RESUMEN
AIM: To determine if the formation of para-chloroaniline (PCA) can be avoided by using an alternative irrigant following sodium hypochlorite but before chlorhexidine. METHODOLOGY: Fifty-five single-rooted teeth were decoronated, instrumented to size 40, .06 taper whilst being irrigated with 14% ethylene-diamine-tetra-acetic acid (EDTA) and 6% NaOCl. Samples were then randomly divided into three experimental and two control groups. Group 1 was irrigated with saline followed by 2% chlorhexidine gluconate (CHX). Group 2 was irrigated with 50% citric acid (CA) followed by 2% CHX. Group 3 was irrigated with 14% EDTA followed by 2% CHX. The chemical identity and quantification of the PCA in the formed precipitate was determined using gas chromatography/mass spectrometry (GC/MS). RESULTS: All experimental groups contained PCA. The mean level of PCA for group 1 (sterile saline) was 229 ng mL(-1), group 2 (citric acid) 72 ng mL(-1) and group 3 (EDTA) 400 ng mL(-1), respectively. A significant difference was found between the saline and EDTA groups and the negative control (P < 0.05). Although no statistical significance was found between the negative control and citric acid group, PCA was still present in this experimental group. CONCLUSIONS: Citric acid used as the intermittent irrigant had the least amount of PCA formation in the canal system. Until the threshold required to cause biological damage in humans is determined, the combination of NaOCl and CHX in root canal treatment should be avoided.
Asunto(s)
Compuestos de Anilina/análisis , Antiinfecciosos Locales/uso terapéutico , Clorhexidina/uso terapéutico , Cavidad Pulpar/metabolismo , Irrigantes del Conducto Radicular/uso terapéutico , Hipoclorito de Sodio/uso terapéutico , Triptófano Hidroxilasa/antagonistas & inhibidores , Compuestos de Anilina/química , Precipitación Química , Ácido Cítrico/uso terapéutico , Cavidad Pulpar/anatomía & histología , Ácido Edético/uso terapéutico , Cromatografía de Gases y Espectrometría de Masas/métodos , Humanos , Ensayo de Materiales , Preparación del Conducto Radicular/métodos , Cloruro de SodioRESUMEN
Cell proliferation requires the coordinated activity of cytosolic and mitochondrial metabolic pathways to provide ATP and building blocks for DNA, RNA and protein synthesis. Many metabolic pathway genes are targets of the c-myc oncogene and cell-cycle regulator. However, the contribution of c-Myc to the activation of cytosolic and mitochondrial metabolic networks during cell-cycle entry is unknown. Here, we report the metabolic fates of [U-(13)C] glucose in serum-stimulated myc(-/-) and myc(+/+) fibroblasts by (13)C isotopomer NMR analysis. We demonstrate that endogenous c-myc increased (13)C labeling of ribose sugars, purines and amino acids, indicating partitioning of glucose carbons into C1/folate and pentose phosphate pathways, and increased tricarboxylic acid cycle turnover at the expense of anaplerotic flux. Myc expression also increased global O-linked N-acetylglucosamine protein modification, and inhibition of hexosamine biosynthesis selectively reduced growth of Myc-expressing cells, suggesting its importance in Myc-induced proliferation. These data reveal a central organizing function for the Myc oncogene in the metabolism of cycling cells. The pervasive deregulation of this oncogene in human cancers may be explained by its function in directing metabolic networks required for cell proliferation.
Asunto(s)
Ciclo Celular/fisiología , Fibroblastos/metabolismo , Redes y Vías Metabólicas/fisiología , Proteínas Proto-Oncogénicas c-myc/metabolismo , Acetilglucosamina/metabolismo , Animales , Western Blotting , Isótopos de Carbono , Ciclo Celular/genética , Línea Celular , Cromatografía Líquida de Alta Presión , Ciclo del Ácido Cítrico , Medios de Cultivo/farmacología , Fibroblastos/citología , Fibroblastos/efectos de los fármacos , Glucosa/metabolismo , Ácido Glutámico/metabolismo , Glucólisis , Espectroscopía de Resonancia Magnética , Redes y Vías Metabólicas/genética , Mitocondrias/metabolismo , Mutación , N-Acetilglucosaminiltransferasas/metabolismo , Oxidación-Reducción/efectos de los fármacos , Fosforilcolina/metabolismo , Procesamiento Proteico-Postraduccional , Proteínas Proto-Oncogénicas c-myc/genética , Ratas , Literatura de Revisión como Asunto , Espectrometría de Masas en TándemAsunto(s)
Aminoácidos Diaminos/metabolismo , Corteza Cerebral/metabolismo , Neurotoxinas/metabolismo , Anciano , Anciano de 80 o más Años , Aminoácidos Diaminos/análisis , Autopsia , Cromatografía Líquida de Alta Presión , Toxinas de Cianobacterias , Enfermedades Endémicas , Femenino , Guam/epidemiología , Humanos , Espectroscopía de Resonancia Magnética , Masculino , Persona de Mediana Edad , Neurotoxinas/análisis , Enfermedad de Parkinson/epidemiología , Enfermedad de Parkinson/metabolismo , Técnica de Dilución de Radioisótopos , Washingtón/epidemiologíaRESUMEN
Mammalian secreted phospholipases A(2) (sPLA2s) comprise a group of at least eight enzymes, including the recently identified group X sPLA2. A bacterial expression system was developed to produce human group X sPLA2 (hGX). Inhibition studies show that the sPLA2 inhibitor LY311727 binds modestly more tightly to human group IIA sPLA2 than to hGX and that a pyrazole-based inhibitor of group IIA sPLA2 is much less active against hGX. The phospholipid head group preference of vesicle-bound hGX was determined. hGX binds tightly to phosphatidylcholine vesicles, which is thought to be required to act efficiently on cells. Tryptophan 67 hGX makes a significant contribution to interfacial binding to zwitterionic vesicles. As little as 10 ng/ml hGX releases arachidonic acid for cyclooxygenase-2- dependent prostaglandin E(2) generation when added exogenously to adherent mammalian cells. In contrast, human group IIA, rat group V, and mouse group IB sPLA2s are virtually inactive at releasing arachidonate when added exogenously to adherent cells. Dislodging cells from the growth surface enhances the ability of all the sPLA2s to release fatty acids. Studies with CHO-K1 cell mutants show that binding of sPLA2s to glycosaminoglycans is not the basis for poor plasma membrane hydrolysis by group IB, IIA, and V sPLA2s.
Asunto(s)
Ácido Araquidónico/metabolismo , Fosfolipasas A/metabolismo , Animales , Células CHO , Adhesión Celular , Cricetinae , Fosfolipasas A2 Grupo II , Humanos , Isoenzimas/metabolismo , Ratones , Unión Proteica , Ratas , Especificidad por SustratoRESUMEN
As recombinant viruses expressing scorpion toxins are moving closer toward the market, it is important to obtain large amounts of pure toxin for biochemical characterization and the evaluation of biological activity in nontarget organisms. In the past, we purified a large amount of Androctonus australis anti-insect toxin (AaIT) present in the venom of A. australis with an analytical reversed-phase column by repeated runs of crude sample. We now report 20 times improved efficiency and speed of the purification by employing a preparative reversed-phase column. In just two consecutive HPLC steps, almost 1 mg of AaIT was obtained from 70 mg crude venom. Furthermore, additional AaIT was obtained from side fractions in a second HPLC run. Recently discovered insect selective toxin, AaIT5, was isolated simultaneously from the same venom batch. It shows different biological toxicity symptoms than the known excitatory and depressant insect toxins. AaIT5 gave 100% mortality with a dose of less than 1.3 micrograms against fourth-instar tobacco budworms Heliothis virescens 24 h after injection. During the purification process, we implemented mass spectrometry in addition to bioassays to monitor the presence of AaIT and AaIT5 in the HPLC fractions. Mass spectrometric screening can unambiguously follow the purification process and can greatly facilitate and expedite the downstream purification of AaIT and AaIT5 eliminating the number of bioassays required. Further, electrospray ionization was compared with matrix-assisted desorption/ionization and evaluated as a method of choice for mass spectrometric characterization of fractions from the venom purification for it provided higher mass accuracy and relative quantitation capability. Molecular models were built for AaIT5, excitatory toxin AaIT4, and depressant toxin LqhIT2. Three-dimensional structure of AaIT5 was compared with structures of the other two toxins, suggesting that AaIT5 is similar to depressant toxins.