Key result
Insulin signaling alters serotonergic neurotransmission, providing mechanistic insights into the comorbidity between diabetes and depression and highlighting new targets for therapeutic options.
Why the study?
The mechanisms underlying how insulin influences emotional behaviours remain unresolved, with no direct and clear-cut evidence demonstrating that such action involves brain serotonergic neurones.
Insulin signaling alters serotonergic neurotransmission, providing mechanistic insights into the comorbidity of diabetes and depression and suggesting new therapeutic targets.
May guide dual-therapy development for comorbid diabetes and depression; leaves open clinical validation of these targets.
The idea that insulin could influence emotional behaviours has long been suggested. However, the underlying mechanisms have yet to be solved and there is no direct and clear-cut evidence demonstrating that such action involves brain serotonergic neurones. Indeed, initial arguments in favour of the association between insulin, serotonin and mood arise from clinical or animal studies showing that impaired insulin action in type 1 or type 2 diabetes causes anxiety- and depressive symptoms along with blunted plasma and brain serotonin levels. The present review synthesises the main mechanistic hypotheses that might explain the comorbidity between diabetes and depression. It also provides a state of knowledge of the direct and indirect experimental evidence that insulin modulates brain serotonergic neurones. Finally, it highlights the literature suggesting that antidiabetic drugs present antidepressant-like effects and, conversely, that serotonergic antidepressants impact glucose homeostasis. Overall, this review provides mechanistic insights into how insulin signalling alters serotonergic neurotransmission and related behaviours bringing new targets for therapeutic options.
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Martin et al. (2021) conducted a review in Diabetes-associated mood disorders. Insulin and antidiabetic drugs was evaluated. Insulin signaling alters serotonergic neurotransmission, providing mechanistic insights into the comorbidity between diabetes and depression and highlighting new targets for therapeutic options.
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