Antimutagenic and free radical scavenger effects of leaf extracts from Accacia salicina

<p>Abstract</p> <p>Background</p> <p>Three extracts were prepared from the leaves of <it>Accacia salicina</it>; ethyl acetate (EA), chloroform (Chl) and petroleum ether (PE) extracts and was designed to examine antimutagenic, antioxidant potenty and oxidative DNA damage protecting activity.</p> <p>Methods</p> <p>Antioxidant activity of <it>A. salicina </it>extracts was determined by the ability of each extract to protect against plasmid DNA strand scission induced by hydroxyl radicals. An assay for the ability of these extracts to prevent mutations induced by various oxidants in <it>Salmonella typhimurium </it>TA102 and TA 104 strains was conducted. In addition, nonenzymatic methods were employed to evaluate anti-oxidative effects of tested extracts.</p> <p>Results</p> <p>These extracts from leaf parts of <it>A. salicina </it>showed no mutagenicity either with or without the metabolic enzyme preparation (S9). The highest protections against methylmethanesulfonate induced mutagenicity were observed with all extracts and especially chloroform extract. This extract exhibited the highest inhibitiory level of the Ames response induced by the indirect mutagen 2- aminoanthracene. All extracts exhibited the highest ability to protect plasmid DNA against hydroxyl radicals induced DNA damages. The ethyl acetate (EA) and chloroform (Chl) extracts showed with high TEAC values radical of 0.95 and 0.81 mM respectively, against the ABTS^.+.</p> <p>Conclusion</p> <p>The present study revealed the antimutagenic and antioxidant potenty of plant extract from <it>Accacia salicina </it>leaves.</p

Evidence of spinal stiffening following fusionless bipolar fixation for neuromuscular scoliosis: a shear wave elastography assessment of lumbar annulus fibrosus

Objectives There are no established criteria for stiffness after fusionless surgery for neuromuscular scoliosis (NMS). As a result, there is no consensus regarding the surgical strategy to propose at long-term follow-up. This study reports the first use of shear wave elastography for assessing the mechanical response of lumbar intervertebral discs (IVDs) after fusionless bipolar fixation (FBF) for NMS and compares them with healthy controls. The aim was to acquire evidence from the stiffness of the spine following FBF. Patients and methods Nineteen NMS operated on with FBF (18 ± 2y at last follow-up, 6 ± 1 y after surgery) were included prospectively. Preoperative Cobb was 89 ± 20° and 35 ± 1° at latest follow-up. All patients had reached skeletal maturity. Eighteen healthy patients (20 ± 4 y) were also included. Shear wave speed (SWS) was measured in the annulus fibrosus of L3L4, L4L5 and L5S1 IVDs and compared between the two groups. A measurement reliability was performed. Results In healthy subjects, average SWS (all disc levels pooled) was 7.5 ± 2.6 m/s. In NMS patients, SWS was significantly higher at 9.9 ± 1.4 m/s (p < 0.05). Differences were significant between L3L4 (9.3 ± 1.8 m/s vs. 7.0 ± 2.5 m/s, p = 0.004) and L4L5 (10.3 ± 2.3 m/s vs. 7.1 ± 1.1 m/s, p = 0.0006). No difference was observed for L5S1 (p = 0.2). No correlation was found with age at surgery, Cobb angle correction and age at the SWE measurement. Conclusions This study shows a significant increase in disc stiffness at the end of growth for NMS patients treated by FBF. These findings are a useful adjunct to CT-scan in assessing stiffness of the spine allowing the avoidance of surgical final fusion at skeletal maturity

Polar extracts from (Tunisian) Acacia salicina Lindl. Study of the antimicrobial and antigenotoxic activities

<p>Abstract</p> <p>Background</p> <p>Methanolic, aqueous and Total Oligomer Flavonoids (TOF)-enriched extracts obtained from the leaves of <it>Acacia salicina </it>'Lindl.' were investigated for antibacterial, antimutagenic and antioxidant activities.</p> <p>Methods</p> <p>The antimicrobial activity was tested on the Gram positive and Gram negative reference bacterial strains. The Mutagenic and antimutagenic activities against direct acting mutagens, methylmethane sulfonate (MMS) and 4-nitro-o-phenylenediamine (NOPD), and indirect acting mutagens, 2-aminoanthracene (2-AA) and benzo[a]pyrene (B(a)P) were performed with <it>S. typhimurium </it>TA102 and TA98 assay systems. In addition, the enzymatic and nonenzymatic methods were employed to evaluate the anti-oxidative effects of the tested extracts.</p> <p>Results</p> <p>A significant effect against the Gram positive and Gram negative reference bacterial strains was observed with all the extracts. The mutagenic and antimutagenic studies revealed that all the extracts decreased the mutagenicity induced by B(a)P (7.5 μg/plate), 2-AA (5 μg/plate), MMS (1.3 mg/plate) and NOPD (10 μg/plate). Likewise, all the extracts showed an important free radical scavenging activity towards the superoxide anion generated by the xanthine/xanthine oxidase assay system, as well as high Trolox Equivalent Antioxidant Capacity (TEAC), against the 2,2'-azino-bis(3-ethylbenzothiazoline-6-sulfonic acid) diammonium salt (ABTS)⁺• radical. TOF-enriched extract exhibited the highest protective effect against free radicals, direct acting-mutagen and metabolically activated S9-dependent mutagens.</p> <p>Conclusions</p> <p>The present study indicates that the extracts from <it>A. salicina </it>leaves are a significant source of compounds with the antimutagenic and antioxidant activities, and this may be useful for developing potential chemopreventive substances.</p

In vitro mutagenicity of Acid Violet 7 and its degradation products by Pseudomonas putida mt-2: Correlation with chemical structures

International audienceAcid Violet 7 (AV7), a very important commercial azo dye used in the textile, food, paper and cosmetic industries, was degraded by Pseudomonas putida mt-2 at a concentration up to 200mg/l. HPLC analysis of the biodegradation media revealed the presence of either 4'-aminoacetanilide (4'-AA) or 5-acetamido-2-amino-1-hydroxy-3,6-naphthalene disulfonic acid (5-ANDS) deriving from AV7 azoreduction which attests the expression of an azoreductase by this bacterium. These amines were identified only in media of static incubation, which is consistent with their biotransformation under shaken incubation (aerobic conditions). Pure azo dye, pure azoreduction products and total lyophilized biodegradation extracts were assayed for their mutagenic properties using Ames test. Mutagenicity of AV7 even with or without the S9 metabolizing system increased significantly after static biodegradation and totally disappeared after shaken incubation. In addition, mutagenicity of pure azo reduction products of AV7 was assessed and compared with that of the parent unsubstituted amines. 4'-AA exhibited a strong mutagenicity which was imputed to the presence of the acetoxy (COCH(3)) substituent on the aromatic amine; however, the presence of sulphonic groups in 5-ANDS limited its mutagenicity

Evaluation of genotoxicity and pro-oxidant effect of the azo dyes: Acids yellow 17, violet 7 and orange 52, and of their degradation products by Pseudomonas putida mt-2

International audienceAcids yellow 17, violet 7 and orange 52, very important commercial azo dyes used in the textile, food, paper and cosmetic industries, were degraded by Pseudomonas putida mt-2 at concentrations up to 100mg/l. The culture media was completely decolorized under static incubation for 60 h, this faster than under continuous shaking incubation. SOS chromotest using Escherichia coli PQ37, with and without metabolic activation (S-9 preparations), was used to assess genotoxicity potential of these dyes before and after biodegradation. None of these dyes or their metabolites was found to be genotoxic in the absence of "Araclor-Induced rat liver microsome" preparations (S-9). However, in presence of the preparation S-9, the genotoxicity of the biodegradation products was highlighted. Metabolites resulting from static cultures were more genotoxic than those obtained in shaken conditions. In addition to genotoxic effects, metabolites have shown a significant ability to induce the formation of superoxide free radical anion (O(2)(*-)). The toxicities generated by the pure azo dyes and the pure azo-reduction products (sulfanilic acid, N,N'-dimethyl-p-phenylenediamine and 4'-aminoacetanilid) were compared. These results suggest that P. putida mt-2 degrades the studied azo dyes in two steps: an azo-reduction followed by an oxygen-dependent metabolization. Some of the derived metabolites would be responsible of genotoxicity and metabolic toxicity

Influence of the chemical structure on the biodegradability of acids yellow 17, violet 7 and orange 52 by Pseudomonas putida

International audienceIn the present study, the textiles azo dyes acids orange 52 (AO52), yellow 17 (AY17) and violet 7 (AV7) were degraded byPseudomonas putida mt-2 in mineral medium at concentration up to 100 mg/l. The culture media were completely (case of AO52) or partially (case of AY17 and AV7) decolourised under static incubation, this faster than under continuous shaking incubation. Decolourisation kinetic by intact cells indicated that AO52 disappeared completely and faster than the two other azo dyes. To understand the differentiated action of this bacterium on the three dyes, cell-free extracts activity was assessed and compared for each couple of dyes “inductor-substrate”. Results showed the same halfsaturation constant Km for a given dye as a substrate whatever the dye inductor, from where the assumption of a same protein with nonspecific azoreductase activity. The enzyme showed slightly more affinity for AO52 than for AY17 and AV7, but especially weaker specific activities against these two last dyes independently of the inductor. Finally, AO52 would be the best azoreductase inductor among the three tested dyes. These results indicated that the level as well the induction as the specificity of the azoreductase activity seems to be strongly dependent on the chemical structure of the dyes

Les colorants textiles sources de contamination de l’eau : CRIBLAGE de la toxicité et des méthodes de traitement

Les colorants sont largement utilisés dans les imprimeries, les produits alimentaires, cosmétiques et cliniques, mais en particulier dans les industries textiles pour leur stabilité chimique et la facilité de leur synthèse et leur variété de couleurs. Cependant, ces colorants sont à l’origine de la pollution une fois évacués dans l’environnement. La production mondiale des colorants est estimée à plus de 800 000 t•an-1 et les colorants azoïques sont majoritaires et représentent 60-70 %. Compte tenu de la composition très hétérogène de ces derniers, leur dégradation conduit souvent à la conception d’une chaîne de traitement physique-chimique et biologique assurant l’élimination des différents polluants par étapes successives. Dés études ont montré que plusieurs colorants azoïques sont toxiques et mutagènes et le traitement biologique de ces colorants semble présenter un intérêt scientifique majeur. Les traitements physico-chimiques communs (adsorption, coagulation/floculation, précipitation etc.) sont couramment utilisés pour les effluents industriels. Malgré leur rapidité, ces méthodes se sont avérées peu efficaces compte tenu des normes exigées sur ces rejets. Le traitement biologique constitue une alternative fiable; en effet, plusieurs microorganismes sont capables de transformer les colorants azoïques en sous-produits incolores. Les bactéries dégradent les colorants azoïques en deux étapes : un clivage de liaison azo, par l’intermédiaire de l’azoréductase, suivi d’une oxydation des amines aromatiques formées lors de la première étape. L’azoréduction constitue alors une étape clé du traitement des effluents chargés de ces colorants.Dyes are widely used for industrial, printing, food, cosmetic and clinical purposes as well as textile dyeing because of their chemical stability, ease of synthesis, and versatility. Their stability, however, causes pollution once the dyes are released into the environment in effluents. More than 800,000 tons of dyes are annually produced worldwide, of which 60 to 70% are azo dyes. Considering the heterogeneous composition of these latter dyes, their degradation usually requires a chain of physical, chemical and biological treatments assuring the elimination of different pollutants in successive steps. In addition, some azo dyes are toxic and mutagenic and thus the biological treatment of these dyes is now of major scientific interest. Physical-chemical treatments (adsorption, coagulation/flocculation precipitation, etc.) are usually used for industrial effluents. In spite of their rapidity, these methods have turned out to be ineffective in attaining the standards required for these discharges. As a viable alternative, biological processes are receiving increasing interest owing to their cost effectiveness and their ability to produce less sludge. It has been found that some microorganisms can transform azo dyes into colourless products. Bacterial degradation of azo dyes is often initiated by an enzymatic biotransformation step that involves cleavage of azo linkages with the aid of an azoreductase and an electron donor. As the azoreductase in some microorganisms can catalyze the reductive cleavage of azo groups, they have potential advantages in developing bio-treatment methods of wastewater containing azo compounds

Comet assay with gill cells of Mytilus galloprovincialis end point tools for biomonitoring of water antibiotic contamination

International audienc