent diabetes mellitus, and 6 patients had familial hypercholesterolemia. Baseline lipid levels were measured after a 4-week placebo period, and these were repeated after 4 weeks of treatment with fluvastatin 20 mg daily, and after 4 weeks of treatment with fluvastatin 40 mg daily. Total cholesterol, low density lipoprotein cholesterol, and apolipoprotein (apo) B were each reduced to the same extent with the 2 doses of fluvastatin (-20%, -26%, and -20%, respectively). Triglycerides and very low density lipoprotein cholesterol were also reduced by about 12% with the 2 doses of fluvastatin. Apo A-I was increased by 7% and high density lipoprotein cholesterol (HDL-C) was increased by 10% with the 40 mg dose. The increase in HDL-C was due to increases in both HDL2-C (18%) and HDL3-C (7%). Lipoprotein(a) levels did not show any significant change with the 2 doses of fluvastatin in this short-term study. One patient developed reversible asymptomatic elevation of liver enzymes with the higher dose of fluvastatin; otherwise the drug was well tolerated and no patients had to be withdrawn from the study.
Asunto(s)
Anticolesterolemiantes/uso terapéutico , Apolipoproteínas/sangre , Ácidos Grasos Monoinsaturados/uso terapéutico , Hidroximetilglutaril-CoA Reductasas/uso terapéutico , Inhibidores de Hidroximetilglutaril-CoA Reductasas , Hipercolesterolemia/tratamiento farmacológico , Indoles/uso terapéutico , Lípidos/sangre , Adulto , Anciano , Anciano de 80 o más Años , Apolipoproteína A-I/sangre , Apolipoproteínas B/sangre , China , Colesterol/sangre , HDL-Colesterol/sangre , LDL-Colesterol/sangre , VLDL-Colesterol/sangre , Femenino , Fluvastatina , Humanos , Hipercolesterolemia/sangre , Hipercolesterolemia/complicaciones , Hipercolesterolemia/dietoterapia , Hiperlipoproteinemia Tipo II/sangre , Hiperlipoproteinemia Tipo II/tratamiento farmacológico , Masculino , Persona de Mediana Edad , Placebos , Triglicéridos/sangreRESUMEN
Our recent investigations have shown that the Eisai compound, E-0722, (2R-4S-6-fluoro-1-2-methylspirochroman 4,4'-imidazolidine 2,5'-dione) is a more potent aldose reductase inhibitor than Sorbinil (D-6-fluorospirochroman 4,4'-imidazolidine 2,5'-dione). In the previous studies these aldose reductase inhibitors were added to the 50% galactose diet fed to rats to determine their effect on galactose-induced alterations in the lens and the development of cataract. In this report we present our results on the effect of prefeeding the aldose reductase inhibitor, E-0722, on the alterations in rat lens following subsequent feeding of galactose. For this study, young Sprague Dawley rats were prefed either rat chow or rat chow plus 50% galactose containing 1mg/day/Kg body weight of E-0722 for 1 or 2 weeks. After this dietary regimen, the animals were transferred to diets containing 50% galactose for different periods. For controls, rats were fed either rat chow or 50% galactose without the prefeeding of E-0722. Our results obtained through gross observation of the lenses, light microscopic studies of lens sections and assay of Na+-K+-ATPase (NPPase) activity show that the prefeeding of E-0722 prior to galactose feeding delays galactose-induced alterations and the development of mature cataract.
Asunto(s)
Aldehído Reductasa/antagonistas & inhibidores , Catarata/etiología , Galactosa/administración & dosificación , Imidazoles/farmacología , Imidazolidinas , Deshidrogenasas del Alcohol de Azúcar/antagonistas & inhibidores , Animales , Catarata/enzimología , Catarata/patología , Dieta , Galactosa/antagonistas & inhibidores , Cristalino/patología , Ratas , Ratas Endogámicas , ATPasa Intercambiadora de Sodio-Potasio/metabolismoRESUMEN
Lenses of rats maintained on a 50% galactose diet displayed the development of a progressive cataract which was cortical at 3-11 days, and progressively internalized (nuclear as well) and mature at 16-20 days of feeding. Lens fiber plasma membranes were isolated from female rats subjected to the galactose diet and from controls at 11, 19, and 31 days of feeding, and analyzed by SDS-PAGE. Examination of the fiber plasma membranes from whole lenses of galactose-fed rats demonstrated the limited proteolysis of MP26 into MP23-24, in both the cortical and mature stages of the resultant cataracts. The limited proteolysis of MP26 was first evident in the lens cortex at 11 days of galactose feeding, and was evident as well, and more severe in proportion, in the lens nucleus at 19 days of feeding. The greatest proportion in MP26 limited proteolysis was observed in whole lenses at 31 days of galactose feeding. The regional progression of MP26 limited proteolysis closely paralleled the morphological progression of the galactose-induced cataract in the rat. The proportion of lens MP26 which underwent limited proteolysis into MP23-24 increased the longer the animals were kept on the galactose diet.
Asunto(s)
Catarata/metabolismo , Proteínas del Ojo/metabolismo , Cristalino/metabolismo , Glicoproteínas de Membrana , Péptido Hidrolasas/metabolismo , Animales , Acuaporinas , Catarata/inducido químicamente , Membrana Celular/metabolismo , Femenino , Galactosa , Ratas , Ratas EndogámicasRESUMEN
Alterations in elemental composition of the normal lens have been reported to accompany galactose cataract development in rats. In this report we present the changes in regional distribution of Na, K, Cl, P, S and Ca during the reversal of galactose-induced cataracts. Elemental X-ray maps of lenses from young female Sprague Dawley rats fed 50% galactose for 20 days were examined at 0, 20, 40 and 90 days following the transfer of galactose fed rats to Purina Rat Chow diet. Reinstatement of normal elemental distribution accompanied the progression of lens transparency. By 90 days on the rat chow diet, K had increased and Na, Cl and Ca had decreased so that a near normal lenticular distribution of these elements was established. The reinstatement of elemental distribution during cataract reversal followed a pattern similar to that observed for alterations during cataract development, initiating near the equatorial surface and expanding centrally. The correlation between the alterations in the distribution of the elements studied and our previously reported morphological investigation of lenses during galactose cataract reversal is discussed in this report.
Asunto(s)
Catarata/metabolismo , Cristalino/metabolismo , Animales , Catarata/inducido químicamente , Cationes/metabolismo , Dieta , Modelos Animales de Enfermedad , Microanálisis por Sonda Electrónica , Femenino , Galactosa , Ratas , Ratas Sprague-DawleyRESUMEN
Previous morphological and biochemical studies indicate that a late appearing hereditary Emory mouse cataract may be a good model for certain human senile cataracts. The development of lenticular opacity in the Emory mouse is a slow process which provides an opportunity to conduct analysis of the progression of alterations that lead to cataract development. Biochemical investigations have not yet demonstrated any specific correlation between alterations in the lens and the extent of opacity. We have conducted studies to determine the role of Na+K+-ATPase in the development of cataract in the Emory mouse. In this report we present results obtained on the site and level of activity of Na+K+-ATPase in six- and twelve-month-old Emory mouse lenses in which visible cataractous changes are beginning to appear. CFW mice (the parent strain) were used for controls in this study. Ultrastructural cytochemistry for the localization of Na+-K+-ATPase exhibited the enzyme reaction product for this enzyme to be present mainly between the lateral epithelial cell membranes and between the apical epithelial cell membranes and superficial cortical fiber membranes. In cortical fibers the reaction product was localized between fiber membranes. Although there was very little or no significant differences in the extent of reaction product in epithelial cells, the reaction product in the cortical fibers of six-month-old Emory mouse was less extensively distributed as compared to lenses from control CFW mice of the same age.(ABSTRACT TRUNCATED AT 250 WORDS)
Asunto(s)
Catarata/enzimología , Cristalino/enzimología , ATPasa Intercambiadora de Sodio-Potasio/metabolismo , Envejecimiento , Animales , Catarata/genética , Catarata/patología , Histocitoquímica , Corteza del Cristalino/ultraestructura , Cristalino/ultraestructura , Ratones/genética , Ratones Endogámicos , Microscopía Electrónica , Monoéster Fosfórico Hidrolasas/metabolismo , ATPasa Intercambiadora de Sodio-Potasio/fisiología , EspectrofotometríaRESUMEN
Lens ultrastructure and Na- K-ATPase activity in the lenses of rats fed galactose and a galactose + sorbinil diet (aldose reductase inhibitor) were studied. Lenses of rats on the galactose diet exhibited development of peripheral opacity within 3-4 days. This opacity progressed with the continuation of the galactose feeding, and by 20 days mature cataracts were observed in these animals. The formation of vacuoles, cysts, membrane disruption in the epithelium and fibers, and swelling of fibers accompanied the development of opacity. With the progression of opacity there was a considerable drop in lens Na- K-ATPase activity in the galactose-fed animals. However, the lenses of rats that were treated with sorbinil did not show any of the alterations in the ultrastructure of the epithelium and fibers that accompany galactose cataractogenesis. The level of Na-K-ATPase activity in the sorbinil-treated animals was similar to that found in lenses from the laboratory chow-fed group of rats. These observations further substantiate the role of aldose reductase in sugar-cataract development.
Asunto(s)
Catarata/prevención & control , Galactosa/antagonistas & inhibidores , Imidazoles/farmacología , Imidazolidinas , Cristalino/efectos de los fármacos , 4-Nitrofenilfosfatasa/metabolismo , Aldehído Reductasa/antagonistas & inhibidores , Animales , Catarata/inducido químicamente , Catarata/patología , Femenino , Cristalino/ultraestructura , Microscopía Electrónica , Ratas , Ratas Endogámicas , ATPasa Intercambiadora de Sodio-Potasio/metabolismoRESUMEN
We have shown that galactose cataract development is delayed or inhibited with the administration of aldose reductase inhibitors (ARIs). Dulcitol forms and accumulates in the lens of rats fed galactose. We undertook investigations to study the effectiveness of ARIs in preventing the formation and accumulation of dulcitol in the lens. Young Sprague Dawley rats were fed Purina Rat Chow with 50% galactose either with or without 15 mg sorbinil, 0.15, 0.5, or 1.0 mg E-0722/day/Kg body weight. At desired intervals following the initiation of diets, the lenses were processed for the determination of galactose and dulcitol levels. The lenticular dulcitol increased significantly in all animals fed galactose reaching a maximum level by approximately 15 days with comparatively lower levels in the groups fed ARIs with galactose; this increase was dose dependent in the groups fed E-0722. There was a subsequent, rapid drop in lenticular dulcitol by 18 days in all dietary groups. Interestingly, a second peak of increased lenticular dulcitol was observed in all groups. The correlation between dulcitol accumulation and cataract development is discussed.
Asunto(s)
Aldehído Reductasa/antagonistas & inhibidores , Galactitol/metabolismo , Imidazoles/farmacología , Imidazolidinas , Cristalino/efectos de los fármacos , Animales , Catarata/inducido químicamente , Catarata/prevención & control , Carbohidratos de la Dieta , Galactosa , Cristalino/metabolismo , Ratas , Ratas Sprague-DawleyRESUMEN
Our previously reported investigations showed that cataracts could be induced in fetal lenses through the maternal feeding of galactose during pregnancy. We also reported that the lens opacity present at birth reverses completely by 30 days of age if there is no further post-natal exposure to galactose. This investigation was designed to investigate if an aldose reductase inhibitor (ARI) has any cross-placental effect in preventing galactose-induced cataracts in fetuses. We have also evaluated if there are any milk-mediated effects of galactose on cataract induction and of galactose and ARI on the maintenance or reversal of opacities induced in utero. Pregnant Sprague-Dawley rats were fed either 50% galactose or rat chow with or without the ARI, (2R,4S)-6-fluoro-2-methyl spirochroman-4,4'-imidazolidine-2',5'-dione (Eisai compound E-0722). Following parturition, pups of mothers from the different dietary groups were either fed by their own mothers or foster fed by lactating females fed either rat chow or 50% galactose with or without the ARI. Lenses of the pups were examined at desired intervals with light and scanning electron microscopes. We observed that: (a) both galactose and the ARI had a cross-placental effect on the fetal lenses in the development and inhibition of cataracts, respectively; (b) galactose had very little, if any, milk-mediated effect on either the induction of cataracts in newborn pups that were born with transparent lenses or the maintenance of cataracts induced in utero; (c) the ARI appeared to have a milk-mediated effect, which accelerates the reversal of cataract associated alterations in lenses of pups with cataracts induced in utero, leading to further reinstatement of lens transparency; and (d) the presence of ARI in the diet of rats during pregnancy and/or post-parturition provided continued protection to the lenses of pups that were exposed to a galactose diet following birth.
Asunto(s)
Aldehído Reductasa/antagonistas & inhibidores , Catarata/prevención & control , Enfermedades Fetales/prevención & control , Imidazolidinas , Leche Humana/fisiología , Animales , Catarata/inducido químicamente , Catarata/patología , Femenino , Galactosa , Imidazoles/metabolismo , Imidazoles/uso terapéutico , Cristalino/ultraestructura , Intercambio Materno-Fetal , Microscopía Electrónica de Rastreo , Embarazo , Ratas , Ratas EndogámicasRESUMEN
Prolactin has been known to affect the water and electrolyte balance. Because increased lens hydration has been shown to be a common phenomenon in most, if not all types of cataracts, we have been interested in investigating a possible role of prolactin in sugar cataract induction and progression. For this study, we have used morphological and biochemical approaches. The prolactin delivery method involved intraperitoneal implantation of one or more pellets in Sprague-Dawley female rats. Following implantation of the desired number of prolactin or control (nonprolactin) pellets, animals were either fed galactose and lab chow, or lab chow diet. Gross morphological observations of whole lenses, slit-lamp examination of lenses and light microscopic analysis of lens sections showed that in the galactose-fed prolactin group, galactose associated alteration progressed faster and total opacification (mature cataract development) was achieved earlier than in the nonprolactin group. The levels of galactose and dulcitol were higher in the lenses of galactose-fed prolactin treated rats as compared to lenses from nonprolactin (control) rats. No significant difference in lens Na+-K+ ATPase activity between the prolactin and nonprolactin group was observed. Our results indicate that prolactin accelerates galactose-induced cataractogenesis in rats.
Asunto(s)
Catarata/inducido químicamente , Prolactina/farmacología , Animales , Catarata/patología , Femenino , Galactitol/metabolismo , Galactosa/metabolismo , Cristalino/enzimología , Cristalino/metabolismo , Ratas , ATPasa Intercambiadora de Sodio-Potasio/metabolismoRESUMEN
A series of rat galactose lenses, from 1 to 20 days on the 50% galactose diet, were frozen in the whole eye, and fractured from pole to pole in the frozen state. Lyophilized half-lenses were prepared for analysis by energy dispersive spectrometry (EDS). Following elemental analysis, some specimens were embedded and sectioned for histological studies. Elemental X-ray maps, and/or profiles, were made for K, Na, Cl, Ca, P, and S. As early as two days on the galactose diet, a crescent-shaped region ("streak") of Cl, Na, and Ca gain, and K loss develops near the equatorial surface. Between this region and the equatorial surface are the nucleated differentiating fiber cells which maintain low Cl, Na, and Ca, and high K (viable equatorial zone, VEZ). With time the "streak" expands anteriorly, centrally and posteriorly, eventually (by 20 days) including most of the lens. The VEZ, including the epithelium, however, is non-reactive to the galactose diet, which is deleterious to the fully differentiated fiber cells. Eventually, the VEZ undergoes a characteristic morphological change, apparently due in part to changes in its physical environment.