Matches in SemOpenAlex for { <https://semopenalex.org/work/W2952023666> ?p ?o ?g. }
- W2952023666 abstract "Background: Disturbance of immunometabolic signaling is a key process involved in the progression of obesity. Microglia-the resident immune cells in the brain, initiate local immune responses. It is known that hypercaloric diets lead to microglial activation. Previously, we observed that hypothalamic microglial cells from mice fed high-fat diet (HFD) lose their day/night rhythm and are constantly activated. However, little is known about daily rhythmicity in microglial circadian, immune and metabolic functions, either in lean or obese conditions. Therefore, we hypothesized that HFD disturbs microglial immunometabolism in a day/night-dependent manner. Methods: Obesity was induced in Wistar rats by feeding them HFD ad libitum for the duration of 8 weeks. Microglia were isolated from HFD- and chow-fed control animals at six time points during 24 h [every 4 h starting 2 h after lights on, i.e., Zeitgeber Time 2 (ZT2)]. Gene expression was evaluated using quantitative RT-PCR. JTK_Cycle software was used to estimate daily rhythmicity. Statistical analysis was performed with two-way ANOVA test. Results: Consumption of the obesogenic diet resulted in a 40 g significantly higher body weight gain in week 8, compared to chow diet (p < 0.0001), associated with increased adiposity. We observed significant rhythmicity of circadian clock genes in microglia under chow conditions, which was partially lost in diet-induced obesity (DIO). Microglial immune gene expression also showed time-of-day differences, which were disrupted in HFD-fed animals. Microglia responded to the obesogenic conditions by a shift of substrate utilization with decreased glutamate and glucose metabolism in the active period of the animals, and an overall increase of lipid metabolism, as indicated by gene expression evaluation. Additionally, data on mitochondria bioenergetics and dynamics suggested an increased energy production in microglia during the inactive period on HFD. Finally, evaluation of monocyte functional gene expression showed small or absent effect of HFD on peripheral myeloid cells, suggesting a cell-specific microglial inflammatory response in DIO. Conclusions: An obesogenic diet affects microglial immunometabolism in a time-of-day dependent manner. Given the central role of the brain in energy metabolism, a better knowledge of daily rhythms in microglial immunometabolism could lead to a better understanding of the pathogenesis of obesity." @default.
- W2952023666 created "2019-06-27" @default.
- W2952023666 creator A5018565033 @default.
- W2952023666 creator A5022312007 @default.
- W2952023666 creator A5047611105 @default.
- W2952023666 creator A5050937491 @default.
- W2952023666 creator A5052298563 @default.
- W2952023666 creator A5067946092 @default.
- W2952023666 creator A5073880325 @default.
- W2952023666 creator A5079692848 @default.
- W2952023666 creator A5082108008 @default.
- W2952023666 creator A5082396860 @default.
- W2952023666 creator A5083304448 @default.
- W2952023666 creator A5090831614 @default.
- W2952023666 date "2019-06-26" @default.
- W2952023666 modified "2023-10-15" @default.
- W2952023666 title "Diet-Induced Obesity Disturbs Microglial Immunometabolism in a Time-of-Day Manner" @default.
- W2952023666 cites W1511961767 @default.
- W2952023666 cites W1544249031 @default.
- W2952023666 cites W1558985734 @default.
- W2952023666 cites W1768846296 @default.
- W2952023666 cites W1828418245 @default.
- W2952023666 cites W1894005404 @default.
- W2952023666 cites W1964562779 @default.
- W2952023666 cites W1967727674 @default.
- W2952023666 cites W1968994158 @default.
- W2952023666 cites W1971656447 @default.
- W2952023666 cites W1972454538 @default.
- W2952023666 cites W1973646302 @default.
- W2952023666 cites W1974191118 @default.
- W2952023666 cites W1982024216 @default.
- W2952023666 cites W1990356805 @default.
- W2952023666 cites W1990757970 @default.
- W2952023666 cites W1996003588 @default.
- W2952023666 cites W1997151200 @default.
- W2952023666 cites W2002353628 @default.
- W2952023666 cites W2025131475 @default.
- W2952023666 cites W2044615101 @default.
- W2952023666 cites W2054717478 @default.
- W2952023666 cites W2056395995 @default.
- W2952023666 cites W2067875627 @default.
- W2952023666 cites W2075792687 @default.
- W2952023666 cites W2075957423 @default.
- W2952023666 cites W2077033935 @default.
- W2952023666 cites W2085667287 @default.
- W2952023666 cites W2086961401 @default.
- W2952023666 cites W2095000147 @default.
- W2952023666 cites W2097722989 @default.
- W2952023666 cites W2098360522 @default.
- W2952023666 cites W2104520325 @default.
- W2952023666 cites W2113328569 @default.
- W2952023666 cites W2114167392 @default.
- W2952023666 cites W2126068729 @default.
- W2952023666 cites W2127700127 @default.
- W2952023666 cites W2129917395 @default.
- W2952023666 cites W2136024338 @default.
- W2952023666 cites W2136735437 @default.
- W2952023666 cites W2144610554 @default.
- W2952023666 cites W2154696002 @default.
- W2952023666 cites W2161737261 @default.
- W2952023666 cites W2184434096 @default.
- W2952023666 cites W2184948420 @default.
- W2952023666 cites W2187903924 @default.
- W2952023666 cites W2261364877 @default.
- W2952023666 cites W2321657373 @default.
- W2952023666 cites W2336534940 @default.
- W2952023666 cites W2465638754 @default.
- W2952023666 cites W2468925656 @default.
- W2952023666 cites W2524985746 @default.
- W2952023666 cites W2535483532 @default.
- W2952023666 cites W2567503091 @default.
- W2952023666 cites W2610528971 @default.
- W2952023666 cites W2612276668 @default.
- W2952023666 cites W2616142271 @default.
- W2952023666 cites W2652575518 @default.
- W2952023666 cites W2735344772 @default.
- W2952023666 cites W2754166148 @default.
- W2952023666 cites W2756001698 @default.
- W2952023666 cites W2757631244 @default.
- W2952023666 cites W2763289233 @default.
- W2952023666 cites W2774325261 @default.
- W2952023666 cites W2784241489 @default.
- W2952023666 cites W2797493687 @default.
- W2952023666 cites W2890187093 @default.
- W2952023666 cites W2891506141 @default.
- W2952023666 cites W39356949 @default.
- W2952023666 cites W4238497443 @default.
- W2952023666 cites W4295101592 @default.
- W2952023666 doi "https://doi.org/10.3389/fendo.2019.00424" @default.
- W2952023666 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/6611391" @default.
- W2952023666 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/31316470" @default.
- W2952023666 hasPublicationYear "2019" @default.
- W2952023666 type Work @default.
- W2952023666 sameAs 2952023666 @default.
- W2952023666 citedByCount "31" @default.
- W2952023666 countsByYear W29520236662019 @default.
- W2952023666 countsByYear W29520236662020 @default.
- W2952023666 countsByYear W29520236662021 @default.
- W2952023666 countsByYear W29520236662022 @default.
- W2952023666 countsByYear W29520236662023 @default.