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AG&M annual report 2018

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The AG&M talent development grant<br />

Charlene Diepenbroek<br />

Ever since starting my PhD research, I have been interested in the role<br />

of the autonomic nervous system in the central regulation of glucose<br />

metabolism. During my PhD, at the department of Endocrinology<br />

& Metabolism of the AMC, I investigated the role of the brain as a<br />

mechanistic link between diet composition and glucose metabolism. I<br />

continued research as a postdoc at Yale University, where I investigated<br />

gastrointestinal-brain signalling, by the vagus nerve, and its role in<br />

ingestive behaviour. This project, and the techniques acquired, bridge the<br />

research from my PhD and the research I work on within the AG&M talent<br />

development grant.<br />

AG&M Grants <strong>2018</strong><br />

The AG&M talent development grant allows me…<br />

… differentiate myself with my own research niche, by generating fundamental knowledge in the innervation of the<br />

endocrine pancreas in diet-induced impaired β cell secretion in the development of type 2 diabetes (T2D).<br />

Although it is known that autonomic innervation is altered in obesity, which is associated with T2D, little is known<br />

about the involvement of the autonomic nervous system in T2D development, e.g. vagal innervation of the β cell.<br />

Furthermore, there is a lack of knowledge in whether dietary components affect vagal-mediated insulin secretion,<br />

thereby contributing to T2D development.<br />

I focus on the (dys)regulation of the brain and autonomous nervous system in the development of diet-induced<br />

impaired insulin secretion. In collaboration with Dr. Daniël van Raalte (Department of Internal Medicine and the<br />

Institute of Cardiovascular Research, VUmc), I will perform ex vivo experiments with isolated pancreatic islets. This<br />

technique enables us to investigate the innervation at the level of the β cell, and to delineate the endocrine from the<br />

exocrine pancreas. I combine this technique with neuroanatomical, chemogenetic, and physiological techniques in<br />

an animal model with a free choice high-fat, high-sugar diet paradigm to further investigate the brain-pancreas-axis<br />

in vivo. Altogether, this will provide novel insights in the development of-, and targeted treatment for T2D.<br />

Charlene Diepenbroek<br />

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