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Biomedical subjects

T Lund

Publications and source records attributed to T Lund.

At least 163 records · Page 9Linked to original sources

Microvascular fluid exchange following thermal skin injury in the rat: changes in extravascular colloid osmotic pressure, albumin mass, and water content.

Microvascular fluid exchange was studied in rats subjected to 0, 10, and 40% body surface area (BSA) full-thickness cutaneous burns without providing fluid substitution. The total amounts of water and of albumin entering the entire burned skin area following 10% BSA burns were similar to that in 40% BSA burns. Colloid osmotic pressure in interstitial fluid (COPi) was around 10 mmHg and did not change in the control group or in burned skin from the 40% BSA burn group. COPi after 10% burns increased to 15 mmHg in injured skin, while plasma COP fell from 16 to 12.5 mmHg. Preburn, the interstitial albumin mass (Qalb) was 14.9 mg/g dry tissue weight (DW) and increased to 42 and 20 mg/g DW in injured skin after 10 and 40% burns, respectively. Extravasation of radiolabeled albumin (Ealb) estimated as plasma equivalents per 30 min increased from 6.0 to 321 microliters/g DW at 30-60 min postburn (PB) in injured skin following 10% BSA burns. At 90-120 and 150-180 min PB Ealb in this group was reduced to approximately 120 microliters/g DW. These levels of Ealb were roughly 6 times higher than those after 40% BSA burns. Total tissue water (TTW) was 1.78 ml/g DW preburn and increased to 3.0 and 2.0 ml X g-1 DW PB in the 10 and 40% burn groups, respectively. TTW and Qalb did not change beyond 60 min PB.

Albumins↗

Upper airway sequelae in burn patients requiring endotracheal intubation or tracheostomy.

During a period of 11 1/2 months, 41 of 217 adult burn patients admitted to the U.S. Army Institute of Surgical Research Burn Center required endotracheal intubation or tracheostomy for management of the airway and/or ventilatory assistance. Permanent upper airway sequelae were recorded and related to presence of inhalation injury, duration of tube placement, cuff pressure, and pulmonary compliance. An "inhalation injury scoring system" based upon history, physical examination, bronchoscopic findings, and abnormalities at 133xenon lung scan correlated well with postinjury alteration in compliance and subsequent sequelae. Significant inhalation injury was found in 35 patients. Seventeen of the study patients survived (Group I) and 24 patients expired (Group II). Group I patients were screened for permanent airway sequelae by fiberoptic bronchoscopy, xeroradiograms, and spirometry undertaken an average of 11 weeks after extubation or decannulation. Four patients developed tracheal stenosis and five patients had significant tracheal scar granuloma formation. Sequelae were generally more frequent and more severe after tracheostomy than after translaryngeal intubation, and duration of tube placement and presence of a tracheal stoma were the most important etiological factors in permanent damage. For initial respiratory support, we favor the use of translaryngeal (nasotracheal) tubes for periods up to 3 weeks. Fiberoptic bronchoscopic examination is the most reliable follow-up method for detecting anatomic damage in such patients. Spirometry can be used as a noninvasive screening test and xeroradiograms are helpful in assessing the degree of tracheal stenosis.

Adolescent↗

Severe hypoxemia without evidence of tissue hypoxia in adult respiratory distress syndrome.

A patient with severe arterial hypoxemia in adult respiratory distress syndrome (ARDS) secondary to a fractured femur is reported. A marked discrepancy between the clinical condition and laboratory findings was observed. At one point, PaO2 was below 4 kPa (30 mm Hg) on F1O2 0.21 without signs of tissue hypoxia. This patient illustrates beneficial effects of a leftward shift of the oxyhemoglobin dissociation curve.

Adult↗

The complete nucleotide sequence of the I-E alpha d immune response gene.

We have isolated and sequenced the complete murine I-E alpha immune response gene of the H-2db haplotype. The I-E alpha d gene consists of 5300 basepairs and is organized into five or possibly six exons that correspond to different domains of the alpha chain. The amino acid sequence deduced from the I-E alpha gene shows 75% homology to its human counterpart, the HLA-DR alpha chain. The absence of I-E antigen in H-2 mice is due to lack of E alpha chain synthesis. We show here that this defect is caused by a deletion in the 5' end of the I-E alpha b gene.

Amino Acid Sequence↗

On the presence of two new high mobility group-like proteins in HeLa S3 cells.

Two phosphorylated HMG-like proteins with Mr approximately 10 000 have been isolated from HeLa S3 cells, one being present in metaphase and one in interphase cells. The amino acid compositions of these proteins are very similar but differ from the known HMG proteins. However, they exhibit similarities being rich in proline, basic and acidic amino acids. A possible role in chromatin condensation of the HMG-like protein characteristic for metaphase cells is suggested.

Chemical Phenomena↗

Structure of the murine immune response I-A beta locus: sequence of the I-A beta gene and an adjacent beta-chain second domain exon.

The murine major histocompatibility complex I region encodes two class II antigens, I-A and I-E. From a mouse spleen DNA cosmid library of the b haplotype, we isolated a clone containing the entire I-A beta gene and a separate exon encoding a beta-chain second domain (A beta 2). The A beta gene, encompassing more than 6 kb, is encoded by six exons corresponding to the different domains of the A beta polypeptide. The translated A beta amino acid sequence displays 73% homology to human DC beta chains; homologies to other subsets of human beta chains are lower, establishing that I-A corresponds structurally to DC. The A beta 2 exon is about 20 kb centromeric to the A beta gene. Its translated amino acid sequence includes all the conserved amino acids of other class II beta-chain second domains. It shows about 60% homology to each of three subsets of human beta chains available for comparison, and to the A beta chain. No A beta 2 first domain exon has been detected with A beta or DC beta probes.

Amino Acid Sequence↗

Control of type I collagen synthesis: evidence for pretranslational coordination of pro alpha 1 (I) and pro alpha 2 (I) chain synthesis in embryonic chick bone.

The normal type I collagen molecule contains two alpha 1 (I) chains and one alpha 2 (I) chain. In embryonic chick calvaria, the two-chains are synthesized in a 2:1 ratio, and total polysomes from this tissue contain twice as much mRNA for pro alpha 1 (I) as for pro alpha 2 (I). To further investigate the mechanism by which synthesis may be coordinated, RNA isolated from various cell fractions of embryonic chick calvaria was translated in a rabbit reticulocyte lysate cell-free system. The procollagen chain products were separated by gel-electrophoresis and densitometrically quantitated from autoradiograms of the gels. Total cellular RNA, total cytoplasmic RNA, and polysomal RNA each directed the synthesis of pro alpha 1 (I) and pro alpha 2 (I) in a proportion of 2:1, whereas no procollagen mRNA activity was found in nonpolysomal cytoplasmic RNA. These results indicate that in the chick bone cells, all compartments contain twice as much pro alpha 1 (I) mRNA as pro alpha (I) mRNA, and that virtually all procollagen mRNA in the cytoplasm in polysome-bound. The coordination of procollagen chain synthesis thus presumably occurs at a pretranslational level, through differential rates of formation and/or degradation of the two mRNAs.

Animals↗

The construction of cosmid libraries which can be used to transform eukaryotic cells.

Cosmid vectors have been developed which carry selective markers for growth in bacteria (beta lactamase gene) and animal cells (the Herpes Simplex virus thymidine kinase gene, the transposon Tn-5 aminoglycosyl 3' phosphotransferase gene and the E. coli guanine phosphoribosyltransferase gene). The design of the cosmids allows the exchange of the eukaryotic markers in recombinant cosmids. Human and mouse cosmid libraries containing DNA inserts of about 40kb have been generated by an improved method. Several clones from the human beta-globin locus were isolated. These cosmids transform mouse L cells at high efficiency in both circular and linear form. The newly introduced genes are expressed accurately in L cells.

Animals↗

Isolation of transforming DNA by cosmid rescue.

A procedure has been developed to allow the recovery of an integrated plasmid genome from a transformed cell, together with large areas of the flanking DNA sequences. DNA from Saccharomyces cerevisiae BAS2, in which the pBR322--ura 3 plasmid (Y1p5) is integrated at the yeast histone H2A and H2B locus, was used to generate a cosmid library, using a new cosmid vector (pTL5) that is ampicillin sensitive and tetracycline resistant. Colonies were selected for ampicillin resistance, which was conferred by the incorporation of the integrated pBR322 beta-lactamase gene into the recombinant cosmid. Restriction enzyme and blot hybridization analyses show that the rescued clones contain the yeast histone genes in addition to the Y1p5 sequences; a total of approximately 50 kilobase pairs of DNA sequences flanking the plasmid was recovered as a series of overlapping cosmids. This approach should allow the recovery of most genes that can be linked to a marker pBR322 sequence and for which a specific phenotype can be selected in a recipient eukaryotic cell.

Bacteriophage lambda↗

In vitro studies on the conversion of the biosynthetic precursor of renin.

The initial translation product of mouse submaxillary gland mRNA has a molecular weight of about 50,000. We have now translated renin mRNA in frog oocytes which are known to be able to remove the so-called "pre"- or "signal"- sequence from products of injected mRNAs. From these injected oocytes, we could precipitate with antirenin a 48,000 dalton polypeptide. Treatment with kallikrein or trypsin of the oocyte product resulted in a decrease in amount of this 48,000 dalton protein and a corresponding increase in a 45,000 dalton protein, precipitable with antirenin. We conclude that the initial translation product of renin mRNA is a preprorenin of molecular weight 50,000, which in oocytes is enzymatically cleaved to render 48,000 dalton prorenin. Although kallikrein may be a physiological activator of renin, it appears to be not the only one since no mature, 40,000 dalton renin was formed.

Animals↗

Comparison of thiopentone and diazepam as induction agents of anaesthesia for Caesarean section.

Clinical effects of thiopentone (3 mg/kg body weight) and diazepam (0.3 mg/kg) were compared for elective caesarean sections in two groups of 43 and 39 women, respectively. They were given general anaesthesia in left lateral tilt. The systolic, diastolic and mean arterial pressures were moderately elevated at onset of surgery in both groups, probably indicating light anaesthesia. Later, a gradual decrease to the preinduction levels was observed. The mean injection-delivery (I-D) interval was 344 s in the thiopentone group and 339 s in the diazepam group. The I-D intervals were shorter than 10 min in 39 of the cases in the thiopentone group and 38 cases in the diazepam group. Low Apgar scores at 1 min (6 or less) occurred in five of the neonates in each group, while all had normal Apgar scores at 5 min ( 7 or mor) As judged by the Apgar scores and the acid-base status of umbilical cord blood, the effects of the induction agents on the neonatal condition were indistinguishable in the two groups. In the thiopentone group, unpleasant recollections were reported in 5 out of 40 patients (12.5%) compared to none in the diazepam group. Diazepam-nitrous oxide anaesthesia is well accepted by the mothers and is alternative to supplementing thiopentone induction with a volatile gas for patients who have previous experienced wakefulness or express fear of awareness. The main drawback with diazepam induction, however, is the slow induction of sleep. Harmful drug effects on the neonates must be expected if the dose has to be increased in order to ensure sleep.

Anesthesia, Intravenous↗

Isolation and characterization of alpha-amylase messenger RNA from bank vole parotid glands. Evidence for two separate messenger RNAs coding for amylase and an amylase-related protein.

Bank vole saliva contains two glycogen-precipitable proteins, both of which show affinity for the alpha-amylase inhibitor cycloheptaamylose. One of these proteins, amylase, has a molecular weight of 55,000, judged from dodecylsulphate/acrylamide gel electrophoresis. The other has an apparent molecular weight of 59,000 and has no amylase activity. We report here that tryptic peptide maps as well as amino-acid composition analyses indicate extensive homology between the two proteins. We have also isolated total poly(A)-containing mRNA from amylase-rich bank vole parotid glands. These mRNAs were translated in the presence of [35S]methionine in an mRNA-dependent cell-free translation system from rabbit reticulocyte lysate. The radioactive translation products were examined by dodecylsulphate/polyacrylamide gel electrophoresis. Two major translation products with apparent molecular weights of approximately 56,500 and 60,500, respectively, were further characterized by tryptic peptide analyses. Our data indicate that the 56,500-Mr product is the biosynthetic precursor of amylase, whereas the 60,500-Mr translation product is a precursor of the 59,000-Mr amylase-like protein. Both precursors appear to contain extra peptide material, presumably as amino-terminal 'pre' or 'signal' peptides, in analogy with that found for other precursors of secretory proteins. Thus, amylase and the 59,000-Mr protein, although very similar, are translated from two separate mRNAs. These two messengers sediment in a sucrose gradient at about 17-S, corresponding to lengths of about 1,800 nucleotides.

Amino Acids↗