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Honours Project Book - Faculty of Health Sciences - University of ...

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Early Life Programming <strong>of</strong> <strong>Health</strong> and Disease<br />

Contact Persons<br />

Pr<strong>of</strong>essor Julie Owens<br />

Phone: 8313 4088<br />

julie.owens@adelaide.edu.au<br />

Dr Kathy Gatford<br />

Phone: 8313 4158<br />

kathy.gatford@adelaide.edu.au<br />

Supervisors<br />

Pr<strong>of</strong>essor Julie Owens<br />

Dr Kathy Gatford<br />

Pr<strong>of</strong>essor Claire Roberts<br />

Dr Miles De Blasio<br />

Ms Patricia Grant<br />

Emeritus Pr<strong>of</strong>essor Jeffrey Robinson<br />

Our research group is part <strong>of</strong> the Research Centre for the Early Origins <strong>of</strong> <strong>Health</strong> and Disease (EOHaD) and an<br />

international leader in the investigation <strong>of</strong> the intergenerational and perinatal origins <strong>of</strong> metabolic and<br />

cardiovascular health in postnatal life. We focus on how our health can be pr<strong>of</strong>oundly influenced by events in early<br />

life and possibly in previous generations, including diabetes, obesity and cardiovascular increasing risk <strong>of</strong> disease.<br />

Common exposures in early life that affect our later health include placental and fetal growth restriction, maternal<br />

vitamin supplementation and maternal obesity and diabetes.<br />

Our aims are to:<br />

• understand how these exposures interact with the genome and affect the epigenome to determine our later<br />

health<br />

• identify interventions to either prevent these conditions that program later health or to overcome or reverse<br />

such programming.<br />

Recent key discoveries include:<br />

• placental restriction<br />

o inducing diabetes in adult <strong>of</strong>fspring via impaired beta cell function and growth and insulin resistance<br />

o causing obesity in <strong>of</strong>fspring via altered appetite control<br />

• altering expression <strong>of</strong> novel small regulatory RNAs that target and repress expression <strong>of</strong> multiple mRNAs to<br />

affect major pathways and funtions<br />

• maternal folate deficiency or folic acid supplementation in changing the epigenome and physiology <strong>of</strong><br />

<strong>of</strong>fspring.<br />

Our research strategies include:<br />

• novel experimental models <strong>of</strong> common early life exposures in non human species<br />

• clinical research <strong>of</strong> human cohorts with exposure to common pregnancy complications<br />

• in vivo characterisation <strong>of</strong> insulin action, glucose and lipid control and other physiological functions<br />

• metabolite and hormone analysis by enzymatic analysis and immunoassay<br />

• quantitative morphmetric analysis <strong>of</strong> tissue structures underpinning function<br />

• molecular analysis <strong>of</strong> expression <strong>of</strong> regulatory RNAs and protein coding genes by quantitative PCR, microarray<br />

and western immunoblotting<br />

• analysis <strong>of</strong> epigenetic state <strong>of</strong> genes by bisulfite treatment <strong>of</strong> DNA and Sequenom or Pyrosequencing<br />

• bioinformatics, including pathway analysis <strong>of</strong> array data <strong>of</strong> microRNA and mRNA expression.<br />

We publish in the top discipline specific and general journals, are highly cited and regularly invite to speak at<br />

leading conferences. Our students publish their work, present at conferences and have gone on to a range <strong>of</strong><br />

careers as researchers, academics, health pr<strong>of</strong>essionals, in the biotechnology and pharmaceutical industry and<br />

management.<br />

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