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Additive antifungal activity of anidulafungin and human neutrophils against Candida parapsilosis biofilms 2011 Laboratory of Infectious Diseases, 3rd Department of Pediatrics, Aristotle University, Hippokration Hospital, 54642 Thessaloniki, Greece.
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Journal Article
Periodical, Full
The Journal of antimicrobial chemotherapy
Periodical, Abbrev.
J.Antimicrob.Chemother.
Pub Date Free Form
Mar
Volume
66
Issue
3
Start Page
588
Other Pages
591
Notes
LR: 20130527; JID: 7513617; 0 (Antifungal Agents); 0 (Echinocandins); 0 (Tetrazolium Salts); 0 (Triazoles); 117038-70-7 (2,3-bis(2-methoxy-4-nitro-5-sulfophenyl)-5-((phenylamino)carbonyl)-2H-tetrazoliu m hydroxide); 9HLM53094I (anidulafungin); 2010/12/07
Place of Publication
England
ISSN/ISBN
1460-2091; 0305-7453
Accession Number
PMID: 21138910
Language
eng
SubFile
Journal Article; Research Support, Non-U.S. Gov't; IM
DOI
10.1093/jac/dkq466 [doi]
Output Language
Unknown(0)
PMID
21138910
Abstract
OBJECTIVES: To investigate the activities of two newer triazoles and two echinocandins combined with human phagocytes against Candida parapsilosis biofilms. METHODS: An in vitro model of C. parapsilosis biofilms was used. Biofilms were grown on silicone elastomer discs in 96-well plates at 37 degrees C for 72 h. Biofilms or planktonic cells were incubated with voriconazole, posaconazole, caspofungin or anidulafungin, at clinically relevant concentrations, and human phagocytes (neutrophils or monocytes) alone or in combination with each of the antifungal agents for a further 22 h. Fungal damage induced by antifungal agents and/or phagocytes was determined by XTT [2,3-bis(2-methoxy-4-nitro-5-sulfophenyl)2H-tetrazolium-5-carboxanilide] metabolic assay. RESULTS: Each of the antifungal agents alone and in combination with human phagocytes induced less damage against C. parapsilosis biofilms compared with planktonic cells. No antagonistic interactions between antifungal agents and phagocytes were found. Furthermore, anidulafungin, but not caspofungin, and neutrophils exerted additive activity against C. parapsilosis biofilms. CONCLUSIONS: Besides a lack of antagonistic interactions between newer antifungal agents and phagocytes, anidulafungin exerts additive immunopharmacological activity against C. parapsilosis biofilms.
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Database
Publisher
Data Source
Authors
Katragkou,A., Chatzimoschou,A., Simitsopoulou,M., Georgiadou,E., Roilides,E.
Original/Translated Title
URL
Date of Electronic
20101207
PMCID
Editors
Caspofungin at catheter lock concentrations eradicates mature biofilms of Candida lusitaniae and Candida guilliermondii 2014 Laboratory of Infectious Diseases, 3rd Department of Pediatrics, Faculty of Medicine, Aristotle University School of Health Sciences, Hippokration Hospital, Thessaloniki, Greece.; Laboratory of Infectious Diseases, 3rd Department of Pediatrics, Faculty of
Source Type
Print(0)
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Journal Article
Periodical, Full
Antimicrobial Agents and Chemotherapy
Periodical, Abbrev.
Antimicrob.Agents Chemother.
Pub Date Free Form
Aug
Volume
58
Issue
8
Start Page
4953
Other Pages
4956
Notes
LR: 20150201; CI: Copyright (c) 2014; JID: 0315061; 0 (Antifungal Agents); 0 (Echinocandins); 0 (Lipopeptides); 0 (liposomal amphotericin B); 7XU7A7DROE (Amphotericin B); 9HLM53094I (anidulafungin); F0XDI6ZL63 (caspofungin); R10H71BSWG (micafungin); OID:
Place of Publication
United States
ISSN/ISBN
1098-6596; 0066-4804
Accession Number
PMID: 24890585
Language
eng
SubFile
Journal Article; Research Support, Non-U.S. Gov't; IM
DOI
10.1128/AAC.03117-14 [doi]
Output Language
Unknown(0)
PMID
24890585
Abstract
The antibiofilm activities of caspofungin, anidulafungin, micafungin, and liposomal amphotericin B were studied against Candida lusitaniae, Candida guilliermondii, and a Candida albicans control strain. While anidulafungin and micafungin (0.007 to 2,048 mg/liter) showed reduced activity against biofilms of both test species, caspofungin displayed concentration-dependent antibiofilm activity, reaching complete and persistent eradication at concentrations achievable during lock therapy (512 to 2,048 mg/liter, P
Descriptors
Links
Book Title
Database
Publisher
American Society for Microbiology. All Rights Reserved
Data Source
Authors
Simitsopoulou,M., Kyrpitzi,D., Velegraki,A., Walsh,T.J., Roilides,E.
Original/Translated Title
URL
Date of Electronic
20140602
PMCID
PMC4136003
Editors
Differential activities of newer antifungal agents against Candida albicans and Candida parapsilosis biofilms 2008 Laboratory of Infectious Diseases, Third Department of Pediatrics, Aristotle University, Hippokration Hospital, 54642 Thessaloniki, Greece.
Source Type
Print(0)
Ref Type
Journal Article
Periodical, Full
Antimicrobial Agents and Chemotherapy
Periodical, Abbrev.
Antimicrob.Agents Chemother.
Pub Date Free Form
Jan
Volume
52
Issue
1
Start Page
357
Other Pages
360
Notes
LR: 20140904; JID: 0315061; 0 (Antifungal Agents); 0 (Azoles); 0 (Echinocandins); OID: NLM: PMC2223899; 2007/10/15 [aheadofprint]; ppublish
Place of Publication
United States
ISSN/ISBN
0066-4804; 0066-4804
Accession Number
PMID: 17938192
Language
eng
SubFile
Journal Article; Research Support, Non-U.S. Gov't; IM
DOI
AAC.00856-07 [pii]
Output Language
Unknown(0)
PMID
17938192
Abstract
The activities of voriconazole, posaconazole, caspofungin, and anidulafungin against Candida albicans and Candida parapsilosis biofilms were evaluated. In contrast to planktonic cells, the MICs for voriconazole and posaconazole for the biofilms of the two species were high (>or=256 and >64 mg/liter, respectively) but relatively low for the echinocandins caspofungin and anidulafungin (<or=1 and <or=2 mg/liter, respectively).
Descriptors
Antifungal Agents/pharmacology, Azoles/pharmacology, Biofilms/drug effects, Candida/classification/drug effects, Candida albicans/drug effects, Echinocandins/pharmacology, Humans, Microbial Sensitivity Tests
Links
Book Title
Database
Publisher
Data Source
Authors
Katragkou,A., Chatzimoschou,A., Simitsopoulou,M., Dalakiouridou,M., Diza-Mataftsi,E., Tsantali,C., Roilides,E.
Original/Translated Title
URL
Date of Electronic
20071015
PMCID
PMC2223899
Editors
Diversity, dynamics, and activity of bacterial communities during production of an artisanal Sicilian cheese as evaluated by 16S rRNA analysis 2002 Laboratory of Microbiology, Department of Agrotechnology and Food Sciences, Wageningen University, 6703 CT Wageningen, The Netherlands.
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Print(0)
Ref Type
Journal Article
Periodical, Full
Applied and Environmental Microbiology
Periodical, Abbrev.
Appl.Environ.Microbiol.
Pub Date Free Form
Apr
Volume
68
Issue
4
Start Page
1882
Other Pages
1892
Notes
LR: 20140612; JID: 7605801; 0 (DNA, Bacterial); 0 (RNA, Ribosomal, 16S); OID: NLM: PMC123848; ppublish
Place of Publication
United States
ISSN/ISBN
0099-2240; 0099-2240
Accession Number
PMID: 11916708
Language
eng
SubFile
Journal Article; Research Support, Non-U.S. Gov't; IM
DOI
Output Language
Unknown(0)
PMID
11916708
Abstract
The diversity and dynamics of the microbial communities during the manufacturing of Ragusano cheese, an artisanal cheese produced in Sicily (Italy), were investigated by a combination of classical and culture-independent approaches. The latter included PCR, reverse transcriptase-PCR (RT-PCR), and denaturing gradient gel electrophoresis (DGGE) of 16S rRNA genes (rDNA). Bacterial and Lactobacillus group-specific primers were used to amplify the V6 to V8 and V1 to V3 regions of the 16S rRNA gene, respectively. DGGE profiles from samples taken during cheese production indicated dramatic shifts in the microbial community structure. Cloning and sequencing of rDNA amplicons revealed that mesophilic lactic acid bacteria (LAB), including species of Leuconostoc, Lactococcus lactis, and Macrococcus caseolyticus were dominant in the raw milk, while Streptococcus thermophilus prevailed during lactic fermentation. Other thermophilic LAB, especially Lactobacillus delbrueckii and Lactobacillus fermentum, also flourished during ripening. Comparison of the rRNA-derived patterns obtained by RT-PCR to the rDNA DGGE patterns indicated a substantially different degree of metabolic activity for the microbial groups detected. Identification of cultivated LAB isolates by phenotypic characterization and 16S rDNA analysis indicated a variety of species, reflecting to a large extent the results obtained from the 16S rDNA clone libraries, with the significant exception of the Lactobacillus delbrueckii species, which dominated in the ripening cheese but was not detected by cultivation. The present molecular approaches combined with culture can effectively describe the complex ecosystem of natural fermented dairy products, giving useful information for starter culture design and preservation of artisanal fermented food technology.
Descriptors
Cheese/microbiology, Colony Count, Microbial, DNA, Bacterial/analysis, Ecosystem, Electrophoresis, Polyacrylamide Gel/methods, Genetic Variation, Gram-Positive Bacteria/classification/genetics/isolation & purification, Lactobacillus, Leuconostoc, Polymerase Chain Reaction, RNA, Ribosomal, 16S/genetics, Reverse Transcriptase Polymerase Chain Reaction, Sequence Analysis, DNA
Links
Book Title
Database
Publisher
Data Source
Authors
Randazzo,C. L., Torriani,S., Akkermans,A. D., de Vos,W. M., Vaughan,E. E.
Original/Translated Title
URL
Date of Electronic
PMCID
PMC123848
Editors
Influence of geographical origin and flour type on diversity of lactic acid bacteria in traditional Belgian sourdoughs 2007 Laboratory of Microbiology, Department of Biochemistry, Physiology and Microbiology, Ghent University, K. L. Ledeganckstraat 35, B-9000 Ghent, Belgium. Ilse.Scheirlinck@ugent.be
Source Type
Print(0)
Ref Type
Journal Article
Periodical, Full
Applied and Environmental Microbiology
Periodical, Abbrev.
Appl.Environ.Microbiol.
Pub Date Free Form
Oct
Volume
73
Issue
19
Start Page
6262
Other Pages
6269
Notes
LR: 20140904; JID: 7605801; 0 (Bacterial Proteins); 0 (DNA, Bacterial); EC 6.1.1.20 (Phenylalanine-tRNA Ligase); OID: NLM: PMC2075033; 2007/08/03 [aheadofprint]; ppublish
Place of Publication
United States
ISSN/ISBN
0099-2240; 0099-2240
Accession Number
PMID: 17675431
Language
eng
SubFile
Journal Article; Research Support, Non-U.S. Gov't; IM
DOI
AEM.00894-07 [pii]
Output Language
Unknown(0)
PMID
17675431
Abstract
A culture-based approach was used to investigate the diversity of lactic acid bacteria (LAB) in Belgian traditional sourdoughs and to assess the influence of flour type, bakery environment, geographical origin, and technological characteristics on the taxonomic composition of these LAB communities. For this purpose, a total of 714 LAB from 21 sourdoughs sampled at 11 artisan bakeries throughout Belgium were subjected to a polyphasic identification approach. The microbial composition of the traditional sourdoughs was characterized by bacteriological culture in combination with genotypic identification methods, including repetitive element sequence-based PCR fingerprinting and phenylalanyl-tRNA synthase (pheS) gene sequence analysis. LAB from Belgian sourdoughs belonged to the genera Lactobacillus, Pediococcus, Leuconostoc, Weissella, and Enterococcus, with the heterofermentative species Lactobacillus paralimentarius, Lactobacillus sanfranciscensis, Lactobacillus plantarum, and Lactobacillus pontis as the most frequently isolated taxa. Statistical analysis of the identification data indicated that the microbial composition of the sourdoughs is mainly affected by the bakery environment rather than the flour type (wheat, rye, spelt, or a mixture of these) used. In conclusion, the polyphasic approach, based on rapid genotypic screening and high-resolution, sequence-dependent identification, proved to be a powerful tool for studying the LAB diversity in traditional fermented foods such as sourdough.
Descriptors
Bacterial Proteins/analysis/genetics, Bacterial Typing Techniques, Belgium, DNA Fingerprinting, DNA, Bacterial, Fermentation, Flour/classification/microbiology, Genetic Variation, Geography, Lactobacillus/classification/genetics/isolation & purification, Phenylalanine-tRNA Ligase/genetics
Links
Book Title
Database
Publisher
Data Source
Authors
Scheirlinck,I., Van der Meulen,R., Van Schoor,A., Vancanneyt,M., De Vuyst,L., Vandamme,P., Huys,G.
Original/Translated Title
URL
Date of Electronic
20070803
PMCID
PMC2075033
Editors
Taxonomic structure and stability of the bacterial community in belgian sourdough ecosystems as assessed by culture and population fingerprinting 2008 Laboratory of Microbiology, Ghent University, K.L. Ledeganckstraat 35, 9000 Ghent, Belgium. ilse.scheirlinck@ugent.be
Source Type
Print(0)
Ref Type
Journal Article
Periodical, Full
Applied and Environmental Microbiology
Periodical, Abbrev.
Appl.Environ.Microbiol.
Pub Date Free Form
Apr
Volume
74
Issue
8
Start Page
2414
Other Pages
2423
Notes
LR: 20140904; GENBANK/AM901454; GENBANK/AM901455; GENBANK/AM901456; GENBANK/AM901457; GENBANK/AM901458; GENBANK/AM901459; GENBANK/AM901460; GENBANK/AM901461; GENBANK/AM901462; GENBANK/AM901463; GENBANK/AM901464; GENBANK/AM901465; GENBANK/AM901466; GENBANK
Place of Publication
United States
ISSN/ISBN
1098-5336; 0099-2240
Accession Number
PMID: 18310426
Language
eng
SubFile
Journal Article; Research Support, Non-U.S. Gov't; IM
DOI
10.1128/AEM.02771-07 [doi]
Output Language
Unknown(0)
PMID
18310426
Abstract
A total of 39 traditional sourdoughs were sampled at 11 bakeries located throughout Belgium which were visited twice with a 1-year interval. The taxonomic structure and stability of the bacterial communities occurring in these traditional sourdoughs were assessed using both culture-dependent and culture-independent methods. A total of 1,194 potential lactic acid bacterium (LAB) isolates were tentatively grouped and identified by repetitive element sequence-based PCR, followed by sequence-based identification using 16S rRNA and pheS genes from a selection of genotypically unique LAB isolates. In parallel, all samples were analyzed by denaturing gradient gel electrophoresis (DGGE) of V3-16S rRNA gene amplicons. In addition, extensive metabolite target analysis of more than 100 different compounds was performed. Both culturing and DGGE analysis showed that the species Lactobacillus sanfranciscensis, Lactobacillus paralimentarius, Lactobacillus plantarum, and Lactobacillus pontis dominated the LAB population of Belgian type I sourdoughs. In addition, DGGE band sequence analysis demonstrated the presence of Acetobacter sp. and a member of the Erwinia/Enterobacter/Pantoea group in some samples. Overall, the culture-dependent and culture-independent approaches each exhibited intrinsic limitations in assessing bacterial LAB diversity in Belgian sourdoughs. Irrespective of the LAB biodiversity, a large majority of the sugar and amino acid metabolites were detected in all sourdough samples. Principal component-based analysis of biodiversity and metabolic data revealed only little variation among the two samples of the sourdoughs produced at the same bakery. The rare cases of instability observed could generally be linked with variations in technological parameters or differences in detection capacity between culture-dependent and culture-independent approaches. Within a sampling interval of 1 year, this study reinforces previous observations that the bakery environment rather than the type or batch of flour largely determines the development of a stable LAB population in sourdoughs.
Descriptors
Acetobacter/chemistry/classification/genetics/isolation & purification, Amino Acids/analysis, Belgium, Biodiversity, Carbohydrates/analysis, DNA Fingerprinting, DNA, Bacterial/chemistry/genetics, DNA, Ribosomal/chemistry/genetics, Ecosystem, Electrophoresis, Polyacrylamide Gel, Enterobacteriaceae/chemistry/classification/genetics/isolation & purification, Flour/microbiology, Food Microbiology, Interspersed Repetitive Sequences, Lactobacillus/chemistry/classification/genetics/isolation & purification, Molecular Sequence Data, Nucleic Acid Denaturation, Polymerase Chain Reaction, RNA, Ribosomal, 16S/genetics, Sequence Analysis, DNA
Links
Book Title
Database
Publisher
Data Source
Authors
Scheirlinck,I., Van der Meulen,R., Van Schoor,A., Vancanneyt,M., De Vuyst,L., Vandamme,P., Huys,G.
Original/Translated Title
URL
Date of Electronic
20080229
PMCID
PMC2293155
Editors
Detailed comparison of Candida albicans and Candida glabrata biofilms under different conditions and their susceptibility to caspofungin and anidulafungin 2011 Laboratory of Molecular Cell Biology, Katholieke Universiteit (KU) Leuven, Leuven, Belgium.
Source Type
Print(0)
Ref Type
Journal Article
Periodical, Full
Journal of medical microbiology
Periodical, Abbrev.
J.Med.Microbiol.
Pub Date Free Form
Sep
Volume
60
Issue
Pt 9
Start Page
1261
Other Pages
1269
Notes
LR: 20130527; JID: 0224131; 0 (Antifungal Agents); 0 (Culture Media); 0 (Echinocandins); 0 (Fungal Proteins); 0 (Polystyrenes); 9HLM53094I (anidulafungin); F0XDI6ZL63 (caspofungin); 2011/05/12 [aheadofprint]; ppublish
Place of Publication
England
ISSN/ISBN
1473-5644; 0022-2615
Accession Number
PMID: 21566087
Language
eng
SubFile
Comparative Study; Journal Article; Research Support, Non-U.S. Gov't; IM
DOI
10.1099/jmm.0.032037-0 [doi]
Output Language
Unknown(0)
PMID
21566087
Abstract
Candida biofilm development can be influenced by diverse factors such as substrate, culture medium, carbohydrate source and pH. We have analysed biofilm formation of Candida albicans SC5314 and Candida glabrata ATCC 2001 wild-type strains in the presence of different media (RPMI 1640 versus YNB) and using different pH values (pH 5.6 or 7.0). We determined adhesion and biofilm formation on polystyrene, changes in the expression of adhesin genes during these processes and the susceptibility of mature biofilms to echinocandins. Biofilms formed on polystyrene by both Candida species proved to be influenced strongly by the composition of the medium rather than pH. C. albicans and C. glabrata formed thicker biofilms in RPMI 1640 medium, whereas in YNB medium, both species manifested adhesion rather than characteristic multilayer biofilm architecture. The stimulated biofilm formation in RPMI 1640 medium at pH 7.0 corroborated positively with increased expression of adhesin genes, essential to biofilm formation in vitro, including ALS3 and EAP1 in C. albicans and EPA6 in C. glabrata. The thicker biofilms grown in RPMI 1640 medium were more tolerant to caspofungin and anidulafungin than YNB-grown biofilms. We also observed that mature C. glabrata biofilms were less susceptible in RPMI 1640 medium to echinocandins than C. albicans biofilms. Environmental conditions, i.e. medium and pH, can significantly affect not only biofilm architecture, but also the expression profile of several genes involved during the different stages of biofilm development. In addition, growth conditions may also influence the antifungal-susceptibility profile of fungal populations within biofilm structures. Therefore, before designing any experimental biofilm set-up, it is important to consider the potential influence of external environmental factors on Candida biofilm development.
Descriptors
Links
Book Title
Database
Publisher
Data Source
Authors
Kucharikova,S., Tournu,H., Lagrou,K., Van Dijck,P., Bujdakova,H.
Original/Translated Title
URL
Date of Electronic
20110512
PMCID
Editors
Lung function profiles and aerobic capacity of adult cigarette and hookah smokers after 12 weeks intermittent training 2015 Laboratory of Pharmacology, Faculty of Medicine of Sfax, University of Sfax, Sfax, Tunisia.; Research Unit (EM2S), Higher Institute of Sport and Physical Education of Sfax, University of Sfax, Sfax, Tunisia.; Laboratory of Cardio-Circulatory, Respiratory,
Source Type
Print(0)
Ref Type
Journal Article
Periodical, Full
The Libyan journal of medicine
Periodical, Abbrev.
Libyan J.Med.
Pub Date Free Form
17-Feb
Volume
10
Issue
Start Page
26680
Other Pages
Notes
LR: 20151028; JID: 101299403; CIN: Libyan J Med. 2015;10:27760. PMID: 25920102; CIN: Libyan J Med. 2015;10:27760. PMID: 25906843; OID: NLM: PMC4332739; OTO: NOTNLM; 2015 [ecollection]; 2014/11/19 [received]; 2015/01/17 [revised]; 2015/01/19 [accepted]; ep
Place of Publication
Sweden
ISSN/ISBN
1819-6357; 1819-6357
Accession Number
PMID: 25694204
Language
eng
SubFile
Journal Article; IM
DOI
10.3402/ljm.v10.26680 [doi]
Output Language
Unknown(0)
PMID
25694204
Abstract
INTRODUCTION: Pulmonary function is compromised in most smokers. Yet it is unknown whether exercise training improves pulmonary function and aerobic capacity in cigarette and hookah smokers and whether these smokers respond in a similar way as do non-smokers. AIM: To evaluate the effects of an interval exercise training program on pulmonary function and aerobic capacity in cigarette and hookah smokers. METHODS: Twelve cigarette smokers, 10 hookah smokers, and 11 non-smokers participated in our exercise program. All subjects performed 30 min of interval exercise (2 min of work followed by 1 min of rest) three times a week for 12 weeks at an intensity estimated at 70% of the subject's maximum aerobic capacity (VO2max). Pulmonary function was measured using spirometry, and maximum aerobic capacity was assessed by maximal exercise testing on a treadmill before the beginning and at the end of the exercise training program. RESULTS: As expected, prior to the exercise intervention, the cigarette and hookah smokers had significantly lower pulmonary function than the non-smokers. The 12-week exercise training program did not significantly affect lung function as assessed by spirometry in the non-smoker group. However, it significantly increased both forced expiratory volume in 1 second and peak expiratory flow (PEF) in the cigarette smoker group, and PEF in the hookah smoker group. Our training program had its most notable impact on the cardiopulmonary system of smokers. In the non-smoker and cigarette smoker groups, the training program significantly improved VO2max (4.4 and 4.7%, respectively), v VO2max (6.7 and 5.6%, respectively), and the recovery index (7.9 and 10.5%, respectively). CONCLUSIONS: After 12 weeks of interval training program, the increase of VO2max and the decrease of recovery index and resting heart rate in the smoking subjects indicated better exercise tolerance. Although the intermittent training program altered pulmonary function only partially, both aerobic capacity and life quality were improved. Intermittent training should be advised in the clinical setting for subjects with adverse health behaviors.
Descriptors
Links
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Database
Publisher
Data Source
Authors
Koubaa,A., Triki,M., Trabelsi,H., Masmoudi,L., Zeghal,K.N., Sahnoun,Z., Hakim,A.
Original/Translated Title
URL
Date of Electronic
20150217
PMCID
PMC4332739
Editors
The effect of a 12-week moderate intensity interval training program on the antioxidant defense capability and lipid profile in men smoking cigarettes or hookah: a cohort study 2015 Laboratory of Pharmacology, Sfax Medicine Faculty SMF, Avenue Majida Boulila, 3029 Sfax, Tunisia ; Laboratory of Cardio-Circulatory, Respiratory, and Hormonal Adaptations to Muscular Exercise, Ibn El Jazzar Medicine Faculty, Avenue Mohamed Karoui, 4002 So
Source Type
Print(0)
Ref Type
Journal Article
Periodical, Full
TheScientificWorldJournal
Periodical, Abbrev.
ScientificWorldJournal
Pub Date Free Form
Volume
2015
Issue
Start Page
639369
Other Pages
Notes
LR: 20150212; JID: 101131163; 0 (Lipids); 4Y8F71G49Q (Malondialdehyde); EC 1.11.1.9 (Glutathione Peroxidase); EC 1.15.1.1 (Superoxide Dismutase); EC 1.8.1.7 (Glutathione Reductase); H4N855PNZ1 (alpha-Tocopherol); OID: NLM: PMC4310461; 2014/07/25 [received
Place of Publication
United States
ISSN/ISBN
1537-744X; 1537-744X
Accession Number
PMID: 25664340
Language
eng
SubFile
Clinical Trial; Journal Article; Research Support, Non-U.S. Gov't; IM
DOI
10.1155/2015/639369 [doi]
Output Language
Unknown(0)
PMID
25664340
Abstract
AIM: To examine the impact of interval training program on the antioxidant defense capability and lipid profile in men smoking cigarettes or hookah unable or unwilling to quit smoking. METHODS: Thirty-five participants performed an interval training (2 : 1 work : rest ratio) 3 times a week for 12 weeks at an intensity of 70% of VO2max. All subjects were subjected to a biochemical test session before and after the training program. RESULTS: The increase of total antioxidant status (TAS), glutathione peroxidase (GPx), and alpha-tocopherol, is significant only for cigarette smokers (CS) and hookah smokers (HS) groups. The decrease of malondialdehyde (MDA) and the increase of glutathione reductase (GR) are more pronounced in smokers groups compared to those of nonsmokers (NS). Superoxide dismutase (SOD) increases in NS, CS, and HS groups by 10.1%, 19.5%, and 13.3%, respectively (P
Descriptors
Links
Book Title
Database
Publisher
Data Source
Authors
Koubaa,A., Triki,M., Trabelsi,H., Baati,H., Sahnoun,Z., Hakim,A.
Original/Translated Title
URL
Date of Electronic
20150114
PMCID
PMC4310461
Editors
Changes in Antioxidant Defense Capability and Lipid Profile after 12-Week Low- Intensity Continuous Training in Both Cigarette and Hookah Smokers: A Follow-Up Study 2015 Laboratory of Pharmacology, Sfax Medicine Faculty SMF, Avenue Majida Boulila, Sfax, 3029, Tunisia; Research Unit (EM2S), Sfax Institute of Sport and Physical Education, Airport Road, P.O Box 384, Sfax, 3000, Tunisia.; Laboratory of cardio-circulatory, res
Source Type
Print(0)
Ref Type
Journal Article
Periodical, Full
PloS one
Periodical, Abbrev.
PLoS One
Pub Date Free Form
29-Jun
Volume
10
Issue
6
Start Page
e0130563
Other Pages
Notes
LR: 20150703; JID: 101285081; 0 (Antioxidants); 0 (Lipids); OID: NLM: PMC4488294; 2015 [ecollection]; 2015/03/27 [received]; 2015/05/21 [accepted]; 2015/06/29 [epublish]; epublish
Place of Publication
United States
ISSN/ISBN
1932-6203; 1932-6203
Accession Number
PMID: 26121249
Language
eng
SubFile
Clinical Trial; Journal Article; Research Support, Non-U.S. Gov't; IM
DOI
10.1371/journal.pone.0130563 [doi]
Output Language
Unknown(0)
PMID
26121249
Abstract
To examine the impact of low-intensity continuous training program on antioxidant defense capability and lipid profile in male cigarette or hookah smokers. Forty-three male adults participated in a 12-week continuous training program at an intensity of 40% of VO2max. All subjects were subjected to anthropometric, physical and biochemical tests before and after the training program. The increase of Glutathione reductase (GR) and Superoxide dismutase (SOD) is significant only for cigarette smokers (CS) and hookah smokers (HS) groups. The Malondialdehyde (MDA) decrease and alpha-tocopherol increase are significant only for HS group. GPx was increased in NS, CS and HS by 2.6% (p
Descriptors
Links
Book Title
Database
Publisher
Data Source
Authors
Koubaa,A., Triki,M., Trabelsi,H., Masmoudi,L., Sahnoun,Z., Hakim,A.
Original/Translated Title
URL
Date of Electronic
20150629
PMCID
PMC4488294
Editors