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Biomedical subjects

S Abrahamsson

Publications and source records attributed to S Abrahamsson.

At least 19 recordsLinked to original sources

Autogenous intrasynovial and extrasynovial tendon grafts: an experimental study of pro alpha 1(I) collagen mRNA expression in dogs.

On the basis of recent evidence that the healing processes of tendon grafts are donor-tissue specific, in situ hybridization, using a 372 bp cDNA fragment complementary to a portion of pro alpha 1(I) collagen mRNA, was utilized to compare the cellular responses to transplantation exhibited by autogenous intrasynovial and extrasynovial flexor tendon grafts. Intrasynovial and extrasynovial tendons from the hindpaw were transferred to synovial sheaths in the forepaw of 12 mongrel dogs (24 tendons) and treated with immediate controlled passive motion. The tendon grafts were harvested at 2, 4, and 6 weeks, and each was divided into a proximal, central (8 mm), and distal portion. Sections from the central portion were embedded in paraffin and subjected to in situ hybridization, autoradiography, and staining; levels of procollagen mRNA then were assessed by microscopic examination. The two types of tendon grafts exhibited different levels of pro alpha 1(I) collagen mRNA expression at all three time points. Intrasynovial tendon grafts displayed no areas of increased type-I procollagen mRNA at 2, 4, and 6 weeks. The extrasynovial tendon grafts displayed increased surface levels of type-I procollagen mRNA at 2 and 4 weeks; the levels decreased to background levels by 6 weeks. The high levels of procollagen mRNA exhibited by the extrasynovial grafts suggest increased collagen synthetic activity, indicative of a cellular response to injury, whereas the preservation of low levels of expression in the intrasynovial grafts may signify a less inflammatory cellular response.

Animals

Prostaglandin-like substances in Propionibacterium acnes. VI. Characterization of the lipid fraction by gas chromatography in conjunction with mass spectrometry.

The lipid fraction of P. acnes was submitted to stepwise purification followed by bioassay in order to localize the prostaglandin-like material. GC-MS analysis revealed the occurrence of substances having a part but not a total molecule in common with the prostaglandin family, suggesting that prostaglandin-like substances represent a new group of prostaglandin compounds.

Gas Chromatography-Mass Spectrometry

Cholesteryl sulphate and phosphate in the solid state and in aqueous systems.

Cholesteryl sodium sulphate (CS) crystallizes as the dihydrate, the crystal structure of which is known. On heating the dihydrate, solid state phase transitions are observed at 65 degrees C and 95 degrees C and melting occurs at 165 degrees C. The structure of the high temperature phase has not been determined. Cholesteryl dihydrogen phosphate (CP) is not isostructural with any phases of CS. It undergoes a phase transition at 50 degrees C and melts at 190 degrees C. In systems with water CS is unstable whereas it was possible to determine the phase diagram of CP. In most of the composition range a crystalline hydrate is in equilibrium with a gel-phase. The latter has remarkable properties in that lamellar order exists with the 46 A lipid bilayer interleaved with water layers up to 1000 A. The monofilm behaviour of CS and CP at different pH levels is also reported.

Cholesterol

The crystal structure of cholesteryl 17-bromoheptadecanoate.

Crystals of cholesteryl-17-bromoheptadecanoate (C44H77BrO2) are monoclinic (P21) with a = 7.663(2), b = 10.311(5), c = 55.96(2) A and beta = 103.10(3 degrees). These are two molecules in the asymmetric unit which have different conformations of the cholesterol side chain and about the ester bond. The molecules pack with regions of only steroid skeleta alternating with regions of hydrocarbon chains. Due to the packing requirements of the skeleta the carbon chains are forced into a hybrid type packing which contains features of the earlier known O perpendicular and T parallel subcells. The subcell (HS1) is orthorhombic with as = 10.3, bs = 7.5 and cs = 2.54 A. The molecular packing is such that the omega-bromine atoms do not continue the trans-carbon chains but adopt a gauche conformation.

Cholesterol Esters