RESUMEN
Acrylamide is known to cause neurotoxicity in the experimental animals and humans. The literature on its neurotoxic effect in the adult animals is huge, but the effect of acrylamide on the embryonic and postnatal development is relatively less understood. The present study examined its effects on the development of external features and cerebellum in albino rats. Acrylamide was orally administered to non-anesthetized pregnant females by gastric intubation 10 mg/kg/day. The animals were divided into three groups as follows. (1) Group A, newborn from control animals; (2) Group B; newborns from mothers treated with acrylamide from day 7 (D7) of gestation till birth (prenatal intoxicated group); (3) Group C; newborns from mothers treated with acrylamide from D7 of gestation till D28 after birth (perinatally intoxicated group). Acrylamide administered either prenatally or perinatally has been shown to induce significant retardation in the newborns' body weights development, increase of thiobarbituric acid-reactive substances (TBARS) and oxidative stress (significant reductions in glutathione reduced [GSH], total thiols, superoxide dismutase [SOD] and peroxidase activities) in the developing cerebellum. Acrylamide treatment delayed the proliferation in the granular layer and delayed both cell migration and differentiation. Purkinje cell loss was also seen in acrylamide-treated animals. Ultrastructural studies of Purkinje cells in the perinatal group showed microvacuolations and cell loss. The results of this study show that prenatal and perinatal acrylamide or its metabolites disrupts the biochemical machinery, cause oxidative stress and induce structural changes in the developing rat cerebellum.
Asunto(s)
Acrilamida/toxicidad , Cerebelo , Desarrollo Embrionario/efectos de los fármacos , Desarrollo Fetal/efectos de los fármacos , Estrés Oxidativo/efectos de los fármacos , Administración Oral , Animales , Animales Recién Nacidos , Conducta Animal/efectos de los fármacos , Conducta Animal/fisiología , Muerte Celular/efectos de los fármacos , Diferenciación Celular/efectos de los fármacos , Movimiento Celular/efectos de los fármacos , Cerebelo/efectos de los fármacos , Cerebelo/embriología , Cerebelo/crecimiento & desarrollo , Cerebelo/metabolismo , Femenino , Glutatión/metabolismo , Crecimiento y Desarrollo/efectos de los fármacos , Crecimiento y Desarrollo/fisiología , Peroxidación de Lípido/efectos de los fármacos , Masculino , Exposición Materna , Oxidorreductasas/antagonistas & inhibidores , Oxidorreductasas/metabolismo , Embarazo , Células de Purkinje/efectos de los fármacos , Células de Purkinje/patología , Células de Purkinje/ultraestructura , Ratas , Aumento de Peso/efectos de los fármacosRESUMEN
A fast transport system of materials is shown in cat sensory fibers of sciatic nerve. After injection of tritiated leucine into the lumbar seventh ganglia, the distribution of activity was measured in the sciatic nerves from 2 to 8 hours afterward. The distribution showed a crest of activity advancing down the fibers at a rate of approximately 410 millimeters per day. An intraaxonic locus of the activity was indicated by a block of the downflow induced by local freezing which causes the fibers to close off. Some of the activity in the nerve was due to free tritiated leucine, with most of it incorporated into polypeptide, soluble protein, and subcellular particulates.
Asunto(s)
Transporte Biológico Activo , Leucina/metabolismo , Nervio Ciático/metabolismo , Animales , Axones/metabolismo , Axones/fisiología , Gatos , Cromatografía en Gel , Congelación , Biosíntesis de Péptidos , Biosíntesis de Proteínas , TritioRESUMEN
Subcellular distribution of 2?,3?-cyclic nucleotide-3?-phosphodiesterase (CNPase) in desheathed, saline perfused cat sciatic nerve is reported. CNPase specific activity was enriched in the total particulate (P(2)) fraction and was low in the soluble (S(2)) fraction. "Light-myelin" floating above the 0.60 M sucrose phase had the highest CNPase activity, 2.5-fold over the crude homogenate (CH). By contrast, enzyme activity in "heavy myelin" floating above the 0.85 M sucrose interface was equal to that of the CH and accounted for only 12% of total activity. CNPase activity in the membranes floating above the 0.25 and 0.60 and 0.85 M sucrose phases comprised nearly 70% of the total CNPase activity. The "light myelin" fraction floating above the 0.60 M sucrose accounted for approx. 51% of the total CNPase activity. SDS-PAGE of membranes individually harvested from above the 0.25 and 0.60 and 0.85 M sucrose phases revealed the presence of myelin-specific proteins (P(0), P(1); and P(2)). Electron microscope examination demonstrated the presence of myelin in each membrane fraction. The results of this study show that the majority of CNPase activity is associated with "light myelin" in cat peripheral nerve.
RESUMEN
Neurological disorders have been reported from parts of Africa with protein-deficient populations and attributed to cyanide (CN-) exposure from prolonged dietary use of cassava, a cyanophoric plant. Cyanide is normally metabolized to thiocyanate (SCN-) by the sulfur-dependent enzyme rhodanese. However, in protein-deficient subjects where sulfur amino acids (SAA) are low, CN may conceivably be converted to cyanate (OCN-), which is known to cause neurodegenerative disease in humans and animals. This study investigates the fate of potassium cyanide administered orally to rats maintained for up to 4 weeks on either a balanced diet (BD) or a diet lacking the SAAs, L-cystine and L-methionine. In both groups, there was a time-dependent increase in plasma cyanate, with exponential OCN- increases in SAA-deficient rats. A strongly positive linear relationship between blood CN- and plasma OCN- concentrations was observed in these animals. These data are consistent with the hypothesis that cyanate is an important mediator of chronic cyanide neurotoxicity during protein-calorie deficiency. The potential role of thiocyanate in cassava-associated konzo is discussed in relationship to the etiology of the comparable pattern of motor-system disease (spastic paraparesis) seen in lathyrism.
Asunto(s)
Cianatos/sangre , Cianuros/sangre , Cistina/deficiencia , Metionina/deficiencia , Cianuro de Potasio/metabolismo , Animales , Peso Corporal/efectos de los fármacos , Diuresis/efectos de los fármacos , Relación Dosis-Respuesta a Droga , Femenino , Humanos , Manihot/toxicidad , Distribución Aleatoria , Ratas , Ratas Sprague-Dawley , Sulfatos/orina , Tiocianatos/orina , Factores de TiempoRESUMEN
A high-performance liquid chromatography (HPLC) method for the determination of picomole levels of polyamines (putrescine, spermidine, and spermine) is described. Amino groups in polyamines react with 9-fluorenylmethyl chloroformate (FMOC) to form stable and highly fluorescent derivatives which can be separated and quantitatively estimated by HPLC in about 12 min. The mean relative elution times (n = 14) for putrescine, spermidine and spermine are 4.21 +/- 0.02, 10.09 +/- 0.02 and 11.19 +/- 0.04 min, respectively. The method has been applied to determine polyamine concentration in rat dorsal root ganglia (DRG) without interference with endogenous amino acids. Polyamine content of individual rat DRG has been calculated and the values are as follows: putrescine, 36.8 +/- 2.01, spermidine, 1652 +/- 131.0 and spermine 388.5 +/- 38.4 pmol/DRG. Information on polyamine concentrations in DRG may be useful in understanding the mechanism of action of toxic chemicals on nervous system.
Asunto(s)
Poliaminas Biogénicas/análisis , Cromatografía Líquida de Alta Presión/métodos , Fluorenos , Ganglios Espinales/análisis , Animales , Putrescina/análisis , Ratas , Ratas Endogámicas , Espermidina/análisis , Espermina/análisisRESUMEN
The effect of n-hexane, 2-hexanol, 5-hydroxy-2-hexanone, 2,5-hexanediol, methyl n-butyl ketone ( MnBK ) and 2,5-hexanedione (2,5-HD) has been studied in vitro on crystalline glyceraldehyde-3-phosphate dehydrogenase (GAPDH), DL-glyceraldehyde-3-phosphate: NAD oxidoreductase (phosphorylating) EC. 1.2.1.12 and phosphofructokinase (PFK) ATP: D-fructose-6-phosphate-1-phosphotransferase; EC. 2.7.1.11 and lactic dehydrogenase (LDH) L-lactate: NAD+ oxidoreductase, EC. 1.1.1.27. MnBK and 2,5-HD both inhibited GAPDH and PFK activities selectively. n-Hexane and 2-hexanol had no effect on GAPDH and PFK activities; 5-hydroxy-2-hexanone and 2,5-hexanediol exhibited a slight inhibitory effect on these enzymes. Neither metabolites of n-hexane have any effect on LDH activity. 2,5-Hexanedione did not inhibit transketolase (D-sedoheptulose-7-phosphate: D-glyceraldehyde-3-phosphate glycolaldehyde transferase, EC. 2.2.1.1) and succinate dehydrogenase (succinate: 2,6-dichlorophenol-indophenol oxidoreductase, EC. 1.3.99.1) activities. The levels of ATP were reduced in 2,5-HD-treated cat sciatic nerves and returned to normal levels by exposing the nerve to sodium pyruvate.
Asunto(s)
Hexanos/farmacología , Oxidorreductasas/metabolismo , Nervios Periféricos/metabolismo , Fosfofructoquinasa-1/metabolismo , Transcetolasa/metabolismo , Adenosina Trifosfato/análisis , Animales , Gatos , Gliceraldehído-3-Fosfato Deshidrogenasas/metabolismo , Técnicas In Vitro , L-Lactato Deshidrogenasa/metabolismo , Fosfocreatina/análisis , Succinato Deshidrogenasa/metabolismoRESUMEN
Single injection of acrylamide (1.3 mmol/kg, i.p.) inhibited retrograde axon transport of [125I]tetanus toxin in hen sensory and motor axons. Retrograde axon transport deficits appeared within hours of dosing with acrylamide. The inhibitory effect of acrylamide on retrograde axon transport was transient since transport deficits were not detectable 35 h after dosing. Acrylamide impaired the retrograde movement but not the uptake of [125I]tetanus toxin in the axon. Multiple doses of acrylamide (0.42 mmol/kg, i.p.) induced progressive clinical signs of acrylamide neuropathy that correlated with increasing deficits in retrograde axon transport of [125I]tetanus toxin to ventral spinal cord. Deficits were also observed in sensory neurons but were not statistically significant. Accumulated decrements in retrograde axon transport may be the underlying cause of degeneration of motor axons in acrylamide neuropathy in fowl.
Asunto(s)
Acrilamidas/toxicidad , Transporte Axonal/efectos de los fármacos , Axones/fisiología , Vías Eferentes/fisiología , Ganglios Espinales/fisiología , Neuronas Motoras/fisiología , Degeneración Nerviosa , Nervio Ciático/fisiología , Médula Espinal/fisiología , Acrilamida , Animales , Axones/efectos de los fármacos , Pollos , Vías Eferentes/efectos de los fármacos , Vías Eferentes/patología , Femenino , Ganglios Espinales/efectos de los fármacos , Ganglios Espinales/patología , Neuronas Motoras/efectos de los fármacos , Nervio Ciático/efectos de los fármacos , Nervio Ciático/patología , Médula Espinal/efectos de los fármacos , Médula Espinal/patología , Toxina TetánicaRESUMEN
The effect of acrylamide on selected glycolytic and citric acid cycle enzymes has been studied in denervated cat sciatic nerves in vitro and in vivo. The enzyme activity of glyceraldehyde-3-phosphate dehydrogenase (GAPDH), neuron specific enolase (NSE), succinate dehydrogenase (SDH), and lactate dehydrogenase (LDH), has been examined in saline-perfused, desheathed and denervated peroneal (P) and tibial (T) nerves from cats treated with acrylamide (15 mg/kg/day, s.c.) or vehicle for 15 days. GAPDH activity in denervated P and T nerve stumps was 2.0- and 2.3-fold higher than normal P and T nerve values. GAPDH activity in Schwann cells in denervated P and T nerves of acrylamide-treated cats was markedly reduced (56% and 61% of untreated denervated nerves, respectively). LDH and SDH activities were unaffected by acrylamide and NSE activity was absent in denervated nerve stumps. Acrylamide (0.5 and 20 mM) inhibited GAPDH activity in denervated nerve homogenates by 67% and 29%, respectively. This study demonstrates that acrylamide inhibits GAPDH in Schwann cells. The significance of GAPDH inhibition by acrylamide in denervated nerves and its relation to distal axonopathy has been discussed.
Asunto(s)
Acrilamidas/farmacología , Enzimas/metabolismo , Nervios Periféricos/enzimología , Acrilamida , Animales , Gatos , Desnervación , Metabolismo Energético/efectos de los fármacos , Femenino , Gliceraldehído-3-Fosfato Deshidrogenasas/metabolismo , Técnicas In Vitro , L-Lactato Deshidrogenasa/metabolismo , Masculino , Fosfopiruvato Hidratasa/metabolismo , Células de Schwann/enzimología , Nervio Ciático/enzimología , Succinato Deshidrogenasa/metabolismoRESUMEN
The effect of single and repeated doses of acrylamide (a neurotoxin) and N,N'-methylene-bis-acrylamide (a non-neurotoxic analogue of acrylamide) on glutathione (GSH), glutathione-S-transferase (GST) and dopamine receptors has been studied in rat brain. In vitro, both acrylamide and bis-acrylamide decreased brain GSH content in a concentration-dependent manner. At equimillimolar concentrations (2-10 mM) bis-acrylamide was more effective than acrylamide in lowering GSH levels. In vitro, GST activity was also inhibited as a function of acrylamide concentration. A single dose of either acrylamide or bis-acrylamide depleted GSH content of rat brain in a concentration-dependent manner without inhibiting GST activity. Repeated administration of either acrylamide or bis-acrylamide in rats (50 mg/kg X 10 days) decreased GSH content in the brain but GST activity was inhibited only by acrylamide and not by bis-acrylamide. Single or repeated injections of acrylamide but not of bis-acrylamide increased brain dopamine receptors ([3H]spiroperidol binding) in a concentration-dependent manner.
Asunto(s)
Acrilamidas/administración & dosificación , Encéfalo/metabolismo , Glutatión Transferasa/metabolismo , Receptores Dopaminérgicos/efectos de los fármacos , Receptores de Péptidos , Acrilamida , Acrilamidas/farmacología , Animales , Esquema de Medicación , Glutatión/metabolismo , Inyecciones Intraperitoneales , Masculino , Ratas , Ratas Endogámicas , Receptores de Superficie Celular/efectos de los fármacos , Receptores Dopaminérgicos/metabolismo , Factores de TiempoRESUMEN
Acrylamide, an occupational neurotoxicant, reduced MAP1 and MAP2 distribution in different regions of rat brain. Different components of the extrapyramidal system (caudate-putamen, globus pallidus, substantia nigra and red nucleus) revealed differential distribution of MAP1 and MAP2 in acrylamide-treated animals. Rats were treated with acrylamide (estimated mean dose: 15 mg/kg/day) for 2 weeks and MAP1 and MAP2 were localized according to Sternberger's peroxidase-anti-peroxidase technique. MAP1 labelled neuronal perikarya and dendrites almost with a similar intensity, but MAP2 immunostaining was more intense in dendrites than neuronal perikarya. Acrylamide caused a near-total loss of MAP1 and MAP2 immunoreactivity in caudate-putamen. Other components of the extrapyramidal system were relatively less affected by acrylamide. These results indicate that caudate-putamen is more susceptible to the action of acrylamide than other components of the extrapyramidal system studied. The depletion of MAP1 and MAP2 immunoreactivity by acrylamide appears to be an early biochemical event preceding peripheral neuropathy. The loss of MAPs immunoreactivity occurs first in dendrites and proceeds toward the perikarya. This study indicates that acrylamide not only causes axonal damage but may also induce dendritic degeneration.
Asunto(s)
Acrilamidas/toxicidad , Tractos Extrapiramidales/efectos de los fármacos , Proteínas Asociadas a Microtúbulos/efectos de los fármacos , Neuronas/efectos de los fármacos , Acrilamida , Animales , Tractos Extrapiramidales/metabolismo , Globo Pálido/efectos de los fármacos , Globo Pálido/metabolismo , Técnicas para Inmunoenzimas , Masculino , Proteínas Asociadas a Microtúbulos/metabolismo , Neostriado/efectos de los fármacos , Neostriado/metabolismo , Ratas , Ratas Sprague-Dawley , Núcleo Rojo/efectos de los fármacos , Núcleo Rojo/metabolismo , Sustancia Negra/efectos de los fármacos , Sustancia Negra/metabolismoRESUMEN
A rapid technique for separating and quantitating the three enolase isozymes present in rodent brain and sciatic nerve was developed using high-pressure liquid anion-exchange chromatography. At pH 7.9, one cationic and two anionic enzyme forms were separated with baseline resolution in an imidazole buffer containing ethylenediaminetetraacetic acid (EDTA) and magnesium. The recovery of enolase activity was 90% or greater for brain and 85% for sciatic nerve. Chromatography of liver and axon-free (degenerated) sciatic nerve allowed the identification of non-neuronal, hybrid, and neuron-specific enolase isozymes. These enzyme forms, respectively, constituted 40%, 29% and 19% of total activity in brain, and 63%, 13% and 4% of total activity in normal sciatic nerve.
Asunto(s)
Encéfalo/enzimología , Isoenzimas/aislamiento & purificación , Fosfopiruvato Hidratasa/aislamiento & purificación , Nervio Ciático/enzimología , Animales , Química Encefálica , Cromatografía Líquida de Alta Presión , Cromatografía por Intercambio Iónico , Isoenzimas/análisis , Masculino , Fosfopiruvato Hidratasa/análisis , Ratas , Ratas EndogámicasRESUMEN
The protective effect of exogenous sodium pyruvate on the distal-proximal progression of experimental acrylamide neuropathy in rats was examined. Incorporation of 2% (w/w) sodium pyruvate powder in the diet of rats receiving subcutaneous injections of an aqueous solution of acrylamide (35 mg/kg/day, 5 days/week) retarded the onset and development of functional, morphological, and biochemical measures of acrylamide neuropathy. Pyruvate supplementation did not alter hexobarbital sleep time or zoxazolamine paralysis time, two in vivo measures of microsomal mixed-function oxidase activity, and the disposition of radioactivity in plasma or sciatic nerve following subcutaneous injection of [14C]acrylamide. Although acrylamide can interfere with energy metabolism at a variety of sites where pyruvate can rescue neurons (axons), the data of this study are consistent with our earlier hypothesis that acrylamide neuropathy may be associated with a glycolytic deficit. The exact site of pyruvate protection is unknown. Exogenous pyruvate is perhaps utilized by axons to circumvent toxin-induced glycolytic inhibition and provide chemical energy for fast axonal transport.
Asunto(s)
Acrilamidas/toxicidad , Enfermedades del Sistema Nervioso/inducido químicamente , Piruvatos/uso terapéutico , Acrilamida , Acrilamidas/farmacocinética , Animales , Masculino , Enfermedades del Sistema Nervioso/tratamiento farmacológico , Enfermedades del Sistema Nervioso/patología , Ácido Pirúvico , Ratas , Ratas EndogámicasRESUMEN
Northern blot analysis was used to study the effects of acrylamide, a potent neurotoxin, on the induction of c-fos and c-jun mRNA in rat brain. Male Sprague-Dawley rats (10-12 weeks old) treated with acrylamide as a single dose (100 mg/kg, i.p.) or via drinking water (0.03% w/v) for 4 weeks, were used to study acute and chronic effects on immediate-early gene expression, respectively. Acute administration of acrylamide caused a statistically significant increase in the expression of c-fos (approx. 37%) and c-jun (approx. 17%) mRNA in rat brain. By contrast, the level of c-fos mRNA in chronic acrylamide treatment was not altered significantly, but the expression of c-jun mRNA was increased almost 100% as compared to control. These data show that the neurotoxin acrylamide induces immediate-early gene expression in the brain. The effects appear to be related to the route of administration, dose and duration of acrylamide treatment.
Asunto(s)
Acrilamidas/farmacología , Química Encefálica/efectos de los fármacos , Expresión Génica/efectos de los fármacos , Genes fos/efectos de los fármacos , Genes jun/efectos de los fármacos , Acrilamida , Animales , Autorradiografía , Northern Blotting , Masculino , Hibridación de Ácido Nucleico , ARN Mensajero/aislamiento & purificación , ARN Mensajero/metabolismo , Ratas , Ratas Sprague-DawleyRESUMEN
Sodium cyanate, a neurotoxic chemical in rodents, primates and humans, is implicated in neurodegenerative disorders in protein-deficient populations subsisting in parts of Africa on the cyanogenic plant cassava. The molecular and cellular mechanisms of cyanate neurotoxicity are not understood. This study investigates the effect of sodium cyanate on glutathione (GSH) homeostasis in rodent brain and liver in vitro and in vivo. GSH levels in mouse brain were rapidly, time- and dose-dependently decreased following intraperitoneal administration of 100, 200 or 300 mg/kg sodium cyanate. By contrast, GSH disulfide (GSSG) levels were increased and GSH/GSSG ratios were decreased in a dose-dependent manner in rat brain. Sodium cyanate depleted GSH levels in all regions of mouse brain. Brain glutathione reductase activity was dose-dependently inhibited, while glutathione peroxidase activity was not affected by sodium cyanate. The disruption of GSH homeotasis, as evidenced by reduced tissue GSH/GSSG ratios, likely results from cyanate-induced inhibition of glutathione reductase activity. The results of this study suggest that cyanate neurotoxicity, and perhaps cassava-associated neurodegenerative diseases, are mediated in part by disruption of glutathione homeostasis in neural tissue.
Asunto(s)
Encéfalo/efectos de los fármacos , Encéfalo/metabolismo , Cianatos/farmacología , Glutatión/metabolismo , Homeostasis/efectos de los fármacos , África , Animales , Cianatos/envenenamiento , Femenino , Disulfuro de Glutatión/metabolismo , Glutatión Reductasa/metabolismo , Humanos , Hígado/efectos de los fármacos , Hígado/metabolismo , Ratones , Ratones Endogámicos , Degeneración Nerviosa/etiología , Degeneración Nerviosa/metabolismo , Trastornos Nutricionales/complicaciones , Deficiencia de Proteína/complicaciones , Ratas , Ratas Sprague-Dawley , Factores de Tiempo , Distribución Tisular/efectos de los fármacosRESUMEN
Nutritional status is an important factor in modulating the metabolic fate of xenobiotics. Sulfur amino acid (SAA) deficiency has been proposed as a risk factor for human neurological diseases among protein-poor populations subsisting on the cyanophoric plant cassava. Female Sprague-Dawley rats were used to develop and define a model of SAA deficiency for use in future studies examining cassava-related neurotoxicity. Rats were kept in metabolic cages for 7-21 d and fed a balanced diet (BD) of known composition or a comparable diet selectively deficient in methionine and cystine (SAA-free diet). Animals fed the SAA-free diet failed to thrive, lost body weight, excreted porphyrinic materials, and showed a steep and persistent reduction of urinary inorganic sulfate. In contrast, animals on the BD gained body weight and maintained baseline output of urinary inorganic sulfate. Urinary thiocyanate excretion did not differ between groups, but plasma thiocyanate concentrations reached double that in SAA-deficient rats. Increased plasma thiocyanate suggests mobilization of sulfur amino acids from endogenous sources. Liver glutathione and blood cyanide concentrations were similar in animals on the BD and the SAA-deficient diet. In summary, a diet free of methionine and cystine results in increased retention of inorganic sulfur as thiocyanate and a near absence of inorganic sulfur excretion in urine.
Asunto(s)
Cianuros/farmacocinética , Cistina/deficiencia , Homeostasis , Metionina/deficiencia , Compuestos de Sulfhidrilo/metabolismo , Animales , Femenino , Inactivación Metabólica , Ratas , Ratas Sprague-Dawley , Sulfatos/orina , Tiocianatos/metabolismoRESUMEN
The in vitro synthesis of myelin proteins has been studied by measuring the incorporation of [3H] lysine in developing rat brain slices. This incorporation system has been used to assay potentially gliotoxic and myelinolytic agents. A reduced incorporation of the labelled amino acid into myelin proteins occurs in the presence of anti-myelin anti-serum and anti-basic protein anti-serum. Diphtheria toxin has been found to inhibit the synthesis of myelin basic and proteolipid protein in the white matter slices of developing rats. Recent experiments with serum samples from multiple sclerosis patients in exacerbation suggest the presence of a factor which interferes with the synthesis of myelin in white matter slices.
Asunto(s)
Esclerosis Múltiple/metabolismo , Proteínas de la Mielina/biosíntesis , Vaina de Mielina/crecimiento & desarrollo , Neuroglía/crecimiento & desarrollo , Oligodendroglía/crecimiento & desarrollo , Animales , Encéfalo/crecimiento & desarrollo , Encéfalo/metabolismo , Toxina Diftérica/farmacología , Humanos , Isoanticuerpos , Proteína Básica de Mielina/inmunología , Vaina de Mielina/inmunología , Neuronas/fisiología , RatasAsunto(s)
Adenosina Trifosfato/metabolismo , Corteza Cerebral/metabolismo , Degeneración Nerviosa/efectos de los fármacos , Neuronas/metabolismo , Neurotoxinas/toxicidad , Propionatos/toxicidad , Animales , Corteza Cerebral/efectos de los fármacos , Corteza Cerebral/patología , Relación Dosis-Respuesta a Droga , Feto , Cinética , Ratones , Neuronas/efectos de los fármacos , Neuronas/patología , Nitrocompuestos , Técnicas de Cultivo de ÓrganosRESUMEN
The aromatic gamma-diketone 1,2-diacetylbenzene (1,2-DAB), the putative active metabolite of the organic solvent 1,2-diethylbenzene, forms blue-colored polymeric protein adducts and induces the formation of amyotrophic lateral sclerosis (ALS)-like giant, intraspinal neurofilamentous axonal swellings in Sprague Dawley rats. The pathogenetic mechanism of this neuropathy has yet to be understood. We assessed whether these pathological changes are also seen in the C57BL/6 mouse, the animal of choice for toxicogenomic studies. Mice were treated intraperitoneally with 30, 35, 50, or 70 mg/kg 1,2-DAB or its inactive isomer 1,3-DAB per day (or on alternate days) for up to 43 days. Animals treated with 30 or 35 mg/kg per day 1,2-DAB, but not with 1,3-DAB, developed muscle spasms and progressive weakness, most prominently in hind limbs. Light microscopy revealed swollen axons in spinal anterior horns and proximal ventral roots, and to a lesser extent in dorsal root ganglia of 1,2-DAB-treated animals. Ultrastructural examination of swollen axons revealed clumps of maloriented 10-nm neurofilaments. Sciatic nerves showed clustering of axonal microtubules and other organelles. These findings are qualitatively comparable to those reported in rats treated with 1,2-DAB and represent a suitable phenotype with which to explore molecular mechanisms of proximal, giant neurofilamentous axonopathy using proteomic and genomic technologies.
Asunto(s)
Acetofenonas/toxicidad , Esclerosis Amiotrófica Lateral/inducido químicamente , Esclerosis Amiotrófica Lateral/patología , Axones/efectos de los fármacos , Modelos Animales de Enfermedad , Esclerosis Amiotrófica Lateral/fisiopatología , Animales , Axones/patología , Axones/ultraestructura , Relación Dosis-Respuesta a Droga , Esquema de Medicación , Masculino , Ratones , Ratones Endogámicos C57BL , Microscopía Electrónica de Transmisión/métodos , Distribución Aleatoria , Médula Espinal/efectos de los fármacos , Médula Espinal/patología , Médula Espinal/ultraestructura , Factores de TiempoRESUMEN
The effect of neurotoxin acrylamide (AC) on energy metabolism has been studied in a purified preparation of the synaptosomes. The synaptosomes were prepared by the flotation technique in a discontinuous Ficoll/sucrose gradient. The purity of the synaptosomes was checked by electron microscopy and by assaying the activity of marker enzymes. By these criterias, free mitochondrial contamination in the synaptosomes was found to be > 2%. Incubation of the synaptosomes with different concentrations of AC (2.5, 5.0, and 10mM) produced a concentration-dependent inhibition (15, 35, and 60%, respectively) of glyceraldehyde-3-phosphate dehydrogenase activity. Acrylamide also produced a time-dependent decrease of ATP concentrations in the synaptosomes; about 25% loss of ATP was seen within 1h, while about 60% ATP was lost after 120 min incubation with 10 mM AC. The effect of known inhibitors of glycolysis-iodoacetic acid (IAA), and of oxidative phophorylation-rotenone and antimycin A, was also studied on ATP synthesis by the synaptosomes. IAA was found to be the most potent inhibitor of ATP synthesis, while both rotenone and antimycin A were equally effective in blocking ATP synthesis in the synaptosomes. These studies show that the synaptosome might be used as a suitable in vitro model to study the effect of neurotoxin such as AC on neuronal energy metabolism.
Asunto(s)
Acrilamidas/farmacología , Adenosina Trifosfato/metabolismo , Gliceraldehído-3-Fosfato Deshidrogenasas/metabolismo , Prosencéfalo/metabolismo , Sinaptosomas/metabolismo , Acrilamida , Animales , Antimicina A/farmacología , Fraccionamiento Celular , Centrifugación Zonal , Relación Dosis-Respuesta a Droga , Ficoll , Yodoacetatos/farmacología , Ácido Yodoacético , Cinética , Microscopía Electrónica , Microsomas/efectos de los fármacos , Microsomas/metabolismo , Mitocondrias/efectos de los fármacos , Mitocondrias/metabolismo , Neurotoxinas/farmacología , Ratas , Ratas Sprague-Dawley , Rotenona/farmacología , Sinaptosomas/efectos de los fármacos , Sinaptosomas/ultraestructuraRESUMEN
The effects of systemically introduced neurotoxic solvents 2,5-hexanedione (2,5-HD) and 3,4-dimethyl-2,5-hexanedione (DMHD) on retrograde axonal transport (RT) of 125I-labeled tetanus toxin (TT) was studied in rat and mouse sciatic nerves. The rate of retrograde transport of TT in control rat sciatic nerves was slightly higher (6.8 +/- 0.4 mm/h) than in mouse sciatic nerves (5.4 +/- 0.5 mm/h). A single high dose of 2,5-HD (1,000 mg/kg, i.p.) produced a time-dependent effect on RT in mouse sciatic nerves. 2,5-HD caused a gradual decrease in the velocity of RT (approximately 65% inhibition between 2.0-2.5 h) with a reversal to normal rate 3-5 h after the toxin administration. The effect of DMHD on RT was examined following semi-chronic treatment in rats. DMHD caused a significant decrease (approximately 50%) in the rate of TT transport, in addition, it produced weight loss and hind-limb paralysis.