Thesis (Ph.D.)--University of Delaware, 2006. / Principal faculty advisor: Richard P. Wool, Dept. of Chemical Engineering. Includes bibliographical references.

Thesis (Ph. D.)--University of Queensland, 2002. / Includes bibliographical references.

No description available.

1. <i>Cis</i> unsaturated fatty acids were shown to inhibit porcine platelet aggregation in response to both collagen and thrombin. Fatty acids with a <i>trans</i> double bond had an anti-aggregatory effect on collagen-induced aggregation but this was significantly less than that observed with the <i>cis</i> equivalent and was diminished as the dose of agonist increased. Thrombin-induced platelet aggregation was unchanged or slightly potentiated by <i>trans</i> isomers. 2. Both the <i>cis</i> and <i>trans</i> isomeric acids inhibited collagen-induced TXB₂ production. The <i>trans</i> unsaturated fatty acids also inhibited TXB₂ production in response to thrombin, even though they did not inhibit thrombin induced platelet aggregation. 3. Unlike arachidonic acid, the <i>cis</i> and <i>trans</i> mono-unsaturated fatty acids were not rapidly incorporated into membrane phospholipids but modified platelet aggregation whilst in the free acid form. 4. Pre-incubation of platelets with either <i>cis</i> or <i>trans</i> delta 13, 18:1, selectivity inhibited the incorporation of radio-labelled arachidonic acid into membrane PS. 5. <i>Cis</i> and <i>trans</i> unsaturated delta 13, 18:1, inhibited the initial turnover of membrane PI in response to thrombin possibly by an inhibitory effect on PI-specific phospholipase C. After 5 minutes, however, the level of arachidonic acid released from both PI and PE was increased in the presence of the isomeric fatty acids. This may have been via a potentiation of the action of phospholipase A₂. 6. An increased release of arachidonic acid could result in the inhibition of aggregation if metabolised via the 12-lipoxygenase pathway, as the end products of this sytem have direct anti-aggregatory activity and inhibit the cyclo-oxygenase enzymes thus reducing TXA₂ synthesis. 7. <i>Cis</i> unsaturated fatty acids, which produce a greater level of membrane disruption than the <i>trans</i>, may lead to more efficient channelling of the released arachidonic acid in the direction of the lipoxygenase pathway, and thereby produce a greater inhibition of aggregation. The possibility remains that the <i>cis</i> isomers have another, as yet unidentified mechanism by which they inhibit platelet aggregation.

Graduation date: 1953

Typescript. / Thesis (Ph. D.)--University of Hawaii, 1969. / Bibliography: leaves 431-437. / xi, 437 l tables

xv, 153 leaves : photos., graphs, tables ; 30 cm. / Title page, contents and abstract only. The complete thesis in print form is available from the University Library. / Thesis (Ph.D.)--University of Adelaide, Dept. of Biochemistry, 1980

Proefschrift--Rijksuniversiteit te Utrecht, 1932. / Includes bibliographical references (p. 74-77).

Thesis (MSc)--University of Stellenbosch, 2007. / Bibliography.

Thesis (Ph.D.)(Botany)--University of Pretoria, 2006. / Includes summary. Includes bibliographical references. Available on the Internet via the World Wide Web.