Author:
Tapia Geronimo P.,Agostinelli Lindsay J.,Chenausky Sarah D.,Salcido Padilla Jessica V.,Navarro Vanessa I.,Alagh Amy,Si Gabriel,Thompson Richard H.,Balivada Sivasai,Khan Arshad M.
Abstract
AbstractRodent studies indicate that impaired glucose utilization or hypoglycemia is associated with cellular activation of neurons in themedulla(Winslow, 1733) (MY) believed to control feeding behavior and glucose counterregulation. However, such activation has been tracked primarily within hours of the challenge, rather than sooner, and has been poorly mapped within standardized brain atlases. Here, we report that within 15 min of receiving 2-deoxy-D-glucose (2-DG; 250 mg/kg, i.v.), which can trigger glucoprivic feeding behavior, marked elevations were observed in the numbers ofrhombic brain(His, 1893) (RB) neuronal cell profiles immunoreactive for the cellular activation marker(s), phosphorylated p44/42 MAP kinases (phospho-ERK1/2), some of which were also catecholaminergic. We mapped their distributions within an open-access rat brain atlas and found that 2-DG-treated rats (compared to their saline-treated controls) displayed greater numbers of phospho-ERK1/2+neurons in thelocus ceruleus(Wenzel & Wenzel, 1812) (LC) and thenucleus of solitary tract (>1840)(NTS). Thus, 2-DG-activation of certain RB neurons is more rapid than perhaps previously realized, engaging neurons that serve multiple functional systems and are of varying cellular phenotypes. Mapping these populations within standardized brain atlas maps streamlines their targeting and/or comparable mapping in preclinical rodent models of disease.
Publisher
Cold Spring Harbor Laboratory