2018
DOI: 10.1038/s41366-018-0133-y
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Reward-representing D1-type neurons in the medial shell of the accumbens nucleus regulate palatable food intake

Abstract: Sensitivity of food reward-representing neurons in the mSh-Nac determines the level of satisfaction that governs cessation of consumption, probably through connections with the LHA. D1R signaling is a key element in this function, and is impaired in obesity-prone rats.

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Cited by 41 publications
(42 citation statements)
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“…Studies have shown that activation of the D1 receptor can inhibit eating of mice (Prado & Luis‐Islas, ). Durst found that intrauterine protein‐restricted mice were prone to hyperphagia, and the expression of D1 receptor in the NAc was significantly reduced (Durst, Konczol, Balazsa, Eyre, & Toth, ). Therefore, the increase in food intake in mice may be associated with a decrease in D1 receptor levels.…”
Section: Discussionmentioning
confidence: 99%
“…Studies have shown that activation of the D1 receptor can inhibit eating of mice (Prado & Luis‐Islas, ). Durst found that intrauterine protein‐restricted mice were prone to hyperphagia, and the expression of D1 receptor in the NAc was significantly reduced (Durst, Konczol, Balazsa, Eyre, & Toth, ). Therefore, the increase in food intake in mice may be associated with a decrease in D1 receptor levels.…”
Section: Discussionmentioning
confidence: 99%
“…Specifically, the genes are enriched to the excitatory and inhibitory cells of D1 medium spiny neurons in the striatum and stellate and basket cells in cerebellum, as well as in cortical neurons. These cells are known to indirectly regulate food-related reward processing and appetite (Durst et al, 2019;Matikainen-Ankney and Kravitz, 2018;Timper and Brüning, 2017;Vong et al, 2011).…”
Section: Transcriptomic Association Analysismentioning
confidence: 99%
“…The S35-UTPlabeled (PerForm Hungaria Kft., Budapest, Hungary) riboprobes were prepared by in vitro transcription as described previously (Konczol et al 2010;Toth et al 2008). The specific sequences used for the hybridizations were: rat prepro-PrRP cDNA (10-240 bp of the coding sequence, accession # AB015418), rat TH cDNA (684-1068 bp of the coding sequence, accession # M23598) (Mezey et al 1998), rat NUCB2 cDNA corresponding to the nesfatin-1 fragment (1-246 bp of the coding sequence, accession # DY314804) and the rat PrRP-R cDNA (189-636 bp of the coding sequence, accession # NM_139193) (Vas et al 2013;Durst et al 2019). The specificity of the cDNAs was verified by sequencing.…”
Section: In Situ Hybridizationmentioning
confidence: 99%