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High-fat diet enhances starvation-induced hyperactivity via sensitizing hunger-sensing neurons in Drosophila.


ABSTRACT: The function of the central nervous system to regulate food intake can be disrupted by sustained metabolic challenges such as high-fat diet (HFD), which may contribute to various metabolic disorders. Previously, we showed that a group of octopaminergic (OA) neurons mediated starvation-induced hyperactivity, an important aspect of food-seeking behavior (Yu et al., 2016). Here we find that HFD specifically enhances this behavior. Mechanistically, HFD increases the excitability of these OA neurons to a hunger hormone named adipokinetic hormone (AKH), via increasing the accumulation of AKH receptor (AKHR) in these neurons. Upon HFD, excess dietary lipids are transported by a lipoprotein LTP to enter these OA+AKHR+ neurons via the cognate receptor LpR1, which in turn suppresses autophagy-dependent degradation of AKHR. Taken together, we uncover a mechanism that links HFD, neuronal autophagy, and starvation-induced hyperactivity, providing insight in the reshaping of neural circuitry under metabolic challenges and the progression of metabolic diseases.

SUBMITTER: Huang R 

PROVIDER: S-EPMC7274782 | biostudies-literature | 2020 Apr

REPOSITORIES: biostudies-literature

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High-fat diet enhances starvation-induced hyperactivity via sensitizing hunger-sensing neurons in <i>Drosophila</i>.

Huang Rui R   Song Tingting T   Su Haifeng H   Lai Zeliang Z   Qin Wusa W   Tian Yinjun Y   Dong Xuan X   Wang Liming L  

eLife 20200423


The function of the central nervous system to regulate food intake can be disrupted by sustained metabolic challenges such as high-fat diet (HFD), which may contribute to various metabolic disorders. Previously, we showed that a group of octopaminergic (OA) neurons mediated starvation-induced hyperactivity, an important aspect of food-seeking behavior (Yu et al., 2016). Here we find that HFD specifically enhances this behavior. Mechanistically, HFD increases the excitability of these OA neurons  ...[more]

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