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Biomedical subjects

C Rey

Publications and source records attributed to C Rey.

At least 307 records · Page 17Linked to original sources
PubMed1987

Phosphatidylethanolamine methyltransferase and cAMP, cGMP phosphodiesterases in lymphocytes and monocytes in sarcoidosis.

Among the various hypotheses proposed to explain immune cell defect in sarcoidosis, we examined thoroughly that of Faguet who described abnormalities of signal transmission at lymphocyte membrane level. Phosphatidylethanolamine methyltransferase and cAMP cGMP phosphodiesterases were studied in blood lymphocytes and monocytes from 8 subjects with sarcoidosis disease. Phosphatidylethanolamine methyltransferase (PMT1) plays an important regulatory role in membrane signal transmission. cAMP and cGMP phosphodiesterases (PDE) regulate cytoplasmic cyclic nucleotide levels and so participate in the modulation of the cell cycle. We observed a decreased PMT1 activity in lymphocytes and monocytes and a decreased cAMP and cGMP PDE activities in monocytes. It is not now possible to say if these abnormalities are primary or secondary. Whatever the origin of this dysfunctioning, these results evoke simultaneous disturbances of membrane signal transmission and cell cycle in monocytes and membrane abnormalities in lymphocytes. These abnormalities could explain some immune cell defects in sarcoidosis disease.

3',5'-Cyclic-AMP Phosphodiesterases↗
PubMed1987

Hepatic extraction, metabolism and biliary excretion of doxorubicin in the isolated perfused rat liver.

The hepatic extraction, metabolism, and biliary excretion of doxorubicin (DX) were studied in the isolated perfused rat liver. Three doses of DX equivalent to 2, 20, and 100 mg/kg in rats were studied over a period of 3 h after bolus injection into the reservoir. DX and metabolites concentration in perfusate, bile, and liver were determined by high-pressure liquid chromatography. The hepatic extraction ratio was low (less than 0.24) and decreased progressively over the 3 h. The hepatic extraction and clearance were significantly lower at the highest dose. Doxorubicinol (DX-OL) was the only metabolite detected in the perfusate, accounting for less than 4% of the total AUC. Thirty-one to thirty-three percent of the dose was excreted into bile over 3 h as unchanged DX. This was reduced to 22% at the highest dose. Only 0.35%-1.33% of the dose was excreted as DX-OL. DX aglycones were found only in the liver, where they represented 20%-30% of the total fluorescence at 3 h. In conclusion, in this model DX has a low extraction ratio, is poorly metabolized and extensively excreted into bile.

Animals↗
PubMed1987

Iatrogenic false aneurysm of the brachial artery in an infant.

A 1-month-old infant was referred for a rapidly expanding mass at the left elbow. Angiography showed contrast extra-vasation from the brachial artery in a 4 X 3 cm pseudo-aneurysm. This false aneurysm was treated surgically with good result. It is probable that accidental arterial puncture during repeated veni punctures in the neonatal period for determination of bilirubinaemia was responsible for pseudo-aneurysm of the brachial artery.

Aneurysm↗
PubMed1987

[Interauricular communication with severe pulmonary hypertension in children. Apropos of 9 cases].

The authors report 9 cases of atrial septal defect with sever pulmonary hypertension in 7 girls and 2 boys under 10 years of age. These cases represent 3.5% of the 255 cases of atrial septal defect in this age group seen at the Hopital Cardiologique of Lille between 1970 and 1985. Group I comprised 3 children with obstructive pulmonary hypertension from the start; two died, one is still alive after 3 years. Group II was composed of 3 children who presented, at first haemodynamic evaluation, with severe but non-obstructive pulmonary hypertension; the hypertension rapidly became obstructive in 2 of them despite digitalis-diuretic therapy; the third child died after surgical correction. The 3 children in group III had normal or slightly raised pulmonary arterial pressure at first haemodynamic evaluation; one of them initially had a right ventricle-pulmonary artery functional gradient of 45 mmHg, which did not prevent the subsequent development of obstructive pulmonary hypertension; the other 2 patients were operated upon 10 months and 4 years later respectively, as they presented with severe pulmonary hypertension; one of these 2 children died postoperatively, the third one developed obstructive pulmonary hypertension. Contrary to what is generally believed, severe pulmonary hypertension is not exceptional in children with atrial septal defect, and it has a poor prognosis. The mechanism underlying the development of this pulmonary hypertension is unclear, but individual susceptibility to excessive blood flow is probable, as is the role played by bronchopulmonary infections frequently noted in these patients' history.

Child↗
PubMed1987

Norepinephrine: a potential modulator of the hepatic transport of taurocholate. a study in the isolated perfused rat liver.

The effects of norepinephrine on portal blood flow hepatic extraction and intrinsic clearance of taurocholate were studied in the isolated perfused rat liver. Livers were perfused at a constant pressure. [14C]Taurocholate was infused continuously at a rate of 0.6 mumol/min. Then, three increasing doses of norepinephrine were added to the perfusate. Norepinephrine induced a significant dose-dependent reduction in portal blood flow. In spite of this reduction, taurocholate extraction did not increase and intrinsic clearance decreased significantly. When portal blood flow was decreased mechanically, intrinsic clearance was, as expected, flow-independent. The effects of norepinephrine on portal blood flow and intrinsic clearance were antagonised by phentolamine but not by propanolol. Norepinephrine decreases independently both portal blood flow and the vectorial transport of taurocholate. These effects are mediated by alpha adrenergic receptors.

Animals↗
PubMed1986

Anomalous unilateral single pulmonary vein mimicking partial anomalous pulmonary venous return.

We report a case in which the clinical findings of a partial anomalous pulmonary venous return were present but with termination of the anomalous pulmonary vein into the left atrium. There was hypoplasia of the right lung, dextroposition of the heart, and a loop-like vascular density in the right lung field. Cardiac catheterization revealed no shunt, and on pulmonary angiograms, a large common right pulmonary vein draining the entire right lung and entering the left atrium by way of a single orifice. Possible embryologic explanations include atresia of the right inferior pulmonary vein and persistence of the ipsilateral superior pulmonary vein.

Cardiac Catheterization↗
PubMed1986

Isolation of dengue 2 and dengue 4 viruses from patients in Senegal.

Dengue 2 and dengue 4 viruses were isolated and re-isolated by inoculation into Aedes pseudoscutellaris continuous cell line (Mos 61) and/or Toxrhynchites brevipalpis. The strain of dengue 2 had been isolated from a patient returning from Casamance (south-western Senegal) and two strains of dengue 4 from patients who lived in Dakar and had not been outside the town in the 15 days before becoming ill. Serological evidence of dengue 4 infection was found in another patient living in Casamance.

Antibodies, Viral↗
PubMed1986

Percutaneous transluminal balloon valvuloplasty in congenital pulmonary valve stenosis.

From March 1984 to September 1986, 49 transluminal balloon valvuloplasties (TBVs) were performed in 44 consecutive patients with congenital pulmonary valve stenosis, aged 1 day to 60 years. Seventeen of the patients were infants aged less than 1 year, five of whom were neonates. The peak systolic gradient was greater than 50 mm Hg (mean, 80.0 mm Hg) in 36 patients and was less than 50 mm Hg (mean, 35.4 mm Hg) in eight. A single balloon catheter was used in 41 cases, and two balloon catheters were used in eight cases. In patients with a gradient greater than 50 mm Hg, the mean right ventricular peak systolic pressure was reduced from 99.8 to 51.8 mm Hg, and the mean transvalvular gradient was reduced from 80.0 to 22.4 mm Hg. In infants and neonates, the mean right ventricular pressure expressed as a percentage of systemic pressure decreased from 122.2% to 63.5%. Follow-up cardiac catheterization 1 to 17 months later (in 19 cases) revealed no significant change in the right ventricular systolic pressure (which had decreased from 53.0 to 48.5 mm Hg) or the peak systolic pressure gradient (which had decreased from 29.0 to 24.5 mm Hg), in comparison with the changes seen immediately after TBV. Thus, TBV is an effective method of relieving pulmonary stenosis in patients of all ages, including neonates.

Journal Article↗
PubMed1986

Takayasu's arteritis--a special form of the aortic arch syndrome. Manifestations of a chronical type III.

The case of a 45-year-old woman with arteritis of Takayasu's type is reported. This disease belongs to the inflammatory diseases of the aortic arch and sometimes shows extensive calcifications of the arterial system. The diagnosis is based on typical anamnesis and characteristic clinical symptoms, as well as on radiologic findings. The clinical signs depend on the extension of the disease. The literature about this rare disease is discussed.

Adolescent↗
PubMed1986

[Congenital subclavian steal syndrome. Apropos of 14 cases. Review of the literature].

Fourteen cases of the congenital subclavian steal syndrome are presented with a review of 99 cases in the literature. This abnormality is usually asymptomatic and a fortuitous finding (clinical: asymmetric blood pressure; radiological: investigation of an associated cardiovascular malformation). The possible malformations are numerous and may be diagnosed by angiography: however, they can be suspected from three simple investigations, clinical examination indicating the side of lower blood pressure, chest X-ray and barium swallow. Seventy one per cent congenital subclavian steal syndromes are associated with a right-sided aortic arch, the steal being then almost always left-sided via a left subclavian artery anomaly. In this group, a left subclavian artery isolated from the aorta represents about a half of the cases. A cardiac malformation is present in one out of two cases and a patent ductus arteriosus uniting the left subclavian artery and the left pulmonary artery is observed in one out of four cases. Twenty nine per cent of congenital subclavian steal syndromes are associated with a left-sided aortic arch. In these cases the abnormalities usually involve the aortic arch (57% of cases) or a right or left subclavian artery. Therefore, in this group, there is no preferential side for the subclavian steal which can be right, left or bilateral. These abnormalities usually only require medical surveillance. When they become symptomatic, vertebro-subclavian revascularisation is justified. The presence of a subclavian steal may have surgical implications: it is important to exclude a subclavian steal before performing a Blalock anastomosis.(ABSTRACT TRUNCATED AT 250 WORDS)

Child↗
PubMed1986

[Aneurysm of the sinus of Valsalva in children and young adults. Apropos of 9 cases].

Nine cases (7 boys and 2 girls) of aneurysm of the sinus of Valsalva (SVA) diagnosed before 19 years of age are reported. Group 1 comprised 5 children aged 5 to 14 years without rupture of the aneurysm; 3 had an associated ventricular septal defect (VSD). The diseased sinus was the right anterior sinus in 4 cases and the posterior sinus in one case. The diagnosis was made by 2D echocardiography, performed in 3 patients for follow-up of a VSD and in 2 patients to investigate a systolic murmur. Group 2 comprised 4 patients under 19 years of age with SVA which ruptured into in the right heart cavities. One of these patients had a known right anterior SVA diagnosed at angiography performed to investigate a VSD when the child was 4 years old. The rupture occurred suddenly when the child was 14. These cases of SVA involved the right anterior sinus with rupture into the right ventricle (3 cases) and the posterior non-coronary sinus with rupture into the right atrium (1 case). A rupture syndrome was observed in 3 of the 4 patients with pulmonary oedema in 2 cases. The authors emphasise the rarity of SVA diagnosed before rupture and the low frequency of rupture before adulthood. Echocardiography is certainly the best method for diagnosing the condition and for following up these patients.

Adolescent↗
PubMed1986

[Continuous electrocardiographic recording with the Holter method in children. Indications and results].

There are relatively few reported studies of continuous electrocardiographic recordings by the Holter method in children. We report our experience of 296 24-hour recordings in 160 patients (average age 10.5 years), investigated for suspected or known cardiac arrhythmias. One hundred and ten patients (68.75%) had no organic heart disease and 6 patients (3.75%) had acquired lesions. Eighty-three patients (52%) were symptomatic. Sixty-three patients (39%) had normal recordings; 97 patients (61%) had a total of 126 arrhythmias. There were 45 cases of atrioventricular block, 24 cases of sinus node dysfunction, 39 cases of supraventricular arrhythmias and 18 cases of ventricular arrhythmias. Overall, 47.6% of these rhythm disturbances were diagnosed by Holter monitoring. This technique was particularly valuable in the diagnosis of arrhythmias in symptomatic patients, patients with arrhythmogenic cardiac lesions and in the detection and surveillance of postoperative arrhythmias in congenital heart disease, of pacemakers, of congenital atrioventricular block and of the chronic arrhythmias of childhood.

Adolescent↗