Journal of Nutrition and Dietetics
Open Access

Hypothalamic mechanisms of depression associated with diabetes (DAD)

Warning: Undefined variable $i in /efsdata/omicsonline.org/httpdocs/peer-reviewed/abstract-page.php on line 156

Warning: Undefined variable $for_cr in /efsdata/omicsonline.org/httpdocs/peer-reviewed/abstract-page.php on line 156
Copyright: © 2021  . This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

To read the full article Peer-reviewed Article PDF

Ample evidence indicates that depression is a common comorbid of diabetes, which represents a major health concern as its rates have been steadily increasing in the world. However, there are still no effective treatments to ameliorate the depression associated with diabetes, which might be attributable to our incomplete understanding of the implicated pathological processes. Agouti- related protein (AgRP) neurons in hypothalamic arcuate nucleus (ARC) play crucial roles in the regulation of glucose levels, and corticotropin-releasing hormone (CRH) neurons in hypothalamic paraventricular nucleus (PVN) modulates hypothalamus-pituitary-adrenal (HPA) functions by terminating the median eminence (ME), a brain region connected to the ARC. It is thus paramount important to define and characterize the AgRP to CRH axonal connections in the ME and potential alterations implicated in depressive-like behaviors associated with diabetes. Our photometry data show that the activity of GABAergic AgRP neurons and the level of AMPK in these neurons are increased in diabetes and depression, and AMPK orchestrates the activity of AgRP neurons. More interestingly, the GABA neurotransmitter exerts excitatory effects in the ME. Together, our results let us propose that sustained stimulated AgRP neurons in diabetes enhance the HPA functions via AgRP-CRH axon connections in the ME, resulting in hypercortisolemia and subsequent hippocampal dysfunctions and depression.

Keywords