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1.
N Z Vet J ; 67(3): 109-116, 2019 May.
Article in English | MEDLINE | ID: mdl-30625279

ABSTRACT

AIMS: To provide herd managers with a set of decision rules allowing them to predict the likelihood that a juvenile bull is ready for Bull Breeding Soundness Evaluation (BBSE), or breeding, if bodyweight and scrotal circumference are known. METHODS: This was a longitudinal study following two groups of young pasture-fed Holstein and Jersey bulls from northwest Tasmania, Australia. Individual scrotal circumference, bodyweight and semen characteristics were recorded at 6-8 weekly intervals, from 6-18 months of age. Classification and regression tree analyses were used to predict the probability that a bull had ≥70% normal sperm morphology based on scrotal circumference and bodyweight measurements. RESULTS: Overall 1,661 scrotal circumference and bodyweight measurements were obtained, and 518 semen samples from 356 bulls were assessed for sperm morphology, from 16 examination sessions that took place between 29 May 2015 and 17 August 2016. Classification and regression tree analyses generated a decision tree for Holstein bulls with four node endpoints, and for Jersey bulls with three node endpoints. Diagnostic test performance showed that for Holstein bulls, using the node endpoints of scrotal circumference ≥27 cm and bodyweight ≥349 kg, 98% had ≥70% normal sperm (positive likelihood ratio 10.4; 95% CI = 2.7-41), and using the node endpoints of scrotal circumference ≥27 cm and bodyweight between 282-349 kg, 89% had ≥70% normal sperm (positive likelihood ratio 1.6; 95% CI = 0.9-2.6). For Jersey bulls, using the node endpoints of bodyweight ≥259 kg and scrotal circumference ≥29 cm, 88% had ≥70% normal sperm (positive likelihood ratio 3.4; 95% CI = 1.6-7.0). CONCLUSIONS: This study provides a set of relatively simple decision rules based on bodyweight and scrotal circumference measurements that allows herd managers to assess the likelihood that juvenile bulls are ready for BBSE or breeding. ABBREVIATIONS: BBSE: Bull breeding soundness evaluation; BRT: Boosted regression tree.


Subject(s)
Body Weight/physiology , Cattle/growth & development , Scrotum/anatomy & histology , Semen Analysis/veterinary , Semen/physiology , Animals , Cattle/anatomy & histology , Longitudinal Studies , Male , Tasmania
2.
Lett Appl Microbiol ; 36(1): 20-4, 2003.
Article in English | MEDLINE | ID: mdl-12485336

ABSTRACT

AIMS: To investigate the occurrence of oxytetracycline (OTC) resistance in Melissococcus plutonius, which causes European foulbrood in honeybee colonies. METHODS AND RESULTS: Strains of M. plutonius were isolated from diseased colonies in England and Wales and tested for resistance to OTC. The minimum inhibitory concentration (MIC) of OTC was also determined for selected isolates. No resistance to the antibiotic was found in any isolate and the average MIC was found to be 3.9 microg ml-1. Melissococcus plutonius was found to be susceptible to both chlortetracycline and tetracycline. CONCLUSIONS: No resistance to OTC was found in M. plutonius. SIGNIFICANCE AND IMPACT OF THE STUDY: This study demonstrated that OTC can continue to be used to treat European foulbrood and that resistance may not explain why some treatments fail.


Subject(s)
Anti-Bacterial Agents/pharmacology , Bees/microbiology , Drug Resistance, Bacterial , Gram-Positive Bacteria/drug effects , Oxytetracycline/pharmacology , Animals , Bees/growth & development , Chlortetracycline/metabolism , Gram-Positive Bacteria/isolation & purification , Gram-Positive Bacteria/pathogenicity , Larva/microbiology , Life Cycle Stages , Microbial Sensitivity Tests , Tetracycline Resistance
4.
Am J Physiol Lung Cell Mol Physiol ; 280(6): L1138-47, 2001 Jun.
Article in English | MEDLINE | ID: mdl-11350792

ABSTRACT

Intrapulmonary veins (PVs) contribute to pulmonary vascular resistance, but the mechanisms controlling PV tone are poorly understood. Although smooth muscle cell (SMC) K(+) channels regulate tone in most vascular beds, their role in PV tone is unknown. We show that voltage-gated (K(V)) and inward rectifier (K(ir)) K(+) channels control resting PV tone in the rat. PVs have a coaxial structure, with layers of cardiomyocytes (CMs) arrayed externally around a subendothelial layer of typical SMCs, thus forming spinchterlike structures. PVCMs have both an inward current, inhibited by low-dose Ba(2+), and an outward current, inhibited by 4-aminopyridine. In contrast, PVSMCs lack inward currents, and their outward current is inhibited by tetraethylammonium (5 mM) and 4-aminopyridine. Several K(V), K(ir), and large-conductance Ca(2+)-sensitive K(+) channels are present in PVs. Immunohistochemistry showed that K(ir) channels are present in PVCMs and PV endothelial cells but not in PVSMCs. We conclude that K(+) channels are present and functionally important in rat PVs. PVCMs form sphincters rich in K(ir) channels, which may modulate venous return both physiologically and in disease states including pulmonary edema.


Subject(s)
Potassium Channels, Inwardly Rectifying , Potassium Channels/metabolism , Pulmonary Veins/metabolism , Vascular Resistance/physiology , 4-Aminopyridine/pharmacology , Animals , Barium/pharmacology , Cell Separation , Endothelium, Vascular/drug effects , Endothelium, Vascular/metabolism , Glyburide/pharmacology , Immunohistochemistry , In Vitro Techniques , Male , Muscle, Smooth, Vascular/drug effects , Muscle, Smooth, Vascular/metabolism , Muscle, Smooth, Vascular/ultrastructure , Myocardium/cytology , Myocardium/metabolism , Patch-Clamp Techniques , Peptides/pharmacology , Potassium Channel Blockers , Pulmonary Circulation/physiology , Pulmonary Veins/cytology , Pulmonary Veins/ultrastructure , Rats , Rats, Sprague-Dawley , Tetraethylammonium/pharmacology , Vasoconstriction/drug effects , Vasoconstriction/physiology , Vasodilation/drug effects , Vasodilation/physiology
5.
Mol Microbiol ; 42(5): 1223-32, 2001 Dec.
Article in English | MEDLINE | ID: mdl-11886554

ABSTRACT

The molecular genetic basis of high-frequency serotype 3 capsule phase variation in Streptococcus pneumoniae (the pneumococcus) was investigated. Pneumococci were grown in sorbarod biofilms at 34 degrees C to mimic nasopharyngeal carriage. Different type 3 pneumococci commonly associated with invasive disease generated apparently random tandem duplications of 11-239 bp segments within the cap3A gene of the type 3 capsule locus. These duplications alone were found to be responsible for high-frequency capsule phase variation, in which (phase off) acapsular variants possessed duplications within cap3A, and (phase on) capsular revertants possessed wild-type cap3A genes, indicating the precise excision of the duplication. Additionally, the frequency of phase reversion (off to on) was found to exhibit a linear relationship between (log) frequency of reversion and (log) length of duplication. This apparently random duplication giving rise to phase variation is in stark contrast to the 'preprogrammed' contingency genes in many Gram-negative organisms that possess homopolymeric sequence repeats or motifs for site-specific recombination.


Subject(s)
Bacterial Capsules , Genetic Variation , Open Reading Frames , Streptococcus pneumoniae/genetics , Bacterial Proteins/genetics , Base Sequence , Biofilms , Gene Duplication , Genes, Bacterial , Molecular Sequence Data , Polymerase Chain Reaction , Serotyping , Streptococcus pneumoniae/classification , Uridine Diphosphate Glucose Dehydrogenase/genetics
6.
Pediatr Neurol ; 22(4): 314-7, 2000 Apr.
Article in English | MEDLINE | ID: mdl-10788751

ABSTRACT

Four young patients with severe unexplained progressive mononeuropathy are described. None had a history of known trauma to the affected limb. In addition to the standard neurologic examination and electrophysiologic studies (nerve conduction studies and electromyography), all underwent neuroimaging of the involved extremity. In three patients, magnetic resonance imaging revealed intrinsic abnormalities of the appropriate nerve. The pattern or absence of magnetic resonance imaging changes directly influenced decisions about surgical exploration of the nerve in all four patients. With the advent of more sophisticated technology, magnetic resonance neurography has become a potent diagnostic tool in the evaluation of disorders of peripheral nerve and muscle.


Subject(s)
Magnetic Resonance Imaging , Peripheral Nervous System Diseases/diagnosis , Peroneal Neuropathies/diagnosis , Ulnar Neuropathies/diagnosis , Adolescent , Child , Electromyography , Female , Humans , Male
7.
Proc Natl Acad Sci U S A ; 96(14): 7944-9, 1999 Jul 06.
Article in English | MEDLINE | ID: mdl-10393927

ABSTRACT

The rapid response to hypoxia in the pulmonary artery (PA), carotid body, and ductus arteriosus is partially mediated by O2-responsive K+ channels. K+ channels in PA smooth muscle cells (SMCs) are inhibited by hypoxia, causing membrane depolarization, increased cytosolic calcium, and hypoxic pulmonary vasoconstriction. We hypothesize that the K+ channels are not themselves "O2 sensors" but rather respond to the reduced redox state created by hypoxic inhibition of candidate O2 sensors (NADPH oxidase or the mitochondrial electron transport chain). Both pathways shuttle electrons from donors, down a redox gradient, to O2. Hypoxia inhibits these pathways, decreasing radical production and causing cytosolic accumulation of unused, reduced, freely diffusible electron donors. PASMC K+ channels are redox responsive, opening when oxidized and closing when reduced. Inhibitors of NADPH oxidase (diphenyleneiodonium) and mitochondrial complex 1 (rotenone) both inhibit PASMC whole-cell K+ current but lack the specificity to identify the O2-sensor pathway. We used mice lacking the gp91 subunit of NADPH oxidase [chronic granulomatous disease (CGD) mice] to assess the hypothesis that NADPH oxidase is a PA O2-sensor. In wild-type lungs, gp91 phox and p22 phox subunits are present (relative expression: macrophages > airways and veins > PASMCs). Deletion of gp91 phox did not alter p22 phox expression but severely inhibited activated O2 species production. Nonetheless, hypoxia caused identical inhibition of whole-cell K+ current (in PASMCs) and hypoxic pulmonary vasoconstriction (in isolated lungs) from CGD vs. wild-type mice. Rotenone vasoconstriction was preserved in CGD mice, consistent with a role for the mitochondrial electron transport chain in O2 sensing. NADPH oxidase, though a major source of lung radical production, is not the pulmonary vascular O2 sensor in mice.


Subject(s)
Granulomatous Disease, Chronic/physiopathology , Lung/physiology , Membrane Glycoproteins/metabolism , Oxygen/analysis , Pulmonary Artery/physiology , Animals , Blood Pressure/drug effects , Blood Pressure/physiology , Granulomatous Disease, Chronic/genetics , Granulomatous Disease, Chronic/pathology , Hemodynamics/drug effects , Hemodynamics/physiology , Hypoxia , In Vitro Techniques , Luminescent Measurements , Lung/blood supply , Lung/physiopathology , Meclofenamic Acid/pharmacology , Membrane Glycoproteins/deficiency , Membrane Glycoproteins/genetics , Mice , Mice, Inbred C57BL , Mice, Knockout , NADPH Oxidase 2 , NADPH Oxidases/deficiency , NADPH Oxidases/genetics , NADPH Oxidases/metabolism , NG-Nitroarginine Methyl Ester/pharmacology , Peptides/pharmacology , Pulmonary Artery/physiopathology , Pulmonary Circulation , Scorpion Venoms/pharmacology , Vascular Resistance/drug effects , Vasoconstriction
8.
J Endod ; 25(3): 206-7, 1999 Mar.
Article in English | MEDLINE | ID: mdl-10321188

ABSTRACT

Straight-line access in mandibular incisors facilitates locating and debridement of the canals. The purpose of this study was to plot where ideal access should be located in mandibular incisors to obtain straight-line access to the apical third of the root canal and to determine if a correlation exists between incisal edge wear and position of access opening. Two hundred and seventy-nine mandibular incisors were radiographed in clinical and proximal views. Straight-line access was determined by finding midpoints in the canal at two levels and extending a line connecting the points through the crown. Teeth were graded as to the condition of the incisal edge. Ideal straight-line access was determined to be at the incisal edge in 72.4% of the teeth, whereas in 27.6% of the teeth it was to the facial of the incisal edge. As the wear of the incisal edge increased, the ideal access moved from the facial toward the incisal.


Subject(s)
Dental Pulp Cavity/anatomy & histology , Incisor/anatomy & histology , Root Canal Preparation , Chi-Square Distribution , Humans , Mandible , Root Canal Therapy , Tooth Attrition , Tooth Crown/anatomy & histology , Tooth Root/anatomy & histology
9.
Acta Virol ; 42(2): 95-101, 1998 Apr.
Article in English | MEDLINE | ID: mdl-9770078

ABSTRACT

The dnaA gene encoding the initiator protein of DNA replication was isolated from the obligate intracellular bacterium, Rickettsia prowazekii. Comparison of the deduced amino acid sequence of R. prowazekii DnaA with other bacterial DnaA proteins revealed extensive similarity. However, the rickettsial sequence is unique in the number of basic lysine residues found within a highly conserved portion of the putative DNA binding region, suggesting that the rickettsial protein may recognize a DNA sequence that differs from the consensus DnaA box sequence identified in other bacteria. Consensus DnaA box sequences, found upstream of many bacterial dnaA genes, were not identified upstream of rickettsial dnaA gene. In addition, gene organization within this region differed from that of other bacteria. The putative start of transcription of the rickettsial dnaA gene was localized to a site 522 nucleotides (nt) upstream of the DnaA start codon.


Subject(s)
Bacterial Proteins/genetics , DNA-Binding Proteins/genetics , Genes, Bacterial/genetics , Rickettsia prowazekii/genetics , Amino Acid Sequence , Base Sequence , Cloning, Molecular , Molecular Sequence Data , Rickettsia prowazekii/classification , Sequence Homology, Amino Acid
10.
J Clin Microbiol ; 36(5): 1176-9, 1998 May.
Article in English | MEDLINE | ID: mdl-9574671

ABSTRACT

The reliability of MYCO/F Lytic medium in the BACTEC 9240 blood culture system was evaluated by comparing its performance to that of the Isolator system for the recovery of fungi and to that of the ESP II system for the recovery of mycobacteria. Of 717 specimens of blood cultured for fungi, 24 were positive; 12 samples were positive with both systems, 7 samples were positive with the Isolator system only, and 5 samples were positive with MYCO/F Lytic medium only. Fourteen samples grew Histoplasma capsulatum; both systems detected H. capsulatum in seven samples but the Isolator system alone detected H. capsulatum in seven samples. The mean times to the detection of H. capsulatum were 8 days (range, 4 to 13 days) for MYCO/F Lytic medium and 9 days (range, 6 to 18 days) for the Isolator system; the mean times to identification were 20 days (range, 15 to 24 days) for isolates recovered with MYCO/F Lytic medium and 11 days (range, 6 to 18 days) for those recovered with the Isolator system (P < 0.05). Cryptococcus neoformans was isolated from 10 fungal cultures; five isolates grew in both systems, and five isolates grew in MYCO/F Lytic medium only. The mean times to detection of C. neoformans were 4 days (range, 2 to 6 days) for MYCO/F Lytic medium and 7 days (range, 5 to 7 days) for the Isolator system (P < 0.05); the mean times to identification were 15 days (range, 7 to 27 days) for isolates recovered with MYCO/F Lytic medium and 8 days (range, 7 to 11 days) for those recovered with the Isolator system. Of the 687 samples of blood cultured for mycobacteria, 64 blood samples from 42 patients grew mycobacteria (58 grew Mycobacterium avium complex, 4 grew Mycobacterium kansasii, and 2 grew Mycobacterium tuberculosis); 42 isolates were recovered with both systems, 18 were isolated with MYCO/F medium only, and 4 were isolated with the ESP II system only alone (P < 0.05). The mean time to detection of mycobacteria with MYCO/F Lytic medium was 14 days, whereas it was 17 days with the ESP II system (P < 0.05). In summary, the combination of MYCO/F Lytic medium and the BACTEC 9240 instrument is an excellent blood culture system for the growth and detection of mycobacteria. A valid assessment of MYCO/F Lytic medium with regard to fungal isolation, however, was not possible due to the small number of isolates recovered.


Subject(s)
Cryptococcosis/diagnosis , Cryptococcus neoformans/isolation & purification , Culture Media , Histoplasma/isolation & purification , Histoplasmosis/diagnosis , Mycobacterium Infections/diagnosis , Mycobacterium/isolation & purification , AIDS-Related Opportunistic Infections/blood , AIDS-Related Opportunistic Infections/diagnosis , Cryptococcosis/blood , Evaluation Studies as Topic , Histoplasmosis/blood , Humans , Mycobacterium Infections/blood , Mycobacterium Infections/microbiology , Reagent Kits, Diagnostic
11.
Clin Immunol Immunopathol ; 86(1): 81-7, 1998 Jan.
Article in English | MEDLINE | ID: mdl-9434799

ABSTRACT

Autoantibodies to EEA1, an antigen on early endosomes, were first reported in the serum of a patient with subacute cutaneous lupus erythematosus (SCLE). Here we have examined 38 sera selected for investigation of autoantibodies to EEA1 on the basis of cytoplasmic vesicle-like reactivity by immunofluorescence. Ten of the sera were reactive to a HeLa cell protein of approximately the same M(r) as human EEA1. Eight of these sera belonged to the IgG1 subclass. Five of the sera reacted with fusion proteins incorporating either the amino (from amino acids 1 to 209) or the carboxyl (incorporating the most C-terminal 300 amino acids) terminus of the human EEA1 protein. Antigens reactive with these 5 sera colocalized with internalized transferrin receptors, indicating their association with early endosomes. The other 5 sera which did not react to both fusion proteins did not colocalize with internalized transferrin receptors. We conclude that 5 of the 38 patients (13%) have autoantibodies to EEA1. None of these patients have SCLE, but have generalized joint pain, polyarthritis, rheumatoid arthritis, or circulating rheumatoid factors.


Subject(s)
Autoantibodies/immunology , Autoimmune Diseases/immunology , Endosomes/immunology , Joint Diseases/immunology , Membrane Proteins/immunology , Aged , Aged, 80 and over , Antibody Specificity , Arthralgia/blood , Arthralgia/immunology , Arthritis/blood , Arthritis/immunology , Arthritis, Rheumatoid/blood , Arthritis, Rheumatoid/immunology , Autoantibodies/blood , Autoimmune Diseases/blood , Biomarkers , Enzyme-Linked Immunosorbent Assay , Female , Fluorescent Antibody Technique, Indirect , HeLa Cells , Humans , Immunoglobulin G/blood , Immunoglobulin G/immunology , Immunoglobulin M/blood , Immunoglobulin M/immunology , Joint Diseases/blood , Male , Receptors, Transferrin/analysis , Recombinant Fusion Proteins/immunology , Rheumatoid Factor/analysis , Vesicular Transport Proteins
12.
J Endod ; 24(10): 648-50, 1998 Oct.
Article in English | MEDLINE | ID: mdl-10023245

ABSTRACT

This study compared the sealing ability of TERM as an interim restoration for the "walking bleach" technique when using either sodium perborate/water or sodium perborate/superoxol. Thirty-three extracted maxillary premolars were restored with TERM after placing either a cotton pellet (control), a paste of sodium perborate and water, or a paste of sodium perborate and superoxol in the chamber. Microleakage was assessed at 24 h, 8 days, and 15 days using a fluid filtration method. Statistical analysis revealed both "walking bleach" groups had significantly higher numbers of teeth demonstrating microleakage than the control group. There was no statistically significant difference in microleakage between the two "walking bleach" groups. The results of this study indicated that the temporary restorative material, TERM, provided an unsatisfactory seal when used with either walking bleach technique. When used over a cotton pellet, TERM provided an excellent seal.


Subject(s)
Composite Resins , Dental Leakage , Root Canal Filling Materials , Tooth Bleaching/methods , Borates , Chi-Square Distribution , Dental Leakage/etiology , Dental Restoration, Temporary/adverse effects , Dental Restoration, Temporary/methods , Evaluation Studies as Topic , Humans , Hydrogen Peroxide , Tooth Bleaching/adverse effects , Tooth, Nonvital
13.
J Clin Microbiol ; 35(5): 1141-3, 1997 May.
Article in English | MEDLINE | ID: mdl-9114396

ABSTRACT

The Captia Syphilis IgG enzyme immunoassay (EIA) was evaluated for use in conjunction with the rapid plasma reagin test (RPR) as a method to test for syphilis. A total of 1,288 serum specimens were tested by the routine laboratory protocol of the RPR followed by microhemagluttination assay for Treponema pallidum (MHA-TP) testing of RPR-reactive sera as well as the EIA-RPR protocol in which the automated EIA followed by a manual RPR test for EIA-positive specimens is used. When using the routine protocol, 131 specimens were initially reactive by the RPR, and 113 of these were reactive by MHA-TP. When using the EIA-RPR protocol, 170 specimens were initially positive by EIA, and of these, 112 were RPR reactive, indicating active disease. When compared to the routine protocol, the EIA-RPR protocol had sensitivity, specificity, and positive and negative predictive values of 96.5, 99.7, 97.3, and 99.7%, respectively. After resolution of discrepancies by additional testing, the adjusted sensitivity, specificity, and positive and negative predictive values were 100, 99.8, 98.3, and 100%, respectively. This evaluation demonstrates that when used in conjunction with the RPR, the Captia Syphilis EIA is a reliable method by which to test for syphilis.


Subject(s)
Antibodies, Bacterial/blood , Immunoassay/methods , Immunoglobulin G/blood , Syphilis/diagnosis , Treponema pallidum/isolation & purification , Humans , Syphilis/blood , Treponema pallidum/immunology
15.
Br J Pharmacol ; 116(4): 2322-6, 1995 Oct.
Article in English | MEDLINE | ID: mdl-8564267

ABSTRACT

1. The effects of the potassium channel opener, pinacidil, on mean arterial pressure (MAP), mean circulatory filling pressure (MCFP), total peripheral resistance (TPR), cardiac output (CO) and resistance to venous return (Rv) were studied in rats. 2. In pentobarbitone-anaesthetized rats given mecamylamine (ganglionic blocker, 3.7 micrograms kg-1) and noradrenaline (1.5 micrograms kg-1 min-1) to suppress autonomic reflexes, pinacidil (60 and 180 micrograms kg-1 min-1), relative to the vehicle, reduced MAP and TPR in a dose-dependent manner but did not significantly alter CO, MCFP or RV. 3. Pinacidil (10-300 micrograms kg-1 min-1) caused similar increases in MCFP, an inverse index of venous compliance, and similar dose-dependent reductions in mean arterial pressure (MAP) in conscious, intact rats and rats infused with the ganglionic blocker, hexamethonium (150 micrograms kg-1 min-1). In rats with vasomotor tone elevated by the infusion of noradrenaline (1.5 micrograms kg-1 min-1), pinacidil caused markedly greater depressor responses but did not significantly alter MCFP. 4. Our results show that pinacidil is an efficacious vasodilator of arterial resistance blood vessels but has little venodilator activity.


Subject(s)
Blood Pressure/drug effects , Guanidines/pharmacology , Vascular Resistance/drug effects , Vasodilator Agents/pharmacology , Anesthesia , Animals , Arteries/drug effects , Arteries/physiology , Cardiac Output/drug effects , Dose-Response Relationship, Drug , Ganglionic Blockers/pharmacology , Heart Rate/drug effects , Male , Microspheres , Pinacidil , Rats , Rats, Sprague-Dawley , Vascular Capacitance/drug effects , Veins/drug effects , Veins/physiology
16.
Am J Cardiol ; 76(2): 41A-46A, 1995 Jul 13.
Article in English | MEDLINE | ID: mdl-7604796

ABSTRACT

Fluvastatin monotherapy up to 40 mg/day over 52 weeks in patients with primary hypercholesterolemia decreased plasma low density lipoprotein cholesterol (LDL-C) by 28%, with varying decreases in plasma triglycerides and increases in high density lipoprotein cholesterol (HDL-C). Patients completing the 52-week study participated in a further trial to assess whether the efficacy of fluvastatin (20-40 mg/day), either as monotherapy or in combination with cholestyramine (CME; 4-16 g/day), taken at least 4 hours prior to fluvastatin, is sustained for up to 3 years. Patients were assessed every 12 weeks on average for safety and efficacy, the latter being calculated as a percent change from baseline of lipids or lipoproteins. During the second year (endpoint up to week 104), 147 patients received monotherapy (estimated mean dose, 30.2 mg/day) and 127 received additional CME (38.1 mg/day fluvastatin plus 10.1 g/day CME). During the third year (endpoint up to week 156), 140 patients received monotherapy (32.5 mg/day) and 67 received additional CME (39.3 mg/day fluvastatin plus 10.3 mg/day CME). Statistically significant reductions in mean total cholesterol and LDL-C and increases in mean HDL-C were achieved in both treatment groups and maintained throughout the study. A significant reduction in triglyceride levels was only observed at the second year endpoint in patients receiving monotherapy (-10.0%).(ABSTRACT TRUNCATED AT 250 WORDS)


Subject(s)
Anticholesteremic Agents/therapeutic use , Cholestyramine Resin/therapeutic use , Fatty Acids, Monounsaturated/therapeutic use , Hydroxymethylglutaryl CoA Reductases/therapeutic use , Hydroxymethylglutaryl-CoA Reductase Inhibitors , Hypercholesterolemia/drug therapy , Indoles/therapeutic use , Anticholesteremic Agents/administration & dosage , Anticholesteremic Agents/adverse effects , Cholesterol/blood , Cholesterol, HDL/blood , Cholesterol, LDL/blood , Cholestyramine Resin/administration & dosage , Cholestyramine Resin/adverse effects , Cohort Studies , Drug Combinations , Fatty Acids, Monounsaturated/administration & dosage , Fatty Acids, Monounsaturated/adverse effects , Female , Fluvastatin , Humans , Hydroxymethylglutaryl CoA Reductases/administration & dosage , Hydroxymethylglutaryl CoA Reductases/adverse effects , Hypercholesterolemia/blood , Indoles/administration & dosage , Indoles/adverse effects , Longitudinal Studies , Male , Middle Aged , Retrospective Studies , Safety , Triglycerides/blood
17.
Gene ; 151(1-2): 191-6, 1994 Dec 30.
Article in English | MEDLINE | ID: mdl-7828873

ABSTRACT

The Rickettsia prowazekii (Rp) gyrA gene, which codes for a subunit of DNA gyrase in this obligate intracellular bacterium, has been isolated and characterized. Nucleotide sequence analysis revealed an open reading frame (ORF), initiating with a GTG start codon, of 2718 bp that could encode a protein of 905 amino acids (aa) with a calculated M(r) of 101,048. The Rp gyrase subunit A (GyrA), when compared to GyrA analogs of other bacterial species, exhibited 43 to 50% identity. Alignment of the Rp GyrA aa sequence with the other analogs revealed the presence of a span of additional aa within the putative DNA-binding domain. The lack of an ORF within 865 bp upstream from the Rp gyrA demonstrates a Rp gene organization different from that of characterized gyrA from other species. Despite the similarity to Escherichia coli GyrA, Rp GyrA did not complement an E. coli gyrA temperature-sensitive mutant. However, Rp gyrA was dominant to an E. coli gyrA96 nalidixic-acid-resistant (NalR) mutant, conferring Nal sensitivity when introduced into the NalR E. coli strain.


Subject(s)
DNA Topoisomerases, Type II/genetics , Genes, Bacterial , Rickettsia prowazekii/genetics , Amino Acid Sequence , Bacteria/enzymology , Bacteria/genetics , Base Sequence , Codon , DNA Gyrase , DNA Topoisomerases, Type II/biosynthesis , Genetic Complementation Test , Genomic Library , Macromolecular Substances , Molecular Sequence Data , Open Reading Frames , Rickettsia prowazekii/enzymology , Sequence Homology, Amino Acid
18.
Blood Press Suppl ; 2: 81-7, 1994.
Article in English | MEDLINE | ID: mdl-8061853

ABSTRACT

In a double-blind, parallel-group study, 260 patients with mild to severe essential hypertension were randomized to treatment with placebo or spirapril at 6, 12 or 24 mg once daily for 6 weeks. When blood pressures were measured at the end of the dosing interval (trough), all spirapril regimens had produced similar reductions in sitting systolic and diastolic blood pressures (siSBP/siDBP) which were significantly greater than those observed in placebo-treated patients. There were no relevant changes in resting heart rate in any of the study groups. At the study endpoint, the mean reductions in siSBP/siDBP were 14.9/11.5 mmHg with spirapril at 6 mg, 15.4/12.0 mmHg with spirapril at 12 mg and 17.8/12.4 mmHg with spirapril at 24 mg/day vs. 3.1/3.6 mmHg with placebo. In a subgroup of 122 patients, blood pressure was recorded at the end of the dosing interval and during the 8 hours immediately postdose to monitor the peak effects on blood pressure. All spirapril dosages produced similar reductions at peak with a mean decrease of siDBP of approximately 20 mmHg in comparison to baseline values vs 6-7 mmHg with placebo. The trough:peak ratios for 6, 12 and 24 mg all lay between 60% and 90% for siSBP and siDBP, indicating that most of the peak effect was maintained at trough. Spirapril was well tolerated; the adverse event profile was not different from that with placebo, and no dose-related adverse events were observed.(ABSTRACT TRUNCATED AT 250 WORDS)


Subject(s)
Angiotensin-Converting Enzyme Inhibitors/administration & dosage , Enalapril/analogs & derivatives , Hypertension/drug therapy , Aged , Analysis of Variance , Angiotensin-Converting Enzyme Inhibitors/adverse effects , Blood Pressure/drug effects , Blood Pressure/physiology , Double-Blind Method , Enalapril/administration & dosage , Enalapril/adverse effects , Female , Humans , Hypertension/physiopathology , Male , Middle Aged , Time Factors
19.
Biol Psychiatry ; 34(1-2): 13-7, 1993.
Article in English | MEDLINE | ID: mdl-8373935

ABSTRACT

This study was designed to ascertain whether individuals with mood disorders are particularly vulnerable to adverse effects of aspartame. Although the protocol required the recruitment of 40 patients with unipolar depression and a similar number of individuals without a psychiatric history, the project was halted by the Institutional Review Board after a total of 13 individuals had completed the study because of the severity of reactions within the group of patients with a history of depression. In a crossover design, subjects received aspartame 30 mg/kg/day or placebo for 7 days. Despite the small n, there was a significant difference between aspartame and placebo in number and severity of symptoms for patients with a history of depression, whereas for individuals without such a history there was not. We conclude that individuals with mood disorders are particularly sensitive to this artificial sweetener and its use in this population should be discouraged.


Subject(s)
Aspartame/adverse effects , Aspartame/therapeutic use , Depressive Disorder/drug therapy , Adult , Cross-Sectional Studies , Depressive Disorder/diagnosis , Depressive Disorder/psychology , Double-Blind Method , Eye Diseases/etiology , Eye Diseases/physiopathology , Female , Headache/etiology , Humans , Male , Middle Aged , Placebos , Psychiatric Status Rating Scales , Vision Disorders/etiology , Vision Disorders/physiopathology
20.
AJR Am J Roentgenol ; 158(3): 591-7, 1992 Mar.
Article in English | MEDLINE | ID: mdl-1739001

ABSTRACT

Stability of the glenohumeral articulation is dependent on the integrity of the rotator cuff, labrum, glenohumeral ligaments, capsular elements, and bony glenoid. The importance of the soft-tissue elements in maintaining stability has been well documented in the surgical literature but has only recently been introduced into the radiologic literature. The purpose of this essay is to illustrate the normal labrum, capsular complex, and glenohumeral ligaments, including common congenital variations as depicted by CT arthrography and MR imaging, and to describe the pathologic findings leading to shoulder instability.


Subject(s)
Ligaments, Articular/pathology , Magnetic Resonance Imaging , Shoulder Joint/pathology , Tomography, X-Ray Computed , Humans , Joint Instability/diagnostic imaging , Joint Instability/etiology , Joint Instability/pathology , Ligaments, Articular/anatomy & histology , Ligaments, Articular/diagnostic imaging , Ligaments, Articular/injuries , Shoulder Injuries , Shoulder Joint/anatomy & histology , Shoulder Joint/diagnostic imaging
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