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Biomedical subjects

C Xiong

Publications and source records attributed to C Xiong.

36 records · Page 2Linked to original sources
PubMed1997

[Clinical efficacy of prolonged therapy with NO on patients with pulmonary hypertension].

OBJECTIVE: To determine the safety and clinical efficacy of prolonged NO administration in patients with pulmonary hypertension. METHOD: Clinical efficacy of prolonged treatment (28 days) with NO (20 ppm) in 17 patients with pulmonary hypertension was observed by chest X-ray film, ECG, Doppler echocardiography, analysis of arterial blood gases and the other laboratory investigations. RESULTS: After prolonged treatment with NO, regurgitation velocity and peak pressure gradient across tricuspid valves during systole reduced by 11.8% and 22.6%, respectively (P < 0.0001). Ejection fraction of right ventricle, stroke volume and cardiac output of left ventricle, partial oxygen pressure and oxygen saturation of arterial blood increased by 29.9%, 60.3%, 37.8%, 21.7% and 3.8% (all statistics; P < 0.0001), respectively. The class of heart function by New York Heart Association (NYHA) was improved dramatically (P < 0.01). Heart rate also reduced from 96 +/- 12 bpm to 83 +/- 10 bpm (P < 0.0001). But systemic artery pressure and the concentration of blood methemoglobin which reflected NO toxicity did not change obviously (P > 0.05). CONCLUSION: Clinical efficacy of prolonged treatment with NO is satisfied in patients with pulmonary hypertension. Significant clinical side effects and toxicities are not seen during prolonged treatment with NO.

Administration, Inhalation↗
PubMed1996

[Expression of myelin basic protein gene in the developing human brain].

The expression of myelin basic protein (MBP) gene in the developing human brain was studied by using Northern dot blot and in situ hybridization with 32P- and biotin-labeled rat MBP cDNA and Diglabeled human MBP cRNA probes so as to explore the relation of temporal and spatial expression of human MBP gene to myelinogenesis and myelination. The results of dot blot analysis showed that the expression of MBP mRNA was near 2.0 A590/microgram of RNA in the fetal brain at 16 weeks of conceptional age, and it increased progressively with development to have 9-fold increment (18 A590/microgram of RNA) in the adult brain. The insitu hybridization was performed with the sections of fetal spinal cord and medulla oblongata at 8-25 weeks of conceptional age, and of pons, midbrain, thalamus, cerebellum and cerebrum at 20, 22 and 25 weeks. The results indicated that the expression of MBP mRNA was found as early as 8-9 weeks and localized within the perinuclear cytoplasm of the scattered cells in the ventral horn of spinal cord and near the basis of the fourth ventricle of medulla oblongata. Whether the above-mentioned labeled cells are neurons or precursors of glial cell remains to be identified because they are larger in size and have more abundant cytoplasm than oligodendrocytes. The labeling of MBP mRNA abruptly increased and spread with the processes of oligodendrocytes to form a network in spinal cord and medulla at 20 weeks; meanwhile, labeling was obvious in pons and scattering in the other brain regions examined.

Adult↗
PubMed1995

A bioacoustic method for timing of respiration at cardiac investigations.

At cardiac investigations Doppler echocardiography is an established technique for the recording of intracardial and intravascular flow velocities. Transvalvular and venous flows are, however, markedly influenced by respiration. Since the start of inspiration is the important time of reference, accurate recording of the respiratory phase is important when analysing these flow velocities. A bioacoustic technique was therefore adopted to meet this demand and was tested in 10 normal subjects. Oesophageal balloon technique was used as a reference, and the bioacoustic technique was compared with a respiratory inductive plethysmograph. The average delay for the acoustic sensor signal compared to the oesophageal pressure changes was 205 +/- 46 (SD) ms, ranging from 160 to 320 ms for normal breathing, and is comparable to that of the respiratory inductive plethysmograph (210 +/- 90 ms). The bioacoustic technique is easier to apply than the respiratory inductive plethysmograph. The sensitivity to disturbances can be further reduced by signal processing and the method has clinical potential for the future.

Adult↗
PubMed1995

Atrial and ventricular function after cardioversion of atrial fibrillation.

OBJECTIVE: Previous studies on atrial recovery after cardioversion of atrial fibrillation have not taken into account new knowledge about the pathophysiology of transmitral and transtricuspid flow velocity patterns. It is possible to shed further light on this problem if atrioventricular inflow velocity, venous filling pattern, and atrioventricular annulus motion are recorded and interpreted together. DESIGN: Prospective examinations of mitral and tricuspid transvalvar flow velocities, superior caval and pulmonary venous filling, and mitral and tricuspid annulus motion were recorded using Doppler echocardiography. Examinations were performed before and 24 hours, 1 month, and 20 months after cardioversion. SETTING: Tertiary referral centre for cardiac disease with facilities for invasive and non-invasive investigation. PATIENTS: 16 patients undergoing cardioversion of atrial fibrillation in whom sinus rhythm had persisted for 24 hours or more. RESULTS: Before conversion there was no identifiable A wave in transvalvar flow recordings. The total motion of the tricuspid and mitral annulus was subnormal and there was no identifiable atrial component. Venous flow patterns in general showed a low systolic velocity. After conversion, A waves and atrial components were seen in all patients and increased significantly (P < 0.01) with time. There was a similar time course for the amplitude of annulus atrial components, an increased systolic component of venous inflow, an increased A wave velocity, and a decreased E/A ratio of the transvalvar velocity curves. The ventricular component of annulus motion was unchanged. Changes in general occurred earlier on the right side than the left. CONCLUSIONS: This study indicates that, in addition to the previously known electromechanical dissociation of atrial recovery that exists after cardioversion of atrial fibrillation, there may also be a transient deterioration of ventricular function modulating the transvalvar inflow velocity recordings. Function on the right side generally becomes normal earlier than on the left. Integration of information from transvalvar inflow curves, annulus motion, and venous filling patterns gives additional insight into cardiac function.

Aged↗
PubMed1995

[Simplified enzyme-linked immunoadsorbent assays for myelin basic protein and antibodies to myelin basic protein].

Synchronous quantitative determination using simplified enzyme-linked immuno adsorbent assay has been developed for myelin basic protein (MBP) and antibodies to myelin basic protein (Anti-MBP). Antisera were prepared by immunizing rabbits with purified MBP from human white matter. Antibodies to MBP was conjugated with horseradish peroxidase (HRP) by using modified periodate oxidation method. Minimum detection amounts of MBP and Anti-MBP are 0.25 ng/ml and 0.20 ng/ml respectively. The activities of Anti-MBP-HRP conjugates are stable (stored at -30 degrees C) for at least 2 years. The detection procedure can be accomplished within 24 hours.

Animals↗
PubMed1992

[Effects of Panax notoginseng saponins on monophasic action potentials of heart and automaticity and contractility of isolated atria].

The effects of Panax notoginseng saponins (PNS) on monophasic action potentials (MAP) recorded from the myocardial surface by means of contact electrode were studied in 30 open-chest rabbits. The MAPA was increased and MAPD50, MAPD90 were prolonged with PNS (100, 200 mg.kg-1, iv), while the Vmax remained unchanged. PNS (300-1200 micrograms.ml-1) inhibited the automaticity of isolated guinea pig right atria and the contractility of the left atria. The positive inotropic action of ouabain (0.2 mumol.L-1) on isolated guinea pig left atria was decreased in the presence of PNS 300 micrograms.ml-1.

Action Potentials↗
PubMed1989

Sindbis virus: an efficient, broad host range vector for gene expression in animal cells.

Sindbis virus, an enveloped virus with a single-stranded RNA genome, was engineered to express a bacterial protein, chloramphenicol acetyltransferase (CAT), in cultured insect, avian, and mammalian cells. The vectors were self-replicating and gene expression was efficient and rapid; up to 10(8) CAT polypeptides were produced per infected cell in 16 to 20 hours. CAT expression could be made temperature-sensitive by means of a derivative that incorporated a temperature-sensitive mutation in viral RNA synthesis. Vector genomic RNAs were packaged into infectious particles when Sindbis helper virus was used to supply virion structural proteins. The vector RNAs were stable to at least seven cycles of infection. The expression of CAT increased about 10(3)-fold, despite a 10(15)-fold dilution during the passaging. Sindbis virus vectors should prove useful for expressing large quantities of gene products in a variety of animal cells.

Aedes↗
PubMed1984

A second cauliflower mosaic virus gene product influences the structure of the viral inclusion body.

We have used electron microscopy of thin sections and experiments on isolated viroplasms to compare the properties of four strains of cauliflower mosaic virus (CaMV), three of which were partially or completely deleted in open reading frame (ORF) II. Our results confirm that this gene is required for aphid transmissibility and show that the product of ORF II influences the firmness with which virions are held within the viroplasm. Analysis of the proteins in the viroplasms showed that a mutant with a partial deletion in ORF II produced a protein smaller than the normal ORF product. This smaller protein was non-functional with respect both to aphid transmissibility and properties of the viroplasms.

Journal Article↗
PubMed1984

Expression of a putative plant viral gene in Escherichia coli.

A recombinant plasmid, pCB300, was constructed which carries a cauliflower mosaic virus (CaMV) DNA insert corresponding to nucleotides 1825-2280, including the coding sequence (1830-2219) of open reading frame III (ORF III). This CaMV DNA insert was fused with the amino-terminal portion of the beta-galactosidase gene. Transcription of the hybrid gene is controlled by the lac promoter, which is repressed in Escherichia coli strain JM103 and can be induced by isopropylthio-beta-D-galactoside (IPTG). When the promoter is derepressed, cells harboring the chimeric plasmid produce an Mr 16 000 fusion protein. This protein is immunodetected by antibodies raised against an amino terminal synthetic peptide of 19 amino acids corresponding to a sequence predicted from the nucleotide sequence of ORF III.

Cloning, Molecular↗
PubMed1984

Detection in vivo of a new gene product (gene III) of cauliflower mosaic virus.

Cauliflower mosaic virus DNA contains six major open reading frames (ORFs). As only the mRNA corresponding to the transcription of gene VI and its translation product have been isolated, the identification in infected plants of products corresponding to the five other putative genes remains to be established. The present paper reports the detection of an ORF III product by means of antibodies raised against an NH(2)-terminal synthetic peptide of 19 amino acids corresponding to a sequence predicted from the nucleotide sequence of ORF III. The detection of this gene product raises the question of the mechanism of its expression.

Journal Article↗
PubMed1982

Identification by immunoprecipitation of cauliflower mosaic virus in vitro major translation product with a specific serum against viroplasm protein.

A highly specific antiserum was prepared against purified cauliflower mosaic virus viroplasm-protein (VmP). A virus specific in vitro major translation product (TPmaj), encoded by the 19S poly(A) RNA fraction from cauliflower mosaic virus infected turnip leaves, was recognized by this antiserum. The N-terminal sequence of TPmaj corresponds to the sequence following the first in-phase initiation codon in gene VI of the cauliflower mosaic virus genome. Both VmP and TPmaj have blocked termini and probably start from the same AUG codon.

Journal Article↗
PubMedDate not supplied

The shape of the proximal isovelocity surface area varies with regurgitant orifice size and distance from orifice: computer simulation and model experiments with color M-mode technique.

The hemispheric proximal isovelocity surface area method for quantification of mitral regurgitant flow (i.e., Qc = 2 pi r2v), where 2 pi r2 is the surface area and v is the velocity at radius r, was investigated as distance from the orifice was increased. Computer simulations and steady flow model experiments were performed for orifices of 4, 6, and 8 mm. Flow rates derived from the centerline velocity and hemispheric assumption were compared with true flow rates. Proximal isovelocity surface area shape varied as distance from each orifice was increased and could only be approximated from the hemispheric equation when a certain distance was exceeded: > 7, > 10, and > 12 mm for the 4, 6, and 8 mm orifices, respectively. Prediction of relative error showed that the best radial zone at which to make measurements was 5 to 9, 6 to 14 and 7 to 17 mm for the 4, 6, and 8 mm orifices, respectively. Although effects of a nonhemispheric shape could be compensated for by use of a correction factor, a radius of 8 to 9 mm can be recommended without the use of a correction factor over all orifices studied if a deviation in calculated as compared with true flow of 15% is considered acceptable. These measurements therefore have implications for the technique in clinical practice.

Blood Flow Velocity↗
PubMedDate not supplied

Problems in timing of respiration with the nasal thermistor technique.

When one analyzes transvalvular and venous flow velocity patterns, it is important to relate them to respiration. For this reason a nasal thermistor technique is often used, although it is known that this signal is delayed in relation to intrathoracic pressure changes. The magnitude and variation in delay have not been investigated previously and were, therefore, studied in a model experiment in 10 normal subjects, in 10 patients with obstructive, and in 10 patients with restrictive pulmonary disease. Esophageal pressure variations measured with an air-filled balloon served as a gold standard for intrathoracic pressure changes. During basal conditions there was, for both patient groups and normal subjects, a considerable delay of the thermistor signal. The average delay for all subjects was 370 msec with a wide variation (from 120 to 720 msec). At higher breathing frequencies the delay shortened to 310 msec (P < 0.01) but there was still a wide variation (ranging from 200 to 470 msec). Theoretic calculations show that the delay caused by the respiratory system accounts for only a minor portion of the total delay. Model experiments confirmed that the response characteristics of the thermistor probes limit the accuracy in timing of respiration. The total delay with the investigated thermistor technique is too long and variable to fulfil clinical demands.

Adult↗