NTS Catecholamine Neurons Mediate Hypoglycemic Hunger via Medial Hypothalamic Feeding Pathways.
NTS Catecholamine Neurons Mediate Hypoglycemic Hunger via Medial Hypothalamic Feeding Pathways.
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DOI:
10.1016/j.cmet.2019.11.016
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发表时间:
2020-02-04
期刊:
影响因子:
29
通讯作者:
Atasoy, Deniz
中科院分区:
文献类型:
--
作者:
Aklan, Iltan;Atasoy, Nilufer Sayar;Yavuz, Yavuz;Ates, Tayfun;Coban, Ilknur;Koksalar, Fulya;Filiz, Gizem;Topcu, Iskalen Cansu;Oncul, Merve;Dilsiz, Pelin;Cebecioglu, Utku;Alp, Muhammed Ikbal;Yilmaz, Bayram;Davis, Deborah R.;Hajdukiewicz, Karolina;Saito, Kenji;Konopka, Witold;Cui, Huxing;Atasoy, Deniz
Glucose is the essential energy source for the brain, whose deficit, triggered by energy deprivation or therapeutic agents, can be fatal. Increased appetite is the key behavioral defense against hypoglycemia; however, the central pathways involved are not well understood. Here, we describe a glucoprivic feeding pathway by tyrosine hydroxylase (TH)-expressing neurons from nucleus of solitary tract (NTS), which project densely to the hypothalamus and elicit feeding through bidirectional adrenergic modulation of agouti-related peptide (AgRP)- and proopiomelanocortin (POMC)-expressing neurons. Acute chemogenetic inhibition of arcuate nucleus (ARC)-projecting NTSTH neurons or their target, AgRP neurons, impaired glucoprivic feeding induced by 2-Deoxy-D-glucose (2DG) injection. Neuroanatomical tracing results suggested that ARC-projecting orexigenic NTSTH neurons are largely distinct from neighboring catecholamine neurons projecting to parabrachial nucleus (PBN) that promotes satiety. Collectively, we describe a circuit organization in which an ascending pathway from brainstem stimulates appetite through key hunger neurons in the hypothalamus in response to hypoglycemia. Increased appetite is a key line of defense against hypoglycemia. Aklan et al. have identified an ascending pathway from the brainstem to the hypothalamus that is required for hypoglycemia-induced food intake.
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影响因子:
29
作者:
Blouet C;Schwartz GJ
通讯作者:
Schwartz GJ
DOI:
10.1152/ajpregu.00604.2003
发表时间:
2004-07-01
影响因子:
2.8
作者:
Blevins, JE;Schwartz, MW;Baskin, DG
通讯作者:
Baskin, DG
影响因子:
4.8
作者:
Gyengesi, Erika;Liu, Zhong-Wu;Diano, Sabrina
通讯作者:
Diano, Sabrina
影响因子:
64.8
作者:
Hsu, Jer-Yuan;Crawley, Suzanne;Allan, Bernard B. .
通讯作者:
Allan, Bernard B. .
影响因子:
56.9
作者:
FLYNN, FW;GRILL, HJ
通讯作者:
GRILL, HJ