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Investigations of the Biological Roles of Substituted Cyclohexadienes

In recent years there have been two cycloterpenals, molecules consisting of a
cyclohexadienal core, isolated from nature. Cyclocitral, the condensation product of
citral, has been isolated from the North Sea bryozoans Flustra foliacea. In the human
eyes, cycloretinal has been isolated and is a toxic by product of the vision cycle. This
retinal dimer is believed to contribute to age related macular degeneration, the leading
cause of blindness in the elderly. In 1992, it was discovered that if [beta]-ionylideneacetaldehyde was incubated with beta-lactoglobulin ([beta]-LG), the principal
whey protein in dairy milk, that it would mediate the formation of cyclo-[beta]-ional. No
follow up studies were performed on this protein mediated reaction or what biological
activities these cycloterpenals may possess.
This dissertation investigates the biological roles of substituted
cyclohexadienes including cycloterpenals and cyclohexadiene enaminonitriles. To
mimic the protein mediated reaction, we developed a synthetic procedure to produce a
wide array of cycloterpenal by utilizing L-proline. Over 100 cycloterpenals were
synthesized and screened for their biological activities against an array of cell based
screens. The phenotypic effects of these cycloterpenals were screened against a PC12 assay where dramatic effects were observed on neurite outgrowth. During the
synthesis of starting materials for the production of our cycloterpenal library, it was
discovered that if excess base was added to the Horner-Wadsworth-Emmons reaction
between a methyl-ketone and diethyl-(cyanomethyl)-phosphonate, conversion of the
[alpha]-[beta]-unsaturated nitrile into an enaminonitrile was observed. This new synthetic
procedure was optimized to generate a library of enaminonitriles as well as their
quinazoline derivatives.
The work within also includes the investigation of the [beta]-LG mediated reaction
formation of cycloterpenals with natural and unnatural [beta]-methyl aldehydes. We were
able to demonstrate that [beta]-LG could mediate the conversion of [alpha],[beta]-unsaturated
aldehydes into their corresponding cycloterpenal. In vitro analysis was also
performed with store bought milks and the [beta]-LG present was able to mediate the
formation of cyclocitral. An in vivo experiment was also performed by utilizing New Zealand White rabbits to demonstrate the formation of cycloretinal within the blood
stream by feeding a source of [beta]-LG with retinal.
Interestingly, in human blood, [beta]-LG is present at concentrations of 0.7-1.2
g/dL. The protein has been identified within drusen pigments and lipofuscin granules
that accumulate in the retina of macular degeneration patients. As humans do not produce beta-lactoglobulin, the source of this protein is from milk and milk products.
With these experiments, we clearly demonstrate that under the appropriate conditions,
cycloretinal can be produced with [beta]-LG. We have clearly established a direct link
between [beta]-LG chemistry and age-related macular degeneration.

Identiferoai:union.ndltd.org:tamu.edu/oai:repository.tamu.edu:1969.1/ETD-TAMU-2009-12-7511
Date2009 December 1900
CreatorsBench, Bennie John
ContributorsWatanabe, Coran
Source SetsTexas A and M University
Languageen_US
Detected LanguageEnglish
TypeBook, Thesis, Electronic Dissertation, text
Formatapplication/pdf

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