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1.
J Stomatol Oral Maxillofac Surg ; 120(1): 11-15, 2019 Feb.
Article in English | MEDLINE | ID: mdl-30739640

ABSTRACT

The objective of the study was to evaluate and compare the relative efficacy of treating linear non-comminuted mandibular fracture of symphysis and parasymphysis region using single 2.0-mm AO locking reconstruction plate or using two conventional miniplates. In this study, 80 patients of symphysis or parasymphysis fracture were divided randomly in two equal groups and treated with open reduction and internal fixation using two 2.5-mm miniplates or with a single 2.0-mm AO locking reconstruction plate. Operating time in case of open reduction and fixation using a single 2.0-mm locking reconstruction plate was significantly less when compared to open reduction and fixation using two conventional miniplates. Both groups showed satisfactory fracture reduction and healing. No postoperative malocclusion was noted, and both groups showed comparable improvement in masticatory efficiency. In conclusion, fracture fixation using a single 2.0-mm AO locking reconstruction plate without use of a second plate at the superior border for treatment of linear non comminuted mandibular fracture in symphysis and parasymphysis region gives comparable results as with treatment by conventional miniplate system and provides significant savings in operating time, ease of use and decrease in amount of hardware incorporated in the body.


Subject(s)
Bone Plates , Mandibular Fractures , Fracture Fixation , Fracture Fixation, Internal , Humans , Mandible
2.
J Immunol ; 161(7): 3242-8, 1998 Oct 01.
Article in English | MEDLINE | ID: mdl-9759838

ABSTRACT

CD20 is a B lymphocyte integral membrane protein with signal-transducing properties. Abs directed toward extracellular CD20 epitopes activate nonreceptor tyrosine kinases and modulate cell cycle progression of B lymphocytes. Recently, we demonstrated that binding of CD20 Abs to B cells induces the rapid redistribution of up to 95% of CD20 molecules to low density, detergent-insoluble membrane microdomains and induces the appearance of an approximately 50-kDa tyrosine-phosphorylated protein in the same compartment. Active relocalization of CD20 may thus be critical to the initiation of signaling events by CD20. The CD20 cDNA sequence predicts a nonglycosylated protein with four transmembrane-spanning regions and intracellular amino and carboxyl termini. Here we provide verification of the location of both the intracellular and extracellular regions of the CD20 molecule and identify a membrane-proximal sequence in the cytoplasmic carboxyl tail that is required for CD20 to redistribute to detergent-insoluble membrane microdomains.


Subject(s)
Antigens, CD20/metabolism , Cell Compartmentation/immunology , Cytoplasm/metabolism , Membrane Proteins/metabolism , Octoxynol , Peptide Fragments/metabolism , Antibody Specificity , Antigens, CD20/genetics , Antigens, CD20/immunology , Cell Membrane/immunology , Cell Membrane/metabolism , Cysteine/metabolism , Cytoplasm/immunology , Humans , Immune Sera/chemistry , Membrane Proteins/genetics , Membrane Proteins/immunology , Palmitic Acid/metabolism , Peptide Fragments/immunology , Protein Structure, Tertiary , Sequence Deletion/immunology , Solubility
3.
Antimicrob Agents Chemother ; 42(4): 762-6, 1998 Apr.
Article in English | MEDLINE | ID: mdl-9559779

ABSTRACT

Newer formulations of amphotericin B (AmB) complexed with liposomes or lipid suspensions have been developed. Preliminary studies have suggested that AmB in Intralipid (IL) may be as effective as, but less toxic than, conventional formulations of AmB, but few data are available regarding its stability, compatibility, or in vitro antifungal activity. A compatibility study was done to evaluate the effects of AmB concentrations in IL containing either 10 or 20% soybean oil. The effects of temperature, shaking, and AmB and IL concentrations on the stability of AmB-IL suspensions were analyzed by visual inspection and liquid chromatography. The in vitro antifungal activity of AmB-IL, compared to that of AmB alone against reference strains of Candida species was determined by using a broth macrodilution method in accordance with National Committee for Clinical Laboratory Standards guidelines (M27-T). Samples of AmB-IL which were lightly shaken retained more than 90% of the AmB concentration over 21 days when stored at either 4 or 23 degrees C. Varying the AmB concentration did not appear to affect the stability of AmB-IL. However, a precipitate was formed when mixtures with more than 30% lipid as a proportion of the total volume were centrifuged. AmB-IL and AmB alone had similar in vitro antifungal activities against reference strains of yeasts. Further pharmacologic and clinical studies with AmB-IL are warranted, although AmB should not be combined with IL in concentrations capable of producing a precipitate.


Subject(s)
Amphotericin B/administration & dosage , Amphotericin B/pharmacology , Antifungal Agents/pharmacology , Amphotericin B/analysis , Antifungal Agents/administration & dosage , Antifungal Agents/analysis , Candida/drug effects , Drug Incompatibility , Drug Stability , Emulsions , Fat Emulsions, Intravenous , Hydrogen-Ion Concentration , Lipids , Microbial Sensitivity Tests , Temperature
4.
Ann Intern Med ; 127(4): 289-93, 1997 Aug 15.
Article in English | MEDLINE | ID: mdl-9265429

ABSTRACT

BACKGROUND: Reports suggest that antituberculosis drugs are malabsorbed in patients with advanced HIV disease. OBJECTIVE: To evaluate the pharmacokinetics of antituberculosis agents in HIV-seropositive patients at different stages of disease. DESIGN: Parallel study. SETTING: Two hospital outpatient clinics. PARTICIPANTS: 12 healthy volunteers, 12 patients with asymptomatic HIV disease, 12 patients with symptomatic HIV disease, and 12 patients with symptomatic HIV disease and diarrhea. MEASUREMENTS: Drug plasma concentrations were measured over 24 hours on day 4 of concurrent therapy. INTERVENTION: Oral isoniazid (300 mg/d), rifampin (600 mg/d), pyrazinamide (1000 mg/d), and ethambutol (1000 mg/d). RESULTS: Reduced total drug exposure to rifampin and pyrazinamide was associated with D-xylose malabsorption in persons with HIV infection or AIDS. Peak drug exposure to isoniazid was lower in patients with diarrhea. CONCLUSIONS: Reduced total drug exposure may be related to malabsorption in persons with HIV infection or AIDS.


Subject(s)
Antitubercular Agents/pharmacokinetics , HIV Infections/blood , Adult , Aged , Case-Control Studies , Diarrhea/blood , Diarrhea/microbiology , Ethambutol/pharmacokinetics , Female , HIV Infections/physiopathology , HIV Seropositivity/blood , Humans , Intestinal Absorption , Isoniazid/pharmacokinetics , Male , Middle Aged , Pyrazinamide/pharmacokinetics , Rifampin/pharmacokinetics
5.
Can J Psychiatry ; 42(3): 310-2, 1997 Apr.
Article in English | MEDLINE | ID: mdl-9114949

ABSTRACT

OBJECTIVE: Traditional monoamine oxidase inhibitors (MAOIs) continue to play an important role in the management of a wide variety of clinical conditions. Accordingly, a practical and safe approach to MAOI dietary restrictions remains an essential component of patient management. METHOD: In an effort to refine MAOI dietary recommendations, we report a case of hypertensive crisis following the consumption of a modest amount of tap beer. RESULTS: A well-documented case report involving tap (draft) beer consumed while on an MAOI supports an earlier study, which recommended that all tap beers be restricted on MAOI diets. The 2 cases were remarkably similar in terms of the offending substance, quantity consumed, and subsequent reaction. CONCLUSIONS: As a result of recent tyramine analyses and 2 well-documented case reports, all tap (draft) beers should now be absolutely restricted on MAOI diets because they represent a very significant risk at modest levels of consumption.


Subject(s)
Beer/adverse effects , Bipolar Disorder/drug therapy , Depressive Disorder/drug therapy , Hypertension, Malignant/chemically induced , Monoamine Oxidase Inhibitors/adverse effects , Phenelzine/adverse effects , Adult , Contraindications , Dose-Response Relationship, Drug , Drug Administration Schedule , Humans , Hypertension, Malignant/prevention & control , Male , Monoamine Oxidase Inhibitors/therapeutic use , Phenelzine/therapeutic use
6.
J Clin Psychopharmacol ; 16(5): 383-8, 1996 Oct.
Article in English | MEDLINE | ID: mdl-8889911

ABSTRACT

Traditional monoamine oxidase inhibitors (MAOIs) remain an important class of drugs for a variety of psychiatric conditions, including depressive illnesses, anxiety, and eating disorders. It was the objective of this study to refine the MAOI diet by determining the tyramine content of a variety of untested and "controversial" foods that continue to appear on MAOI diet-restricted food lists. A secondary objective of the study was to evaluate the effect of freshness on the tyramine content of some foods. Fifty-one food samples were evaluated for tyramine content by liquid chromatography. Food samples included a selection of sausages, beverages, sliced meat products, including chicken liver, and some fruits, including raspberries, bananas, and banana peels. Foods that were found to have dangerously high concentrations of tyramine (> or = 6 mg/serving) included chicken liver aged 9 days (63.84 mg/30 g), air-dried sausage (7.56 g/30 g), soy sauce (0.941 mg/ml), and sauerkraut (7.75 mg/250 g). Of the foods analyzed in this study, only those with high tyramine content per serving should continue to be absolutely restricted. All other foods are either safe for consumption or safe in moderation. The data provided should be combined with the data from other similar analytical studies to develop a list of foods that should be absolutely restricted. A more accurate list of restricted foods may enhance patient dietary compliance.


Subject(s)
Diet Therapy , Food Analysis , Monoamine Oxidase Inhibitors/administration & dosage , Tyramine/analysis , Humans , Time Factors
8.
J Clin Psychiatry ; 57(3): 99-104, 1996 Mar.
Article in English | MEDLINE | ID: mdl-8617704

ABSTRACT

BACKGROUND: Many monoamine oxidase inhibitor (MAOI) diets are considered to be excessively restrictive and founded on poor scientific evidence. We present a safe and practical MAOI diet based on the related clinical and analytic data. METHOD: We used a critical review of the literature and our own tyramine assay results to categorize foods to be restricted absolutely, taken in moderation only, or unrestricted. RESULTS: We recommend that users avoid aged cheese; aged or cured meats (e.g., air-dried sausage); any potentially spoiled meat, poultry, or fish; broad (fava) bean pods; Marmite concentrated yeast extract; sauerkraut; soy sauce and soy bean condiments; and tap beer. Wine and domestic bottled or canned beer are considered safe when consumed in moderation. Other foods not mentioned are considered unrestricted. CONCLUSION: The concerns about perpetuating an overly restrictive MAOI diet include the avoidance by prescribers of a potentially useful treatment option, excessive limitations on lifestyle for patients, and increased risk to patients secondary to noncompliance with the diet. We propose an MAOI diet that has a solid scientific and clinical basis and that is, above all, practical.


Subject(s)
Diet/adverse effects , Food-Drug Interactions , Hypertension/prevention & control , Monoamine Oxidase Inhibitors/adverse effects , Acute Disease , Animals , Beer , Cheese/adverse effects , Depressive Disorder/drug therapy , Fishes , Fruit , Humans , Hypertension/chemically induced , Meat , Monoamine Oxidase Inhibitors/therapeutic use , Poultry , Tyramine/adverse effects , Vegetables
9.
J Clin Psychopharmacol ; 14(1): 5-14, 1994 Feb.
Article in English | MEDLINE | ID: mdl-8151003

ABSTRACT

A case report of a hypertensive crisis resulting from the ingestion of tap beer in a patient on an irreversible monamine oxidase inhibitor (MAOI; phenelzine) stimulated the investigation of different kinds of beer for tyramine concentration. The objective was to determine the tyramine concentration in tap and bottled beers. A total of 98 beer samples (79 different brands of beer) were analyzed by high-performance liquid chromatography for tyramine. Of these 98 beers, 49 were bottled or canned beers and 49 were beers on tap. All of the bottled beers analyzed had safe tyramine concentrations (< or = 10 mg/liter; range, 0 to 3.16 mg/liter) and, thus, do not require restriction in patients receiving MAOIs. Therefore, the consumption of canned or bottled beer, including dealcoholized beer, in moderation (fewer than four bottles or cans; 1.5 liters within a 4-hour period) appears to be safe and does not require restriction in patients receiving MAOIs. Only 4 of 98 beer samples studied were found to have a dangerous (> 10 mg/liter) tyramine concentration, one of which was the index beer. The tyramine concentration in these four beers ranged from 26.34 to 112.91 mg/liter. All four of these beers were tap beers produced by bottom fermentation (lagers) and brewed by a secondary fermentation process. Although we did not find any visible bacterial growth in the tap beers with high tyramine content, this finding does not preclude the possibility that bacterial contamination, bacterial growth, production of tyramine, and eventually bacterial death occurred at some earlier time. Therefore, to err on the side of caution, it is recommended that patients on irreversible MAOIs avoid beers on tap.


Subject(s)
Beer/adverse effects , Depressive Disorder/drug therapy , Hypertension/chemically induced , Phenelzine/adverse effects , Adult , Beer/analysis , Blood Pressure/drug effects , Depressive Disorder/psychology , Heart Rate/drug effects , Humans , Male , Phenelzine/therapeutic use , Tyramine/adverse effects , Tyramine/analysis
10.
Ann Pharmacother ; 27(10): 1231-42, 1993 Oct.
Article in English | MEDLINE | ID: mdl-8251694

ABSTRACT

OBJECTIVE: To review the bacterial genus Enterococcus with respect to its epidemiology, specific infections in humans, mechanisms of resistance and tolerance, and antimicrobial treatment. DATA SOURCES: A MEDLINE search of English-language journal articles published from 1977 to 1992 was completed. Articles published prior to 1977 were identified through Index Medicus and from references appearing in the bibliographies of other journal articles. Information also was acquired from abstracts, personal communication with infectious disease specialists with active research in the area of enterococcal infection, and conference proceedings. STUDY SELECTION: In vitro data; animal models of enterococcal infection; case reports; and case-controlled, cohort, and randomized controlled trials in humans were evaluated for relevant information. DATA EXTRACTION: Studies were evaluated by their methodologic strength (e.g., randomized controlled trial), reporting of clinically relevant outcomes (e.g., clinical response to antimicrobial therapy), statistical analyses, and accountability of all patients who entered the study. DATA SYNTHESIS: The incidence of enterococcal infections has increased in recent years and enterococci are now the second most frequently reported nosocomial pathogens. Enterococcus faecalis is the pathogen responsible for most enterococcal infections seen today; it has been implicated as an important cause of endocarditis, bacteremia, urinary tract infections, and intraabdominal infections. CONCLUSIONS: Enterococcal infection is of particular concern clinically because of its resistance to several antibiotics. Controlled comparative clinical trials of antimicrobial therapy in humans are lacking for several enterococcal infections. Therefore, the recommendations for antimicrobial therapy presented in this review are guidelines that reflect our current understanding of antibiotics used for enterococcal infection.


Subject(s)
Enterococcus , Gram-Positive Bacterial Infections , Abdomen/microbiology , Anti-Bacterial Agents/therapeutic use , Bacteremia/microbiology , Drug Resistance, Microbial , Endocarditis, Bacterial/microbiology , Gram-Positive Bacterial Infections/drug therapy , Gram-Positive Bacterial Infections/microbiology , Humans , Randomized Controlled Trials as Topic , Urinary Tract Infections/microbiology
11.
Cancer Genet Cytogenet ; 40(1): 89-94, 1989 Jul 01.
Article in English | MEDLINE | ID: mdl-2758403

ABSTRACT

The murine c-raf-1 gene was localized by in situ hybridization to 6C3, proximal to c-ki-ras-2 and distal to the Igk locus. The localization of this protooncogene may be relevant to the correlation of chromosome breakpoints in neoplastic disease.


Subject(s)
Chromosome Mapping , Genetic Markers , Proto-Oncogenes , Animals , DNA/genetics , Humans , Karyotyping , Leukemia, Myeloid/genetics , Mice , Nucleic Acid Hybridization , Translocation, Genetic
12.
Cytogenet Cell Genet ; 50(2-3): 165-7, 1989.
Article in English | MEDLINE | ID: mdl-2776484

ABSTRACT

The chromosomal localization of the gene for creatine kinase M has been determined to be on rabbit chromosome 19 at q11----q12 by in situ molecular hybridization. The results show significant cross-hybridization of the creatine kinase, muscle (CKMM) probe to the previously mapped creatine kinase, brain (CKBB) locus at 20q13----qter, and therefore provide independent support for the localization of CKBB at that site.


Subject(s)
Creatine Kinase/genetics , Animals , Chromosome Mapping , Chromosomes , Nucleic Acid Hybridization , Rabbits
13.
Steroids ; 42(5): 493-501, 1983 Nov.
Article in English | MEDLINE | ID: mdl-6689627

ABSTRACT

The total synthesis of (+/-)-8,13-diaza-3-thia-A-norgona-1,5(10)-dien-17-one (XII) was achieved starting from 2-(2-thienyl) ethylamine (VII) and 3-succinimidopropionyl chloride (IX) as the A and D ring precursors respectively.


Subject(s)
Steroids, Heterocyclic/chemical synthesis , Magnetic Resonance Spectroscopy , Methods , Spectrophotometry , Stereoisomerism
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