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Biomedical subjects

H Gilljam

Publications and source records attributed to H Gilljam.

34 records · Page 2Linked to original sources

Bronchial exudation of bulk plasma at allergen challenge in allergic asthma.

This study examined plasma exudation into the bronchial lumen after allergen challenge. A novel low-trauma technique was developed to challenge and lavage a medium-sized lingular or middle lobe bronchus. Eleven subjects with challenge-assessed pollen-sensitive asthma were allocated to fiberbronchoscopy in the supine position. In the control bronchus 0.5 ml diluent was instilled. The bronchus was occluded proximally 3 min later by inflation of a balloon, and lavage was carried out twice with 25 ml saline. Incremental doses of allergen solution (0.5 ml) were then instilled in the contralateral lung. The challenge continued until a clearly visible bronchial reaction occurred and was immediately followed by the same lavage as on the control side. The lavage liquids were analyzed for the presence of plasma exudation and mast cell activation indices. On the allergen-challenged side, tryptase, reflecting mast cell activation, was increased by 150% (p < 0.01) compared with the control side. Fibrinogen (mol wt 340,000), reflecting large protein exudation, was increased by 840% (p < 0.05), and N-alpha-tosyl-L-arginine-methyl esterase activity, reflecting both large protein exudation and mast cell activation, increased by 480% (p < 0.01). The level of albumin (mol wt 69,000), the major luminal protein under baseline conditions, increased but not significantly. We conclude that activation of mast cells and luminal entry of little sieved plasma exudates occur early after endobronchial allergen provocation in human subjects with allergic asthma.

Albumins↗

Smoking and reproduction. Short and long term effects and benefits of smoking cessation.

There have been many attempts during the last years to restrict smoking because of the significant health hazards. In particular the high prevalence of smoking among women in their reproductive years has been a matter of concern. This review was prompted in order to make the medical profession, and gynecologists in particular, confident with the underlying data. This will hopefully result in enabling them to provide balanced information to their patients, not overemphasizing the dangers of smoking, but rather presenting ways to properly recognize and treat tobacco dependence. It is a widely held view that the various risks imposed by smoking are very modest. A doubling of the risk for a rare problem may not prevent many women from continuing to smoke. However, a doubling of the risk for early miscarriage or a significant reduction of success rate in the treatment of infertility may be much more discouraging. The purpose of this review is to list the various effects smoking may have on the different phases of reproduction and to present an overview of the explanation models which have been suggested. Late effects on the child and its development will also be discussed. Hopefully, this will lead to proper concern about the problems and thus increase the motivation to quit smoking even before attempting a pregnancy. In addition, we give some hints on smoking cessation programs.

Child Development↗

Passive smoking in cystic fibrosis.

The families of 32 children with cystic fibrosis (CF) were interviewed about both their tobacco consumption and their childrens physical activities. Hospital records informed about treatment frequency, lung function and clinical score. Cystic fibrosis families smoked far more than the Swedish average and the passive smokers among our patients seemed to fare less well in all parameters. The children of smoking mothers required significantly longer periods of intravenous antibiotic treatment (P greater than 0.05). Frequent physical exercise seemed to compensate for the potential harmful effects of passive smoking and children with high physical activity living in families who smoked needed significantly less frequent antibiotic treatment than the inactive children (P greater than 0.02). Although this series is small, the results indicate that a smoke-free environment may be important for CF patients. General information is insufficient and extensive psychological support to the families is probably necessary.

Adolescent↗

Plasma calcitonin levels in patients with cystic fibrosis.

Plasma levels of calcitonin were investigated in patients with cystic fibrosis and compared with age- and sex-matched healthy controls. About forty per cent of the cystic fibrosis patients had plasma calcitonin levels that were markedly higher than normal. Elevated levels were found predominantly in female patients. In general, patients with marked pulmonary involvement had high plasma calcitonin levels. Immunoextraction and gel chromatography, carried out on plasma of one of the patients demonstrated monomer-like forms of calcitonin similar to those found in the healthy subjects.

Adolescent↗

Increased bronchial chloride concentration in cystic fibrosis.

Ten patients with cystic fibrosis (CF) and 10 patients with severe chronic bronchitis were analysed for bronchial electrolyte composition. Samples aspirated from the left main bronchus by a fibre-optic bronchoscope were dissolved in an iso-osmolar solution of N-acetylcysteine, and separated from cells and bacteria by gentle centrifugation. The concentrations of potassium and calcium were measured by flame emission and atomic absorption spectrometry, and found to be similar in both groups of patients. The mean concentration of chloride, measured by coulometric titration, was significantly higher in patients with CF than in patients with chronic bronchitis (170 vs. 85 mmol l-1, p less than 0.01). The findings are consistent with a functional abnormality of the chloride channels of the airway epithelium in patients with CF.

Adult↗

Composition and surface properties of the bronchial lipids in adult patients with cystic fibrosis.

Bronchial secretions from seven patients with cystic fibrosis (CF) were aspirated by fibreoptic bronchoscopy and analysed for lipid composition. The total lipid fraction was also used to measure dynamic surface tension. Pooled samples from 'normal' patients, healthy volunteers, patients with chronic bronchitis, and individual samples from two patients with bronchiectasis were used as controls. Increased bronchial inflammation and infection correlated with a decrease of the phospholipid fraction, and an increase of the cholesterol, diglyceride and triglyceride fractions. When individual phospholipids were analysed, patients with clinically severe CF showed a markedly decreased phosphatidylcholine fraction, whereas the phosphatidylinositol fraction was significantly higher in CF patients than in controls (p less than 0.05). Minimum surface tension was higher in CF patients compared to patients with chronic bronchitis (p less than 0.05). This might be related to earlier reported specific changes in the pattern of fatty acids of the CF bronchial phospholipids.

Adult↗

Relation between defective regulation of arachidonic acid release and symptoms in cystic fibrosis.

A hypothesis is formed about the basic defect in CF based on the findings of 1) a defective inhibition of AA release by dexamethasone stimulation of lymphocytes from patients with CF, probably due to a defect in or absence of lipocortin and 2) the essential fatty acid deficiency (EFAD) in CF reported by different authors for 25 years. Both in lymphocytes and fibroblasts from patients with CF increased AA release has been demonstrated. AA, substrate for the eicosanoid system (prostaglandins, leukotrienes, hydroxyeicosatetraenoic acids, thromboxanes), has been shown to increase mucus release, influence chloride transport and the stimulus-secretion coupling (Ca++ balance), all factors suggested as basic defects in CF. The increased release of AA might explain the development of EFAD, since AA is synthesized from linoleic acid. In animals EFAD gives rise to symptoms similar to those in CF, e.g. defect Na transport, liver steatosis, increased caloric need, disturbed insulin release, increased bacterial colonization of airways, and decreased immune response. Regular supplementation with fat emulsion (Intralipid) to CF patients normalizes the renal Na transport and prevents liver steatosis. We suggest that the basic defect in CF is a defect in or absence of lipocortin, causing an increased release of AA, which regulates synthesis in the eicosanoid system. An increase of the products in this system gives rise to the basic signs and symptoms of CF. The resulting EFAD is dependent on the rate of AA turnover and could explain most of the clinical symptoms and the progression of the disease.

Annexins↗

Ultrastructure of the bronchial epithelium in adult patients with cystic fibrosis.

The respiratory epithelium of large airways was studied in biopsy specimens obtained by bronchoscopy in seven patients with cystic fibrosis (CF). All but one of these patients were chronically colonised with Pseudomonas aeruginosa. Biopsy specimens were also obtained from the large airways of 10 control patients with or without signs of chronic bronchitis. All samples were studied by transmission electron microscopy. Morphometry was applied to assess the volume density of various cell types and intercellular spaces and for quantification of microvilli of ciliated cells. In CF patients, the average number of microvilli per ciliated cell was decreased by 17% compared to patients with chronic bronchitis and by 34% compared to patients with apparently normal bronchi (p less than 0.02, respectively), but otherwise no abnormalities were found. In particular, the volume density of goblet cells was not increased. Thus the ultrastructure of the airway epithelium may be nearly normal in CF, even in adult patients with chronic respiratory infection.

Adult↗

Conformity of bacterial growth in sputum and contamination free endobronchial samples in patients with cystic fibrosis.

The use of sputum cultures to guide the antimicrobial treatment of patients with cystic fibrosis has been questioned. Bacterial growth and antibiotic susceptibility patterns of 33 culture pairs from sputum and contamination free endobronchial swabs from 14 patients with cystic fibrosis were compared. As expected, Pseudomonas aeruginosa of the mucoid and non-mucoid type, Staphylococcus aureus, and Haemophilus influenzae were the organisms most frequently found. Absolute or good agreement was found in 73% of the culture pairs. The accuracy of the sputum cultures improved with the duration of antimicrobial treatment. The extra information gained from the endobronchial culture did not change the antimicrobial strategy from that based on the sputum culture alone. It is concluded that sputum cultures provide accurate information about the bacterial colonisation of the lower respiratory tract in patients with cystic fibrosis and therefore can be trusted both at onset of treatment and during the entire treatment period.

Adult↗

Increased mole fraction of arachidonic acid in bronchial phospholipids in patients with cystic fibrosis.

The fatty acid pattern of the phospholipids in the bronchial secretion of patients with cystic fibrosis (CF) showed an increase of the mole fraction of arachidonic acid (AA) in most phospholipid classes compared to normals. Increase of AA in some classes was also found in patients with chronic bronchitis and in patients chronically colonized with Pseudomonas aeruginosa but in the diphosphatidylglycerol, lysophosphatidylethanolamine and sphingomyelin phospholipids, high fractions of AA was found exclusively in CF patients. Arachidonic acid was found to attain the highest ratios in CF in seven of the nine major bronchial phospholipids compared to the controls. There was no difference in the ratio saturated/unsaturated fatty acids between the CF patients and the control groups. A tendency towards unsaturation of the fatty acids in the bronchial secretion seems to be characteristic of infection and inflammation but AA appears to be more markedly increased in CF. Thus, the recorded changes may be characteristic for CF and not secondary to infection and/or inflammation in general, nor to P. aeruginosa colonization.

Arachidonic Acids↗

X-ray microanalysis of goblet cells in bronchial epithelium of patients with cystic fibrosis.

The elemental composition of goblet cells in bronchial epithelium was investigated by X-ray microanalysis. Biopsies were obtained from the left main bronchus, shock-frozen and freeze-substituted. In comparison to the control group (patients with chronic bronchitis), the goblet cells of patients with cystic fibrosis (CF) contained significantly more calcium. The analysis also indicated higher sulphur levels and lower potassium levels in the goblet cells of CF patients. Detailed analysis of a control biopsy showed that the calcium level in the mucous cells of the submucosal glands was considerably higher than that in the goblet cells. Although the data point to a higher calcium content of goblet cell mucus in CF patients, the significance of this finding for the calcium content of the tracheobronchial secretions in CF patients is unclear.

Adult↗

The effect of cimetidine in meal-stimulated gastric functions measured with a new method.

A new method to measure gastric functions after meal-stimulation without infusion of bicarbonate into the stomach is presented. Six healthy volunteers were investigated after stimulation of the gastric functions with a 300-ml fluid test meal with and without cimetidine infusion. Cimetidine reduced the acid output substantially but had no effect on gastric emptying.

Adolescent↗