RESUMEN
Cadmium is a non-physiological heavy metal released into the environment and workplace as a result of industrial, municipal, and agricultural activities. The association of Cd with pulmonary, prostatic and testicular cancer may be related to the ability of Cd to induce oxidative stress, which could in turn cause oxidative damage to DNA. This study examines the response of antioxidant enzymes and metabolites to Cd-induced oxidative stress in normal liver cells. We found a definite concentration-dependent increase in ROS when CRL-1439 normal liver cells were exposed to various concentrations of Cd2+ (100-300 microM). An increase in ROS production is an indication of oxidative stress, which is known to impact on the performance of antioxidant enzymes and metabolites in the cell. In fact, we found that superoxide dismutase (SOD), catalase (CAT), glutathione reductase (GR) and glutathione peroxidase (GPx) lost activities upon a 4-h exposure of liver cells to levels of Cd2+ ranging from 100 to 300 microM. After exposure of cells for 8 h, the activity of SOD and GPx increased while those of CAT and GR decreased substantially. The metabolites glutathione (GSH), oxidized glutathione (GSSG) and total thiols showed a decrease in concentration after 4 or 8 h of incubation of liver cells with Cd (100-300 microM). Malondialdehyde (MDA) on the other hand, showed an increase in concentration after 4-8 h of incubation of liver cells with Cd due to lipid peroxidation. The relationships of these fluxes to oxidative stress as well as intracellular redox homeostasis are discussed.
Asunto(s)
Antioxidantes/metabolismo , Cloruro de Cadmio/farmacología , Hepatocitos/efectos de los fármacos , Estrés Oxidativo , Oxidorreductasas/metabolismo , Especies Reactivas de Oxígeno/metabolismo , Animales , Catalasa/metabolismo , Línea Celular , Disulfuro de Glutatión/análisis , Glutatión Reductasa/metabolismo , Hepatocitos/enzimología , Hepatocitos/metabolismo , Malondialdehído/análisis , Estructura Molecular , Oxidación-Reducción , Ratas , Especies Reactivas de Oxígeno/análisis , Superóxido Dismutasa/metabolismoRESUMEN
We previously showed that S-adenosylmethionine (SAM) induces movement impairments similar to those observed in Parkinson's disease (PD) apparently by prenylated protein methylation; 5 kDa molecules being methylated and the symptoms being inhibited by prenylcysteine (PC) analogs. In the present study, we explore the biochemical mechanism of action of the PC analogs. N-acetylgeranylcysteine (AGC), N-acetylfarnesylcysteine (AFC), N-acetylgeranylgeranylcysteine (AGGC), farnesylthioacetic acid (FTA), farnesyl-2-ethanesulfonic acid (FTE) and farnesylsuccinic acid (FMS), but not farnesylthiotriazole (FTT) and farnesylthiolactic acid (FTL), inhibited the SAM-induced motor impairments. Incubation of the respective analogs with rat brain membranes containing prenylated protein methyltransferase (PPMTase) resulted in the methylation of AGC, AFC and AGGC. FTA, FTE, FMS and FTT, but not FTL, inhibited the enzyme activity. A single injection of the active analogs remained effective for at least 3 days against repeated injections of 1 micromol SAM. Amphetamine-induced hyperactivity in rats was inhibited by SAM but potentiated by FTE. During 60 min, the movement time for amphetamine-treated rats was 1477 s compared with 633 and 1664 s for amphetamine+SAM- and amphetamine+FTE-treated rats, respectively. The total distance for amphetamine+FTE-treated rats was 82% higher than for amphetamine. The horizontal activity was 30,728 (amphetamine), 15,430 (FTE), 18,526 (amphetamine+SAM), 41,736 (amphetamine+FTE) and 7004 (SAM) as compared to the PBS control (4726). The intricate relationship between the actions of SAM, which speeds up prenylated protein methylation and impairs movement, amphetamine, which increases synaptic dopamine levels and movement, and the PC analogs, which prevent the SAM-induced movement impairments, suggests a SAM-induced defect on dopamine signaling as the likely cause of the symptoms. The data reveal that interaction of PC analogs with PPMTase may not be an indicator of anti-PD-like activity.
Asunto(s)
Cistina/análogos & derivados , Discinesia Inducida por Medicamentos/prevención & control , S-Adenosilmetionina/farmacología , Anfetamina/antagonistas & inhibidores , Anfetamina/farmacología , Animales , Temperatura Corporal/efectos de los fármacos , Estimulantes del Sistema Nervioso Central/antagonistas & inhibidores , Estimulantes del Sistema Nervioso Central/farmacología , Cistina/farmacología , Sinergismo Farmacológico , Inhibidores Enzimáticos/farmacología , Hipercinesia/inducido químicamente , Hipercinesia/prevención & control , Técnicas In Vitro , Masculino , Metilación , Proteína Metiltransferasas/antagonistas & inhibidores , Proteína Metiltransferasas/metabolismo , Ratas , Ratas Sprague-Dawley , Relación Estructura-Actividad , Triazoles/farmacologíaRESUMEN
Polyisoprenylation is a set of secondary modifications involving proteins whose aberrant activities are implicated in cancers and degenerative disorders. The last step of the pathway involves an ester-forming polyisoprenylated protein methyl transferase- and hydrolytic polyisoprenylated methylated protein methyl esterase (PMPMEase)-catalyzed reactions. Omega-3 and omega-6 polyunsaturated fatty acids (PUFAs) have been linked with antitumorigeneis and tumorigenesis, respectively. PUFAs are structurally similar to the polyisoprenyl groups and may interfere with polyisoprenylated protein metabolism. It was hypothesized that PUFAs may be more potent inhibitors of PMPMEase than their more polar oxidative metabolites, the prostaglandins. As such, the relative effects of PUFAs and prostaglandins on PMPMEase could explain the association between cyclooxygenase-2 (COX-2) expression in tumors, the chemopreventive effects of the non-steroidal anti-inflammatory (NSAIDs) COX-2 inhibitors and PUFAs. PUFAs such as arachidonic (AA), eicosapentaenoic (EPA) and docosahexaenoic (DHA) acids inhibited PMPMEase activity with Ki values of 0.12 to 3.7 µM. The most potent prostaglandin was 63-fold less potent than AA. The PUFAs were also more effective at inducing neuroblastoma cell death at physiologically equivalent concentrations. The lost PMPMEase activity in AA-treated degenerating cells was restored by incubating the lysates with COX-1 or COX-2. PUFAs may thus be physiological regulators of cell growth and could owe these effects to PMPMEase inhibition.
RESUMEN
Cadmium is an environmental toxicant, which causes cancer in different organs. It was found that it damages DNA in the various tissues and cultured cell lines. To investigate the mechanism of DNA damage, we have studied the effect of cadmium-induced DNA damage in plasmid pBR322 DNA, and the possible ameliorative effects of antioxidative agents under in vitro conditions. It was observed that cadmium alone did not cause DNA damage. However, it caused DNA damage in the presence of hydrogen peroxide, in a dose dependent manner, because of production of hydroxyl radicals. Findings from this study show the conversion of covalently closed circular double-stranded pBR 322 DNA to the open circular and linear forms of DNA when treated with 10 muM cadmium and various concentrations of H(2)O(2). The conversion was due to nicking in DNA strands. The observed rate of DNA strand breakage was dependent on H(2)O(2) concentration, temperature, and time. Metallothionein I failed to prevent cadmium-induced DNA nicking in the presence of H(2)O(2). Of the two antioxidant enzymes (catalase and superoxide dismutase) studied, only catalase conferred significant (50-60%) protection. EDTA and DMSO exhibited protection similar to catalase, while mannitol showed only about 20% protection against DNA damage. Ethyl alcohol failed to ameliorate cadmium-induced DNA strands break. From this study, it is plausible to infer that cadmium in the presence of hydrogen peroxide causes DNA damage probably by the formation of hydroxyl ions. These results may indicate that cadmium in vivo could play a major role in the DNA damage induced by oxidative stress.