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1.
Benef Microbes ; 9(4): 629-641, 2018 Jun 15.
Article in English | MEDLINE | ID: mdl-29695181

ABSTRACT

We evaluated the effect of oral administration of Bifidobacterium animalis subsp. lactis CECT 8145 strain in Zücker fatty rats. The Zücker fatty rats were randomly divided into two groups (n=10 each) and administered either B. animalis subsp. lactis CECT 8145 (1010 cfu/day) suspended in skim milk, or skim milk alone (control group). Each treatment was administered in drinking bottles from week 5 until week 17 of age. A lean Zücker rat group (standard group) was included to provide normal values for the Zücker strain. This group was administered skim milk in the drinking bottle for the same experimental period as Zücker fatty rats. Body weight gain was greater in the fatty control group than in the fatty rats treated daily with B. animalis subsp. lactis CECT 8145. Furthermore, dry and liquid food intake significantly decreased in the treated Zücker fatty group and these rats also showed decreased plasma ghrelin levels as compared with the Zücker fatty control group. B. animalis subsp. lactis CECT 8145 intake also decreased plasma tumour necrosis factor-α (a proinflammatory cytokine) and plasma malondialdehyde (a biomarker of oxidative stress). Moreover, the ratio plasma total cholesterol/plasma cholesterol transported by high-density lipoproteins, considered as an index for cardiovascular disease, also significantly decreased in the Zücker fatty rats treated with B. animalis subsp. lactis CECT 8145. By contrast, this bacterial strain significantly increased plasma adiponectin (an insulin-sensitising adipokine), but did not produce significant effects on triglyceride levels or glucose metabolism biomarkers. Although further research is required to confirm B. animalis subsp. lactis CECT 8145 is an efficient anti-obesity treatment in humans, the results obtained in this study are promising and point to the health and anti-obesity properties of this bacterial strain.


Subject(s)
Bifidobacterium animalis , Obesity/therapy , Probiotics/pharmacology , Animals , Appetite Depressants/pharmacology , Disease Models, Animal , Eating/drug effects , Ghrelin/blood , Glucose/metabolism , Humans , Lipid Metabolism , Male , Malondialdehyde/blood , Obesity/microbiology , Probiotics/administration & dosage , Rats , Rats, Zucker , Tumor Necrosis Factor-alpha/blood , Weight Gain/drug effects
2.
Benef Microbes ; 8(2): 193-206, 2017 Apr 26.
Article in English | MEDLINE | ID: mdl-28343402

ABSTRACT

The objective of this study is to analyse the effect of the ingestion of two selected antioxidant probiotics strains (Lactobacillus rhamnosus CECT8361 and Bifidobacterium longum CECT7347) on sperm quality parameters in asthenozoospermic males after three and six weeks of administration. Nine asthenozoospermic men without any medical treatment under similar diet conditions participated in the study. The quality of individual sperm samples was evaluated before (previous to ingestion), during (after 3 and 6 weeks of ingestion) and after probiotic administration (3 and 6 weeks after finishing the treatment). Sperm motility was evaluated by computer-assisted sperm analysis system, DNA fragmentation by sperm chromatin structure assay, cell viability by flow cytometry and measurement of intracellular H2O2 (reactive oxygen species; ROS) by flow cytometry using dichloro-dihydrofluorescein diacetate. Sperm motility was drastically improved after the treatment (approximately 6 fold change), DNA fragmentation was statistically reduced after probiotic administration from (approximately 1.2 fold change) and intracellular H2O2 level was decreased (approximately 3.5 fold change). Cell viability was not affected by the treatment. The significant improvement in sperm motility and the decrease in DNA fragmentation reported in this study provide preliminary evidence that probiotics could be administrated to improve motility and decrease DNA fragmentation and ROS levels in asthenozoospermic human males.


Subject(s)
Asthenozoospermia/therapy , Bifidobacterium longum , Lacticaseibacillus rhamnosus , Probiotics/therapeutic use , Semen Analysis , Sperm Motility/drug effects , Cell Survival/drug effects , Chromatin/physiology , DNA Fragmentation/drug effects , Humans , Hydrogen Peroxide/analysis , Male
3.
Benef Microbes ; 7(1): 83-93, 2016 Feb.
Article in English | MEDLINE | ID: mdl-26565081

ABSTRACT

Inflammatory bowel diseases (IBDs) are complex affections with increasing incidence worldwide. Multiple factors are involved in the development and maintenance of the symptoms including enhanced oxidative stress in intestinal mucosa. The conventional therapeutic approaches for IBDs are based on the use anti-inflammatory drugs with important collateral effects and partial efficacy. In the present work we tested the anti-inflammatory capacity of Kluyveromyces marxianus CIDCA 8154 in different models. In vitro, we showed that the pretreatment of epithelial cells with the yeast reduce the levels of intracellular reactive oxygen species. Furthermore, in a murine model of trinitro benzene sulfonic acid-induced colitis, yeast-treated animals showed a reduced histopathological score (P<0.05) and lower levels of circulating interleukin 6 (P<0.05). The capacity to modulate oxidative stress in vivo was assessed using a Caenorhabditis elegans model. The yeast was able to protect the nematodes from oxidative stress by modulating the SKN-1 transcription factor trough the DAF-2 pathway. These results indicate that K. marxianus CIDCA 8154 could control the intestinal inflammation and cellular oxidative stress. Deciphering the mechanisms of action of different probiotics might be useful for the rational formulation of polymicrobial products containing microorganisms targeting different anti-inflammatory pathways.


Subject(s)
Anti-Inflammatory Agents, Non-Steroidal/pharmacology , Colitis/prevention & control , Kluyveromyces , Oxidative Stress , Probiotics/pharmacology , Animals , Caco-2 Cells , Caenorhabditis elegans , HT29 Cells , Humans , Male , Mice , Mice, Inbred BALB C , Reactive Oxygen Species/metabolism
4.
Food Microbiol ; 50: 5-11, 2015 Sep.
Article in English | MEDLINE | ID: mdl-25998809

ABSTRACT

The aim of this study was to evaluate the effect of two antimicrobial substances, carvacrol and citral, on Listeria monocytogenes and Listeria innocua cells, as well as possible virulence changes in injured cells, using Caenorhabditis elegans as a model test. The results indicated that the percentage of sublethal damage was higher in L. monocytogenes than in L. innocua. The results of the study carried out by using C. elegans indicated that C. elegans fed in a lawn of L. monocytogenes previously treated with carvacrol showed a loss in life span (p ≤ 0.05) as compared with L. monocytogenes treated with citral, Escherichia coli OP50 as a negative control, and treated and untreated L. innocua. Egg laying was also affected: worms fed in a lawn of treated and untreated L. monocytogenes laid fewer eggs than those fed in a lawn of treated and untreated L. innocua or fed with OP50 as a negative control. Worms fed in a lawn of treated and untreated L. innocua also laid fewer eggs than those fed with OP50 as a negative control. A phenotype named bag of worms and an undescribed new one, "vulva inflammation", were also observed.


Subject(s)
Anti-Bacterial Agents/pharmacology , Caenorhabditis elegans/microbiology , Listeria monocytogenes/drug effects , Listeria/drug effects , Monoterpenes/pharmacology , Acyclic Monoterpenes , Animals , Caenorhabditis elegans/drug effects , Caenorhabditis elegans/physiology , Cymenes , Escherichia coli/drug effects , Escherichia coli/pathogenicity , Listeria/pathogenicity , Listeria monocytogenes/pathogenicity , Models, Animal , Oviposition/drug effects , Phenotype , Virulence
5.
Genome Announc ; 2(2)2014 Mar 27.
Article in English | MEDLINE | ID: mdl-24675853

ABSTRACT

Bifidobacterium animalis subsp. lactis strain CECT 8145 is able to reduce body fat content and improve metabolic syndrome biomarkers. Here, we report the draft genome sequence of this strain, which may provide insights into its safety status and functional role.

6.
Appl Environ Microbiol ; 77(4): 1335-43, 2011 Feb.
Article in English | MEDLINE | ID: mdl-21169430

ABSTRACT

Helicobacter pylori is considered one of the major risk factors underlying the development of gastritis and gastric and duodenal ulcers. Moreover, 50% of the population carries this bacterium, and consequently, when it is detected, eradication of H. pylori is strongly recommended. Regarding the use of probiotics as functional agents, several studies have shown that there is a direct relationship between the addition of certain probiotic bacteria and in vitro inhibition of H. pylori; however, in vivo studies showing bifidobacterial activity against H. pylori remain scarce. In this study, a Bifidobacterium bifidum strain which proved active in vitro against H. pylori has been isolated, with inhibition levels reaching 81.94% in the case of the supernatant and even 94.77% inhibition for supernatant purified by cationic exchange followed by an inverse phase. In vivo studies using a BALB/c mouse model have proved that this strain partially relieves damage to gastric tissues caused by the pathogen and also decreases the H. pylori pathogenicity ratio. This novel strain fulfills the main properties required of a probiotic (resistance to gastrointestinal juices, biliary salts, NaCl, and low pH; adhesion to intestinal mucus; and sensitivity to antibiotics). Furthermore, the absence of undesirable metabolites has been demonstrated, and its food safety status has been confirmed by acute ingestion studies in mice. In summary, the results presented here demonstrate that Bifidobacterium bifidum CECT 7366 can be considered a probiotic able to inhibit H. pylori both in vitro and in vivo.


Subject(s)
Antibiosis , Bifidobacterium/physiology , Helicobacter Infections/therapy , Helicobacter pylori/physiology , Probiotics , Animals , Base Sequence , Bifidobacterium/classification , Bifidobacterium/isolation & purification , Gastrointestinal Diseases/microbiology , Gastrointestinal Diseases/therapy , Gastrointestinal Diseases/veterinary , Helicobacter Infections/microbiology , Helicobacter pylori/pathogenicity , Intestinal Mucosa/microbiology , Mice , Molecular Sequence Data , Polymerase Chain Reaction , RNA, Ribosomal, 16S/genetics , Sequence Analysis, DNA , Sequence Analysis, RNA
7.
Gac Med Mex ; 116(5): 197-9, 1980 May.
Article in Spanish | MEDLINE | ID: mdl-7192229

Subject(s)
Violence , Humans
8.
Gac Med Mex ; 116(5): 210-2, 1980 May.
Article in Spanish | MEDLINE | ID: mdl-7192232

Subject(s)
Violence , Humans
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