4.6 Article

Functional and Neurochemical Identification of Ghrelin Receptor (GHSR)-Expressing Cells of the Lateral Parabrachial Nucleus in Mice

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FRONTIERS IN NEUROSCIENCE
卷 15, 期 -, 页码 -

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FRONTIERS MEDIA SA
DOI: 10.3389/fnins.2021.633018

关键词

GHSR; ghrelin; parabrachial nucleus; body weight; food intake and food choice; glutamate; PACAP; CGRP

资金

  1. Vetenskapsradet [2018-02588, 2019-01051]
  2. Hjarnfonden [FO2017-0180, FO20190086]
  3. Novo Nordisk Fonden [NNF17OC0027206, NNF19OC0056694]
  4. Avtal om Lakarutbildning och Forskning [ALFGBG-723681]
  5. Forte [2019-01051] Funding Source: Forte
  6. Vinnova [2018-02588] Funding Source: Vinnova
  7. Swedish Research Council [2018-02588, 2019-01051] Funding Source: Swedish Research Council

向作者/读者索取更多资源

Studies have shown that GHSR cells in the lateral parabrachial nucleus play a crucial role in regulating diet-induced weight gain and adiposity, as well as food intake and food choice. These cells are predominantly glutamatergic and do not belong to the well-characterized anorexigenic CGRP cell population.
The lateral parabrachial nucleus (lPBN), located in the pons, is a well-recognized anorexigenic center harboring, amongst others, the calcitonin gene-related peptide (CGRP)-expressing neurons that play a key role. The receptor for the orexigenic hormone ghrelin (the growth hormone secretagogue receptor, GHSR) is also abundantly expressed in the lPBN and ghrelin delivery to this site has recently been shown to increase food intake and alter food choice. Here we sought to explore whether GHSR-expressing cells in the lPBN (GHSR(lPBN) cells) contribute to feeding control, food choice and body weight gain in mice offered an obesogenic diet, involving studies in which GHSR(lPBN) cells were silenced. We also explored the neurochemical identity of GHSR(lPBN) cells. To silence GHSR(lPBN) cells, Ghsr-IRES-Cre male mice were bilaterally injected intra-lPBN with a Cre-dependent viral vector expressing tetanus toxin-light chain. Unlike control wild-type littermates that significantly increased in body weight on the obesogenic diet (i.e., high-fat high-sugar free choice diet comprising chow, lard and 9% sucrose solution), the heterozygous mice with silenced GHSR(lPBN) cells were resistant to diet-induced weight gain with significantly lower food intake and fat weight. The lean phenotype appeared to result from a decreased food intake compared to controls and caloric efficiency was unaltered. Additionally, silencing the GHSR(lPBN) cells altered food choice, significantly reducing palatable food consumption. RNAscope and immunohistochemical studies of the lPBN revealed considerable co-expression of GHSR with glutamate and pituitary adenylate cyclase-activating peptide (PACAP), and much less with neurotensin, substance P and CGRP. Thus, the GHSR(lPBN) cells are important for diet-induced weight gain and adiposity, as well as in the regulation of food intake and food choice. Most GHSR(lPBN) cells were found to be glutamatergic and the majority (76%) do not belong to the well-characterized anorexigenic CGRP cell population.

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