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Energy Homeostasis-Associated (Enho) MRNA Expression and Energy Homeostasis in the Acute Stress Versus Chronic Unpredictable Mild Stress Rat Models

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Journal Biomedicines
Date 2023 Feb 25
PMID 36830976
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Abstract

The energy homeostasis-associated (Enho) gene, the transcript for the Adropin peptide, is usually linked to energy homeostasis, adiposity, glycemia, and insulin resistance. Studies on Enho expression in stressful conditions are lacking. This work aimed to investigate Enho mRNA expression and energy homeostasis in acute stress (AS) versus chronic unpredictable mild stress (CUMS) rat models. A total of thirty male Wistar rats (180-220 g) were fed a balanced diet with free access to water. Rats were divided into three equal groups ( = 10): (a) the normal control (NC) group; (b) the AS group, where one episode of stress for 2 h was applied; and (c) the CUMS group, in which rats were exposed to a variable program of mild stressors for 4 weeks. Energy homeostasis was analyzed by the PhenoMaster system for the automatic measuring of food intake (FI), respiratory O volume (VO), CO volume (VCO), respiratory quotient (RQ), and total energy expenditure (TEE). Finally, liver, whole brain, and adipose (WAT) tissue samples were collected, total RNA was prepared, and RT-PCR analysis of the Enho gene was performed. The CUMS group showed higher VO consumption and VCO production, and a higher RQ than the AS group. Furthermore, the TEE and FI were higher in the CUMS group compared to the AS group. Enho gene expression in the liver, brain, and WAT was significantly higher in the CUMS group than in the AS and NC groups. We can conclude that in the chew-fed AS rats, hypophagia was evident, with a shift in the RQ toward fat utilization, with no changes in body weight despite the increase in Enho mRNA expression in all studied tissues. In the CUMS group, the marked rise in Enho mRNA expression may have contributed to weight loss despite increased FI and TEE.

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References
1.
Even P, Nadkarni N . Indirect calorimetry in laboratory mice and rats: principles, practical considerations, interpretation and perspectives. Am J Physiol Regul Integr Comp Physiol. 2012; 303(5):R459-76. DOI: 10.1152/ajpregu.00137.2012. View

2.
Benchimol de Souza D, Silva D, Marinho Costa Silva C, Sampaio F, Costa W, Cortez C . Effects of immobilization stress on kidneys of Wistar male rats: a morphometrical and stereological analysis. Kidney Blood Press Res. 2011; 34(6):424-9. DOI: 10.1159/000328331. View

3.
DE SOUZA E, Van Loon G . Differential plasma beta-endorphin, beta-lipotropin, and adrenocorticotropin responses to stress in rats. Endocrinology. 1985; 116(4):1577-86. DOI: 10.1210/endo-116-4-1577. View

4.
Gao S, Ghoshal S, Zhang L, Stevens J, McCommis K, Finck B . The peptide hormone adropin regulates signal transduction pathways controlling hepatic glucose metabolism in a mouse model of diet-induced obesity. J Biol Chem. 2019; 294(36):13366-13377. PMC: 6737218. DOI: 10.1074/jbc.RA119.008967. View

5.
Armario A . The hypothalamic-pituitary-adrenal axis: what can it tell us about stressors?. CNS Neurol Disord Drug Targets. 2006; 5(5):485-501. DOI: 10.2174/187152706778559336. View