Physiological effects of an herbal extract mixture containing Acanthopanax senticosus Harms on the development, reproduction, and lipid metabolism of Caenorhabditis elegans

2011 ◽  
Vol 2 (4) ◽  
pp. 173
Author(s):  
Kazuichi Sakamoto ◽  
Hiroyuki Hano
Aging Cell ◽  
2020 ◽  
Vol 19 (6) ◽  
Author(s):  
Anubhuti Dixit ◽  
Anjali Sandhu ◽  
Souvik Modi ◽  
Meghana Shashikanth ◽  
Sandhya P. Koushika ◽  
...  

2020 ◽  
Vol 4 (Supplement_2) ◽  
pp. 38-38
Author(s):  
Jang Miran ◽  
Zhang Yuan ◽  
Bai Juan ◽  
Jun-Bae An ◽  
Park Yeonhwa ◽  
...  

Abstract Objectives Lipolysis is the catabolic process that hydrolyzes triglyceride (TG) to free fatty acids (FFAs) and glycerol under negative energy balance such as fasting. In adipocytes, adipose TG lipase (ATGL), hormone-sensitive lipase (HSL), and monoglyceride lipase play key roles in a series of TG hydrolysis reactions in mammals. However, overly activated adipose lipolysis is believed to contribute to link between obesity and systemic inflammation and oxidative stress. We previously demonstrated that piceatannol (PIC), a natural resveratrol analogue, inhibits adipogenesis in cultured adipocytes and lipogenesis in Caenorhabditis elegans. Furthermore, we showed that PIC extends the lifespan of C. elegans via the insulin/IGF-1 signaling. However, the effects of PIC on lipid metabolism during fasting state is unknown. Methods We conducted Oil-Red-O assay, Enzyme assay (TG and Free glycerol contents), PCR analysis and lifespan assay. Results In this study, we demonstrated that PIC-treated C. elegans exhibited suppressed lipolysis under fasting as judged by increased lipid accumulation and TG levels with decreased free glycerol level. Consistent with these findings, PIC treatment resulted in decreased mRNA levels of genes involved lipolysis such as atgl-1, hosl-1 and aak-2 in fasted C. elegans. Also, PIC treatment augmented fasting-induced lifespan of C. elegans by an increased daf-16 gene expression. However, such effect was abolished when atgl-1, aak-2, and daf-16 mutants were treated with PIC. In addition, we also found that autophagy is required for PIC-induced lifespan in C. elegans during fasting since autophagy inhibitor treatments and autophagy gene deficient worms resulted in blunting the lifespan extension effect of PIC. Conclusions Collectively, our results indicate that PIC contributes to lifespan extension in C. elegans during fasting possibly through regulating lipolysis- and/or autophagy-dependent lipid metabolism. Funding Sources 1. The National Research Foundation of Korea (NRF) grant funded by the Korea government (MSIP) (2019R1A2C1086146) and (2019R1A6A3A03033878) 2. The Rural Development Administration of the Republic of Korea.


2015 ◽  
Vol 211 (2) ◽  
pp. 261-271 ◽  
Author(s):  
Vineet Choudhary ◽  
Namrata Ojha ◽  
Andy Golden ◽  
William A. Prinz

Lipid droplets (LDs) are found in all cells and play critical roles in lipid metabolism. De novo LD biogenesis occurs in the endoplasmic reticulum (ER) but is not well understood. We imaged early stages of LD biogenesis using electron microscopy and found that nascent LDs form lens-like structures that are in the ER membrane, raising the question of how these nascent LDs bud from the ER as they grow. We found that a conserved family of proteins, fat storage-inducing transmembrane (FIT) proteins, is required for proper budding of LDs from the ER. Elimination or reduction of FIT proteins in yeast and higher eukaryotes causes LDs to remain in the ER membrane. Deletion of the single FIT protein in Caenorhabditis elegans is lethal, suggesting that LD budding is an essential process in this organism. Our findings indicated that FIT proteins are necessary to promote budding of nascent LDs from the ER.


2021 ◽  
Vol 339 ◽  
pp. 127813
Author(s):  
Xiang Xiao ◽  
Xiaowei Zhang ◽  
Juan Bai ◽  
Jie Li ◽  
Caiqin Zhang ◽  
...  

PLoS Genetics ◽  
2017 ◽  
Vol 13 (5) ◽  
pp. e1006806 ◽  
Author(s):  
Rosalind Hussey ◽  
Jon Stieglitz ◽  
Jaleh Mesgarzadeh ◽  
Tiffany T. Locke ◽  
Ying K. Zhang ◽  
...  

2018 ◽  
Vol 8 (1) ◽  
Author(s):  
Emelyne Teo ◽  
Krishna Chaithanya Batchu ◽  
Diogo Barardo ◽  
Linfan Xiao ◽  
Amaury Cazenave-Gassiot ◽  
...  

2019 ◽  
Vol 3 (Supplement_1) ◽  
Author(s):  
Renalison Farias-Pereira ◽  
Yeonhwa Park

Abstract Objectives Cafestol, a diterpene found in coffee beans, is reported to be an agonist of farnesoid X receptors (FXR), nuclear hormone receptors involved in cholesterol homeostasis. It is also known that FXR plays critical roles in other metabolic pathways, including lipid metabolism; however, little is known about cafestol's effects on lipid metabolism. The goal of the current study was to investigate the effects of cafestol on lipid metabolism using Caenorhabditis elegans as a model system. Methods C. elegans was treated for 2 days with cafestol or 0.2% dimethyl sulfoxide (vehicle control). Triglycerides, locomotor behavior (an indicator of energy expenditure) and lipid metabolism-related gene expressions were measured. Results Cafestol at 60 µM significantly reduced fat accumulation by 20% compared to the control. Cafestol increased locomotor activity by 38% compared to the control. The effects of cafestol on fat accumulation were dependent on daf-12 (a functional homolog of the human FXR) and further confirmed by the upregulation of a DAF-12-target gene, fard-1 (the homolog of the human fatty acid reductase 1). Cafestol's fat-lowering effects were also dependent on tub-1 (an ortholog of the human TUBBY), which is involved in the neurological regulation of energy expenditure. Cafestol upregulated the expression of ech-1.1, involved in fatty acid β-oxidation; however, no effects of cafestol were observed on lipogenesis, lipolysis or lipid uptake and transport. Conclusions In conclusion, cafestol regulates lipid metabolism in C. elegans by increasing fatty acid β-oxidation and energy expenditure dependent on daf-12/FXR. Funding Sources Brazilian National Counsel of Technological and Scientific Development (CNPq).


FEBS Journal ◽  
2009 ◽  
Vol 276 (18) ◽  
pp. 5030-5040 ◽  
Author(s):  
Elise Petit ◽  
Xavier Michelet ◽  
Claudine Rauch ◽  
Justine Bertrand-Michel ◽  
François Tercé ◽  
...  

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