Literature DB >> 30703063

Vagal afferents contribute to sympathoexcitation-driven metabolic dysfunctions.

L Francisco Lorenzo-Martín1,2,3, Mauricio Menacho-Márquez1,2,3, Salvatore Fabbiano1,2, Omar Al-Massadi4,5,6, Antonio Abad1,2,3, Sonia Rodríguez-Fdez1,2, María A Sevilla1,2, María J Montero1,2, Carlos Diéguez4,5,6, Rubén Nogueiras4,5,6, Xosé R Bustelo1,2.   

Abstract

Multiple crosstalk between peripheral organs and the nervous system are required to maintain physiological and metabolic homeostasis. Using Vav3-deficient mice as a model for chronic sympathoexcitation-associated disorders, we report here that afferent fibers of the hepatic branch of the vagus nerve are needed for the development of the peripheral sympathoexcitation, tachycardia, tachypnea, insulin resistance, liver steatosis and adipose tissue thermogenesis present in those mice. This neuronal pathway contributes to proper activity of the rostral ventrolateral medulla, a sympathoregulatory brainstem center hyperactive in Vav3-/- mice. Vagal afferent inputs are also required for the development of additional pathophysiological conditions associated with deregulated rostral ventrolateral medulla activity. By contrast, they are dispensable for other peripheral sympathoexcitation-associated disorders sparing metabolic alterations in liver.

Entities:  

Keywords:  GABAergic signals; adipose tissue; brainstem; diabetes; hypertension; liver; metabolic syndrome; sympathetic system; thermogenesis; ventrolateral medulla

Mesh:

Substances:

Year:  2019        PMID: 30703063      PMCID: PMC6368248          DOI: 10.1530/JOE-18-0623

Source DB:  PubMed          Journal:  J Endocrinol        ISSN: 0022-0795            Impact factor:   4.286


  38 in total

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8.  Chronic sympathoexcitation through loss of Vav3, a Rac1 activator, results in divergent effects on metabolic syndrome and obesity depending on diet.

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10.  Hypothalamic kappa opioid receptor mediates both diet-induced and melanin concentrating hormone-induced liver damage through inflammation and endoplasmic reticulum stress.

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