Abstract

White adipose tissue (WAT) is present in different depots throughout the body. Although all depots are exposed to systemic humoral signals, they are not functionally identical. Studies in clock gene knockout animals and in shift workers suggest that daily rhythmicity may play an important role in lipid metabolism. Differences in rhythmicity between fat depots might explain differences in depot function; therefore, we measured mRNA expression of clock genes and metabolic genes on a 3-h interval over a 24-h period in the subcutaneous inguinal depot and in the intra-abdominal perirenal, epididymal, and mesenteric depots of male Wistar rats. We analyzed rhythmicity using CircWave software. Additionally, we measured plasma concentrations of glucose, insulin, corticosterone, and leptin. The clock genes (Bmal1/Per2/Cry1/Cry2/RevErbα/DBP) showed robust daily gene expression rhythms, which did not vary between WAT depots. Metabolic gene expression rhythms (SREBP1c/PPARα/PPARγ/FAS/LPL/Glut4/HSL/CPT1b/leptin/visfatin/resistin) were more variable between depots. However, no distinct differences between intra-abdominal and subcutaneous rhythms were found. Concluding, specific fat depots are not associated with differences in clock gene expression rhythms and, therefore, do not provide a likely explanation for the differences in metabolic function between different fat depots.

Highlights

  • Sustained disturbances in daily rhythmicity increase the risk to develop obesity and related metabolic disease [1]

  • We conclude that differences in the molecular clock or clock-controlled genes do not provide a major explanation for the differences in metabolic function between the different fat depots

  • Clock gene and metabolic gene expression per white adipose tissue (WAT) depot, r2 and amplitude are plotted for each gene in Figures 1 and 2

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Summary

Introduction

Sustained disturbances in daily rhythmicity (e.g., shift work, jet lag) increase the risk to develop obesity and related metabolic disease [1]. Storage in and release of lipids from white adipose tissue (WAT) are regulated processes that anticipate rest-activity and feeding cycles. WAT is abundantly present throughout the body in different fat depots. The main depots are located underneath the skin in the inguinal area [subcutaneous white adipose tissue (sWAT)], and in the abdominal cavity (intra-abdominal depots): perirenal- (pWAT, retroperitoneal, next to the kidney), epididymal- (eWAT, connected to and lining the epididymis), and mesenteric WAT (mWAT, intraperitoneal, lining the gastrointestinal tract). Frontiers in Endocrinology | www.frontiersin.org van der Spek et al

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