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1.
J Periodontal Res ; 53(1): 73-79, 2018 Feb.
Article in English | MEDLINE | ID: mdl-29044521

ABSTRACT

OBJECTIVE: To examine the effect of tongue cleaning with a tongue scraper (TS) or toothbrush (TB) in patients with periodontitis. BACKGROUND: The tongue is a possible reservoir for bacterial (re)colonization of the periodontal tissues in patients with periodontitis. To date, it is not known what the influence of tongue cleaning is on the tongue coating of patients with periodontitis. MATERIAL AND METHODS: Eighteen systemically healthy, untreated moderate to severe adult patients with periodontitis with some degree of tongue coating were randomly assigned to the use of a TS or TB for cleaning the tongue. Microbial load of the saliva and tongue dorsum, amount of tongue coating and patient perception about tongue cleaning were studied at baseline and 2 weeks later. RESULTS: Two weeks of tongue cleaning with either a TB or a TS, did not influence the microbiological counts, neither in the saliva, nor in the tongue coating, even though tongue coating was significantly less. The patients themselves experienced no differences in breath odour or taste sensation after 2 weeks of tongue cleaning; however, they felt that their tongue was cleaner at the end of the study compared to baseline. No differences could be detected between the uses of a TS vs a TB. CONCLUSION: In patients with periodontitis, tongue cleaning does not influence the bacterial load in the saliva or on the tongue dorsum.


Subject(s)
Dental Devices, Home Care , Oral Hygiene/methods , Periodontitis/microbiology , Saliva/microbiology , Tongue/microbiology , Adult , Bacterial Load , Female , Humans , Male , Middle Aged , Oral Hygiene/instrumentation
2.
Colorectal Dis ; 16(10): O360-6, 2014 Oct.
Article in English | MEDLINE | ID: mdl-24629060

ABSTRACT

AIM: Nitric oxide donors, such as isosorbide dinitrate ointment (ISDN), are considered as first-choice agents in the treatment of chronic anal fissure. Injection with botulinum toxin A in the internal anal sphincter is often used as a second-line therapy, although it may give better results and fewer side effects than nitric oxide donors. The aim of this randomized clinical trial was to investigate whether botulinum toxin A (Dysport) is more effective than ISDN in the primary treatment of chronic anal fissure. METHOD: From April 2005 until October 2009, 60 patients (32 men) with a median age of 42 (25-82) years were randomized to receive either ISDN 10 mg/ml (1%) (n = 33) or injection with 60 units of Dysport (n = 27). The primary end-point was the percentage of complete fissure healing after 8 weeks. RESULTS: After a median of 9 weeks complete fissure healing was noted in 18 of 27 patients in the Dysport group and in 11 of 33 patients in the ISDN group (P = 0.010). Absolute improvement of pain scores after 9 weeks was similar in both groups (P = 0.733). Patients treated with Dysport had fewer side effects than patients treated with ISDN (P = 0.028). Of the patients with a healed fissure, 28% of the Dysport group and 50% of the ISDN group had a recurrence within 1 year (P = 0.286; hazard ratio 2.08; 95% CI = 0.54-7.97). CONCLUSION: Dysport is more effective than ISDN ointment and has fewer side effects in the primary treatment of chronic anal fissure. The recurrence rate within 1 year in both treatment groups is high.


Subject(s)
Acetylcholine Release Inhibitors/therapeutic use , Botulinum Toxins, Type A/therapeutic use , Fissure in Ano/drug therapy , Isosorbide Dinitrate/therapeutic use , Nitric Oxide Donors/therapeutic use , Administration, Topical , Adult , Aged , Aged, 80 and over , Anal Canal , Chronic Disease , Female , Fissure in Ano/complications , Humans , Injections, Intramuscular , Male , Middle Aged , Ointments , Pain/etiology , Recurrence
3.
Colorectal Dis ; 12(7 Online): e163-9, 2010 Jul.
Article in English | MEDLINE | ID: mdl-19832866

ABSTRACT

INTRODUCTION: Chemical sphincterotomy, the use of pharmacological agents to reduce anal sphincter resting pressure, has become more and more popular in the treatment of chronic anal fissures (CAFs). It offers the possibility to avoid a lateral internal sphincterotomy and its associated risk of incontinence. In our hospital, patient with a chronic anal fissure are consecutively treated with isosorbide dinitrate 1% ointment, applied 6 times a day for 8 weeks, followed by diltiazem 2% ointment, applied 2 times a day for 8 weeks and Botulin Toxin A injections (Dysport; Ipsen, Hoofddorp, the Netherlands) in the internal anal sphincter. In a previous study (1), we describe high healing rates with this regime. Objective The objective of this study is to evaluate the effect of the combination of fissurectomy and Botulin Toxin A in the treatment of CAFs. METHODS: Twenty-one patients (10 male patients, median age 48 years) with persistent symptoms of chronic anal fissures after following the above mentioned treatment, were enrolled in this study. Fissurectomy was combined with Botulinum Toxin A (80 U of Dysport) under regional anaesthesia in day care. Results After 12 weeks 19/21 CAFs (90%) had healed. Median follow-up was 16 (9-30) months. No recurrences were seen. CONCLUSION: Fissurectomy in combination with Botulinum Toxin A injection in the internal anal sphincter is an effective treatment for medically resistant CAFs.


Subject(s)
Anal Canal/surgery , Botulinum Toxins, Type A/administration & dosage , Digestive System Surgical Procedures/methods , Fissure in Ano/therapy , Neuromuscular Agents/administration & dosage , Adult , Anal Canal/drug effects , Chronic Disease , Defecation , Female , Fissure in Ano/physiopathology , Follow-Up Studies , Humans , Injections, Intramuscular , Male , Middle Aged , Prospective Studies , Treatment Outcome
4.
Mol Cell Biol ; 18(1): 233-9, 1998 Jan.
Article in English | MEDLINE | ID: mdl-9418870

ABSTRACT

The transcription factor IID (TFIID) complex is highly conserved between the Drosophila and mammalian systems. A mammalian homolog has been described for all the Drosophila TATA box-binding protein-associated factors (TAFs), with the exception of dTAF(II)150. We previously reported the identification of CIF, an essential cofactor for TFIID-dependent transcription from promoters containing initiator (Inr) elements. Here we describe the molecular cloning of CIF150, the human homolog of dTAF(II)150, and present biochemical evidence that this factor is involved in Inr activity. CIF150 is capable of mediating TFIID-dependent Inr activity in a complementation assay, and a protein fraction lacking Inr activity lacks detectable amounts of CIF150. Despite the striking similarity to dTAF(II)150, CIF150 does not appear to be associated with human TFIID. However, in vitro binding assays revealed a specific and direct interaction between CIF150 and hTAF(II)135. This interaction might be structurally important for the functional interaction between CIF150 and human TFIID, since CIF150 stabilizes TFIID binding to a core promoter.


Subject(s)
DNA-Binding Proteins/genetics , Promoter Regions, Genetic , TATA-Binding Protein Associated Factors , Transcription Factors, TFII/genetics , Transcription Factors/genetics , Transcription, Genetic , Amino Acid Sequence , HeLa Cells , Humans , Molecular Sequence Data , Sequence Alignment , TATA Box , Transcription Factor TFIID
5.
J Med Life ; 10(1): 38-43, 2017.
Article in English | MEDLINE | ID: mdl-28255374

ABSTRACT

Introduction. The aim of this study was to determine whether the use of primary health care differs between students enrolled in Belgian and German government-funded universities. The secondary aim of the study was to determine the factors that might explain such a difference. Methods. Participants were recruited through all Belgian and German government-funded universities. Because not all the universities agreed to participate, recruiting was also done through social media groups of the universities. An anonymous online survey was used for data collection. Results. In total, 2238 completed surveys were evaluated, of which 544 from students in Belgium and 1694 from students in Germany. In Belgium, more students had a family physician (87%) as compared to the students in Germany (73%) (p < 0.001). During the two months prior to the study, 37% of the Belgian students and 35% of the German students attended a family physician (p = 0.37). More German students attended a specialist (40%) as compared to the Belgian students (24%) (p<0.001). The German students also attended the emergency department more frequently (6%) as compared to their Belgian counterparts (3%) (p = 0.004). Conclusion. Belgian university students were more likely to attend a primary care physician than the German students. The health care seemed to be better organized for Belgian students and they were more satisfied with the delivered care.


Subject(s)
Patient Acceptance of Health Care , Students/statistics & numerical data , Universities/statistics & numerical data , Adult , Belgium/epidemiology , Emergency Medical Services , Female , Germany/epidemiology , Health Status , Humans , Insurance, Health , Male , Patient Satisfaction , Physicians, Family , Specialization , Surveys and Questionnaires , Young Adult
6.
Nucleic Acids Res ; 27(16): e11, 1999 Aug 15.
Article in English | MEDLINE | ID: mdl-10454648

ABSTRACT

Negatively supercoiled plasmids can be assembled into dynamic minichromosomes using Drosophila embryo extract as a source of histones and chromatin assembly factors. However, analysis of such mini-chromosomes is often difficult due to the presence in the crude extract of a large excess of macromolecules and low molecular weight molecules including ATP. Several techniques have been used to partially purify the minichromosomes based on either sizing columns or centrifugation on sucrose gradients. We have developed a single-step method employing a 30 min ultracentrifugation through a glycerol cushion. In contrast to chromatin purified in sucrose-containing buffers, the minichromosomes obtained with this method are suitable for transcriptional analysis. This method is fast, quantitative, flexible, can deal with several samples simultaneously and leads to concentration of the chromatin. As centrifugation through glycerol yields chromatin free of ATP and several characterized chromatin remodeling complexes, this method should be useful for structural and functional studies in vitro.


Subject(s)
CCAAT-Enhancer-Binding Proteins , Chromatin/isolation & purification , Chromosomes , Glycerol , Transcription Factors , Ultracentrifugation/methods , Animals , Chromatin/metabolism , DNA-Binding Proteins/genetics , DNA-Binding Proteins/metabolism , Drosophila , HeLa Cells , Humans , NFI Transcription Factors , Nuclear Proteins , Plasmids , Y-Box-Binding Protein 1
7.
Nucleic Acids Res ; 29(24): 4994-5000, 2001 Dec 15.
Article in English | MEDLINE | ID: mdl-11812829

ABSTRACT

Sp3 is a ubiquitous transcription factor closely related to Sp1. Previous analyses showed that, unlike Sp1, Sp3 fails to activate transcription in certain promoter settings. This is due to the presence of an inhibitory domain located between the second glutamine-rich activation domain and the DNA-binding domain. To further analyze the transcriptional properties of Sp3, we have expressed and purified recombinant Sp3 and Sp1 as epitope-tagged proteins from stable transfected insect cells. We found that Sp3 does act as a strong activator similar to Sp1 in an in vitro transcription assay using Sp1/Sp3-depleted HeLa nuclear extract. However, on the same promoter Sp3 is almost inactive when transfected into cells. Mutational studies demonstrate that a single lysine residue is responsible for the low transcriptional activity of Sp3 in vivo. We show that Sp3, but not a mutant of Sp3 that lacks this lysine residue, is highly acetylated in vivo. Our results strongly suggest that the transcriptional activity of Sp3 is regulated by acetylation. The consequences of acetylation for the activity of Sp3 are discussed.


Subject(s)
DNA-Binding Proteins/metabolism , Transcription Factors/metabolism , Acetylation , Animals , Binding Sites/genetics , Cell Line , DNA-Binding Proteins/genetics , Gene Expression , HeLa Cells , Histone Acetyltransferases , Humans , Lysine/genetics , Nuclear Receptor Coactivator 3 , Point Mutation , Recombinant Proteins/genetics , Recombinant Proteins/metabolism , Sp1 Transcription Factor/genetics , Sp1 Transcription Factor/metabolism , Sp3 Transcription Factor , Trans-Activators/genetics , Trans-Activators/metabolism , Transcription Factors/genetics
8.
J Cancer Res Clin Oncol ; 120(6): 359-64, 1994.
Article in English | MEDLINE | ID: mdl-8138561

ABSTRACT

A rapid assay system for measuring the potential of estrogenic drugs is introduced. Luciferase induction could be measured in estrogen-receptor-positive human MCF-7 breast cancer cells, which had been transfected with a novel luciferase reporter plasmid ERE luc. The minimal requirement was 1 h exposure to the inducing drug and 3.5 h of incubation after removal of the drug. The assay system was used to measure the stability of the drug diaqua-[1,2-bis (2,6-dichloro-4-hydroxyphenyl) ethylenediamine] platinum(II) sulfate, containing an estrogenic ligand and reactive platinum. Luciferase activity was observed only when the drug was in the culture medium and cells for short times, whereas the estrogenic ligand alone remained active. It is assumed that binding of the platinum moiety to macromolecular constituents of the culture or cells renders the drug inaccessible for binding to the estrogen receptor.


Subject(s)
Antineoplastic Agents/pharmacology , Estrogens, Non-Steroidal/pharmacology , Luciferases/genetics , Organoplatinum Compounds/pharmacology , Breast Neoplasms/metabolism , Enzyme Activation/drug effects , Estradiol/pharmacology , Female , Humans , Receptors, Estrogen/drug effects , Transcription, Genetic/drug effects , Transfection , Tumor Cells, Cultured
9.
J Steroid Biochem Mol Biol ; 49(1): 51-62, 1994 May.
Article in English | MEDLINE | ID: mdl-8003439

ABSTRACT

The 2-phenylindole system has proved to be a versatile structure for the design of potent antiestrogens, especially when functional groups have been introduced into the alkyl side chain in position 1. In analogy to steroidal structures such as ICI 164,384 a number of 2-phenylindoles with carbamoylalkyl and aminoalkyl side chains were synthesized. They bind to the calf uterine estrogen receptor with relative binding affinities between 2.1 and 21 (estradiol = 100). The antiestrogenic effect of these compounds was demonstrated by the inhibition of transcriptional activity which was measured in a new luciferase assay with the EREwtc luc as reporter plasmid. The derivative with a methyl-n-propyldodecanamide side chain (4h) antagonized the effect of estradiol (10(-9) M) completely at concentrations of 10(-7) M and higher. As a sensitive model for quantification of estrogenic and antiestrogenic effects in vitro we used HeLa-cells cotransfected both with the reporter plasmid and estrogen receptor expression vectors HEG0 and HE0. In cells transfected with these vectors transcriptional activity was strongly dependent on side chain structure. With mutated receptors we were able to show that this activity was mainly due to TAF-1 whereas TAF-2 remained silent. When we studied the effect of some of the new compounds in vivo using the mouse uterine weight assay, we observed a correlation between transcriptional activity in transfected HeLa cells and estrogenic effects in mice. Two of the 1-carbamoylalkyl-2-phenylindoles (4f, 4h) proved to be "pure" antiestrogens both in vitro and in vivo. In estrogen-sensitive MCF-7 breast cancer cells, they strongly inhibit cellular growth. Some of the IC50-values were close to 10(-8) M.


Subject(s)
Estrogen Antagonists/chemistry , Estrogen Antagonists/pharmacology , Indoles/chemistry , Indoles/pharmacology , Animals , Breast Neoplasms/metabolism , Cell Division/drug effects , Estradiol/analogs & derivatives , Estradiol/metabolism , Estradiol/pharmacology , Estrogen Antagonists/metabolism , Female , HeLa Cells , Humans , Indoles/metabolism , Mice , Organ Size/drug effects , Polyunsaturated Alkamides , Radioligand Assay , Receptors, Estrogen/genetics , Receptors, Estrogen/metabolism , Sequence Deletion , Structure-Activity Relationship , Tamoxifen/pharmacology , Transcriptional Activation , Tumor Cells, Cultured , Uterus/drug effects
10.
Case Rep Gastroenterol ; 7(2): 208-13, 2013 May.
Article in English | MEDLINE | ID: mdl-23741208

ABSTRACT

A relatively new therapy in the treatment of hemorrhoids is transanal hemorrhoidal dearterialization (THD). We report a case of brain abscess caused by Streptococcus milleri following THD. Although a brain abscess after drainage of a perianal abscess has been described in the literature, no report exists of a brain abscess following treatment of hemorrhoids. A healthy 51-year-old man with hemorrhoids underwent THD. Two weeks later he presented with a headache, bradyphrenia, flattened behavior and a left hemiplegia. No perianal complaint and/or perianal abscess was present. A contrast CT scan of the cerebrum showed a right temporoparieto-occipital abscess, with edema and compression of the surrounding tissue and lateral ventricles. MRI showed an abscess with leakage in the right lateral ventricle. Treatment with dexamethasone and intravenous antibiotics was started. Because of progression of symptoms, 3 weeks later ventriculoscopy was performed and the abscess was drained. Culture of the punctuate showed S. milleri. Because of developing hydrocephalus 3 days after ventriculoscopy, first an external ventricle drain and later a ventriculoperitoneal drain was placed. Hereafter the hemiplegia and cognitive disorders improved. This case report describes a severe complication following treatment of hemorrhoids with THD which until now, to our knowledge, has never been described in the literature.

12.
Z Ernahrungswiss ; 22(4): 271-86, 1983 Dec.
Article in German | MEDLINE | ID: mdl-6659595

ABSTRACT

In experiments with male Wistar rats the influence of the non-saponifiable constituents of dietary fats: dl-alpha-tocopherol (60 ppm), dl-gamma-tocopherol (480 ppm), ubiquinone (96 ppm) and beta-sitosterol (3035 ppm) on the tocopherol status was investigated, considering the fatty acid composition of the tested fats. For a test period of eight weeks the animals were fed isoenergetic diets containing three types of dietary fats: corn oil (60% PUFA), a kind of "stripped corn oil" (60% PUFA) and butter (nearly 5% PUFA). Independent of the PUFA-content of the diet, the tocopherol supplementations were able to stabilize the erythrocyte membrane; the calculated hemolysis rates were about 2%. The absence of tocopherols in the diets ("stripped corn oil", butter) caused an increase of the hemolysis rate up to 70% after two weeks. The original amounts of tocopherols in corn oil tended to minimize the hemolysis. Ubiquinone and beta-sitosterol did not reduce the hemolysis rates when they were applied without tocopherols. With respect to creatine-phosphokinase activity, creatine and creatinine excretion the results were similar. Plasma and erythrocyte levels of alpha- and gamma-tocopherol were determined in all groups and discussed in connection with the other examined parameters of tocopherol status. The ultimate result of this experiment is that the content of tocopherols in dietary fats is not always adequate to keep vitamin E status normal, especially if polyunsaturated fatty acid content is high in the diet. Reflecting the vitamin E adequacy of dietary fats, not only alpha-tocopherol but also gamma-tocopherol should be much more considered than previously.


Subject(s)
Dietary Fats/administration & dosage , Sitosterols/administration & dosage , Ubiquinone/administration & dosage , Vitamin E/metabolism , Animals , Butter , Dose-Response Relationship, Drug , Fatty Acids, Unsaturated/administration & dosage , Hemolysis/drug effects , Male , Rats , Rats, Inbred Strains , Structure-Activity Relationship , Triglycerides/administration & dosage , Vitamin E/administration & dosage , Zea mays
13.
Mol Cell ; 4(1): 45-54, 1999 Jul.
Article in English | MEDLINE | ID: mdl-10445026

ABSTRACT

In contrast to its behavior as naked DNA, the MMTV promoter assembled in minichromosomes can be activated synergistically by the progesterone receptor and NF1 in a process involving ATP-dependent chromatin remodeling. The DNA-binding domain of NF1 is required and sufficient for stable occupancy of all receptor-binding sites and for functional synergism. Activation of purified minichromosomes is observed in the absence of SWI/SNF and can be enhanced by recombinant ISWI. Receptor binding to minichromosomes recruits ISWI and NURF38, but not brahma. We propose a two-step synergism in which the receptor triggers a chromatin remodeling event that facilitates access of NF1, which in turn stabilizes an open nucleosomal conformation required for efficient binding of further receptor molecules and full transactivation.


Subject(s)
CCAAT-Enhancer-Binding Proteins , Cell Cycle Proteins , Chromosomes/genetics , DNA-Binding Proteins/genetics , Drosophila Proteins , Pyrophosphatases , Receptors, Progesterone/genetics , Adenosine Triphosphatases/genetics , Adenosine Triphosphate/metabolism , Animals , Chromatin/metabolism , DNA Footprinting , Drosophila/embryology , Humans , Insect Proteins/metabolism , Mammary Tumor Virus, Mouse/genetics , NFI Transcription Factors , Nuclear Proteins , Nucleic Acid Conformation , Nucleosomes/genetics , Promoter Regions, Genetic , Recombinant Proteins/genetics , Trans-Activators/metabolism , Transcription Factors/genetics , Transcription, Genetic , Y-Box-Binding Protein 1
14.
Article in English | MEDLINE | ID: mdl-10384288

ABSTRACT

Adenovirus large E1A, Epstein-Barr virus Zebra, and herpes simplex virus VP16 were studied as models of animal cell transcriptional activators. Large E1A can activate transcription from a TATA box, a result that leads us to suggest that it interacts with a general transcription factor. Initial studies showed that large E1A binds directly to the TBP subunit of TFIID. However, analysis of multiple E1A and TBP mutants failed to support the significance of this in vitro interaction for the mechanism of activation. Recent studies to be reported elsewhere indicate that conserved region 3 of large E1A, which is required for its activation function, binds to one subunit of a multisubunit protein that stimulates in vitro transcription in response to large E1A and other activators. A method was developed for the rapid purification of TFIID approximately 25,000-fold to near homogeneity from a cell line engineered to express an epitope-tagged form of TBP. Purified TFIID contains 11 major TAFs ranging in mass from approximately 250 to 20 kD. Zta and VP16, but not large E1A, greatly stimulate the rate and extent of assembly of a TFIID-TFIIA complex on promoter DNA (DA complex). For VP16, this is a function of the carboxy-terminal activation subdomain. An excellent correlation was found between the ability of VP16C mutants to stimulate DA complex assembly and their ability to activate transcription in vivo. Consequently, for a subset of activation domains, DA complex assembly activity is an important component of the overall mechanism of activation.


Subject(s)
Trans-Activators/metabolism , Transcription Factors/metabolism , Transcription, Genetic , Viral Proteins , Viruses/genetics , Adenovirus E1A Proteins/metabolism , Animals , DNA-Binding Proteins/metabolism , HeLa Cells , Herpes Simplex Virus Protein Vmw65/metabolism , Humans , Transcription Factor TFIID , Transcription Factors, TFII/metabolism , Transcriptional Activation , Viruses/metabolism
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